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BMC Medical Genomics
|
March 27, 2009
Correlation of microRNA levels during hypoxia with predicted target mRNAs through genome-wide microarray analysis
Jennifer S Guimbellot, Stephen W Erickson, Tapan Mehta, et al.
Annals of Human Genetics
|
November 28, 2015
A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects
Ming Li, Jingyun Li, Changshuai Wei, et al.
Plos One
|
February 8, 2011
Maternal genome-wide DNA methylation patterns and congenital heart defects
Shimul Chowdhury, Stephen W Erickson, Stewart L MacLeod, et al.
British Journal of Haematology
|
November 17, 2015
A common genetic variant in 19q13·3 is associated with outcome of multiple myeloma patients treated with Total Therapy 2 and 3
Stephen W Erickson, Owen W Stephens, Shweta S Chavan, et al.
Vascular Health and Risk Management
|
May 11, 2013
Platelet function testing to predict hyporesponsiveness to clopidogrel in patients with chest pain seen in the emergency department
Rakesh K Sharma, Stephen W Erickson, Rohit Sharma, et al.
Journal of Neuromuscular Diseases
|
August 29, 2018
Bone Health and Endocrine Care of Boys with Duchenne Muscular Dystrophy: Data from the MD STARnet
David R Weber, Shiny Thomas, Stephen W Erickson, et al.
Toxicology Letters
|
August 25, 2016
Chronic exposure to trichloroethylene increases DNA methylation of the Ifng promoter in CD4<sup>+</sup> T cells
Kathleen M Gilbert, Sarah J Blossom, Stephen W Erickson, et al.
Genetic Epidemiology
|
March 4, 2014
Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression
Ming Li, Stephen W Erickson, Charlotte A Hobbs, et al.
Molecular Genetics and Metabolism
|
October 13, 2012
Associations between maternal genotypes and metabolites implicated in congenital heart defects
Shimul Chowdhury, Charlotte A Hobbs, Stewart L MacLeod, et al.
Human Genetics
|
June 5, 2014
A genetic association study detects haplotypes associated with obstructive heart defects
Ming Li, Mario A Cleves, Himel Mallick, et al.
Page
of 7
Search research articles
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Showing results (11-20 of 65) with videos related to
Sort By:
Page
of 7
BMC Medical Genomics
|
March 27, 2009
Correlation of microRNA levels during hypoxia with predicted target mRNAs through genome-wide microarray analysis
Jennifer S Guimbellot, Stephen W Erickson, Tapan Mehta, et al.
Annals of Human Genetics
|
November 28, 2015
A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects
Ming Li, Jingyun Li, Changshuai Wei, et al.
Plos One
|
February 8, 2011
Maternal genome-wide DNA methylation patterns and congenital heart defects
Shimul Chowdhury, Stephen W Erickson, Stewart L MacLeod, et al.
British Journal of Haematology
|
November 17, 2015
A common genetic variant in 19q13·3 is associated with outcome of multiple myeloma patients treated with Total Therapy 2 and 3
Stephen W Erickson, Owen W Stephens, Shweta S Chavan, et al.
Vascular Health and Risk Management
|
May 11, 2013
Platelet function testing to predict hyporesponsiveness to clopidogrel in patients with chest pain seen in the emergency department
Rakesh K Sharma, Stephen W Erickson, Rohit Sharma, et al.
Journal of Neuromuscular Diseases
|
August 29, 2018
Bone Health and Endocrine Care of Boys with Duchenne Muscular Dystrophy: Data from the MD STARnet
David R Weber, Shiny Thomas, Stephen W Erickson, et al.
Toxicology Letters
|
August 25, 2016
Chronic exposure to trichloroethylene increases DNA methylation of the Ifng promoter in CD4<sup>+</sup> T cells
Kathleen M Gilbert, Sarah J Blossom, Stephen W Erickson, et al.
Genetic Epidemiology
|
March 4, 2014
Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression
Ming Li, Stephen W Erickson, Charlotte A Hobbs, et al.
Molecular Genetics and Metabolism
|
October 13, 2012
Associations between maternal genotypes and metabolites implicated in congenital heart defects
Shimul Chowdhury, Charlotte A Hobbs, Stewart L MacLeod, et al.
Human Genetics
|
June 5, 2014
A genetic association study detects haplotypes associated with obstructive heart defects
Ming Li, Mario A Cleves, Himel Mallick, et al.
Page
of 7