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Research 301–330 of 1000+
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- A kindred with mutant IKAROS and autoimmunity
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Polymorphism of keratin-associated protein (KAP) 7 gene and its association with wool traits in Rambouillet sheep
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- The Genetics of Acne
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Oral Presentation Abstracts
- Comparative Antioxidant Activity and Volatile Oil Composition of Leaves and Fruits of Thuja orientalis Growing in Egypt
- Development of a Chitosan Nanofibrillar Scaffold for Skin Repair and Regeneration
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Thyroid disorders: An overview of causes and treatment
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia