Search
for
Sort by
Research 91–120 of 1000+
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Regulation of Keratin Gene Expression in Hair Follicle Differentiation<sup>a</sup>
- The Proteins of Normal and Aberrant Hair Keratins
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Ageing processes influence keratin and KAP expression in human hair follicles
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Structural features and sites of expression of a new murine 65 kD and 48 kD hair-related keratin pair, associated with a special type of parakeratotic epithelial differentiation
- Sequence, expression, and evolutionary conservation of a gene encoding a glycine/tyrosine-rich keratin-associated protein of hair.
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Sequence and expression of human hair keratin genes
- Monilethrix in three generations
- Ribonucleic Acids Coding for the Keratin Complex of Hair
- [Genetic and biochemical aspects of keratin synthesis by hair follicles].
- 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
- Human hair keratins
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Two-dimensional electrophoretic analysis of human hair keratins, especially hair matrix proteins
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Spiny Keratoderma
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Genes for intermediate filament proteins and the draft sequence of the human genome
- A newborn presenting with congenital blistering
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Hypotrichosis and Hair Loss on the Occipital Scalp