Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Elizabeth A. O'Hare"'
Autor:
Elizabeth A. O'Hare, Xiaochun Wang, May E. Montasser, Yen-Pei C. Chang, Braxton D. Mitchell, Norann A. Zaghloul
Publikováno v:
Journal of Lipid Research, Vol 55, Iss 11, Pp 2242-2253 (2014)
Hyperlipidemia and arterial cholesterol accumulation are primary causes of cardiovascular events. Monogenic forms of hyperlipidemia and recent genome-wide association studies indicate that genetics plays an important role. Zebrafish are a useful mode
Externí odkaz:
https://doaj.org/article/6bba27102e094cd08cc2d3ba2a3f6ca8
Autor:
Erin L Cadwalader, Elizabeth D O’Hare
Publikováno v:
Annals of the Entomological Society of America. 112:71-74
Publikováno v:
Frontiers in Neuroscience, Vol 3 (2009)
Fluid reasoning is a cornerstone of human cognition, both during development and in adulthood. In spite of this, the neural mechanisms underlying the development of fluid reasoning are largely unknown. Here we provide an overview of this important co
Externí odkaz:
https://doaj.org/article/4fef85a9b7ac4366a7f3abbbecb7b069
Autor:
Elizabeth A. O'Hare, Janet D. Robishaw, Kathy Ryan, Shilpa Narina, Laura M. Yerges-Armstrong, Glenn S. Gerhard, Rongze Yang, Rebecca McFarland, Alan R. Shuldiner, Norann A. Zaghloul, Alexis Gorden, Christopher D. Still, Steve A. Farber, Meredith H. Wilson, Urmila Sreenivasan, G. Craig Wood, Carmen C. Leitch, Carole Sztalryd
Publikováno v:
Hepatology. 65:1526-1542
The transmembrane 6 superfamily member 2 (TM6SF2) loss-of-function variant rs58542926 is a genetic risk factor for nonalcoholic fatty liver disease and progression to fibrosis but is paradoxically associated with lower levels of hepatically derived t
Autor:
Norann A. Zaghloul, Alan R. Shuldiner, Laura M. Yerges-Armstrong, James A. Perry, Elizabeth A. O'Hare
Publikováno v:
Molecular Endocrinology. 30:429-445
Type 2 diabetes (T2D) has been associated with a large number of genomic loci, many of which encompass multiple genes without a definitive causal gene. This complexity has hindered efforts to clearly identify functional candidate genes and interpret
Autor:
Fred Santoni, Valerie M. Schwitzgebel, Jean-Louis Blouin, Norann A. Zaghloul, Caroline Stekelenburg, Elizabeth A. O'Hare
Publikováno v:
Diabetes. 67
Background/Introduction: Using whole exome sequencing we identified a truncating mutation in the KIAA2022 gene in a child with mental retardation and antibody-negative diabetes. The KIAA2022 gene encodes a large protein of 1516 amino acids, which has
Publikováno v:
Journal of Heredity
Next-generation sequencing (NGS) and expression technologies were utilized to investigate the genes and sequence elements in a 586 kb region of chicken chromosome 1 associated with the autosomal recessive diplopodia-1 (dp-1) mutation. This mutation s
Autor:
James A. Perry, Rebecca McFarland, Elizabeth A. O'Hare, Alicia D. Howard, Alan R. Shuldiner, Kenneth Rice, Cashell E. Jaquish, Kathleen A. Ryan, Yen Pei C. Chang, Braxton D. Mitchell, Norann A. Zaghloul, Xiaochun Wang, May E. Montasser, Michael Miller
Publikováno v:
Circulation. 138(13)
Background: Elevated levels of low-density lipoprotein cholesterol (LDL-C) are a major risk factor for cardiovascular disease via its contribution to the development and progression of atherosclerotic lesions. Although the genetic basis of LDL-C has
Autor:
Thomas Haaf, Christopher M. Ashwell, Qing Wang, Craig A. Smith, Michael E. Persia, Harry Noyes, Stefan A. Muljo, David W. Burt, Parker B. Antin, Huaijun Zhou, Martien A. M. Groenen, Anne Nitsche, Darren K. Griffin, Jonathan Wood, Darek Kedra, Paul Flicek, Sheila C. Ommeh, Denis M. Larkin, Raman Akinyanju Lawal, Mary E. Delany, Bronwen Aken, David P. Froman, Kerstin Howe, Richard P. M. A. Crooijmans, Tammy E. Steeves, Wesley C. Warren, Akira Motegi, Michael S. Neuberger, Andrea Münsterberg, Heather McCormack, Liang Sun, Matthew Dunn, Helio Pais, Jacqueline Smith, Cedric Notredame, Almas Gheyas, Alisa Sophia Schneider, Olivier Hanotte, Pablo Prieto Barja, Elizabeth A. O'Hare, Richard V. N. Davis, Pierre-François Roux, Katie E. Fowler, Rishi Nag, Likit Preeyanon, Mario Fasold, Thomas Derrien, Frédérique Pitel, Marta Farré, Alan Hart, Kalmia E. Kniel, Lel Eory, Joana Damas, Max F. Rothschild, Susan J. Lamont, Perry J. Blackshear, Damarius S. Fleming, Julien Häsler, Peter K. Kaiser, Stephen J. Kemp, Alan Archibald, S. Blair Hedges, Sandrine Lagarrigue, Igor Ulitsky, C. Titus Brown, Michael Schmid, Peter F. Stadler, Dirk-Jan de Koning, Fiona M. McCarthy, Valerie Garceau, Hans Ellegren, David A. Hume, Carl J. Schmidt, Richard Kuo, Takele T Desta, Douglas D. Rhoads, Clarissa Boschiero, Marla C. McPherson, Shane C. Burgess, Claus Steinlein, Andrew J. Oler, Paul P. Gardner, William Chow, Charmaine M. Robinson, Elizabeth M. Pritchett, Christophe Klopp, Michael N Romanov, I. Nanda, Ian C. Dunn, Sarah M. Markland, Steve Searle, David Wragg, Jana Hertel, Allen Hubbard, Ying Wang, Rebecca E. O’Connor, Michael A. Skinner, Ionas Erb, Laure Fresard, Minoru Takata, Hans H. Cheng, Derrick Coble, Matthew G. Schwartz, Amanda M. Cooksey
Publikováno v:
ResearcherID
Cytogenetic and Genome Research 145 (2015) 2
Cytogenetic and Genome Research, 145(2), 78-179
Schmid, M, Smith, J, Burt, D W, Aken, B L, Antin, P B, Archibald, A L, Ashwell, C, Blackshear, P J, Boschiero, C, Brown, C T, Burgess, S C, Cheng, H H, Chow, W, Coble, D J, Cooksey, A, Crooijmans, R P M A, Damas, J, Davis, R V N, De Koning, D, Delany, M E, Derrien, T, Desta, T T, Dunn, I C, Dunn, M, Ellegren, H, Eory, L, Erb, I, Farre, M, Fasold, M, Fleming, D, Flicek, P, Fowler, K E, Fresard, L, Froman, D P, Garceau, V, Gardner, P P, Gheyas, A A, Griffin, D K, Groenen, M A M, Haaf, T, Hanotte, O, Hart, A, Hasler, J, Hedges, S B, Hertel, J, Howe, K, Hubbard, A, Hume, D A, Kaiser, P, Kedra, D, Kemp, S, Klopp, C, Kniel, K E, Kuo, R, Lagarrigue, S, Lamont, S J, Larkin, D M, Lawal, R A, Markland, S M, Mccarthy, F, Mccormack, H A, Mcpherson, M C, Motegi, A, Muljo, S A, Munsterberg, A, Nag, R, Nanda, I, Neuberger, M, Nitsche, A, Notredame, C, Noyes, H, O''connor, R, O''hare, E A, Oler, A J, Ommeh, S C, Pais, H, Persia, M, Pitel, F, Preeyanon, L, Prieto Barja, P, Pritchett, E M, Rhoads, D D, Robinson, C M, Romanov, M N, Rothschild, M, Roux, P, Schmidt, C J, Schneider, A, Schwartz, M, Searle, S M, Skinner, M A, Smith, C A, Stadler, P F, Steeves, T E, Steinlein, C, Sun, L, Takata, M, Ulitsky, I, Wang, Q, Wang, Y, Warren, W C, Wood, J M D, Wragg, D & Zhou, H 2015, ' Third Report on Chicken Genes and Chromosomes 2015 ', Cytogenetic and Genome Research, vol. 145, no. 2, pp. 78-179 . https://doi.org/10.1159/000430927
Cytogenetic and Genome Research 145 (2015) 2
Cytogenetic and Genome Research, 145(2), 78-179
Schmid, M, Smith, J, Burt, D W, Aken, B L, Antin, P B, Archibald, A L, Ashwell, C, Blackshear, P J, Boschiero, C, Brown, C T, Burgess, S C, Cheng, H H, Chow, W, Coble, D J, Cooksey, A, Crooijmans, R P M A, Damas, J, Davis, R V N, De Koning, D, Delany, M E, Derrien, T, Desta, T T, Dunn, I C, Dunn, M, Ellegren, H, Eory, L, Erb, I, Farre, M, Fasold, M, Fleming, D, Flicek, P, Fowler, K E, Fresard, L, Froman, D P, Garceau, V, Gardner, P P, Gheyas, A A, Griffin, D K, Groenen, M A M, Haaf, T, Hanotte, O, Hart, A, Hasler, J, Hedges, S B, Hertel, J, Howe, K, Hubbard, A, Hume, D A, Kaiser, P, Kedra, D, Kemp, S, Klopp, C, Kniel, K E, Kuo, R, Lagarrigue, S, Lamont, S J, Larkin, D M, Lawal, R A, Markland, S M, Mccarthy, F, Mccormack, H A, Mcpherson, M C, Motegi, A, Muljo, S A, Munsterberg, A, Nag, R, Nanda, I, Neuberger, M, Nitsche, A, Notredame, C, Noyes, H, O''connor, R, O''hare, E A, Oler, A J, Ommeh, S C, Pais, H, Persia, M, Pitel, F, Preeyanon, L, Prieto Barja, P, Pritchett, E M, Rhoads, D D, Robinson, C M, Romanov, M N, Rothschild, M, Roux, P, Schmidt, C J, Schneider, A, Schwartz, M, Searle, S M, Skinner, M A, Smith, C A, Stadler, P F, Steeves, T E, Steinlein, C, Sun, L, Takata, M, Ulitsky, I, Wang, Q, Wang, Y, Warren, W C, Wood, J M D, Wragg, D & Zhou, H 2015, ' Third Report on Chicken Genes and Chromosomes 2015 ', Cytogenetic and Genome Research, vol. 145, no. 2, pp. 78-179 . https://doi.org/10.1159/000430927
It is now over 10 years since the first avian genome [International Chicken Genome Sequencing Consortium, 2004] and the first complete avian karyotype [Masabanda et al., 2004] were both published; however, until 2014, avian cytogenetics has focused h
Autor:
A.E. Webb, B. May, Elizabeth A. O'Hare, C.L. Gitter, Mary E. Delany, Ingrid A. Youngworth, Hans H. Cheng, Muhammet Kaya
Publikováno v:
Poultry Science
Wingless-2 (wg-2) is an autosomal recessive mutation in chicken that results in an embryonic lethal condition. Affected individuals exhibit a multisystem syndrome characterized by absent wings, truncated legs, and craniofacial, kidney, and feather ma