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Val C Sheffield

Showing results (171-180 of 193) with videos related to

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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.
Visual Neuroscience|December 8, 2005
Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouseLawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
Human Genetics|October 29, 2010
Genome-wide analysis of copy number variants in age-related macular degenerationKacie J Meyer, Lea K Davis, Emily I Schindler, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Copy number variations and primary open-angle glaucomaLea K Davis, Kacie J Meyer, Emily I Schindler, et al.
Free Radical Biology & Medicine|February 8, 2020
Disulfiram causes selective hypoxic cancer cell toxicity and radio-chemo-sensitization via redox cycling of copperKelly C Falls-Hubert, Aimee L Butler, Kai Gui, 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.
BMC Genomics|June 27, 2021
Exome-based investigation of the genetic basis of human pigmentary glaucomaCarly van der Heide, Wes Goar, Kacie J Meyer, et al.
Genome Research|October 19, 2004
1274 full-open reading frames of transcripts expressed in the developing mouse nervous systemMaria F Bonaldo, Thomas B Bair, Todd E Scheetz, et al.
Pageof 20

Showing results (171-180 of 193) with videos related to

Sort By:
Pageof 20
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.
Visual Neuroscience|December 8, 2005
Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouseLawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
Human Genetics|October 29, 2010
Genome-wide analysis of copy number variants in age-related macular degenerationKacie J Meyer, Lea K Davis, Emily I Schindler, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Copy number variations and primary open-angle glaucomaLea K Davis, Kacie J Meyer, Emily I Schindler, et al.
Free Radical Biology & Medicine|February 8, 2020
Disulfiram causes selective hypoxic cancer cell toxicity and radio-chemo-sensitization via redox cycling of copperKelly C Falls-Hubert, Aimee L Butler, Kai Gui, 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.
BMC Genomics|June 27, 2021
Exome-based investigation of the genetic basis of human pigmentary glaucomaCarly van der Heide, Wes Goar, Kacie J Meyer, et al.
Genome Research|October 19, 2004
1274 full-open reading frames of transcripts expressed in the developing mouse nervous systemMaria F Bonaldo, Thomas B Bair, Todd E Scheetz, et al.
Pageof 20