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Research 151–180 of 1000+
- Hypertrichosis and topical corticosteroid use
- Osteopontin regulatory functions in the hair follicle open a therapeutic approach for hypertrichosis
- 1371 FGF7-dependent inhibition of human hair growth byan osteopontin-derived peptide: A novel solution for hirsutism and hypertrichosis?
- Generalized Hypertrichosis Due to Topical Minoxidil
- Hypertrichosis and Hyperpigmentation in the Periocular Area Associated with Travoprost Treatment
- Hypertrichosis and hirsutism
- Hypertrichosis Secondry to Minoxidil
- Hypertrichosis Cubiti Presenting in a Female Child: A Case Report
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Effects of Hypertrichotic Agents on Follicular and Nonfollicular Cells in vitro
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood