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Research 301–330 of 1000+
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Diagnostic approach to low‐renin hypertension
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Congenital adrenal hyperplasia
- 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
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- Evaluation of Hair Density and Hair Diameter in the Adult Thai Population Using Quantitative Trichoscopic Analysis
- Hair Changes Caused by Aging
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Hair and nail involvement in lupus erythematosus
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Biology of Human Hair: Know Your Hair to Control It
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- British Society for Dermatopathology
- Psychometric validation of the Spanish alopecia areata–life impact questionnaire
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Skin precancer.
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Chronic overlapping pain conditions and nociplastic pain
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets