Výsledky vyhledávání - Scott Smemo
- Zobrazuji výsledky 1 - 10 z 10
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TBX5 drives Scn5a expression to regulate cardiac conduction system function Autor David E. Arnolds, Fang Liu, John Fahrenbach, Gene Kim, Kurt J. Schillinger, Scott Smemo, Elizabeth M. McNally, Marcelo A. Nóbrega, Vickas V. Patel, Ivan P. Moskowitz
Vydáno 2012Artigo -
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FTO-mediated formation of N6-hydroxymethyladenosine and N6-formyladenosine in mammalian RNA Autor Ye Fu, Guifang Jia, Xueqin Pang, Richard N. Wang, Xiao Wang, Charles J. Li, Scott Smemo, Qing Dai, Kathleen A. Bailey, Marcelo A. Nóbrega, Keli Han, Qiang Cui, Chuan He
Vydáno 2013Artigo -
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Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1polymorphisms Autor Suzanne E. Wahrle, Aarti R. Shah, Anne M. Fagan, Scott Smemo, John SK Kauwe, Andrew Grupe, Anthony L. Hinrichs, Kevin H. Mayo, Hong Jiang, Leon J. Thal, Alison Goate, David M. Holtzman
Vydáno 2007Artigo -
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Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function Autor Tao Shen, Ivy Aneas, Noboru J. Sakabe, Ralf J. Dirschinger, Gang Wang, Scott Smemo, John M. Westlund, Hongqiang Cheng, Nancy Dalton, Yusu Gu, Cornelis J. Boogerd, Chen‐Leng Cai, Kirk L. Peterson, Ju Chen, Marcelo A. Nóbrega, Sylvia Μ. Evans
Vydáno 2011Artigo -
6
A common genetic variant within SCN10A modulates cardiac SCN5A expression Autor Malou van den Boogaard, Scott Smemo, Ozanna Burnicka-Turek, David E. Arnolds, Harmen J.G. van de Werken, Petra Klous, David McKean, Jochen D. Muehlschlegel, Julia Moosmann, Okan Toka, Xinan Yang, Tamara T. Koopmann, Michiel Adriaens, Connie R. Bezzina, Wouter de Laat, Christine E. Seidman, J.G. Seidman, Vincent M. Christoffels, Marcelo A. Nóbrega, Phil Barnett, Ivan P. Moskowitz
Vydáno 2014Artigo -
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DAPK1 variants are associated with Alzheimer's disease and allele-specific expression Autor Yonghong Li, Andrew Grupe, Charles M. Rowland, Petra Nowotny, John Kauwe, Scott Smemo, Anthony L. Hinrichs, Kristina Tacey, Timothy A. Toombs, Shirley Kwok, Joseph J. Catanese, Thomas J. White, Taylor J. Maxwell, Paul Hollingworth, Richard Abraham, David C. Rubinsztein, Carol Brayne, Fabienne Wavrant‐De Vrièze, John Hardy, Michael O’Donovan, Simon Lovestone, Christopher M. Morris, Leon J. Thal, Michael J. Owen, Julie Williams, Alison Goate
Vydáno 2006Artigo -
8
Obesity-associated variants within FTO form long-range functional connections with IRX3 Autor Scott Smemo, Juan J. Tena, Kyoung-Han Kim, Eric R. Gamazon, Noboru J. Sakabe, Carlos Gómez-Marín, Ivy Aneas, Flavia L. Credidio, Débora R. Sobreira, Nora Wasserman, Ju Hee Lee, Vijitha Puviindran, Davis Tam, Michael M. Shen, Joe Eun Son, N Alizadeh Vakili, Hoon‐Ki Sung, Silvia Naranjo, Rafael D. Acemel, Miguel Manzanares, András Nagy, Nancy J. Cox, Chi-chung Hui, José Luis Gómez-Skármeta, Marcelo A. Nóbrega
Vydáno 2014Artigo -
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Association of late-onset Alzheimer's disease with genetic variation in multiple members of the <i>GAPD</i> gene family Autor Yonghong Li, Petra Nowotny, Peter Holmans, Scott Smemo, John Kauwe, Anthony L. Hinrichs, Kristina Tacey, Lisa Doil, Ryan van Luchene, Verónica García, Charles M. Rowland, Steven J. Schrodi, Diane U. Leong, Goran Gogic, Joanne Chan, Anibal Cravchik, David A. Ross, Kit Lau, Shirley Kwok, Sheng-Yung Chang, Joe Catanese, John J. Sninsky, Thomas J. White, John Hardy, John Powell, Simon Lovestone, Christopher M. Morris, Leon J. Thal, Michael J. Owen, Julie Williams, Alison Goate, Andrew Grupe
Vydáno 2004Artigo -
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A Scan of Chromosome 10 Identifies a Novel Locus Showing Strong Association with Late-Onset Alzheimer Disease Autor Andrew Grupe, Yonghong Li, Charles M. Rowland, Petra Nowotny, Anthony L. Hinrichs, Scott Smemo, John Kauwe, Taylor J. Maxwell, Sara Cherny, Lisa Doil, Kristina Tacey, Ryan van Luchene, Amanda Myers, Fabienne Wavrant‐De Vrièze, Mona Kaleem, Paul Hollingworth, Luke Jehu, Catherine Foy, Nicola Archer, Gillian Hamilton, Peter Holmans, Christopher M. Morris, Joseph J. Catanese, John J. Sninsky, Thomas J. White, John Powell, John Hardy, Michael O’Donovan, Simon Lovestone, Lesley Jones, Christopher M. Morris, Leon J. Thal, Michael J. Owen, Julie Williams, Alison Goate
Vydáno 2005Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Internal medicine
Genotype
Single-nucleotide polymorphism
Cell biology
Disease
Enhancer
Locus (genetics)
Phenotype
Transcription factor
Allele
Apolipoprotein E
Bioinformatics
Brugada syndrome
Chemistry
Embryonic stem cell
Endocrinology
Gene expression
Genetic association
Genetic linkage
Heart development
Neuroscience
SNP
ABCA1
Allele frequency
Biochemistry
Cardiomyopathy