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Research 151–180 of 1000+
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- A rare hair loss in children: Monilethrix
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Genetic Hair Disorders: A Review
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Desmogleins: Hair perspective
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Laser Hair Removal
- Growth Hormone and the Human Hair Follicle
- Becker's Nevus Syndrome
- Topically applied glycyrrhizic acid causes hair removal in rats
- Fibroblast bioelectric signaling drives hair growth
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Effects of Hormones and Endocrine Disorders on Hair Growth
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- New clinico‐genetic classification of trichothiodystrophy
- Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Alopezien und Hypotrichosen im Kindesalter
- Characterization and Management of Adverse Events of Low-Dose Oral Minoxidil Treatment for Alopecia: A Narrative Review
- A missense mutation in Lama3 causes androgen alopecia
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis