Christine Van Broeckhoven

Christine Van Broeckhoven (born 9 April 1953) is a Belgian molecular biologist and professor in Molecular genetics at the University of Antwerp (Antwerp, Belgium). She is also leading the VIB Department of Molecular Genetics, University of Antwerp of the Flanders Institute for Biotechnology (VIB). Christine Van Broeckhoven does research on Alzheimer dementia, bipolar mental disorders and other neurological diseases. Since 1983 she has had her own laboratory for molecular genetics at the University of Antwerp, and since 2005 is focussing her research on neurodegenerative brain diseases. She is an associate editor of the scientific journal ''Genes, Brain and Behavior''. Provided by Wikipedia
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  1. 1
    Genetic perspective on the synergistic connection between vesicular transport, lysosomal and mitochondrial pathways associated with Parkinson’s disease pathogenesis

    Genetic perspective on the synergistic connection between vesicular transport, lysosomal and mitochondrial pathways associated with Parkinson’s disease pathogenesis by Stefanie Smolders, Christine Van Broeckhoven

    Published 2020-05-01
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  2. 2
    Proteasome degrades soluble expanded polyglutamine completely and efficiently

    Proteasome degrades soluble expanded polyglutamine completely and efficiently by Andrej Michalik, Christine Van Broeckhoven

    Published 2004-06-01
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  3. 3
    The role of ATP-binding cassette subfamily A in the etiology of Alzheimer’s disease

    The role of ATP-binding cassette subfamily A in the etiology of Alzheimer’s disease by Liene Bossaerts, Rita Cacace, Christine Van Broeckhoven

    Published 2022-04-01
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  4. 4
    Insight into the genetic etiology of Alzheimer's disease: A comprehensive review of the role of rare variants

    Insight into the genetic etiology of Alzheimer's disease: A comprehensive review of the role of rare variants by Julie Hoogmartens, Rita Cacace, Christine Van Broeckhoven

    Published 2021-01-01
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  5. 5
    Advances in Charcot–Marie–Tooth Disease Research: Cellular Function of CMT-Related Proteins, Transgenic Animal Models, and Pathomechanisms

    Advances in Charcot–Marie–Tooth Disease Research: Cellular Function of CMT-Related Proteins, Transgenic Animal Models, and Pathomechanisms by Hans W. Müller, Ueli Suter, Christine Van Broeckhoven

    Published 2000-06-01
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  6. 6
    Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant?

    Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant? by Geert Van Gassen, Wim Annaert, Christine Van Broeckhoven

    Published 2000-06-01
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  7. 7
    Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant?

    Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant? by Geert Van Gassen, Wim Annaert, Christine Van Broeckhoven

    Published 2000-12-01
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  8. 8
    Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum

    Stress granule mediated protein aggregation and underlying gene defects in the FTD-ALS spectrum by Yalda Baradaran-Heravi, Christine Van Broeckhoven, Julie van der Zee

    Published 2020-02-01
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  9. 9
    Rare missense mutations in ABCA7 might increase Alzheimer’s disease risk by plasma membrane exclusion

    Rare missense mutations in ABCA7 might increase Alzheimer’s disease risk by plasma membrane exclusion by Liene Bossaerts, Elisabeth Hendrickx Van de Craen, Rita Cacace, Bob Asselbergh, Christine Van Broeckhoven

    Published 2022-03-01
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  10. 10
    Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity

    Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in Comorbidity by Eva Parobkova, Eva Parobkova, Julie van der Zee, Julie van der Zee, Lubina Dillen, Lubina Dillen, Christine Van Broeckhoven, Christine Van Broeckhoven, Robert Rusina, Robert Rusina, Radoslav Matej, Radoslav Matej, Radoslav Matej, Radoslav Matej

    Published 2020-11-01
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  11. 11
    Lymphoblast-derived integration-free ISRM-CON9 iPS cell line from a 75 year old female

    Lymphoblast-derived integration-free ISRM-CON9 iPS cell line from a 75 year old female by Soraia Martins, Martina Bohndorf, Friederike Schröter, Fatima Assar, Wasco Wruck, Kristel Sleegers, Christine Van Broeckhoven, James Adjaye

    Published 2018-01-01
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  12. 12
    Peripheral myelin protein 2 – a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy

    Peripheral myelin protein 2 – a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy by Paulius Palaima, Teodora Chamova, Sebastian Jander, Vanyo Mitev, Christine Van Broeckhoven, Ivailo Tournev, Kristien Peeters, Albena Jordanova

    Published 2019-08-01
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  13. 13
    Lymphoblast-derived integration-free iPSC line AD-TREM2-1 from a 67 year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant

    Lymphoblast-derived integration-free iPSC line AD-TREM2-1 from a 67 year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant by Soraia Martins, Hatice Yigit, Martina Bohndorf, Nina Graffmann, Aurelian Robert Fiszl, Wasco Wruck, Kristel Sleegers, Christine Van Broeckhoven, James Adjaye

    Published 2018-05-01
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  14. 14
    IPSC-Derived Neuronal Cultures Carrying the Alzheimer’s Disease Associated <i>TREM2</i> R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network

    IPSC-Derived Neuronal Cultures Carrying the Alzheimer’s Disease Associated <i>TREM2</i> R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network by Soraia Martins, Andreas Müller-Schiffmann, Lars Erichsen, Martina Bohndorf, Wasco Wruck, Kristel Sleegers, Christine Van Broeckhoven, Carsten Korth, James Adjaye

    Published 2020-06-01
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  15. 15
    Lymphoblast-derived integration-free iPSC line AD-TREM2-3 from a 74 year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant

    Lymphoblast-derived integration-free iPSC line AD-TREM2-3 from a 74 year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant by Soraia Martins, Hatice Yigit, Martina Bohndorf, Nina Graffmann, Aurelian Robert Fiszl, Wasco Wruck, Kristel Sleegers, Christine Van Broeckhoven, James Adjaye

    Published 2018-07-01
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  16. 16
    Evidence That Aβ42 Plasma Levels in Presenilin-1 Mutation Carriers Do not Allow for Prediction of Their Clinical Phenotype

    Evidence That Aβ42 Plasma Levels in Presenilin-1 Mutation Carriers Do not Allow for Prediction of Their Clinical Phenotype by Chris De Jonghe, Patrick Cras, Hugo Vanderstichele, Marc Cruts, Inge Vanderhoeven, Iris Smouts, Eugeen Vanmechelen, Jean-Jaques Martin, Lydia Hendriks, Christine Van Broeckhoven

    Published 1999-08-01
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  17. 17
    Alzheimer's Disease Associated Presenilin 1 Interacts with HC5 and ZETA, Subunits of the Catalytic 20S Proteasome

    Alzheimer's Disease Associated Presenilin 1 Interacts with HC5 and ZETA, Subunits of the Catalytic 20S Proteasome by Geert Van Gassen, Chris De Jonghe, Stefan Pype, Wim Van Criekinge, Ann Julliams, Inge Vanderhoeven, Sarah Woodrow, Rudi Beyaert, Danny Huylebroeck, Christine Van Broeckhoven

    Published 1999-10-01
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  18. 18
    Longer leukocyte telomere length is associated with smaller hippocampal volume among non-demented APOE ε3/ε3 subjects.

    Longer leukocyte telomere length is associated with smaller hippocampal volume among non-demented APOE ε3/ε3 subjects. by Mikael Wikgren, Thomas Karlsson, Johanna Lind, Therese Nilbrink, Johan Hultdin, Kristel Sleegers, Christine Van Broeckhoven, Göran Roos, Lars-Göran Nilsson, Lars Nyberg, Rolf Adolfsson, Karl-Fredrik Norrback

    Published 2012-01-01
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  19. 19
    In Vitro Studies of Flemish, Dutch, and Wild-Type β-Amyloid Provide Evidence for Two-Staged Neurotoxicity

    In Vitro Studies of Flemish, Dutch, and Wild-Type β-Amyloid Provide Evidence for Two-Staged Neurotoxicity by Samir Kumar-Singh, Ann Julliams, Rony Nuydens, Chantal Ceuterick, Christine Labeur, Sally Serneels, Krist'l Vennekens, Peter Van Osta, Hugo Geerts, Bart De Strooper, Christine Van Broeckhoven

    Published 2002-11-01
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  20. 20
    Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

    Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene by Håkan Thonberg, Huei-Hsin Chiang, Lena Lilius, Charlotte Forsell, Anna-Karin Lindström, Charlotte Johansson, Jenny Björkström, Steinunn Thordardottir, Kristel Sleegers, Christine Van Broeckhoven, Annica Rönnbäck, Caroline Graff

    Published 2017-06-01
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