Results 241 to 250 of about 5,711 (254)

Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing

Journal of Investigative Dermatology, 2009
Hans Christian Hennies
exaly  

A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis

Journal of Investigative Dermatology, 2012
Muhammad Farooq, Asuka Inoue, Manabu Ohyama   +2 more
exaly  

Congenital hypotrichosis in two dogs

Journal of the American Veterinary Medical Association, 1984
openaire   +2 more sources

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Nature Genetics, 2009
Yaran Wen, Sven Cichon, Markus M Nöthen
exaly  

Hypotrichosis simplex of the scalp

Journal of the European Academy of Dermatology and Venereology, 2007
openaire   +2 more sources

A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis

Human Genetics, 2007
Ghazanfar Ali, Wasim Ahmad
exaly  

A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats

PLoS ONE, 2015
Marie Abitbol, Laurent Tiret
exaly  

Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin

British Journal of Dermatology, 2020
exaly  

Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions

Journal of Investigative Dermatology, 2006
Hisham Bazzi
exaly  

Long‐term safety and efficacy of bimatoprost solution 0·03% application to the eyelid margin for the treatment of idiopathic and chemotherapy‐induced eyelash hypotrichosis: a randomized controlled trial

British Journal of Dermatology, 2015
exaly