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P L Beales

Showing results (11-20 of 19) with videos related to

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Osteoarthritis and Cartilage|March 30, 2019
Mechanical loading inhibits cartilage inflammatory signalling via an HDAC6 and IFT-dependent mechanism regulating primary cilia elongationS Fu, C L Thompson, A Ali, et al.
Journal of Immunological Methods|February 4, 2012
An enzyme-linked immunosorbent assay (ELISA) for quantification of human collectin 11 (CL-11, CL-K1)L Selman, M L Henriksen, J Brandt, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndromeN Katsanis, P L Beales, M O Woods, et al.
European Cells & Materials|September 21, 2017
Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signallingC L Thompson, J C Plant, A K Wann, 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.
Clinical Genetics|March 12, 2014
Genetic predictors of cardiovascular morbidity in Bardet-Biedl syndromeE Forsythe, K Sparks, B E Hoskins, et al.
Journal of Medical Genetics|October 3, 2009
Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mappingH M Harville, S Held, A Diaz-Font, et al.
Human Mutation|April 3, 2007
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Osteoarthritis and Cartilage|March 30, 2019
Mechanical loading inhibits cartilage inflammatory signalling via an HDAC6 and IFT-dependent mechanism regulating primary cilia elongationS Fu, C L Thompson, A Ali, et al.
Journal of Immunological Methods|February 4, 2012
An enzyme-linked immunosorbent assay (ELISA) for quantification of human collectin 11 (CL-11, CL-K1)L Selman, M L Henriksen, J Brandt, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndromeN Katsanis, P L Beales, M O Woods, et al.
European Cells & Materials|September 21, 2017
Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signallingC L Thompson, J C Plant, A K Wann, 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.
Clinical Genetics|March 12, 2014
Genetic predictors of cardiovascular morbidity in Bardet-Biedl syndromeE Forsythe, K Sparks, B E Hoskins, et al.
Journal of Medical Genetics|October 3, 2009
Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mappingH M Harville, S Held, A Diaz-Font, et al.
Human Mutation|April 3, 2007
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.
Pageof 2