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    Research 271–300 of 1000+

    1. Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome Biomedicines · 2023 · 3 citations
    2. Aging skin and non-surgical procedures: a basic science overview Plastic and Aesthetic Research · 2020 · 3 citations
    3. Moxibustion improves ovarian function based on the regulation of the androgen balance Experimental and Therapeutic Medicine · 2021 · 2 citations
    4. Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients Medicina · 2024 · 1 citations
    5. An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review Heliyon · 2023 · 1 citations
    6. Novel Insights into TSC22D Family Genes in Metabolic Diseases and Cancer Biomolecules · 2026
    7. Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock BMC Pediatrics · 2025
    8. Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways Preprints.org · 2025
    9. A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene 2024
    10. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    11. Carcinogenesis of the Human Scalp. An Immunometabolic Centered View Preprints.org · 2024
    12. Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review Frontiers in endocrinology · 2024
    13. Ehlers-Danlos syndrome: From bedside to bench Frontiers research topics · 2024
    14. Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study Journal of Thoracic Disease · 2023
    15. Proteome Analysis of Alpine Merino Sheep Skin Reveals New Insights into the Mechanisms Involved in Regulating Wool Fiber Diameter International journal of molecular sciences · 2023
    16. Endocrinology Clinical Chemistry and Laboratory Medicine · 2023
    17. Author response: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ 2017
    18. Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology Medizinische Genetik · 2023
    19. Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter Animals · 2022 · 2 citations
    20. Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review Mammalian Genome · 2025 · 7 citations
    21. Genes and Immune Response in Alopecia Areata: Review of the Alopecia Areata Research Summit First Day Proceedings Journal of Investigative Dermatology Symposium Proceedings · 2013 · 6 citations
    22. Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes Animals · 2024 · 4 citations
    23. Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis Dermatology and Therapy · 2024 · 3 citations
    24. A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome Annals of Dermatology · 2022 · 1 citations
    25. Pathogenesis and management of TRPV3-related Olmsted syndrome Frontiers in Genetics · 2024
    26. Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles Clinical, cosmetic and investigational dermatology · 2023 · 1 citations
    27. A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene Clinical Case Reports · 2025
    28. Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients Journal of endocrinological investigation · 2021 · 31 citations
    29. Inflammatory bowel disease: pathogenesis, diagnosis and current therapeutic approach Journal of Mind and Medical Sciences · 2022 · 13 citations
    30. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations