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Results: 1 to 20 of 97

Similar articles for PubMed (Select 11161814)

1.

Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.

Hadano S, Yanagisawa Y, Skaug J, Fichter K, Nasir J, Martindale D, Koop BF, Scherer SW, Nicholson DW, Rouleau GA, Ikeda J, Hayden MR.

Genomics. 2001 Jan 15;71(2):200-13.

PMID:
11161814
2.

A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34.

Hadano S, Nichol K, Brinkman RR, Nasir J, Martindale D, Koop BF, Nicholson DW, Scherer SW, Ikeda JE, Hayden MR.

Genomics. 1999 Jan 1;55(1):106-12.

PMID:
9889004
3.

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE.

Nat Genet. 2001 Oct;29(2):166-73.

PMID:
11586298
4.

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.

Hosler BA, Sapp PC, Berger R, O'Neill G, Bejaoui K, Hamida MB, Hentati F, Chin W, McKenna-Yasek D, Haines JL, Patterson D, Horvitz HR, Brown RH Jr, Day CB.

Neurogenetics. 1998 Dec;2(1):34-42.

PMID:
9933298
5.

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, Hentati F, Siddique T.

Nat Genet. 2001 Oct;29(2):160-5.

PMID:
11586297
6.

Cell death attenuation by 'Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex.

Rasper DM, Vaillancourt JP, Hadano S, Houtzager VM, Seiden I, Keen SL, Tawa P, Xanthoudakis S, Nasir J, Martindale D, Koop BF, Peterson EP, Thornberry NA, Huang J, MacPherson DP, Black SC, Hornung F, Lenardo MJ, Hayden MR, Roy S, Nicholson DW.

Cell Death Differ. 1998 Apr;5(4):271-88.

7.

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C, et al.

Nat Genet. 1994 Jul;7(3):425-8.

PMID:
7920663
8.
9.

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.

Gros-Louis F, Kriz J, Kabashi E, McDearmid J, Millecamps S, Urushitani M, Lin L, Dion P, Zhu Q, Drapeau P, Julien JP, Rouleau GA.

Hum Mol Genet. 2008 Sep 1;17(17):2691-702. doi: 10.1093/hmg/ddn171. Epub 2008 Jun 16.

10.

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.

Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, Bouchard JP, Camu W, Hayden MR, Rouleau GA.

Arch Neurol. 2003 Dec;60(12):1768-71.

PMID:
14676054
11.

Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP).

Herzfeld T, Wolf N, Winter P, Hackstein H, Vater D, Müller U.

Neurogenetics. 2009 Feb;10(1):59-64. doi: 10.1007/s10048-008-0148-y. Epub 2008 Sep 23.

PMID:
18810511
12.

Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis.

Belzil VV, Langlais JS, Daoud H, Dion PA, Brais B, Rouleau GA.

Arch Neurol. 2012 May;69(5):653-6.

PMID:
22248478
13.

Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis.

Berger R, Mezey E, Clancy KP, Harta G, Wright RM, Repine JE, Brown RH, Brownstein M, Patterson D.

Somat Cell Mol Genet. 1995 Mar;21(2):121-31.

PMID:
7570184
14.

Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degeneration.

Hadano S, Kunita R, Otomo A, Suzuki-Utsunomiya K, Ikeda JE.

Neurochem Int. 2007 Jul-Sep;51(2-4):74-84. Epub 2007 May 4. Review.

PMID:
17566607
15.

Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis.

Parboosingh JS, Meininger V, McKenna-Yasek D, Brown RH Jr, Rouleau GA.

Arch Neurol. 1999 Jun;56(6):710-2.

PMID:
10369311
16.

Genetic inroads in familial ALS.

Shaw PJ.

Nat Genet. 2001 Oct;29(2):103-4.

PMID:
11586285
17.

Variation in CASP10 gene is associated with idiopathic talipes equinovarus.

Heck AL, Bray MS, Scott A, Blanton SH, Hecht JT.

J Pediatr Orthop. 2005 Sep-Oct;25(5):598-602.

PMID:
16199938
18.

Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.

Cooper PR, Nowak NJ, Higgins MJ, Church DM, Shows TB.

Genomics. 1998 May 1;49(3):419-29.

PMID:
9615227
19.

Novel mutation in the ALS2 gene in juvenile amyotrophic lateral sclerosis.

Kress JA, Kühnlein P, Winter P, Ludolph AC, Kassubek J, Müller U, Sperfeld AD.

Ann Neurol. 2005 Nov;58(5):800-3.

PMID:
16240357
20.

Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.

Eymard-Pierre E, Lesca G, Dollet S, Santorelli FM, di Capua M, Bertini E, Boespflug-Tanguy O.

Am J Hum Genet. 2002 Sep;71(3):518-27. Epub 2002 Jul 26.

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