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Research 121–150 of 1000+
- Cell Polarization Defects in Early Heart Development
- In This Issue
- Nonclassic 21-hydroxylase deficiency
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Human Skin is a Steroidogenic Tissue: Steroidogenic Enzymes and Cofactors Are Expressed in Epidermis, Normal Sebocytes, and an Immortalized Sebocyte Cell Line (SEB-1)
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Deciphering the Insulin Link: Exploring Metabolic Interplay in Polycystic Ovary Syndrome
- Sexual Dysfunction in Polycystic Ovary Syndrome (PCOS): A Biopsychosocial Approach to Assessment and Management
- Approach to the Patient: Diagnostic Challenges in the Work Up for Polycystic Ovary Syndrome
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Women with PCOS have a heightened risk of cardiometabolic and cardiovascular diseases: statement from the Experts Group on Inositol in Basic and Clinical Research and PCOS (EGOI-PCOS) and Italian Association of Hospital Cardiologists (ANMCO)
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Visualizing Integrative Functioning in the Human Brainstem and Spinal Cord With Spinal Functional Magnetic Resonance Imaging
- Polycystic ovary syndrome
- Current Guidelines for Diagnosing PCOS
- Natural killer cells in atopic and autoimmune diseases of the skin
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Rapidly progressing mycosis fungoides presenting as follicular mucinosis
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Criteria for Diagnosis of Polycystic Ovary Syndrome during Adolescence: Literature Review
- A rational approach to the diagnosis of polycystic ovarian syndrome during adolescence
- Early embryonic exposure of freshwater gastropods to pharmaceutical 5-alpha-reductase inhibitors results in a surprising open-coiled “banana-shaped” shell
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis