Bibliografias temáticas / Mạc family

Literatura científica selecionada sobre o tema "Mạc family"

Autor: Grafiati
Publicado: 27 de julho de 2024

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Artigos de revistas sobre o assunto "Mạc family"

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Holm, David. "The Brigands’ Song among the Ngạn People in Northern Vietnam". MANUSYA: Journal of Humanities 26, n.º 1 (17 de outubro de 2023): 1–26. http://dx.doi.org/10.1163/26659077-26010009.

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Abstract The Ngạn people are a small local population of Tai-language speakers now living in the eastern districts of Cao Bằng province in northern Vietnam. They are said to be descendants of mercenary soldiers hired by the Mạc royal court during the 17th century. It is the aim of this article to investigate where they came from, using Vietnamese and Chinese ethnological studies, on-site fieldwork and analysis of song texts, supplemented by information from a ritual text and a family register. My conclusion is that the original homeland of the Ngạn was in the Youjiang River valley in west-central Guangxi. Numerous strands of evidence point to a strong connection with the native chieftaincy of Tianzhou and the neighbouring chieftaincy of Si’en.
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Credito, Kim, Klaudia Kosowska-Shick e Peter C. Appelbaum. "Mutant Prevention Concentrations of Four Carbapenems against Gram-Negative Rods". Antimicrobial Agents and Chemotherapy 54, n.º 6 (22 de março de 2010): 2692–95. http://dx.doi.org/10.1128/aac.00033-10.

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ABSTRACT We tested the propensities of four carbapenems to select for resistant Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii mutants by determining the mutant prevention concentrations (MPCs) for 100 clinical strains with various ß-lactam phenotypes. Among the members of the Enterobacteriaceae family and A. baumannii strains, the MPC/MIC ratios were mostly 2 to 4. In contrast, for P. aeruginosa the MPC/MIC ratios were 4 to ≥16. The MPC/MIC ratios for β-lactamase-positive K. pneumoniae and E. coli isolates were much higher (range, 4 to >16 μg/ml) than those for ß-lactamase-negative strains.
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Kuma, Dominic Nkwantabisa, Alex Boye, Godwin Kwakye-Nuako, Yaw Duah Boakye, Justice Kwaku Addo, Ernest Amponsah Asiamah, Eugene Agyei Aboagye, Orleans Martey, Mainprice Akuoko Essuman e Victor Yao Atsu Barku. "Wound Healing Properties and Antimicrobial Effects of Parkia clappertoniana Keay Fruit Husk Extract in a Rat Excisional Wound Model". BioMed Research International 2022 (23 de julho de 2022): 1–18. http://dx.doi.org/10.1155/2022/9709365.

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Background. Parkia clappertoniana Keay (Family: Fabaceae) (P. clappertoniana) fruit husk is commonly used in northern Ghana for wound treatment. However, this folk claim remains to be confirmed scientifically. Objective. This study investigated wound healing and antimicrobial effects of P. clappertoniana fruit husk extract (PCFHE) by using excision wound model in rats. Materials and Methods. After preparation and phytochemical analysis of PCFHE, it was reconstituted in purified water and emulsifying ointment yielding a wound healing formula (0.3, 1, and 3%). Excision wounds were established in healthy male Sprague-Dawley rats (aged 8-10 weeks; weighing 150–200 g). Rats were randomly assigned into six groups (model, 1% silver sulfadiazine [SSD], vehicle, and PCFHE [0.3, 1, and 3%, respectively]) and topically treated daily until complete wound healing. The endpoints (period of epithelialization, wound contraction, collagen content, erythema index, oedema index, inflammatory cell infiltration, and antimicrobial activity) were assessed for all groups. Minimum fungicidal concentration (MFC), minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and time-kill were assessed. Results. Quercetin and catechin were detected in PCFHE. Compared to model and vehicle groups, PCFHE-treatment groups improved wound healing and antimicrobial (MBC, MFC, and MIC) endpoints. PCFHE demonstrated bacteriostatic and fungicidal effects against identified wound contaminants (Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, and Candida albicans). Conclusion. P. clappertoniana fruit husk possesses wound healing and antimicrobial effects in excisional wounds in rats that confirms its folk use, and the reported pharmacological properties of PCFHE are attributable to its quercetin and catechin phyto-constituents.
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Schmidt, Emmett V. "MYC family ties". Nature Genetics 14, n.º 1 (setembro de 1996): 8–10. http://dx.doi.org/10.1038/ng0996-8.

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Hidayatullah, Hidayatullah, Syariful Anam e Muhamad Rinaldhi Tandah. "PROFIL KANDUNGAN KIMIA DAN AKTIVITAS ANTIBAKTERI EKSTRAK METANOL DAUN BAMBAN (Donax canniformis (G. Forst.) K. Schum.) TERHADAP Staphylococcus aureus". Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) 1, n.º 2 (28 de outubro de 2015): 141–48. http://dx.doi.org/10.22487/j24428744.2015.v1.i2.7899.

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Bamban (Donax canniformis (G. Forst.) K. Schum.) is one of the family Marantaceae plant that has many uses such as traditional medicine. Methanol extract of bamban leaves contains phenolic, tannins and saponins compounds. The purpose of this research is to determine the class of compounds that has antibacterial activity against Staphylococcus aureus and determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) methanol extract of bamban leaves. This extract was prepared using maceration method with methanol solvent. Determination the class of compounds was initiated by bioautografi test in order to determine spots which has have antibacterial activity. Subsequently, the spot were identified the class of compound using reagent spray FeCl3 and H2SO4 10%. The determination of MIC and MBC using dilution method. Research showed there are three compounds that had antibacterial activity. These compounds were predicted as spot I and spot II which were phenolic compounds and spot III as a saponin compound. MIC and MBC value of the methanol extract of leaves bamban leaves 8% and 13%, respectively.
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Bappah, Adamu Maryam, Muthasir Qossim, Zakari Nusayba Dambam, Adamu Shehu Usman e Uba Awalu. "Antibacterial Activity of Alkaloid, Flavonoids and Lipids from Crude Extracts of Azadirachta indica on Some Selected Medically Important Bacteria". Journal of Biochemistry, Microbiology and Biotechnology 10, n.º 2 (31 de dezembro de 2022): 20–24. http://dx.doi.org/10.54987/jobimb.v10i2.752.

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Most tropical climates are home to the green perennial tree Azadirachta indica, which belongs to the Meliaceae family of Mahogany, and has long been known to have therapeutic effects. Secondary metabolites in plants cause biological activity in both humans and animals, which explains why they are used as herbs. For the investigation of the lipid, alkaloids, and flavonoids present in the A. indica extracts, thin-layer chromatography was carried out using several solvent systems. The thin layer chromatography-separated active components were tested for antibacterial efficacy against three multi-drug resistance pathogens namely: Salmonella typhi, P. aeruginosa and S. aureus. Alkaloids showed the highest antibacterial activity on Salmonella spp. (15 mm) and 12 mm Staphylococcus aureus isolates while lipids showed the least activity on the tested isolates. The minimum bactericidal concentration (MBC) and minimum inhibitory concentration (MIC) were calculated. The outcomes of the MIC and MBC revealed that the inhibitory concentrations of different plant extracts for certain bacteria varied. Values of MIC for Salmonella typhi were found in the range of 25 to 50 mg/mL, MBC 100 to 200 mg/mL and for Staphylococcus aureus MIC values ranged between 50 and 200 mg/mL, MBC 100 to 400 mg/mL and for Pseudomonas aeruginosa MIC values were found in the range of 100 to 200 mg/mL and MIC values ranged between 200 and 400 mg/mL using a different part of the plant extracted using three different solvents. The finding suggests that crude extract of A. indica might work well for the treatment of illnesses brought on by these microbes and that the activity of the crude extract is more than that of an individual component.
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Bahram, S., e T. Spies. "The MIC gene family". Human Immunology 47, n.º 1-2 (abril de 1996): 64. http://dx.doi.org/10.1016/0198-8859(96)85038-5.

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Bahram, S., e T. Spies. "The MIC gene family". Research in Immunology 147, n.º 5 (janeiro de 1996): 328–33. http://dx.doi.org/10.1016/0923-2494(96)89646-5.

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Daniel, Paulo Sergio, Emerson Luiz Botelho Lourenço, Rayane Monique Sete da Cruz, Carlos Henrique De Souza Gonçalves, Luiz Renato Marques Das Almas, Jaqueline Hoscheid, Camila da Silva, Ezilda Jacomassi, Liberato Brum Junior e Odair Alberton. "Composition and antimicrobial activity of essential oil of yarrow (Achillea millefolium L.)". March 2020, n.º 14(03):2020 (20 de março de 2020): 545–50. http://dx.doi.org/10.21475/ajcs.20.14.03.p2325.

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The medicinal plant yarrow (Achillea millefolium L.) belongs to the Asteracea family. It is being used in the pharmacological, food, and cosmetic industry. The economic importance of yarrow resides in its essential oil (EO). This plant is used in traditional medicine as the EO has properties which range from antibacterial, antifungal, anti-inflammatory, anti-oxidant and antitumor activities. The objective of this study was to identify chemical components and EO content of yarrow, as well as its antimicrobial activity against some micro-organisms in vitro. The fresh leaves were collected in a morning in October (2018) at the UNIPAR Medicinal Plants Garden, Umuarama-Paraná State, Brazil. The EO was obtained by hydrodistillation of the modified Clevenger type. After that, the content (m/m%) was calculated. The chemical composition of the EO was identified by gas chromatography/mass spectrometry (GC/MS). The minimal inhibitory concentration (MIC), minimal bactericidal concentration (MBC) and minimal fungicidal concentration (MFC) were determined by a microdilution method in 96-well microtitre plates and effect of EO was assessed on four micro-organisms (Candida albicans, Staphylococcus epidermidis, Escherechia coli and Klebsiella pneumoniae). The EO content (yield) in the plant shoots was 0.4% (four grams of EO kg-1 of plant fresh shoots) and presented 20 chemical compounds such as α-farnesene (31.66%), followed by chamazulene (17.17%), β-caryophyllene (10.27%) and sabinene (8.77%). The majority class was hydrocarbon sesquiterpene with 74.29%. The antimicrobial activity tests showed that the EO had low antimicrobial activity against the analyzed species with MIC for all species above 1.5 mg mL-1. It was concluded that the EO content was 0.4%. The major component was α-farnesene (31.66%) and EO presented low MIC.
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Raho, G. Bachir, M. Otsmane e F. Sebaa. "Antimicrobial activity of essential oils of Juniperus phoenicea from North Western Algeria". Journal of Medicinal Botany 1 (1 de junho de 2017): 01. http://dx.doi.org/10.25081/jmb.2017.v1.41.

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Juniperus phoenicea (Family: Cupressaceae) is an evergreen tree widely distributed in North Africa including Algeria. The aim of this investigation was to analyse the antimicrobial potential of essential oils from J. phoenicea on Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumonia, Streptococcus sp, Bacillus sp and Candida albicans using wells and discs diffusion methods. Broth dilution method was utilized to study the minimum inhibitory concentrations (MIC) and minimum bactericidal concentrations (MBC). The results showed a variable degree of antimicrobial activity. The diameters of inhibition zones for all test organisms were in the ranges of 7–21 mm, while MIC was from 62.5 to >500µl/ml and MBC from 250 to >500µl/ml. The highest antimicrobial activities were observed against Gram positive bacteria followed by Gram negative ones then Candida albicans. The findings provide the evidence that J. phoenicea as a good medicinal plant for further investigations.
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Teses / dissertações sobre o assunto "Mạc family"

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Jopling, Catherine L. "Internal ribosome entry in the myc gene family". Thesis, University of Leicester, 2001. http://hdl.handle.net/2381/29662.

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The proto-oncogene c-myc is encoded by a transcript in which the 5' UTR contains a potent internal ribosome entry segment (IRES). The N-myc gene shows considerable homology to c-myc and also possesses a 5' UTR that is long and structured. Thus, the potential for internal ribosome entry within this UTR was examined. N-myc was found to contain an IRES that was of comparable activity to that of c-myc in non-neuronal cells, but was specifically activated relative to the c-myc IRES in neuronal cells in which the N-myc transcription is expressed. Furthermore, the activity of the N-myc IRES was specifically inhibited during neuronal differentiation, when N-myc expression is reduced. The trans-acting factor requirements for N-myc IRES function were examined and a candidate protein was found, although not characterised. An IRES was also identified in the 5' UTR of the third well-studied member of the myc gene family, L-myc. An alternative form of the UTR exists in which an intron is retained, but it was not possible to draw any definite conclusions on the IRES activity of this UTR. Translation of both c- and N-myc mRNAs can occur by both cap-dependent and IRES-dependent mechanisms, so the existence of IRESs within these transcripts was intriguing. c-Myc protein levels were analysed during apoptosis and were maintained, despite the apoptotic inhibition of protein synthesis and the short half-life of c-Myc. The activity of the c-myc IRES was maintained during apoptosis and was responsible for this effect. The c-myc IRES was also shown to lie downstream of the p38 mitogen-activated protein kinase signalling pathway.
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Bull, Camilla Louise. "Localisation and expression of epididymal apical protein I". Thesis, University of Bristol, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319142.

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Foster, Helen Elisabeth. "A family study of primary Sjogren's syndrome in north east England". Thesis, University of Newcastle Upon Tyne, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309065.

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Liang, Rebecca Yue. "Probing Protein Interactions with Stapled Peptides: Myc Family and Insulin Receptor". Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:11063.

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One of the most exciting frontiers of expanding pharmacopeia to combat currently untreatable diseases is achieving specifically and potently disruption of unwanted protein-protein interactions where traditional small molecule drugs tend to fall short. Our laboratory has developed the methodology of peptide stapling and pioneered successful applications in multiple disease models since its induction over a decade ago. One common feature of past applications is the use of a single stapled peptide in helical form, derived from the natural binding interface of target proteins. This dissertation ventures into protein interactions that involve multiple components and sites and explores the extended use of stapled peptides in these volatile settings.
Chemistry and Chemical Biology
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Lee, Sun Young. "The search for Myc-family genes in lepidopteran insects, strategies and applications". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq62172.pdf.

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Rice, Jerome Lee. "Examining Family Hierarchy Through the Eyes of Former Mac Baller Gang Members". ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/7952.

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Criminal gang membership is growing, which corresponds to a continued breakdown of the family unit in the United States. Most of the young people who form gangs come from broken families or single-parent-headed households. This study explored the role of family hierarchy on gang membership. A qualitative case study approach was used to gather information on what motivates young people to join criminal gangs. A random sampling technique was used to recruit seven former members of the Mac Baller Brim gang. Ethical concerns were addressed to minimize the risks to the participants. The collected data from interviews were analyzed using an interpretive research philosophy to determine the contribution of family hierarchy on motivating the participants to join gangs. Interpretive research philosophy indicates that reality can only be understood by subjective interpretation and intervention. An action research strategy was also used in an attempt to provide a practical solution for the people studied while adding to existing theories. The findings of the study indicated that there are 5 reasons why young people join gangs: protection, respect, money, fun, and because a friend was in the gang. This study may contribute to social change by identifying factors that lead to gang membership to aid policy and program interventions that lower the likelihood of youth joining gangs.
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Ryan, Sarra Louise. "The clinical and biological roles of MYC gene family amplification in childhood medulloblastoma". Thesis, University of Newcastle Upon Tyne, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512113.

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To make a comprehensive assessment of the incidence, nature and significance of MYC gene family amplification in medulloblastoma, we first developed a quantitative real-time PCR (qPCR) assay to identify MYCC, MYCN and MYCL amplification in a large patient cohort (n=292), which included 178 children entered into the SIOP/UKCCSG PNET3 clinical trial. MYCC, MYCN and MYCL copy number elevation was identified in 6% (17/292), 6% (18/292), and 1% (3/292) of medulloblastomas, respectively. No evidence of co-incident copy number elevation of more than one MYC family member was identified in any sample. The transcript expression of genes frequently harboured within the MYCC and MYCN amplicons was assessed and a correlation was identified between gene copy number and transcript expression of four genes (TRIB2, DDX1, NESE2 and AK093424) neighbouring the MYCC and MYCN loci, suggesting that these genes may represent amplification targets and play a role in medulloblastoma. In cases where RNA was available (n=60), a correlation was identified between MYCC copy number elevation (n=8) and elevated expression of its transcript; however the relationship between MYCN copy number and transcript expression was less clear. MYCL expression was assessed in a smaller number (n=18) of medulloblastoma primary tumours and was found to be significantly overexpressed in cases with MYCL amplification (n=2). All three MYC family members were more highly expressed in medulloblastomas with a deregulated Shh- or Wnt- signalling pathway, suggesting that these pathways also play a role in the regulation of MYC family member expression in medulloblastoma. Comprehensive assessment of the clinico-histopathological significance of MYCC and MYCN amplification (HCN ≥5.00) identified an association with the large cell anaplastic (LCA) medulloblastoma and all tumours with an elevated copy number of MYCC (n=17) and MYCN (n=18) were derived from patients greater than three years of age. Log-rank tests identified MYCC or MYCN amplifications as a marker of poor prognosis and Cox proportional hazards models revealed that MYCC and MYCN amplification had similar hazard ratios (hazard ratio (HR); 299) to establish markers fo disease risk (Metastatic (M) stage ≥2 (HR; 3.33) and the LCA subtype (HR; 3.63)). Multivariate analyses identified MYCC or MYCN amplification as independent markers of poor prognosis and together with LCA histology and M stage ≥2, formed a combined high risk group of patients with a significantly poorer prognosis (29.4% (75/255); p<0.0001).
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Koneni, Rupa. "The Biological Function of Interacting Partners of ZXD Family Proteins". Cleveland State University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=csu1250261050.

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PELLANDA, PAOLA. "STRUCTURE-FUNCTION ANALYSIS OF MYC/MAX-DNA BINDING". Doctoral thesis, Università degli Studi di Milano, 2018. http://hdl.handle.net/2434/556180.

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The c-Myc oncoprotein (or Myc) is a transcription factor of the basic-Helix-Loop-Helix Leucine-zipper (bHLH-LZ) family, whose transcriptional activity depends on dimerization with the bHLH-LZ partner Max and DNA binding, mediated by the basic regions of both proteins. Myc/Max dimers bind preferentially to the hexanucleotide motif CACGTG (known as E-box) and variants thereof. The ability of Myc to bind DNA in vivo, however, is not stringently regulated by the presence of the E-box, since many genomic sites targeted by Myc do not contain this motif. Hence, we still need to fully comprehend how Myc recognizes its genomic targets and to what extent sequence-specific DNA binding contributes to this process. Based on the crystal structure of the DNA-bound Myc/Max dimer, we generated a Myc mutant in which two basic region residues engaged in sequence-specific contacts (H359 and E363) were mutated to Alanine (Myc HEA), and compared this with a mutant in which three Arginine residues involved in DNA backbone interactions were mutated to Alanine (Myc RA). While both mutants showed impaired E-box recognition in vitro, their over-expression in murine fibroblasts revealed very different genome-interaction profiles, Myc RA showing no detectable DNA binding, and Myc HEA retaining about half of the binding sites seen with Myc wt. The analysis of the binding intensity of Myc wt and Myc HEA at their binding sites revealed that, as expected, Myc wt bound more strongly the sites containing the E-box, while Myc HEA bound the sites with an E-box as well as the sites without it, confirming that the mutant lost the sequence-specific recognition ability. The interactions retained by the Myc HEA were dramatically reduced with the protein expressed from the endogenous c-myc locus, though genome engineering. Thus, unlike Myc RA, the Myc HEA mutant retained non-specific interactions with genomic DNA (detectable at elevated protein levels) but failed to engage more stably through sequence-specific DNA contacts. In spite of this residual DNA-binding activity, Myc HEA was profoundly impaired in its biological function, undistinguishable from Myc RA: in particular, neither mutant could substitute for wild-type Myc in supporting cell proliferation in murine fibroblasts, whether at normal or supra-physiological levels. While the assessment of transcriptional activities is still ongoing, we conclude that E-box recognition is essential for Myc’s biological function.
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Su, Yingtao. "Function and regulation of myc-family bHLHZip transcription factors during the animal and plant cell cycle /". Uppsala : Dept. of Plant Biology and Forest Genetics, Swedish University of Agricultural Sciences, 2008. http://epsilon.slu.se/200836.pdf.

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Livros sobre o assunto "Mạc family"

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Chương trình nghiên cứu gia phả Việt Nam, ed. Hà Tiên trấn hiệp trấn Mạc Thị gia phả: Hà Tiên - Kiên Giang = Hexian zhen Ye zhen Zheng shi jia pu. Hà Nội: Nhà xuất bản Thế giới, 2006.

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Macalou, Ousmane Abdoul. Mac, the African country boy. Berkeley, CA: OMAC International Distributors, 1989.

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Drisko, Frances Sterling. MackIntosh, Mac Intosh, Mc Intosh: Descendants of Alexander-1 Mac Intosh and his wife, Clara Younkhause/Junghans. Bowie, Md: Heritage Books, 1993.

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Smith, Russell Kirk. Regulation of the Myc family genes during B lymphoid development. [New York]: [Columbia University], 1993.

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McAmis, Edward C. Family military records of the Sept Mac Hamish. St. Leonard, MD (6041 Locust Rd., St. Leonard 20685): E.C. McAmis, 1994.

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Leger, Alicia St. Mac Carthy: People and places. Whitegate, Co. Clare, Ireland: Ballinakella Press, 1990.

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Hamilton, Virginia. M.C. Higgins, the great. New York, N.Y: Simon & Schuster, 1999.

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Hamilton, Virginia. M.C. Higgins, the great. New York: Aladdin Books, 1993.

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Hamilton, Virginia. M.C. Higgins, the great. Waterville, Me: Thorndike Press, 2005.

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Hamilton, Virginia. M.C. Higgins, the great. Santa Barbara, Calif: ABC-CLIO, 1988.

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Capítulos de livros sobre o assunto "Mạc family"

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Lee, William M. F. "The myc family of nuclear proto-oncogenes". In Cancer Treatment and Research, 37–71. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-1599-5_3.

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Groth, P., Ursula Zarmstorf, Irmtraud Stoll e R. Reincke. "Family screening in medullary thyroid carcinoma (MTC)". In New Aspects in Thyroid Diseases, editado por H. F. Deckart e E. Strehlau, 324–29. Berlin, Boston: De Gruyter, 1992. http://dx.doi.org/10.1515/9783110874051-042.

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Laari-Salmela, Sari, Tuija Mainela, Elina Pernu e Vesa Puhakka. "One Family Firm, Four Families: Developing Management Models of a Family Values-Based MNC". In The Palgrave Handbook of Family Firm Internationalization, 173–97. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-66737-5_6.

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Wheeler, C., D. Maloney, S. Watts, J. Vogel, J. Towner, D. Baldwin, J. Rufer et al. "Microgene Conversion in the Evolution of the MHC Class I Multigene Family". In Transgenic Mice and Mutants in MHC Research, 14–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75442-5_2.

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Matsuoka, Rumiko. "Study of the Vertebrate MHC Multigene Family During Heart Development". In Advances in Experimental Medicine and Biology, 17–30. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-9029-7_2.

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Dildrop, R., K. Zimmerman, R. A. DePinho, G. D. Yancopoulos, A. Tesfaye e F. W. Alt. "Differential Expression of myc-family Genes During Development: Normal and Deregulated N-myc Expression in Transgenic Mice". In Current Topics in Microbiology and Immunology, 100–109. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-74006-0_14.

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Shin, Sang Uk, Kyung Hyune Rhee, Dae Hyun Ryu e Sang Jin Lee. "A new hash function based on MDx-family and its application to MAC". In Public Key Cryptography, 234–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/bfb0054028.

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Thompson, E. Brad, Y.-S. Yuh, D. Harbour, J. Ashraf, B. Johnson e J. M. Harmon. "Growth Inhibition of CEM Cells by Glucocorticoids: c-myc down Regulation, and the Topology of the Glucocorticoid Receptor". In The Steroid/Thyroid Hormone Receptor Family and Gene Regulation, 127–45. Basel: Birkhäuser Basel, 1989. http://dx.doi.org/10.1007/978-3-0348-5466-5_9.

