Literatura académica sobre el tema "Transcript variants"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Transcript variants".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Transcript variants"
Ouyang, Hongjia, Jiao Yu, Xiaolan Chen, Zhijun Wang y Qinghua Nie. "A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken". PeerJ 8 (4 de febrero de 2020): e8351. http://dx.doi.org/10.7717/peerj.8351.
Texto completoAhmed Elnour, Abdalla Abdelrahman y Mahdi H. A. Abdalla. "P210 and P190 BCR-ABL fusion transcripts variants frequencies among Philadelphia chromosome-positive chronic myeloid leukemia in Sudan". International Journal of Biomedical Research 9, n.º 5 (29 de mayo de 2018): 172. http://dx.doi.org/10.7439/ijbr.v9i5.4736.
Texto completoMorales, Joannella, Shashikant Pujar, Jane E. Loveland, Alex Astashyn, Ruth Bennett, Andrew Berry, Eric Cox et al. "A joint NCBI and EMBL-EBI transcript set for clinical genomics and research". Nature 604, n.º 7905 (6 de abril de 2022): 310–15. http://dx.doi.org/10.1038/s41586-022-04558-8.
Texto completoCook, Taylor W., Amy M. Wilstermann, Jackson T. Mitchell, Nicholas E. Arnold, Surender Rajasekaran, Caleb P. Bupp y Jeremy W. Prokop. "Understanding Insulin in the Age of Precision Medicine and Big Data: Under-Explored Nature of Genomics". Biomolecules 13, n.º 2 (30 de enero de 2023): 257. http://dx.doi.org/10.3390/biom13020257.
Texto completoRosa, Villegas-Ruíz, Caballero-Palacios, Pérez-López, Murata, Zapata-Tarres, Cárdenas-Cardos, Paredes-Aguilera, Rivera-Luna y Juárez-Méndez. "Expression of ZNF695 Transcript Variants in Childhood B-Cell Acute Lymphoblastic Leukemia". Genes 10, n.º 9 (16 de septiembre de 2019): 716. http://dx.doi.org/10.3390/genes10090716.
Texto completoValenzuela-Palomo, Alberto, Lara Sanoguera-Miralles, Elena Bueno-Martínez, Ada Esteban-Sánchez, Inés Llinares-Burguet, Alicia García-Álvarez, Pedro Pérez-Segura, Susana Gómez-Barrero, Miguel de la Hoya y Eladio A. Velasco-Sampedro. "Splicing Analysis of 16 PALB2 ClinVar Variants by Minigene Assays: Identification of Six Likely Pathogenic Variants". Cancers 14, n.º 18 (19 de septiembre de 2022): 4541. http://dx.doi.org/10.3390/cancers14184541.
Texto completoJohn, Miya y Caroline E. Ford. "Pan-Tissue and -Cancer Analysis of ROR1 and ROR2 Transcript Variants Identify Novel Functional Significance for an Alternative Splice Variant of ROR1". Biomedicines 10, n.º 10 (13 de octubre de 2022): 2559. http://dx.doi.org/10.3390/biomedicines10102559.
Texto completoGermeshausen, Manuela, Magda Grudzien, Cornelia Zeidler, Hengameh Abdollahpour, Sevgi Yetgin, Nima Rezaei, Matthias Ballmaier, Bodo Grimbacher, Karl Welte y Christoph Klein. "Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations". Blood 111, n.º 10 (15 de mayo de 2008): 4954–57. http://dx.doi.org/10.1182/blood-2007-11-120667.
Texto completoBueno-Martínez, Elena, Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Víctor Lorca, Alicia Gómez-Sanz, Sara Carvalho, Jamie Allen et al. "RAD51D Aberrant Splicing in Breast Cancer: Identification of Splicing Regulatory Elements and Minigene-Based Evaluation of 53 DNA Variants". Cancers 13, n.º 11 (7 de junio de 2021): 2845. http://dx.doi.org/10.3390/cancers13112845.
Texto completoDe la Cruz-Hernández, Erick, Alejandro García-Carrancá, Alejandro Mohar-Betancourt, Alfonso Dueñas-González, Adriana Contreras-Paredes, Enrique Pérez-Cardenas, Roberto Herrera-Goepfert y Marcela Lizano-Soberón. "Differential splicing of E6 within human papillomavirus type 18 variants and functional consequences". Journal of General Virology 86, n.º 9 (1 de septiembre de 2005): 2459–68. http://dx.doi.org/10.1099/vir.0.80945-0.
