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A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesis.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 595, doi. 10.1002/gcc.22743
By:
- Penther, Dominique;
- Viailly, Pierre‐Julien;
- Latour, Sylvain;
- Etancelin, Pascaline;
- Bohers, Elodie;
- Vellemans, Hélène;
- Camus, Vincent;
- Menard, Anne Lise;
- Coutant, Sophie;
- Lanic, Hélène;
- Lemasle, Emilie;
- Drieux, Fanny;
- Veresezan, Liana;
- Ruminy, Philippe;
- Raimbault, Anna;
- Soulier, Jean;
- Frebourg, Thierry;
- Tilly, Hervé;
- Jardin, Fabrice
Publication type:
Article
RNA sequencing identifies a novel USP9X‐USP6 promoter swap gene fusion in a primary aneurysmal bone cyst.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 589, doi. 10.1002/gcc.22742
By:
- Blackburn, Patrick R.;
- Davila, Jaime I.;
- Jackson, Rory A.;
- Fadra, Numrah;
- Atiq, Mazen A.;
- Pitel, Beth A.;
- Nair, Asha A.;
- VanDeWalker, Todd J.;
- Hessler, Mark G.;
- Hovel, Sara K.;
- Wehrs, Rebecca N.;
- Fritchie, Karen J.;
- Jenkins, Robert B.;
- Halling, Kevin C.;
- Geiersbach, Katherine B.
Publication type:
Article
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 567, doi. 10.1002/gcc.22741
By:
- Peterson, Jess F.;
- Sukov, William R.;
- Pitel, Beth A.;
- Smoley, Stephanie A.;
- Pearce, Kathryn E.;
- Meyer, Reid G.;
- Williamson, Cynthia M.;
- Smadbeck, James B.;
- Vasmatzis, George;
- Hoppman, Nicole L.;
- Greipp, Patricia T.;
- Baughn, Linda B.;
- Ketterling, Rhett P.
Publication type:
Article
Pediatric acute myeloid leukemia with t(7;21)(p22;q22).
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 551, doi. 10.1002/gcc.22740
By:
- Paulraj, Prabakaran;
- Diamond, Steven;
- Razzaqi, Faisal;
- Ozeran, J. Daniel;
- Longhurst, Maria;
- Andersen, Erica F.;
- Toydemir, Reha M.;
- Hong, Bo
Publication type:
Article
Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 541, doi. 10.1002/gcc.22739
By:
- Ten Broek, Roel W.;
- Eijkelenboom, Astrid;
- Vleuten, Carine J. M.;
- Kamping, Eveline J.;
- Kets, Marleen;
- Verhoeven, Bas H.;
- Grünberg, Katrien;
- Schultze Kool, Leo J.;
- Tops, Bastiaan B. J.;
- Ligtenberg, Marjolijn J. L.;
- Flucke, Uta
Publication type:
Article
Newly diagnosed multiple myeloma patients carrying monoallelic deletion of the whole locus of immunoglobulin heavy chain gene have a better prognosis compared to those with t(4;14) and t(14;16).
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 516, doi. 10.1002/gcc.22738
By:
- Duek, Adrian;
- Trakhtenbrot, Luba;
- Amariglio, Ninette;
- Benyamini, Noam;
- Zilbershats, Itay;
- Ganzel, Chezi;
- Shevetz, Olga;
- Leiba, Ronit;
- Rozic, Gabriela;
- Nagler, Arnon;
- Leiba, Merav
Publication type:
Article
Novel TG‐FGFR1 and TRIM33‐NTRK1 transcript fusions in papillary thyroid carcinoma.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 558, doi. 10.1002/gcc.22737
By:
- Pfeifer, Aleksandra;
- Rusinek, Dagmara;
- Żebracka‐Gala, Jadwiga;
- Czarniecka, Agnieszka;
- Chmielik, Ewa;
- Zembala‐Nożyńska, Ewa;
- Wojtaś, Bartosz;
- Gielniewski, Bartłomiej;
- Szpak‐Ulczok, Sylwia;
- Oczko‐Wojciechowska, Małgorzata;
- Krajewska, Jolanta;
- Polańska, Joanna;
- Jarząb, Barbara
Publication type:
Article
Characterization of human telomerase reverse transcriptase promoter methylation and transcription factor binding in differentiated thyroid cancer cell lines.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 530, doi. 10.1002/gcc.22735
By:
- Avin, Brittany A.;
- Wang, Yongchun;
- Gilpatrick, Timothy;
- Workman, Rachael E.;
- Lee, Isac;
- Timp, Winston;
- Umbricht, Christopher B.;
- Zeiger, Martha A.
Publication type:
Article
Early detection of the PAX3‐FOXO1 fusion gene in circulating tumor‐derived DNA in a case of alveolar rhabdomyosarcoma.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 521, doi. 10.1002/gcc.22734
By:
- Eguchi‐Ishimae, Minenori;
- Tezuka, Mari;
- Kokeguchi, Tomoki;
- Nagai, Kozo;
- Moritani, Kyoko;
- Yonezawa, Sachiko;
- Tauchi, Hisamichi;
- Tokuda, Kiriko;
- Ishida, Yasushi;
- Ishii, Eiichi;
- Eguchi, Mariko
Publication type:
Article
Tumor mutational burden standardization initiatives: Recommendations for consistent tumor mutational burden assessment in clinical samples to guide immunotherapy treatment decisions.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 578, doi. 10.1002/gcc.22733
By:
- Stenzinger, Albrecht;
- Allen, Jeffrey D.;
- Maas, Jörg;
- Stewart, Mark D.;
- Merino, Diana M.;
- Wempe, Madison M.;
- Dietel, Manfred
Publication type:
Article
5q21 deletion is often heterogeneous in prostate cancer.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 509, doi. 10.1002/gcc.22730
By:
- Kluth, Martina;
- Al Kilani, Zaid;
- Özden, Cansu;
- Hussein, Khakan;
- Frogh, Sohall;
- Möller‐Koop, Christina;
- Burandt, Eike;
- Steurer, Stefan;
- Büscheck, Franziska;
- Jacobsen, Frank;
- Luebke, Andreas M.;
- Minner, Sarah;
- Tsourlakis, Maria Christina;
- Hoeflmayer, Doris;
- Wittmer, Corinna;
- Schlomm, Thorsten;
- Sauter, Guido;
- Simon, Ronald;
- Wilczak, Waldemar
Publication type:
Article
Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 602, doi. 10.1002/gcc.22728
By:
- Kock, Leanne;
- Hillmer, Morten;
- Wagener, Rabea;
- Soglio, Dorothée Bouron‐Dal;
- Sabbaghian, Nelly;
- Siebert, Reiner;
- Priest, John R.;
- Miller, Michal;
- Foulkes, William D.
Publication type:
Article
Table of Content Volume 58, Number 8, August 2019.
Published in:
Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 507, doi. 10.1002/gcc.22658
Publication type:
Article

Found: 13