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Human Molecular Genetics
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April 19, 2013
Glucocorticoid receptor is required for foetal heart maturation
Eva A Rog-Zielinska, Adrian Thomson, Christopher J Kenyon, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
February 25, 2009
Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development
Alexander Ermakov, Jonathan L Stevens, Elaine Whitehill, et al.
The Journal of Biological Chemistry
|
June 4, 2002
Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural family
Kirsty S Hewitson, Luke A McNeill, Madeline V Riordan, et al.
Scientific Reports
|
July 12, 2018
A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity
Iain M Dykes, Dorota Szumska, Linta Kuncheria, et al.
Elife
|
July 7, 2015
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
Romaric Bouveret, Ashley J Waardenberg, Nicole Schonrock, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 22, 2015
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect
Lisa C A D'Alessandro, Saeed Al Turki, Ashok Kumar Manickaraj, et al.
Plos One
|
March 4, 2014
Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects
Emilie A Bard-Chapeau, Dorota Szumska, Bindya Jacob, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 28, 2012
Nprl3 is required for normal development of the cardiovascular system
Monika S Kowalczyk, Jim R Hughes, Christian Babbs, et al.
Nature Genetics
|
May 3, 2011
Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes
Erik Engelen, Umut Akinci, Jan Christian Bryne, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 9, 2006
A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice
Leah C Solberg, William Valdar, Dominique Gauguier, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 97) with videos related to
Sort By:
Page
of 10
Human Molecular Genetics
|
April 19, 2013
Glucocorticoid receptor is required for foetal heart maturation
Eva A Rog-Zielinska, Adrian Thomson, Christopher J Kenyon, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
February 25, 2009
Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development
Alexander Ermakov, Jonathan L Stevens, Elaine Whitehill, et al.
The Journal of Biological Chemistry
|
June 4, 2002
Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural family
Kirsty S Hewitson, Luke A McNeill, Madeline V Riordan, et al.
Scientific Reports
|
July 12, 2018
A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity
Iain M Dykes, Dorota Szumska, Linta Kuncheria, et al.
Elife
|
July 7, 2015
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
Romaric Bouveret, Ashley J Waardenberg, Nicole Schonrock, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 22, 2015
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect
Lisa C A D'Alessandro, Saeed Al Turki, Ashok Kumar Manickaraj, et al.
Plos One
|
March 4, 2014
Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects
Emilie A Bard-Chapeau, Dorota Szumska, Bindya Jacob, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 28, 2012
Nprl3 is required for normal development of the cardiovascular system
Monika S Kowalczyk, Jim R Hughes, Christian Babbs, et al.
Nature Genetics
|
May 3, 2011
Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes
Erik Engelen, Umut Akinci, Jan Christian Bryne, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 9, 2006
A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice
Leah C Solberg, William Valdar, Dominique Gauguier, et al.
Page
of 10