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Research 481–510 of 1000+
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- SEXUAL DIMORPHISM IN MAMMALS
- Male-pattern baldness susceptibility locus at 20p11
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Toxicological Studies on Procyanidin B-2 for Extern?al Application as a Hair Growing Agent
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Bloom's syndrome–‐a first report from India
- The hair shaft: normality, abnormality, and genetics
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Validation of Replacement of the Synthetic Food Dye 'Sunset Yellow'-Induced Hepatotoxicity and Genotoxicity with the Nutraceutical 'Curcumin' in Mice
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Pigmentary mosaicism: An update
- Acromegaloid Facial Appearance: Case Report and Literature Review
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Homologous recombination induced by doxazosin mesylate and saw palmetto in the <i>Drosophila</i> wing‐spot test
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Primary Amenorrhoea
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Immunolocalization of telomerases in human hairs identifies proliferating cells in the bulb matrix and outer root sheath
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair