Search
for
Sort by
Research 61–90 of 1000+
- Molecular genetics of androgen insensitivity
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Alopecia Areata
- Androgen receptors and their biology
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Predominant expression of 5 alpha-reductase type 1 in pubic skin from normal subjects and hirsute patients.
- Androgen Dependence of Hirsutism, Acne, and Alopecia in Women
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- 5-Alpha reductase deficiency
- Transcriptomic analysis reveals critical genes for the hair follicle of Inner Mongolia cashmere goat from catagen to telogen
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Target-Adverse Events and Fear of Cancer Progression, Anxiety, and Depression in Patients with Advanced Non-Small Cell Lung Cancer
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements