Mandahl N - Search Results

1

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: mandahl n. Hum Mol Genet. 2002 Dec 1;11(25):3221-9. doi: 10.1093/hmg/11.25.3221. Hum Mol Genet. 2002. PMID: 12444106

2

Characteristic chromosome abnormalities, including rearrangements of 6p, del(7q), +12, and t(12;14), in 44 uterine leiomyomas.

Nilbert M, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F. Nilbert M, et al. Among authors: mandahl n. Hum Genet. 1990 Oct;85(6):605-11. doi: 10.1007/BF00193583. Hum Genet. 1990. PMID: 2227952

3

In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1.

Arheden K, Rønne M, Mandahl N, Heim S, Kinzler KW, Vogelstein B, Mitelman F. Arheden K, et al. Among authors: mandahl n. Hum Genet. 1989 Apr;82(1):1-2. doi: 10.1007/BF00288260. Hum Genet. 1989. PMID: 2497059

4

Trisomy 7 and sex chromosome loss in human brain tissue.

Heim S, Mandahl N, Jin Y, Strömblad S, Lindström E, Salford LG, Mitelman F. Heim S, et al. Among authors: mandahl n. Cytogenet Cell Genet. 1989;52(3-4):136-8. doi: 10.1159/000132863. Cytogenet Cell Genet. 1989. PMID: 2630185

5

Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization.

Arheden K, Mandahl N, Strömbeck B, Isaksson M, Mitelman F. Arheden K, et al. Among authors: mandahl n. Cytogenet Cell Genet. 1988;47(1-2):86-7. doi: 10.1159/000132513. Cytogenet Cell Genet. 1988. PMID: 3281802

6

Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas.

Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F. Mandahl N, et al. Hum Genet. 1988 Jul;79(3):203-8. doi: 10.1007/BF00366238. Hum Genet. 1988. PMID: 3402992

7

Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients.

Mertens F, Johansson B, Heim S, Mandahl N, Rydholm A, Mitelman F. Mertens F, et al. Among authors: mandahl n. Hum Genet. 1988 Aug;79(4):309-14. doi: 10.1007/BF00282167. Hum Genet. 1988. PMID: 3410455

8

Evidence of somatic mutations in osteoarthritis.

Mertens F, Pålsson E, Lindstrand A, Toksvig-Larsen S, Knuutila S, Larramendy ML, el-Rifai W, Limon J, Mitelman F, Mandahl N. Mertens F, et al. Among authors: mandahl n. Hum Genet. 1996 Dec;98(6):651-6. doi: 10.1007/s004390050278. Hum Genet. 1996. PMID: 8931694

9

Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma.

Simon MP, Pedeutour F, Sirvent N, Grosgeorge J, Minoletti F, Coindre JM, Terrier-Lacombe MJ, Mandahl N, Craver RD, Blin N, Sozzi G, Turc-Carel C, O'Brien KP, Kedra D, Fransson I, Guilbaud C, Dumanski JP. Simon MP, et al. Among authors: mandahl n. Nat Genet. 1997 Jan;15(1):95-8. doi: 10.1038/ng0197-95. Nat Genet. 1997. PMID: 8988177

10

Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis.

Broberg K, Limon J, Pålsson E, Lindstrand A, Toksvig-Larsen S, Mandahl N, Mertens F. Broberg K, et al. Among authors: mandahl n. Hum Genet. 1997 Dec;101(3):295-8. doi: 10.1007/s004390050631. Hum Genet. 1997. PMID: 9439657

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