-
1
-
-
0036164342
-
Incidence of adult brain arteriovenous malformation hemorrhage in a prospective population-based stroke survey
-
Stapf C, Labovitz DL, Sciacca RR, et al. Incidence of adult brain arteriovenous malformation hemorrhage in a prospective population-based stroke survey. Cerebrovasc Dis 2002;13:43-6.
-
(2002)
Cerebrovasc Dis
, vol.13
, pp. 43-46
-
-
Stapf, C.1
Labovitz, D.L.2
Sciacca, R.R.3
-
2
-
-
0343527474
-
Cerebral arteriovenous malformations and associated aneurysms: Analysis of 305 cases from a series of 662 patients
-
Meisel HJ, Mansmann U, Alvarez H, et al. Cerebral arteriovenous malformations and associated aneurysms: analysis of 305 cases from a series of 662 patients. Neurosurgery 2000;46:793-800.
-
(2000)
Neurosurgery
, vol.46
, pp. 793-800
-
-
Meisel, H.J.1
Mansmann, U.2
Alvarez, H.3
-
3
-
-
39149085980
-
Outcome after interventional or conservative management of unruptured brain arteriovenous malformations: A prospective, population-based cohort study
-
Wedderburn CJ, van Beijnum J, Bhattacharya JJ, et al . Outcome after interventional or conservative management of unruptured brain arteriovenous malformations: a prospective, population-based cohort study. Lancet Neurol 2008;7:223-30.
-
(2008)
Lancet Neurol
, vol.7
, pp. 223-230
-
-
Wedderburn, C.J.1
Van Beijnum, J.2
Bhattacharya, J.J.3
-
4
-
-
85052609523
-
Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations
-
Kim H, Marchuk DA, Pawlikowska L, et al. Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations. Acta Neurochir Suppl 2008;105:199-206.
-
(2008)
Acta Neurochir Suppl
, vol.105
, pp. 199-206
-
-
Kim, H.1
Marchuk, D.A.2
Pawlikowska, L.3
-
5
-
-
73449088332
-
Biology of vascular malformations of the brain NINDS Workshop Collaborators. Biology of vascular malformations of the brain
-
Leblanc GG, Golanov E, Awad IA, et al. Biology of vascular malformations of the brain NINDS Workshop Collaborators. Biology of vascular malformations of the brain. Stroke 2009;40:694-702.
-
(2009)
Stroke
, vol.40
, pp. 694-702
-
-
Leblanc, G.G.1
Golanov, E.2
Awad, I.A.3
-
6
-
-
33744741661
-
Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system
-
Simon M, Franke D, Ludwig M, et al. Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system. J Neurosurg 2006;104:945-9.
-
(2006)
J Neurosurg
, vol.104
, pp. 945-949
-
-
Simon, M.1
Franke, D.2
Ludwig, M.3
-
7
-
-
84874290488
-
Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations: Where do we stand?
-
Sturiale CL, Puca A, Sebastiani P, et al. Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations: where do we stand? Brain 2013;136:665-81.
-
(2013)
Brain
, vol.136
, pp. 665-681
-
-
Sturiale, C.L.1
Puca, A.2
Sebastiani, P.3
-
8
-
-
79952193044
-
Polymorphisms of the vascular endothelial growth factor A gene and susceptibility to sporadic brain arteriovenous malformation in a Chinese population
-
Chen H, Gu Y, Wu W, et al. Polymorphisms of the vascular endothelial growth factor A gene and susceptibility to sporadic brain arteriovenous malformation in a Chinese population. J Clin Neurosci 2011;18:549-53.
-
(2011)
J Clin Neurosci
, vol.18
, pp. 549-553
-
-
Chen, H.1
Gu, Y.2
Wu, W.3
-
9
-
-
78049460953
-
The rs522616 polymorphism in the matrix metalloproteinase-3 (MMP-3) gene is associated with sporadic brain arteriovenous malformation in a Chinese population
-
Zhao Y, Li P, Fan W, et al. The rs522616 polymorphism in the matrix metalloproteinase-3 (MMP-3) gene is associated with sporadic brain arteriovenous malformation in a Chinese population. J Clin Neurosci 2010;17:1568-72.
-
(2010)
J Clin Neurosci
, vol.17
, pp. 1568-1572
-
-
Zhao, Y.1
Li, P.2
Fan, W.3
-
10
-
-
57649126477
-
Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation
-
Kim H, Hysi PG, Pawlikowska L, et al. Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation. Cerebrovasc Dis 2009;27:176-82.