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Siegel, D. S., J. A. Terry, J. Koury, B. Barlogie, J. Epstein e R. Feinman. "Myc/Max Family of Transcription Factors and bcl-2 are Involved in Drug-induced Apoptosis of Myeloma Cells". In Current Topics in Microbiology and Immunology, 257–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60801-8_26.

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Barman, Bikash, e Pradip Chouhan. "Utilization of MHC Services in Empowered Action Group (EAG) States of India: Evidence from National Family Health Survey (NFHS)-4". In Population, Sanitation and Health, 297–320. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-40128-2_19.

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Trabalhos de conferências sobre o assunto "Mạc family"

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Jianghua Ge, Chuanxiao Yang, Tiequn Duan e Yongqiu Chen. "Research on method of construction and configuration of product family based on ontology". In 2013 2nd International Conference on Measurement, Information and Control (ICMIC). IEEE, 2013. http://dx.doi.org/10.1109/mic.2013.6758228.

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Resetca, Diana, Dharmesh Dingar, Manpreet Kalkat, Brian Raught e Linda Z. Penn. "Abstract 2010: Charactering the interactomes of the Myc family of oncogenes". In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-2010.

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Jong, Yongsop, Wei Zhang e Weisheng Xu. "Guard Time Settings in TDMA Family MAC Protocol for Underwater Sensor Networks". In The 7th International Conference on Computer Engineering and Networks. Trieste, Italy: Sissa Medialab, 2017. http://dx.doi.org/10.22323/1.299.0034.

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Dammert, Marcel A., e Martin L. Sos. "Abstract 3340: Endogenous, CRISPR-mediated overexpression of MYC family members as a framework to discover MYC-specific vulnerabilities". In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-3340.

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Shatat, M. A., E. Yuan e R. T. Lee. "Mistletoe Lectin as Treatment for Small Cell Lung Cancer Expressing Myc Family Oncoproteins". In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a3950.

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Patel, Ayushi S., Seungyeul Yoo, Ranran Kong, Takashi Sato, Maya Fridrikh, German Nudelman, Charles A. Powell, Jun Zhu e Hideo Watanabe. "Abstract 1295: Myc family members differentially regulate lineage plasticity in small cell lung cancer". In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-1295.

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Durbin, Adam D., Guillaume Kugener, Mark W. Zimmerman, Chuan Yan, Neekesh V. Dharia, Elizabeth S. Frank, Xiang Chen et al. "Abstract B10: Rhabdomyosarcoma requires MYC family genomic events to pathogenically subvert core-regulatory circuitry". In Abstracts: AACR Special Conference on the Advances in Pediatric Cancer Research; September 17-20, 2019; Montreal, QC, Canada. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.pedca19-b10.

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Valli, Emanuele, Chengyuan Xue, Leanna Cheung, Laura Gamble, Ruby Pandher, Simone Di Giacomo, Catherine Burkhart et al. "Abstract 2616: A novel iron-chelating agent reduces MYC transcription via E2F gene family regulation". In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-2616.

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Valli, Emanuele, Chengyuan Xue, Leanna Cheung, Laura Gamble, Ruby Pandher, Simone Di Giacomo, Catherine Burkhart et al. "Abstract 2616: A novel iron-chelating agent reduces MYC transcription via E2F gene family regulation". In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-2616.

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Yu, Shiqiang, Pai Zheng, Chunyang Yu e Xun Xu. "Product-Service Family Enabled Product Configuration System for Cloud Manufacturing". In ASME 2017 12th International Manufacturing Science and Engineering Conference collocated with the JSME/ASME 2017 6th International Conference on Materials and Processing. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/msec2017-2987.

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Rapid responsiveness to diverse customer needs is considered a competitive advantage in manufacturing business. To shrink the inquiry-to-order process, manufacturing firms will benefit a lot from building a product configuration system (PCS) which is the enabler of mass customisation (MC). PCS has matured in consumer businesses for decades but in capital goods industries, typically operating in engineer-to-order (ETO) manner, things differ a lot. It is for the reason that conventional PCS is incapable of extending customisation from order-delivery processes to the design/engineering phase. Cloud manufacturing, which is an emerging service-oriented manufacturing paradigms enabled by cyber-physical system, the Internet of Things and the Internet of Service, is promising to break the bottleneck of “ETO PCS” by the provision of technical infrastructure for product, service and data customisation. With the introducing of manufacturing-as-a-service (MaaS) concept, a product family is extended to a product-service family (PSF) in this paper for implementing in-depth product configuration process with scalable customisation depth (i.e., the degree of customisation freedom). Additionally, an approach of service delegation in product configuration process is proposed to support customer-centric product customisation. At last, the methodology proposed in this paper is validated by a case study in which the product configuration process of a complex ETO product is performed.
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Relatórios de organizações sobre o assunto "Mạc family"

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McClure, Michael A., Yitzhak Spiegel, David M. Bird, R. Salomon e R. H. C. Curtis. Functional Analysis of Root-Knot Nematode Surface Coat Proteins to Develop Rational Targets for Plantibodies. United States Department of Agriculture, outubro de 2001. http://dx.doi.org/10.32747/2001.7575284.bard.

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The goal of this research was to provide a better understanding of the interface between root-knot nematodes, Meloidogyne spp., and their host in order to develop rational targets for plantibodies and other novel methods of nematode control directed against the nematode surface coat (SC). Specific objectives were: 1. To produce additional monoclonal SC antibodies for use in Objectives 2, 3, and 4 and as candidates for development of plantibodies. 2. To determine the production and distribution of SC proteins during the infection process. 3. To use biochemical and immunological methods to perturbate the root-knot nematode SC in order to identify SC components that will serve as targets for rationally designed plantibodies. 4. To develop SC-mutant nematodes as additional tools for defining the role of the SC during infection. The external cuticular layer of nematodes is the epicuticle. In many nematodes, it is covered by a fuzzy material termed "surface coat" (SC). Since the SC is the outermost layer, it may playa role in the interaction between the nematode and its surroundings during all life stages in soil and during pathogenesis. The SC is composed mainly of proteins, carbohydrates (which can be part of glycoproteins), and lipids. SC proteins and glycoproteins have been labeled and extracted from preparasitic second-stage juveniles and adult females of Meloidogyne and specific antibodies have been raised against surface antigens. Antibodies can be used to gain more information about surface function and to isolate genes encoding for surface antigens. Characterization of surface antigens and their roles in different life-stages may be an important step towards the development of alternative control. Nevertheless, the role of the plant- parasitic nematode's surface in plant-nematode interaction is still not understood. Carbohydrates or carbohydrate-recognition domains (CROs) on the nematode surface may interact with CROs or carbohydrate molecules, on root surfaces or exudates, or be active after the nematode has penetrated into the root. Surface antigens undoubtedly play an important role in interactions with microorganisms that adhere to the nematodes. Polyclonal (PC) and monoclonal (MC) antibodies raised against Meloidogyne javanica, M. incognita and other plant-parasitic nematodes, were used to characterize the surface coat and secreted-excreted products of M. javanica and M. incognita. Some of the MC and PC antibodies raised against M. incognita showed cross-reactivity with the surface coat of M. javanica. Further characterization, in planta, of the epitopes recognized by the antibodies, showed that they were present in the parasitic juvenile stages and that the surface coat is shed during root penetration by the nematode and its migration between root cells. At the molecular level, we have followed two lines of experimentation. The first has been to identify genes encoding surface coat (SC) molecules, and we have isolated and characterized a small family of mucin genes from M. incognita. Our second approach has been to study host genes that respond to the nematode, and in particular, to the SC. Our previous work has identified a large suite of genes expressed in Lycopersicon esculentum giant cells, including the partial cDNA clone DB#131, which encodes a serine/threonine protein kinase. Isolation and predicted translation of the mature cDNA revealed a frame shift mutation in the translated region of nematode sensitive plants. By using primers homologous to conserved region of DB#131 we have identified the orthologues from three (nematode-resistant) Lycopersicon peruvianum strains and found that these plants lacked the mutation.
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L’union fait la force ! La mise en oeuvre de la Politique de la famille et de développement social dans la MRC des Maskoutains : Quelques constats pour préparer l’avenir. Institut national de santé publique du Québec, 2024. http://dx.doi.org/10.51644/nqfa1268.

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