Academic literature on the topic 'GITC'

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Journal articles on the topic "GITC":

1

Nocero, M., T. Isshiki, M. Yamamoto, and C. S. Hoffman. "Glucose repression of fbp1 transcription of Schizosaccharomyces pombe is partially regulated by adenylate cyclase activation by a G protein alpha subunit encoded by gpa2 (git8)." Genetics 138, no. 1 (September 1, 1994): 39–45. http://dx.doi.org/10.1093/genetics/138.1.39.

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Abstract In the fission yeast Schizosaccharomyces pombe, genetic studies have identified genes that are required for glucose repression of fbp1 transcription. The git2 gene, also known as cyr1, encodes adenylate cyclase. Adenylate cyclase converts ATP into the second messenger cAMP as part of many eukaryotic signal transduction pathways. The git1, git3, git5, git7, git8 and git10 genes act upstream of adenylate cyclase, presumably encoding an adenylate cyclase activation pathway. In mammalian cells, adenylate cyclase enzymatic activity is regulated by heterotrimeric guanine nucleotide-binding proteins (G proteins). In the budding yeast Saccharomyces cerevisiae, adenylate cyclase enzymatic activity is regulated by monomeric, guanine nucleotide-binding Ras proteins. We show here that git8 is identical to the gpa2 gene that encodes a protein homologous to the alpha subunit of a G protein. Mutations in two additional genes, git3 and git5 are suppressed by gpa2+ in high copy number. Furthermore, a mutation in either git3 or git5 has an additive effect in strains deleted for gpa2 (git8), as it significantly increases expression of an fbp1-lacZ reporter gene. Therefore, git3 and git5 appear to act either in concert with or independently from gpa2 (git8) to regulate adenylate cyclase activity.
2

Welton, Robert M., and Charles S. Hoffman. "Glucose Monitoring in Fission Yeast via the gpa2 Gα, the git5 Gβ and the git3 Putative Glucose Receptor." Genetics 156, no. 2 (October 1, 2000): 513–21. http://dx.doi.org/10.1093/genetics/156.2.513.

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Abstract The fission yeast Schizosaccharomyces pombe responds to environmental glucose by activating adenylate cyclase. The resulting cAMP signal activates protein kinase A (PKA). PKA inhibits glucose starvation-induced processes, such as conjugation and meiosis, and the transcription of the fbp1 gene that encodes the gluconeogenic enzyme fructose-1,6-bisphosphatase. We previously identified a collection of git genes required for glucose repression of fbp1 transcription, including pka1/git6, encoding the PKA catalytic subunit, git2/cyr1, encoding adenylate cyclase, and six “upstream” genes required for adenylate cyclase activation. The git8 gene, identical to gpa2, encodes the alpha subunit of a heterotrimeric guanine-nucleotide binding protein (Gα) while git5 encodes a Gβ subunit. Multicopy suppression studies with gpa2+ previously indicated that S. pombe adenylate cyclase activation may resemble that of the mammalian type II enzyme with sequential activation by Gα followed by βγ. We show here that an activated allele of gpa2 (gpa2R176H, carrying a mutation in the coding region for the GTPase domain) fully suppresses mutations in git3 and git5, leading to a refinement in our model. We describe the cloning of git3 and show that it encodes a putative seven-transmembrane G protein-coupled receptor. A git3 deletion confers the same phenotypes as deletions of other components of the PKA pathway, including a germination delay, constitutive fbp1 transcription, and starvation-independent conjugation. Since the git3 deletion is fully suppressed by the gpa2R176H allele with respect to fbp1 transcription, git3 appears to encode a G protein-coupled glucose receptor responsible for adenylate cyclase activation in S. pombe.
3

Hoffman, C. S. "Glucose sensing via the protein kinase A pathway in Schizosaccharomyces pombe." Biochemical Society Transactions 33, no. 1 (February 1, 2005): 257–60. http://dx.doi.org/10.1042/bst0330257.

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The fission yeast Schizosaccharomyces pombe primarily detects glucose via a cAMP-signalling pathway. Components of this pathway include the Git3 G-protein-coupled receptor and a heterotrimeric G-protein, from which the Gpa2 Gα subunit activates adenylate cyclase (Git2/Cyr1). Three additional proteins, Git1, Git7 and Git10 are required to generate a cAMP response even in a strain expressing an activated form of Gpa2, which is capable of bypassing the loss of the GPCR and Gβγ dimer. Therefore, Git1, Git7 and Git10 either act in a G-protein-independent manner or are required to stabilize or assemble a functional signalling complex. Although prior data suggested that the Cgs2 cAMP phosphodiesterase (PDE) does not regulate the cAMP response, we now have evidence that along with adenylate cyclase regulation, PDE activation is important for limiting the response to glucose. Finally, regulation of protein kinase A activation appears to involve both traditional post-translational regulation of the function of the components of the cAMP pathway and glucose-dependent transcriptional regulation of some of these cAMP pathway genes.
4

Gilleland, Rebecca C., and Richard D. Hockett. "Stability of RNA Molecules Stored in GITC." BioTechniques 25, no. 6 (December 1998): 944–48. http://dx.doi.org/10.2144/98256bm03.

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Anike, US, I. A. Nwannadi, I. Okpala, and AJ Madu. "The Role of Micro-RNA 466i on Vaso-Occlusive Complications of Sickle Cell Anaemia." Journal of BioMedical Research and Clinical Practice 2, no. 2 (July 6, 2019): 144–49. http://dx.doi.org/10.46912/2i2.2019111.

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Vaso-occlusion in sickle cell anaemia (SCA) is mediated via increased expression of adhesion molecules. Micro-RNA 466i up regulates the expression of interleukin-10 and may contribute to the pathogenesis of the complications in SCA. We sought to investigate the relationship between changes in the level of micro-RNA 466i and the frequency of vaso-occlusive complications in SCA patients. Red blood cells were lysed using ammonium chloride. The resulting white blood cell pellets were lysed in guanidiumisothiocyanate (GITC) lyses buffer. From the GITC lysate, total RNA was extracted. Thereafter, the amount of micro-RNA 466i was quantified. There were no relationships between microRNA 466i and the frequency of complications in SCA patients. (p=0.066) There was also no significant difference in the levels of micro-RNA 466i between patients who had vaso-occlusive complications and those that did not.(p=0.9307) Micro-RNA 466i increased with age (p=0.03) but there was no significant difference between the males and the females patients.(p= 0.370) Micro-RNA 466i (a pro-inflammatory nucleotide) play little or no role in the pathogenesis of vaso-occlusive complications in SCA. Its assay in this group of patients may is not useful in the overall management of these patients.
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Anike, US, I. A. Nwannadi, I. Okpala, and AJ Madu. "The Role of Micro-RNA 466i on Vaso-Occlusive Complications of Sickle Cell Anaemia." Journal of BioMedical Research and Clinical Practice 2, no. 2 (July 6, 2019): 144–49. http://dx.doi.org/10.46912/jbrcp.111.

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Vaso-occlusion in sickle cell anaemia (SCA) is mediated via increased expression of adhesion molecules. Micro-RNA 466i up regulates the expression of interleukin-10 and may contribute to the pathogenesis of the complications in SCA. We sought to investigate the relationship between changes in the level of micro-RNA 466i and the frequency of vaso-occlusive complications in SCA patients. Red blood cells were lysed using ammonium chloride. The resulting white blood cell pellets were lysed in guanidiumisothiocyanate (GITC) lyses buffer. From the GITC lysate, total RNA was extracted. Thereafter, the amount of micro-RNA 466i was quantified. There were no relationships between microRNA 466i and the frequency of complications in SCA patients. (p=0.066) There was also no significant difference in the levels of micro-RNA 466i between patients who had vaso-occlusive complications and those that did not.(p=0.9307) Micro-RNA 466i increased with age (p=0.03) but there was no significant difference between the males and the females patients.(p= 0.370) Micro-RNA 466i (a pro-inflammatory nucleotide) play little or no role in the pathogenesis of vaso-occlusive complications in SCA. Its assay in this group of patients may is not useful in the overall management of these patients.
7

Anike, US, I. A. Nwannadi, I. Okpala, and AJ Madu. "The Role of Micro-RNA 466i on Vaso-Occlusive Complications of Sickle Cell Anaemia." Journal of BioMedical Research and Clinical Practice 2, no. 2 (July 6, 2019): 144–49. http://dx.doi.org/10.46912/jbrcp.v2.i2.2019.111.

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Vaso-occlusion in sickle cell anaemia (SCA) is mediated via increased expression of adhesion molecules. Micro-RNA 466i up regulates the expression of interleukin-10 and may contribute to the pathogenesis of the complications in SCA. We sought to investigate the relationship between changes in the level of micro-RNA 466i and the frequency of vaso-occlusive complications in SCA patients. Red blood cells were lysed using ammonium chloride. The resulting white blood cell pellets were lysed in guanidiumisothiocyanate (GITC) lyses buffer. From the GITC lysate, total RNA was extracted. Thereafter, the amount of micro-RNA 466i was quantified. There were no relationships between microRNA 466i and the frequency of complications in SCA patients. (p=0.066) There was also no significant difference in the levels of micro-RNA 466i between patients who had vaso-occlusive complications and those that did not.(p=0.9307) Micro-RNA 466i increased with age (p=0.03) but there was no significant difference between the males and the females patients.(p= 0.370) Micro-RNA 466i (a pro-inflammatory nucleotide) play little or no role in the pathogenesis of vaso-occlusive complications in SCA. Its assay in this group of patients may is not useful in the overall management of these patients.
8

Schadick, Kevin, H. Matthew Fourcade, Peter Boumenot, Jeffrey J. Seitz, Jennifer L. Morrell, Louise Chang, Kathleen L. Gould, et al. "Schizosaccharomyces pombe Git7p, a Member of the Saccharomyces cerevisiae Sgt1p Family, Is Required for Glucose and Cyclic AMP Signaling, Cell Wall Integrity, and Septation." Eukaryotic Cell 1, no. 4 (August 2002): 558–67. http://dx.doi.org/10.1128/ec.1.4.558-567.2002.

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ABSTRACT The Schizosaccharomyces pombe fbp1 gene, encoding fructose-1,6-bisphosphatase, is transcriptionally repressed by glucose. Mutations that confer constitutive fbp1 transcription identify git (glucose-insensitive transcription) genes that encode components of a cyclic AMP (cAMP) signaling pathway required for adenylate cyclase activation. Four of these genes encode the three subunits of a heterotrimeric G protein (gpa2, git5, and git11) and a G protein-coupled receptor (git3). Three additional genes, git1, git7, and git10, act in parallel to or downstream from the G protein genes. Here, we describe the cloning and characterization of the git7 gene. The Git7p protein is a member of the Saccharomyces cerevisiae Sgt1p protein family. In budding yeast, Sgt1p associates with Skp1p and plays an essential role in kinetochore assembly, while in Arabidopsis, a pair of SGT1 proteins have been found to be involved in plant disease resistance through an interaction with RAR1. Like S. cerevisiae Sgt1p, Git7p is essential, but this requirement appears to be due to roles in septation and cell wall integrity, which are unrelated to cAMP signaling, as S. pombe cells lacking either adenylate cyclase or protein kinase A are viable. In addition, git7 mutants are sensitive to the microtubule-destabilizing drug benomyl, although they do not display a chromosome stability defect. Two alleles of git7 that are functional for cell growth and septation but defective for glucose-triggered cAMP signaling encode proteins that are altered in the highly conserved carboxy terminus. The S. cerevisiae and human SGT1 genes both suppress git7-93 but not git7-235 for glucose repression of fbp1 transcription and benomyl sensitivity. This allele-specific suppression indicates that the Git7p/Sgt1p proteins may act as multimers, such that Git7-93p but not Git7-235p can deliver the orthologous proteins to species-specific targets. Our studies suggest that members of the Git7p/Sgt1p protein family may play a conserved role in the regulation of adenylate cyclase activation in S. pombe, S. cerevisiae, and humans.
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Schmalzigaug, Robert, Hyewon Phee, Collin E. Davidson, Arthur Weiss, and Richard T. Premont. "Differential Expression of the ARF GAP Genes GIT1 and GIT2 in Mouse Tissues." Journal of Histochemistry & Cytochemistry 55, no. 10 (October 2007): 1039–48. http://dx.doi.org/10.1369/jhc.7a7207.2007.

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GIT1 and GIT2 belong to the family of ADP-ribosylation factor GTPase-activating proteins (ARF-GAP) and have been implicated in the regulation of G protein-coupled receptor sequestration, cell migration, T-cell activation, neuronal spine formation, and aggregate formation in Huntington's disease. Examination of endogenous GIT protein expression in tissues, however, has been hampered by the lack of GIT2-specific antibodies. To visualize GIT1 and GIT2 gene expression in mouse tissues, we created mice with β-galactosidase (β-Gal) reporters inserted into the two GIT genes. β-Gal staining confirmed the broad tissue distribution of GIT1 and GIT2 in the mouse but also revealed striking differences. GIT2 is expressed in most cells of the body, whereas GIT1 is restricted to only a subset of cells. For example, GIT2 is uniformly expressed throughout lung and liver, whereas GIT1 is restricted to cells lining blood vessels, bronchi, and bile ducts. Expression of GIT1 and GIT2 is mutually exclusive in the testes, where a developmental expression shift occurs, with GIT2 present in spermatogonia but GIT1 in mature spermatids. In conclusion, analysis of endogenous GIT expression revealed a nearly ubiquitous distribution of GIT2, whereas GIT1 is restricted to specific cell types even in tissues with apparently high GIT1 expression and is entirely absent from some tissues. (J Histochem Cytochem 55: 1039–1048, 2007)
10

Hartono, Indra K., Novan Zulkarnain, and Rudy Tjahyadi. "Prototype of Dashboard Business Intelligent for Employees Training Effectiveness." Advanced Science Letters 21, no. 4 (April 1, 2015): 661–66. http://dx.doi.org/10.1166/asl.2015.5931.

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Employees training in a company is considered as expenditure rather than as a long-term investment by company. The company needs to monitor the training of employees in order to take advantage of the training results by using Business Intelligent (BI). The object of research conducted at Garuda Indonesia Training Center (GITC). Methods of the research is a quantitative, analyze correlation and regression and the variables need to be examine in this research, are as follows: Nature of Training, Management Involvement, Management Motivation, Training Outcome and Firm Performance. Based on this research findings, the hypothesis can be accepted or rejected and hence, a better of prototype of Dashboard Business Intelligent can be well designed and make Employees Training more effective.

Dissertations / Theses on the topic "GITC":

1

Khalid, Fahad. "Magnetic Resonance Imaging and Genomic Mutation in Diffuse Intrinsic Pontine Glioma : Machine Learning Approaches for a Comprehensive Analysis." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPAST006.

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Le diagnostic du gliome infiltrant du tronc cérébral (GITC) chez les enfants est l'un des plus éprouvants en oncologie pédiatrique. Malgré de nombreux essais cliniques explorant divers traitements, le pronostic reste sombre, la plupart des patients succombant entre 9 et 11 mois après le diagnostic. Les mutations génétiques clé associées au GITC incluent H3K27M, ACVR1 et TP53. Chaque mutation a des caractéristiques distinctes, poussant les médecins à suggérer des thérapies personnalisées, soulignant l'importance d'une détection précise des mutations pour guider le traitement. Situées dans la région cruciale du tronc cérébral, les tumeurs GITC présentent des risques significatifs liés à la biopsie en raison de potentiels dommages neurologiques. L'IRM est une méthode indispensable pour le diagnostic de ces tumeurs, évaluant leur extension et permettant de mesurer l'évolution de la maladie au cours de la thérapie. Une prédiction des mutations, combinée à l'identification des patients survivant plus de deux ans, pourrait améliorer la thérapie proposée à ces patients. Dans ce contexte, la radiomique transforme les images en vastes sources de données, extrayant des caractéristiques comme la forme et la texture pour aider à la prise de décision. L'objectif de cette thèse est de prédire les principales mutations génétiques et d'identifier les survivants à long terme, en mettant l'accent sur la normalisation des images et l'applicabilité des modèles radiomiques. Notre étude a utilisé une base de données rétrospective de l'Institut Gustave Roussy, comprenant les données IRM de 80 patients et leurs données cliniques respectives. Les données d'IRM ont mis en évidence des problèmes pour les études radiomiques, tels que l'inhomogénéité du champ de biais et l'effet "scanner". Pour répondre à ces défis, un pipeline de normalisation d'images IRM a été mis en place, et les caractéristiques radiomiques ont été harmonisées par la méthode ComBat. Pour faire face au problème de modalités manquantes dans l'ensemble de données, une stratégie multi-modèles a été employée, conduisant à 16 modèles distincts reposant sur diverses combinaisons de caractéristiques radiomiques et cliniques. Cette approche a ensuite été rationalisée en une méthode multimodale, réduisant le nombre de modèles à cinq, après une phase de sélection de caractéristiques indépendantes. Les résultats de l'approche multimodale se sont avérés être prometteurs. Cette stratégie multimodale a été essentielle pour identifier les patients survivant plus de deux ans et a été complétée par l'approche ICARE pour une analyse de survie détaillée
The diagnosis of diffuse intrinsic pontine glioma (DIPG) in children stands as one of the most harrowing within pediatric oncology. Despite numerous clinical trials exploring various treatments, the prognosis remains bleak, with most patients succumbing between 9 to 11 months post-diagnosis. Key gene mutations linked to DIPG include H3K27M, ACVR1, and TP53. Each mutation has distinct characteristics, leading physicians to suggest tailored therapies, underscoring the importance of accurate mutation detection in guiding treatment. Located in the crucial region of the brainstem, the pons, DIPG tumors pose significant biopsy risks due to potential neurological damage. Hence, MRI could become a primordial diagnostic tool for these tumors, assessing their spread and gauging therapy responses. Its use to predict accurate gene mutation, and identify long-term survivors, could enhance patient care significantly. Within this framework, radiomics transforms images into vast data sources, extracting features like shape and texture to aid decision-making. The objective of this thesis is to refine mutation prediction and pinpoint long-term survivors, emphasizing image normalization and the applicability of radiomic models. Our study utilized a retrospective database from Gustave Roussy Institute, encompassing 80 patients MRI data and their respective clinical data. These MRI images highlighted issues in radiomic studies, such as bias field inhomogeneity and the "scanner effect". To address these challenges, a dedicated MR image normalization pipeline was implemented, and radiomic features underwent ComBat harmonization. Given the dataset's missing modalities, a multi-model strategy was employed, leading to 16 distinct models based on various radiomic and clinical feature combinations. This approach was then streamlined into a multi-modal method, reducing the number of models to five. The results from the ensemble of these models proved to be the most promising. This multi-modal strategy incorporated a feature selection phase, pinpointing the most pertinent features. Additionally, this method was applied to identify long-term survivors and was complemented by the ICARE framework for a nuanced survival analysis output
2

Turci, Rubens Younger Paul. "Sraddha in the Bhagavad Gita." *McMaster only, 2007.

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3

Nautiyal, Jaishikha. "Rhetorical Agency in the Bhagavad Gita." Thesis, North Dakota State University, 2013. https://hdl.handle.net/10365/27021.

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This M.A. thesis presents a rhetorical analysis of the Indian philosophical and religious text, The Bhagavad Gita. Utilizing Kenneth Burke's Pentad of act, scene, agent, agency and purpose as a primary interpretive lens for uncovering universal human motivations, this rhetorical critique conceptualizes the idea of rhetorical agency as a model for action in the Gita's dialogical progression between Krishna and Arjuna. Rhetorical agency in the Gita differs from a traditional understanding of agency in that the former amalgamates competing yet co-existing pragmatic and consummatory agencies that Arjuna may utilize to act in the here and now but also relinquish the control on the fruits of his act, to ultimately transcend all human action by breaking the cycle of birth and death. In that sense, by virtue of rhetorical agency, the Gita may be considered in Burke's words Equipment for Living, because it provides a template for life across the universe.
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Cataldo, Yáñez Cristóbal, and Pineda Ronald Mella. "Plan de negocio E-GIT." Tesis, Universidad de Chile, 2016. http://repositorio.uchile.cl/handle/2250/138602.

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Tesis para optar al grado de Magíster en Administración
Cataldo Yañez, Cristobál [Parte I], Mella Pineda, Ronald [Parte II]
Hoy en día existe un número importante de industrias que tienen establecimientos y/o sucursales de atención presencial a lo largo de todo Chile para sus clientes y usuarios. Muchos de ellos, poseen una alta demanda de servicios que se traduce en un gran volumen de usuarios que requieren ser atendidos. El mercado ante esta demanda, ha implementado sistemas de atención con el fin de dar un orden y secuencia. Muchos de los sistemas implementados son de carácter presencial y consideran un rollo de papel enumerado y un display que muestra el número actual de atención, esto obliga al usuario a encontrarse presencialmente esperando que sea su turno, sin poder utilizar su tiempo para lo que estime mejor. En base a este contexto, se ha detectado una oportunidad de negocio que da origen a e-GIT que nace cómo una solución al problema de optimización en el uso del tiempo que tienen las atareadas personas actualmente en Chile. Con el sistema de gestión inteligente de ticket de atención diseñado por e-GIT, el usuario puede solicitar su número virtualmente, puede mantenerse informado, ver el avance de la fila y en qué número de atención se encuentra, sin tener que estar en forma presencial, con lo cual puede manejar de mejor manera su valioso tiempo, adicionalmente el usuario se puede mantener en distintas filas, las cuales puede seguir desde una misma aplicación. Y la incorporación de alertas simplifica la experiencia del cliente, ya que es avisado del tiempo restante para su atención según la configuración que el usuario haya ingresado. Desde el punto de vista de la empresa se facilita el uso de sus espacios, reduce la cantidad de clientes que no aparecen, se reduce el tiempo de espera percibido por el cliente, lo que se traduce en una mejor percepción del servicio. La aplicación de gestión para la empresa provee gran cantidad de estadísticas fácil de obtener en función de la data generada, por ejemplo, tiempo de espera promedio, número de clientes atendidos, número de clientes que desertan, atenciones por empleado, sucursal con mayor número de atenciones, y mucho más.
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ROVEDA, GIANLUCA. "Mining Git based Software Repositories." Doctoral thesis, Università degli studi di Pavia, 2018. http://hdl.handle.net/11571/1214877.

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The proposed thesis analyzes on the methods of analyzing Git-based software repositories, and focuses on mining GitHub based repositories. The introduction includes a summary of VCS history and usage, with many details that cover the interactions between users, Git and GitHub. The “related works” chapter presents the methods used by other researchers to mine Git data. Four different datasets are used in this thesis: the historical MSR14, and other three ad-hoc collected datasets. The datasets are analyzed and compared, both for a deeper understanding of the data and to validate the three “new” datasets with the already researched MSR14. Interesting findings are presented, and include considerations on the identification of a commit author. The main objective of the thesis is to present a graphic approach to analyze the interactions between different repositories through users. The results are shown to the researcher as an animated network graph through Gephi. Many examples are shown to investigate on the approach performances and capabilities, and are compared to expert knowledge on the repositories.
The proposed thesis analyzes on the methods of analyzing Git-based software repositories, and focuses on mining GitHub based repositories. The introduction includes a summary of VCS history and usage, with many details that cover the interactions between users, Git and GitHub. The “related works” chapter presents the methods used by other researchers to mine Git data. Four different datasets are used in this thesis: the historical MSR14, and other three ad-hoc collected datasets. The datasets are analyzed and compared, both for a deeper understanding of the data and to validate the three “new” datasets with the already researched MSR14. Interesting findings are presented, and include considerations on the identification of a commit author. The main objective of the thesis is to present a graphic approach to analyze the interactions between different repositories through users. The results are shown to the researcher as an animated network graph through Gephi. Many examples are shown to investigate on the approach performances and capabilities, and are compared to expert knowledge on the repositories.
6

Moreira, Juliana Baptista. "Aspectos das alterações climáticas nas estratégias europeias de GIZC." Master's thesis, Universidade de Aveiro, 2010. http://hdl.handle.net/10773/679.

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Mestrado em Engenharia do Ambiente
Portugal possui uma enorme e vulnerável faixa costeira. Estas zonas têm vindo a ser afectadas por actividade humanas exercendo uma forte pressão sobre o meio marinho. As zonas costeiras estão também associadas a actividades socioeconómicas significativas, tornando-se desta forma zonas bastante sensíveis. Surge assim, como pressão adicional a estas zonas, as alterações climáticas. Estas estão ligadas à subida do nível do mar, a alterações da frequência e/ou da intensidade das tempestades e furacões associados às consequentes cheias. Os impactes das alterações climáticas nas zonas costeiras serão assim provavelmente agravados pelo facto de nestas se localizarem as principais áreas metropolitanas do país. Assim o potencial para afectar um número elevado de pessoas é, nesta faixa, particularmente alto, tornando-se também um risco acrescido para os ecossistemas, e para a saúde humana. Com a realização deste trabalho, pretende-se, verificar as medidas de adaptação existentes na estratégia de gestão integrada portuguesa, no âmbito das alterações climáticas, efectuando uma comparação entre as medidas existentes em algumas das estratégias existentes no espaço Europeu e propondo algumas medidas a aplicar na estratégia existente em Portugal. ABSTRACT: Portugal posses a huge and vulnerable coastline that has been affected by human activities, putting its sea life to a high stress. The coastal areas are also associated with significant socio-economic activities, thus making them very sensitive areas. Therefore and as an additional problem comes the climate changes.These are combined with the rising sea levels, changes in frequency and/or intensity of storms and hurricanes associated with the resulting flood. Thus, the impacts of climate change on coastal areas will be, probably, aggravated by the fact that these areas are located in the major metropolitan areas of the country. As a result, the probability to affect a large number of people is particularly high, making it also increase the risk for ecosystems as for human health. The purpose of this thesis is to verify the adaptation measures, relative to the climate changes, within IZCM’s strategy. This is achieved by making a comparison between the existing measures in Portugal and in other European zones, and also, proposing some measures to implement to the current national strategy.
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Leaney, Sarah J. "GIT : glycosylation 'via' inter/intramolecular transfer." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.409812.

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Perez, De Rosso Santiago (Santiago Nicolas). "A conceptual design analysis of Git." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/97817.

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Thesis: S.M., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2015.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 75-77).
It is commonly asserted that the success of a software development project, and the usability of the final product, depend on the quality of the concepts that underlie its design. Yet this hypothesis has not been systematically explored by researchers, and conceptual design has not played the central role in the research and teaching of software engineering that one might expect. As part of a new research project to explore conceptual design, we are engaging in a series of case studies. This thesis reports on our case study on Git, a popular-yet sometimes puzzling-version control system. In an attempt to understand the root causes of its complexity, we analyze its conceptual model and identify some undesirable properties; we then present a reworking of the conceptual model that forms the basis of Gitless, our redesign of Git.
by Santiago Perez De Rosso.
S.M.
9

Hamadeh, Awni. "Learning Git Through Serious Educational Game." Thesis, Malmö universitet, Fakulteten för teknik och samhälle (TS), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-20823.

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Git is a distributed version control system that tracks changes to a project overtime and is used to save these changes. Today it is being used by millions of people and is becoming a demand on the job market. For this reason it has become important to learn the version control system. Learning Git however may be difficult for beginners and learning it through tutorials may not always be effective. Learning it through a serious educational game (SEG) may be more effective as a SEG can provide motivation and feedback which are two factors for successful learning. This study seeks to assess how effective a SEG is in teaching Git by looking at the amount of knowledge gained from playing a SEG. This study also seeks to assess how much participants learned Git using a tutorial compared to participants who used a serious educational game. From the results, the study found that the SEG expanded the understanding of Git. The study also found that there was no significant difference in the amount of understanding gained from the SEG and the tutorial.
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Guarnera, Drew T. "Merge Commit Contributions in Git Repositories." University of Akron / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=akron1436528894.

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Books on the topic "GITC":

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Gilmore, Rachna. Laydhadhkii Gita =: Lights for Gita. London: Mantra Publishing, 1994.

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Else, Chris. Gith. Auckland, N.Z: Vintage, 2008.

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Padmanabhacharya, C. M. A critical study of Bhagavad Geeta. Tiruchanur: Sriman Madhwa Siddhantonnahini Sabha, 2007.

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Mohandas. Gita: Letters on the Bhagavad Gita. Santa Barbara: Bandanna Books, 1989.

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Gilmore, Rachna. Gita için ş klar =: Lights for Gita. London: Mantra Publishing, 1994.

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Narasimhan, Iyer Raghavan, ed. The Bhagavad Gita, with the Uttara Gita. London: Concord Grove Press, 1985.

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Vinoda, Vinoda Candra Pāṇḍeya. Gita sataka. Lakhanaū: Sumitrā Sāhitya Sadana, 1992.

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Āsthā, (Organization :. Udaipur Rajasthan India). Gita gunjana. 4th ed. Udayapura: Astha Samsthana, 2011.

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Pai, Anant. The Gita. Bombay: H.G. Mirchandani for India Book House Education Trust, 1992.

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Maharaj, Ravishankar, and Shah Krishnavadan, eds. Gita bodhvani. Ahmedabad: R.M. Seva Trist, 1988.

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Book chapters on the topic "GITC":

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Katoh, Masaru. "GIPC." In Encyclopedia of Signaling Molecules, 2067–72. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101607.

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Katoh, Masaru. "GIPC." In Encyclopedia of Signaling Molecules, 1–6. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6438-9_101607-1.

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Halligan, Fredrica R. "Bhagavad Gita." In Encyclopedia of Psychology and Religion, 208–9. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-24348-7_70.

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Halligan, Fredrica R. "Bhagavad Gita." In Encyclopedia of Psychology and Religion, 165–67. Boston, MA: Springer US, 2014. http://dx.doi.org/10.1007/978-1-4614-6086-2_70.

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Popovsky, Mark, Benjamin Beit-Hallahmi, David A. Leeming, Fredrica R. Halligan, Jeffrey B. Pettis, Kalman J. Kaplan, Matthew B. Schwartz, et al. "Bhagavad Gita." In Encyclopedia of Psychology and Religion, 94–96. Boston, MA: Springer US, 2010. http://dx.doi.org/10.1007/978-0-387-71802-6_70.

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Gajda, Włodzimierz. "Hosting git Git Repositories." In Git Recipes, 279–325. Berkeley, CA: Apress, 2013. http://dx.doi.org/10.1007/978-1-4302-6104-9_11.

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Hagos, Ted. "Git." In Android Studio IDE Quick Reference, 95–115. Berkeley, CA: Apress, 2019. http://dx.doi.org/10.1007/978-1-4842-4953-6_9.

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Gamble, Adam, Cloves Carneiro, and Rida Al Barazi. "Git." In Beginning Rails 4, 281–83. Berkeley, CA: Apress, 2013. http://dx.doi.org/10.1007/978-1-4302-6035-6_15.

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Gamble, Adam, Cloves Carneiro, and Rida Al Barazi. "Git." In Beginning Rails 4, 285–96. Berkeley, CA: Apress, 2013. http://dx.doi.org/10.1007/978-1-4302-6035-6_16.

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Kaplan, Jacob. "Git." In A Criminologist's Guide to R, 107–26. Boca Raton: Chapman and Hall/CRC, 2022. http://dx.doi.org/10.1201/9781003279211-9.

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Conference papers on the topic "GITC":

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Rosenbloom, Arnold, Sadia Sharmin, and Andrew Wang. "GIT." In ITiCSE '17: Innovation and Technology in Computer Science Education. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3059009.3072980.

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Mandell, John F., Douglas S. Cairns, Daniel D. Samborsky, Robert B. Morehead, and Darrin H. Haugen. "Prediction of Delamination in Wind Turbine Blade Structural Details." In ASME 2003 Wind Energy Symposium. ASMEDC, 2003. http://dx.doi.org/10.1115/wind2003-697.

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Delamination between plies is the root cause of many failures of composite materials structures such as wind turbine blades. Design methodologies to prevent such failures have not been widely available for the materials and processes used in blades. This paper presents simplified methodologies for the prediction of delamination under both static and fatigue loading at typical structural details in blades. The methodology is based on fracture mechanics. The critical strain energy release rate, GIC and GIIC, are determined for opening mode (I) and shearing mode (II) delamination cracks; fatigue crack growth in each mode is also characterized. These data can be used directly for matrix selection, and as properties for the prediction of delamination in structural details. The strain energy release rates are then determined for an assumed interlaminar flaw in the structural detail. The flaw is positioned based on finite element analysis (FEA), and the strain energy release rates are calculated using the virtual crack closure feature available in codes like ANSYS. The methodology has been validated for a skin-stiffener intersection. Two prediction methods differing in complexity and data requirements have been explored. Results for both methods show good agreement between predicted and experimental delamination loads under both static and fatigue loading.
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Cavallaro, Paul V., Andrew Hulton, Mahmoud Salama, and Melvin W. Jee. "Effects of Crimped Fiber Paths on Mixed Mode Delamination Behaviors in Woven Fabric Composites." In ASME 2016 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/imece2016-65646.

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This research investigated the fracture toughness and crack propagation behaviors of woven fabric reinforced polymer (WFRP) composite laminates subjected to single and mixed mode loadings using numerical models. The objectives were to characterize the fracture behaviors and toughness properties at the fiber/matrix interfaces and to identify mechanisms that can be exploited for increasing delamination resistance. The mode-I and mode-II strain energy release rates GI and GII, the effective critical strain energy release rate, Gc_eff, (also known as the mixed mode fracture toughness) and crack growth stabilities were determined as functions of crimped fiber paths using meso-scale, 2D multi-continuum finite element models. Three variations of a plain-woven fabric architecture were considered; each having different crimped fiber paths. The presence of mixed-mode strain energy release rates at the meso-scale due to the curvilinear fiber paths was shown to influence the interlaminar fracture toughness and was explored for pure single-mode and mixed-mode global loadings. It was concluded that woven fabric composites provided a Fracture Toughness Conversion Mechanism (FTCM) and their toughness properties were dependent upon and varied with positon along the crimped fiber paths. The FTCM was identified as an advanced tailoring mechanism that can be further utilized to improve toughness and damage tolerance thresholds especially when the mode-II fracture toughness GIIc is greater than the mode-I fracture toughness GIc.
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Fabris, E., M. Meneghini, C. De Santi, M. Borga, G. Meneghesso, E. Zanoni, Y. Kinoshita, K. Tanaka, H. Ishida, and T. Ueda. "Hot-Electron Effects in GaN GITs and HD-GITs: A Comprehensive Analysis." In 2019 IEEE International Reliability Physics Symposium (IRPS). IEEE, 2019. http://dx.doi.org/10.1109/irps.2019.8720472.

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Gonzalez, Ana M., Mariana L. Manrique, Lukasz Swiech, Thomas Horn, Jeremy Waight, Yuqi Liu, Shiwen Lin, et al. "Abstract 3643: INCAGN1876, a unique GITR agonist antibody that facilitates GITR oligomerization." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3643.

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Hojelse, K., T. Kilbak, J. Rossum, E. Japelt, L. Merino, and M. Lungu. "Git-Truck: Hierarchy-Oriented Visualization of Git Repository Evolution." In 2022 Working Conference on Software Visualization (VISSOFT). IEEE, 2022. http://dx.doi.org/10.1109/vissoft55257.2022.00021.

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Ding, Yifeng, Yimeng Dai, Hai-Tao Zheng, and Rui Zhang. "GiTS: Gist-driven Text Segmentation." In 2022 International Joint Conference on Neural Networks (IJCNN). IEEE, 2022. http://dx.doi.org/10.1109/ijcnn55064.2022.9892668.

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Markovtsev, Vadim, and Waren Long. "Public git archive." In ICSE '18: 40th International Conference on Software Engineering. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3196398.3196464.

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Afzali, Hammad, Santiago Torres-Arias, Reza Curtmola, and Justin Cappos. "le-git-imate." In ASIA CCS '18: ACM Asia Conference on Computer and Communications Security. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3196494.3196523.

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Dauber, Edwin, Aylin Caliskan, Richard Harang, and Rachel Greenstadt. "Git blame who?" In ICSE '18: 40th International Conference on Software Engineering. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3183440.3195007.

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Reports on the topic "GITC":

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Godinez Vazquez, Humberto C. Data Assimilation with GITM. Office of Scientific and Technical Information (OSTI), February 2013. http://dx.doi.org/10.2172/1062701.

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Thompson, Timothy C. GIT2 Gene: Androgenic Regulation of White Adipose Tissue-Prostate Cancer Interactions. Fort Belvoir, VA: Defense Technical Information Center, May 2014. http://dx.doi.org/10.21236/ada609906.

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Trichtchenko, L., and L. Nikitina. Forecasting of GIC indices for Canadian power utilities. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/329423.

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O'Neill, H. B., S. A. Wolfe, and C. Duchesne. Preliminary modelling of ground ice abundance in the Slave Geological Province, Northwest Territories and Nunavut. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/329815.

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New infrastructure corridors within the Slave Geological Province could provide transportation, electric, and communications links to mineral-rich areas of northern Canada, and connect southern highway systems and Arctic shipping routes. Relatively little information on permafrost and ground ice is available compared to other regions, particularly in the north of the corridor. Improved knowledge of permafrost and ground ice conditions is required to inform planning and management of infrastructure. Work within the Geological Survey of Canada's (GSC) GEM-GeoNorth program includes mapping periglacial terrain features, synthesizing existing permafrost and surficial data, and modelling ground ice conditions along the Yellowknife-Grays Bay corridor. Here we present initial modelling of ground ice abundance in the region using a methodology developed for the national scale Ground ice map of Canada (GIMC), and higher resolution surficial geology mapping. The results highlight the increased estimated abundance of potentially ice-rich deposits compared to the GIMC when using more detailed surficial geology as model inputs.
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Auclair, M., and M. Gauthier. Eastern Metals Un Gite a Ni - Cu - Zn - Co - Au Au Sein D'une Serpentinite Alteree [Listwaenite]. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1990. http://dx.doi.org/10.4095/130892.

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Kuwabara, Fumio, Kuniki Kanayama, Hiroki Arai, Jin Kusaka, Tomoyuki Wakisaka, and Yasuhiro Daisho. Numerical Analysis of Diesel Combustion by GIT Code Account for Detailed Chemical Reactions. Warrendale, PA: SAE International, May 2005. http://dx.doi.org/10.4271/2005-08-0316.

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Kulesza, Joel. Workshop on Using a Git-based Repository for ASTM Committee Technical Knowledge Capture. Office of Scientific and Technical Information (OSTI), October 2021. http://dx.doi.org/10.2172/1825393.

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Tinel, M., D. Boteler, and L. Trichtchenko. Evaluating the impact of earth transfer function on the geoelectric field for GIC modelling. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2016. http://dx.doi.org/10.4095/298818.

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Trichtchenko, L., P. A. Fernberg, and D. H. Boteler. One-dimensional layered Earth models of Canada for GIC applications, part 1: General description. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2019. http://dx.doi.org/10.4095/314804.

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Trichtchenko, L., P. A. Fernberg, and D. H. Boteler. One-dimensional layered Earth models of Canada for GIC applications, part 2: Detailed description. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2019. http://dx.doi.org/10.4095/314805.

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