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Research 661–690 of 1000+
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Curcumin derivatives inhibit testicular 17β-hydroxysteroid dehydrogenase 3
- Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia.
- Alopecia: Association with Resistance to Thyroid Hormones
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Evaluation of Hair Loss
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Hair Loss: A Harbinger of the Morbidities to Come!
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- Ischemic onycholysis of the hands
- 9. Immunology and Genetics
- Abstracts Pt.30
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Male Pattern Baldness
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Delayed Puberty
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Association of Benign Prostatic Hyperplasia with Male Pattern Baldness
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Hair Shafts in Trichoscopy
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Alopecia Areata
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Pseudoacromegaly induced by the long-term use of minoxidil