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Research 31–60 of 523
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Solid state NMR of isotope labelled murine fur: a powerful tool to study atomic level keratin structure and treatment effects
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- Developing Optical Biometrics Using Optical Coherence Tomography for Medical Screening and Diagnosis
- Beyond Expectations
- The human keratins: biology and pathology
- Mechanical forces in skin disorders
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Australasian Society for Dermatology Research Meeting, May 2007
- The Genetics of Human Skin Disease
- A discourse on human hair fibers and reflections on the conservation of drug molecules
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Ethnic Hair Disorders
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Hair today, gone tomorrow: the degradation and conservation of archaeological hair fibers
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Structural changes in trichocyte keratin intermediate filaments during keratinization
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- The role of disulfide bond formation in the structural transition observed in the intermediate filaments of developing hair
- Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus