-
1
-
-
0035929575
-
Deaths: Final data for 1999.
-
Hoyert DL, Arias E, Smith BL, Murphy SL, Kochanek KD, Deaths: final data for 1999. Natl Vital Stat Rep 2001 49 1 113
-
(2001)
Natl Vital Stat Rep
, vol.49
, pp. 1-113
-
-
Hoyert, D.L.1
Arias, E.2
Smith, B.L.3
Murphy, S.L.4
Kochanek, K.D.5
-
2
-
-
84875452770
-
Diseases of the thoracic aorta in women.
-
Huynh TT, Starr JE, Diseases of the thoracic aorta in women. J Vasc Surg 2013 57 11S 17S. doi: 10.1016/j.jvs.2012.08.126
-
(2013)
J Vasc Surg
, vol.57
, pp. 11S-17S
-
-
Huynh, T.T.1
Starr, J.E.2
-
3
-
-
70349956433
-
Finding the missing heritability of complex diseases.
-
doi: 10.1038/nature08494
-
Manolio TA, Collins FS, Cox NJ, Finding the missing heritability of complex diseases. Nature 2009 461 747 753. doi: 10.1038/nature08494
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
4
-
-
84928209346
-
Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
-
Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL, ACMG Laboratory Quality Assurance Committee Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015 17 405 424. doi: 10.1038/gim.2015.30
-
(2015)
Genet Med
, vol.17
, pp. 405-424
-
-
Richards, S.1
Aziz, N.2
Bale, S.3
Bick, D.4
Das, S.5
Gastier-Foster, J.6
Grody, W.W.7
Hegde, M.8
Lyon, E.9
Spector, E.10
Voelkerding, K.11
Rehm, H.L.12
-
5
-
-
84876286561
-
Histological features of carotid plaque in patients with ocular ischemia versus cerebral events.
-
Howard DP, van Lammeren GW, Redgrave JN, Moll FL, de Vries JP, de Kleijn DP, de Borst GJ, Pasterkamp G, Rothwell PM, Histological features of carotid plaque in patients with ocular ischemia versus cerebral events. Stroke 2013 44 734 739. doi: 10.1161/STROKEAHA.112.678672
-
(2013)
Stroke
, vol.44
, pp. 734-739
-
-
Howard, D.P.1
Van Lammeren, G.W.2
Redgrave, J.N.3
Moll, F.L.4
De Vries, J.P.5
De Kleijn, D.P.6
De Borst, G.J.7
Pasterkamp, G.8
Rothwell, P.M.9
-
6
-
-
80052361779
-
Susceptibility to acute thoracic aortic dissections in patients dying outside the hospital: An autopsy study.
-
Prakash SK, Haden-Pinneri K, Milewicz DM, Susceptibility to acute thoracic aortic dissections in patients dying outside the hospital: an autopsy study. Am Heart J 2011 162 474 479. doi: 10.1016/j.ahj.2011.06.020
-
(2011)
Am Heart J
, vol.162
, pp. 474-479
-
-
Prakash, S.K.1
Haden-Pinneri, K.2
Milewicz, D.M.3
-
7
-
-
0028876793
-
Marfan syndrome. Long-term survival and complications after aortic aneurysm repair.
-
Finkbohner R, Johnston D, Crawford ES, Coselli J, Milewicz DM, Marfan syndrome. Long-term survival and complications after aortic aneurysm repair. Circulation 1995 91 728 733
-
(1995)
Circulation
, vol.91
, pp. 728-733
-
-
Finkbohner, R.1
Johnston, D.2
Crawford, E.S.3
Coselli, J.4
Milewicz, D.M.5
-
8
-
-
0028854314
-
Life expectancy in the Marfan syndrome.
-
Silverman DI, Burton KJ, Gray J, Bosner MS, Kouchoukos NT, Roman MJ, Boxer M, Devereux RB, Tsipouras P, Life expectancy in the Marfan syndrome. Am J Cardiol 1995 75 157 160
-
(1995)
Am J Cardiol
, vol.75
, pp. 157-160
-
-
Silverman, D.I.1
Burton, K.J.2
Gray, J.3
Bosner, M.S.4
Kouchoukos, N.T.5
Roman, M.J.6
Boxer, M.7
Devereux, R.B.8
Tsipouras, P.9
-
9
-
-
77950185458
-
2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine.
-
Hiratzka LF, Bakris GL, Beckman JA, American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines; American Association for Thoracic Surgery; American College of Radiology; American Stroke Association; Society of Cardiovascular Anesthesiologists; Society for Cardiovascular Angiography and Interventions; Society of Interventional Radiology; Society of Thoracic Surgeons; Society for Vascular Medicine 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine. J Am Coll Cardiol 2010 55 e27 e129. doi: 10.1016/j.jacc.2010.02.015
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. e27-e129
-
-
Hiratzka, L.F.1
Bakris, G.L.2
Beckman, J.A.3
-
10
-
-
34548385845
-
Aortic diameter >or = 5.5 cm is not a good predictor of type A aortic dissection: Observations from the International Registry of Acute Aortic Dissection (IRAD).
-
Pape LA, Tsai TT, Isselbacher EM, Oh JK, O'gara PT, Evangelista A, Fattori R, Meinhardt G, Trimarchi S, Bossone E, Suzuki T, Cooper JV, Froehlich JB, Nienaber CA, Eagle KA, International Registry of Acute Aortic Dissection (IRAD) Investigators Aortic diameter >or = 5.5 cm is not a good predictor of type A aortic dissection: observations from the International Registry of Acute Aortic Dissection (IRAD). Circulation 2007 116 1120 1127. doi: 10.1161/CIRCULATIONAHA.107.702720
-
(2007)
Circulation
, vol.116
, pp. 1120-1127
-
-
Pape, L.A.1
Tsai, T.T.2
Isselbacher, E.M.3
Oh, J.K.4
O'Gara, P.T.5
Evangelista, A.6
Fattori, R.7
Meinhardt, G.8
Trimarchi, S.9
Bossone, E.10
Suzuki, T.11
Cooper, J.V.12
Froehlich, J.B.13
Nienaber, C.A.14
Eagle, K.A.15
-
11
-
-
85007271243
-
International registry of patients carrying TGFBR1 or TGFBR2 mutations: Results of the MAC (Montalcino Aortic Consortium).
-
Jondeau G, Ropers J, Regalado E, Montalcino Aortic Consortium International registry of patients carrying TGFBR1 or TGFBR2 mutations: results of the MAC (Montalcino Aortic Consortium). Circ Cardiovasc Genet 2016 9 548 558. doi: 10.1161/CIRCGENETICS.116.001485
-
(2016)
Circ Cardiovasc Genet
, vol.9
, pp. 548-558
-
-
Jondeau, G.1
Ropers, J.2
Regalado, E.3
-
12
-
-
84936947295
-
Aortic disease presentation and outcome associated with ACTA2 mutations.
-
Regalado ES, Guo DC, Prakash S, Montalcino Aortic Consortium Aortic disease presentation and outcome associated with ACTA2 mutations. Circ Cardiovasc Genet 2015 8 457 464. doi: 10.1161/CIRCGENETICS.114.000943
-
(2015)
Circ Cardiovasc Genet
, vol.8
, pp. 457-464
-
-
Regalado, E.S.1
Guo, D.C.2
Prakash, S.3
-
13
-
-
78649294102
-
Treatment guidelines for thoracic aortic aneurysms and dissections based on the underlying causative gene.
-
discussion S45
-
Milewicz DM, Regalado ES, Guo DC, Treatment guidelines for thoracic aortic aneurysms and dissections based on the underlying causative gene. J Thorac Cardiovasc Surg 2010 140 S2 S4; discussion S45. doi: 10.1016/j.jtcvs.2010.07.027
-
(2010)
J Thorac Cardiovasc Surg
, vol.140
, pp. S2-S4
-
-
Milewicz, D.M.1
Regalado, E.S.2
Guo, D.C.3
-
14
-
-
0025886783
-
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.
-
doi: 10.1038/352337a0
-
Dietz HC, Cutting GR, Pyeritz RE, Maslen CL, Sakai LY, Corson GM, Puffenberger EG, Hamosh A, Nanthakumar EJ, Curristin SM, Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 1991 352 337 339. doi: 10.1038/352337a0
-
(1991)
Nature
, vol.352
, pp. 337-339
-
-
Dietz, H.C.1
Cutting, G.R.2
Pyeritz, R.E.3
Maslen, C.L.4
Sakai, L.Y.5
Corson, G.M.6
Puffenberger, E.G.7
Hamosh, A.8
Nanthakumar, E.J.9
Curristin, S.M.10
-
15
-
-
33747812887
-
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
-
doi: 10.1056/NEJMoa055695
-
Loeys BL, Schwarze U, Holm T, Aneurysm syndromes caused by mutations in the TGF-beta receptor. N Engl J Med 2006 355 788 798. doi: 10.1056/NEJMoa055695
-
(2006)
N Engl J Med
, vol.355
, pp. 788-798
-
-
Loeys, B.L.1
Schwarze, U.2
Holm, T.3
-
16
-
-
3543013177
-
Heterozygous TGFBR2 mutations in Marfan syndrome.
-
doi: 10.1038/ng1392
-
Mizuguchi T, Collod-Beroud G, Akiyama T, Heterozygous TGFBR2 mutations in Marfan syndrome. Nat Genet 2004 36 855 860. doi: 10.1038/ng1392
-
(2004)
Nat Genet
, vol.36
, pp. 855-860
-
-
Mizuguchi, T.1
Collod-Beroud, G.2
Akiyama, T.3
-
17
-
-
33748752789
-
Familial thoracic aortic aneurysms and dissections-incidence, modes of inheritance, and phenotypic patterns.
-
Albornoz G, Coady MA, Roberts M, Davies RR, Tranquilli M, Rizzo JA, Elefteriades JA, Familial thoracic aortic aneurysms and dissections-incidence, modes of inheritance, and phenotypic patterns. Ann Thorac Surg 2006 82 1400 1405. doi: 10.1016/j.athoracsur.2006.04.098
-
(2006)
Ann Thorac Surg
, vol.82
, pp. 1400-1405
-
-
Albornoz, G.1
Coady, M.A.2
Roberts, M.3
Davies, R.R.4
Tranquilli, M.5
Rizzo, J.A.6
Elefteriades, J.A.7
-
18
-
-
0030946538
-
Familial thoracic aortic dilatations and dissections: A case control study.
-
Biddinger A, Rocklin M, Coselli J, Milewicz DM, Familial thoracic aortic dilatations and dissections: a case control study. J Vasc Surg 1997 25 506 511
-
(1997)
J Vasc Surg
, vol.25
, pp. 506-511
-
-
Biddinger, A.1
Rocklin, M.2
Coselli, J.3
Milewicz, D.M.4
-
19
-
-
0031823564
-
Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections.
-
Milewicz DM, Chen H, Park ES, Petty EM, Zaghi H, Shashidhar G, Willing M, Patel V, Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections. Am J Cardiol 1998 82 474 479
-
(1998)
Am J Cardiol
, vol.82
, pp. 474-479
-
-
Milewicz, D.M.1
Chen, H.2
Park, E.S.3
Petty, E.M.4
Zaghi, H.5
Shashidhar, G.6
Willing, M.7
Patel, V.8
-
20
-
-
85050346506
-
Evaluation of the clinical validity of genes for heritable thoracic aortic aneurysm and dissections: Application of the clinical genome resource framework.
-
Renard M, Francis CA, Ghosh R, Evaluation of the clinical validity of genes for heritable thoracic aortic aneurysm and dissections: Application of the clinical genome resource framework. J Am Coll Cardiol 2018 72 605 615
-
(2018)
J Am Coll Cardiol
, vol.72
, pp. 605-615
-
-
Renard, M.1
Francis, C.A.2
Ghosh, R.3
-
21
-
-
84864411184
-
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.
-
Boileau C, Guo DC, Hanna N, National Heart, Lung, and Blood Institute (NHLBI) Go Exome Sequencing Project TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome. Nat Genet 2012 44 916 921. doi: 10.1038/ng.2348
-
(2012)
Nat Genet
, vol.44
, pp. 916-921
-
-
Boileau, C.1
Guo, D.C.2
Hanna, N.3
-
22
-
-
0019436388
-
Altered secretion of type III procollagen in a form of type IV Ehlers-Danlos syndrome. Biochemical studies in cultured fibroblasts.
-
Byers PH, Holbrook KA, Barsh GS, Smith LT, Bornstein P, Altered secretion of type III procollagen in a form of type IV Ehlers-Danlos syndrome. Biochemical studies in cultured fibroblasts. Lab Invest 1981 44 336 341
-
(1981)
Lab Invest
, vol.44
, pp. 336-341
-
-
Byers, P.H.1
Holbrook, K.A.2
Barsh, G.S.3
Smith, L.T.4
Bornstein, P.5
-
23
-
-
36549071997
-
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
-
Guo DC, Pannu H, Tran-Fadulu V, Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. Nat Genet 2007 39 1488 1493. doi: 10.1038/ng.2007.6
-
(2007)
Nat Genet
, vol.39
, pp. 1488-1493
-
-
Guo, D.C.1
Pannu, H.2
Tran-Fadulu, V.3
-
24
-
-
84881662678
-
Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.
-
Guo DC, Regalado E, Casteel DE, GenTAC Registry Consortium; National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections. Am J Hum Genet 2013 93 398 404. doi: 10.1016/j.ajhg.2013.06.019
-
(2013)
Am J Hum Genet
, vol.93
, pp. 398-404
-
-
Guo, D.C.1
Regalado, E.2
Casteel, D.E.3
-
25
-
-
84954424738
-
LOX mutations predispose to thoracic aortic aneurysms and dissections.
-
Guo DC, Regalado ES, Gong L, University of Washington Center for Mendelian Genomics LOX mutations predispose to thoracic aortic aneurysms and dissections. Circ Res 2016 118 928 934. doi: 10.1161/CIRCRESAHA.115.307130
-
(2016)
Circ Res
, vol.118
, pp. 928-934
-
-
Guo, D.C.1
Regalado, E.S.2
Gong, L.3
-
26
-
-
80052584397
-
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.
-
Regalado ES, Guo DC, Villamizar C, Avidan N, Gilchrist D, McGillivray B, Clarke L, Bernier F, Santos-Cortez RL, Leal SM, Bertoli-Avella AM, Shendure J, Rieder MJ, Nickerson DA, Milewicz DM, NHLBI GO Exome Sequencing Project Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms. Circ Res 2011 109 680 686. doi: 10.1161/CIRCRESAHA.111.248161
-
(2011)
Circ Res
, vol.109
, pp. 680-686
-
-
Regalado, E.S.1
Guo, D.C.2
Villamizar, C.3
Avidan, N.4
Gilchrist, D.5
McGillivray, B.6
Clarke, L.7
Bernier, F.8
Santos-Cortez, R.L.9
Leal, S.M.10
Bertoli-Avella, A.M.11
Shendure, J.12
Rieder, M.J.13
Nickerson, D.A.14
Milewicz, D.M.15
-
27
-
-
79251602475
-
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis.
-
van de Laar IM, Oldenburg RA, Pals G, Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis. Nat Genet 2011 43 121 126
-
(2011)
Nat Genet
, vol.43
, pp. 121-126
-
-
Van De Laar, I.M.1
Oldenburg, R.A.2
Pals, G.3
-
28
-
-
78249244459
-
Mutations in myosin light chain kinase cause familial aortic dissections.
-
Wang L, Guo DC, Cao J, Gong L, Kamm KE, Regalado E, Li L, Shete S, He WQ, Zhu MS, Offermanns S, Gilchrist D, Elefteriades J, Stull JT, Milewicz DM, Mutations in myosin light chain kinase cause familial aortic dissections. Am J Hum Genet 2010 87 701 707. doi: 10.1016/j.ajhg.2010.10.006
-
(2010)
Am J Hum Genet
, vol.87
, pp. 701-707
-
-
Wang, L.1
Guo, D.C.2
Cao, J.3
Gong, L.4
Kamm, K.E.5
Regalado, E.6
Li, L.7
Shete, S.8
He, W.Q.9
Zhu, M.S.10
Offermanns, S.11
Gilchrist, D.12
Elefteriades, J.13
Stull, J.T.14
Milewicz, D.M.15
-
29
-
-
33644627494
-
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus.
-
doi: 10.1038/ng1721
-
Zhu L, Vranckx R, Khau Van Kien P, Lalande A, Boisset N, Mathieu F, Wegman M, Glancy L, Gasc JM, Brunotte F, Bruneval P, Wolf JE, Michel JB, Jeunemaitre X, Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus. Nat Genet 2006 38 343 349. doi: 10.1038/ng1721
-
(2006)
Nat Genet
, vol.38
, pp. 343-349
-
-
Zhu, L.1
Vranckx, R.2
Khau Van Kien, P.3
Lalande, A.4
Boisset, N.5
Mathieu, F.6
Wegman, M.7
Glancy, L.8
Gasc, J.M.9
Brunotte, F.10
Bruneval, P.11
Wolf, J.E.12
Michel, J.B.13
Jeunemaitre, X.14
-
30
-
-
65149088429
-
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
-
Guo DC, Papke CL, Tran-Fadulu V, Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. Am J Hum Genet 2009 84 617 627. doi: 10.1016/j.ajhg.2009.04.007
-
(2009)
Am J Hum Genet
, vol.84
, pp. 617-627
-
-
Guo, D.C.1
Papke, C.L.2
Tran-Fadulu, V.3
-
31
-
-
0027402602
-
Smooth muscle cell to elastic lamina connections in developing mouse aorta. Role in aortic medial organization.
-
Davis EC, Smooth muscle cell to elastic lamina connections in developing mouse aorta. Role in aortic medial organization. Lab Invest 1993 68 89 99
-
(1993)
Lab Invest
, vol.68
, pp. 89-99
-
-
Davis, E.C.1
-
32
-
-
84900298561
-
Cell biology. Dysfunctional mechanosensing in aneurysms.
-
Humphrey JD, Milewicz DM, Tellides G, Schwartz MA, Cell biology. Dysfunctional mechanosensing in aneurysms. Science 2014 344 477 479. doi: 10.1126/science.1253026
-
(2014)
Science
, vol.344
, pp. 477-479
-
-
Humphrey, J.D.1
Milewicz, D.M.2
Tellides, G.3
Schwartz, M.A.4
-
33
-
-
84930211518
-
Role of mechanotransduction in vascular biology: Focus on thoracic aortic aneurysms and dissections.
-
Humphrey JD, Schwartz MA, Tellides G, Milewicz DM, Role of mechanotransduction in vascular biology: focus on thoracic aortic aneurysms and dissections. Circ Res 2015 116 1448 1461. doi: 10.1161/CIRCRESAHA.114.304936
-
(2015)
Circ Res
, vol.116
, pp. 1448-1461
-
-
Humphrey, J.D.1
Schwartz, M.A.2
Tellides, G.3
Milewicz, D.M.4
-
34
-
-
0027257818
-
Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5' end.
-
Corson GM, Chalberg SC, Dietz HC, Charbonneau NL, Sakai LY, Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5' end. Genomics 1993 17 476 484. doi: 10.1006/geno.1993.1350
-
(1993)
Genomics
, vol.17
, pp. 476-484
-
-
Corson, G.M.1
Chalberg, S.C.2
Dietz, H.C.3
Charbonneau, N.L.4
Sakai, L.Y.5
-
35
-
-
0018393854
-
The Marfan syndrome: Diagnosis and management.
-
doi: 10.1056/NEJM197904053001406
-
Pyeritz RE, McKusick VA, The Marfan syndrome: diagnosis and management. N Engl J Med 1979 300 772 777. doi: 10.1056/NEJM197904053001406
-
(1979)
N Engl J Med
, vol.300
, pp. 772-777
-
-
Pyeritz, R.E.1
McKusick, V.A.2
-
36
-
-
84991059632
-
WES/WGS reporting of mutations from cardiovascular "actionable" genes in clinical practice: A key role for UMD knowledgebases in the era of big databases.
-
Pinard A, Salgado D, Desvignes JP, Rai G, Hanna N, Arnaud P, Guien C, Martinez M, Faivre L, Jondeau G, Boileau C, Zaffran S, Béroud C, Collod-Béroud G, WES/WGS reporting of mutations from cardiovascular "Actionable" genes in clinical practice: a key role for UMD knowledgebases in the era of big databases. Hum Mutat 2016 37 1308 1317. doi: 10.1002/humu.23119
-
(2016)
Hum Mutat
, vol.37
, pp. 1308-1317
-
-
Pinard, A.1
Salgado, D.2
Desvignes, J.P.3
Rai, G.4
Hanna, N.5
Arnaud, P.6
Guien, C.7
Martinez, M.8
Faivre, L.9
Jondeau, G.10
Boileau, C.11
Zaffran, S.12
Béroud, C.13
Collod-Béroud, G.14
-
37
-
-
52949141431
-
Genetic basis of thoracic aortic aneurysms and dissections: Focus on smooth muscle cell contractile dysfunction.
-
Milewicz DM, Guo DC, Tran-Fadulu V, Lafont AL, Papke CL, Inamoto S, Kwartler CS, Pannu H, Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunction. Annu Rev Genomics Hum Genet 2008 9 283 302. doi: 10.1146/annurev.genom.8.080706.092303
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 283-302
-
-
Milewicz, D.M.1
Guo, D.C.2
Tran-Fadulu, V.3
Lafont, A.L.4
Papke, C.L.5
Inamoto, S.6
Kwartler, C.S.7
Pannu, H.8
-
38
-
-
0028203457
-
Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders.
-
Milewicz DM, Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders. Tex Heart Inst J 1994 21 22 29
-
(1994)
Tex Heart Inst J
, vol.21
, pp. 22-29
-
-
Milewicz, D.M.1
-
39
-
-
0025335330
-
Immunohistologic abnormalities of the microfibrillar-fiber system in the Marfan syndrome.
-
doi: 10.1056/NEJM199007193230303
-
Hollister DW, Godfrey M, Sakai LY, Pyeritz RE, Immunohistologic abnormalities of the microfibrillar-fiber system in the Marfan syndrome. N Engl J Med 1990 323 152 159. doi: 10.1056/NEJM199007193230303
-
(1990)
N Engl J Med
, vol.323
, pp. 152-159
-
-
Hollister, D.W.1
Godfrey, M.2
Sakai, L.Y.3
Pyeritz, R.E.4
-
40
-
-
0026585419
-
Marfan syndrome: Defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts.
-
doi: 10.1172/JCI115589
-
Milewicz DM, Pyeritz RE, Crawford ES, Byers PH, Marfan syndrome: defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts. J Clin Invest 1992 89 79 86. doi: 10.1172/JCI115589
-
(1992)
J Clin Invest
, vol.89
, pp. 79-86
-
-
Milewicz, D.M.1
Pyeritz, R.E.2
Crawford, E.S.3
Byers, P.H.4
-
41
-
-
0027035013
-
Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domains.
-
Dietz HC, Saraiva JM, Pyeritz RE, Cutting GR, Francomano CA, Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domains. Hum Mutat 1992 1 366 374. doi: 10.1002/humu.1380010504
-
(1992)
Hum Mutat
, vol.1
, pp. 366-374
-
-
Dietz, H.C.1
Saraiva, J.M.2
Pyeritz, R.E.3
Cutting, G.R.4
Francomano, C.A.5
-
43
-
-
10944263184
-
Structural consequences of cysteine substitutions C1977Y and C1977R in calcium-binding epidermal growth factor-like domain 30 of human fibrillin-1.
-
doi: 10.1074/jbc.M408156200
-
Suk JY, Jensen S, McGettrick A, Willis AC, Whiteman P, Redfield C, Handford PA, Structural consequences of cysteine substitutions C1977Y and C1977R in calcium-binding epidermal growth factor-like domain 30 of human fibrillin-1. J Biol Chem 2004 279 51258 51265. doi: 10.1074/jbc.M408156200
-
(2004)
J Biol Chem
, vol.279
, pp. 51258-51265
-
-
Suk, J.Y.1
Jensen, S.2
McGettrick, A.3
Willis, A.C.4
Whiteman, P.5
Redfield, C.6
Handford, P.A.7
-
44
-
-
50549084575
-
Transforming growth factor-beta signaling in thoracic aortic aneurysm development: A paradox in pathogenesis.
-
doi: 10.1159/000151766
-
Jones JA, Spinale FG, Ikonomidis JS, Transforming growth factor-beta signaling in thoracic aortic aneurysm development: a paradox in pathogenesis. J Vasc Res 2009 46 119 137. doi: 10.1159/000151766
-
(2009)
J Vasc Res
, vol.46
, pp. 119-137
-
-
Jones, J.A.1
Spinale, F.G.2
Ikonomidis, J.S.3
-
46
-
-
0035910615
-
Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome.
-
Bunton TE, Biery NJ, Myers L, Gayraud B, Ramirez F, Dietz HC, Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome. Circ Res 2001 88 37 43
-
(2001)
Circ Res
, vol.88
, pp. 37-43
-
-
Bunton, T.E.1
Biery, N.J.2
Myers, L.3
Gayraud, B.4
Ramirez, F.5
Dietz, H.C.6
-
47
-
-
84982705733
-
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans.
-
Lee VS, Halabi CM, Hoffman EP, Carmichael N, Leshchiner I, Lian CG, Bierhals AJ, Vuzman D, Mecham RP, Frank NY, Stitziel NO, Brigham Genomic Medicine Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans. Proc Natl Acad Sci USA 2016 113 8759 8764. doi: 10.1073/pnas.1601442113
-
(2016)
Proc Natl Acad Sci USA
, vol.113
, pp. 8759-8764
-
-
Lee, V.S.1
Halabi, C.M.2
Hoffman, E.P.3
Carmichael, N.4
Leshchiner, I.5
Lian, C.G.6
Bierhals, A.J.7
Vuzman, D.8
Mecham, R.P.9
Frank, N.Y.10
Stitziel, N.O.11
-
48
-
-
41549090795
-
Connective tissue disorders in dissections of the carotid or vertebral arteries.
-
Gdynia HJ, Kühnlein P, Ludolph AC, Huber R, Connective tissue disorders in dissections of the carotid or vertebral arteries. J Clin Neurosci 2008 15 489 494. doi: 10.1016/j.jocn.2007.10.001
-
(2008)
J Clin Neurosci
, vol.15
, pp. 489-494
-
-
Gdynia, H.J.1
Kühnlein, P.2
Ludolph, A.C.3
Huber, R.4
-
49
-
-
85044932875
-
LTBP3 pathogenic variants predispose individuals to thoracic aortic aneurysms and dissections.
-
Guo DC, Regalado ES, Pinard A, University of Washington Center for Mendelian Genomics LTBP3 pathogenic variants predispose individuals to thoracic aortic aneurysms and dissections. Am J Hum Genet 2018 102 706 712. doi: 10.1016/j.ajhg.2018.03.002
-
(2018)
Am J Hum Genet
, vol.102
, pp. 706-712
-
-
Guo, D.C.1
Regalado, E.S.2
Pinard, A.3
-
50
-
-
84943664666
-
Latent TGF-β-binding proteins.
-
Robertson IB, Horiguchi M, Zilberberg L, Dabovic B, Hadjiolova K, Rifkin DB, Latent TGF-β-binding proteins. Matrix Biol 2015 47 44 53. doi: 10.1016/j.matbio.2015.05.005
-
(2015)
Matrix Biol
, vol.47
, pp. 44-53
-
-
Robertson, I.B.1
Horiguchi, M.2
Zilberberg, L.3
Dabovic, B.4
Hadjiolova, K.5
Rifkin, D.B.6
-
51
-
-
0037165615
-
Latent TGF-beta binding protein-3 (LTBP-3) requires binding to TGF-beta for secretion.
-
Chen Y, Dabovic B, Annes JP, Rifkin DB, Latent TGF-beta binding protein-3 (LTBP-3) requires binding to TGF-beta for secretion. FEBS Lett 2002 517 277 280
-
(2002)
FEBS Lett
, vol.517
, pp. 277-280
-
-
Chen, Y.1
Dabovic, B.2
Annes, J.P.3
Rifkin, D.B.4
-
52
-
-
84865408942
-
Specificity of latent TGF-β binding protein (LTBP) incorporation into matrix: Role of fibrillins and fibronectin.
-
Zilberberg L, Todorovic V, Dabovic B, Horiguchi M, Couroussé T, Sakai LY, Rifkin DB, Specificity of latent TGF-β binding protein (LTBP) incorporation into matrix: role of fibrillins and fibronectin. J Cell Physiol 2012 227 3828 3836. doi: 10.1002/jcp.24094
-
(2012)
J Cell Physiol
, vol.227
, pp. 3828-3836
-
-
Zilberberg, L.1
Todorovic, V.2
Dabovic, B.3
Horiguchi, M.4
Couroussé, T.5
Sakai, L.Y.6
Rifkin, D.B.7
-
53
-
-
84919695467
-
MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.
-
Barbier M, Gross MS, Aubart M, MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections. Am J Hum Genet 2014 95 736 743. doi: 10.1016/j.ajhg.2014.10.018
-
(2014)
Am J Hum Genet
, vol.95
, pp. 736-743
-
-
Barbier, M.1
Gross, M.S.2
Aubart, M.3
-
54
-
-
84954367131
-
Diagnostic exome sequencing identifies a novel gene, EMILIN1, associated with autosomal-dominant hereditary connective tissue disease.
-
Capuano A, Bucciotti F, Farwell KD, Tippin Davis B, Mroske C, Hulick PJ, Weissman SM, Gao Q, Spessotto P, Colombatti A, Doliana R, Diagnostic exome sequencing identifies a novel gene, EMILIN1, associated with autosomal-dominant hereditary connective tissue disease. Hum Mutat 2016 37 84 97. doi: 10.1002/humu.22920
-
(2016)
Hum Mutat
, vol.37
, pp. 84-97
-
-
Capuano, A.1
Bucciotti, F.2
Farwell, K.D.3
Tippin Davis, B.4
Mroske, C.5
Hulick, P.J.6
Weissman, S.M.7
Gao, Q.8
Spessotto, P.9
Colombatti, A.10
Doliana, R.11
-
55
-
-
33645125433
-
Aortic aneurysmal disease and cutis laxa caused by defects in the elastin gene.
-
Szabo Z, Crepeau MW, Mitchell AL, Stephan MJ, Puntel RA, Yin Loke K, Kirk RC, Urban Z, Aortic aneurysmal disease and cutis laxa caused by defects in the elastin gene. J Med Genet 2006 43 255 258. doi: 10.1136/jmg.2005.034157
-
(2006)
J Med Genet
, vol.43
, pp. 255-258
-
-
Szabo, Z.1
Crepeau, M.W.2
Mitchell, A.L.3
Stephan, M.J.4
Puntel, R.A.5
Yin Loke, K.6
Kirk, R.C.7
Urban, Z.8
-
56
-
-
84861197972
-
Recessively inherited severe aortic aneurysm caused by mutated EFEMP2.
-
Al-Hassnan ZN, Almesned AR, Tulbah S, Hakami A, Al-Omrani A, Al Sehly A, Mohammed S, Majid S, Meyer B, Al-Fayyadh M, Recessively inherited severe aortic aneurysm caused by mutated EFEMP2. Am J Cardiol 2012 109 1677 1680. doi: 10.1016/j.amjcard.2012.01.394
-
(2012)
Am J Cardiol
, vol.109
, pp. 1677-1680
-
-
Al-Hassnan, Z.N.1
Almesned, A.R.2
Tulbah, S.3
Hakami, A.4
Al-Omrani, A.5
Al Sehly, A.6
Mohammed, S.7
Majid, S.8
Meyer, B.9
Al-Fayyadh, M.10
-
57
-
-
84992472531
-
Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxa.
-
Sasaki T, Hanisch FG, Deutzmann R, Sakai LY, Sakuma T, Miyamoto T, Yamamoto T, Hannappel E, Chu ML, Lanig H, von der Mark K, Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxa. Matrix Biol 2016 56 132 149. doi: 10.1016/j.matbio.2016.06.003
-
(2016)
Matrix Biol
, vol.56
, pp. 132-149
-
-
Sasaki, T.1
Hanisch, F.G.2
Deutzmann, R.3
Sakai, L.Y.4
Sakuma, T.5
Miyamoto, T.6
Yamamoto, T.7
Hannappel, E.8
Chu, M.L.9
Lanig, H.10
Von Der Mark, K.11
-
58
-
-
85041291286
-
Ascending aortic aneurysm in a child with fibulin-4 deficiency.
-
Hibino M, Sakai Y, Kato W, Tanaka K, Tajima K, Yokoyama T, Iwasa M, Morisaki H, Tsuzuki T, Usui A, Ascending aortic aneurysm in a child with fibulin-4 deficiency. Ann Thorac Surg 2018 105 e59 e61. doi: 10.1016/j.athoracsur.2017.08.041
-
(2018)
Ann Thorac Surg
, vol.105
, pp. e59-e61
-
-
Hibino, M.1
Sakai, Y.2
Kato, W.3
Tanaka, K.4
Tajima, K.5
Yokoyama, T.6
Iwasa, M.7
Morisaki, H.8
Tsuzuki, T.9
Usui, A.10
-
59
-
-
78349242484
-
De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction.
-
Milewicz DM, Østergaard JR, Ala-Kokko LM, Khan N, Grange DK, Mendoza-Londono R, Bradley TJ, Olney AH, Adès L, Maher JF, Guo D, Buja LM, Kim D, Hyland JC, Regalado ES, De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction. Am J Med Genet A 2010 152A 2437 2443. doi: 10.1002/ajmg.a.33657
-
(2010)
Am J Med Genet A
, vol.152
, pp. 2437-2443
-
-
Milewicz, D.M.1
Østergaard, J.R.2
Ala-Kokko, L.M.3
Khan, N.4
Grange, D.K.5
Mendoza-Londono, R.6
Bradley, T.J.7
Olney, A.H.8
Adès, L.9
Maher, J.F.10
Guo, D.11
Buja, L.M.12
Kim, D.13
Hyland, J.C.14
Regalado, E.S.15
-
60
-
-
84938652684
-
Vascular disease-causing mutation R258C in ACTA2 disrupts actin dynamics and interaction with myosin.
-
Lu H, Fagnant PM, Bookwalter CS, Joel P, Trybus KM, Vascular disease-causing mutation R258C in ACTA2 disrupts actin dynamics and interaction with myosin. Proc Natl Acad Sci USA 2015 112 E4168 E4177. doi: 10.1073/pnas.1507587112
-
(2015)
Proc Natl Acad Sci USA
, vol.112
, pp. E4168-E4177
-
-
Lu, H.1
Fagnant, P.M.2
Bookwalter, C.S.3
Joel, P.4
Trybus, K.M.5
-
61
-
-
79959889715
-
Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.
-
Kuang SQ, Guo DC, Prakash SK, GenTAC Investigators Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections. PLoS Genet 2011 7 e1002118. doi: 10.1371/journal.pgen.1002118
-
(2011)
PLoS Genet
, vol.7
, pp. e1002118
-
-
Kuang, S.Q.1
Guo, D.C.2
Prakash, S.K.3
-
62
-
-
85043767070
-
Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: Delineation of the clinical phenotype.
-
doi: 10.1186/s13023-018-0769-7
-
Shalata A, Mahroom M, Milewicz DM, Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype. Orphanet J Rare Dis 2018 13 41. doi: 10.1186/s13023-018-0769-7
-
(2018)
Orphanet J Rare Dis
, vol.13
, pp. 41
-
-
Shalata, A.1
Mahroom, M.2
Milewicz, D.M.3
-
63
-
-
85048728966
-
MYLK pathogenic variants aortic disease presentation, pregnancy risk, and characterization of pathogenic missense variants.
-
doi: 10.1038/s41436-018-0038-0
-
Wallace SE, Regalado ES, Gong L, MYLK pathogenic variants aortic disease presentation, pregnancy risk, and characterization of pathogenic missense variants. Genet Med 2019 21 144 151. doi: 10.1038/s41436-018-0038-0
-
(2019)
Genet Med
, vol.21
, pp. 144-151
-
-
Wallace, S.E.1
Regalado, E.S.2
Gong, L.3
-
64
-
-
0033697283
-
Smooth muscle myosin light chain kinase expression in cardiac and skeletal muscle.
-
C1656
-
Herring BP, Dixon S, Gallagher PJ, Smooth muscle myosin light chain kinase expression in cardiac and skeletal muscle. Am J Physiol Cell Physiol 2000 279 C1656 C1664. doi: 10.1152/ajpcell.2000.279.5.C1656
-
(2000)
Am J Physiol Cell Physiol
, vol.279
, pp. C1656-C1664
-
-
Herring, B.P.1
Dixon, S.2
Gallagher, P.J.3
-
65
-
-
19944432730
-
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.
-
doi: 10.1212/01.WNL.0000149512.79621.DF
-
Sheen VL, Jansen A, Chen MH, Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome. Neurology 2005 64 254 262. doi: 10.1212/01.WNL.0000149512.79621.DF
-
(2005)
Neurology
, vol.64
, pp. 254-262
-
-
Sheen, V.L.1
Jansen, A.2
Chen, M.H.3
-
66
-
-
85040725769
-
Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations.
-
Chen MH, Choudhury S, Hirata M, Khalsa S, Chang B, Walsh CA, Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations. Am J Med Genet A 2018 176 337 350. doi: 10.1002/ajmg.a.38580
-
(2018)
Am J Med Genet A
, vol.176
, pp. 337-350
-
-
Chen, M.H.1
Choudhury, S.2
Hirata, M.3
Khalsa, S.4
Chang, B.5
Walsh, C.A.6
-
67
-
-
20144367207
-
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
-
doi: 10.1038/ng1511
-
Loeys BL, Chen J, Neptune ER, A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet 2005 37 275 281. doi: 10.1038/ng1511
-
(2005)
Nat Genet
, vol.37
, pp. 275-281
-
-
Loeys, B.L.1
Chen, J.2
Neptune, E.R.3
-
68
-
-
0024593190
-
Familial aortic dissecting aneurysm.
-
Nicod P, Bloor C, Godfrey M, Hollister D, Pyeritz RE, Dittrich H, Polikar R, Peterson KL, Familial aortic dissecting aneurysm. J Am Coll Cardiol 1989 13 811 819
-
(1989)
J Am Coll Cardiol
, vol.13
, pp. 811-819
-
-
Nicod, P.1
Bloor, C.2
Godfrey, M.3
Hollister, D.4
Pyeritz, R.E.5
Dittrich, H.6
Polikar, R.7
Peterson, K.L.8
-
69
-
-
69749113581
-
Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.
-
Tran-Fadulu V, Pannu H, Kim DH, Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations. J Med Genet 2009 46 607 613. doi: 10.1136/jmg.2008.062844
-
(2009)
J Med Genet
, vol.46
, pp. 607-613
-
-
Tran-Fadulu, V.1
Pannu, H.2
Kim, D.H.3
-
70
-
-
23044438103
-
Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections.
-
Pannu H, Fadulu VT, Chang J, Lafont A, Hasham SN, Sparks E, Giampietro PF, Zaleski C, Estrera AL, Safi HJ, Shete S, Willing MC, Raman CS, Milewicz DM, Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections. Circulation 2005 112 513 520. doi: 10.1161/CIRCULATIONAHA.105.537340
-
(2005)
Circulation
, vol.112
, pp. 513-520
-
-
Pannu, H.1
Fadulu, V.T.2
Chang, J.3
Lafont, A.4
Hasham, S.N.5
Sparks, E.6
Giampietro, P.F.7
Zaleski, C.8
Estrera, A.L.9
Safi, H.J.10
Shete, S.11
Willing, M.C.12
Raman, C.S.13
Milewicz, D.M.14
-
71
-
-
78149350496
-
TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections.
-
doi: 10.1093/cvr/cvq230
-
Inamoto S, Kwartler CS, Lafont AL, TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections. Cardiovasc Res 2010 88 520 529. doi: 10.1093/cvr/cvq230
-
(2010)
Cardiovasc Res
, vol.88
, pp. 520-529
-
-
Inamoto, S.1
Kwartler, C.S.2
Lafont, A.L.3
-
72
-
-
84864415173
-
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.
-
Lindsay ME, Schepers D, Bolar NA, Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm. Nat Genet 2012 44 922 927. doi: 10.1038/ng.2349
-
(2012)
Nat Genet
, vol.44
, pp. 922-927
-
-
Lindsay, M.E.1
Schepers, D.2
Bolar, N.A.3
-
73
-
-
78649726867
-
Quantitative analysis of TGFBR2 mutations in Marfan-syndrome-related disorders suggests a correlation between phenotypic severity and Smad signaling activity.
-
Horbelt D, Guo G, Robinson PN, Knaus P, Quantitative analysis of TGFBR2 mutations in Marfan-syndrome-related disorders suggests a correlation between phenotypic severity and Smad signaling activity. J Cell Sci 2010 123 4340 4350. doi: 10.1242/jcs.074773
-
(2010)
J Cell Sci
, vol.123
, pp. 4340-4350
-
-
Horbelt, D.1
Guo, G.2
Robinson, P.N.3
Knaus, P.4
-
74
-
-
84947042087
-
SMAD2 mutations are associated with arterial aneurysms and dissections.
-
Micha D, Guo DC, Hilhorst-Hofstee Y, SMAD2 mutations are associated with arterial aneurysms and dissections. Hum Mutat 2015 36 1145 1149. doi: 10.1002/humu.22854
-
(2015)
Hum Mutat
, vol.36
, pp. 1145-1149
-
-
Micha, D.1
Guo, D.C.2
Hilhorst-Hofstee, Y.3
-
75
-
-
85043291458
-
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3.
-
Schepers D, Tortora G, Morisaki H, A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3. Hum Mutat 2018 39 621 634. doi: 10.1002/humu.23407
-
(2018)
Hum Mutat
, vol.39
, pp. 621-634
-
-
Schepers, D.1
Tortora, G.2
Morisaki, H.3
-
76
-
-
79961025097
-
Increased vertebral artery tortuosity index is associated with adverse outcomes in children and young adults with connective tissue disorders.
-
Morris SA, Orbach DB, Geva T, Singh MN, Gauvreau K, Lacro RV, Increased vertebral artery tortuosity index is associated with adverse outcomes in children and young adults with connective tissue disorders. Circulation 2011 124 388 396. doi: 10.1161/CIRCULATIONAHA.110.990549
-
(2011)
Circulation
, vol.124
, pp. 388-396
-
-
Morris, S.A.1
Orbach, D.B.2
Geva, T.3
Singh, M.N.4
Gauvreau, K.5
Lacro, R.V.6
-
77
-
-
33645672459
-
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.
-
Habashi JP, Judge DP, Holm TM, Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome. Science 2006 312 117 121. doi: 10.1126/science.1124287
-
(2006)
Science
, vol.312
, pp. 117-121
-
-
Habashi, J.P.1
Judge, D.P.2
Holm, T.M.3
-
78
-
-
84933677647
-
Dimorphic effects of transforming growth factor-β signaling during aortic aneurysm progression in mice suggest a combinatorial therapy for Marfan syndrome.
-
Cook JR, Clayton NP, Carta L, Galatioto J, Chiu E, Smaldone S, Nelson CA, Cheng SH, Wentworth BM, Ramirez F, Dimorphic effects of transforming growth factor-β signaling during aortic aneurysm progression in mice suggest a combinatorial therapy for Marfan syndrome. Arterioscler Thromb Vasc Biol 2015 35 911 917. doi: 10.1161/ATVBAHA.114.305150
-
(2015)
Arterioscler Thromb Vasc Biol
, vol.35
, pp. 911-917
-
-
Cook, J.R.1
Clayton, N.P.2
Carta, L.3
Galatioto, J.4
Chiu, E.5
Smaldone, S.6
Nelson, C.A.7
Cheng, S.H.8
Wentworth, B.M.9
Ramirez, F.10
-
79
-
-
85035789399
-
Aortopathy in a mouse model of Marfan syndrome is not mediated by altered transforming growth factor beta signaling.
-
Wei H, Hu JH, Angelov SN, Fox K, Yan J, Enstrom R, Smith A, Dichek DA, Aortopathy in a mouse model of Marfan syndrome is not mediated by altered transforming growth factor beta signaling. J Am Heart Assoc 2017 6 e004968
-
(2017)
J Am Heart Assoc
, vol.6
, pp. e004968
-
-
Wei, H.1
Hu, J.H.2
Angelov, S.N.3
Fox, K.4
Yan, J.5
Enstrom, R.6
Smith, A.7
Dichek, D.A.8
-
80
-
-
84959904216
-
FOXE3 mutations predispose to thoracic aortic aneurysms and dissections.
-
doi: 10.1172/JCI83778
-
Kuang SQ, Medina-Martinez O, Guo DC, FOXE3 mutations predispose to thoracic aortic aneurysms and dissections. J Clin Invest 2016 126 948 961. doi: 10.1172/JCI83778
-
(2016)
J Clin Invest
, vol.126
, pp. 948-961
-
-
Kuang, S.Q.1
Medina-Martinez, O.2
Guo, D.C.3
-
81
-
-
84920737567
-
MAT2A mutations predispose individuals to thoracic aortic aneurysms.
-
Guo DC, Gong L, Regalado ES, GenTAC Investigators, National Heart, Lung, and Blood Institute Go Exome Sequencing Project; Montalcino Aortic Consortium MAT2A mutations predispose individuals to thoracic aortic aneurysms. Am J Hum Genet 2015 96 170 177. doi: 10.1016/j.ajhg.2014.11.015
-
(2015)
Am J Hum Genet
, vol.96
, pp. 170-177
-
-
Guo, D.C.1
Gong, L.2
Regalado, E.S.3
-
82
-
-
84884417889
-
Pleiotropic effects of methionine adenosyltransferases deregulation as determinants of liver cancer progression and prognosis.
-
Frau M, Feo F, Pascale RM, Pleiotropic effects of methionine adenosyltransferases deregulation as determinants of liver cancer progression and prognosis. J Hepatol 2013 59 830 841. doi: 10.1016/j.jhep.2013.04.031
-
(2013)
J Hepatol
, vol.59
, pp. 830-841
-
-
Frau, M.1
Feo, F.2
Pascale, R.M.3
-
83
-
-
0034868436
-
Relevance of folate metabolism in the pathogenesis of colorectal cancer.
-
Ryan BM, Weir DG, Relevance of folate metabolism in the pathogenesis of colorectal cancer. J Lab Clin Med 2001 138 164 176. doi: 10.1067/mlc.2001.117161
-
(2001)
J Lab Clin Med
, vol.138
, pp. 164-176
-
-
Ryan, B.M.1
Weir, D.G.2
-
84
-
-
58049211966
-
Mechanotransduction at a distance: Mechanically coupling the extracellular matrix with the nucleus.
-
doi: 10.1038/nrm2594
-
Wang N, Tytell JD, Ingber DE, Mechanotransduction at a distance: mechanically coupling the extracellular matrix with the nucleus. Nat Rev Mol Cell Biol 2009 10 75 82. doi: 10.1038/nrm2594
-
(2009)
Nat Rev Mol Cell Biol
, vol.10
, pp. 75-82
-
-
Wang, N.1
Tytell, J.D.2
Ingber, D.E.3
-
85
-
-
85045537499
-
Ari-1 regulates myonuclear organization together with parkin and is associated with aortic aneurysms.
-
Tan KL, Haelterman NA, Kwartler CS, Regalado ES, Lee PT, Nagarkar-Jaiswal S, Guo DC, Duraine L, Wangler MF, Bamshad MJ, Nickerson DA, Lin G, Milewicz DM, Bellen HJ, University of Washington Center for Mendelian Genomics Ari-1 regulates myonuclear organization together with parkin and is associated with aortic aneurysms. Dev Cell 2018 45 226.e8 244.e8. doi: 10.1016/j.devcel.2018.03.020
-
(2018)
Dev Cell
, vol.45
, pp. 226e8-244e8
-
-
Tan, K.L.1
Haelterman, N.A.2
Kwartler, C.S.3
Regalado, E.S.4
Lee, P.T.5
Nagarkar-Jaiswal, S.6
Guo, D.C.7
Duraine, L.8
Wangler, M.F.9
Bamshad, M.J.10
Nickerson, D.A.11
Lin, G.12
Milewicz, D.M.13
Bellen, H.J.14
-
86
-
-
80053385386
-
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.
-
LeMaire SA, McDonald ML, Guo DC, Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1. Nat Genet 2011 43 996 1000. doi: 10.1038/ng.934
-
(2011)
Nat Genet
, vol.43
, pp. 996-1000
-
-
Lemaire, S.A.1
McDonald, M.L.2
Guo, D.C.3
-
87
-
-
85002620872
-
Genetic variants in LRP1 and ULK4 are associated with acute aortic dissections.
-
Guo DC, Grove ML, Prakash SK, GenTAC Investigators; BAVCon Investigators Genetic variants in LRP1 and ULK4 are associated with acute aortic dissections. Am J Hum Genet 2016 99 762 769. doi: 10.1016/j.ajhg.2016.06.034
-
(2016)
Am J Hum Genet
, vol.99
, pp. 762-769
-
-
Guo, D.C.1
Grove, M.L.2
Prakash, S.K.3
-
88
-
-
85033670701
-
Heritable thoracic aortic disease genes in sporadic aortic dissection.
-
Guo DC, Hostetler EM, Fan Y, Kulmacz RJ, Zhang D, Nickerson DA, Leal SM, LeMaire SA, Regalado ES, Milewicz DM, GenTAC Investigators Heritable thoracic aortic disease genes in sporadic aortic dissection. J Am Coll Cardiol 2017 70 2728 2730. doi: 10.1016/j.jacc.2017.09.1094
-
(2017)
J Am Coll Cardiol
, vol.70
, pp. 2728-2730
-
-
Guo, D.C.1
Hostetler, E.M.2
Fan, Y.3
Kulmacz, R.J.4
Zhang, D.5
Nickerson, D.A.6
Leal, S.M.7
Lemaire, S.A.8
Regalado, E.S.9
Milewicz, D.M.10
-
89
-
-
85048703358
-
Variants of unknown significance in genes associated with heritable thoracic aortic disease can be low penetrant "risk variants".
-
Kwartler CS, Gong L, Chen J, Wang S, Kulmacz R, Duan XY, Janda A, Huang J, Kamm KE, Stull JT, Guo D, Milewicz DM, Variants of unknown significance in genes associated with heritable thoracic aortic disease can be low penetrant "risk variants". Am J Hum Genet 2018 103 138 143. doi: 10.1016/j.ajhg.2018.05.012
-
(2018)
Am J Hum Genet
, vol.103
, pp. 138-143
-
-
Kwartler, C.S.1
Gong, L.2
Chen, J.3
Wang, S.4
Kulmacz, R.5
Duan, X.Y.6
Janda, A.7
Huang, J.8
Kamm, K.E.9
Stull, J.T.10
Guo, D.11
Milewicz, D.M.12
-
90
-
-
65649094104
-
In the clinic. Abdominal aortic aneurysm.
-
doi: 10.7326/0003-4819-150-9-200905050-01005
-
Lederle FA, In the clinic. Abdominal aortic aneurysm. Ann Intern Med 2009 150 ITC5 ITC1. doi: 10.7326/0003-4819-150-9-200905050-01005
-
(2009)
Ann Intern Med
, vol.150
, pp. ITC5-ITC1
-
-
Lederle, F.A.1
-
91
-
-
84893826277
-
Diabetes and abdominal aortic aneurysms.
-
De Rango P, Farchioni L, Fiorucci B, Lenti M, Diabetes and abdominal aortic aneurysms. Eur J Vasc Endovasc Surg 2014 47 243 261. doi: 10.1016/j.ejvs.2013.12.007
-
(2014)
Eur J Vasc Endovasc Surg
, vol.47
, pp. 243-261
-
-
De Rango, P.1
Farchioni, L.2
Fiorucci, B.3
Lenti, M.4
-
92
-
-
77952308573
-
Abdominal aortic aneurysms, or a relatively large diameter of non-aneurysmal aortas, increase total and cardiovascular mortality: The Tromsø study.
-
doi: 10.1093/ije/dyp320
-
Forsdahl SH, Solberg S, Singh K, Jacobsen BK, Abdominal aortic aneurysms, or a relatively large diameter of non-aneurysmal aortas, increase total and cardiovascular mortality: the Tromsø study. Int J Epidemiol 2010 39 225 232. doi: 10.1093/ije/dyp320
-
(2010)
Int J Epidemiol
, vol.39
, pp. 225-232
-
-
Forsdahl, S.H.1
Solberg, S.2
Singh, K.3
Jacobsen, B.K.4
-
93
-
-
72549087148
-
Genetic and environmental contributions to abdominal aortic aneurysm development in a twin population.
-
discussion 7
-
Wahlgren CM, Larsson E, Magnusson PK, Hultgren R, Swedenborg J, Genetic and environmental contributions to abdominal aortic aneurysm development in a twin population. J Vasc Surg 2010 51 3 7; discussion 7. doi: 10.1016/j.jvs.2009.08.036
-
(2010)
J Vasc Surg
, vol.51
, pp. 3-7
-
-
Wahlgren, C.M.1
Larsson, E.2
Magnusson, P.K.3
Hultgren, R.4
Swedenborg, J.5
-
94
-
-
0022518005
-
Familial tendency for abdominal aortic aneurysms.
-
Johansen K, Koepsell T, Familial tendency for abdominal aortic aneurysms. JAMA 1986 256 1934 1936
-
(1986)
JAMA
, vol.256
, pp. 1934-1936
-
-
Johansen, K.1
Koepsell, T.2
-
95
-
-
84979300084
-
Comparison of three targeted approaches to screening for abdominal aortic aneurysm based on cardiovascular risk.
-
Jones GT, Hill BG, Curtis N, Kabir TD, Wong LE, Tilyard MW, Williams MJ, van Rij AM, Comparison of three targeted approaches to screening for abdominal aortic aneurysm based on cardiovascular risk. Br J Surg 2016 103 1139 1146. doi: 10.1002/bjs.10224
-
(2016)
Br J Surg
, vol.103
, pp. 1139-1146
-
-
Jones, G.T.1
Hill, B.G.2
Curtis, N.3
Kabir, T.D.4
Wong, L.E.5
Tilyard, M.W.6
Williams, M.J.7
Van Rij, A.M.8
-
96
-
-
0037326089
-
Familial abdominal aortic aneurysms: Collection of 233 multiplex families.
-
Kuivaniemi H, Shibamura H, Arthur C, Familial abdominal aortic aneurysms: collection of 233 multiplex families. J Vasc Surg 2003 37 340 345. doi: 10.1067/mva.2003.71
-
(2003)
J Vasc Surg
, vol.37
, pp. 340-345
-
-
Kuivaniemi, H.1
Shibamura, H.2
Arthur, C.3
-
97
-
-
27644586450
-
The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: An analysis of 187 aneurysm families in Nova Scotia, Canada.
-
Ogata T, MacKean GL, Cole CW, Arthur C, Andreou P, Tromp G, Kuivaniemi H, The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: an analysis of 187 aneurysm families in Nova Scotia, Canada. J Vasc Surg 2005 42 891 897. doi: 10.1016/j.jvs.2005.08.002
-
(2005)
J Vasc Surg
, vol.42
, pp. 891-897
-
-
Ogata, T.1
Mackean, G.L.2
Cole, C.W.3
Arthur, C.4
Andreou, P.5
Tromp, G.6
Kuivaniemi, H.7
-
98
-
-
0035037959
-
Familial abdominal aortic aneurysms in the Otago region of New Zealand.
-
Rossaak JI, Hill TM, Jones GT, Phillips LV, Harris EL, van Rij AM, Familial abdominal aortic aneurysms in the Otago region of New Zealand. Cardiovasc Surg 2001 9 241 248
-
(2001)
Cardiovasc Surg
, vol.9
, pp. 241-248
-
-
Rossaak, J.I.1
Hill, T.M.2
Jones, G.T.3
Phillips, L.V.4
Harris, E.L.5
Van Rij, A.M.6
-
99
-
-
58549108408
-
A population-based case-control study of the familial risk of abdominal aortic aneurysm.
-
discussion 51
-
Larsson E, Granath F, Swedenborg J, Hultgren R, A population-based case-control study of the familial risk of abdominal aortic aneurysm. J Vasc Surg 2009 49 47 50; discussion 51. doi: 10.1016/j.jvs.2008.08.012
-
(2009)
J Vasc Surg
, vol.49
, pp. 47-50
-
-
Larsson, E.1
Granath, F.2
Swedenborg, J.3
Hultgren, R.4
-
100
-
-
33847354330
-
The genetic basis of abdominal aortic aneurysms: A review.
-
Sandford RM, Bown MJ, London NJ, Sayers RD, The genetic basis of abdominal aortic aneurysms: a review. Eur J Vasc Endovasc Surg 2007 33 381 390. doi: 10.1016/j.ejvs.2006.10.025
-
(2007)
Eur J Vasc Endovasc Surg
, vol.33
, pp. 381-390
-
-
Sandford, R.M.1
Bown, M.J.2
London, N.J.3
Sayers, R.D.4
-
101
-
-
0017752744
-
Familial abdominal aortic aneurysms.
-
Clifton MA, Familial abdominal aortic aneurysms. Br J Surg 1977 64 765 766
-
(1977)
Br J Surg
, vol.64
, pp. 765-766
-
-
Clifton, M.A.1
-
102
-
-
84864439539
-
High prevalence of abdominal aortic aneurysms in brothers and sisters of patients despite a low prevalence in the population.
-
Linné A, Lindström D, Hultgren R, High prevalence of abdominal aortic aneurysms in brothers and sisters of patients despite a low prevalence in the population. J Vasc Surg 2012 56 305 310. doi: 10.1016/j.jvs.2012.01.061
-
(2012)
J Vasc Surg
, vol.56
, pp. 305-310
-
-
Linné, A.1
Lindström, D.2
Hultgren, R.3
-
103
-
-
78751654000
-
High frequency of thoracic aneurysms in patients with abdominal aortic aneurysms.
-
b013e3181d96498
-
Larsson E, Vishnevskaya L, Kalin B, Granath F, Swedenborg J, Hultgren R, High frequency of thoracic aneurysms in patients with abdominal aortic aneurysms. Ann Surg 2011 253 180 184. doi: 10.1097/SLA.0b013e3181d96498
-
(2011)
Ann Surg
, vol.253
, pp. 180-184
-
-
Larsson, E.1
Vishnevskaya, L.2
Kalin, B.3
Granath, F.4
Swedenborg, J.5
Hultgren, R.6
-
104
-
-
0030048971
-
Thoracic and thoracoabdominal aortic aneurysm and dissection: An investigation based on autopsy.
-
Svensjö S, Bengtsson H, Bergqvist D, Thoracic and thoracoabdominal aortic aneurysm and dissection: an investigation based on autopsy. Br J Surg 1996 83 68 71
-
(1996)
Br J Surg
, vol.83
, pp. 68-71
-
-
Svensjö, S.1
Bengtsson, H.2
Bergqvist, D.3
-
105
-
-
85018786631
-
Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms.
-
van 't Hof FN, Ruigrok YM, Lee CH, Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms. J Am Heart Assoc 2016 5 e002603
-
(2016)
J Am Heart Assoc
, vol.5
, pp. e002603
-
-
Van 'T Hof, F.N.1
Ruigrok, Y.M.2
Lee, C.H.3
-
106
-
-
38649091662
-
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
-
Helgadottir A, Thorleifsson G, Magnusson KP, The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet 2008 40 217 224. doi: 10.1038/ng.72
-
(2008)
Nat Genet
, vol.40
, pp. 217-224
-
-
Helgadottir, A.1
Thorleifsson, G.2
Magnusson, K.P.3
-
107
-
-
84956593164
-
Abdominal aortic aneurysm genetic associations: Mostly false? A systematic review and meta-analysis.
-
Bradley DT, Badger SA, McFarland M, Hughes AE, Abdominal aortic aneurysm genetic associations: mostly false? A systematic review and meta-analysis. Eur J Vasc Endovasc Surg 2016 51 64 75. doi: 10.1016/j.ejvs.2015.09.006
-
(2016)
Eur J Vasc Endovasc Surg
, vol.51
, pp. 64-75
-
-
Bradley, D.T.1
Badger, S.A.2
McFarland, M.3
Hughes, A.E.4
-
108
-
-
2442493147
-
Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13.
-
doi: 10.1161/01.CIR.0000127857.77161.A1
-
Shibamura H, Olson JM, van Vlijmen-Van Keulen C, Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13. Circulation 2004 109 2103 2108. doi: 10.1161/01.CIR.0000127857.77161.A1
-
(2004)
Circulation
, vol.109
, pp. 2103-2108
-
-
Shibamura, H.1
Olson, J.M.2
Van Vlijmen-Van Keulen, C.3
-
109
-
-
84942987885
-
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
-
Nikpay M, Goel A, Won HH, A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet 2015 47 1121 1130. doi: 10.1038/ng.3396
-
(2015)
Nat Genet
, vol.47
, pp. 1121-1130
-
-
Nikpay, M.1
Goel, A.2
Won, H.H.3
-
110
-
-
79960697023
-
A single nucleotide polymorphism in exon 3 of the kallikrein 1 gene is associated with large but not small abdominal aortic aneurysm.
-
Biros E, Norman PE, Walker PJ, Nataatmadja M, West M, Golledge J, A single nucleotide polymorphism in exon 3 of the kallikrein 1 gene is associated with large but not small abdominal aortic aneurysm. Atherosclerosis 2011 217 452 457. doi: 10.1016/j.atherosclerosis.2011.04.017
-
(2011)
Atherosclerosis
, vol.217
, pp. 452-457
-
-
Biros, E.1
Norman, P.E.2
Walker, P.J.3
Nataatmadja, M.4
West, M.5
Golledge, J.6
-
111
-
-
85002194690
-
Meta-analysis of genome-wide association studies for abdominal aortic aneurysm identifies four new disease-specific risk loci.
-
Jones GT, Tromp G, Kuivaniemi H, Meta-analysis of genome-wide association studies for abdominal aortic aneurysm identifies four new disease-specific risk loci. Circ Res 2017 120 341 353. doi: 10.1161/CIRCRESAHA.116.308765
-
(2017)
Circ Res
, vol.120
, pp. 341-353
-
-
Jones, G.T.1
Tromp, G.2
Kuivaniemi, H.3
-
112
-
-
84945173643
-
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.
-
Bown MJ, Jones GT, Harrison SC, CARDIoGRAM Consortium; Global BPgen Consortium; DIAGRAM Consortium; VRCNZ Consortium Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. Am J Hum Genet 2011 89 619 627. doi: 10.1016/j.ajhg.2011.10.002
-
(2011)
Am J Hum Genet
, vol.89
, pp. 619-627
-
-
Bown, M.J.1
Jones, G.T.2
Harrison, S.C.3
-
113
-
-
84947899513
-
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.
-
Gretarsdottir S, Baas AF, Thorleifsson G, Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nat Genet 2010 42 692 697. doi: 10.1038/ng.622
-
(2010)
Nat Genet
, vol.42
, pp. 692-697
-
-
Gretarsdottir, S.1
Baas, A.F.2
Thorleifsson, G.3
-
114
-
-
84891514939
-
Interleukin-6 receptor pathways in abdominal aortic aneurysm.
-
doi: 10.1093/eurheartj/ehs354
-
Harrison SC, Smith AJ, Jones GT, Aneurysm Consortium Interleukin-6 receptor pathways in abdominal aortic aneurysm. Eur Heart J 2013 34 3707 3716. doi: 10.1093/eurheartj/ehs354
-
(2013)
Eur Heart J
, vol.34
, pp. 3707-3716
-
-
Harrison, S.C.1
Smith, A.J.2
Jones, G.T.3
-
115
-
-
84880305065
-
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.
-
doi: 10.1093/hmg/ddt141
-
Jones GT, Bown MJ, Gretarsdottir S, A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm. Hum Mol Genet 2013 22 2941 2947. doi: 10.1093/hmg/ddt141
-
(2013)
Hum Mol Genet
, vol.22
, pp. 2941-2947
-
-
Jones, G.T.1
Bown, M.J.2
Gretarsdottir, S.3
-
116
-
-
84892385162
-
A variant in LDLR is associated with abdominal aortic aneurysm.
-
Bradley DT, Hughes AE, Badger SA, A variant in LDLR is associated with abdominal aortic aneurysm. Circ Cardiovasc Genet 2013 6 498 504. doi: 10.1161/CIRCGENETICS.113.000165
-
(2013)
Circ Cardiovasc Genet
, vol.6
, pp. 498-504
-
-
Bradley, D.T.1
Hughes, A.E.2
Badger, S.A.3
-
117
-
-
16644377930
-
Could medical intervention work for aortic aneurysms?
-
Baxter BT, Could medical intervention work for aortic aneurysms? Am J Surg 2004 188 628 632. doi: 10.1016/j.amjsurg.2004.08.034
-
(2004)
Am J Surg
, vol.188
, pp. 628-632
-
-
Baxter, B.T.1
-
118
-
-
0029089366
-
Inflammation and matrix metalloproteinases in the enlarging abdominal aortic aneurysm.
-
Freestone T, Turner RJ, Coady A, Higman DJ, Greenhalgh RM, Powell JT, Inflammation and matrix metalloproteinases in the enlarging abdominal aortic aneurysm. Arterioscler Thromb Vasc Biol 1995 15 1145 1151
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 1145-1151
-
-
Freestone, T.1
Turner, R.J.2
Coady, A.3
Higman, D.J.4
Greenhalgh, R.M.5
Powell, J.T.6
-
119
-
-
85033982572
-
Two C-C family chemokines, eotaxin and RANTES, are novel independent plasma biomarkers for abdominal aortic aneurysm.
-
Jones GT, Phillips LV, Williams MJ, van Rij AM, Kabir TD, Two C-C family chemokines, eotaxin and RANTES, are novel independent plasma biomarkers for abdominal aortic aneurysm. J Am Heart Assoc 2016 5 e002993
-
(2016)
J Am Heart Assoc
, vol.5
, pp. e002993
-
-
Jones, G.T.1
Phillips, L.V.2
Williams, M.J.3
Van Rij, A.M.4
Kabir, T.D.5
-
120
-
-
84919768683
-
The pathohistology of abdominal aortic aneurysm.
-
Rijeka, Croatia InTech
-
Jones GT, Grundmann RT, The pathohistology of abdominal aortic aneurysm. In: Diagnosis, Screening and Treatment of Abdominal, Thoracoabdominal and Thoracic Aortic Aneurysms 2011 Rijeka, Croatia InTech 414
-
(2011)
In: Diagnosis, Screening and Treatment of Abdominal, Thoracoabdominal and Thoracic Aortic Aneurysms
, pp. 414
-
-
Jones, G.T.1
Grundmann, R.T.2
-
121
-
-
85021756461
-
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.
-
Howson JMM, Zhao W, Barnes DR, CARDIoGRAMplusC4D; EPIC-CVD Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nat Genet 2017 49 1113 1119. doi: 10.1038/ng.3874
-
(2017)
Nat Genet
, vol.49
, pp. 1113-1119
-
-
Howson, J.M.M.1
Zhao, W.2
Barnes, D.R.3
-
122
-
-
85047752186
-
Identification of 64 novel genetic loci provides an expanded view on the genetic architecture of coronary artery disease.
-
van der Harst P, Verweij N, Identification of 64 novel genetic loci provides an expanded view on the genetic architecture of coronary artery disease. Circ Res 2018 122 433 443. doi: 10.1161/CIRCRESAHA.117.312086
-
(2018)
Circ Res
, vol.122
, pp. 433-443
-
-
Van Der Harst, P.1
Verweij, N.2
-
123
-
-
84865125773
-
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.
-
Helgadottir A, Gretarsdottir S, Thorleifsson G, Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. J Am Coll Cardiol 2012 60 722 729. doi: 10.1016/j.jacc.2012.01.078
-
(2012)
J Am Coll Cardiol
, vol.60
, pp. 722-729
-
-
Helgadottir, A.1
Gretarsdottir, S.2
Thorleifsson, G.3
-
124
-
-
34147211127
-
Plasma lipoprotein(a) indicates risk for 4 distinct forms of vascular disease.
-
Jones GT, van Rij AM, Cole J, Williams MJ, Bateman EH, Marcovina SM, Deng M, McCormick SP, Plasma lipoprotein(a) indicates risk for 4 distinct forms of vascular disease. Clin Chem 2007 53 679 685. doi: 10.1373/clinchem.2006.079947
-
(2007)
Clin Chem
, vol.53
, pp. 679-685
-
-
Jones, G.T.1
Van Rij, A.M.2
Cole, J.3
Williams, M.J.4
Bateman, E.H.5
Marcovina, S.M.6
Deng, M.7
McCormick, S.P.8
-
125
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
-
Schunkert H, König IR, Kathiresan S, Cardiogenics; CARDIoGRAM Consortium Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 43 333 338. doi: 10.1038/ng.784
-
(2011)
Nat Genet
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
König, I.R.2
Kathiresan, S.3
-
126
-
-
77949775636
-
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.
-
doi: 10.1038/nature08801
-
Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, Blow MJ, Cohen JC, Rubin EM, Pennacchio LA, Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature 2010 464 409 412. doi: 10.1038/nature08801
-
(2010)
Nature
, vol.464
, pp. 409-412
-
-
Visel, A.1
Zhu, Y.2
May, D.3
Afzal, V.4
Gong, E.5
Attanasio, C.6
Blow, M.J.7
Cohen, J.C.8
Rubin, E.M.9
Pennacchio, L.A.10
-
127
-
-
84863113857
-
The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues.
-
Pilbrow AP, Folkersen L, Pearson JF, The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues. PLoS One 2012 7 e39574. doi: 10.1371/journal.pone.0039574
-
(2012)
PLoS One
, vol.7
-
-
Pilbrow, A.P.1
Folkersen, L.2
Pearson, J.F.3
-
128
-
-
84903817603
-
The contribution of the functional IL6R polymorphism rs2228145, eQTLs and other genome-wide SNPs to the heritability of plasma sIL-6R levels.
-
doi: 10.1007/s10519-014-9656-8
-
van Dongen J, Jansen R, Smit D, Hottenga JJ, Mbarek H, Willemsen G, Kluft C, Penninx BW, Ferreira MA, Boomsma DI, de Geus EJ, AAGC Collaborators The contribution of the functional IL6R polymorphism rs2228145, eQTLs and other genome-wide SNPs to the heritability of plasma sIL-6R levels. Behav Genet 2014 44 368 382. doi: 10.1007/s10519-014-9656-8
-
(2014)
Behav Genet
, vol.44
, pp. 368-382
-
-
Van Dongen, J.1
Jansen, R.2
Smit, D.3
Hottenga, J.J.4
Mbarek, H.5
Willemsen, G.6
Kluft, C.7
Penninx, B.W.8
Ferreira, M.A.9
Boomsma, D.I.10
De Geus, E.J.11
-
129
-
-
80052721297
-
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.
-
doi: 10.1016/S0140-6736(11)60874-X
-
Ferreira MA, Matheson MC, Duffy DL, Australian Asthma Genetics Consortium Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet 2011 378 1006 1014. doi: 10.1016/S0140-6736(11)60874-X
-
(2011)
Lancet
, vol.378
, pp. 1006-1014
-
-
Ferreira, M.A.1
Matheson, M.C.2
Duffy, D.L.3
-
130
-
-
77955499945
-
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus.
-
doi: 10.1038/nature09266
-
Musunuru K, Strong A, Frank-Kamenetsky M, From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature 2010 466 714 719. doi: 10.1038/nature09266
-
(2010)
Nature
, vol.466
, pp. 714-719
-
-
Musunuru, K.1
Strong, A.2
Frank-Kamenetsky, M.3
-
131
-
-
77956327982
-
Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export.
-
Kjolby M, Andersen OM, Breiderhoff T, Fjorback AW, Pedersen KM, Madsen P, Jansen P, Heeren J, Willnow TE, Nykjaer A, Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export. Cell Metab 2010 12 213 223. doi: 10.1016/j.cmet.2010.08.006
-
(2010)
Cell Metab
, vol.12
, pp. 213-223
-
-
Kjolby, M.1
Andersen, O.M.2
Breiderhoff, T.3
Fjorback, A.W.4
Pedersen, K.M.5
Madsen, P.6
Jansen, P.7
Heeren, J.8
Willnow, T.E.9
Nykjaer, A.10
-
132
-
-
85044438628
-
The miR-182/SORT1 axis regulates vascular smooth muscle cell calcification in vitro and in vivo.
-
Zhang Z, Jiang W, Yang H, Lin Q, Qin X, The miR-182/SORT1 axis regulates vascular smooth muscle cell calcification in vitro and in vivo. Exp Cell Res 2018 362 324 331. doi: 10.1016/j.yexcr.2017.11.033
-
(2018)
Exp Cell Res
, vol.362
, pp. 324-331
-
-
Zhang, Z.1
Jiang, W.2
Yang, H.3
Lin, Q.4
Qin, X.5
-
133
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids.
-
doi: 10.1038/nature09270
-
Teslovich TM, Musunuru K, Smith AV, Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010 466 707 713. doi: 10.1038/nature09270
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
-
134
-
-
85041475144
-
Genetic association of lipids and lipid drug targets with abdominal aortic aneurysm: A meta-analysis.
-
Harrison SC, Holmes MV, Burgess S, Genetic association of lipids and lipid drug targets with abdominal aortic aneurysm: a meta-analysis. JAMA Cardiol 2018 3 26 33. doi: 10.1001/jamacardio.2017.4293
-
(2018)
JAMA Cardiol
, vol.3
, pp. 26-33
-
-
Harrison, S.C.1
Holmes, M.V.2
Burgess, S.3
-
135
-
-
85045462568
-
Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization study.
-
Weng LC, Roetker NS, Lutsey PL, Alonso A, Guan W, Pankow JS, Folsom AR, Steffen LM, Pankratz N, Tang W, Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: a Mendelian randomization study. PLoS One 2018 13 e0195719. doi: 10.1371/journal.pone.0195719
-
(2018)
PLoS One
, vol.13
-
-
Weng, L.C.1
Roetker, N.S.2
Lutsey, P.L.3
Alonso, A.4
Guan, W.5
Pankow, J.S.6
Folsom, A.R.7
Steffen, L.M.8
Pankratz, N.9
Tang, W.10
-
136
-
-
0029115532
-
Production and localization of 92-kilodalton gelatinase in abdominal aortic aneurysms. An elastolytic metalloproteinase expressed by aneurysm-infiltrating macrophages.
-
doi: 10.1172/JCI118037
-
Thompson RW, Holmes DR, Mertens RA, Liao S, Botney MD, Mecham RP, Welgus HG, Parks WC, Production and localization of 92-kilodalton gelatinase in abdominal aortic aneurysms. An elastolytic metalloproteinase expressed by aneurysm-infiltrating macrophages. J Clin Invest 1995 96 318 326. doi: 10.1172/JCI118037
-
(1995)
J Clin Invest
, vol.96
, pp. 318-326
-
-
Thompson, R.W.1
Holmes, D.R.2
Mertens, R.A.3
Liao, S.4
Botney, M.D.5
Mecham, R.P.6
Welgus, H.G.7
Parks, W.C.8
-
137
-
-
85045055605
-
Plasma lipid transfer proteins: The role of PLTP and CETP in atherogenesis.
-
doi: 10.17219/acem/67968
-
Chowaniec Z, Skoczyńska A, Plasma lipid transfer proteins: the role of PLTP and CETP in atherogenesis. Adv Clin Exp Med 2018 27 429 436. doi: 10.17219/acem/67968
-
(2018)
Adv Clin Exp Med
, vol.27
, pp. 429-436
-
-
Chowaniec, Z.1
Skoczyńska, A.2
-
138
-
-
46249107650
-
Acute elevation of plasma PLTP activity strongly increases pre-existing atherosclerosis.
-
Moerland M, Samyn H, van Gent T, van Haperen R, Dallinga-Thie G, Grosveld F, van Tol A, de Crom R, Acute elevation of plasma PLTP activity strongly increases pre-existing atherosclerosis. Arterioscler Thromb Vasc Biol 2008 28 1277 1282. doi: 10.1161/ATVBAHA.108.165084
-
(2008)
Arterioscler Thromb Vasc Biol
, vol.28
, pp. 1277-1282
-
-
Moerland, M.1
Samyn, H.2
Van Gent, T.3
Van Haperen, R.4
Dallinga-Thie, G.5
Grosveld, F.6
Van Tol, A.7
De Crom, R.8
-
139
-
-
84901049772
-
Cathepsin G degradation of phospholipid transfer protein (PLTP) augments pulmonary inflammation.
-
246843
-
Brehm A, Geraghty P, Campos M, Garcia-Arcos I, Dabo AJ, Gaffney A, Eden E, Jiang XC, D'Armiento J, Foronjy R, Cathepsin G degradation of phospholipid transfer protein (PLTP) augments pulmonary inflammation. FASEB J 2014 28 2318 2331. doi: 10.1096/fj.13-246843
-
(2014)
FASEB J
, vol.28
, pp. 2318-2331
-
-
Brehm, A.1
Geraghty, P.2
Campos, M.3
Garcia-Arcos, I.4
Dabo, A.J.5
Gaffney, A.6
Eden, E.7
Jiang, X.C.8
D'Armiento, J.9
Foronjy, R.10
-
140
-
-
84954398045
-
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.
-
Coleman C, Quinn EM, Ryan AW, Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. Eur J Hum Genet 2016 24 291 297. doi: 10.1038/ejhg.2015.87
-
(2016)
Eur J Hum Genet
, vol.24
, pp. 291-297
-
-
Coleman, C.1
Quinn, E.M.2
Ryan, A.W.3
-
141
-
-
84859608366
-
Meta-analysis of individual patient data to examine factors affecting growth and rupture of small abdominal aortic aneurysms.
-
Sweeting MJ, Thompson SG, Brown LC, Powell JT, RESCAN collaborators Meta-analysis of individual patient data to examine factors affecting growth and rupture of small abdominal aortic aneurysms. Br J Surg 2012 99 655 665. doi: 10.1002/bjs.8707
-
(2012)
Br J Surg
, vol.99
, pp. 655-665
-
-
Sweeting, M.J.1
Thompson, S.G.2
Brown, L.C.3
Powell, J.T.4
-
142
-
-
84906078639
-
SMYD proteins: Key regulators in skeletal and cardiac muscle development and function.
-
Du SJ, Tan X, Zhang J, SMYD proteins: key regulators in skeletal and cardiac muscle development and function. Anat Rec (Hoboken) 2014 297 1650 1662. doi: 10.1002/ar.22972
-
(2014)
Anat Rec (Hoboken)
, vol.297
, pp. 1650-1662
-
-
Du, S.J.1
Tan, X.2
Zhang, J.3
-
143
-
-
84924059414
-
The histone methyltransferase Smyd2 is a negative regulator of macrophage activation by suppressing interleukin 6 (IL-6) and tumor necrosis factor α (TNF-α) production.
-
doi: 10.1074/jbc.M114.610345
-
Xu G, Liu G, Xiong S, Liu H, Chen X, Zheng B, The histone methyltransferase Smyd2 is a negative regulator of macrophage activation by suppressing interleukin 6 (IL-6) and tumor necrosis factor α (TNF-α) production. J Biol Chem 2015 290 5414 5423. doi: 10.1074/jbc.M114.610345
-
(2015)
J Biol Chem
, vol.290
, pp. 5414-5423
-
-
Xu, G.1
Liu, G.2
Xiong, S.3
Liu, H.4
Chen, X.5
Zheng, B.6
-
144
-
-
84867844538
-
The role of extracellular signal-related kinase during abdominal aortic aneurysm formation.
-
Ghosh A, DiMusto PD, Ehrlichman LK, Sadiq O, McEvoy B, Futchko JS, Henke PK, Eliason JL, Upchurch GR Jr, The role of extracellular signal-related kinase during abdominal aortic aneurysm formation. J Am Coll Surg 2012 215 668.e1 680.e1. doi: 10.1016/j.jamcollsurg.2012.06.414
-
(2012)
J Am Coll Surg
, vol.215
, pp. 668e1-680e1
-
-
Ghosh, A.1
Dimusto, P.D.2
Ehrlichman, L.K.3
Sadiq, O.4
McEvoy, B.5
Futchko, J.S.6
Henke, P.K.7
Eliason, J.L.8
Upchurch, R.G.9
-
145
-
-
84871763644
-
Importance of endothelial NF-κB signalling in vascular remodelling and aortic aneurysm formation.
-
doi: 10.1093/cvr/cvs298
-
Saito T, Hasegawa Y, Ishigaki Y, Yamada T, Gao J, Imai J, Uno K, Kaneko K, Ogihara T, Shimosawa T, Asano T, Fujita T, Oka Y, Katagiri H, Importance of endothelial NF-κB signalling in vascular remodelling and aortic aneurysm formation. Cardiovasc Res 2013 97 106 114. doi: 10.1093/cvr/cvs298
-
(2013)
Cardiovasc Res
, vol.97
, pp. 106-114
-
-
Saito, T.1
Hasegawa, Y.2
Ishigaki, Y.3
Yamada, T.4
Gao, J.5
Imai, J.6
Uno, K.7
Kaneko, K.8
Ogihara, T.9
Shimosawa, T.10
Asano, T.11
Fujita, T.12
Oka, Y.13
Katagiri, H.14
-
146
-
-
84927946719
-
Heat shock protein 90 inhibition by 17-DMAG attenuates abdominal aortic aneurysm formation in mice.
-
Qi J, Yang P, Yi B, Huo Y, Chen M, Zhang J, Sun J, Heat shock protein 90 inhibition by 17-DMAG attenuates abdominal aortic aneurysm formation in mice. Am J Physiol Heart Circ Physiol 2015 308 H841 H852. doi: 10.1152/ajpheart.00470.2014
-
(2015)
Am J Physiol Heart Circ Physiol
, vol.308
, pp. H841-H852
-
-
Qi, J.1
Yang, P.2
Yi, B.3
Huo, Y.4
Chen, M.5
Zhang, J.6
Sun, J.7
-
147
-
-
85042881652
-
SMYD2 promoter DNA methylation is associated with abdominal aortic aneurysm (AAA) and SMYD2 expression in vascular smooth muscle cells.
-
doi: 10.1186/s13148-018-0460-9
-
Toghill BJ, Saratzis A, Freeman PJ, Sylvius N, Bown MJ, UKAGS collaborators SMYD2 promoter DNA methylation is associated with abdominal aortic aneurysm (AAA) and SMYD2 expression in vascular smooth muscle cells. Clin Epigenetics 2018 10 29. doi: 10.1186/s13148-018-0460-9
-
(2018)
Clin Epigenetics
, vol.10
, pp. 29
-
-
Toghill, B.J.1
Saratzis, A.2
Freeman, P.J.3
Sylvius, N.4
Bown, M.J.5
-
148
-
-
70349093134
-
LRP1 regulates architecture of the vascular wall by controlling PDGFRbeta-dependent phosphatidylinositol 3-kinase activation.
-
Zhou L, Takayama Y, Boucher P, Tallquist MD, Herz J, LRP1 regulates architecture of the vascular wall by controlling PDGFRbeta-dependent phosphatidylinositol 3-kinase activation. PLoS One 2009 4 e6922. doi: 10.1371/journal.pone.0006922
-
(2009)
PLoS One
, vol.4
-
-
Zhou, L.1
Takayama, Y.2
Boucher, P.3
Tallquist, M.D.4
Herz, J.5
-
149
-
-
0037432766
-
LRP: Role in vascular wall integrity and protection from atherosclerosis.
-
Boucher P, Gotthardt M, Li WP, Anderson RG, Herz J, LRP: role in vascular wall integrity and protection from atherosclerosis. Science 2003 300 329 332. doi: 10.1126/science.1082095
-
(2003)
Science
, vol.300
, pp. 329-332
-
-
Boucher, P.1
Gotthardt, M.2
Li, W.P.3
Anderson, R.G.4
Herz, J.5
-
150
-
-
58149215681
-
Fibroblast growth factor 9 signaling inhibits airway smooth muscle differentiation in mouse lung.
-
Yi L, Domyan ET, Lewandoski M, Sun X, Fibroblast growth factor 9 signaling inhibits airway smooth muscle differentiation in mouse lung. Dev Dyn 2009 238 123 137. doi: 10.1002/dvdy.21831
-
(2009)
Dev Dyn
, vol.238
, pp. 123-137
-
-
Yi, L.1
Domyan, E.T.2
Lewandoski, M.3
Sun, X.4
-
151
-
-
84949292738
-
Fibroblast growth factor-9 activates c-kit progenitor cells and enhances angiogenesis in the infarcted diabetic heart.
-
doi: 10.1155/2016/5810908
-
Singla D, Wang J, Fibroblast growth factor-9 activates c-kit progenitor cells and enhances angiogenesis in the infarcted diabetic heart. Oxid Med Cell Longev 2016 2016 5810908. doi: 10.1155/2016/5810908
-
(2016)
Oxid Med Cell Longev
, vol.2016
, pp. 5810908
-
-
Singla, D.1
Wang, J.2
-
152
-
-
33747379850
-
Abdominal aortic aneurysm rupture is associated with increased medial neovascularization and overexpression of proangiogenic cytokines.
-
doi: 10.1161/01.ATV.0000234944.22509.f9
-
Choke E, Thompson MM, Dawson J, Wilson WR, Sayed S, Loftus IM, Cockerill GW, Abdominal aortic aneurysm rupture is associated with increased medial neovascularization and overexpression of proangiogenic cytokines. Arterioscler Thromb Vasc Biol 2006 26 2077 2082. doi: 10.1161/01.ATV.0000234944.22509.f9
-
(2006)
Arterioscler Thromb Vasc Biol
, vol.26
, pp. 2077-2082
-
-
Choke, E.1
Thompson, M.M.2
Dawson, J.3
Wilson, W.R.4
Sayed, S.5
Loftus, I.M.6
Cockerill, G.W.7
-
153
-
-
84859499801
-
The transcription factor Erg controls endothelial cell quiescence by repressing activity of nuclear factor (NF)-κB p65.
-
doi: 10.1074/jbc.M112.346791
-
Dryden NH, Sperone A, Martin-Almedina S, Hannah RL, Birdsey GM, Khan ST, Layhadi JA, Mason JC, Haskard DO, Göttgens B, Randi AM, The transcription factor Erg controls endothelial cell quiescence by repressing activity of nuclear factor (NF)-κB p65. J Biol Chem 2012 287 12331 12342. doi: 10.1074/jbc.M112.346791
-
(2012)
J Biol Chem
, vol.287
, pp. 12331-12342
-
-
Dryden, N.H.1
Sperone, A.2
Martin-Almedina, S.3
Hannah, R.L.4
Birdsey, G.M.5
Khan, S.T.6
Layhadi, J.A.7
Mason, J.C.8
Haskard, D.O.9
Göttgens, B.10
Randi, A.M.11
-
154
-
-
84880512956
-
ETS factors regulate Vegf-dependent arterial specification.
-
Wythe JD, Dang LT, Devine WP, Boudreau E, Artap ST, He D, Schachterle W, Stainier DY, Oettgen P, Black BL, Bruneau BG, Fish JE, ETS factors regulate Vegf-dependent arterial specification. Dev Cell 2013 26 45 58. doi: 10.1016/j.devcel.2013.06.007
-
(2013)
Dev Cell
, vol.26
, pp. 45-58
-
-
Wythe, J.D.1
Dang, L.T.2
Devine, W.P.3
Boudreau, E.4
Artap, S.T.5
He, D.6
Schachterle, W.7
Stainier, D.Y.8
Oettgen, P.9
Black, B.L.10
Bruneau, B.G.11
Fish, J.E.12
-
155
-
-
76349107344
-
Site specificity of aneurysmal disease.
-
Norman PE, Powell JT, Site specificity of aneurysmal disease. Circulation 2010 121 560 568. doi: 10.1161/CIRCULATIONAHA.109.880724
-
(2010)
Circulation
, vol.121
, pp. 560-568
-
-
Norman, P.E.1
Powell, J.T.2
-
156
-
-
84899649184
-
Identification of novel TMPRSS2:ERG mechanisms in prostate cancer metastasis: Involvement of MMP9 and PLXNA2.
-
Tian TV, Tomavo N, Huot L, Flourens A, Bonnelye E, Flajollet S, Hot D, Leroy X, de Launoit Y, Duterque-Coquillaud M, Identification of novel TMPRSS2:ERG mechanisms in prostate cancer metastasis: involvement of MMP9 and PLXNA2. Oncogene 2014 33 2204 2214. doi: 10.1038/onc.2013.176
-
(2014)
Oncogene
, vol.33
, pp. 2204-2214
-
-
Tian, T.V.1
Tomavo, N.2
Huot, L.3
Flourens, A.4
Bonnelye, E.5
Flajollet, S.6
Hot, D.7
Leroy, X.8
De Launoit, Y.9
Duterque-Coquillaud, M.10
-
157
-
-
0026544808
-
Are aortic aneurysms caused by atherosclerosis?
-
Reed D, Reed C, Stemmermann G, Hayashi T, Are aortic aneurysms caused by atherosclerosis? Circulation 1992 85 205 211
-
(1992)
Circulation
, vol.85
, pp. 205-211
-
-
Reed, D.1
Reed, C.2
Stemmermann, G.3
Hayashi, T.4
-
158
-
-
84928021248
-
Genetically determined height and coronary artery disease.
-
doi: 10.1056/NEJMoa1404881
-
Nelson CP, Hamby SE, Saleheen D, CARDIoGRAM+C4D Consortium Genetically determined height and coronary artery disease. N Engl J Med 2015 372 1608 1618. doi: 10.1056/NEJMoa1404881
-
(2015)
N Engl J Med
, vol.372
, pp. 1608-1618
-
-
Nelson, C.P.1
Hamby, S.E.2
Saleheen, D.3
-
159
-
-
77954772383
-
Short stature is associated with coronary heart disease: A systematic review of the literature and a meta-analysis.
-
doi: 10.1093/eurheartj/ehq155
-
Paajanen TA, Oksala NK, Kuukasjärvi P, Karhunen PJ, Short stature is associated with coronary heart disease: a systematic review of the literature and a meta-analysis. Eur Heart J 2010 31 1802 1809. doi: 10.1093/eurheartj/ehq155
-
(2010)
Eur Heart J
, vol.31
, pp. 1802-1809
-
-
Paajanen, T.A.1
Oksala, N.K.2
Kuukasjärvi, P.3
Karhunen, P.J.4
-
160
-
-
77951748276
-
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.
-
Thorgeirsson TE, Gudbjartsson DF, Surakka I, ENGAGE Consortium Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet 2010 42 448 453. doi: 10.1038/ng.573
-
(2010)
Nat Genet
, vol.42
, pp. 448-453
-
-
Thorgeirsson, T.E.1
Gudbjartsson, D.F.2
Surakka, I.3
-
161
-
-
84983111414
-
The potential role of DNA methylation in the pathogenesis of abdominal aortic aneurysm.
-
Toghill BJ, Saratzis A, Harrison SC, Verissimo AR, Mallon EB, Bown MJ, The potential role of DNA methylation in the pathogenesis of abdominal aortic aneurysm. Atherosclerosis 2015 241 121 129. doi: 10.1016/j.atherosclerosis.2015.05.001
-
(2015)
Atherosclerosis
, vol.241
, pp. 121-129
-
-
Toghill, B.J.1
Saratzis, A.2
Harrison, S.C.3
Verissimo, A.R.4
Mallon, E.B.5
Bown, M.J.6
-
162
-
-
85020660311
-
Loss of smooth muscle α-actin leads to NF-κB-dependent increased sensitivity to angiotensin II in smooth muscle cells and aortic enlargement.
-
Chen J, Peters A, Papke CL, Loss of smooth muscle α-actin leads to NF-κB-dependent increased sensitivity to angiotensin II in smooth muscle cells and aortic enlargement. Circ Res 2017 120 1903 1915. doi: 10.1161/CIRCRESAHA.117.310563
-
(2017)
Circ Res
, vol.120
, pp. 1903-1915
-
-
Chen, J.1
Peters, A.2
Papke, C.L.3
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