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Research 30 of 42
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- 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
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Hair follicle differentiation and regulation.
- Biology and Genetics of Hair
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Congenital hair loss disorders: Rare, but not too rare
- Genetics of Structural Hair Disorders
- Characteristic Localization of Neuronatin in Rat Testis, Hair Follicle, Tongue, and Pancreas
- Woolly Antics between the Sheaths
- The human keratins: biology and pathology
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Krt6a-Cre Transgenic Mice Direct LoxP-Mediated Recombination to the Companion Cell Layer of the Hair Follicle and Following Induction by Retinoic Acid to the Interfollicular Epidermis
- In this Issue
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses