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Research 301–330 of 1000+
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Treatment of alopecia areata: “What is new on the horizon?”
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Atrichia with papular lesions
- Disease causing homozygous variants in the human hairless gene
- Expression of novel keratin associated protein 5 genes in the cuticle layer of human hair follicles
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Congenital atrichia with papular lesions
- Marie-unna hereditary hypotrichosis
- Monilethrix
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Frontal Fibrosing Alopecia
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Familial congenital generalized hypertrichosis
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Natural variation in trichome density and biochemistry in Antirrhinum