Similar articles for PMID: 9124215

Year	Number of Results
1976	1
1984	1
1989	2
1990	3
1991	12
1992	3
1993	11
1994	15
1995	13
1996	13
1997	14
1998	16
1999	10
2000	11
2001	10
2002	10
2003	5
2004	11
2005	7
2006	5
2007	8
2008	3
2009	9
2010	8
2011	5
2012	4
2013	8
2014	5
2015	11
2016	13
2017	10
2018	9
2019	16
2020	14
2021	8
2022	15
2023	10
2024	0

1

Molecular genetic analysis of the von Hippel-Lindau disease tumor suppressor gene in familial and sporadic cerebellar hemangioblastomas.

Tse JY, Wong JH, Lo KW, Poon WS, Huang DP, Ng HK. Tse JY, et al. Am J Clin Pathol. 1997 Apr;107(4):459-66. doi: 10.1093/ajcp/107.4.459. Am J Clin Pathol. 1997. PMID: 9124215

2

Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system.

Gläsker S, Bender BU, Apel TW, van Velthoven V, Mulligan LM, Zentner J, Neumann HP. Gläsker S, et al. J Neurol Neurosurg Psychiatry. 2001 May;70(5):644-8. doi: 10.1136/jnnp.70.5.644. J Neurol Neurosurg Psychiatry. 2001. PMID: 11309459 Free PMC article.

3

Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas.

Kanno H, Kondo K, Ito S, Yamamoto I, Fujii S, Torigoe S, Sakai N, Hosaka M, Shuin T, Yao M. Kanno H, et al. Cancer Res. 1994 Sep 15;54(18):4845-7. Cancer Res. 1994. PMID: 8069849

4

Loss of heterozygosity and somatic mutations of the VHL tumor suppressor gene in sporadic cerebellar hemangioblastomas.

Lee JY, Dong SM, Park WS, Yoo NJ, Kim CS, Jang JJ, Chi JG, Zbar B, Lubensky IA, Linehan WM, Vortmeyer AO, Zhuang Z. Lee JY, et al. Cancer Res. 1998 Feb 1;58(3):504-8. Cancer Res. 1998. PMID: 9458097

5

Analysis of von hippel-lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity.

Gijtenbeek JM, Jacobs B, Sprenger SH, Eleveld MJ, van Kessel AG, Kros JM, Sciot R, van Calenbergh F, Wesseling P, Jeuken JW. Gijtenbeek JM, et al. J Neurosurg. 2002 Oct;97(4):977-82. doi: 10.3171/jns.2002.97.4.0977. J Neurosurg. 2002. PMID: 12405390

6

Loss of heterozygosity at 6q is frequent and concurrent with 3p loss in sporadic and familial capillary hemangioblastomas.

Lemeta S, Pylkkänen L, Sainio M, Niemelä M, Saarikoski S, Husgafvel-Pursiainen K, Böhling T. Lemeta S, et al. J Neuropathol Exp Neurol. 2004 Oct;63(10):1072-9. doi: 10.1093/jnen/63.10.1072. J Neuropathol Exp Neurol. 2004. PMID: 15535134

7

Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis.

Clifford SC, Prowse AH, Affara NA, Buys CH, Maher ER. Clifford SC, et al. Genes Chromosomes Cancer. 1998 Jul;22(3):200-9. doi: 10.1002/(sici)1098-2264(199807)22:3<200::aid-gcc5>3.0.co;2-#. Genes Chromosomes Cancer. 1998. PMID: 9624531

8

Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.

Rasmussen A, Nava-Salazar S, Yescas P, Alonso E, Revuelta R, Ortiz I, Canizales-Quinteros S, Tusié-Luna MT, López-López M. Rasmussen A, et al. J Neurosurg. 2006 Mar;104(3):389-94. doi: 10.3171/jns.2006.104.3.389. J Neurosurg. 2006. PMID: 16572651

9

Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.

Prowse AH, Webster AR, Richards FM, Richard S, Olschwang S, Resche F, Affara NA, Maher ER. Prowse AH, et al. Am J Hum Genet. 1997 Apr;60(4):765-71. Am J Hum Genet. 1997. PMID: 9106522 Free PMC article.

10

Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH.

Decker HJ, Neuhaus C, Jauch A, Speicher M, Ried T, Bujard M, Brauch H, Störkel S, Stöckle M, Seliger B, Huber C. Decker HJ, et al. Hum Genet. 1996 Jun;97(6):770-6. doi: 10.1007/BF02346188. Hum Genet. 1996. PMID: 8641695

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