Dumanski JP - Search Results

1

Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.

Hansson CM, Buckley PG, Grigelioniene G, Piotrowski A, Hellström AR, Mantripragada K, Jarbo C, Mathiesen T, Dumanski JP. Hansson CM, et al. Among authors: dumanski jp. BMC Genomics. 2007 Jan 12;8:16. doi: 10.1186/1471-2164-8-16. BMC Genomics. 2007. PMID: 17222329 Free PMC article.

2

Molecular genetic analysis of chromosome 22 in 81 cases of meningioma.

Dumanski JP, Rouleau GA, Nordenskjöld M, Collins VP. Dumanski JP, et al. Cancer Res. 1990 Sep 15;50(18):5863-7. Cancer Res. 1990. PMID: 2393856

3

Deletions on chromosome 22 in sporadic meningioma.

Ruttledge MH, Xie YG, Han FY, Peyrard M, Collins VP, Nordenskjöld M, Dumanski JP. Ruttledge MH, et al. Among authors: dumanski jp. Genes Chromosomes Cancer. 1994 Jun;10(2):122-30. doi: 10.1002/gcc.2870100207. Genes Chromosomes Cancer. 1994. PMID: 7520265

4

Structure of the promoter and genomic organization of the human beta'-adaptin gene (BAM22) from chromosome 22q12.

Peyrard M, Pan HQ, Kedra D, Fransson I, Swahn S, Hartman K, Clifton SW, Roe BA, Dumanski JP. Peyrard M, et al. Among authors: dumanski jp. Genomics. 1996 Aug 15;36(1):112-7. doi: 10.1006/geno.1996.0431. Genomics. 1996. PMID: 8812422

5

A high ratio of insulin-like growth factor II/insulin-like growth factor binding protein 2 messenger RNA as a marker for anaplasia in meningiomas.

Nordqvist AC, Peyrard M, Pettersson H, Mathiesen T, Collins VP, Dumanski JP, Schalling M. Nordqvist AC, et al. Among authors: dumanski jp. Cancer Res. 1997 Jul 1;57(13):2611-4. Cancer Res. 1997. PMID: 9205065

6

Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity.

Sulman EP, Dumanski JP, White PS, Zhao H, Maris JM, Mathiesen T, Bruder C, Cnaan A, Brodeur GM. Sulman EP, et al. Among authors: dumanski jp. Cancer Res. 1998 Aug 1;58(15):3226-30. Cancer Res. 1998. PMID: 9699646

7

A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene.

Bruder CE, Ichimura K, Tingby O, Hirakawa K, Komatsuzaki A, Tamura A, Yuasa Y, Collins VP, Dumanski JP. Bruder CE, et al. Among authors: dumanski jp. Hum Genet. 1999 May;104(5):418-24. doi: 10.1007/s004390050978. Hum Genet. 1999. PMID: 10394935

8

Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia.

Grigelioniene G, Eklöf O, Ivarsson SA, Westphal O, Neumeyer L, Kedra D, Dumanski J, Hagenäs L. Grigelioniene G, et al. Hum Genet. 2000 Aug;107(2):145-9. doi: 10.1007/s004390000352. Hum Genet. 2000. PMID: 11030412

9

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH.

Bruder CE, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Rask-Andersen H, Kluwe L, Mautner V, Sainio M, Hung G, Mathiesen T, Möller C, Pulst SM, Harder H, Heiberg A, Honda M, Niimura M, Sahlén S, Blennow E, Albertson DG, Pinkel D, Dumanski JP. Bruder CE, et al. Among authors: dumanski jp. Hum Mol Genet. 2001 Feb 1;10(3):271-82. doi: 10.1093/hmg/10.3.271. Hum Mol Genet. 2001. PMID: 11159946 Free article.

10

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.

Buckley PG, Mantripragada KK, Benetkiewicz M, Tapia-Páez I, Diaz De Ståhl T, Rosenquist M, Ali H, Jarbo C, De Bustos C, Hirvelä C, Sinder Wilén B, Fransson I, Thyr C, Johnsson BI, Bruder CE, Menzel U, Hergersberg M, Mandahl N, Blennow E, Wedell A, Beare DM, Collins JE, Dunham I, Albertson D, Pinkel D, Bastian BC, Faruqi AF, Lasken RS, Ichimura K, Collins VP, Dumanski JP. Buckley PG, et al. Among authors: dumanski jp. Hum Mol Genet. 2002 Dec 1;11(25):3221-9. doi: 10.1093/hmg/11.25.3221. Hum Mol Genet. 2002. PMID: 12444106

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