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Research 61–90 of 1000+
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Hoxc13 and homologs of mammalian hair keratins are required for the cornification of nuptial pads in Xenopus frogs
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Few Simple Sequence Repeats in Human Hair
- Whole transcriptome sequencing of different hair types in inner Mongolian cashmere goats
- Construction and Verification of Recombinant Follicle-specific Expression Vector
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- Monilethrix: Beaded hair and hypotrichosis in a child
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Office Diagnosis of Hair Shaft Defects
- Association analysis of polymorphisms in six keratin genes with wool traits in sheep
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Keratin 17 Impacts Global Gene Expression and Controls G2/M Cell Cycle Transition in Ionizing Radiation–Induced Skin Damage
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- 604 DNA dioxygenases TET regulate keratin gene expression and enhancer networks within lineage-specific gene loci during epidermal and hair follicle-specific keratinocyte differentiation
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.