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Research 361–390 of 1000+
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- SEXUAL DIMORPHISM IN MAMMALS
- BIOACTIVE AND PERIPHERAL ANDROGENS IN PREPUBERTAL SIMPLE HYPERTRICHOSIS
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- An Update of Congenital Adrenal Hyperplasia
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- Hair and Scalp Dermatoscopy (Trichoscopy)
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Modelling androgen synthesis and action during human sexual differentiation
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Hairless is a nuclear receptor corepressor essential for skin function
- INCIDENCE OF VIRILISATION IN SEX CORD STROMAL TUMOURS OF OVARY, A 5- YEAR EXPERIENCE IN A TERTIARY CARE GYNAECOLOGICAL CENTRE
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- Congenital atrichia associated with situs inversus and mesocardia
- Hyperandrogenism and Cardiometabolic Risk in Pre- and Postmenopausal Women—What Is the Evidence?
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Multidimensional assessment of adverse events of finasteride：a real-world pharmacovigilance analysis based on FDA Adverse Event Reporting System (FAERS) from 2004 to April 2024
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Weight Changes Are Linked to Adipose Tissue Genes in Overweight Women with Polycystic Ovary Syndrome
- Pubertal Acne
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Metabolic features of the reproductive phenotypes of polycystic ovary syndrome
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency