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Michael A Simpson

Showing results (111-120 of 168) with videos related to

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Nature Communications|February 8, 2022
Genome-wide association meta-analysis identifies 29 new acne susceptibility lociBrittany L Mitchell, Jake R Saklatvala, Nick Dand, et al.
Nature Communications|June 14, 2014
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgarisAlexander A Navarini, Michael A Simpson, Michael Weale, et al.
American Journal of Human Genetics|May 14, 2011
Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomaliesLaura Southgate, Rajiv D Machado, Katie M Snape, et al.
Human Mutation|August 6, 2016
Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic ParaplegiaGaurav V Harlalka, Meriel E McEntagart, Neerja Gupta, et al.
Nature Communications|December 14, 2018
Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acneChristos Petridis, Alexander A Navarini, Nick Dand, et al.
Annals of the Rheumatic Diseases|August 20, 2017
Cross-phenotype association mapping of the MHC identifies genetic variants that differentiate psoriatic arthritis from psoriasisJohn Bowes, James Ashcroft, Nick Dand, et al.
American Journal of Human Genetics|May 6, 2014
AP1S3 mutations are associated with pustular psoriasis and impaired Toll-like receptor 3 traffickingNiovi Setta-Kaffetzi, Michael A Simpson, Alexander A Navarini, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
The Journal of Allergy and Clinical Immunology|December 31, 2013
Genetic variation in schlafen genes in a patient with a recapitulation of the murine Elektra phenotypeMike Recher, Marja-Liisa Karjalainen-Lindsberg, Mikael Lindlöf, et al.
Pageof 17

Showing results (111-120 of 168) with videos related to

Sort By:
Pageof 17
Nature Communications|February 8, 2022
Genome-wide association meta-analysis identifies 29 new acne susceptibility lociBrittany L Mitchell, Jake R Saklatvala, Nick Dand, et al.
Nature Communications|June 14, 2014
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgarisAlexander A Navarini, Michael A Simpson, Michael Weale, et al.
American Journal of Human Genetics|May 14, 2011
Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomaliesLaura Southgate, Rajiv D Machado, Katie M Snape, et al.
Human Mutation|August 6, 2016
Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic ParaplegiaGaurav V Harlalka, Meriel E McEntagart, Neerja Gupta, et al.
Nature Communications|December 14, 2018
Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acneChristos Petridis, Alexander A Navarini, Nick Dand, et al.
Annals of the Rheumatic Diseases|August 20, 2017
Cross-phenotype association mapping of the MHC identifies genetic variants that differentiate psoriatic arthritis from psoriasisJohn Bowes, James Ashcroft, Nick Dand, et al.
American Journal of Human Genetics|May 6, 2014
AP1S3 mutations are associated with pustular psoriasis and impaired Toll-like receptor 3 traffickingNiovi Setta-Kaffetzi, Michael A Simpson, Alexander A Navarini, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
The Journal of Allergy and Clinical Immunology|December 31, 2013
Genetic variation in schlafen genes in a patient with a recapitulation of the murine Elektra phenotypeMike Recher, Marja-Liisa Karjalainen-Lindsberg, Mikael Lindlöf, et al.
Pageof 17