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Items: 10

1.

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
2.

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
3.
4.

[From gene to disease: amyotrophic lateral sclerosis].

van Vught PW, Veldink JH, Baas F, van Muiswinkel FL, van den Berg LH.

Ned Tijdschr Geneeskd. 2004 Oct 23;148(43):2125-7. Review. Dutch.

PMID:
15553356
5.

Alsin and the molecular pathways of amyotrophic lateral sclerosis.

Chandran J, Ding J, Cai H.

Mol Neurobiol. 2007 Dec;36(3):224-31. Epub 2007 Jul 10. Review.

6.

Cytoskeletal defects in amyotrophic lateral sclerosis (motor neuron disease).

Julien JP, Millecamps S, Kriz J.

Novartis Found Symp. 2005;264:183-92; discussion 192-6, 227-30. Review.

PMID:
15773754
7.

A molecular genetic approach to amyotrophic lateral sclerosis.

Siddique T, Hu P, Hentati A, Deng G, Hung WY, McInnis MG, Warren AC, Rimmler J, Antonarakis S, Pericak-Vance MA.

Int J Neurol. 1991-1992;25-26:60-9. Review.

PMID:
11980064
8.

ALS2/alsin knockout mice and motor neuron diseases.

Cai H, Shim H, Lai C, Xie C, Lin X, Yang WJ, Chandran J.

Neurodegener Dis. 2008;5(6):359-66. doi: 10.1159/000151295. Epub 2008 Aug 20. Review.

9.

[Causative genes for familial amyotrophic lateral sclerosis].

Hadano S.

Seikagaku. 2002 Jun;74(6):483-9. Review. Japanese. No abstract available.

PMID:
12138710
10.

[Genetic defects in neurodegenerative diseases].

Davidson B, Nass D.

Harefuah. 1997 Apr 1;132(7):481-5. Review. Hebrew. No abstract available.

PMID:
9153920

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