Nordling M - Search Results

1

Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis.

Rohlin A, Engwall Y, Fritzell K, Göransson K, Bergsten A, Einbeigi Z, Nilbert M, Karlsson P, Björk J, Nordling M. Rohlin A, et al. Among authors: nordling m. Oncogene. 2011 Dec 15;30(50):4977-89. doi: 10.1038/onc.2011.201. Epub 2011 Jun 6. Oncogene. 2011. PMID: 21643010 Free PMC article. Clinical Trial.

2

Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.

Kanter-Smoler G, Fritzell K, Rohlin A, Engwall Y, Hallberg B, Bergman A, Meuller J, Grönberg H, Karlsson P, Björk J, Nordling M. Kanter-Smoler G, et al. Among authors: nordling m. BMC Med. 2008 Apr 24;6:10. doi: 10.1186/1741-7015-6-10. BMC Med. 2008. PMID: 18433509 Free PMC article.

3

Identification of genomic deletions of the APC gene in familial adenomatous polyposis by two independent quantitative techniques.

Meuller J, Kanter-Smoler G, Nygren AO, Errami A, Grönberg H, Holmberg E, Björk J, Wahlström J, Nordling M. Meuller J, et al. Among authors: nordling m. Genet Test. 2004 Fall;8(3):248-56. doi: 10.1089/gte.2004.8.248. Genet Test. 2004. PMID: 15727247

4

Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization.

Kanter-Smoler G, Björk J, Fritzell K, Engwall Y, Hallberg B, Karlsson G, Grönberg H, Karlsson P, Wallgren A, Wahlström J, Hultcrantz R, Nordling M. Kanter-Smoler G, et al. Among authors: nordling m. Clin Gastroenterol Hepatol. 2006 Apr;4(4):499-506. doi: 10.1016/j.cgh.2006.01.005. Clin Gastroenterol Hepatol. 2006. PMID: 16616356

5

Parallel sequencing used in detection of mosaic mutations: comparison with four diagnostic DNA screening techniques.

Rohlin A, Wernersson J, Engwall Y, Wiklund L, Björk J, Nordling M. Rohlin A, et al. Among authors: nordling m. Hum Mutat. 2009 Jun;30(6):1012-20. doi: 10.1002/humu.20980. Hum Mutat. 2009. PMID: 19347965

6

Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.

Rohlin A, Rambech E, Kvist A, Törngren T, Eiengård F, Lundstam U, Zagoras T, Gebre-Medhin S, Borg Å, Björk J, Nilbert M, Nordling M. Rohlin A, et al. Among authors: nordling m. Fam Cancer. 2017 Apr;16(2):195-203. doi: 10.1007/s10689-016-9934-0. Fam Cancer. 2017. PMID: 27696107 Free PMC article.

7

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.

Olkinuora A, Nieminen TT, Mårtensson E, Rohlin A, Ristimäki A, Koskenvuo L, Lepistö A; Swedish Extended Genetic Analysis of Colorectal Neoplasia (SWEN) Study Group; Gebre-Medhin S, Nordling M, Peltomäki P. Olkinuora A, et al. Among authors: nordling m. Genet Med. 2019 Aug;21(8):1868-1873. doi: 10.1038/s41436-018-0405-x. Epub 2018 Dec 21. Genet Med. 2019. PMID: 30573798 Free PMC article.

8

Novel mutations in the APC gene and clinical features in Swedish patients with polyposis coli.

Nordling M, Engwall Y, Wahlström J, Wiklund L, Eriksson MA, Gustavsson B, Fasth S, Larsson PA, Martinsson T. Nordling M, et al. Anticancer Res. 1997 Nov-Dec;17(6D):4275-80. Anticancer Res. 1997. PMID: 9494520

9

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.

Nordling M, Karlsson P, Wahlström J, Engwall Y, Wallgren A, Martinsson T. Nordling M, et al. Cancer Res. 1998 Apr 1;58(7):1372-5. Cancer Res. 1998. PMID: 9537232

10

Periampullary adenomas and adenocarcinomas in familial adenomatous polyposis: cumulative risks and APC gene mutations.

Björk J, Akerbrant H, Iselius L, Bergman A, Engwall Y, Wahlström J, Martinsson T, Nordling M, Hultcrantz R. Björk J, et al. Among authors: nordling m. Gastroenterology. 2001 Nov;121(5):1127-35. doi: 10.1053/gast.2001.28707. Gastroenterology. 2001. PMID: 11677205

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