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R Beier

Showing results (181-190 of 236) with videos related to

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Plos One|December 24, 2010
A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic developmentBryan C Bjork, Yuko Fujiwara, Shannon W Davis, et al.
Nature Genetics|January 31, 2002
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesisBruce J Herron, Weining Lu, Cherie Rao, et al.
Plos Genetics|August 26, 2025
A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defectsGist H Farr, Whitaker Reid, Eva H Hasegawa, et al.
Genomics|March 24, 1999
A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouseK P Brady, H Dushkin, D Förnzler, et al.
Nature Genetics|October 1, 1995
Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J miceG T De Sanctis, M Merchant, D R Beier, et al.
Genomics|September 1, 1994
The genes encoding alpha 2(IX) collagen (COL9A2) map to human chromosome 1p32.3-p33 and mouse chromosome 4M L Warman, M T McCarthy, M Perälä, et al.
Development (Cambridge, England)|August 20, 2003
A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutationCherie Rao, Dorothee Foernzler, Stacie K Loftus, et al.
Human Molecular Genetics|January 22, 2005
A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 miceBruce J Herron, Cherie Rao, Shanming Liu, et al.
Growth Factors (Chur, Switzerland)|January 1, 1994
Isolation of a receptor tyrosine kinase (DTK) from embryonic stem cells: structure, genetic mapping and analysis of expressionP S Crosier, P M Lewis, L R Hall, et al.
Journal of Muscle Research and Cell Motility|September 21, 2022
Mammalian organ regeneration in spiny miceDaryl M Okamura, Elizabeth D Nguyen, Sarah J Collins, et al.
Pageof 24

Showing results (181-190 of 236) with videos related to

Sort By:
Pageof 24
Plos One|December 24, 2010
A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic developmentBryan C Bjork, Yuko Fujiwara, Shannon W Davis, et al.
Nature Genetics|January 31, 2002
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesisBruce J Herron, Weining Lu, Cherie Rao, et al.
Plos Genetics|August 26, 2025
A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defectsGist H Farr, Whitaker Reid, Eva H Hasegawa, et al.
Genomics|March 24, 1999
A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouseK P Brady, H Dushkin, D Förnzler, et al.
Nature Genetics|October 1, 1995
Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J miceG T De Sanctis, M Merchant, D R Beier, et al.
Genomics|September 1, 1994
The genes encoding alpha 2(IX) collagen (COL9A2) map to human chromosome 1p32.3-p33 and mouse chromosome 4M L Warman, M T McCarthy, M Perälä, et al.
Development (Cambridge, England)|August 20, 2003
A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutationCherie Rao, Dorothee Foernzler, Stacie K Loftus, et al.
Human Molecular Genetics|January 22, 2005
A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 miceBruce J Herron, Cherie Rao, Shanming Liu, et al.
Growth Factors (Chur, Switzerland)|January 1, 1994
Isolation of a receptor tyrosine kinase (DTK) from embryonic stem cells: structure, genetic mapping and analysis of expressionP S Crosier, P M Lewis, L R Hall, et al.
Journal of Muscle Research and Cell Motility|September 21, 2022
Mammalian organ regeneration in spiny miceDaryl M Okamura, Elizabeth D Nguyen, Sarah J Collins, et al.
Pageof 24