Cerebral Microvascular Amyloid β Protein Deposition Induces Vascular Degeneration and Neuroinflammation in Transgenic Mice Expressing Human Vasculotropic Mutant Amyloid β Precursor...

Por Miao, Jianting, Xu, Feng, Davis, Judianne, Otte-Höller, Irene, Verbeek, Marcel M., Van Nostrand, William E.
Publicado em 2005

Lithium Causes G2 Arrest of Renal Principal Cells

Por de Groot, Theun, Alsady, Mohammad, Jaklofsky, Marcel, Otte-Höller, Irene, Baumgarten, Ruben, Giles, Rachel H., Deen, Peter M.T.
Publicado em 2014

Apolipoprotein E Genotype Regulates Amyloid-β Cytotoxicity

Por Wilhelmus, Micha M. M., Otte-Höller, Irene, Davis, Judianne, Van Nostrand, William E., de Waal, Robert M. W., Verbeek, Marcel M.
Publicado no J Neurosci (2005)

Agrin Is a Major Heparan Sulfate Proteoglycan Accumulating in Alzheimer’s Disease Brain

Por Verbeek, Marcel M., Otte-Höller, Irene, van den Born, Jacob, van den Heuvel, Lambert P. W. J., David, Guido, Wesseling, Pieter, de Waal, Robert M. W.
Publicado em 1999

Lipoprotein Receptor-Related Protein-1 Mediates Amyloid-β-Mediated Cell Death of Cerebrovascular Cells

Por Wilhelmus, Micha M.M., Otte-Höller, Irene, van Triel, Jos J.J., Veerhuis, Robert, Maat-Schieman, Marion L.C., Bu, Guojun, de Waal, Robert M.W., Verbeek, Marcel M.
Publicado em 2007

Increased mitochondrial activity in a novel IDH1-R132H mutant human oligodendroglioma xenograft model: in situ detection of 2-HG and α-KG

Por Navis, Anna C, Niclou, Simone P, Fack, Fred, Stieber, Daniel, van Lith, Sanne, Verrijp, Kiek, Wright, Alan, Stauber, Jonathan, Tops, Bastiaan, Otte-Holler, Irene, Wevers, Ron A, van Rooij, Arno, Pusch, Stefan, von Deimling, Andreas, Tigchelaar, Wikky, van Noorden, Cornelis JF, Wesseling, Pieter, Leenders, William PJ
Publicado em 2013

HER2, chromosome 17 polysomy and DNA ploidy status in breast cancer; a translational study

Por Halilovic, Altuna, Verweij, Dagmar I., Simons, Annet, Stevens-Kroef, Marian J. P. L., Vermeulen, Susan, Elsink, Janet, Tops, Bastiaan B. J., Otte-Höller, Irene, van der Laak, Jeroen A. W. M., van de Water, Carlijn, Boelens, Oliver B. A., Schlooz-Vries, Margrethe S., Dijkstra, Jeroen R., Nagtegaal, Iris D., Tol, Jolien, van Cleef, Patricia H. J., Span, Paul N., Bult, Peter
Publicado no Sci Rep (2019)

Mutations in DDHD2, Encoding an Intracellular Phospholipase A(1), Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Por Schuurs-Hoeijmakers, Janneke H.M., Geraghty, Michael T., Kamsteeg, Erik-Jan, Ben-Salem, Salma, de Bot, Susanne T., Nijhof, Bonnie, van de Vondervoort, Ilse I.G.M., van der Graaf, Marinette, Nobau, Anna Castells, Otte-Höller, Irene, Vermeer, Sascha, Smith, Amanda C., Humphreys, Peter, Schwartzentruber, Jeremy, Ali, Bassam R., Al-Yahyaee, Saeed A., Tariq, Said, Pramathan, Thachillath, Bayoumi, Riad, Kremer, Hubertus P.H., van de Warrenburg, Bart P., van den Akker, Willem M.R., Gilissen, Christian, Veltman, Joris A., Janssen, Irene M., Vulto-van Silfhout, Anneke T., van der Velde-Visser, Saskia, Lefeber, Dirk J., Diekstra, Adinda, Erasmus, Corrie E., Willemsen, Michèl A., Vissers, Lisenka E.L.M., Lammens, Martin, van Bokhoven, Hans, Brunner, Han G., Wevers, Ron A., Schenck, Annette, Al-Gazali, Lihadh, de Vries, Bert B.A., de Brouwer, Arjan P.M.
Publicado em 2012