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Results: 1 to 20 of 120

1.

Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis.

Aoki M, Lin CL, Rothstein JD, Geller BA, Hosler BA, Munsat TL, Horvitz HR, Brown RH Jr.

Ann Neurol. 1998 May;43(5):645-53.

PMID:
9585360
[PubMed - indexed for MEDLINE]
2.

Polymorphisms in the glutamate transporter gene EAAT2 in European ALS patients.

Jackson M, Steers G, Leigh PN, Morrison KE.

J Neurol. 1999 Dec;246(12):1140-4.

PMID:
10653305
[PubMed - indexed for MEDLINE]
3.

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis.

Lin CL, Bristol LA, Jin L, Dykes-Hoberg M, Crawford T, Clawson L, Rothstein JD.

Neuron. 1998 Mar;20(3):589-602.

PMID:
9539131
[PubMed - indexed for MEDLINE]
Free Article
4.

Intron 7 retention and exon 9 skipping EAAT2 mRNA variants are not associated with amyotrophic lateral sclerosis.

Flowers JM, Powell JF, Leigh PN, Andersen P, Shaw CE.

Ann Neurol. 2001 May;49(5):643-9.

PMID:
11357955
[PubMed - indexed for MEDLINE]
5.

The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia.

Meyer T, Münch C, Völkel H, Booms P, Ludolph AC.

J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):594-6.

PMID:
9771796
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

The RNA of the glutamate transporter EAAT2 is variably spliced in amyotrophic lateral sclerosis and normal individuals.

Meyer T, Fromm A, Münch C, Schwalenstöcker B, Fray AE, Ince PG, Stamm S, Grön G, Ludolph AC, Shaw PJ.

J Neurol Sci. 1999 Nov 15;170(1):45-50.

PMID:
10540035
[PubMed - indexed for MEDLINE]
7.

SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.

Battistini S, Giannini F, Greco G, Bibbò G, Ferrera L, Marini V, Causarano R, Casula M, Lando G, Patrosso MC, Caponnetto C, Origone P, Marocchi A, Del Corona A, Siciliano G, Carrera P, Mascia V, Giagheddu M, Carcassi C, Orrù S, Garrè C, Penco S.

J Neurol. 2005 Jul;252(7):782-8. Epub 2005 Mar 29.

PMID:
15789135
[PubMed - indexed for MEDLINE]
8.

Glutamate transporter EAAT2 splice variants occur not only in ALS, but also in AD and controls.

Honig LS, Chambliss DD, Bigio EH, Carroll SL, Elliott JL.

Neurology. 2000 Oct 24;55(8):1082-8.

PMID:
11071482
[PubMed - indexed for MEDLINE]
9.

Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.

Gellera C, Castellotti B, Riggio MC, Silani V, Morandi L, Testa D, Casali C, Taroni F, Di Donato S, Zeviani M, Mariotti C.

Neuromuscul Disord. 2001 May;11(4):404-10.

PMID:
11369193
[PubMed - indexed for MEDLINE]
10.

Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.

Jackson M, Al-Chalabi A, Enayat ZE, Chioza B, Leigh PN, Morrison KE.

Ann Neurol. 1997 Nov;42(5):803-7.

PMID:
9392581
[PubMed - indexed for MEDLINE]
11.

Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.

Parboosingh JS, Rouleau GA, Meninger V, McKenna-Yasek D, Brown RH Jr, Figlewicz DA.

Neuromuscul Disord. 1995 Jan;5(1):7-10.

PMID:
7719145
[PubMed - indexed for MEDLINE]
12.

Alternative splicing of the 5'-sequences of the mouse EAAT2 glutamate transporter and expression in a transgenic model for amyotrophic lateral sclerosis.

Münch C, Ebstein M, Seefried U, Zhu B, Stamm S, Landwehrmeyer GB, Ludolph AC, Schwalenstöcker B, Meyer T.

J Neurochem. 2002 Aug;82(3):594-603.

PMID:
12153483
[PubMed - indexed for MEDLINE]
13.

Alternative splicing of the glutamate transporter EAAT2 (GLT-1).

Meyer T, Münch C, Knappenberger B, Liebau S, Völkel H, Ludolph AC.

Neurosci Lett. 1998 Jan 23;241(1):68-70.

PMID:
9502218
[PubMed - indexed for MEDLINE]
14.

Glutamate transporter gene expression in amyotrophic lateral sclerosis motor cortex.

Bristol LA, Rothstein JD.

Ann Neurol. 1996 May;39(5):676-9.

PMID:
8619555
[PubMed - indexed for MEDLINE]
15.

Genetics of ALS in Italian families.

Gellera C.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2001 Mar;2 Suppl 1:S43-6.

PMID:
11465924
[PubMed - indexed for MEDLINE]
16.

[Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis].

Shi SG, Li LS, Chen KN, Liu X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):149-52. Chinese.

PMID:
15079798
[PubMed - indexed for MEDLINE]
17.

An analysis of the entire SOD1 gene in sporadic ALS.

Luquin N, Yu B, Trent RJ, Morahan JM, Pamphlett R.

Neuromuscul Disord. 2008 Jul;18(7):545-52. doi: 10.1016/j.nmd.2008.04.013. Epub 2008 May 27.

PMID:
18504130
[PubMed - indexed for MEDLINE]
18.

A novel two-base mutation in the Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan.

Morita M, Aoki M, Abe K, Hasegawa T, Sakuma R, Onodera Y, Ichikawa N, Nishizawa M, Itoyama Y.

Neurosci Lett. 1996 Feb 23;205(2):79-82.

PMID:
8907321
[PubMed - indexed for MEDLINE]
19.

Increased expression of the glial glutamate transporter EAAT2 modulates excitotoxicity and delays the onset but not the outcome of ALS in mice.

Guo H, Lai L, Butchbach ME, Stockinger MP, Shan X, Bishop GA, Lin CL.

Hum Mol Genet. 2003 Oct 1;12(19):2519-32. Epub 2003 Aug 5.

PMID:
12915461
[PubMed - indexed for MEDLINE]
Free Article
20.

Sporadic ALS is not associated with VAPB gene mutations in Southern Italy.

Conforti FL, Sprovieri T, Mazzei R, Ungaro C, Tessitore A, Tedeschi G, Patitucci A, Magariello A, Gabriele A, Labella V, Simone IL, Majorana G, Monsurrò MR, Valentino P, Muglia M, Quattrone A.

J Negat Results Biomed. 2006 May 29;5:7.

PMID:
16729899
[PubMed - indexed for MEDLINE]
Free PMC Article

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