Terms: = Germ cell tumor AND CAMTA1, ENSG00000171735, 23261, Q9Y6Y1, KIAA0833
14 results:
1. The role of Calmodulin Binding Transcription Activator 1 (camta1) gene and its putative genetic partners in the human nervous system.
Alves G; Ornellas MH; Liehr T
Psychogeriatrics; 2022 Nov; 22(6):869-878. PubMed ID: 35949142
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2. camta1, a novel antitumor gene, regulates proliferation and the cell cycle in glioma by inhibiting AKT phosphorylation.
He Z; Yang C; He Y; Gong B; Yin C; Feng J; Chen L; Tang J; Chen Y
Cell Signal; 2021 Mar; 79():109882. PubMed ID: 33316386
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3. Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene.
Juhlin CC; Stenman A; Haglund F; Clark VE; Brown TC; Baranoski J; Bilguvar K; Goh G; Welander J; Svahn F; Rubinstein JC; Caramuta S; Yasuno K; Günel M; Bäckdahl M; Gimm O; Söderkvist P; Prasad ML; Korah R; Lifton RP; Carling T
Genes Chromosomes Cancer; 2015 Sep; 54(9):542-54. PubMed ID: 26032282
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4. [Diagnostics and therapy for neuroendocrine neoplasia of an unknown primary - a plea for open exploration].
Begum N; Hubold C; Buchmann I; Thorns C; Bouchard R; Lubienski A; Schlöricke E; Zimmermann M; Lehnert H; Bruch HP; Bürk CG
Zentralbl Chir; 2014 Jun; 139(3):284-91. PubMed ID: 23508839
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5. Delineating the cytogenomic and epigenomic landscapes of glioma stem cell lines.
Baronchelli S; Bentivegna A; Redaelli S; Riva G; Butta V; Paoletta L; Isimbaldi G; Miozzo M; Tabano S; Daga A; Marubbi D; Cattaneo M; Biunno I; Dalprà L
PLoS One; 2013; 8(2):e57462. PubMed ID: 23468990
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6. camta1 is a novel tumour suppressor regulated by miR-9/9* in glioblastoma stem cells.
Schraivogel D; Weinmann L; Beier D; Tabatabai G; Eichner A; Zhu JY; Anton M; Sixt M; Weller M; Beier CP; Meister G
EMBO J; 2011 Aug; 30(20):4309-22. PubMed ID: 21857646
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7. camta1, a 1p36 tumor suppressor candidate, inhibits growth and activates differentiation programs in neuroblastoma cells.
Henrich KO; Bauer T; Schulte J; Ehemann V; Deubzer H; Gogolin S; Muth D; Fischer M; Benner A; König R; Schwab M; Westermann F
Cancer Res; 2011 Apr; 71(8):3142-51. PubMed ID: 21385898
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8. Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.
Isidor B; Le Cunff M; Boceno M; Boisseau P; Thomas C; Rival JM; David A; Le Caignec C
Eur J Med Genet; 2008; 51(6):679-84. PubMed ID: 18672103
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9. Expression and sequence analysis of candidates for the 1p36.31 tumor suppressor gene deleted in neuroblastomas.
Okawa ER; Gotoh T; Manne J; Igarashi J; Fujita T; Silverman KA; Xhao H; Mosse YP; White PS; Brodeur GM
Oncogene; 2008 Jan; 27(6):803-10. PubMed ID: 17667943
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10. Allelic variants of camta1 and FLJ10737 within a commonly deleted region at 1p36 in neuroblastoma.
Henrich KO; Claas A; Praml C; Benner A; Mollenhauer J; Poustka A; Schwab M; Westermann F
Eur J Cancer; 2007 Feb; 43(3):607-16. PubMed ID: 17222547
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11. Reduced expression of camta1 correlates with adverse outcome in neuroblastoma patients.
Henrich KO; Fischer M; Mertens D; Benner A; Wiedemeyer R; Brors B; Oberthuer A; Berthold F; Wei JS; Khan J; Schwab M; Westermann F
Clin Cancer Res; 2006 Jan; 12(1):131-8. PubMed ID: 16397034
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12. Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of camta1 as a candidate tumor suppressor gene.
Barbashina V; Salazar P; Holland EC; Rosenblum MK; Ladanyi M
Clin Cancer Res; 2005 Feb; 11(3):1119-28. PubMed ID: 15709179
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13. cell cycle-dependent transcriptional regulation of calmodulin-binding transcription activator 1 in neuroblastoma cells.
Nakatani K; Nishioka J; Itakura T; Nakanishi Y; Horinouchi J; Abe Y; Wada H; Nobori T
Int J Oncol; 2004 Jun; 24(6):1407-12. PubMed ID: 15138581
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14. Identification and characterization of FLJ10737 and camta1 genes on the commonly deleted region of neuroblastoma at human chromosome 1p36.31-p36.23.
Katoh M; Katoh M
Int J Oncol; 2003 Oct; 23(4):1219-24. PubMed ID: 12964007
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