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Hepatology Research : the Official Journal of the Japan Society of Hepatology
|
October 29, 2020
Single nucleus transcriptomics data integration recapitulates the major cell types in human liver
Klev Diamanti, Juan Salvador Inda Díaz, Amanda Raine, et al.
Omics : a Journal of Integrative Biology
|
September 14, 2021
The Thioesterase <i>ACOT1</i> as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver
Marco Cavalli, Klev Diamanti, Yonglong Dang, et al.
Investigative Ophthalmology & Visual Science
|
July 29, 2003
Expression and localization of bestrophin during normal mouse development
Benjamin Bakall, Lihua Y Marmorstein, George Hoppe, et al.
Epigenetics
|
March 12, 2009
Histone H3 lysine 27 trimethylation in adult differentiated colon associated to cancer DNA hypermethylation
Alvaro Rada-Iglesias, Stefan Enroth, Robin Andersson, et al.
Nature Medicine
|
September 11, 2019
Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease
Torgny Karlsson, Mathias Rask-Andersen, Gang Pan, et al.
Clinical Pharmacology and Therapeutics
|
August 9, 2005
Functional role of P-glycoprotein in the human blood-placental barrier
Melissa Mölsä, Tuija Heikkinen, Jukka Hakkola, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 12, 2005
Expression of bestrophin-1, the product of the VMD2 gene, modulates voltage-dependent Ca2+ channels in retinal pigment epithelial cells
Rita Rosenthal, Benjamin Bakall, Tyson Kinnick, et al.
Nucleic Acids Research
|
September 15, 2016
Maps of context-dependent putative regulatory regions and genomic signal interactions
Klev Diamanti, Husen M Umer, Marcin Kruczyk, et al.
Genome Research
|
January 31, 2008
Whole-genome maps of USF1 and USF2 binding and histone H3 acetylation reveal new aspects of promoter structure and candidate genes for common human disorders
Alvaro Rada-Iglesias, Adam Ameur, Philipp Kapranov, et al.
Human Genetics
|
April 6, 2002
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism
Bodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson, et al.
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of 8
Search research articles
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Showing results (31-40 of 80) with videos related to
Sort By:
Page
of 8
Hepatology Research : the Official Journal of the Japan Society of Hepatology
|
October 29, 2020
Single nucleus transcriptomics data integration recapitulates the major cell types in human liver
Klev Diamanti, Juan Salvador Inda Díaz, Amanda Raine, et al.
Omics : a Journal of Integrative Biology
|
September 14, 2021
The Thioesterase <i>ACOT1</i> as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver
Marco Cavalli, Klev Diamanti, Yonglong Dang, et al.
Investigative Ophthalmology & Visual Science
|
July 29, 2003
Expression and localization of bestrophin during normal mouse development
Benjamin Bakall, Lihua Y Marmorstein, George Hoppe, et al.
Epigenetics
|
March 12, 2009
Histone H3 lysine 27 trimethylation in adult differentiated colon associated to cancer DNA hypermethylation
Alvaro Rada-Iglesias, Stefan Enroth, Robin Andersson, et al.
Nature Medicine
|
September 11, 2019
Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease
Torgny Karlsson, Mathias Rask-Andersen, Gang Pan, et al.
Clinical Pharmacology and Therapeutics
|
August 9, 2005
Functional role of P-glycoprotein in the human blood-placental barrier
Melissa Mölsä, Tuija Heikkinen, Jukka Hakkola, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 12, 2005
Expression of bestrophin-1, the product of the VMD2 gene, modulates voltage-dependent Ca2+ channels in retinal pigment epithelial cells
Rita Rosenthal, Benjamin Bakall, Tyson Kinnick, et al.
Nucleic Acids Research
|
September 15, 2016
Maps of context-dependent putative regulatory regions and genomic signal interactions
Klev Diamanti, Husen M Umer, Marcin Kruczyk, et al.
Genome Research
|
January 31, 2008
Whole-genome maps of USF1 and USF2 binding and histone H3 acetylation reveal new aspects of promoter structure and candidate genes for common human disorders
Alvaro Rada-Iglesias, Adam Ameur, Philipp Kapranov, et al.
Human Genetics
|
April 6, 2002
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidism
Bodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson, et al.
Page
of 8