Works matching IS 10452257 AND DT 2019 AND VI 58 AND IP 9

Results: 13

The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 657, doi. 10.1002/gcc.22759
By:
- Pinheiro, Manuela;
- Francisco, Inês;
- Pinto, Carla;
- Peixoto, Ana;
- Veiga, Isabel;
- Filipe, Bruno;
- Santos, Catarina;
- Maia, Sofia;
- Silva, João;
- Pinto, Pedro;
- Santos, Rui;
- Claro, Isabel;
- Lage, Pedro;
- Lopes, Paula;
- Ferreira, Sara;
- Rosa, Isadora;
- Fonseca, Ricardo;
- Rodrigues, Paula;
- Henrique, Rui;
- Chaves, Paula
Publication type:
Article
S100 and CD34 positive spindle cell tumor with prominent perivascular hyalinization and a novel NCOA4‐RET fusion.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 680, doi. 10.1002/gcc.22758
By:
- Michal, Michael;
- Ptáková, Nikola;
- Martínek, Petr;
- Gatalica, Zoran;
- Kazakov, Dmitry V.;
- Michalová, Květoslava;
- Stoláriková, Lýdia;
- Švajdler, Marián;
- Michal, Michal
Publication type:
Article
Radiation‐induced genomic instability in breast carcinomas of the Swedish hemangioma cohort.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 627, doi. 10.1002/gcc.22757
By:
- Biermann, Jana;
- Langen, Britta;
- Nemes, Szilárd;
- Holmberg, Erik;
- Parris, Toshima Z.;
- Werner Rönnerman, Elisabeth;
- Engqvist, Hanna;
- Kovács, Anikó;
- Helou, Khalil;
- Karlsson, Per
Publication type:
Article
Novel recurrent PHF1‐TFE3 fusions in ossifying fibromyxoid tumors.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 643, doi. 10.1002/gcc.22755
By:
- Suurmeijer, Albert J. H.;
- Song, Wangzhao;
- Sung, Yun‐Shao;
- Zhang, Lei;
- Swanson, David;
- Fletcher, Christopher D. M.;
- Dickson, Brendan C.;
- Antonescu, Cristina R.
Publication type:
Article
Double minute chromosomes harboring MDM2 amplification in a pediatric atypical lipomatous tumor.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 673, doi. 10.1002/gcc.22754
By:
- Dadone‐Montaudié, Bérengère;
- Burel‐Vandenbos, Fanny;
- Soler, Christine;
- Rosello, Olivier;
- Boyer, Corinne;
- Fabas, Thibault;
- Bianchini, Laurence;
- Pedeutour, Florence
Publication type:
Article
Gain of FGF4 is a frequent event in KIT/PDGFRA/SDH/RAS‐P WT GIST.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 636, doi. 10.1002/gcc.22753
By:
- Urbini, Milena;
- Indio, Valentina;
- Tarantino, Giuseppe;
- Ravegnini, Gloria;
- Angelini, Sabrina;
- Nannini, Margherita;
- Saponara, Maristella;
- Santini, Donatella;
- Ceccarelli, Claudio;
- Fiorentino, Michelangelo;
- Vincenzi, Bruno;
- Fumagalli, Elena;
- Casali, Paolo Giovanni;
- Grignani, Giovanni;
- Pession, Andrea;
- Ardizzoni, Andrea;
- Astolfi, Annalisa;
- Pantaleo, Maria Abbondanza
Publication type:
Article
Germline large deletion of BAP1 and decreased expression in non‐tumor choroid in uveal melanoma patients with high risk for inherited cancer.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 650, doi. 10.1002/gcc.22752
By:
- Boru, Getachew;
- Grosel, Timothy W.;
- Pilarski, Robert;
- Stautberg, Meredith;
- Massengill, James B.;
- Jeter, Joanne;
- Singh, Arun;
- Marino, Meghan J.;
- McElroy, Joseph P.;
- Davidorf, Frederick H.;
- Cebulla, Colleen M.;
- Abdel‐Rahman, Mohamed H.
Publication type:
Article
Whole transcriptome sequencing reveals a KMT2A‐USP2 fusion in infant acute myeloid leukemia.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 669, doi. 10.1002/gcc.22751
By:
- Ikeda, Junji;
- Shiba, Norio;
- Tsujimoto, Shin‐ichi;
- Yoshida, Masanori;
- Nakabayashi, Kazuhiko;
- Ogata‐Kawata, Hiroko;
- Okamura, Kohji;
- Takeuchi, Masanobu;
- Osumi, Tomoo;
- Tomizawa, Daisuke;
- Hata, Kenichiro;
- Kiyokawa, Nobutaka;
- Ito, Shuichi;
- Kato, Motohiro
Publication type:
Article
Metastatic risk stratification of clear cell renal cell carcinoma patients based on genomic aberrations.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 612, doi. 10.1002/gcc.22749
By:
- Grimm, Julia;
- Zeuschner, Philip;
- Janssen, Martin;
- Wagenpfeil, Stefan;
- Hartmann, Arndt;
- Stöhr, Christine;
- Keck, Bastian;
- Kahlmeyer, Andreas;
- Stöckle, Michael;
- Junker, Kerstin
Publication type:
Article
Most gene fusions in cancer are stochastic events.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 607, doi. 10.1002/gcc.22745
By:
- Johansson, Bertil;
- Mertens, Fredrik;
- Schyman, Tommy;
- Björk, Jonas;
- Mandahl, Nils;
- Mitelman, Felix
Publication type:
Article
A near‐haploid clone harboring a BCR/ABL1 gene fusion in an adult patient with newly diagnosed B‐lymphoblastic leukemia.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 665, doi. 10.1002/gcc.22744
By:
- Peterson, Jess F.;
- Ketterling, Rhett P.;
- Huang, Li;
- Finn, Laura E.;
- Shi, Min;
- Hoppman, Nicole L.;
- Greipp, Patricia T.;
- Baughn, Linda B.
Publication type:
Article
Table of Content Volume 58, Number 9, September 2019.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 605, doi. 10.1002/gcc.22659
Publication type:
Article
GATA3 germline variant is associated with CRLF2 expression and predicts outcome in pediatric B‐cell precursor acute lymphoblastic leukemia.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 619, doi. 10.1002/gcc.22748
By:
- Madzio, Joanna;
- Pastorczak, Agata;
- Sedek, Lukasz;
- Braun, Marcin;
- Taha, Joanna;
- Wypyszczak, Kamila;
- Trelinska, Joanna;
- Lejman, Monika;
- Muszynska‐Roslan, Katarzyna;
- Tomasik, Bartlomiej;
- Derwich, Katarzyna;
- Koltan, Andrzej;
- Kazanowska, Bernarda;
- Irga‐Jaworska, Nina;
- Badowska, Wanda;
- Matysiak, Michal;
- Kowalczyk, Jerzy;
- Styczynski, Jan;
- Fendler, Wojciech;
- Szczepanski, Tomasz
Publication type:
Article