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Research 91–120 of 1000+
- 563 CsA-induced hypertrichosis might be caused in part by inhibition of TGF-β2 expression in dermal papilla cells.
- Hypertrichosis and topical corticosteroid use
- A rare clinical image of hypertrichosis (Werewolf syndrome)
- 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
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Hypertrichosis and hirsutism
- Hypertrichosis Secondry to Minoxidil
- Hypertrichosis Cubiti Presenting in a Female Child: A Case Report
- Hypertrichosis Lanuginosa Acquisita: When Hair Unravels the Unseen
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- A case of hypertrichosis lanuginosa acquisita as a sign of malignancy
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Androgenetic alopecia, hirsutism and hypertrichosis
- 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