-
1
-
-
65449167582
-
Long-term prognosis of Chinese patients with a lacunar infarct associated with small vessel disease: A 5 year longitudinal study
-
Mok VC, Lau AY, Wong A, Lam WW, Chan A, Leung H, et al. Long-term prognosis of Chinese patients with a lacunar infarct associated with small vessel disease: A 5 year longitudinal study. Int J Stroke 2009;4:81-88.
-
(2009)
Int J Stroke
, vol.4
, pp. 81-88
-
-
Mok, V.C.1
Lau, A.Y.2
Wong, A.3
Lam, W.W.4
Chan, A.5
Leung, H.6
-
2
-
-
0037534908
-
Evaluating the genetic component of ischemic stroke subtypes: A family history study
-
Jerrard-Dunne P, Cloud G, Hassan A, Markus HS. Evaluating the genetic component of ischemic stroke subtypes: A family history study. Stroke 2003;34:1364-1369.
-
(2003)
Stroke
, vol.34
, pp. 1364-1369
-
-
Jerrard-Dunne, P.1
Cloud, G.2
Hassan, A.3
Markus, H.S.4
-
3
-
-
0037196888
-
Family history of stroke in stroke types and subtypes
-
Polychronopoulos P, Gioldasis G, Ellul J, Metallinos IC, Lekka NP, Paschalis C, Papapetropoulos T. Family history of stroke in stroke types and subtypes. J Neurol Sci 2002;195:117-122.
-
(2002)
J Neurol Sci
, vol.195
, pp. 117-122
-
-
Polychronopoulos, P.1
Gioldasis, G.2
Ellul, J.3
Metallinos, I.C.4
Lekka, N.P.5
Paschalis, C.6
Papapetropoulos, T.7
-
4
-
-
80053212602
-
The genetics of white matter lesions
-
Assareh A, Mather KA, Schofield PR, Kwok JB, Sachdev PS. The genetics of white matter lesions. CNS Neurosci Ther 2011;17(5):525-40.
-
(2011)
CNS Neurosci Ther
, vol.17
, Issue.5
, pp. 525-540
-
-
Assareh, A.1
Mather, K.A.2
Schofield, P.R.3
Kwok, J.B.4
Sachdev, P.S.5
-
5
-
-
66849141259
-
Genetic determinants of white matter hyperintensities on brain scans: A systematic assessment of 19 candidate gene polymorphisms in 46 studies in 19,000 subjects
-
Paternoster L, Chen W, Sudlow CL. Genetic determinants of white matter hyperintensities on brain scans: A systematic assessment of 19 candidate gene polymorphisms in 46 studies in 19, 000 subjects. Stroke 2009;40:2020-2026.
-
(2009)
Stroke
, vol.40
, pp. 2020-2026
-
-
Paternoster, L.1
Chen, W.2
Sudlow, C.L.3
-
6
-
-
64549160555
-
Endothelial dysfunction in lacunar stroke: A systematic review
-
Knottnerus IL, Ten Cate H, Lodder J, Kessels F, van Oostenbrugge RJ. Endothelial dysfunction in lacunar stroke: A systematic review. Cerebrovasc Dis 2009;27:519-526.
-
(2009)
Cerebrovasc Dis
, vol.27
, pp. 519-526
-
-
Knottnerus, I.L.1
Ten Cate, H.2
Lodder, J.3
Kessels, F.4
van Oostenbrugge, R.J.5
-
8
-
-
41149158733
-
Changes in background blood-brain barrier integrity between lacunar and cortical ischemic stroke subtypes
-
Wardlaw JM, Farrall A, Armitage PA, Carpenter T, Chappell F, Doubal F, et al. Changes in background blood-brain barrier integrity between lacunar and cortical ischemic stroke subtypes. Stroke 2008;39:1327-1332.
-
(2008)
Stroke
, vol.39
, pp. 1327-1332
-
-
Wardlaw, J.M.1
Farrall, A.2
Armitage, P.A.3
Carpenter, T.4
Chappell, F.5
Doubal, F.6
-
9
-
-
0037228838
-
Increased blood-brain barrier permeability in type II diabetes demonstrated by gadolinium magnetic resonance imaging
-
Starr JM, Wardlaw J, Ferguson K, MacLullich A, Deary IJ, Marshall I. Increased blood-brain barrier permeability in type II diabetes demonstrated by gadolinium magnetic resonance imaging. J Neurol Neurosurg Psychiatry 2003;74:70-76.
-
(2003)
J Neurol Neurosurg Psychiatry
, vol.74
, pp. 70-76
-
-
Starr, J.M.1
Wardlaw, J.2
Ferguson, K.3
MacLullich, A.4
Deary, I.J.5
Marshall, I.6
-
10
-
-
77954326094
-
Myosin light chain kinase in microvascular endothelial barrier function
-
Shen Q, Rigor RR, Pivetti CD, Wu MH, Yuan SY. Myosin light chain kinase in microvascular endothelial barrier function. Cardiovasc Res 2010;87:272-280.
-
(2010)
Cardiovasc Res
, vol.87
, pp. 272-280
-
-
Shen, Q.1
Rigor, R.R.2
Pivetti, C.D.3
Wu, M.H.4
Yuan, S.Y.5
-
11
-
-
0031729852
-
Regulation of cytoskeletal mechanics and cell growth by myosin light chainphosphorylation
-
Cai S, Pestic-Dragovich L, O'Donnell ME, Wang N, Ingber D, Elson E, et al. Regulation of cytoskeletal mechanics and cell growth by myosin light chainphosphorylation. Am J Physiol 1998;275:C1349-C1356.
-
(1998)
Am J Physiol
, vol.275
-
-
Cai, S.1
Pestic-Dragovich, L.2
O'Donnell, M.E.3
Wang, N.4
Ingber, D.5
Elson, E.6
-
12
-
-
34447342541
-
Microvascular permeability in diabetes and insulin resistance
-
Yuan SY, Breslin JW, Perrin R, Gaudreault N, Guo M, Kargozaran H, et al. Microvascular permeability in diabetes and insulin resistance. Microcirculation 2007;14:363-373.
-
(2007)
Microcirculation
, vol.14
, pp. 363-373
-
-
Yuan, S.Y.1
Breslin, J.W.2
Perrin, R.3
Gaudreault, N.4
Guo, M.5
Kargozaran, H.6
-
13
-
-
69149101976
-
Molecular mechanisms of endothelial hyperpermeability: Implications in inflammation
-
Kumar P, Shen Q, Pivetti CD, Lee ES, Wu MH, Yuan SY. Molecular mechanisms of endothelial hyperpermeability: Implications in inflammation. Expert Rev Mol Med 2009;11:e19.
-
(2009)
Expert Rev Mol Med
, vol.11
-
-
Kumar, P.1
Shen, Q.2
Pivetti, C.D.3
Lee, E.S.4
Wu, M.H.5
Yuan, S.Y.6
-
14
-
-
78650518134
-
CysLT2 receptor-mediated AQP4 up-regulation is involved in ischemic-like injury through activation of ERK and p38 MAPK in rat astrocytes
-
Qi LL, Fang SH, Shi WZ, Huang XQ, Zhang XY, Lu YB, et al. CysLT2 receptor-mediated AQP4 up-regulation is involved in ischemic-like injury through activation of ERK and p38 MAPK in rat astrocytes. Life Sci 2011;88:50-56.
-
(2011)
Life Sci
, vol.88
, pp. 50-56
-
-
Qi, L.L.1
Fang, S.H.2
Shi, W.Z.3
Huang, X.Q.4
Zhang, X.Y.5
Lu, Y.B.6
-
16
-
-
0041703033
-
Inhibition of aquaporin-4 expression in astrocytes by RNAi determines alteration in cell morphology, growth, and water transport and induces changes in ischemia-related genes
-
Nicchia GP, Frigeri A, Liuzzi GM, Svelto M. Inhibition of aquaporin-4 expression in astrocytes by RNAi determines alteration in cell morphology, growth, and water transport and induces changes in ischemia-related genes. FASEB J 2003;17:1508-1510.
