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Volumn 70, Issue 6, 2011, Pages 964-973

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

(56)  Van Es, Michael A a   Schelhaas, Helenius J b   Van Vught, Paul W J a   Ticozzi, Nicola c,d   Andersen, Peter M e   Groen, Ewout J N a   Schulte, Claudia f   Blauw, Hylke M a   Koppers, Max a   Diekstra, Frank P a   Fumoto, Katsumi a   Leclerc, Ashley Lyn c   Keagle, Pamela c   Bloem, Bastiaan R b   Scheffer, Hans g   Van Nuenen, Bart F L b   Van Blitterswijk, Marka a   Van Rheenen, Wouter a   Wills, Anne Marie h   Lowe, Patrick P c   more..


Author keywords

[No Author keywords available]

Indexed keywords

ANGIOGENIN; DNA;

EID: 84255163614     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.22611     Document Type: Review
Times cited : (166)

References (50)
  • 1
    • 0028097839 scopus 로고
    • A controlled trial of riluzole in amyotrophic lateral sclerosis
    • DOI 10.1056/NEJM199403033300901
    • Bensimon G, Lacomblez L, Meininger V,. A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group. N Engl J Med 1994; 330: 585-591. (Pubitemid 24065791)
    • (1994) New England Journal of Medicine , vol.330 , Issue.9 , pp. 585-591
    • Bensimon, G.1    Lacomblez, L.2    Meininger, V.3
  • 3
    • 78649632679 scopus 로고    scopus 로고
    • An estimate of amyotrophic lateral sclerosis heritability using twin data
    • Al-Chalabi A, Fang F, Hanby MF, et al. An estimate of amyotrophic lateral sclerosis heritability using twin data. J Neurol Neurosurg Psychiatry 2010; 81: 1324-1326.
    • (2010) J Neurol Neurosurg Psychiatry , vol.81 , pp. 1324-1326
    • Al-Chalabi, A.1    Fang, F.2    Hanby, M.F.3
  • 4
    • 70349592269 scopus 로고    scopus 로고
    • Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
    • van Es MA, Veldink JH, Saris CG, et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat Genet 2009; 41: 1083-1087.
    • (2009) Nat Genet , vol.41 , pp. 1083-1087
    • Van Es, M.A.1    Veldink, J.H.2    Saris, C.G.3
  • 5
    • 70350075024 scopus 로고    scopus 로고
    • Genetics of motor neuron disorders: New insights into pathogenic mechanisms
    • Dion PA, Daoud H, Rouleau GA,. Genetics of motor neuron disorders: new insights into pathogenic mechanisms. Nat Rev Genet 2009; 10: 769-782.
    • (2009) Nat Rev Genet , vol.10 , pp. 769-782
    • Dion, P.A.1    Daoud, H.2    Rouleau, G.A.3
  • 6
    • 77954038587 scopus 로고    scopus 로고
    • Paraoxonase gene mutations in amyotrophic lateral sclerosis
    • Ticozzi N, LeClerc AL, Keagle PJ, et al. Paraoxonase gene mutations in amyotrophic lateral sclerosis. Ann Neurol 2010; 68: 102-107.
    • (2010) Ann Neurol , vol.68 , pp. 102-107
    • Ticozzi, N.1    Leclerc, A.L.2    Keagle, P.J.3
  • 8
    • 78649941297 scopus 로고    scopus 로고
    • Exome sequencing reveals VCP mutations as a cause of familial ALS
    • Johnson JO, Mandrioli J, Benatar M, et al. Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 2010; 68: 857-864.
    • (2010) Neuron , vol.68 , pp. 857-864
    • Johnson, J.O.1    Mandrioli, J.2    Benatar, M.3
  • 9
    • 77952419246 scopus 로고    scopus 로고
    • Mutations of optineurin in amyotrophic lateral sclerosis
    • Maruyama H, Morino H, Ito H, et al. Mutations of optineurin in amyotrophic lateral sclerosis. Nature 2010; 465: 223-226.
    • (2010) Nature , vol.465 , pp. 223-226
    • Maruyama, H.1    Morino, H.2    Ito, H.3
  • 12
    • 72749106555 scopus 로고    scopus 로고
    • Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: Increased susceptibility in male carriers of the -2578AA genotype
