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Research 241–270 of 1000+
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Expression of novel keratin associated protein 5 genes in the cuticle layer of human hair follicles
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Monilethrix
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Human tissue kallikreins as promiscuous modulators of homeostatic skin barrier functions
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Runx1 transcription factor is involved in the regulation of KAP5 gene expression in human hair follicles
- The role of vitamin D receptor mutations in the development of alopecia
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- In this Issue
- Hair Anomalies in a 6-Year-Old Girl
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- The Catalog of Human Hair Keratins