Works matching IS 10452257 AND DT 2018 AND VI 57 AND IP 12

Results: 10

Putative new childhood leukemia cancer predisposition syndrome caused by germline bi‐allelic missense mutations in DDX41.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 670, doi. 10.1002/gcc.22680
By:
- Diness, Birgitte R.;
- Risom, Lotte;
- Frandsen, Thomas L.;
- Hansen, Bente;
- Andersen, Mette K.;
- Schmiegelow, Kjeld;
- Wadt, Karin A. W.
Publication type:
Article
Genomic analysis reveals recurrent deletion of JAK‐STAT signaling inhibitors HNRNPK and SOCS1 in mycosis fungoides.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 653, doi. 10.1002/gcc.22679
By:
- Bastidas Torres, Armando N.;
- Cats, Davy;
- Mei, Hailiang;
- Szuhai, Karoly;
- Willemze, Rein;
- Vermeer, Maarten H.;
- Tensen, Cornelis P.
Publication type:
Article
Clonal evolution analysis of paired anaplastic and well‐differentiated thyroid carcinomas reveals shared common ancestor.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 645, doi. 10.1002/gcc.22678
By:
- Dong, Weilai;
- Nicolson, Norman G.;
- Choi, Jungmin;
- Barbieri, Andrea L.;
- Kunstman, John W.;
- Abou Azar, Sara;
- Knight, James;
- Bilguvar, Kaya;
- Mane, Shrikant M.;
- Lifton, Richard P.;
- Korah, Reju;
- Carling, Tobias
Publication type:
Article
Expanding the spectrum of translocations in sclerosing epitheloid fibrosarcoma: A new case with EWSR1‐CREB3L3 fusion.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 675, doi. 10.1002/gcc.22677
By:
- Dong, Fei;
- Quade, Bradley J.;
- Dal Cin, Paola;
- Jo, Vickie Y.
Publication type:
Article
Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 665, doi. 10.1002/gcc.22676
By:
- Kudo, Ko;
- Ueno, Hiroo;
- Sato, Tomohiko;
- Kubo, Kaori;
- Kanezaki, Rika;
- Kobayashi, Akie;
- Kamio, Takuya;
- Sasaki, Shinya;
- Terui, Kiminori;
- Kurose, Akira;
- Yoshida, Kenichi;
- Shiozawa, Yusuke;
- Toki, Tsutomu;
- Ogawa, Seishi;
- Ito, Etsuro
Publication type:
Article
Nuclear factor I X is a recurrent target for HPV16 insertions in anal carcinomas.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 638, doi. 10.1002/gcc.22675
By:
- Jeannot, Emmanuelle;
- Harlé, Alexandre;
- Holmes, Allyson;
- Sastre‐Garau, Xavier
Publication type:
Article
Colorectal cancer susceptibility loci and influence on survival.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 630, doi. 10.1002/gcc.22674
By:
- Song, Nan;
- Kim, Kyeezu;
- Shin, Aesun;
- Park, Ji Won;
- Chang, Hee Jin;
- Shi, Jiajun;
- Cai, Qiuyin;
- Kim, Dae Yong;
- Zheng, Wei;
- Oh, Jae Hwan
Publication type:
Article
Array‐based CGH of primary cutaneous CD8+ aggressive EPIDERMO‐tropic cytotoxic T‐cell lymphoma.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 622, doi. 10.1002/gcc.22673
By:
- Fanoni, Daniele;
- Corti, Laura;
- Alberti‐Violetti, Silvia;
- Tensen, Cornelis P.;
- Venegoni, Luigia;
- Vermeer, Maarten;
- Willemze, Rein;
- Berti, Emilio
Publication type:
Article
A novel group of spindle cell tumors defined by S100 and CD34 co‐expression shows recurrent fusions involving RAF1, BRAF, and NTRK1/2 genes.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 611, doi. 10.1002/gcc.22671
By:
- Suurmeijer, Albert J. H.;
- Dickson, Brendan C.;
- Swanson, David;
- Zhang, Lei;
- Sung, Yun‐Shao;
- Cotzia, Paolo;
- Fletcher, Christopher D. M.;
- Antonescu, Cristina R.
Publication type:
Article
Table of Content Volume 57, Number 12, December 2018.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 609, doi. 10.1002/gcc.22500
Publication type:
Article