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Human Molecular Genetics|July 3, 2003
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locusJose L Badano, Jun Chul Kim, Bethan E Hoskins, et al.Proceedings of the National Academy of Sciences of the United States of America|March 4, 2024
Decoupling of bird migration from the changing phenology of spring green-upEllen P Robertson, Frank A La Sorte, Jonathan D Mays, et al.Science (New York, N.Y.)|September 22, 2001
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorderN Katsanis, S J Ansley, J L Badano, et al.American Journal of Human Genetics|February 17, 2001
Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other lociP L Beales, N Katsanis, R A Lewis, et al.American Journal of Human Genetics|April 5, 2003
Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndromePhilip L Beales, Jose L Badano, Alison J Ross, et al.Nature Genetics|April 27, 2004
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progressionJun Chul Kim, Jose L Badano, Sonja Sibold, et al.Nature|October 2, 2003
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndromeStephen J Ansley, Jose L Badano, Oliver E Blacque, et al.Genes & Development|July 3, 2004
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transportOliver E Blacque, Michael J Reardon, Chunmei Li, et al.Nature Genetics|August 18, 2004
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndromeYanli Fan, Muneer A Esmail, Stephen J Ansley, et al.Pageof 3