    • Lambrechts D, Poesen K, Fernandez-Santiago R, et al. Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype. J Med Genet 2009; 46: 840-846.
    • (2009) J Med Genet , vol.46 , pp. 840-846
    • Lambrechts, D.1    Poesen, K.2    Fernandez-Santiago, R.3
  • 14
    • 33645422711 scopus 로고    scopus 로고
    • ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
    • Greenway MJ, Andersen PM, Russ C, et al. ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. Nat Genet 2006; 38: 411-413.
    • (2006) Nat Genet , vol.38 , pp. 411-413
    • Greenway, M.J.1    Andersen, P.M.2    Russ, C.3
  • 15
    • 38449113556 scopus 로고    scopus 로고
    • Genetics of sporadic amyotrophic lateral sclerosis
    • Schymick JC, Talbot K, Traynor BJ,. Genetics of sporadic amyotrophic lateral sclerosis. Hum Mol Genet 2007; 16: R233-R242.
    • (2007) Hum Mol Genet , vol.16
    • Schymick, J.C.1    Talbot, K.2    Traynor, B.J.3
  • 16
    • 69949186725 scopus 로고    scopus 로고
    • Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation
    • Seilhean D, Cazeneuve C, Thuries V, et al. Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation. Acta Neuropathol 2009; 118: 561-573.
    • (2009) Acta Neuropathol , vol.118 , pp. 561-573
    • Seilhean, D.1    Cazeneuve, C.2    Thuries, V.3
  • 17
    • 59649128986 scopus 로고    scopus 로고
    • A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation
    • van Es MA, Diekstra FP, Veldink JH, et al. A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation. Neurology 2009; 72: 287-288.
    • (2009) Neurology , vol.72 , pp. 287-288
    • Van Es, M.A.1    Diekstra, F.P.2    Veldink, J.H.3
  • 19
    • 77956881000 scopus 로고    scopus 로고
    • Coexistence of parkinsonism, dementia and upper motor neuron syndrome in four Czech patients
    • Farnikova K, Kanovsky P, Nestrasil I, et al. Coexistence of parkinsonism, dementia and upper motor neuron syndrome in four Czech patients. J Neurol Sci 2010; 296: 47-54.
    • (2010) J Neurol Sci , vol.296 , pp. 47-54
    • Farnikova, K.1    Kanovsky, P.2    Nestrasil, I.3
  • 20
    • 77956801164 scopus 로고    scopus 로고
    • Parkinsonism and motor neuron diseases: Twenty-seven patients with diverse overlap syndromes
    • Gilbert RM, Fahn S, Mitsumoto H, et al. Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes. Mov Disord 2010; 25: 1868-1875.
    • (2010) Mov Disord , vol.25 , pp. 1868-1875
    • Gilbert, R.M.1    Fahn, S.2    Mitsumoto, H.3
  • 22
    • 37749020600 scopus 로고    scopus 로고
    • Descriptive epidemiology of amyotrophic lateral sclerosis: New evidence and unsolved issues
    • Logroscino G, Traynor BJ, Hardiman O, et al. Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues. J Neurol Neurosurg Psychiatry 2008; 79: 6-11.
    • (2008) J Neurol Neurosurg Psychiatry , vol.79 , pp. 6-11
    • Logroscino, G.1    Traynor, B.J.2    Hardiman, O.3
  • 23
    • 0028046648 scopus 로고
    • Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: Evidence of shared genetic susceptibility
    • Majoor-Krakauer D, Ottman R, Johnson WG, et al. Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility. Neurology 1994; 44: 1872-1877. (Pubitemid 24319214)
    • (1994) Neurology , vol.44 , Issue.10 , pp. 1872-1877
    • Majoor-Krakauer, D.1    Ottman, R.2    Johnson, W.G.3    Rowland, L.P.4
  • 24
    • 80052726999 scopus 로고    scopus 로고
    • Broadening the phenotype of TARDBP mutations: The TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia
    • Quadri M, Cossu G, Saddi V, et al. Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia. Neurogenetics 2011; 12: 203-209.
    • (2011) Neurogenetics , vol.12 , pp. 203-209
    • Quadri, M.1    Cossu, G.2    Saddi, V.3
