Search
for
Sort by
Research 511–540 of 1000+
- Pregnancy, hair loss, and the pill.
- INTERFERONS IN DERMATOLOGY
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Is there any relationship between decreased AgNOR protein synthesis and human hair loss?
- The probable destructive mechanisms behind COVID-19 on male reproduction system and fertility
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Progranulin, a secreted tumorigenesis and dementia-related factor, regulates mouse hair growth
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Function of KLF4 in Stem Cell Biology
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- How a Bird Gets Its Feathers: Insights from Chromatin Looping
- Disorders of ovulation
- New Three-dimensional Moving Field Radiation Therapy for Brain Tumors
- Anaesthetics and platelets.
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Research progress on mechanisms of skin aging and anti-aging strategies
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Assessment of scalp hair survivin in patients with premature greying of hair
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- 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