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Research 271–300 of 1000+
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- 9. Immunology and Genetics
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- De Novo Production of Dermal Papilla Cells during the Anagen Phase of the Hair Cycle
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Besnoitiosis in donkeys: an emerging parasitic disease of equids in Italy
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- 864 Catalytic-dependent and -independent activities of Polycomb repressive complex 1 differentially regulate skin stem cell specification
- 860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies
- 865 Conditional ablation of JAK-STAT5 signaling induces anagen hair growth
- Gut microbiota in alopecia areata
- The Genetics of Human Skin Disease
- Androgen receptor CAG repeat length is associated with ovarian reserve but not with ovarian response
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- ATP-dependent chromatin remodeling during mammalian development
- Mechanical stretch induces hair regeneration through the alternative activation of macrophages
- Human Scalp Hair Follicles Are Both a Target and a Source of Prolactin, which Serves as an Autocrine and/or Paracrine Promoter of Apoptosis-Driven Hair Follicle Regression
- Skin Adipocyte Stem Cell Self-Renewal Is Regulated by a PDGFA/AKT-Signaling Axis
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Steroid 5α-Reductase as a Novel Therapeutic Target for Schizophrenia and Other Neuropsychiatric Disorders
- Tinea genitalis: a new entity of sexually transmitted infection? Case series and review of the literature
- Choreographing Immunity in the Skin Epithelial Barrier
- The prostamide‐related glaucoma therapy, bimatoprost, offers a novel approach for treating scalp alopecias