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Research 511–540 of 1000+
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- The Hidden Link between Polycystic Ovary Syndrome and Kidney Stones: Finding from the Tehran Lipid and Glucose Study (TLGS)
- Transgneic Endothelin 3 Regulates Murine Pigment Production and Coat Color
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- WNT Signaling in the Control of Hair Growth and Structure
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration
- Síndrome dos ovários policísticos: correlação dos fenótipos com as manifestações metabólicas
- An Unusual Cause of Primary Amenorrhea
- AB0163 ANTI-KU ANTIBODIES: MUCH MORE THAN SCLEROMYOSITIS
- Polycystic Ovary Syndrome: Explaining the Gynecological Aspects and Treatment Options to Patients
- Role of Basti in Artavshaya w.s.r. to Lean and Obese Polycystic Ovarian Syndrome
- Diagnosis and Treatment of PCOS- A Comparative Review
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Cell Proteomic Footprinting: Advances in the Quality of Cellular and Cell-Derived Cancer Vaccines
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Fibroblasts in Diabetic Foot Ulcers
- Modulation of Macrophage Function by Bioactive Wound Dressings with an Emphasis on Extracellular Matrix-Based Scaffolds and Nanofibrous Composites
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- Dynamic immunomodulatory nanoarchitectonics: Rewiring tissue regenerative microenvironment via intelligent regulation