Mérel P - Search Results

1

Molecular analysis of genetic changes in ependymomas.

Bijlsma EK, Voesten AM, Bijleveld EH, Troost D, Westerveld A, Mérel P, Thomas G, Hulsebos TJ. Bijlsma EK, et al. Among authors: merel p. Genes Chromosomes Cancer. 1995 Aug;13(4):272-7. doi: 10.1002/gcc.2870130407. Genes Chromosomes Cancer. 1995. PMID: 7547635

2

Analysis of mutations in the SCH gene in schwannomas.

Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Bijlsma EK, et al. Among authors: merel p. Genes Chromosomes Cancer. 1994 Sep;11(1):7-14. doi: 10.1002/gcc.2870110103. Genes Chromosomes Cancer. 1994. PMID: 7529050

3

Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene.

Bijlsma EK, Merel P, Fleury P, van Asperen CJ, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Bijlsma EK, et al. Among authors: merel p. Hum Genet. 1995 Jul;96(1):1-5. doi: 10.1007/BF00214177. Hum Genet. 1995. PMID: 7607639

4

Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas.

Mérel P, Hoang-Xuan K, Sanson M, Moreau-Aubry A, Bijlsma EK, Lazaro C, Moisan JP, Resche F, Nishisho I, Estivill X, et al. Mérel P, et al. Genes Chromosomes Cancer. 1995 Jul;13(3):211-6. doi: 10.1002/gcc.2870130311. Genes Chromosomes Cancer. 1995. PMID: 7669741

5

Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas.

Hoang-Xuan K, Merel P, Vega F, Hugot JP, Cornu P, Delattre JY, Poisson M, Thomas G, Delattre O. Hoang-Xuan K, et al. Among authors: merel p. Int J Cancer. 1995 Feb 8;60(4):478-81. doi: 10.1002/ijc.2910600409. Int J Cancer. 1995. PMID: 7829260

6

Screening for germ-line mutations in the NF2 gene.

Mérel P, Hoang-Xuan K, Sanson M, Bijlsma E, Rouleau G, Laurent-Puig P, Pulst S, Baser M, Lenoir G, Sterkers JM, et al. Mérel P, et al. Genes Chromosomes Cancer. 1995 Feb;12(2):117-27. doi: 10.1002/gcc.2870120206. Genes Chromosomes Cancer. 1995. PMID: 7535084

7

Neurofibromatosis type 2 in an adolescent boy with polyneuropathy and a mutation in the NF2 gene.

Overweg-Plandsoen WC, Brouwer-Mladin R, Merel P, de Vries L, Bijlsma EK. Overweg-Plandsoen WC, et al. Among authors: merel p. J Neurol. 1996 Oct;243(10):724-6. doi: 10.1007/BF00873979. J Neurol. 1996. PMID: 8923306 No abstract available.

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: merel p. Nat Genet. 1994 Feb;6(2):180-4. doi: 10.1038/ng0294-180. Nat Genet. 1994. PMID: 8162072

9

Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors.

Thomas G, Delattre O, Zucman J, Merel P, Desmaze C, Melot T, Sanson M, Hoang-Xuan K, Plougastel B, Dejong P, et al. Thomas G, et al. Among authors: merel p. Cold Spring Harb Symp Quant Biol. 1994;59:555-64. doi: 10.1101/sqb.1994.059.01.062. Cold Spring Harb Symp Quant Biol. 1994. PMID: 7587112 No abstract available.

10

The neurofibromatosis type 2 gene is inactivated in schwannomas.

Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA. Twist EC, et al. Among authors: merel p. Hum Mol Genet. 1994 Jan;3(1):147-51. doi: 10.1093/hmg/3.1.147. Hum Mol Genet. 1994. PMID: 8162016

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