-
(2009)
Cerebrovasc Dis
, vol.27
, pp. 176-182
-
-
Kim, H.1
Hysi, P.G.2
Pawlikowska, L.3
-
11
-
-
77951768060
-
Genome-wide association study of intracranial aneurysm identifies three new risk loci
-
Yasuno K, Bilguvar K, Bijlenga P, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010;42:420-5.
-
(2010)
Nat Genet
, vol.42
, pp. 420-425
-
-
Yasuno, K.1
Bilguvar, K.2
Bijlenga, P.3
-
12
-
-
33749172559
-
Stem-cell ageing modified by the cyclin-dependent kinase inhibitor p16INK4a
-
Janzen V, Forkert R, Fleming HE, et al. Stem-cell ageing modified by the cyclin-dependent kinase inhibitor p16INK4a. Nature 2006;443:421-6.
-
(2006)
Nature
, vol.443
, pp. 421-426
-
-
Janzen, V.1
Forkert, R.2
Fleming, H.E.3
-
13
-
-
27244455897
-
Deleted in liver cancer 2 (DLC2) suppresses cell transformation by means of inhibition of RhoA activity
-
Leung TH, Ching YP, Yam JW, et al. Deleted in liver cancer 2 (DLC2) suppresses cell transformation by means of inhibition of RhoA activity. Proc Natl Acad Sci USA 2005;102:15207-12.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 15207-15212
-
-
Leung, T.H.1
Ching, Y.P.2
Yam, J.W.3
-
14
-
-
33749423324
-
Redundant roles of Sox17 and Sox18 in postnatal angiogenesis in mice
-
Matsui T, Kanai-Azuma M, Hara K, et al. Redundant roles of Sox17 and Sox18 in postnatal angiogenesis in mice. J Cell Sci 2006;119:3513-26.
-
(2006)
J Cell Sci
, vol.119
, pp. 3513-3526
-
-
Matsui, T.1
Kanai-Azuma, M.2
Hara, K.3
-
15
-
-
34447265321
-
Redundant roles of Sox17 and Sox18 in early cardiovascular development of mouse embryos
-
Sakamoto Y, Hara K, Kanai-Azuma M, et al. Redundant roles of Sox17 and Sox18 in early cardiovascular development of mouse embryos. Biochem Biophys Res Commun 2007;360:539-44.
-
(2007)
Biochem Biophys Res Commun
, vol.360
, pp. 539-544
-
-
Sakamoto, Y.1
Hara, K.2
Kanai-Azuma, M.3
-
16
-
-
67349246802
-
CtIP-BRCA1 modulates the choice of DNA double-strand-break repair pathway throughout the cell cycle
-
Yun MH, Hiom K. CtIP-BRCA1 modulates the choice of DNA double-strand-break repair pathway throughout the cell cycle. Nature 2009;459:460-3.
-
(2009)
Nature
, vol.459
, pp. 460-463
-
-
Yun, M.H.1
Hiom, K.2
-
17
-
-
25144506445
-
Functional characterization of ACDP2 (ancient conserved domain protein), a divalent metal transporter
-
Goytain A, Quamme GA. Functional characterization of ACDP2 (ancient conserved domain protein), a divalent metal transporter. Physiol Genomics 2005;22:382-9.
-
(2005)
Physiol Genomics
, vol.22
, pp. 382-389
-
-
Goytain, A.1
Quamme, G.A.2
-
18
-
-
84881543884
-
Association between the rs1333040 polymorphism on the chromosomal 9p21 locus and sporadic brain arteriovenous malformations
-
Sturiale CL, Gatto I, Puca A, et al . Association between the rs1333040 polymorphism on the chromosomal 9p21 locus and sporadic brain arteriovenous malformations. J Neurol Neurosurg Psychiatry 2013;84:1059-62.
-
(2013)
J Neurol Neurosurg Psychiatry
, vol.84
, pp. 1059-1062
-
-
Sturiale, C.L.1
Gatto, I.2
Puca, A.3
-
19
-
-
84898731854
-
Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms
-
Bendjilali N, Nelson J, Weinsheimer S, et al. Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms. J Neurol Neurosurg Psychiatry 2014;85:1280-3.
-
(2014)
J Neurol Neurosurg Psychiatry
, vol.85
, pp. 1280-1283
-
-
Bendjilali, N.1
Nelson, J.2
Weinsheimer, S.3
-
20
-
-
70349592269
-
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;41:1083-7.
-
(2009)
Nat Genet
, vol.41
, pp. 1083-1087
-
-
Van Es, M.A.1
Veldink, J.H.2
Saris, C.G.3
-
21
-
-
78651245467
-
Common variants in P2RY11 are associated with narcolepsy
-
Kornum BR, Kawashima M, Faraco J, et al. Common variants in P2RY11 are associated with narcolepsy. Nat Genet 2011;43:66-71.
-
(2011)
Nat Genet
, vol.43
, pp. 66-71
-
-
Kornum, B.R.1
Kawashima, M.2
Faraco, J.3
-
22
-
-
56749157973
-
Susceptibility loci for intracranial aneurysm in European and Japanese populations
-
Bilguvar K, Yasuno K, Niemela M, et al. Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nat Genet 2008;40:1472-7.
-
(2008)
Nat Genet
, vol.40
, pp. 1472-1477
-
-
Bilguvar, K.1
Yasuno, K.2
Niemela, M.3
-
23
-
-
78649508578
-
MaCH: Using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li Y, Willer CJ, Ding J, et al. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 2010;34: 816-34.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 816-834
-
-
Li, Y.1
Willer, C.J.2
Ding, J.3
-
25
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007;81: 559-75.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
-
26
-
-
66349110366
-
Sox17 promotes cell cycle progression and inhibits TGF-beta/Smad3 signaling to initiate progenitor cell behavior in the respiratory epithelium
-
Lange AW, Keiser AR, Wells JM, et al. Sox17 promotes cell cycle progression and inhibits TGF-beta/Smad3 signaling to initiate progenitor cell behavior in the respiratory epithelium. PLoS ONE 2009;4:5711.
-
(2009)
PLoS ONE
, vol.4
, pp. 5711
-
-
Lange, A.W.1
Keiser, A.R.2
Wells, J.M.3
-
27
-
-
79957653357
-
Sox17 regulates proliferation and cell cycle during gastric cancer progression
-
Ye YW, Wu JH, Wang CM, et al. Sox17 regulates proliferation and cell cycle during gastric cancer progression. Cancer Lett 2011;307:124-31.
-
(2011)
Cancer Lett
, vol.307
, pp. 124-131
-
-
Ye, Y.W.1
Wu, J.H.2
Wang, C.M.3
-
28
-
-
84873843115
-
Sox17 promotes tumor angiogenesis and destabilizes tumor vessels in mice
-
Yang H, Lee S, Lee S, et al . Sox17 promotes tumor angiogenesis and destabilizes tumor vessels in mice. J Clin Invest 2013;123:418-31.
-
(2013)
J Clin Invest
, vol.123
, pp. 418-431
-
-
Yang, H.1
Lee, S.2
Lee, S.3
-
29
-
-
80055077904
-
CtIP mutations cause seckel and jawad syndromes
-
Qvist P, Huertas P, Nimeno S, et al. CtIP Mutations Cause Seckel and Jawad Syndromes. PLoS Genet 2011;7:e1002310.
-
(2011)
PLoS Genet
, vol.7
, pp. e1002310
-
-
Qvist, P.1
Huertas, P.2
Nimeno, S.3
-
30
-
-
0034973265
-
Evidence of increased endothelial cell turnover in brain arteriovenous malformations
-
Hashimoto T, Mesa-Tejada R, Quick CM, et al. Evidence of increased endothelial cell turnover in brain arteriovenous malformations. Neurosurgery 2001;49: 124-31.
-
(2001)
Neurosurgery
, vol.49
, pp. 124-131
-
-
Hashimoto, T.1
Mesa-Tejada, R.2
Quick, C.M.3
-
31
-
-
83355166837
-
Gene expression profiling of blood in brain arteriovenous malformation patients
-
Weinsheimer S, Xu H, Achrol AS, et al. Gene expression profiling of blood in brain arteriovenous malformation patients. Transl Stroke Res 2011;2:575-87.
-
(2011)
Transl Stroke Res
, vol.2
, pp. 575-587
-
-
Weinsheimer, S.1
Xu, H.2
Achrol, A.S.3
-
32
-
-
10744232469
-
Gene microarray analysis of human brain arteriovenous malformations
-
Hashimoto T, Lawton MT, Wen G, et al. Gene microarray analysis of human brain arteriovenous malformations. Neurosurg 2004;54:410-23.
-
(2004)
Neurosurg
, vol.54
, pp. 410-423
-
-
Hashimoto, T.1
Lawton, M.T.2
Wen, G.3
|