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Research 31–60 of 936
- Guidelines for the diagnosis and treatment of male-pattern and female-pattern hair loss, 2017 version
- Identification of a preferred substrate peptide for transglutaminase 3 and detection of <i>in situ</i> activity in skin and hair follicles
- Hair Cycle-Dependent Expression of Hepatocyte Growth Factor (HGF) Activator, Other Proteinases, and Proteinase Inhibitors Correlates with the Expression of HGF in Rat Hair Follicles
- Partial Purification and Characterization of Two Distinct Types of Caspases from Human Epidermis
- Multivariate analysis of prognostic factors in patients with rapidly progressive alopecia areata
- Oral finasteride improved the quality of life of androgenetic alopecia patients
- Hair growth stimulatory effect by a combination of 5-aminolevulinic acid and iron ion
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Epimorphin expression during human foetal hair follicle development
- Tardily accelerated neurologic deterioration in two-step thallium intoxication
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Finasteride in the treatment of Japanese men with male pattern hair loss.
- Spironolactone, a Classic Potassium-Sparing Diuretic, Reduces Survivin Expression and Chemosensitizes Cancer Cells to Non-DNA-Damaging Anticancer Drugs
- Topical adenosine increases thick hair ratio in Japanese men with androgenetic alopecia
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Biological characteristics of age-related changes in C57BL/6 mice sub-strains in the national center for geriatrics and gerontology aging farm
- Polymorphic CAG repeat numbers in the androgen receptor gene of female pattern hair loss patients
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Granulomatous pigmented purpuric dermatosis containing Propionibacterium acnes
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Potential of polar lipids from bovine milk to regulate the rodent dorsal hair cycle
- An Update on the Roles of the Complement System in Autoimmune Diseases and the Therapeutic Possibilities of Anti-Complement Agents
- Antisense oligonucleotide targeting fibroblast growth factor receptor (FGFR)-1 stimulates cellular activity of hair follicles in an<i>in vitro</i>organ culture system
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- The five-year effects of testosterone replacement therapy on lipid profile and glucose tolerance among hypogonadal men in Japan: a case control study
- Progenitor-derived endothelin controls dermal sheath contraction for hair follicle regression
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation