Works matching IS 10452257 AND DT 2017 AND VI 56 AND IP 1

Results: 9

Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K-AKT pathway.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 11, doi. 10.1002/gcc.22396
By:
- Volckmar, Anna‐Lena;
- Leichsenring, Jonas;
- Flechtenmacher, Christa;
- Pfarr, Nicole;
- Siebolts, Udo;
- Kirchner, Martina;
- Budczies, Jan;
- Bockmayr, Michael;
- Ridinger, Kathrin;
- Lorenz, Katja;
- Herpel, Esther;
- Noske, Aurelia;
- Weichert, Wilko;
- Klauschen, Frederick;
- Schirmacher, Peter;
- Penzel, Roland;
- Endris, Volker;
- Stenzinger, Albrecht
Publication type:
Article
Table of Content Volume 56, Number 1, January 2017.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 1, doi. 10.1002/gcc.22403
Publication type:
Article
Heterogeneity of MYCN amplification in neuroblastoma at diagnosis, treatment, relapse, and metastasis.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 28, doi. 10.1002/gcc.22398
By:
- Marrano, Paula;
- Irwin, Meredith S.;
- Thorner, Paul S.
Publication type:
Article
Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 75, doi. 10.1002/gcc.22418
By:
- Herold, Tobias;
- Metzeler, Klaus H.;
- Vosberg, Sebastian;
- Hartmann, Luise;
- Jurinovic, Vindi;
- Opatz, Sabrina;
- Konstandin, Nikola P.;
- Schneider, Stephanie;
- Zellmeier, Evelyn;
- Ksienzyk, Bianka;
- Graf, Alexander;
- Krebs, Stefan;
- Blum, Helmut;
- Cristina Sauerland, Maria;
- Büchner, Thomas;
- Berdel, Wolfgang E.;
- Wörmann, Bernhard J.;
- Mansmann, Ulrich;
- Hiddemann, Wolfgang;
- Bohlander, Stefan K.
Publication type:
Article
Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 51, doi. 10.1002/gcc.22401
By:
- Nacci, Lucia;
- Valli, Roberto;
- Maria Pinto, Rita;
- Zecca, Marco;
- Cipolli, Marco;
- Morini, Jacopo;
- Cesaro, Simone;
- Boveri, Emanuela;
- Rosti, Vittorio;
- Corti, Paola;
- Ambroni, Maura;
- Pasquali, Francesco;
- Danesino, Cesare;
- Maserati, Emanuela;
- Minelli, Antonella
Publication type:
Article
MicroRNAs role as potential biomarkers and key regulators in melanoma.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 3, doi. 10.1002/gcc.22402
By:
- Varamo, Chiara;
- Occelli, Marcella;
- Vivenza, Daniela;
- Merlano, Marco;
- Lo Nigro, Cristiana
Publication type:
Article
Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 18, doi. 10.1002/gcc.22397
By:
- Sticca, Tiberio;
- Caberg, Jean‐Hubert;
- Wenric, Stephane;
- Poulet, Christophe;
- Herens, Christian;
- Jamar, Mauricette;
- Josse, Claire;
- El Guendi, Sonia;
- Max, Stéphanie;
- Beguin, Yves;
- Gothot, André;
- Caers, Jo;
- Bours, Vincent
Publication type:
Article
Common fragile sites (CFS) and extremely large CFS genes are targets for human papillomavirus integrations and chromosome rearrangements in oropharyngeal squamous cell carcinoma.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 59, doi. 10.1002/gcc.22415
By:
- Gao, Ge;
- Johnson, Sarah H;
- Vasmatzis, George;
- Pauley, Christina E;
- Tombers, Nicole M.;
- Kasperbauer, Jan L;
- Smith, David I.
Publication type:
Article
Expanding the molecular signature of ossifying fibromyxoid tumors with two novel gene fusions: CREBBP-BCORL1 and KDM2A-WWTR1.
Published in:
Genes, Chromosomes & Cancer, 2017, v. 56, n. 1, p. 42, doi. 10.1002/gcc.22400
By:
- Kao, Yu‐Chien;
- Sung, Yun‐Shao;
- Zhang, Lei;
- Chen, Chun‐Liang;
- Huang, Shih‐Chiang;
- Antonescu, Cristina R.
Publication type:
Article