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Darryl Y Nishimura

Showing results (21-30 of 26) with videos related to

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Nature Medicine|November 20, 2012
Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse modelCalvin S Carter, Timothy W Vogel, Qihong Zhang, et al.
American Journal of Human Genetics|April 20, 2010
Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71Darryl Y Nishimura, Lisa M Baye, Rahat Perveen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Annie P Chiang, John S Beck, Hsan-Jan Yen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2007
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityRoger E Davis, Ruth E Swiderski, Kamal Rahmouni, et al.
Nature Genetics|July 16, 2002
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeKirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
American Journal of Human Genetics|January 14, 2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
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Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Nature Medicine|November 20, 2012
Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse modelCalvin S Carter, Timothy W Vogel, Qihong Zhang, et al.
American Journal of Human Genetics|April 20, 2010
Discovery and functional analysis of a retinitis pigmentosa gene, C2ORF71Darryl Y Nishimura, Lisa M Baye, Rahat Perveen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Annie P Chiang, John S Beck, Hsan-Jan Yen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2007
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityRoger E Davis, Ruth E Swiderski, Kamal Rahmouni, et al.
Nature Genetics|July 16, 2002
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeKirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
American Journal of Human Genetics|January 14, 2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
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