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Research 961–990 of 1000+
- Clinical and Demographic Characteristics of Patients Diagnosed with Polycystic Ovary Syndrome: A Cross-Sectional Observational Study
- The Hidden Link between Polycystic Ovary Syndrome and Kidney Stones: Finding from the Tehran Lipid and Glucose Study (TLGS)
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- PO:17:252 | The choice between belimumab and anifrolumab: analysis of a monocentric cohort
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Clinical Usefulness of Non-Invasive Metabolic-Associated Fatty Liver Disease Risk Assessment Methods in Patients with Full-Blown Polycystic Ovary Syndrome in Relation to the MRI Examination with the Ideal IQ Sequence
- An Unusual Cause of Primary Amenorrhea
- AB0163 ANTI-KU ANTIBODIES: MUCH MORE THAN SCLEROMYOSITIS
- Effects of the bovine slick mutation on heat stress responses and hair growth in mice
- Transgneic Endothelin 3 Regulates Murine Pigment Production and Coat Color
- Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration
- Molecular and Functional Characterization of Clonogenic Human Thymic Epithelial Cells
- The effects of sonic, desert and Indian hedgehog signalling in skin
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- THERAPY OF ENDOCRINE DISEASE: Treatment of hirsutism in the polycystic ovary syndrome
- Interfacial Adipose Tissue in Systemic Sclerosis
- 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
- Polycystic Ovary Syndrome: A Literature Review With a Focus on Diagnosis, Pathophysiology, and Management
- Mechanism of Vitamin D Receptor Action
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Comparison of two ASC-derived therapeutics in an in vitro OA model: secretome versus extracellular vesicles
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure