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Research 121–150 of 1000+
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- 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
- 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
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- Natural variation in trichome density and biochemistry in Antirrhinum
- Immunolocalization of telomerases in human hairs identifies proliferating cells in the bulb matrix and outer root sheath
- Hox demarcates regional regeneration of adult hair follicle stem cells
- A mouse with bad hair and poor taste
- Genetics of blond hair
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Screening of Sheep Fibroblast Cell Line with the Spider Dragline Silk Protein Gene
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Letter To Editor-Alopecia universalis in Down syndrome: Response totherapy
- BRITISH ASSOCIATION OF DERMATOLOGY.
- Genetic and molecular aspects of androgenetic alopecia
- Cosmeceutical Treatments for Androgenetic Alopecia
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters