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Research 271–300 of 1000+
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Progeroide Syndrome
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Cepharanthine: a review of the antiviral potential of a Japanese-approved alopecia drug in COVID-19
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- 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*
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Molecular Genetics of Alopecias
- 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.
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- 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
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- Expression of AKT1 along with AKT2 in granulosa-lutein cells of hyperandrogenic PCOS patients
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview