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Research 631–660 of 1000+
- Redefining hormone resistance in prostate cancer
- Manipulation of outer root sheath cell survival perturbs the hair-growth cycle
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat
- The bright side of fibroblasts: molecular signature and regenerative cues in major organs
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Pathophysiology of the Behçet's Disease
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
- <i>In vivo </i>CD44‐CD49d complex formation in autoimmune disease has consequences on T cell activation and apoptosis resistance
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Nonclassic congenital adrenal hyperplasia
- Through the lens of hair follicle neogenesis, a new focus on mechanisms of skin regeneration after wounding
- Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet
- Ovarian SAHA syndrome is associated with a more insulin-resistant profile and represents an independent risk factor for glucose abnormalities in women with polycystic ovary syndrome: A prospective controlled study
- Phenotypic comparison of Caucasian and Asian women with polycystic ovary syndrome: a cross-sectional study
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- State-dependent signaling by Ca<sub>v</sub>1.2 regulates hair follicle stem cell function
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- The impact of VDR expression and regulation in vivo
- The Genetics of Human Skin Disease
- Expression Profiles of Reproduction- and Thyroid Hormone-Related Transcripts in the Brains of Chemically-Induced Intersex Frogs
- The Wave complex controls epidermal morphogenesis and proliferation by suppressing Wnt–Sox9 signaling
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity