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Research 751–780 of 795
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- A descriptive study of alopecia patterns and their relation to thyroid dysfunction
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- The Mixed Lineage Kinase Leucine-Zipper Protein Kinase Exhibits a Differentiation-Associated Localization in Normal Human Skin and Induces Keratinocyte Differentiation upon Overexpression
- Targeted Delivery of Zinc Pyrithione to Skin Epithelia
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Ultrastructure of the contrasting types of keratinization seen in the tail epidermis of the laboratory mouseMus musculus
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- Eyebrow and Eyelash Alopecia: A Clinical Review
- The Scientific Legacy of Stephen Rothman
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- A rare complication of follicular hair unit extraction: Kaposi’s varicelliform eruption
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- Immunostaining study of cytokeratins in human hair follicle development
- Nutrition and Hair Anomalies
- A clinical investigation of early‐onset alopecia areata in children: Onset earlier than 4 years of age might have a better short‐term prognosis
- Treatments for Dissecting Cellulitis of the Scalp: A Systematic Review and Treatment Algorithm
- Lipid signaling in keratinocytes: Lipin-1 plays a PArt
- Trichothiodystrophy