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Research 61–90 of 1000+
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Alopecia Areata
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Alopecia Areata
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Ingredients of Trichological Shampoos with Alleged Beneficial Effects on Hair—What Is Really Known About Their Efficacy? A Scoping Review of an Area with More Unknowns than Knowns
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Insertional mutation of the hairless locus on mouse Chromosome 14
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- THE PATHOGENESIS OF ALOPECIA AREATA
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Piecing together the pigment-type switching puzzle
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases