Search
for
Sort by
Research 391–420 of 1000+
- Congenital Adrenal Hyperplasia
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Prolactin and Its Receptor Are Expressed in Murine Hair Follicle Epithelium, Show Hair Cycle-Dependent Expression, and Induce Catagen
- Biology and Genetics of Hair
- Learning from nudity: lessons from the nude phenotype
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- What causes hidradenitis suppurativa ?—15 years after
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Trichoscopy in genetic hair shaft abnormalities
- HRT for women with premature ovarian insufficiency: a comprehensive review
- Influence of TRPV3 mutation on hair growth cycle in mice
- Nonclassic adrenal hyperplasia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Congenital hair loss disorders: Rare, but not too rare
- The nude gene and the skin
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Morphological Approach to Hair Disorders
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Dihydrotestosterone inhibits hair growth in mice by inhibiting insulin-like growth factor-I production in dermal papillae
- Diagnostic approach to low‐renin hypertension
- Dietary isoflavone increases insulin-like growth factor-I production, thereby promoting hair growth in mice
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Hair Loss in Children
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Alopecia Areata
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat