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Research 121–150 of 1000+
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- Faculty Opinions recommendation of A new classification of pattern hair loss that is universal for men and women: basic and specific (BASP) classification.
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Minoxidil 5% Solution for Topical Treatment of Loose Anagen Hair Syndrome
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Development of a New Grading Scale for Evaluating Overall Hair Density
- Transcriptional Governance of Hair Follicle Stem Cell Quiescence and Niche Maintenance in Long-Term Tissue Regeneration
- 889 Trpv3 gain-of-function mutation impairs differentiation of hair follicle inner root sheath
- A rare hair loss in children: Monilethrix
- Expression of a dominant negative mutant of epidermal growth factor receptor in the epidermis of transgenic mice elicits striking alterations in hair follicle development and skin structure.
- Philosophy and technique in hair restoration surgery
- Diagnostic challenge: Loose anagen hair syndrome
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- The Gross Morphology and Scanning Electron Microscopic Evaluation of the Skin Surface in Congenic Strains of Hairless Mice
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A diagnostic clue: New onset alopecia sparing white hairs
- Biotinidase deficiency characterized by skin and hair findings
- オルニチン・トランスカルバミラーゼ(OTC)欠損(spf・ash)マウスへのOTC遺伝子導入
- Você conhece esta síndrome? * Do you know this syndrome? *
- The ‘Watch Sign’ – Another Observation in the Course of Male Frontal Fibrosing Alopecia
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Monilethrix
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Monilethrix in three generations
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Renbök phenomenon: Alopecia areata sparing psoriasis plaques