441 related articles for article (PubMed ID: 2142531)
1. Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.
Menon AG; Anderson KM; Riccardi VM; Chung RY; Whaley JM; Yandell DW; Farmer GE; Freiman RN; Lee JK; Li FP
Proc Natl Acad Sci U S A; 1990 Jul; 87(14):5435-9. PubMed ID: 2142531
[TBL] [Abstract][Full Text] [Related]
2. Loss of heterozygosity on chromosome arm 17p in small cell lung carcinomas, but not in neurofibromas, in a patient with von Recklinghausen neurofibromatosis.
Shimizu E; Shinohara T; Mori N; Yokota J; Tani K; Izumi K; Obashi A; Ogura T
Cancer; 1993 Feb; 71(3):725-8. PubMed ID: 8094318
[TBL] [Abstract][Full Text] [Related]
3. Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis.
Glover TW; Stein CK; Legius E; Andersen LB; Brereton A; Johnson S
Genes Chromosomes Cancer; 1991 Jan; 3(1):62-70. PubMed ID: 1906341
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the p53 gene occur in diverse human tumour types.
Nigro JM; Baker SJ; Preisinger AC; Jessup JM; Hostetter R; Cleary K; Bigner SH; Davidson N; Baylin S; Devilee P
Nature; 1989 Dec; 342(6250):705-8. PubMed ID: 2531845
[TBL] [Abstract][Full Text] [Related]
5. Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1.
Rasmussen SA; Overman J; Thomson SA; Colman SD; Abernathy CR; Trimpert RE; Moose R; Virdi G; Roux K; Bauer M; Rojiani AM; Maria BL; Muir D; Wallace MR
Genes Chromosomes Cancer; 2000 Aug; 28(4):425-31. PubMed ID: 10862051
[TBL] [Abstract][Full Text] [Related]
6. Formation of a minichromosome by excision of the proximal region of 17q in a patient with von Recklinghausen neurofibromatosis.
Andersen LB; Tommerup N; Koch J
Cytogenet Cell Genet; 1990; 53(4):206-10. PubMed ID: 2119939
[TBL] [Abstract][Full Text] [Related]
7. Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type I.
Gutmann DH; Cole JL; Stone WJ; Ponder BA; Collins FS
Genes Chromosomes Cancer; 1994 May; 10(1):55-8. PubMed ID: 7519874
[TBL] [Abstract][Full Text] [Related]
8. Loss of distinct regions on the short arm of chromosome 17 associated with tumorigenesis of human astrocytomas.
el-Azouzi M; Chung RY; Farmer GE; Martuza RL; Black PM; Rouleau GA; Hettlich C; Hedley-Whyte ET; Zervas NT; Panagopoulos K
Proc Natl Acad Sci U S A; 1989 Sep; 86(18):7186-90. PubMed ID: 2571151
[TBL] [Abstract][Full Text] [Related]
9. The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.
Skuse GR; Kosciolek BA; Rowley PT
Am J Hum Genet; 1991 Sep; 49(3):600-7. PubMed ID: 1715669
[TBL] [Abstract][Full Text] [Related]
10. Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis.
Xu W; Mulligan LM; Ponder MA; Liu L; Smith BA; Mathew CG; Ponder BA
Genes Chromosomes Cancer; 1992 Jun; 4(4):337-42. PubMed ID: 1377942
[TBL] [Abstract][Full Text] [Related]
11. Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors.
Beert E; Brems H; Daniëls B; De Wever I; Van Calenbergh F; Schoenaers J; Debiec-Rychter M; Gevaert O; De Raedt T; Van Den Bruel A; de Ravel T; Cichowski K; Kluwe L; Mautner V; Sciot R; Legius E
Genes Chromosomes Cancer; 2011 Dec; 50(12):1021-32. PubMed ID: 21987445
[TBL] [Abstract][Full Text] [Related]
12. Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.
Baker SJ; Fearon ER; Nigro JM; Hamilton SR; Preisinger AC; Jessup JM; vanTuinen P; Ledbetter DH; Barker DF; Nakamura Y; White R; Vogelstein B
Science; 1989 Apr; 244(4901):217-21. PubMed ID: 2649981
[TBL] [Abstract][Full Text] [Related]
13. Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.
Fang Y; Elahi A; Denley RC; Rao PH; Brennan MF; Jhanwar SC
Anticancer Res; 2009 Apr; 29(4):1255-62. PubMed ID: 19414372
[TBL] [Abstract][Full Text] [Related]
14. Mechanisms of loss of heterozygosity in neurofibromatosis type 1-associated plexiform neurofibromas.
Steinmann K; Kluwe L; Friedrich RE; Mautner VF; Cooper DN; Kehrer-Sawatzki H
J Invest Dermatol; 2009 Mar; 129(3):615-21. PubMed ID: 18800150
[TBL] [Abstract][Full Text] [Related]
15. Losses in chromosomes 17, 19, and 22q in neurofibromatosis type 1 and sporadic neurofibromas: a comparative genomic hybridization analysis.
Koga T; Iwasaki H; Ishiguro M; Matsuzaki A; Kikuchi M
Cancer Genet Cytogenet; 2002 Jul; 136(2):113-20. PubMed ID: 12237234
[TBL] [Abstract][Full Text] [Related]
16. Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations.
Serra E; Ars E; Ravella A; Sánchez A; Puig S; Rosenbaum T; Estivill X; Lázaro C
Hum Genet; 2001 May; 108(5):416-29. PubMed ID: 11409870
[TBL] [Abstract][Full Text] [Related]
17. A search for evidence of somatic mutations in the NF1 gene.
John AM; Ruggieri M; Ferner R; Upadhyaya M
J Med Genet; 2000 Jan; 37(1):44-9. PubMed ID: 10633134
[TBL] [Abstract][Full Text] [Related]
18. Alterations at chromosome 17 loci in peripheral nerve sheath tumors.
Lothe RA; Slettan A; Saeter G; Brøgger A; Børresen AL; Nesland JM
J Neuropathol Exp Neurol; 1995 Jan; 54(1):65-73. PubMed ID: 7815081
[TBL] [Abstract][Full Text] [Related]
19. Absence of cutaneous neurofibromas in an NF1 patient with an atypical deletion partially overlapping the common 1.4 Mb microdeleted region.
Kehrer-Sawatzki H; Schmid E; Fünsterer C; Kluwe L; Mautner VF
Am J Med Genet A; 2008 Mar; 146A(6):691-9. PubMed ID: 18265407
[TBL] [Abstract][Full Text] [Related]
20. Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17.
Skuse GR; Kosciolek BA; Rowley PT
Genes Chromosomes Cancer; 1989 Sep; 1(1):36-41. PubMed ID: 2577271
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
