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Research 481–510 of 607
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Plastic surgery : indications, operations, and outcomes
- Male infertility and genitourinary birth defects: there is more than meets the eye
- The impact of VDR expression and regulation in vivo
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Systematic analyses of murine masculinization processes based on genital sex differentiation parameters
- Comparison of prevalence of periodontal disease in women with polycystic ovary syndrome and healthy controls
- Current evaluation of amenorrhea
- New and Consolidated Therapeutic Options for Pubertal Induction in Hypogonadism: In-depth Review of the Literature
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Altered FGF expression profile in human scalp-derived fibroblasts upon WNT activation: implication of their role to provide folliculogenetic microenvironment
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Best Practices for FACE-Q Aesthetics Research: A Systematic Review of Study Methodology
- Impaired Keratinocyte Proliferative and Clonogenic Potential in Transgenic Mice Overexpressing 14-3-3σ in the Epidermis
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Vanillic Acid Stimulates Anagen Signaling via the PI3K/Akt/ β-Catenin Pathway in Dermal Papilla Cells
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- β-Catenin Signaling Evokes Hair Follicle Senescence by Accelerating the Differentiation of Hair Follicle Mesenchymal Progenitors
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder