Martinsson T - Search Results

1

Loss of Chromosome Y in Neuroblastoma Is Associated With High-Risk Disease, 11q-Deletion, and Telomere Maintenance.

Djos A, Svensson J, Gaarder J, Umapathy G, Nilsson S, Ek T, Vogt H, Georgantzi K, Öra I, Träger C, Kogner P, Martinsson T, Fransson S. Djos A, et al. Among authors: martinsson t. Genes Chromosomes Cancer. 2024 Jul;63(7):e23260. doi: 10.1002/gcc.23260. Genes Chromosomes Cancer. 2024. PMID: 39031441

2

Neuroblastoma consensus deletion maps to 1p36.1-2.

Weith A, Martinsson T, Cziepluch C, Brüderlein S, Amler LC, Berthold F, Schwab M. Weith A, et al. Among authors: martinsson t. Genes Chromosomes Cancer. 1989 Nov;1(2):159-66. doi: 10.1002/gcc.2870010209. Genes Chromosomes Cancer. 1989. PMID: 2487156

3

Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms.

Martinsson T, Sjöberg RM, Hedborg F, Kogner P. Martinsson T, et al. Cancer Res. 1995 Dec 1;55(23):5681-6. Cancer Res. 1995. PMID: 7585654

4

Homozygous deletion of the neurofibromatosis-1 gene in the tumor of a patient with neuroblastoma.

Martinsson T, Sjöberg RM, Hedborg F, Kogner P. Martinsson T, et al. Cancer Genet Cytogenet. 1997 Jun;95(2):183-9. doi: 10.1016/s0165-4608(96)00259-2. Cancer Genet Cytogenet. 1997. PMID: 9169039

5

Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours.

Martinsson T, Sjöberg RM, Hallstensson K, Nordling M, Hedborg F, Kogner P. Martinsson T, et al. Eur J Cancer. 1997 Oct;33(12):1997-2001. doi: 10.1016/s0959-8049(97)00278-5. Eur J Cancer. 1997. PMID: 9516841

6

Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumour-suppressor locus distal to the FHIT gene.

Ejeskär K, Aburatani H, Abrahamsson J, Kogner P, Martinsson T. Ejeskär K, et al. Among authors: martinsson t. Br J Cancer. 1998 Jun;77(11):1787-91. doi: 10.1038/bjc.1998.297. Br J Cancer. 1998. PMID: 9667647 Free PMC article.

7

The use of fine-needle aspiration cytology in the molecular characterization of neuroblastoma in children.

Fröstad B, Martinsson T, Tani E, Falkmer U, Darnfors C, Skoog L, Kogner P. Fröstad B, et al. Among authors: martinsson t. Cancer. 1999 Apr 25;87(2):60-8. Cancer. 1999. PMID: 10227595

8

Variable expression and absence of mutations in p73 in primary neuroblastoma tumors argues against a role in neuroblastoma development.

Ejeskär K, Sjöberg RM, Kogner P, Martinsson T. Ejeskär K, et al. Among authors: martinsson t. Int J Mol Med. 1999 Jun;3(6):585-9. doi: 10.3892/ijmm.3.6.585. Int J Mol Med. 1999. PMID: 10341287

9

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: martinsson t. Br J Cancer. 1999 Dec;81(8):1402-9. doi: 10.1038/sj.bjc.6692231. Br J Cancer. 1999. PMID: 10604740 Free PMC article.

10

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. Among authors: martinsson t. Cytogenet Cell Genet. 2000;89(1-2):62-6. doi: 10.1159/000015566. Cytogenet Cell Genet. 2000. PMID: 10894940

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