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Research 241–270 of 1000+
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- The character “hairless” in the mouse
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Molecular Genetics of Alopecias
- Antisense oligonucleotide targeting fibroblast growth factor receptor (FGFR)-1 stimulates cellular activity of hair follicles in an<i>in vitro</i>organ culture system
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Hierarchical patterning modes orchestrate hair follicle morphogenesis
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Wnt and Notch signaling pathway involved in wound healing by targeting c-Myc and Hes1 separately