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Lynn M Boyden

Showing results (1-10 of 19) with videos related to

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The Journal of Investigative Dermatology|April 17, 2017
The Molecular Revolution in Cutaneous Biology: Identification of Skin Disease GenesLynn M Boyden, Keith A Choate
Pediatric Dermatology|May 14, 2013
Capillary malformation--arteriovenous malformation syndrome: review of the literature, proposed diagnostic criteria, and recommendations for managementCharisse M Orme, Lynn M Boyden, Keith A Choate, et al.
Journal of the American Academy of Dermatology|November 20, 2012
Capillary malformation-arteriovenous malformation syndrome: identification of a family with a novel mutationLynn M Boyden, Charisse M Orme, Richard J Antaya, et al.
The New England Journal of Medicine|May 17, 2002
High bone density due to a mutation in LDL-receptor-related protein 5Lynn M Boyden, Junhao Mao, Joseph Belsky, et al.
Nature Genetics|April 15, 2008
Skint1, the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal gammadelta T cellsLynn M Boyden, Julia M Lewis, Susannah D Barbee, et al.
Cutis|September 30, 2022
Focal Palmoplantar Keratoderma and Gingival Keratosis Caused by a KRT16 MutationTheodore D Zaki, Lynn M Boyden, Erin Mathes, et al.
American Journal of Human Genetics|June 10, 2020
Mutations in ASPRV1 Cause Dominantly Inherited IchthyosisLynn M Boyden, Jing Zhou, Ronghua Hu, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2011
Skint-1 is a highly specific, unique selecting component for epidermal T cellsSusannah D Barbee, Martin J Woodward, Gleb Turchinovich, et al.
The Journal of Investigative Dermatology|November 15, 2014
Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital DysplasiaLynn M Boyden, Brittany G Craiglow, Jing Zhou, et al.
American Journal of Human Genetics|October 22, 2019
Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and PhotophobiaLynn M Boyden, Lihi Atzmony, Claire Hamilton, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
The Journal of Investigative Dermatology|April 17, 2017
The Molecular Revolution in Cutaneous Biology: Identification of Skin Disease GenesLynn M Boyden, Keith A Choate
Pediatric Dermatology|May 14, 2013
Capillary malformation--arteriovenous malformation syndrome: review of the literature, proposed diagnostic criteria, and recommendations for managementCharisse M Orme, Lynn M Boyden, Keith A Choate, et al.
Journal of the American Academy of Dermatology|November 20, 2012
Capillary malformation-arteriovenous malformation syndrome: identification of a family with a novel mutationLynn M Boyden, Charisse M Orme, Richard J Antaya, et al.
The New England Journal of Medicine|May 17, 2002
High bone density due to a mutation in LDL-receptor-related protein 5Lynn M Boyden, Junhao Mao, Joseph Belsky, et al.
Nature Genetics|April 15, 2008
Skint1, the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal gammadelta T cellsLynn M Boyden, Julia M Lewis, Susannah D Barbee, et al.
Cutis|September 30, 2022
Focal Palmoplantar Keratoderma and Gingival Keratosis Caused by a KRT16 MutationTheodore D Zaki, Lynn M Boyden, Erin Mathes, et al.
American Journal of Human Genetics|June 10, 2020
Mutations in ASPRV1 Cause Dominantly Inherited IchthyosisLynn M Boyden, Jing Zhou, Ronghua Hu, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2011
Skint-1 is a highly specific, unique selecting component for epidermal T cellsSusannah D Barbee, Martin J Woodward, Gleb Turchinovich, et al.
The Journal of Investigative Dermatology|November 15, 2014
Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital DysplasiaLynn M Boyden, Brittany G Craiglow, Jing Zhou, et al.
American Journal of Human Genetics|October 22, 2019
Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and PhotophobiaLynn M Boyden, Lihi Atzmony, Claire Hamilton, et al.
Pageof 2