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L Beales

Showing results (121-130 of 194) with videos related to

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Biomolecules|December 24, 2021
Gut Metabolite Trimethylamine N-Oxide Protects INS-1 β-Cell and Rat Islet Function under Diabetic Glucolipotoxic ConditionsEmily S Krueger, Joseph L Beales, Kacie B Russon, et al.
Nature|December 6, 2005
Dissection of epistasis in oligogenic Bardet-Biedl syndromeJose L Badano, Carmen C Leitch, Stephen J Ansley, et al.
Nature Genetics|August 24, 2004
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouseHeather M Kulaga, Carmen C Leitch, Erica R Eichers, et al.
European Journal of Medical Genetics|September 6, 2017
Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literatureDinu Antony, Narayanan Nampoory, Chiara Bacchelli, et al.
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.
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.
Nature Communications|November 7, 2014
Ciliary dysfunction impairs beta-cell insulin secretion and promotes development of type 2 diabetes in rodentsJantje M Gerdes, Sonia Christou-Savina, Yan Xiong, et al.
Journal of the American Society of Nephrology : JASN|September 24, 2016
Risk Factors for Severe Renal Disease in Bardet-Biedl SyndromeElizabeth Forsythe, Kathryn Sparks, Sunayna Best, 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.
Plos Genetics|March 17, 2017
COLEC10 is mutated in 3MC patients and regulates early craniofacial developmentMustafa M Munye, Anna Diaz-Font, Louise Ocaka, et al.
Pageof 20

Showing results (121-130 of 194) with videos related to

Sort By:
Pageof 20
Biomolecules|December 24, 2021
Gut Metabolite Trimethylamine N-Oxide Protects INS-1 β-Cell and Rat Islet Function under Diabetic Glucolipotoxic ConditionsEmily S Krueger, Joseph L Beales, Kacie B Russon, et al.
Nature|December 6, 2005
Dissection of epistasis in oligogenic Bardet-Biedl syndromeJose L Badano, Carmen C Leitch, Stephen J Ansley, et al.
Nature Genetics|August 24, 2004
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouseHeather M Kulaga, Carmen C Leitch, Erica R Eichers, et al.
European Journal of Medical Genetics|September 6, 2017
Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literatureDinu Antony, Narayanan Nampoory, Chiara Bacchelli, et al.
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.
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.
Nature Communications|November 7, 2014
Ciliary dysfunction impairs beta-cell insulin secretion and promotes development of type 2 diabetes in rodentsJantje M Gerdes, Sonia Christou-Savina, Yan Xiong, et al.
Journal of the American Society of Nephrology : JASN|September 24, 2016
Risk Factors for Severe Renal Disease in Bardet-Biedl SyndromeElizabeth Forsythe, Kathryn Sparks, Sunayna Best, 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.
Plos Genetics|March 17, 2017
COLEC10 is mutated in 3MC patients and regulates early craniofacial developmentMustafa M Munye, Anna Diaz-Font, Louise Ocaka, et al.
Pageof 20