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Research 61–90 of 1000+
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- Cutaneous Reactions to Drugs
- Policistisko olnīcu sindroms pusaudzēm – starppaaudžu, ģenētiskie, dzīves kvalitātes un negausīgas ēšanas aspekti. Promocijas darbs
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Characterisation of the Ovine KRTAP36-1 Gene in Chinese Tan Lambs and Its Impact on Selected Wool Traits
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Registrars’ Symposium: Summaries of Papers
- 5‐Alpha reductase inhibitor related litigation: A legal database review
- Shorter CAG repeats in the androgen receptor gene may enhance hyperandrogenicity in polycystic ovary syndrome
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Antihelminthic Drugs
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- A population pharmacokinetic model for individualized regimens of finasteride according to CYP3A5 genotype and liver function
- Vaccines, Infections, and Alopecia Areata
- Buschke-Ollendorff syndrome
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Keratin disorders: from gene to therapy
- THE PATHOGENESIS OF ALOPECIA AREATA
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Ulcerative colitis and total alopecia in a mother and her son
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia