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Medicine

D-Index
79
Citations
18965
World Ranking
17733
National Ranking
668

Overview

Dirk Troost is affiliated with the University of Amsterdam in the Netherlands. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, as well as Medicine. Troost's work addresses several subfields including Molecular Biology, Cell Biology, Physiology, and Epidemiology.

The scientist's research topics focus on areas such as Heat Shock Proteins research, Endoplasmic Reticulum Stress and Disease, Alzheimer's disease research and treatments, and Autophagy in Disease and Therapy.

Troost has contributed to a number of publications. Notable recent papers include:

  • Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling, 2021, published in EMBO Reports
  • Aggregates of RNA Binding Proteins and ER Chaperones Linked to Exosomes in Granulovacuolar Degeneration of the Alzheimer's Disease Brain, 2020, published in Journal of Alzheimer s Disease

Frequent co-authors in Troost's work are:

  • Priyanka Tripathi
  • Eleonora Aronica
  • Anand Goswami
  • Laura Mediani
  • Francesco Antoniani

The main publication venues where Troost's work appears include EMBO Reports and the Journal of Alzheimer s Disease.

Best Publications

  • Integrated Genomics Identifies Five Medulloblastoma Subtypes with Distinct Genetic Profiles, Pathway Signatures and Clinicopathological Features

    Marcel Kool;Jan Koster;Jens Bunt;Nancy E. Hasselt

  • Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

    Manuela Neumann;Manuela Neumann;Linda K. Kwong;Edward B. Lee;Elisabeth Kremmer

  • TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.

    Nigel J. Cairns;Manuela Neumann;Manuela Neumann;Eileen H. Bigio;Ida E. Holm

  • IDH1 mutations at residue p.R132 (IDH1(R132)) occur frequently in high-grade gliomas but not in other solid tumors.

    Fonnet E. Bleeker;Simona Lamba;Sieger Leenstra;Dirk Troost

  • Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3

    Caroline Vance;Ammar Al-Chalabi;Deborah Ruddy;Bradley N. Smith

  • The IL-1β system in epilepsy-associated malformations of cortical development

    T. Ravizza;K. Boer;S. Redeker;W.G.M. Spliet

  • Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations

    Ian R. Mackenzie;Thomas Arzberger;Thomas Arzberger;Elisabeth Kremmer;Elisabeth Kremmer;Dirk Troost

  • Upregulation of metabotropic glutamate receptor subtype mGluR3 and mGluR5 in reactive astrocytes in a rat model of mesial temporal lobe epilepsy.

    Eleonora Aronica;Erwin A. Van Vliet;Oleg A. Mayboroda;Dirk Troost

  • Expression and functional role of mGluR3 and mGluR5 in human astrocytes and glioma cells: opposite regulation of glutamate transporter proteins.

    Eleonora Aronica;Jan A. Gorter;Helen Ijlst-Keizers;Annemieke J. Rozemuller

  • The prognostic IDH1 R132 mutation is associated with reduced NADP + -dependent IDH activity in glioblastoma

    Fonnet E. Bleeker;Nadia A. Atai;Simona Lamba;Ard Jonker

  • NLRP3 Inflammasome Is Expressed by Astrocytes in the SOD1 Mouse Model of ALS and in Human Sporadic ALS Patients

    Sonja Johann;Marius Heitzer;Mithila Kanagaratnam;Anand Goswami

  • Expression and Cellular Distribution of Multidrug Resistance–related Proteins in the Hippocampus of Patients with Mesial Temporal Lobe Epilepsy

    Eleonora Aronica;Jan A. Gorter;Marja Ramkema;Sandra Redeker

  • Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex.

    K. Boer;F. Jansen;M. Nellist;S. Redeker

  • Expression and cellular distribution of multidrug transporter proteins in two major causes of medically intractable epilepsy: focal cortical dysplasia and glioneuronal tumors.

    E.M.A. Aronica;J.A. Gorter;G.H. Jansen;C.W.M. van Veelen

  • Toll-like receptor signaling in amyotrophic lateral sclerosis spinal cord tissue.

    M. Casula;A.M. Iyer;W.G.M. Spliet;J.J. Anink

  • Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation

    Marcel Naumann;Arun Pal;Anand Goswami;Xenia Lojewski

  • Complement activation in experimental and human temporal lobe epilepsy.

    E. Aronica;K. Boer;E.A. van Vliet;S. Redeker

  • The combination of IDH1 mutations and MGMT methylation status predicts survival in glioblastoma better than either IDH1 or MGMT alone

    Remco J. Molenaar;Dagmar Verbaan;Simona Lamba;Carlo Zanon

  • The genomic profile of human malignant glioma is altered early in primary cell culture and preserved in spheroids

    P C De Witt Hamer;A A G Van Tilborg;P P Eijk;P Sminia

  • Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers

    Ian R. A. Mackenzie;Petra Frick;Friedrich A. Grässer;Tania F. Gendron

Frequent Co-Authors

Eleonora Aronica
Eleonora Aronica University of Amsterdam
Jan A. Gorter
Jan A. Gorter University of Amsterdam
Frank Baas
Frank Baas Leiden University Medical Center
Joachim Weis
Joachim Weis RWTH Aachen University
Peter C. van Rijen
Peter C. van Rijen Utrecht University
Manuela Neumann
Manuela Neumann University of Tübingen
Cornelis J.F. Van Noorden
Cornelis J.F. Van Noorden University of Amsterdam
Dick F. Swaab
Dick F. Swaab Royal Netherlands Academy of Arts and Sciences
Alberto Bardelli
Alberto Bardelli University of Turin
Erwin A. van Vliet
Erwin A. van Vliet University of Amsterdam

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