يعرض 1 - 9 نتائج من 9 نتيجة بحث عن '"Pagnon de la Vega, María"', وقت الاستعلام: 1.12s تنقيح النتائج
  1. 1
    Altered amyloid-β structure markedly reduces gliosis in the brain of mice harboring the Uppsala APP deletion

    المؤلفون: Pagnon de la Vega, María, Syvänen, Stina, Giedraitis, Vilmantas, Hooley, Monique, Konstantinidis, Evangelos, 1990, Meier, Silvio R., Rokka, Johanna, Eriksson, Jonas, Aguilar, Ximena, Spires-Jones, Tara L., Lannfelt, Lars, Nilsson, Lars N. G., Erlandsson, Anna, Hultqvist, Greta, 1980, Ingelsson, Martin, Sehlin, Dag, 1976

    المصدر: Acta neuropathologica communications. 12(1)

    مصطلحات موضوعية: Alzheimer's disease (AD), Amyloid precursor protein (APP), Amyloid-beta (A beta), PET imaging, Microglia, Astrocytes, Immunotherapy

    وصف الملف: electronic

    URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-523728
    https://doi.org/10.1186/s40478-024-01734-x
    https://uu.diva-portal.org/smash/get/diva2:1840756/FULLTEXT01.pdf

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  2. 2
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

    View this record from ISI Web of Science
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  3. 3
    دورية أكاديمية
    Mutation analysis of disease causing genes in patients with early onset or familial forms of Alzheimer’s disease and frontotemporal dementia

    المؤلفون: Pagnon de la Vega, María, Näslund, Carl, Brundin, RoseMarie, Lannfelt, Lars, Löwenmark, Malin, Kilander, Lena, Ingelsson, MartinAff1, Aff2, Aff3, Giedraitis, VilmantasAff1, IDs12864022083439_cor8

    المصدر: BMC Genomics. 23(1)

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest Full Text Finder
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  4. 4
    Characterization of the novel “Uppsala mutation” causing a familial form of early onset Alzheimer’s disease

    المؤلفون: Pagnon de la Vega, María, 1994

    المساهمون: Ingelsson, Martin, Professor, Senior consultant, Sehlin, Dag, Associate Professor, Giedraitis, Vilmantas, PhD, Researcher, Gouras, Gunnar, Professor

    المصدر: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine.

    مصطلحات موضوعية: Alzheimer's disease, neurodegeneration, amyloid precursor protein, APP processing, amyloid beta, transgenic mouse model

    وصف الملف: electronic

    URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-446916
    https://uu.diva-portal.org/smash/get/diva2:1571680/FULLTEXT01.pdf
    https://uu.diva-portal.org/smash/get/diva2:1571680/PREVIEW01.jpg

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  5. 5
    دورية أكاديمية
    The Uppsala APP deletion causes early onset autosomal dominant Alzheimer's disease by altering APP processing and increasing amyloid β fibril formation.

    المؤلفون: Pagnon de la Vega, María, Giedraitis, Vilmantas, Michno, Wojciech, Kilander, Lena, Güner, Gökhan, Zielinski, Mara, Löwenmark, Malin, Brundin, RoseMarie, Danfors, Torsten, Söderberg, Linda, Alafuzoff, Irina, Nilsson, Lars N.G., Erlandsson, Anna, Willbold, Dieter, Müller, Stephan A., Schröder, Gunnar F., Hanrieder, Jörg, Lichtenthaler, Stefan F., Lannfelt, Lars, Sehlin, Dag

    المصدر: Science Translational Medicine; 8/11/2021, Vol. 13 Issue 606, p1-13, 13p

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  6. 6
    دورية
    The Uppsala APPdeletion causes early onset autosomal dominant Alzheimer’s disease by altering APP processing and increasing amyloid β fibril formation

    المؤلفون: Pagnon de la Vega, María, Giedraitis, Vilmantas, Michno, Wojciech, Kilander, Lena, Güner, Gökhan, Zielinski, Mara, Löwenmark, Malin, Brundin, RoseMarie, Danfors, Torsten, Söderberg, Linda, Alafuzoff, Irina, Nilsson, Lars N.G., Erlandsson, Anna, Willbold, Dieter, Müller, Stephan A., Schröder, Gunnar F., Hanrieder, Jörg, Lichtenthaler, Stefan F., Lannfelt, Lars, Sehlin, Dag, Ingelsson, Martin

    المصدر: Science Translational Medicine; August 2021, Vol. 13 Issue: 606

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  7. 7
    Transgenic mice harboring the Uppsala APP mutation display altered APP processing and accelerated Aβ42 pathology with distinct structural features

    المؤلفون: Pagnon de la Vega, María, 1994, Syvänen, Stina, Hooley, Monique, Giedraitis, Vilmantas, Kostantinidis, Evangelos, Meier, Silvio R., Rokka, Johanna, Eriksson, Jonas, Aguilar, Ximena, Spires-Jones, Tara, Hultqvist, Greta, 1980, Nilsson, Lars, Lannfelt, Lars, Ingelsson, Martin, Sehlin, Dag, 1976

    وصف الملف: print

    URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-446865

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  8. 8
    The Uppsala APP deletion causes early onset autosomal dominant Alzheimer’s disease by altering APP processing and increasing amyloid-β fibril formation

    المؤلفون: Pagnon de la Vega, María, 1994, Giedraitis, Vilmantas, Michno, Wojciech, Kilander, Lena, Güner, Gökhan, Zielinski, Mara, Löwenmark, Malin, Brundin, RoseMarie, Danfors, Torsten, 1964, Söderberg, Linda, Alafuzoff, Irina, Nilsson, Lars, Erlandsson, Anna, Willbold, Dieter, Müller, Stephan A., Schöder, Gunnar F., Hanrieder, Jörg, Lichtenthaler, Stefan F., Lannfelt, Lars, Sehlin, Dag, 1976, Ingelsson, Martin

    المصدر: Science Translational Medicine.

    وصف الملف: print

    URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-446824

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  9. 9
    The Uppsala APP mutation promotes wildtype Aβ aggregation and deposition in vivo

    المؤلفون: Pagnon de la Vega, María, 1994, Ge, Junyue, Giedraitis, Vilmantas, Syvänen, Stina, Lannfelt, Lars, Hanrieder, Jörg, Ingelsson, Martin, Sehlin, Dag, 1976

    وصف الملف: print

    URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-446874

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