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Michael E March

Showing results (41-50 of 54) with videos related to

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Nature Communications|March 31, 2025
Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitisMeritxell Oliva, Mrinal K Sarkar, Michael E March, et al.
Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.
Nature Communications|September 29, 2016
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing geneGijs van Ingen, Jin Li, André Goedegebure, et al.
Nature Medicine|July 3, 2019
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorDong Li, Michael E March, Alvaro Gutierrez-Uzquiza, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 29, 2022
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic AnalysisJin Li, Yun R Li, Joseph T Glessner, et al.
American Journal of Human Genetics|June 18, 2021
Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylationDaniel L Polla, Andrew C Edmondson, Sandrine Duvet, et al.
Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.
JCI Insight|May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibitionSarah E Sheppard, Michael E March, Christoph Seiler, et al.
Nature Genetics|November 19, 2013
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbationsKlaus Bønnelykke, Patrick Sleiman, Kasper Nielsen, et al.
Science Advances|May 13, 2021
Pathogenic variants in <i>SMARCA5</i>, a chromatin remodeler, cause a range of syndromic neurodevelopmental featuresDong Li, Qin Wang, Naihua N Gong, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Nature Communications|March 31, 2025
Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitisMeritxell Oliva, Mrinal K Sarkar, Michael E March, et al.
Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.
Nature Communications|September 29, 2016
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing geneGijs van Ingen, Jin Li, André Goedegebure, et al.
Nature Medicine|July 3, 2019
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorDong Li, Michael E March, Alvaro Gutierrez-Uzquiza, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 29, 2022
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic AnalysisJin Li, Yun R Li, Joseph T Glessner, et al.
American Journal of Human Genetics|June 18, 2021
Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylationDaniel L Polla, Andrew C Edmondson, Sandrine Duvet, et al.
Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.
JCI Insight|May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibitionSarah E Sheppard, Michael E March, Christoph Seiler, et al.
Nature Genetics|November 19, 2013
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbationsKlaus Bønnelykke, Patrick Sleiman, Kasper Nielsen, et al.
Science Advances|May 13, 2021
Pathogenic variants in <i>SMARCA5</i>, a chromatin remodeler, cause a range of syndromic neurodevelopmental featuresDong Li, Qin Wang, Naihua N Gong, et al.
Pageof 6