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Search Results - Popitsch, N.
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Next-Generation Sequencing-based genomic profiling of brain metastases of primary ovarian cancer identifies high number of BRCA-mutations
by
Balendran, S.
,
Liebmann-Reindl, S.
,
Berghoff, A. S.
,
Reischer, T.
,
Popitsch, N.
,
Geier, C. B.
,
Kenner, L.
,
Birner, P.
,
Streubel, B.
,
Preusser, M.
Published in
Journal of neuro-oncology
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Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia
by
Klintman, Jenny
,
Appleby, Niamh
,
Stamatopoulos, Basile
,
Ridout, Katie
,
Eyre, Toby A.
,
Robbe, Pauline
,
Pascua, Laura Lopez
,
Knight, Samantha J.L.
,
Dreau, Helene
,
Cabes, Maite
,
Popitsch, Niko
,
Ehinger, Mats
,
Martín-Subero, Jose I.
,
Campo, Elías
,
Månsson, Robert
,
Rossi, Davide
,
Taylor, Jenny C.
,
Vavoulis, Dimitrios V.
,
Schuh, Anna
Published in
Blood
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Impaired plasticity of macrophages in X-linked adrenoleukodystrophy
by
Weinhofer, Isabelle
,
Zierfuss, Bettina
,
Hametner, Simon
,
Wagner, Magdalena
,
Popitsch, Niko
,
Machacek, Christian
,
Bartolini, Barbara
,
Zlabinger, Gerhard
,
Ohradanova-Repic, Anna
,
Stockinger, Hannes
,
Köhler, Wolfgang
,
Höftberger, Romana
,
Regelsberger, Günther
,
Forss-Petter, Sonja
,
Lassmann, Hans
,
Berger, Johannes
Published in
Brain (London, England : 1878)
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DSNotify - Detecting and Fixing Broken Links in Linked Data Sets
by
Haslhofer, B.
,
Popitsch, N.
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Conference Proceeding
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An Evaluation Approach for Dynamics-Aware Applications Using Linked Data
by
Popitsch, N
,
Haslhofer, B
,
Roochi, E M
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Identifikation einer Heterozygoten RIT1-Mutation in einem fetalen Fall von Noonan Syndrom mit gonadoblastoider, testiculärer Dysplasie mittels Exom-Sequenzierung
by
Reischer, T
,
Schmid, M
,
Vodopiutz, J
,
Krampl-Bettlheim, E
,
Popitsch, N
,
Streubel, B
Published in
Geburtshilfe und Frauenheilkunde
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Identifikation einer Heterozygoten RIT1-Mutation in einem fetalen Fall von Noonan Syndrom mit gonadoblastoider, testiculärer Dysplasie mittels Exom-Sequenzierung
by
Reischer, T
,
Schmid, M
,
Vodopiutz, J
,
Krampl-Bettlheim, E
,
Popitsch, N
,
Streubel, B
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Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies
by
Ilkovski, Biljana
,
Pagnamenta, Alistair T
,
O'Grady, Gina L
,
Kinoshita, Taroh
,
Howard, Malcolm F
,
Lek, Monkol
,
Thomas, Brett
,
Turner, Anne
,
Christodoulou, John
,
Sillence, David
,
Knight, Samantha J L
,
Popitsch, Niko
,
Keays, David A
,
Anzilotti, Consuelo
,
Goriely, Anne
,
Waddell, Leigh B
,
Brilot, Fabienne
,
North, Kathryn N
,
Kanzawa, Noriyuki
,
Macarthur, Daniel G
,
Taylor, Jenny C
,
Kini, Usha
,
Murakami, Yoshiko
,
Clarke, Nigel F
Published in
Human molecular genetics
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Microcavity Lasing from Block Peptide Hierarchically Assembled Quantum Dot Spherical Resonators
by
Cha, Jennifer N
,
Bartl, Michael H
,
Wong, Michael S
,
Popitsch, Alois
,
Deming, Timothy J
,
Stucky, Galen D
Published in
Nano letters
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CD371 cell surface expression: a unique feature of DUX4 -rearranged acute lymphoblastic leukemia
by
Schinnerl, Dagmar
,
Mejstrikova, Ester
,
Schumich, Angela
,
Zaliova, Marketa
,
Fortschegger, Klaus
,
Nebral, Karin
,
Attarbaschi, Andishe
,
Fiser, Karel
,
Kauer, Maximilian O
,
Popitsch, Niko
,
Haslinger, Sabrina
,
Inthal, Andrea
,
Buldini, Barbara
,
Basso, Giuseppe
,
Bourquin, Jean-Pierre
,
Gaipa, Giuseppe
,
Brüggemann, Monika
,
Feuerstein, Tamar
,
Maurer-Granofszky, Margarita
,
Panzer-Grümayer, Renate
,
Trka, Jan
,
Mann, Georg
,
Haas, Oskar A
,
Hrusak, Ondrej
,
Dworzak, Michael N
,
Strehl, Sabine
Published in
Haematologica (Roma)
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