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Michael A Simpson

Showing results (121-130 of 168) with videos related to

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The Journal of Clinical Investigation|July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalisSilvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.
The EMBO Journal|March 14, 2013
Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative diseaseReza Sharifi, Rosa Morra, C Denise Appel, et al.
The Journal of Investigative Dermatology|April 3, 2014
Epithelial inflammation resulting from an inherited loss-of-function mutation in EGFRPatrick Campbell, Penny E Morton, Takuya Takeichi, et al.
The Journal of Allergy and Clinical Immunology|May 27, 2026
Multi-cytokine based TWAS for seven inflammatory skin disorders identify candidate causal genes in keratinocytesHaihan Zhang, Matthew T Patrick, Mrinal K Sarkar, et al.
The Journal of Allergy and Clinical Immunology|December 23, 2018
HLA-C*06:02 genotype is a predictive biomarker of biologic treatment response in psoriasisNick Dand, Michael Duckworth, David Baudry, et al.
The Journal of Investigative Dermatology|August 5, 2017
Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with ThrombocytopeniaTakuya Takeichi, Antonio Torrelo, John Y W Lee, et al.
The Journal of Investigative Dermatology|November 12, 2021
Differences in Clinical Features and Comorbid Burden between HLA-C∗06:02 Carrier Groups in >9,000 People with PsoriasisKonstantinos Douroudis, Ravi Ramessur, Ines A Barbosa, et al.
American Journal of Human Genetics|January 31, 2012
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathyPia Ostergaard, Michael A Simpson, Antonella Mendola, et al.
The Journal of Investigative Dermatology|June 2, 2018
Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk GenesManuela Pigors, John E A Common, Xuan Fei Colin C Wong, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
Pageof 17

Showing results (121-130 of 168) with videos related to

Sort By:
Pageof 17
The Journal of Clinical Investigation|July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalisSilvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.
The EMBO Journal|March 14, 2013
Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative diseaseReza Sharifi, Rosa Morra, C Denise Appel, et al.
The Journal of Investigative Dermatology|April 3, 2014
Epithelial inflammation resulting from an inherited loss-of-function mutation in EGFRPatrick Campbell, Penny E Morton, Takuya Takeichi, et al.
The Journal of Allergy and Clinical Immunology|May 27, 2026
Multi-cytokine based TWAS for seven inflammatory skin disorders identify candidate causal genes in keratinocytesHaihan Zhang, Matthew T Patrick, Mrinal K Sarkar, et al.
The Journal of Allergy and Clinical Immunology|December 23, 2018
HLA-C*06:02 genotype is a predictive biomarker of biologic treatment response in psoriasisNick Dand, Michael Duckworth, David Baudry, et al.
The Journal of Investigative Dermatology|August 5, 2017
Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with ThrombocytopeniaTakuya Takeichi, Antonio Torrelo, John Y W Lee, et al.
The Journal of Investigative Dermatology|November 12, 2021
Differences in Clinical Features and Comorbid Burden between HLA-C∗06:02 Carrier Groups in >9,000 People with PsoriasisKonstantinos Douroudis, Ravi Ramessur, Ines A Barbosa, et al.
American Journal of Human Genetics|January 31, 2012
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathyPia Ostergaard, Michael A Simpson, Antonella Mendola, et al.
The Journal of Investigative Dermatology|June 2, 2018
Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk GenesManuela Pigors, John E A Common, Xuan Fei Colin C Wong, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
Pageof 17