Works matching IS 10452257 AND DT 2022 AND VI 61 AND IP 12

Results: 7

Loss of ALK hotspot mutations in relapsed neuroblastoma.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 747, doi. 10.1002/gcc.23093
By:
- Allinson, Lisa M.;
- Potts, Aaron;
- Goodman, Angharad;
- Bown, Nick;
- Bashton, Matthew;
- Thompson, Dean;
- Basta, Nermine O.;
- Gabriel, Alem S.;
- McCorkindale, Michael;
- Ng, Antony;
- McNally, Richard J. Q.;
- Tweddle, Deborah A.
Publication type:
Article
Successful treatment with MEK‐inhibitor in a patient with NRAS‐related cutaneous skeletal hypophosphatemia syndrome.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 740, doi. 10.1002/gcc.23092
By:
- Carli, Diana;
- Cardaropoli, Simona;
- Tessaris, Daniele;
- Coppo, Paola;
- La Selva, Roberta;
- Cesario, Claudia;
- Lepri, Francesca Romana;
- Pullano, Verdiana;
- Palumbo, Martina;
- Ramenghi, Ugo;
- Brusco, Alfredo;
- Medico, Enzo;
- De Sanctis, Luisa;
- Ferrero, Giovanni Battista;
- Mussa, Alessandro
Publication type:
Article
AGAP3: A novel BRAF fusion partner in pediatric pancreatic‐type acinar cell carcinoma.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 734, doi. 10.1002/gcc.23091
By:
- Paoli, Charlotte;
- Burel‐Vandenbos, Fanny;
- Coulomb‐l'Hermine, Aurore;
- Cros, Jérôme;
- Pondrom, Morgane;
- Kubiniek, Valérie;
- Pedeutour, Florence;
- Dadone‐Montaudié, Bérengère
Publication type:
Article
Multiomics to investigate the mechanisms contributing to repression of PTPRC and SOCS2 in pediatric T‐ALL: Focus on miR‐363‐3p and promoter methylation.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 720, doi. 10.1002/gcc.23085
By:
- Drobna‐Śledzińska, Monika;
- Maćkowska‐Maślak, Natalia;
- Jaksik, Roman;
- Kosmalska, Maria;
- Szarzyńska, Bronisława;
- Lejman, Monika;
- Sędek, Łukasz;
- Szczepański, Tomasz;
- Taghon, Tom;
- Van Vlierberghe, Pieter;
- Witt, Michał;
- Dawidowska, Małgorzata
Publication type:
Article
Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 710, doi. 10.1002/gcc.23084
By:
- Koleilat, Alaa;
- Smadbeck, James B.;
- Zepeda‐Mendoza, Cinthya J.;
- Williamson, Cynthia M.;
- Pitel, Beth A.;
- Golden, Crystal L.;
- Xu, Xinjie;
- Greipp, Patricia T.;
- Ketterling, Rhett P.;
- Hoppman, Nicole L.;
- Peterson, Jess F.;
- Harrison, Christine J.;
- Akkari, Yassmine M. N.;
- Tsuchiya, Karen D.;
- Shago, Mary;
- Baughn, Linda B.
Publication type:
Article
Recurrent VGLL3 fusions define a distinctive subset of spindle cell rhabdomyosarcoma with an indolent clinical course and striking predilection for the head and neck.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 701, doi. 10.1002/gcc.23083
By:
- Agaimy, Abbas;
- Dermawan, Josephine K.;
- Leong, Iona;
- Stoehr, Robert;
- Swanson, David;
- Weinreb, Ilan;
- Zhang, Lingxin;
- Antonescu, Cristina R.;
- Dickson, Brendan C.
Publication type:
Article
Issue Information.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 697, doi. 10.1002/gcc.22969
Publication type:
Article

Works matching IS 10452257 AND DT 2022 AND VI 61 AND IP 12

Loss of ALK hotspot mutations in relapsed neuroblastoma.

Successful treatment with MEK‐inhibitor in a patient with NRAS‐related cutaneous skeletal hypophosphatemia syndrome.

AGAP3: A novel BRAF fusion partner in pediatric pancreatic‐type acinar cell carcinoma.

Multiomics to investigate the mechanisms contributing to repression of PTPRC and SOCS2 in pediatric T‐ALL: Focus on miR‐363‐3p and promoter methylation.

Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group.

Recurrent VGLL3 fusions define a distinctive subset of spindle cell rhabdomyosarcoma with an indolent clinical course and striking predilection for the head and neck.

Issue Information.