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Research 631–660 of 1000+
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- ROR2 regulates self-renewal and maintenance of hair follicle stem cells
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Alopecia Areata, Primary Sclerosing Cholangitis, and Ulcerative Colitis: Autoimmunity and Apoptosis as Common Links?
- 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
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Adipose and Hair Function: An aPPARent Connection
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Antisense oligonucleotide targeting fibroblast growth factor receptor (FGFR)-1 stimulates cellular activity of hair follicles in an<i>in vitro</i>organ culture system
- Linking allergy to mercury to HLA and burning mouth syndrome
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Advances in Hair Diseases
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Diffuse idiopathic skeletal hyperostosis in a 33-year-old woman with PCOS and metabolic syndrome: a rare scenario
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- HHV-6A and HHV-6B in Drug-Induced Hypersensitivity Syndrome/Drug Reaction with Eosinophilia and Systemic Symptoms
- To study hypoactive sexual desire disorder in a fragile X carrier female successfully treated with local testosterone application
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Antihelminthic Drugs