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Research 31–60 of 1000+
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Keratin Gene Expression Differences in Wool Follicles and Sequence Diversity of High Glycine-Tyrosine Keratin-Associated Proteins (Kaps) in Magra Sheep of India
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- The Catalog of Human Hair Keratins
- Sequence Analysis and Expression of a TypeIHair Keratin Gene in Goat Skin
- Hoxc13 and homologs of mammalian hair keratins are required for the cornification of nuptial pads in Xenopus frogs
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- 723 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and three-dimensional chromatin topology in lineage-specific loci to control hair growth
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- 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
- Monilethrix: Beaded hair and hypotrichosis in a child
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Office Diagnosis of Hair Shaft Defects
- Evolution of Trichocyte Keratins
- Few Simple Sequence Repeats in Human Hair
- Whole transcriptome sequencing of different hair types in inner Mongolian cashmere goats
- Structure and expression of the ovine Hoxc-13 gene
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1