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Research 391–420 of 1000+
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Epigenetic control of adult stem cell function
- Why Some Women Look Young for Their Age
- Molecular Mechanisms Regulating Hair Follicle Development
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Regulatory T Cells in Autoimmune Diseases and their Potential
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Hyperandrogenism and Cardiometabolic Risk in Pre- and Postmenopausal Women—What Is the Evidence?
- Weight Changes Are Linked to Adipose Tissue Genes in Overweight Women with Polycystic Ovary Syndrome
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Real-world pharmacovigilance insights into drug-induced risk of alopecia
- Unhealthy diet and lifestyle factors linked to female androgenetic alopecia: a community-based study from Jidong study, China
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Levodopa-induced skin disorders in patients with Parkinson disease: a systematic literature review approach
- Thrombocytopenia and Leukopenia Associated with Itraconazole
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Evaluation of COVID-19 risk in patients on systemic retinoid therapy