  • 25
    • 79960811611 scopus 로고    scopus 로고
    • Ataxin-2 repeat-length variation and neurodegeneration
    • Ross OA, Rutherford NJ, Baker M, et al. Ataxin-2 repeat-length variation and neurodegeneration. Hum Mol Genet 2011; 20: 3207-3212.
    • (2011) Hum Mol Genet , vol.20 , pp. 3207-3212
    • Ross, O.A.1    Rutherford, N.J.2    Baker, M.3
  • 30
    • 37549038185 scopus 로고    scopus 로고
    • Absence of angiogenic genes modification in Italian ALS patients
    • Del BR, Scarlato M, Ghezzi S, et al. Absence of angiogenic genes modification in Italian ALS patients. Neurobiol Aging 2008; 29: 314-316.
    • (2008) Neurobiol Aging , vol.29 , pp. 314-316
    • Del, B.R.1    Scarlato, M.2    Ghezzi, S.3
  • 31
    • 68449084458 scopus 로고    scopus 로고
    • Identification of novel angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis
    • Fernandez-Santiago R, Hoenig S, Lichtner P, et al. Identification of novel angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis. J Neurol 2009; 256: 1337-1342.
    • (2009) J Neurol , vol.256 , pp. 1337-1342
    • Fernandez-Santiago, R.1    Hoenig, S.2    Lichtner, P.3
  • 32
    • 38649105800 scopus 로고    scopus 로고
    • Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis
    • Gellera C, Colombrita C, Ticozzi N, et al. Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis. Neurogenetics 2008; 9: 33-40.
    • (2008) Neurogenetics , vol.9 , pp. 33-40
    • Gellera, C.1    Colombrita, C.2    Ticozzi, N.3
  • 33
    • 54049119245 scopus 로고    scopus 로고
    • Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis
    • Paubel A, Violette J, Amy M, et al. Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis. Arch Neurol 2008; 65: 1333-1336.
    • (2008) Arch Neurol , vol.65 , pp. 1333-1336
    • Paubel, A.1    Violette, J.2    Amy, M.3
  • 34
    • 35248844678 scopus 로고    scopus 로고
    • Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis
    • Wu D, Yu W, Kishikawa H, et al. Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis. Ann Neurol 2007; 62: 609-617.
    • (2007) Ann Neurol , vol.62 , pp. 609-617
    • Wu, D.1    Yu, W.2    Kishikawa, H.3
  • 35
    • 57649136554 scopus 로고    scopus 로고
    • Progress and challenges in genome-wide association studies in humans
    • Donnelly P,. Progress and challenges in genome-wide association studies in humans. Nature 2008; 456: 728-731.
    • (2008) Nature , vol.456 , pp. 728-731
    • Donnelly, P.1
  • 36
    • 70349956433 scopus 로고    scopus 로고
    • Finding the missing heritability of complex diseases
    • Manolio TA, Collins FS, Cox NJ, et al. Finding the missing heritability of complex diseases. Nature 2009; 461: 747-753.
    • (2009) Nature , vol.461 , pp. 747-753
    • Manolio, T.A.1    Collins, F.S.2    Cox, N.J.3
  • 37
    • 77958102016 scopus 로고    scopus 로고
    • Statistical analysis strategies for association studies involving rare variants
    • Bansal V, Libiger O, Torkamani A, et al. Statistical analysis strategies for association studies involving rare variants. Nat Rev Genet 2010; 11: 773-785.
    • (2010) Nat Rev Genet , vol.11 , pp. 773-785
    • Bansal, V.1    Libiger, O.2    Torkamani, A.3
  • 38
    • 61449168010 scopus 로고    scopus 로고
    • A groupwise association test for rare mutations using a weighted sum statistic
    • Madsen BE, Browning SR,. A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet 2009; 5: e1000384.
    • (2009) PLoS Genet , vol.5
    • Madsen, B.E.1    Browning, S.R.2
  • 39
    • 77953121877 scopus 로고    scopus 로고
    • Pooled association tests for rare variants in exon-resequencing studies
    • Price AL, Kryukov GV, de Bakker PI, et al. Pooled association tests for rare variants in exon-resequencing studies. Am J Hum Genet 2010; 86: 832-838.
    • (2010) Am J Hum Genet , vol.86 , pp. 832-838
    • Price, A.L.1    Kryukov, G.V.2    De Bakker, P.I.3
  • 40
    • 70549112253 scopus 로고    scopus 로고
    • Evidence for a common pathway linking neurodegenerative diseases
    • Shulman JM, De Jager PL,. Evidence for a common pathway linking neurodegenerative diseases. Nat Genet 2009; 41: 1261-1262.
    • (2009) Nat Genet , vol.41 , pp. 1261-1262
    • Shulman, J.M.1    De Jager, P.L.2
  • 41
    • 67249139655 scopus 로고    scopus 로고
    • SNCA variants are associated with increased risk for multiple system atrophy
    • Scholz SW, Houlden H, Schulte C, et al. SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol 2009; 65: 610-614.
    • (2009) Ann Neurol , vol.65 , pp. 610-614
    • Scholz, S.W.1    Houlden, H.2    Schulte, C.3
  • 43
    • 70350319531 scopus 로고    scopus 로고
    • Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
    • Sidransky E, Nalls MA, Aasly JO, et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med 2009; 361: 1651-1661.
    • (2009) N Engl J Med , vol.361 , pp. 1651-1661
    • Sidransky, E.1    Nalls, M.A.2    Aasly, J.O.3
  • 44
    • 37549019664 scopus 로고    scopus 로고
    • Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons
    • Subramanian V, Crabtree B, Acharya KR,. Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons. Hum Mol Genet 2008; 17: 130-149.
    • (2008) Hum Mol Genet , vol.17 , pp. 130-149
    • Subramanian, V.1    Crabtree, B.2    Acharya, K.R.3
  • 45
    • 58149373936 scopus 로고    scopus 로고
    • Control of motoneuron survival by angiogenin
    • Kieran D, Sebastia J, Greenway MJ, et al. Control of motoneuron survival by angiogenin. J Neurosci 2008; 28: 14056-14061.
    • (2008) J Neurosci , vol.28 , pp. 14056-14061
    • Kieran, D.1    Sebastia, J.2    Greenway, M.J.3
  • 46
    • 69049110867 scopus 로고    scopus 로고
    • Angiogenin protects motoneurons against hypoxic injury
    • Sebastia J, Kieran D, Breen B, et al. Angiogenin protects motoneurons against hypoxic injury. Cell Death Differ 2009; 16: 1238-1247.
    • (2009) Cell Death Differ , vol.16 , pp. 1238-1247
    • Sebastia, J.1    Kieran, D.2    Breen, B.3
  • 47
    • 34447317537 scopus 로고    scopus 로고
    • A new role for angiogenin in neurite growth and pathfinding: Implications for amyotrophic lateral sclerosis
    • DOI 10.1093/hmg/ddm095
    • Subramanian V, Feng Y,. A new role for angiogenin in neurite growth and pathfinding: implications for amyotrophic lateral sclerosis. Hum Mol Genet 2007; 16: 1445-1453. (Pubitemid 47055116)
    • (2007) Human Molecular Genetics , vol.16 , Issue.12 , pp. 1445-1453
    • Subramanian, V.1    Feng, Y.2
  • 49
    • 39249084455 scopus 로고    scopus 로고
    • Transcriptional dysregulation in a transgenic model of Parkinson disease
    • Yacoubian TA, Cantuti-Castelvetri I, Bouzou B, et al. Transcriptional dysregulation in a transgenic model of Parkinson disease. Neurobiol Dis 2008; 29: 515-528.
    • (2008) Neurobiol Dis , vol.29 , pp. 515-528
    • Yacoubian, T.A.1    Cantuti-Castelvetri, I.2    Bouzou, B.3
  • 50
    • 78651282742 scopus 로고    scopus 로고
    • A neuroprotective role for angiogenin in models of Parkinson's disease
    • Steidinger TU, Standaert DG, Yacoubian TA,. A neuroprotective role for angiogenin in models of Parkinson's disease. J Neurochem 2011; 116: 334-341.
    • (2011) J Neurochem , vol.116 , pp. 334-341
    • Steidinger, T.U.1    Standaert, D.G.2    Yacoubian, T.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.