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Results: 1 to 20 of 123

Similar articles for PubMed (Select 16501576)

1.

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

Greenway MJ, Andersen PM, Russ C, Ennis S, Cashman S, Donaghy C, Patterson V, Swingler R, Kieran D, Prehn J, Morrison KE, Green A, Acharya KR, Brown RH Jr, Hardiman O.

Nat Genet. 2006 Apr;38(4):411-3. Epub 2006 Feb 26.

PMID:
16501576
2.

Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis.

Gellera C, Colombrita C, Ticozzi N, Castellotti B, Bragato C, Ratti A, Taroni F, Silani V.

Neurogenetics. 2008 Feb;9(1):33-40. Epub 2007 Dec 18.

PMID:
18087731
3.

A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy.

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

Neuromuscul Disord. 2008 Jan;18(1):68-70. Epub 2007 Aug 20.

PMID:
17703939
4.

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.

Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Vande Velde C, Bouchard JP, Lacomblez L, Pochigaeva K, Salachas F, Pradat PF, Camu W, Meininger V, Dupre N, Rouleau GA.

Nat Genet. 2008 May;40(5):572-4. doi: 10.1038/ng.132. Epub 2008 Mar 30.

PMID:
18372902
6.

Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort.

Zou ZY, Wang XN, Liu MS, Sun Q, Li XG, Cui LY, Kong J.

Amyotroph Lateral Scler. 2012 May;13(3):270-5. doi: 10.3109/17482968.2011.643900. Epub 2012 Jan 31.

PMID:
22292798
7.

Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis.

Wu D, Yu W, Kishikawa H, Folkerth RD, Iafrate AJ, Shen Y, Xin W, Sims K, Hu GF.

Ann Neurol. 2007 Dec;62(6):609-17.

8.

Characterization of human angiogenin variants implicated in amyotrophic lateral sclerosis.

Crabtree B, Thiyagarajan N, Prior SH, Wilson P, Iyer S, Ferns T, Shapiro R, Brew K, Subramanian V, Acharya KR.

Biochemistry. 2007 Oct 23;46(42):11810-8. Epub 2007 Sep 27.

PMID:
17900154
9.

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis.

Fernández-Santiago R, Hoenig S, Lichtner P, Sperfeld AD, Sharma M, Berg D, Weichenrieder O, Illig T, Eger K, Meyer T, Anneser J, Münch C, Zierz S, Gasser T, Ludolph A.

J Neurol. 2009 Aug;256(8):1337-42. doi: 10.1007/s00415-009-5124-4. Epub 2009 Apr 12.

10.

Mutations of optineurin in amyotrophic lateral sclerosis.

Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H.

Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28.

PMID:
20428114
11.

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Paubel A, Violette J, Amy M, Praline J, Meininger V, Camu W, Corcia P, Andres CR, Vourc'h P; French Amyotrophic Lateral Sclerosis (ALS) Study Group.

Arch Neurol. 2008 Oct;65(10):1333-6. doi: 10.1001/archneur.65.10.1333.

PMID:
18852347
12.

SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.

Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noël L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V.

J Med Genet. 2010 Aug;47(8):554-60. doi: 10.1136/jmg.2010.077180. Epub 2010 Jun 24.

PMID:
20577002
13.

Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population.

Corrado L, Battistini S, Penco S, Bergamaschi L, Testa L, Ricci C, Giannini F, Greco G, Patrosso MC, Pileggi S, Causarano R, Mazzini L, Momigliano-Richiardi P, D'Alfonso S.

J Neurol Sci. 2007 Jul 15;258(1-2):123-7. Epub 2007 Apr 25.

PMID:
17462671
14.

Prediction of functional loss of human angiogenin mutants associated with ALS by molecular dynamics simulations.

Padhi AK, Jayaram B, Gomes J.

Sci Rep. 2013;3:1225. doi: 10.1038/srep01225. Epub 2013 Feb 7.

15.

Angiogenin protects motoneurons against hypoxic injury.

Sebastià J, Kieran D, Breen B, King MA, Netteland DF, Joyce D, Fitzpatrick SF, Taylor CT, Prehn JH.

Cell Death Differ. 2009 Sep;16(9):1238-47. doi: 10.1038/cdd.2009.52. Epub 2009 May 15.

16.

Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.

Zou ZY, Peng Y, Feng XH, Wang XN, Sun Q, Liu MS, Li XG, Cui LY.

Eur J Neurol. 2012 Jul;19(7):977-83. doi: 10.1111/j.1468-1331.2012.03662.x. Epub 2012 Feb 16.

PMID:
22340366
17.

TDP-43 mutation in familial amyotrophic lateral sclerosis.

Yokoseki A, Shiga A, Tan CF, Tagawa A, Kaneko H, Koyama A, Eguchi H, Tsujino A, Ikeuchi T, Kakita A, Okamoto K, Nishizawa M, Takahashi H, Onodera O.

Ann Neurol. 2008 Apr;63(4):538-42. doi: 10.1002/ana.21392.

PMID:
18438952
18.

A novel candidate region for ALS on chromosome 14q11.2.

Greenway MJ, Alexander MD, Ennis S, Traynor BJ, Corr B, Frost E, Green A, Hardiman O.

Neurology. 2004 Nov 23;63(10):1936-8.

PMID:
15557516
19.

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
20.

TARDBP in amyotrophic lateral sclerosis: identification of a novel variant but absence of copy number variation.

Bäumer D, Parkinson N, Talbot K.

J Neurol Neurosurg Psychiatry. 2009 Nov;80(11):1283-5. doi: 10.1136/jnnp.2008.166512.

PMID:
19864663
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