Texto completoTesis sobre el tema "Transcript variants"
Chandra, Shubhra. "Delineating the role of Hepatocyte nuclear factor 1 beta (HNF1B) transcript variants in prostate cancer". Thesis, Queensland University of Technology, 2020. https://eprints.qut.edu.au/135713/1/Shubhra_Chandra_Thesis.pdf.
Texto completoMARRANCI, ANDREA. "Analysis of the expression of all BRAF transcript variants and of their implication in post-transcriptional regulation mediated by miRNAs in melanoma". Doctoral thesis, Università di Siena, 2017. http://hdl.handle.net/11365/1005876.
Texto completoHeller, Susanne. "Molecular mechanisms involved in glioma cell interactions in vitro and studies of PDGF B transcript variants". Doctoral thesis, Uppsala University, Department of Genetics and Pathology, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1252.
Texto completoGlioblastoma multiforme is a malignant brain tumor characterized by heterogeneity.Interactions between heterogeneous tumor cells are supposed to affect the behavior of awhole tumor cell population. In this thesis an in vitro model system of clonal glioma celllines originating from one glioblastoma tumor was used, and the behavior of cells incocultures was studied and compared the behavior of cells grown separately. The resultsindicate the presence of two types of interactions. In one, paracrine signals acted via extra-cellular media. This was associated with increased growth of the whole co-culture followedby a selective force driving one clone to dominance. In the other type, the cell clones grewside by side without signs of paracrine signalling, in a balance resulting in an increasedterminal cell density. Further investigations focused on mechanisms of interactions in thiscombination.
Two cell clones were chosen, a GFAP+ and a GFAP-, for further experiments. Withdifferential display PCR it was possible to investigate their specific gene expressionpatterns. Seventeen cDNA fragments were differentially expressed, among them twocorresponded to known transcription factors, ATF3 and prox-1, one to a cytoskeletal protein,α-tropomyosin. The collection also contained eight ESTs (Expressed Sequence Tags) wherethe corresponding genes are unknown at present. Expression of the isolated sequences werealso analyzed in a panel of 12 different glioma cell lines and the results illustrate thecomplexity of gene expression and of tumor heterogeneity. Genes, the expression levels ofwhich were modulated in co-cultures and/or were cell density dependent, were alsoidentified.
PDGF B is suggested to play a role in sarcomas. The gene codes for an mRNA transcriptwith long UTRs, parts of which are deleted in the homologous oncogene v-sis. The UTRs ofPDGF B mRNAs in human sarcomas were investigated for deletions similar to v-sis thatmight result in increased protein levels. A new transcript variant was identified, lacking a149 base region in the 3'UTR, but its presence was not associated with increased levels ofprotein. Alterations in the 5'UTR were found more likely to be associated with increasedprotein levels.
CAPUA, G. DI. "CHARACTERIZATION OF HUMAN TENEURIN-4 TRANSCRIPT IN OVARIAN CANCER DERIVED CELL LINES". Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/171959.
Texto completoHaghighat, Roya. "Identification of unique CD44 variant transcripts in human colon cancer". Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=23892.
Texto completoMartin, Juliette. "Le Gene Agouti Bovin : Organisation Structurale et expression tissulaire : Production par génie génétique de trois variants protéiques". Limoges, 2001. http://www.theses.fr/2001LIMO0048.
Texto completoThe work presented in this report was begun within the framework of a research program for genetic markers of the French bovine species in association with INRA and UPRA. .
Ross, Heather Hamilton. "Characterization and Functional Analysis of a Newly Identified Human MT5-MMP Transcript Variant Isolated from Multipotent NT2 Cells". VCU Scholars Compass, 2006. http://hdl.handle.net/10156/1498.
Texto completoGriffith, Malachi. "Methods for transcript variant discovery and alternative expression analysis : application to the study of fluorouracil resistance in colorectal cancer". Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/18621.
Texto completoYoung, Kyle E. "Alternative splicing of the zebrafish myosin phosphatase targeting subunit, MYPT1, produces a novel isoform". Scholarly Commons, 2016. https://scholarlycommons.pacific.edu/uop_etds/173.
Texto completoIwai, Akio. "Siah-1L, a novel transcript variant belonging to the human Siah family of proteins, regulates β-catenin activity in a p53-dependent manner". Kyoto University, 2005. http://hdl.handle.net/2433/144711.
Texto completoLibros sobre el tema "Transcript variants"
Ginsberg, Allen. Howl: Original draft facsimile, transcript & variant versions, fully annotated by author, with contemporaneous correspondence, account of first public reading, legal skirmishes, precursor texts & bibliography. New York: Harper & Row, 1986.
Buscar texto completo1943-, Miles Barry, ed. Howl: Original draft facsimile, transcript & variant versions, fully annotated by author, with contemporaneous correspondence, account of first public reading, legal skirmishes, percusor texts & bibliography. (Harmondsworth): Viking, 1987.
Buscar texto completoAllen, Ginsberg. Howl: Original draft facsimile, transcript & variant versions, fully annotated by author, with contemporaneous correspondence, account of first public reading, legal skirmishes, precursor texts & bibliography. New York: Harper & Row, 1986.
Buscar texto completoAllen, Ginsberg. Howl: Original draft facsimile, transcript and variant versions, fully annotated by author, with contemporaneous correspondence, account of first public reading, legal skirmishes, precursor texts and bibliography. New York, NY: Harper Perennial Modern Classics, 2006.
Buscar texto completoAllen, Ginsberg. Howl: Original Draft Facsimile, Transcript and Variant Versions. HarperCollins, 1988.
Buscar texto completoAllen, Ginsberg. Howl: Original Draft Facsimile, Transcript and Variant Versions. HarperCollins, 1988.
Buscar texto completoSieburg, Heinz, ed. Vielfalt der Sprachen - Varianz der Perspektiven. transcript Verlag, 2013. http://dx.doi.org/10.1515/transcript.9783839420300.
Texto completoSieburg, Heinz, ed. Vielfalt der Sprachen - Varianz der Perspektiven. transcript-Verlag, 2013. http://dx.doi.org/10.14361/transcript.9783839420300.
Texto completoAllen, Ginsberg. Howl: Original draft facsimile, transcript & variant versions, fully annotated by author, with contemporaneous correspondence, account of first public ... skirmishes, precursor texts & bibliography. Harper & Row, 1986.
Buscar texto completoAllen, Ginsberg. Howl: Original draft facsimile, transcript & variant versions, fully annotated by author, with contemporaneous correspondence, account of first public ... skirmishes, precursor texts & bibliography. Harper & Row, 1986.
Buscar texto completoCapítulos de libros sobre el tema "Transcript variants"
Freeman, Lita A. "Cloning Full-Length Transcripts and Transcript Variants Using 5′ and 3′ RACE". En Methods in Molecular Biology, 3–17. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-60327-369-5_1.
Texto completoSun, Cong, Qiang Wu, Ye-chao Han, Ting-ting Tang y Li-li Wang. "Prediction of Three-Dimensional Structure of PPARγ Transcript Variant 1 Protein". En Lecture Notes in Electrical Engineering, 2813–19. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7618-0_355.
Texto completoVilla, E., A. Dugani, L. Cammellini, P. Buttafuoco, A. Grottola, I. Ferretti, A. Ferrari y F. Manenti. "Prevalence of Wild-Type and Variant Transcripts of Liver Estrogen Receptors in Chronic Liver Disease". En New Trends in Hepatology, 197–203. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0357-9_22.
Texto completoMottaz, Anaïs, Emilie Pasche, Pierre-André Michel, Luc Mottin, Douglas Teodoro y Patrick Ruch. "Designing an Optimal Expansion Method to Improve the Recall of a Genomic Variant Curation-Support Service". En Studies in Health Technology and Informatics. IOS Press, 2022. http://dx.doi.org/10.3233/shti220603.
Texto completoSoileau, Jeanne Pitre. "Running and Imaginative Games". En What the Children Said, 214–47. University Press of Mississippi, 2021. http://dx.doi.org/10.14325/mississippi/9781496835734.003.0007.
Texto completoEndo, Shiho, Kenta Motomura, Masakazu Tsuhako, Yuki Kakazu, Morikazu Nakamura y Joji M. Otaki. "Search for Human-Specific Proteins Based on Availability Scores of Short Constituent Sequences: Identification of a WRWSH Protein in Human Testis". En Computational Biology and Chemistry. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89653.
Texto completoColombo, Mara, Paolo Radice y Miguel de la Hoya. "Functional evidence (I) transcripts and RNA-splicing outline". En Clinical DNA Variant Interpretation, 121–44. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-820519-8.00004-1.
Texto completoLucchesi, John C. "Epigenetic chromatin changes and the transcription cycle". En Epigenetics, Nuclear Organization & Gene Function, 57–68. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198831204.003.0005.
Texto completo"Le multilinguisme comme caractéristique et défi de la littérature au Luxembourg". En Vielfalt der Sprachen - Varianz der Perspektiven, 107–42. transcript-Verlag, 2013. http://dx.doi.org/10.14361/transcript.9783839420300.107.
Texto completo"Schreiben in mehr als einer Sprache". En Vielfalt der Sprachen - Varianz der Perspektiven, 143–66. transcript-Verlag, 2013. http://dx.doi.org/10.14361/transcript.9783839420300.143.
Texto completoActas de conferencias sobre el tema "Transcript variants"
Hoff, Andreas M., Sen Zhao, Bjarne Johannessen y Rolf I. Skotheim. "Abstract 2700: Transcriptome analyses reveal fusion transcripts and transcript variants that are recurrent across sample series of testicular germ cell tumors". En 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.am2016-2700.
Texto completoAzmi, Muhammad Bilal. "In Silico Basis to Understand the Molecular Interaction of Human NNATGene With Therapeutic Compounds of Anorexia Nervosa". En INTERNATIONAL CONFERENCE ON BIOLOGICAL RESEARCH AND APPLIED SCIENCE. Jinnah University for Women, Karachi,Pakistan, 2022. http://dx.doi.org/10.37962/ibras/2022/1-2.
Texto completoCaswell, Jennifer L., Scott Huntsman, Donglei Hu y Elad Ziv. "Abstract P2-03-13: Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors". En Thirty-Seventh Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 9-13, 2014; San Antonio, TX. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.sabcs14-p2-03-13.
Texto completoShurr, AYL, C. Maurer, IG Turbin, M. Bernabeu-Herrero, M. Aldred, D. Patel y CL Shovlin. "P112 Addressing the problem of variants of uncertain significance in genetic diagnosis of vascular pulmonary disease: a role for transcript expression in blood monocytes?" En British Thoracic Society Winter Meeting 2019, QEII Centre, Broad Sanctuary, Westminster, London SW1P 3EE, 4 to 6 December 2019, Programme and Abstracts. BMJ Publishing Group Ltd and British Thoracic Society, 2019. http://dx.doi.org/10.1136/thorax-2019-btsabstracts2019.255.
Texto completoStanoszek, Lauren, Thomas Blomquist, Erin L. Crawford, Bradly Austermiller, Casey Spitzer, Paige FS Willey y James C. Willey. "Abstract 2232: Effectiveness evaluation of an in vitro nucleic acid amplification test for quantification of BCR-ABL fusion transcript variants in human whole blood". En Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-2232.
Texto completoBlanchard, Anne AA, Xiuli Ma, Teresa Zelinski, Jiuyong Xie, Steven Cooper y Yvonne Myal. "Abstract 751: Identification of variant claudin 1 transcripts in human breast tumors." En Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-751.
Texto completoSeidel, MF, MP Junier y H. Vetter. "THU0028 Different variants of tnf-alpha mrna transcripts are expressed in rats with collagen-induced arthritis". En Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.825.
Texto completoFagan-Solis, Katerina D., David A. McDonald, Lynnelle W. Thorpe y Jodie M. Fleming. "Abstract 1193: LSR transcript variant iota drives nuclear localization and altered transcriptome regulation in breast cancer". En Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1193.
Texto completoSarver, Nava y George A. Ricca. "SUSTAINED EXPRESSION OF FULL LENGTH AND VARIANT RECOMBINANT FACTOR VIII IN GENETICALLY ENGINEERED CELLS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643875.
Texto completoHoff, Andreas M., Torfinn Nome, Anne Cathrine Bakken, Torleiv O. Rognum, Arild Nesbakken y Rolf I. Skotheim. "Abstract 2235: High frequency of fusion transcripts involving TCF7L2 in colorectal cancer: Novel fusion partner and splice variants". En Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-2235.
Texto completoInformes sobre el tema "Transcript variants"
Dubcovsky, Jorge, Tzion Fahima y Ann Blechl. Molecular characterization and deployment of the high-temperature adult plant stripe rust resistance gene Yr36 from wheat. United States Department of Agriculture, noviembre de 2013. http://dx.doi.org/10.32747/2013.7699860.bard.
Texto completoRafaeli, Ada y Russell Jurenka. Molecular Characterization of PBAN G-protein Coupled Receptors in Moth Pest Species: Design of Antagonists. United States Department of Agriculture, diciembre de 2012. http://dx.doi.org/10.32747/2012.7593390.bard.
Texto completo