Collins VP - Search Results

1

Chromosome 17 abnormalities and lack of TP53 mutations in paediatric central nervous system tumours.

Phelan CM, Liu L, Ruttledge MH, Müntzning K, Ridderheim PA, Collins VP. Phelan CM, et al. Among authors: collins vp. Hum Genet. 1995 Dec;96(6):684-90. doi: 10.1007/BF00210300. Hum Genet. 1995. PMID: 8522328

2

Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter.

Dumanski JP, Geurts van Kessel AH, Ruttledge M, Wladis A, Sugawa N, Collins VP, Nordenskjöld M. Dumanski JP, et al. Among authors: collins vp. Hum Genet. 1990 Feb;84(3):219-22. doi: 10.1007/BF00200562. Hum Genet. 1990. PMID: 1968030 Free article.

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: collins vp. Genes Chromosomes Cancer. 1994 Jun;10(2):122-30. doi: 10.1002/gcc.2870100207. Genes Chromosomes Cancer. 1994. PMID: 7520265

4

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene.

Peyrard M, Fransson I, Xie YG, Han FY, Ruttledge MH, Swahn S, Collins JE, Dunham I, Collins VP, Dumanski JP. Peyrard M, et al. Among authors: collins vp, collins je. Hum Mol Genet. 1994 Aug;3(8):1393-9. doi: 10.1093/hmg/3.8.1393. Hum Mol Genet. 1994. PMID: 7987321

5

Chromosome 7 rearrangements in glioblastomas; loci adjacent to EGFR are independently amplified.

Liu L, Ichimura K, Pettersson EH, Collins VP. Liu L, et al. Among authors: collins vp. J Neuropathol Exp Neurol. 1998 Dec;57(12):1138-45. doi: 10.1097/00005072-199812000-00005. J Neuropathol Exp Neurol. 1998. PMID: 9862636

6

Mutations in Rb1 pathway-related genes are associated with poor prognosis in anaplastic astrocytomas.

Bäcklund LM, Nilsson BR, Liu L, Ichimura K, Collins VP. Bäcklund LM, et al. Among authors: collins vp. Br J Cancer. 2005 Jul 11;93(1):124-30. doi: 10.1038/sj.bjc.6602661. Br J Cancer. 2005. PMID: 15970925 Free PMC article.

7

Loss of genetic information in central nervous system tumors common to children and young adults.

James CD, He J, Carlbom E, Mikkelsen T, Ridderheim PA, Cavenee WK, Collins VP. James CD, et al. Among authors: collins vp. Genes Chromosomes Cancer. 1990 Jul;2(2):94-102. doi: 10.1002/gcc.2870020204. Genes Chromosomes Cancer. 1990. PMID: 1980610

8

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.

Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins VP, et al. Ruttledge MH, et al. Among authors: collins vp. Nat Genet. 1994 Feb;6(2):180-4. doi: 10.1038/ng0294-180. Nat Genet. 1994. PMID: 8162072

9

Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression.

Lindblom A, Ruttledge M, Collins VP, Nordenskjöld M, Dumanski JP. Lindblom A, et al. Among authors: collins vp. Int J Cancer. 1994 Feb 1;56(3):354-7. doi: 10.1002/ijc.2910560310. Int J Cancer. 1994. PMID: 8314321

10

Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers.

Ruttledge MH, Narod SA, Dumanski JP, Parry DM, Eldridge R, Wertelecki W, Parboosingh J, Faucher MC, Lenoir GM, Collins VP, et al. Ruttledge MH, et al. Among authors: collins vp. Neurology. 1993 Sep;43(9):1753-60. doi: 10.1212/wnl.43.9.1753. Neurology. 1993. PMID: 8414026

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