يعرض 1 - 6 نتائج من 6 نتيجة بحث عن '"LYSOSOMAL storage diseases"', وقت الاستعلام: 0.73s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Unique molecular signature in mucolipidosis type IV microglia.

    المؤلفون: Cougnoux, Antony1 (AUTHOR), Drummond, Rebecca A.2 (AUTHOR), Fellmeth, Mason1 (AUTHOR), Navid, Fatemeh3 (AUTHOR), Collar, Amanda L.2 (AUTHOR), Iben, James4 (AUTHOR), Kulkarni, Ashok B.5 (AUTHOR), Pickel, James6 (AUTHOR), Schiffmann, Raphael7 (AUTHOR), Wassif, Christopher A.1 (AUTHOR), Cawley, Niamh X.1 (AUTHOR), Lionakis, Michail S.2 (AUTHOR), Porter, Forbes D.1 (AUTHOR) fdporter@mail.nih.gov

    المصدر: Journal of Neuroinflammation. 12/28/2019, Vol. 16 Issue 1, p1-12. 12p.

    مصطلحات موضوعية: *LYSOSOMAL storage diseases, *ANGIOKERATOMA corporis diffusum, *HUNTINGTON disease, *AMYOTROPHIC lateral sclerosis, *NIEMANN-Pick diseases

    النص الكامل

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  2. 2
    دورية أكاديمية
    Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease

    المؤلفون: Ayelet Vardi, Shifra Ben-Dor, Soo Min Cho, Ulrich Kalinke, Julia Spanier, Anthony H. Futerman

    المصدر: Journal of Neuroinflammation, Vol 17, Iss 1, Pp 1-13 (2020)

    مصطلحات موضوعية: Gaucher disease, Pathogen recognition receptors, Type 1 interferon, Neurodegenerative diseases, Lipid metabolism, Lysosomal storage diseases, Neurology. Diseases of the nervous system, RC346-429

    وصف الملف: electronic resource

    العلاقة: http://link.springer.com/article/10.1186/s12974-020-01934-xTest; https://doaj.org/toc/1742-2094Test

    الوصول الحر: https://doaj.org/article/5d0995bc6334429eae1931e23d6e8d7dTest

    View record in DOAJ النص الكامل

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  3. 3
    دورية أكاديمية
    Inhibition of microglial β-glucocerebrosidase hampers the microglia-mediated antioxidant and protective response in neurons.

    المؤلفون: Brunialti, Electra, Villa, Alessandro, Mekhaeil, Marianna, Mornata, Federica, Vegeto, Elisabetta, Maggi, Adriana, Di Monte, Donato A., Ciana, Paolo

    المصدر: Journal of Neuroinflammation; 9/22/2021, Vol. 18 Issue 1, p1-18, 18p

    مصطلحات موضوعية: MICROGLIA, GAUCHER'S disease, NEUROTOXIC agents, NEURONS, PARKINSON'S disease, LYSOSOMAL storage diseases, ASTROCYTES

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  4. 4
    دورية أكاديمية
    Mucopolysaccharidosis IIIB, a lysosomal storage disease, triggers a pathogenic CNS autoimmune response.

    المؤلفون: Killedar, Smruti1,2, DiRosario, Julianne1, Divers, Erin1, Popovich, Phillip G.3,4,5, McCarty, Douglas M.1,2, Haiyan Fu1,2 haiyan.fu@nationwidechildrens.org

    المصدر: Journal of Neuroinflammation. 2010, Vol. 7, p39-46. 8p.

    مصطلحات موضوعية: *MUCOPOLYSACCHARIDOSIS, *LYSOSOMAL storage diseases, *LYMPHOCYTES, *INBORN errors of metabolism, *NEUROLOGICAL disorders

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  5. 5
    Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease

    المؤلفون: Shifra Ben-Dor, Anthony H. Futerman, Soo Min Cho, Ulrich Kalinke, Ayelet Vardi, Julia Spanier

    المساهمون: TWINCORE, Zentrum für experimentelle und klinische Infektionsforschung GmbH,Feodor-Lynen Str. 7, 30625 Hannover, Germany.

    المصدر: Journal of Neuroinflammation, Vol 17, Iss 1, Pp 1-13 (2020)
    Journal of Neuroinflammation
    Journal of neuroinflammation
    England

    مصطلحات موضوعية: 0301 basic medicine, Chemokine, Pathogen recognition receptors, Immunology, Gaucher disease, Type 1 interferon, lcsh:RC346-429, Mice, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Interferon, hemic and lymphatic diseases, Lysosomal storage diseases, medicine, Animals, Receptor, Neuroinflammation, lcsh:Neurology. Diseases of the nervous system, Mice, Knockout, Neurons, Innate immune system, biology, Microglia, Research, General Neuroscience, Neurodegenerative diseases, Sphingolipid, Disease Models, Animal, 030104 developmental biology, medicine.anatomical_structure, Lipid metabolism, Neurology, Interferon Type I, Cancer research, biology.protein, Glucosylceramidase, Tumor necrosis factor alpha, 030217 neurology & neurosurgery, Signal Transduction, medicine.drug

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ba497013484225939efc07c4580b25Test
    http://link.springer.com/article/10.1186/s12974-020-01934-xTest


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  6. 6
    دورية أكاديمية
    Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease.

    المؤلفون: Vardi, Ayelet, Ben-Dor, Shifra, Cho, Soo Min, Kalinke, Ulrich, Spanier, Julia, Futerman, Anthony H.

    المصدر: Journal of Neuroinflammation; 9/7/2020, Vol. 17 Issue 1, pN.PAG-N.PAG, 1p

    مصطلحات موضوعية: TYPE I interferons, INTERFERONS, GLYCOGEN storage disease type II, MICE, LYSOSOMAL storage diseases, BETA-glucosidase, CELL metabolism, BIOLOGICAL models, NEURONS, CELLULAR signal transduction, GLYCOSIDASES, GAUCHER'S disease, ANIMALS

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