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Research 121–150 of 1000+
- Phenotype of Normal Hairline Maturation
- The ‘bald’ phenotype (androgenetic alopecia) is caused by the high glycaemic, high cholesterol and low mineral ‘western diet’
- FORENSIC DNA PHENOTYPING FOR CRIMINAL IDENTIFICATION
- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Phenotypic variation in biotinidase deficiency
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Variation and Heritability in Hair Diameter and Curvature in an Australian Twin Sample
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- 516 Functional annotation of genes underlying hair disorders
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Hair follicle-derived mesenchymal cells support undifferentiated growth of embryonic stem cells
- The Frequency of Various Phenotypes of Polycystic Ovarian Syndrome in Adolescents, Based on Rotterdam Criteria
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Enhancing Quercetin Bioavailability Attenuates Aging Phenotypes via the Gut Microbiota–Intestinal Barrier Axis in Aged Mice
- Spectrum of Phenotypes Associated with Human MC1R Variations
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- 1349 Inducing fate changes at the hair follicle stem cell nice
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- 1250 Development of an ex vivo human skin explant model to examine candidate gene functions in the hair follicle and epidermis
- Keratin 15 Promoter Targets Putative Epithelial Stem Cells in the Hair Follicle Bulge
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Amelanocytic Anhidrotic Alopecia Areata-like Phenotype After Allogeneic Hematopoietic Cell Transplant
- LB1672 Senescent melanocytes in nevus skin stimulate hair growth
- ZNF750 safeguards upper hair follicle homeostasis to prevent inflammatory skin disease
- Laser-assisted hair removal: Side effects of Q-switched Nd:YAG, long-pulsed ruby, and alexandrite lasers
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family