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Research 271–300 of 1000+
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 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
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Keratin disorders: from gene to therapy
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Congenital adrenal hyperplasia
- Cantú syndrome with coexisting familial pituitary adenoma
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Disease causing homozygous variants in the human hairless gene
- Australasian Society for Dermatology Research Meeting, May 2006
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Identifying molecular targets for reverse aging using integrated network analysis of transcriptomic and epigenomic changes during aging
- Inducible, reversible hair loss in transgenic mice.
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Polycystic ovary syndrome and impact on health
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- Association between male pattern baldness and testicular germ cell tumor: a meta-analysis
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Skin signs of systemic diseases
- New Biomarkers to Evaluate Hyperandrogenemic Women and Hypogonadal Men