Ejeskär K - Search Results

1

Discovery of a rare GKAP1-NTRK2 fusion in a pediatric low-grade glioma, leading to targeted treatment with TRK-inhibitor larotrectinib.

Deland L, Keane S, Olsson Bontell T, Sjögren H, Fagman H, Øra I, De La Cuesta E, Tisell M, Nilsson JA, Ejeskär K, Sabel M, Abel F. Deland L, et al. Among authors: ejeskar k. Cancer Biol Ther. 2021 Mar 4;22(3):184-195. doi: 10.1080/15384047.2021.1899573. Epub 2021 Apr 5. Cancer Biol Ther. 2021. PMID: 33820494 Free PMC article.

2

Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24.

Abel F, Ejeskär K, Kogner P, Martinsson T. Abel F, et al. Among authors: ejeskar k. Br J Cancer. 1999 Dec;81(8):1402-9. doi: 10.1038/sj.bjc.6692231. Br J Cancer. 1999. PMID: 10604740 Free PMC article.

3

Fine mapping of the human preprocortistatin gene (CORT) to neuroblastoma consensus deletion region 1p36.3-->p36.2, but absence of mutations in primary tumors.

Ejeskär K, Abel F, Sjöberg R, Bäckström J, Kogner P, Martinsson T. Ejeskär K, et al. Cytogenet Cell Genet. 2000;89(1-2):62-6. doi: 10.1159/000015566. Cytogenet Cell Genet. 2000. PMID: 10894940

4

Fine mapping of a tumour suppressor candidate gene region in 1p36.2-3, commonly deleted in neuroblastomas and germ cell tumours.

Ejeskär K, Sjöberg RM, Abel F, Kogner P, Ambros PF, Martinsson T. Ejeskär K, et al. Med Pediatr Oncol. 2001 Jan;36(1):61-6. doi: 10.1002/1096-911X(20010101)36:1<61::AID-MPO1016>3.0.CO;2-0. Med Pediatr Oncol. 2001. PMID: 11464908

5

Analyses of apoptotic regulators CASP9 and DFFA at 1P36.2, reveal rare allele variants in human neuroblastoma tumours.

Abel F, Sjöberg RM, Ejeskär K, Krona C, Martinsson T. Abel F, et al. Among authors: ejeskar k. Br J Cancer. 2002 Feb 12;86(4):596-604. doi: 10.1038/sj.bjc.6600111. Br J Cancer. 2002. PMID: 11870543 Free PMC article.

6

Screening for gene mutations in a 500 kb neuroblastoma tumor suppressor candidate region in chromosome 1p; mutation and stage-specific expression in UBE4B/UFD2.

Krona C, Ejeskär K, Abel F, Kogner P, Bjelke J, Björk E, Sjöberg RM, Martinsson T. Krona C, et al. Among authors: ejeskar k. Oncogene. 2003 Apr 17;22(15):2343-51. doi: 10.1038/sj.onc.1206324. Oncogene. 2003. PMID: 12700669

7

A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours.

Krona C, Ejeskär K, Carén H, Abel F, Sjöberg RM, Martinsson T. Krona C, et al. Among authors: ejeskar k. Br J Cancer. 2004 Sep 13;91(6):1119-30. doi: 10.1038/sj.bjc.6602083. Br J Cancer. 2004. PMID: 15328517 Free PMC article.

8

Stage-dependent expression of PI3K/Akt‑pathway genes in neuroblastoma.

Fransson S, Abel F, Kogner P, Martinsson T, Ejeskär K. Fransson S, et al. Among authors: ejeskar k. Int J Oncol. 2013 Feb;42(2):609-16. doi: 10.3892/ijo.2012.1732. Epub 2012 Dec 12. Int J Oncol. 2013. PMID: 23232578

9

Low DLG2 gene expression, a link between 11q-deleted and MYCN-amplified neuroblastoma, causes forced cell cycle progression, and predicts poor patient survival.

Keane S, Améen S, Lindlöf A, Ejeskär K. Keane S, et al. Among authors: ejeskar k. Cell Commun Signal. 2020 Apr 20;18(1):65. doi: 10.1186/s12964-020-00553-6. Cell Commun Signal. 2020. PMID: 32312269 Free PMC article.

10

MYO5B mutations in pheochromocytoma/paraganglioma promote cancer progression.

Tomić TT, Olausson J, Rehammar A, Deland L, Muth A, Ejeskär K, Nilsson S, Kristiansson E, Wassén ON, Abel F. Tomić TT, et al. Among authors: ejeskar k. PLoS Genet. 2020 Jun 8;16(6):e1008803. doi: 10.1371/journal.pgen.1008803. eCollection 2020 Jun. PLoS Genet. 2020. PMID: 32511227 Free PMC article.

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