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Research 421–450 of 1000+
- Function of KLF4 in Stem Cell Biology
- Hormonal, Medical, and Nonsurgical Aspects of Gender Affirmation
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- Association of follicle-stimulating hormone receptor gene ser680 asn (rs6166) polymorphism with polycystic ovarian syndrome
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Increased expression of psoriasin (S100A7) and interleukin 17 (IL-17) in lesional skin in lichen planopilaris
- Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia
- The role of versican in the skin ECM and its interaction with hyaluronic acid
- Bio-Catalytic Action of Pseudomonas DL17 on Environmental Contaminant Sunset Yellow FCF
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Assessment of scalp hair survivin in patients with premature greying of hair
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Pictorial Essay on Hair Loss; the Result of Head Bones Displacement
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- Study on Changes of 19 Steroids in Plasma From 9 Diagnosed Patients With P450 Oxidoreductase Deficiency
- Inherited Epidermolysis Bullosa: A Clinical Case
- 公表学術論文等リスト 2018
- WNT10B (wingless-type MMTV integration site family)
- Study of Skin Expression of MicroRNA-146a in Patients with Alopacia Areata
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Androgen effects on the skin
- Comparative study of efficacy of excimer light therapy vs intralesional triamcinolone vs topical 5% minoxidil: an observational study
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- British Society for Dermatopathology: Summaries of Papers