Sjöberg RM - Search Results

1

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. Among authors: sjoberg rm. Cancer Genet Cytogenet. 1997 Jun;95(2):183-9. doi: 10.1016/s0165-4608(96)00259-2. Cancer Genet Cytogenet. 1997. PMID: 9169039

2

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. Among authors: sjoberg rm. Cancer Res. 1995 Dec 1;55(23):5681-6. Cancer Res. 1995. PMID: 7585654

3

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. Among authors: sjoberg rm. Eur J Cancer. 1997 Oct;33(12):1997-2001. doi: 10.1016/s0959-8049(97)00278-5. Eur J Cancer. 1997. PMID: 9516841

4

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: sjoberg rm. Int J Mol Med. 1999 Jun;3(6):585-9. doi: 10.3892/ijmm.3.6.585. Int J Mol Med. 1999. PMID: 10341287

5

Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors.

Jögi A, Abel F, Sjöberg RM, Toftgård R, Zaphiropoulos PG, Påhlman S, Martinsson T, Axelson H. Jögi A, et al. Among authors: sjoberg rm. Int J Oncol. 2000 May;16(5):943-9. doi: 10.3892/ijo.16.5.943. Int J Oncol. 2000. PMID: 10762630

6

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. Among authors: sjoberg rm. 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

7

A genome-wide scan to locate regions associated with familial vesicoureteral reflux.

Bartik Z, Sillén U, Östensson M, Fransson S, Djos A, Sjöberg R, Martinsson T. Bartik Z, et al. Exp Ther Med. 2022 Jan;23(1):92. doi: 10.3892/etm.2021.11015. Epub 2021 Nov 28. Exp Ther Med. 2022. PMID: 34976134 Free PMC article.

8

Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.

Fransson S, Martinez-Monleon A, Johansson M, Sjöberg RM, Björklund C, Ljungman G, Ek T, Kogner P, Martinsson T. Fransson S, et al. Among authors: sjoberg rm. Sci Rep. 2020 Dec 31;10(1):22432. doi: 10.1038/s41598-020-78370-7. Sci Rep. 2020. PMID: 33384420 Free PMC article.

9

11q Deletion or ALK Activity Curbs DLG2 Expression to Maintain an Undifferentiated State in Neuroblastoma.

Siaw JT, Javanmardi N, Van den Eynden J, Lind DE, Fransson S, Martinez-Monleon A, Djos A, Sjöberg RM, Östensson M, Carén H, Trøen G, Beiske K, Berbegall AP, Noguera R, Lai WY, Kogner P, Palmer RH, Hallberg B, Martinsson T. Siaw JT, et al. Among authors: sjoberg rm. Cell Rep. 2020 Sep 22;32(12):108171. doi: 10.1016/j.celrep.2020.108171. Cell Rep. 2020. PMID: 32966799 Free article.

10

Low Frequency ALK Hotspots Mutations In Neuroblastoma Tumours Detected By Ultra-deep Sequencing: Implications For ALK Inhibitor Treatment.

Javanmardi N, Fransson S, Djos A, Sjöberg RM, Nilsson S, Truvé K, Kogner P, Martinsson T. Javanmardi N, et al. Among authors: sjoberg rm. Sci Rep. 2019 Feb 18;9(1):2199. doi: 10.1038/s41598-018-37240-z. Sci Rep. 2019. PMID: 30778092 Free PMC article.

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