Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Karrie D. Dudek"'
Autor:
Anna B Osipovich, Karrie D Dudek, Linh T Trinh, Lily H Kim, Shristi Shrestha, Jean-Philippe Cartailler, Mark A Magnuson
Publikováno v:
PLoS Genetics, Vol 19, Iss 5, p e1010729 (2023)
Repressive KRAB domain-containing zinc-finger proteins (KRAB-ZFPs) are abundant in mammalian genomes and contribute both to the silencing of transposable elements (TEs) and to the regulation of developmental stage- and cell type-specific gene express
Externí odkaz:
https://doaj.org/article/958a757243fb446dbbf604462b38535d
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 11, Iss 11 (2021)
Abstract Insm1Neurod1Pax6Insm1Neurod1Pax6Insm1Neurod1Pax6Syt14Snap25Syt14Insm1Pax6Snap25Insm1Neurod1Pax6
Externí odkaz:
https://doaj.org/article/97e3448da97c4d6cbd1e0a4a3fc6f1fc
Autor:
Hui-Young Lee, Hye Rim Jang, Hui Li, Varman T. Samuel, Karrie D. Dudek, Anna B. Osipovich, Mark A. Magnuson, Jeffrey Sklar, Gerald I. Shulman
Publikováno v:
Proceedings of the National Academy of Sciences. 119
Single-nucleotide polymorphisms in the human juxtaposed with another zinc finger protein 1 ( JAZF1 ) gene have repeatedly been associated with both type 2 diabetes (T2D) and height in multiple genome-wide association studies (GWAS); however, the mech
Autor:
Hui-Young, Lee, Hye Rim, Jang, Hui, Li, Varman T, Samuel, Karrie D, Dudek, Anna B, Osipovich, Mark A, Magnuson, Jeffrey, Sklar, Gerald I, Shulman
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 119(49)
Single-nucleotide polymorphisms in the human juxtaposed with another zinc finger protein 1 (
Autor:
Karrie D. Dudek, Anna B. Osipovich, Jennifer S. Stancill, Mark A. Magnuson, Jean-Philippe Cartailler
Publikováno v:
Diabetes
A sustained increase in intracellular Ca2+ concentration (referred to hereafter as excitotoxicity), brought on by chronic metabolic stress, may contribute to pancreatic β-cell failure. To determine the additive effects of excitotoxicity and overnutr
Publikováno v:
G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 11, Iss 11 (2021)
G3: Genes, Genomes, Genetics, Vol 11, Iss 11 (2021)
Insm1, Neurod1, and Pax6 are essential for the formation and function of pancreatic endocrine cells. Here, we report comparative immunohistochemical, transcriptomic, functional enrichment, and RNA splicing analyses of these genes using gene knock-out
Autor:
Karrie D. Dudek, Christian J. Stoeckert, Jean-Philippe Cartailler, Leah Potter Case, Hannah W. Clayton, Anna B. Osipovich, Guoqiang Gu, Emily Greenfest-Allen, Eun-Young Choi, Mark A. Magnuson, Austin Chapman, Elisabetta Manduchi
Publikováno v:
Development. 148
To gain a deeper understanding of pancreatic β-cell development, we used iterative weighted gene correlation network analysis to calculate a gene co-expression network (GCN) from 11 temporally and genetically defined murine cell populations. The GCN
Autor:
Anna B, Osipovich, Karrie D, Dudek, Emily, Greenfest-Allen, Jean-Philippe, Cartailler, Elisabetta, Manduchi, Leah, Potter Case, Eunyoung, Choi, Austin G, Chapman, Hannah W, Clayton, Guoqiang, Gu, Christian J, Stoeckert, Mark A, Magnuson
Publikováno v:
Development
To gain a deeper understanding of pancreatic β-cell development, we used iterative weighted gene correlation network analysis to calculate a gene co-expression network (GCN) from 11 temporally and genetically defined murine cell populations. The GCN
Autor:
Vittorio Maglione, M. Diana Neely, Timothy Halbesma, Alba Di Pardo, Preethi Umashanker, Hunter K. Holt, Nicole M. Fisher, Terry Jo Bichell, Gunnar F. Kwakye, Emma M. Bradley, Miles R. Bryan, Roger J. Colbran, Alexander P. Osmand, Kyle J. Horning, K. Grace Tipps, Michael Aschner, Karrie D. Dudek, Michael A. Uhouse, Andrew D. Stubbs, Aaron B. Bowman, Andrew M. Tidball, Michal Wegrzynowicz
Publikováno v:
Biochimica et biophysica acta. Molecular basis of disease. 1863(6)
Huntington's disease (HD) is caused by a mutation in the huntingtin gene (HTT), resulting in profound striatal neurodegeneration through an unknown mechanism. Perturbations in the urea cycle have been reported in HD models and in HD patient blood and