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Research 691–720 of 718
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Utility of dermoscopy in alopecia areata
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Epidermal Wnt/β-catenin signaling regulates adipocyte differentiation via secretion of adipogenic factors
- Ejaculations and Benign Prostatic Hyperplasia: An Impossible Compromise? A Comprehensive Review
- Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Clinical Conditions Targeted by OnabotulinumtoxinA in Different Ways in Medicine
- Mesenchymal Stem Cells Pretreated with Collagen Promote Skin Wound-Healing
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- Epimedium brevicornum Maxim. Extract exhibits pigmentation by melanin biosynthesis and melanosome biogenesis/transfer
- Single-Cell Sequencing Technology in Ruminant Livestock: Challenges and Opportunities
- Retinoic acid exerts sexually dimorphic effects on muscle energy metabolism and function
- Regional Variation in Androgen Receptor Expression and Biomechanical Properties May Contribute to Cryptorchidism Susceptibility in the LE/orl Rat
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- Effective treatment with afoxolaner (NexGard) of <i>Trixacarus caviae</i> in a pet guinea pig
- Illness and femininity in Hilary Mantel’s Giving Up the Ghost (2003)
- Olympic and Board Game Dermatology: Exploring Eponyms Linking Skin Conditions to Sports and Strategy Games
- Prevalence of skin lesions in a sample of Brazilian patients with inflammatory bowel disease
- Mineral Deficiencies: A Root Cause for Reduced Longevity in Mammals
- The molecular basis of human keratin disorders
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- The AR/miR-221/IGF-1 pathway mediates the pathogenesis of androgenetic alopecia
- Prevalence and Predictors of Impaired Glucose Tolerance and Diabetes Mellitus Type 2 in Patients with Polycystic Ovary Syndrome
- GUNJA (ABRUS PRECATORIUS LINN.): COMPREHENSIVE INSIGHTS INTO ITS PHARMACOLOGICAL POTENTIAL
- Evaluation of hair surface structure and morphology of patients with lichen planopilaris (LPP) by atomic force microscopy (AFM)
- Evaluation of Surface Structure and Morphological Phenomena of Caucasian Virgin Hair with Atomic Force Microscopy