Showing 1,121 - 1,140 results of 1,178 for search '"Genetic disorder', query time: 0.07s Refine Results
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    Predicting amyloid proteins using attention-based long short-term memory by Zhuowen Li

    Published 2025-02-01
    “…Alzheimer’s disease (AD) is one of the genetically inherited neurodegenerative disorders that mostly occur when people get old. …”
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    The endocytic adaptor AP-2 maintains Purkinje cell function by balancing cerebellar parallel and climbing fiber synapses by Marianna Tolve, Janine Tutas, Ebru Özer-Yildiz, Ines Klein, Anne Petzold, Veronika J. Fritz, Melina Overhoff, Quinn Silverman, Ellie Koletsou, Filip Liebsch, Guenter Schwarz, Tatiana Korotkova, Silvana Valtcheva, Graziana Gatto, Natalia L. Kononenko

    Published 2025-02-01
    “…Summary: The loss of cerebellar Purkinje cells is a hallmark of neurodegenerative movement disorders, but the mechanisms remain enigmatic. We show that endocytic adaptor protein complex 2 (AP-2) is crucial for Purkinje cell survival. …”
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    Deep Venous Thrombosis and Bilateral Pulmonary Embolism Revealing Silent Celiac Disease: Case Report and Review of the Literature by Igor Dumic, Scott Martin, Nadim Salfiti, Robert Watson, Tamara Alempijevic

    Published 2017-01-01
    “…Celiac disease (CD) is a systemic, chronic autoimmune disease that occurs in genetically predisposed individuals following dietary gluten exposure. …”
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    Review article: key aspects of mammal microbiome development by E. V. Semenova, O. A. Manzhurina, Yu. S. Parkhomenko

    Published 2021-03-01
    “…Even different modes of delivery (caesarean or vaginal delivery) may determine the initial colonization of the newborn. The animal genetics, nutrition and environment also influence the intestinal microbiota development. …”
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    Neuronal heterogeneity in the ventral tegmental area: Distinct contributions to reward circuitry and motivated behavior by N. Dalton Fitzgerald, Jeremy J. Day

    Published 2025-03-01
    “…Understanding VTA cell type heterogeneity may yield new insights into the reward system, offering potential avenues for treating substance use disorders and other related conditions.…”
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    Idiopathic Generalized Epilepsy and Hypokalemic Periodic Paralysis in a Family of South Indian Descent by Muthiah Subramanian, N. Senthil, S. Sujatha

    Published 2015-01-01
    “…Inherited channelopathies are a heterogeneous group of disorders resulting from dysfunction of ion channels in cellular membranes. …”
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    Calcitonin and Bone Physiology: In Vitro, In Vivo, and Clinical Investigations by Jingbo Xie, Jian Guo, Zaeema Kanwal, Mingzheng Wu, Xiangyang Lv, Nihal Abdalla Ibrahim, Ping Li, Manal Ali Buabeid, El-Shaimaa A. Arafa, Qingshan Sun

    Published 2020-01-01
    “…This is the reason why calcitonin has been used widely in clinics for the treatment of bone disorders such as osteoporosis, hypercalcemia, and Paget’s disease. …”
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    Cellular therapies in rheumatic and musculoskeletal diseases by Pedro Franco-Fuquen, Juana Figueroa-Aguirre, David A. Martínez, Eider F. Moreno-Cortes, Juan E. Garcia-Robledo, Fabio Vargas-Cely, Daniela A. Castro-Martínez, Mustafa Almaini, Januario E. Castro

    Published 2025-06-01
    “…These diseases, which include autoimmune disorders such as multiple sclerosis, rheumatoid arthritis, and systemic lupus erythematosus, are marked by the presence of autoreactive B cells that play a critical role in their pathogenesis. …”
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