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Michael A Simpson

Showing results (141-150 of 168) with videos related to

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Plos Genetics|February 12, 2015
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genesNatalie J Prescott, Benjamin Lehne, Kristina Stone, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 4, 2022
Comparative Genetic Analysis of Psoriatic Arthritis and Psoriasis for the Discovery of Genetic Risk Factors and Risk Prediction ModelingMehreen Soomro, Michael Stadler, Nick Dand, et al.
Nature Genetics|September 24, 2013
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical developmentSilvia Cappello, Mary J Gray, Caroline Badouel, et al.
The European Respiratory Journal|January 19, 2019
The ADAMTS13-VWF axis is dysregulated in chronic thromboembolic pulmonary hypertensionMichael Newnham, Kieron South, Marta Bleda, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Science Signaling|August 21, 2014
The ErbB4 CYT2 variant protects EGFR from ligand-induced degradation to enhance cancer cell motilityTai Kiuchi, Elena Ortiz-Zapater, James Monypenny, et al.
American Journal of Human Genetics|April 16, 2019
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-DyskinesiaKathleen M Gorman, Esther Meyer, Detelina Grozeva, et al.
The Journal of Investigative Dermatology|June 22, 2019
Semidominant GPNMB Mutations in Amyloidosis Cutis DyschromicaAlexandros Onoufriadis, Chao-Kai Hsu, Cindy R Eide, et al.
American Journal of Human Genetics|July 30, 2013
Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesiaDaniel J Moore, Alexandros Onoufriadis, Amelia Shoemark, et al.
JAMA Dermatology|February 12, 2025
Epistasis of ERAP1 With 4 Major Histocompatibility Complex Class I Alleles in Frontal Fibrosing Alopecia: A Genome-Wide Association Study Meta-AnalysisTuntas Rayinda, Nick Dand, Sheila M McSweeney, et al.
Pageof 17

Showing results (141-150 of 168) with videos related to

Sort By:
Pageof 17
Plos Genetics|February 12, 2015
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genesNatalie J Prescott, Benjamin Lehne, Kristina Stone, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 4, 2022
Comparative Genetic Analysis of Psoriatic Arthritis and Psoriasis for the Discovery of Genetic Risk Factors and Risk Prediction ModelingMehreen Soomro, Michael Stadler, Nick Dand, et al.
Nature Genetics|September 24, 2013
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical developmentSilvia Cappello, Mary J Gray, Caroline Badouel, et al.
The European Respiratory Journal|January 19, 2019
The ADAMTS13-VWF axis is dysregulated in chronic thromboembolic pulmonary hypertensionMichael Newnham, Kieron South, Marta Bleda, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Science Signaling|August 21, 2014
The ErbB4 CYT2 variant protects EGFR from ligand-induced degradation to enhance cancer cell motilityTai Kiuchi, Elena Ortiz-Zapater, James Monypenny, et al.
American Journal of Human Genetics|April 16, 2019
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-DyskinesiaKathleen M Gorman, Esther Meyer, Detelina Grozeva, et al.
The Journal of Investigative Dermatology|June 22, 2019
Semidominant GPNMB Mutations in Amyloidosis Cutis DyschromicaAlexandros Onoufriadis, Chao-Kai Hsu, Cindy R Eide, et al.
American Journal of Human Genetics|July 30, 2013
Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesiaDaniel J Moore, Alexandros Onoufriadis, Amelia Shoemark, et al.
JAMA Dermatology|February 12, 2025
Epistasis of ERAP1 With 4 Major Histocompatibility Complex Class I Alleles in Frontal Fibrosing Alopecia: A Genome-Wide Association Study Meta-AnalysisTuntas Rayinda, Nick Dand, Sheila M McSweeney, et al.
Pageof 17