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Research 331–360 of 1000+
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Identification of SNPs and expression patterns of FZD3 gene and its effect on wool traits in Chinese Merino sheep (Xinjiang Type)
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Genomic Characterization of Quality Wool Traits in Spanish Merino Sheep
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Cells to Surgery Quiz: April 2020
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- Frontal Fibrosing Alopecia
- Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA
- Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield