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Research 181–210 of 1000+
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Early onset androgenic alopecia: not a cosmetic problem but a sign of life time risk factors. Male phenotypic equivalent of polycystic ovarian syndrome: Is There a Male Phenotype of PCOS
- Comparing the Efficacy of Myo-Inositol Plus α-Lactalbumin vs. Myo-Inositol Alone on Reproductive and Metabolic Disturbances of Polycystic Ovary Syndrome
- Spontaneous Lesions of Endangered Geriatric Julia Creek Dunnarts (Sminthopsis douglasi, Archer 1979) with Emphasis in Reproductive Pathology
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Spatiotemporal regulation of acute wound healing by the NLRP3 inflammasome: dual roles in macrophage-fibroblast chemotaxis and phenotype during wound repair
- Reconsidering the Polycystic Ovary Syndrome (PCOS)
- Health-related quality of life in women with polycystic ovary syndrome attending to a tertiary hospital in Southeastern Spain: a case-control study.
- A systematic review of models of care for polycystic ovary syndrome highlights the gap in the literature, especially in developing countries
- Endocrine intervention for transsexuals
- A mutation in MAP2 is associated with prenatal hair follicle density
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Skin deep: dermatologic challenges in PCOS through the female lifespan
- New clinico‐genetic classification of trichothiodystrophy
- Nitric Oxide: Physiological Functions, Delivery, and Biomedical Applications
- Polycystic ovary syndrome and mental health: a call to action
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- 516 Functional annotation of genes underlying hair disorders
- Increased rate of hair keratin gene loss in the cetacean lineage
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- A missense mutation in Lama3 causes androgen alopecia
- Epidemiology, diagnosis, and management of polycystic ovary syndrome
- Follicular Fluid: A Powerful Tool for the Understanding and Diagnosis of Polycystic Ovary Syndrome
- Polycystic ovary syndrome and infertility: an update
- Global Impact of Coronavirus Disease 2019 (COVID-19)
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Morphometric-stereological and functional epididymal alterations and a decrease in fertility in rats treated with finasteride and after a 30-day post-treatment recovery period
- Biomaterial-based mechanical regulation facilitates scarless wound healing with functional skin appendage regeneration