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Experimental Dermatology|April 29, 2017
Genetics and other factors in the aetiology of female pattern hair lossSilke Redler, Andrew G Messenger, Regina C BetzEuropean Journal of Medical Genetics|April 16, 2019
Novel EXOSC3 pathogenic variant results in a mild course of neurologic disease with cerebellum involvementDiana Le Duc, Susanne Horn, Rami Abou Jamra, et al.American Journal of Medical Genetics. Part A|September 4, 2010
Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutationAyse Tulin Mansur, Nursel H Elcioglu, Silke Redler, et al.Journal of the American Academy of Dermatology|July 28, 2010
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 reportSilke Redler, Roland Kruse, Sibylle Eigelshoven, et al.Experimental Dermatology|June 18, 2026
Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?Leonie Rieger-Molitor, Carlo Maj, Silke Redler, et al.Molecular and Cellular Biology|September 2, 2024
De Novo Missense Variations of ATP8B2 Impair Its Phosphatidylcholine Flippase ActivityHiroyuki Takatsu, Narumi Nishimura, Yusuke Kosugi, et al.Clinical Genetics|October 3, 2020
QRICH1 variants in Ververi-Brady syndrome-delineation of the genotypic and phenotypic spectrumMelanie Föhrenbach, Rami Abou Jamra, Arndt Borkhardt, et al.Cancer Gene Therapy|May 28, 2021
Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategiesEvgeniya Denisova, Dana Westphal, Harald M Surowy, et al.Frontiers in Immunology|May 4, 2026
Genome-wide association study of atopic and autoimmune comorbidities in alopecia areataMarisol Herrera-Rivero, Yasmina Gossmann, Swapnil Awasthi, et al.BMJ Open|July 20, 2025
Psychosocial outcomes of risk-adapted prevention for prostate cancer predisposition: study protocol for a longitudinal observational mixed-methods studyMaike K Klett, Peter Albers, Jale Lakes, et al.Pageof 4