Gravel RA - Search Results

1

Mice deficient in Neu4 sialidase exhibit abnormal ganglioside catabolism and lysosomal storage.

Seyrantepe V, Canuel M, Carpentier S, Landry K, Durand S, Liang F, Zeng J, Caqueret A, Gravel RA, Marchesini S, Zwingmann C, Michaud J, Morales CR, Levade T, Pshezhetsky AV. Seyrantepe V, et al. Among authors: gravel ra. Hum Mol Genet. 2008 Jun 1;17(11):1556-68. doi: 10.1093/hmg/ddn043. Epub 2008 Feb 11. Hum Mol Genet. 2008. PMID: 18270209

2

Mice doubly-deficient in lysosomal hexosaminidase A and neuraminidase 4 show epileptic crises and rapid neuronal loss.

Seyrantepe V, Lema P, Caqueret A, Dridi L, Bel Hadj S, Carpentier S, Boucher F, Levade T, Carmant L, Gravel RA, Hamel E, Vachon P, Di Cristo G, Michaud JL, Morales CR, Pshezhetsky AV. Seyrantepe V, et al. Among authors: gravel ra. PLoS Genet. 2010 Sep 16;6(9):e1001118. doi: 10.1371/journal.pgen.1001118. PLoS Genet. 2010. PMID: 20862357 Free PMC article.

3

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases.

Phaneuf D, Wakamatsu N, Huang JQ, Borowski A, Peterson AC, Fortunato SR, Ritter G, Igdoura SA, Morales CR, Benoit G, Akerman BR, Leclerc D, Hanai N, Marth JD, Trasler JM, Gravel RA. Phaneuf D, et al. Among authors: gravel ra. Hum Mol Genet. 1996 Jan;5(1):1-14. doi: 10.1093/hmg/5.1.1. Hum Mol Genet. 1996. PMID: 8789434

4

Apoptotic cell death in mouse models of GM2 gangliosidosis and observations on human Tay-Sachs and Sandhoff diseases.

Huang JQ, Trasler JM, Igdoura S, Michaud J, Hanal N, Gravel RA. Huang JQ, et al. Among authors: gravel ra. Hum Mol Genet. 1997 Oct;6(11):1879-85. doi: 10.1093/hmg/6.11.1879. Hum Mol Genet. 1997. PMID: 9302266

5

Cloning of the cDNA and gene encoding mouse lysosomal sialidase and correction of sialidase deficiency in human sialidosis and mouse SM/J fibroblasts.

Igdoura SA, Gafuik C, Mertineit C, Saberi F, Pshezhetsky AV, Potier M, Trasler JM, Gravel RA. Igdoura SA, et al. Among authors: gravel ra. Hum Mol Genet. 1998 Jan;7(1):115-21. doi: 10.1093/hmg/7.1.115. Hum Mol Genet. 1998. PMID: 9384611

6

Altered gene expression in cells from patients with lysosomal storage disorders suggests impairment of the ubiquitin pathway.

Bifsha P, Landry K, Ashmarina L, Durand S, Seyrantepe V, Trudel S, Quiniou C, Chemtob S, Xu Y, Gravel RA, Sladek R, Pshezhetsky AV. Bifsha P, et al. Among authors: gravel ra. Cell Death Differ. 2007 Mar;14(3):511-23. doi: 10.1038/sj.cdd.4402013. Epub 2006 Aug 4. Cell Death Differ. 2007. PMID: 16888648

7

Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis.

Pshezhetsky AV, Richard C, Michaud L, Igdoura S, Wang S, Elsliger MA, Qu J, Leclerc D, Gravel R, Dallaire L, Potier M. Pshezhetsky AV, et al. Nat Genet. 1997 Mar;15(3):316-20. doi: 10.1038/ng0397-316. Nat Genet. 1997. PMID: 9054950

8

Sialidase-mediated depletion of GM2 ganglioside in Tay-Sachs neuroglia cells.

Igdoura SA, Mertineit C, Trasler JM, Gravel RA. Igdoura SA, et al. Among authors: gravel ra. Hum Mol Genet. 1999 Jun;8(6):1111-6. doi: 10.1093/hmg/8.6.1111. Hum Mol Genet. 1999. PMID: 10332044

9

Impact of premature stop codons on mRNA levels in infantile Sandhoff disease.

Zhang ZX, Wakamatsu N, Mules EH, Thomas GH, Gravel RA. Zhang ZX, et al. Among authors: gravel ra. Hum Mol Genet. 1994 Jan;3(1):139-45. doi: 10.1093/hmg/3.1.139. Hum Mol Genet. 1994. PMID: 8162015

10

Neuronal apoptosis in sudden infant death syndrome.

Waters KA, Meehan B, Huang JQ, Gravel RA, Michaud J, Côté A. Waters KA, et al. Among authors: gravel ra. Pediatr Res. 1999 Feb;45(2):166-72. doi: 10.1203/00006450-199902000-00002. Pediatr Res. 1999. PMID: 10022585

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