Similar articles for PMID: 17209131

Year	Number of Results
1992	1
1995	2
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2000	2
2001	2
2002	1
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2004	4
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2006	19
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2017	22
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2019	18
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2022	15
2023	5
2024	0

1

Mitotic recombination as evidence of alternative pathogenesis of gastrointestinal stromal tumours in neurofibromatosis type 1.

Stewart DR, Corless CL, Rubin BP, Heinrich MC, Messiaen LM, Kessler LJ, Zhang PJ, Brooks DG. Stewart DR, et al. J Med Genet. 2007 Jan;44(1):e61. doi: 10.1136/jmg.2006.043075. J Med Genet. 2007. PMID: 17209131 Free PMC article.

2

Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients.

Maertens O, Prenen H, Debiec-Rychter M, Wozniak A, Sciot R, Pauwels P, De Wever I, Vermeesch JR, de Raedt T, De Paepe A, Speleman F, van Oosterom A, Messiaen L, Legius E. Maertens O, et al. Hum Mol Genet. 2006 Mar 15;15(6):1015-23. doi: 10.1093/hmg/ddl016. Epub 2006 Feb 6. Hum Mol Genet. 2006. PMID: 16461335

3

Multiple gastrointestinal stromal tumors: Clinicopathologic and genetic analysis of 12 patients.

Kang DY, Park CK, Choi JS, Jin SY, Kim HJ, Joo M, Kang MS, Moon WS, Yun KJ, Yu ES, Kang H, Kim KM. Kang DY, et al. Am J Surg Pathol. 2007 Feb;31(2):224-32. doi: 10.1097/01.pas.0000213318.66800.94. Am J Surg Pathol. 2007. PMID: 17255767

4

Quadruple-Negative GIST Is a Sentinel for Unrecognized Neurofibromatosis Type 1 Syndrome.

Gasparotto D, Rossi S, Polano M, Tamborini E, Lorenzetto E, Sbaraglia M, Mondello A, Massani M, Lamon S, Bracci R, Mandolesi A, Frate E, Stanzial F, Agaj J, Mazzoleni G, Pilotti S, Gronchi A, Dei Tos AP, Maestro R. Gasparotto D, et al. Clin Cancer Res. 2017 Jan 1;23(1):273-282. doi: 10.1158/1078-0432.CCR-16-0152. Epub 2016 Jul 7. Clin Cancer Res. 2017. PMID: 27390349

5

Gastrointestinal stromal tumors of neurofibromatosis type I (von Recklinghausen's disease).

Takazawa Y, Sakurai S, Sakuma Y, Ikeda T, Yamaguchi J, Hashizume Y, Yokoyama S, Motegi A, Fukayama M. Takazawa Y, et al. Am J Surg Pathol. 2005 Jun;29(6):755-63. doi: 10.1097/01.pas.0000163359.32734.f9. Am J Surg Pathol. 2005. PMID: 15897742

6

Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA.

de Raedt T, Cools J, Debiec-Rychter M, Brems H, Mentens N, Sciot R, Himpens J, de Wever I, Schöffski P, Marynen P, Legius E. de Raedt T, et al. Gastroenterology. 2006 Dec;131(6):1907-12. doi: 10.1053/j.gastro.2006.07.002. Gastroenterology. 2006. PMID: 17087943

7

V600E BRAF mutations are alternative early molecular events in a subset of KIT/PDGFRA wild-type gastrointestinal stromal tumours.

Agaimy A, Terracciano LM, Dirnhofer S, Tornillo L, Foerster A, Hartmann A, Bihl MP. Agaimy A, et al. J Clin Pathol. 2009 Jul;62(7):613-6. doi: 10.1136/jcp.2009.064550. J Clin Pathol. 2009. PMID: 19561230

8

Neurofibromatosis type 1-related gastrointestinal stromal tumors: a special reference to loss of heterozygosity at 14q and 22q.

Yamamoto H, Tobo T, Nakamori M, Imamura M, Kojima A, Oda Y, Nakamura N, Takahira T, Yao T, Tsuneyoshi M. Yamamoto H, et al. J Cancer Res Clin Oncol. 2009 Jun;135(6):791-8. doi: 10.1007/s00432-008-0514-z. Epub 2008 Nov 20. J Cancer Res Clin Oncol. 2009. PMID: 19020900

9

Diagnostic significance of DOG-1 and PKC-θ expression and c-Kit/PDGFRA mutations in gastrointestinal stromal tumours.

Wang C, Jin MS, Zou YB, Gao JN, Li XB, Peng F, Wang HY, Wu ZD, Wang YP, Duan XM. Wang C, et al. Scand J Gastroenterol. 2013 Sep;48(9):1055-65. doi: 10.3109/00365521.2013.816770. Epub 2013 Jul 17. Scand J Gastroenterol. 2013. PMID: 23862765

10

Clinical significance of oncogenic KIT and PDGFRA mutations in gastrointestinal stromal tumours.

Lasota J, Miettinen M. Lasota J, et al. Histopathology. 2008 Sep;53(3):245-66. doi: 10.1111/j.1365-2559.2008.02977.x. Epub 2008 Feb 28. Histopathology. 2008. PMID: 18312355 Review.

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