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Research 211–240 of 873
- Interventions for female pattern hair loss
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Role of stem/progenitor cells in reparative disorders
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Hirsutism: diagnosis and treatment
- Male pattern baldness and its association with coronary heart disease: a meta-analysis
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- The Genetics of Human Skin Disease
- INTERFERONS IN DERMATOLOGY
- Ovarian morphology is associated with insulin resistance in women with polycystic ovary syndrome: a cross sectional study
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Case 21-2012
- Expansion and characterization of epithelial stem cells with potential for cyclical hair regeneration
- Efficacy of stem cell therapy for burn wounds: a systematic review and meta-analysis of preclinical studies
- QR 678 & QR678 Neo Vs PRP—A randomised, comparative, prospective study
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Isolation and Characterization of a Fetal-Maternal Microchimeric Stem Cell Population in Maternal Hair Follicles Long after Parturition
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- The use of cyproterone acetate/ethinyl estradiol in hyperandrogenic skin symptoms – a review
- The hair shaft: normality, abnormality, and genetics
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Fibroblast heterogeneity and tertiary lymphoid tissues in the kidney
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Non‐infective mucocutaneous presentations of human immunodeficiency virus infection