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Research 61–90 of 1000+
- Unexpected hair growth induced by gefitinib treatment in two patients with EGFR gene mutation-positive adenocarcinoma of the lung
- Prostaglandin D2 Inhibits Wound-Induced Hair Follicle Neogenesis through the Receptor, Gpr44
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Structure of human type II 5 alpha-reductase gene
- 5 alpha-reductase-2 gene mutations in the Dominican Republic.
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A second <i>KRT</i>71 allele in curly coated dogs
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Detection of five substitution TPO mutations in Polycystic Ovary Syndrome (PCOS) and thyroid hormones disturbance patients
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- 851 The role of astrotactin2 in regulating mammalian skin polarity
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Matrix Stiffness-driven FAK Splicing Tunes Cell Mechanosensing
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- COVID‐19, androgens, and androgenic alopecia
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis