Rouleau GA - Search Results

1

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: rouleau ga. Hum Mol Genet. 1994 Jan;3(1):147-51. doi: 10.1093/hmg/3.1.147. Hum Mol Genet. 1994. PMID: 8162016

2

Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus.

Twist EC, Farrer LA, Macleod PM, Radvany J, Chamberlain S, Rosenberg RN, Rouleau GA. Twist EC, et al. Among authors: rouleau ga. Hum Genet. 1994 Mar;93(3):335-8. doi: 10.1007/BF00212034. Hum Genet. 1994. PMID: 8125487

3

Dinucleotide repeat polymorphism at the D22S268 locus.

Marineau C, Baron C, Delattre O, Zucman J, Thomas G, Rouleau GA. Marineau C, et al. Among authors: rouleau ga. Hum Mol Genet. 1993 Mar;2(3):336. doi: 10.1093/hmg/2.3.336-a. Hum Mol Genet. 1993. PMID: 8499931 No abstract available.

4

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.

Ruttledge MH, Andermann AA, Phelan CM, Claudio JO, Han FY, Chretien N, Rangaratnam S, MacCollin M, Short P, Parry D, Michels V, Riccardi VM, Weksberg R, Kitamura K, Bradburn JM, Hall BD, Propping P, Rouleau GA. Ruttledge MH, et al. Among authors: rouleau ga. Am J Hum Genet. 1996 Aug;59(2):331-42. Am J Hum Genet. 1996. PMID: 8755919 Free PMC article.

5

Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene.

Watkins D, Ruttledge MH, Sarrazin J, Rangaratnam S, Poisson M, Delattre JY, Rouleau GA. Watkins D, et al. Among authors: rouleau ga. Cancer Genet Cytogenet. 1996 Nov;92(1):73-8. doi: 10.1016/s0165-4608(96)00149-5. Cancer Genet Cytogenet. 1996. PMID: 8956876

6

Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus.

Twist EC, Casaubon LK, Ruttledge MH, Rao VS, Macleod PM, Radvany J, Zhao Z, Rosenberg RN, Farrer LA, Rouleau GA. Twist EC, et al. Among authors: rouleau ga. J Med Genet. 1995 Jan;32(1):25-31. doi: 10.1136/jmg.32.1.25. J Med Genet. 1995. PMID: 7897622 Free PMC article.

7

Mapping of human gamma-glutamyl transpeptidase genes on chromosome 22 and other human autosomes.

Figlewicz DA, Delattre O, Guellaen G, Krizus A, Thomas G, Zucman J, Rouleau GA. Figlewicz DA, et al. Among authors: rouleau ga. Genomics. 1993 Aug;17(2):299-305. doi: 10.1006/geno.1993.1325. Genomics. 1993. PMID: 8104871

8

The mouse homologue of the neurofibromatosis type 2 gene is highly conserved.

Claudio JO, Marineau C, Rouleau GA. Claudio JO, et al. Among authors: rouleau ga. Hum Mol Genet. 1994 Jan;3(1):185-90. doi: 10.1093/hmg/3.1.185. Hum Mol Genet. 1994. PMID: 8162023

9

Isolation and mapping of 45 NotI linking clones to chromosome 22.

Sanson M, Zhang F, Demczuk S, Delattre O, DeJong P, Aurias A, Thomas G, Rouleau GA. Sanson M, et al. Among authors: rouleau ga. Genomics. 1993 Sep;17(3):776-9. doi: 10.1006/geno.1993.1407. Genomics. 1993. PMID: 8244398

10

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2.

Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B, et al. Rouleau GA, et al. Nature. 1993 Jun 10;363(6429):515-21. doi: 10.1038/363515a0. Nature. 1993. PMID: 8379998

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