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Journal of Lipid Research
|
February 8, 2014
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias
Christopher T Johansen, Joseph B Dubé, Melissa N Loyzer, et al.
CJC Open
|
June 25, 2021
Evaluating Polygenic Risk Scores in "Lone" Atrial Fibrillation
Julieta Lazarte, Jacqueline S Dron, Adam D McIntyre, et al.
Circulation. Genomic and Precision Medicine
|
February 1, 2021
Role of Common Genetic Variation in Lone Atrial Fibrillation
Julieta Lazarte, Jacqueline S Dron, Adam D McIntyre, et al.
BMC Health Services Research
|
August 5, 2017
Health service changes to address diabetes in pregnancy in a complex setting: perspectives of health professionals
R Kirkham, J A Boyle, C Whitbread, et al.
Journal of Cellular Physiology
|
October 1, 1989
Cytotoxicity of gelonin and its conjugates with antibodies is determined by the extent of their endocytosis
V S Goldmacher, C F Scott, J M Lambert, et al.
Journal of Clinical Lipidology
|
November 24, 2018
Severe hypertriglyceridemia is primarily polygenic
Jacqueline S Dron, Jian Wang, Henian Cao, et al.
Journal of Clinical Lipidology
|
December 11, 2020
Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia
Praneet K Gill, Jacqueline S Dron, Allison A Dilliott, et al.
Journal of Lipid Research
|
September 10, 2017
The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation
Meenakshi Sundaram, Kaitlin R Curtis, Mohsen Amir Alipour, et al.
Canadian Journal of Diabetes
|
October 4, 2020
Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the Young
Amanda J Berberich, Jian Wang, Henian Cao, et al.
Journal of Medical Genetics
|
March 21, 1998
P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population
A Gilfillan, J P Warner, J M Kirk, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 284) with videos related to
Sort By:
Page
of 29
Journal of Lipid Research
|
February 8, 2014
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias
Christopher T Johansen, Joseph B Dubé, Melissa N Loyzer, et al.
CJC Open
|
June 25, 2021
Evaluating Polygenic Risk Scores in "Lone" Atrial Fibrillation
Julieta Lazarte, Jacqueline S Dron, Adam D McIntyre, et al.
Circulation. Genomic and Precision Medicine
|
February 1, 2021
Role of Common Genetic Variation in Lone Atrial Fibrillation
Julieta Lazarte, Jacqueline S Dron, Adam D McIntyre, et al.
BMC Health Services Research
|
August 5, 2017
Health service changes to address diabetes in pregnancy in a complex setting: perspectives of health professionals
R Kirkham, J A Boyle, C Whitbread, et al.
Journal of Cellular Physiology
|
October 1, 1989
Cytotoxicity of gelonin and its conjugates with antibodies is determined by the extent of their endocytosis
V S Goldmacher, C F Scott, J M Lambert, et al.
Journal of Clinical Lipidology
|
November 24, 2018
Severe hypertriglyceridemia is primarily polygenic
Jacqueline S Dron, Jian Wang, Henian Cao, et al.
Journal of Clinical Lipidology
|
December 11, 2020
Ancestry-specific profiles of genetic determinants of severe hypertriglyceridemia
Praneet K Gill, Jacqueline S Dron, Allison A Dilliott, et al.
Journal of Lipid Research
|
September 10, 2017
The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation
Meenakshi Sundaram, Kaitlin R Curtis, Mohsen Amir Alipour, et al.
Canadian Journal of Diabetes
|
October 4, 2020
Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the Young
Amanda J Berberich, Jian Wang, Henian Cao, et al.
Journal of Medical Genetics
|
March 21, 1998
P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population
A Gilfillan, J P Warner, J M Kirk, et al.
Page
of 29