-
(2003)
FASEB J
, vol.17
, pp. 1508-1510
-
-
Nicchia, G.P.1
Frigeri, A.2
Liuzzi, G.M.3
Svelto, M.4
-
17
-
-
65949090748
-
Genomewide association studies of stroke
-
Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, et al. Genomewide association studies of stroke. N Engl J Med 2009;360:1718-1728.
-
(2009)
N Engl J Med
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
Seshadri, S.2
Bis, J.C.3
Fornage, M.4
DeStefano, A.L.5
Aulchenko, Y.S.6
-
18
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14, 000 cases of seven common diseases and 3000 shared controls. Nature 2007;447:661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
19
-
-
34147144860
-
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease
-
Wang L, Hauser ER, Shah SH, Pericak-Vance MA, Haynes C, Crosslin D, et al. Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease. Am J Hum Genet 2007;80:650-663.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 650-663
-
-
Wang, L.1
Hauser, E.R.2
Shah, S.H.3
Pericak-Vance, M.A.4
Haynes, C.5
Crosslin, D.6
-
20
-
-
58649090901
-
Targeted epithelial tight junction dysfunction causes immune activation and contributes to development of experimental colitis
-
Su L, Shen L, Clayburgh DR, Nalle SC, Sullivan EA, Meddings JB, et al. Targeted epithelial tight junction dysfunction causes immune activation and contributes to development of experimental colitis. Gastroenterology 2009;136:551-563.
-
(2009)
Gastroenterology
, vol.136
, pp. 551-563
-
-
Su, L.1
Shen, L.2
Clayburgh, D.R.3
Nalle, S.C.4
Sullivan, E.A.5
Meddings, J.B.6
-
21
-
-
42649086167
-
Genetic polymorphisms and human aging: Association studies deliver
-
Melzer D. Genetic polymorphisms and human aging: Association studies deliver. Rejuvenation Res 2008;11:523-526.
-
(2008)
Rejuvenation Res
, vol.11
, pp. 523-526
-
-
Melzer, D.1
-
22
-
-
44449176689
-
Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21
-
Matarin M, Brown WM, Singleton A, Hardy JA, Meschia JF. Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21. Stroke 2008;39:1586-1589.
-
(2008)
Stroke
, vol.39
, pp. 1586-1589
-
-
Matarin, M.1
Brown, W.M.2
Singleton, A.3
Hardy, J.A.4
Meschia, J.F.5
-
23
-
-
34548153747
-
How stem cells age and why this makes us grow old
-
Sharpless NE, DePinho RA. How stem cells age and why this makes us grow old. Nat Rev Mol Cell Biol 2007;18:703-713.
-
(2007)
Nat Rev Mol Cell Biol
, vol.18
, pp. 703-713
-
-
Sharpless, N.E.1
DePinho, R.A.2
-
24
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, et al. Genomewide association analysis of coronary artery disease. N Engl J Med 2007;357(5):443-453.
-
(2007)
N Engl J Med
, vol.357
, Issue.5
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
-
25
-
-
66249120705
-
The impact of newly identified loci on coronary heart disease, stroke, and total mortality in the MORGAM prospective cohorts
-
Karvanen J, Silander K, Kee F, Tiret L, Salomaa V, Kuulasmaa K, et al. The impact of newly identified loci on coronary heart disease, stroke, and total mortality in the MORGAM prospective cohorts. Genet Epidemiol 2009;33(3):237-246.
-
(2009)
Genet Epidemiol
, vol.33
, Issue.3
, pp. 237-246
-
-
Karvanen, J.1
Silander, K.2
Kee, F.3
Tiret, L.4
Salomaa, V.5
Kuulasmaa, K.6
-
26
-
-
80051800851
-
Association between two key SNPs on chromosome 12p13 and ischemic stroke in Chinese Han population
-
Tong Y, Zhang Y, Zhang R, Geng Y, Lin L, Wang Z, et al. Association between two key SNPs on chromosome 12p13 and ischemic stroke in Chinese Han population. Pharmacogenet Genomics 2011;21(9):572-578.
-
(2011)
Pharmacogenet Genomics
, vol.21
, Issue.9
, pp. 572-578
-
-
Tong, Y.1
Zhang, Y.2
Zhang, R.3
Geng, Y.4
Lin, L.5
Wang, Z.6
-
27
-
-
77954972947
-
Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population
-
Matsushita T, Umeno J, Hirakawa Y, Yonemoto K, Ashikawa K, Amitani H, et al. Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population. J Hum Genet 2010;55(7):473-476.
-
(2010)
J Hum Genet
, vol.55
, Issue.7
, pp. 473-476
-
-
Matsushita, T.1
Umeno, J.2
Hirakawa, Y.3
Yonemoto, K.4
Ashikawa, K.5
Amitani, H.6
-
28
-
-
77958517452
-
No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic stroke
-
Lotta LA, Giusti B, Saracini C, Vestrini A, Volpe M, Rubattu S, et al. No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic stroke. J Thromb Haemost 2010;8(8):1858-1860.
-
(2010)
J Thromb Haemost
, vol.8
, Issue.8
, pp. 1858-1860
-
-
Lotta, L.A.1
Giusti, B.2
Saracini, C.3
Vestrini, A.4
Volpe, M.5
Rubattu, S.6
-
29
-
-
79451468882
-
Genetic variant on chromosome 12p13 does not show association to ischemic stroke in 3 Swedish case-control studies
-
Olsson S, Melander O, Jood K, Smith JG, Lövkvist H, Sjögren M, et al. Genetic variant on chromosome 12p13 does not show association to ischemic stroke in 3 Swedish case-control studies. Stroke 2011;42(1):214-216.
-
(2011)
Stroke
, vol.42
, Issue.1
, pp. 214-216
-
-
Olsson, S.1
Melander, O.2
Jood, K.3
Smith, J.G.4
Lövkvist, H.5
Sjögren, M.6
-
30
-
-
79957988152
-
No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population
-
Ding H, Tu X, Xu Y, Xu C, Wang X, Cui G, Bao X, et al. No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population. Atherosclerosis 2011;216(2):381-3812.
-
(2011)
Atherosclerosis
, vol.216
, Issue.2
, pp. 381-3812
-
-
Ding, H.1
Tu, X.2
Xu, Y.3
Xu, C.4
Wang, X.5
Cui, G.6
Bao, X.7
-
31
-
-
77951427974
-
Failure to validate association between 12p13 variants and ischemic stroke
-
International Stroke Genetics Consortium; Wellcome Trust Case-Control Consortium 2.
-
International Stroke Genetics Consortium; Wellcome Trust Case-Control Consortium 2. Failure to validate association between 12p13 variants and ischemic stroke. N Engl J Med 2010;362(16):1547-1550.
-
(2010)
N Engl J Med
, vol.362
, Issue.16
, pp. 1547-1550
-
-
-
33
-
-
60849084449
-
Polymorphic mature microRNAs from passenger strand of pre-miR146a contribute to thyroid cancer
-
Jazdzewski K, Liyanarachchi S, Swierniak M, Pachucki J, Ringel MD, Jarzab B, et al. Polymorphic mature microRNAs from passenger strand of pre-miR146a contribute to thyroid cancer. Proc Natl Acad Sci USA 2009;106(5):1502-1505.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.5
, pp. 1502-1505
-
-
Jazdzewski, K.1
Liyanarachchi, S.2
Swierniak, M.3
Pachucki, J.4
Ringel, M.D.5
Jarzab, B.6
-
34
-
-
70350102890
-
Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk
-
Cui R, Kamatani Y, Takahashi A, Usami M, Hosono N, Kawaguchi T, et al. Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. Gastroenterology 2009;137(5):1768-1775.
-
(2009)
Gastroenterology
, vol.137
, Issue.5
, pp. 1768-1775
-
-
Cui, R.1
Kamatani, Y.2
Takahashi, A.3
Usami, M.4
Hosono, N.5
Kawaguchi, T.6
-
35
-
-
80053198167
-
From hypertension to stroke: Mechanisms and potential prevention strategies
-
Yu JG, Zhou RR, Cai GJ. From hypertension to stroke: Mechanisms and potential prevention strategies. CNS Neurosci Ther 2011;17(5):577-84.
-
(2011)
CNS Neurosci Ther
, vol.17
, Issue.5
, pp. 577-584
-
-
Yu, J.G.1
Zhou, R.R.2
Cai, G.J.3
|