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Research 511–540 of 1000+
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Madarosis: A marker of many Maladies
- Prevalence, comorbidities, and treatment patterns of Japanese patients with alopecia areata: A descriptive study using Japan medical data center claims database
- Necl2 regulates epidermal adhesion and wound repair
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Eyebrow Loss
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- The Proteins of Normal and Aberrant Hair Keratins
- New developments in the molecular treatment of ichthyosis: review of the literature
- Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles
- Palatogenesis and cutaneous repair: A two‐headed coin
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Diversity of Trichocyte Keratins and Keratin Associated Proteins
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Differences between ultrastructure and protein composition in straight hair fibres
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Hair follicles modulate skin barrier function
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Congenital atrichia with papular lesions
- Frontal fibrosing alopecia: a review of eleven patients