| Year |
Citation |
Score |
| 2007 |
Jaźwińska A, Badakov R, Keating MT. Activin-betaA signaling is required for zebrafish fin regeneration. Current Biology : Cb. 17: 1390-5. PMID 17683938 DOI: 10.1016/J.Cub.2007.07.019 |
0.394 |
|
| 2007 |
Decher N, Renigunta V, Zuzarte M, Soom M, Heinemann SH, Timothy KW, Keating MT, Daut J, Sanguinetti MC, Splawski I. Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndrome. Cardiovascular Research. 75: 748-57. PMID 17568571 DOI: 10.1016/J.Cardiores.2007.05.010 |
0.363 |
|
| 2006 |
Schebesta M, Lien CL, Engel FB, Keating MT. Transcriptional profiling of caudal fin regeneration in zebrafish. Thescientificworldjournal. 6: 38-54. PMID 17205186 DOI: 10.1100/Tsw.2006.326 |
0.381 |
|
| 2006 |
Engel FB, Hsieh PC, Lee RT, Keating MT. FGF1/p38 MAP kinase inhibitor therapy induces cardiomyocyte mitosis, reduces scarring, and rescues function after myocardial infarction. Proceedings of the National Academy of Sciences of the United States of America. 103: 15546-51. PMID 17032753 DOI: 10.1073/Pnas.0607382103 |
0.317 |
|
| 2006 |
Tseng AS, Engel FB, Keating MT. The GSK-3 inhibitor BIO promotes proliferation in mammalian cardiomyocytes. Chemistry & Biology. 13: 957-63. PMID 16984885 DOI: 10.1016/J.Chembiol.2006.08.004 |
0.321 |
|
| 2006 |
Lien CL, Schebesta M, Makino S, Weber GJ, Keating MT. Gene expression analysis of zebrafish heart regeneration. Plos Biology. 4: e260. PMID 16869712 DOI: 10.1371/Journal.Pbio.0040260 |
0.384 |
|
| 2006 |
Splawski I, Yoo DS, Stotz SC, Cherry A, Clapham DE, Keating MT. CACNA1H mutations in autism spectrum disorders. The Journal of Biological Chemistry. 281: 22085-91. PMID 16754686 DOI: 10.1074/Jbc.M603316200 |
0.344 |
|
| 2006 |
Bayliss PE, Bellavance KL, Whitehead GG, Abrams JM, Aegerter S, Robbins HS, Cowan DB, Keating MT, O'Reilly T, Wood JM, Roberts TM, Chan J. Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrafish. Nature Chemical Biology. 2: 265-73. PMID 16565716 DOI: 10.1038/Nchembio778 |
0.33 |
|
| 2006 |
Kiehl TR, Nechiporuk A, Figueroa KP, Keating MT, Huynh DP, Pulst SM. Generation and characterization of Sca2 (ataxin-2) knockout mice. Biochemical and Biophysical Research Communications. 339: 17-24. PMID 16293225 DOI: 10.1016/J.Bbrc.2005.10.186 |
0.629 |
|
| 2005 |
Whitehead GG, Makino S, Lien CL, Keating MT. fgf20 is essential for initiating zebrafish fin regeneration. Science (New York, N.Y.). 310: 1957-60. PMID 16373575 DOI: 10.1126/Science.1117637 |
0.424 |
|
| 2005 |
Makino S, Whitehead GG, Lien CL, Kim S, Jhawar P, Kono A, Kawata Y, Keating MT. Heat-shock protein 60 is required for blastema formation and maintenance during regeneration. Proceedings of the National Academy of Sciences of the United States of America. 102: 14599-604. PMID 16204379 DOI: 10.1073/Pnas.0507408102 |
0.402 |
|
| 2005 |
Engel FB, Schebesta M, Duong MT, Lu G, Ren S, Madwed JB, Jiang H, Wang Y, Keating MT. p38 MAP kinase inhibition enables proliferation of adult mammalian cardiomyocytes. Genes & Development. 19: 1175-87. PMID 15870258 DOI: 10.1101/Gad.1306705 |
0.344 |
|
| 2005 |
Splawski I, Timothy KW, Decher N, Kumar P, Sachse FB, Beggs AH, Sanguinetti MC, Keating MT. Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations. Proceedings of the National Academy of Sciences of the United States of America. 102: 8089-96; discussion . PMID 15863612 DOI: 10.1073/Pnas.0502506102 |
0.373 |
|
| 2004 |
Ackerman MJ, Splawski I, Makielski JC, Tester DJ, Will ML, Timothy KW, Keating MT, Jones G, Chadha M, Burrow CR, Stephens JC, Xu C, Judson R, Curran ME. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 1: 600-7. PMID 15851227 DOI: 10.1016/J.Hrthm.2004.07.013 |
0.377 |
|
| 2004 |
Philippar U, Schratt G, Dieterich C, Müller JM, Galgóczy P, Engel FB, Keating MT, Gertler F, Schüle R, Vingron M, Nordheim A. The SRF target gene Fhl2 antagonizes RhoA/MAL-dependent activation of SRF. Molecular Cell. 16: 867-80. PMID 15610731 DOI: 10.1016/J.Molcel.2004.11.039 |
0.324 |
|
| 2004 |
Zhang L, Vincent GM, Baralle M, Baralle FE, Anson BD, Benson DW, Whiting B, Timothy KW, Carlquist J, January CT, Keating MT, Splawski I. An intronic mutation causes long QT syndrome. Journal of the American College of Cardiology. 44: 1283-91. PMID 15364333 DOI: 10.1016/J.Jacc.2004.06.045 |
0.345 |
|
| 2004 |
Keating MT. Genetic approaches to disease and regeneration. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 359: 795-8. PMID 15293807 DOI: 10.1098/Rstb.2004.1469 |
0.33 |
|
| 2004 |
Poss KD, Nechiporuk A, Stringer KF, Lee C, Keating MT. Germ cell aneuploidy in zebrafish with mutations in the mitotic checkpoint gene mps1. Genes & Development. 18: 1527-32. PMID 15231734 DOI: 10.1101/Gad.1182604 |
0.72 |
|
| 2004 |
Mohler PJ, Splawski I, Napolitano C, Bottelli G, Sharpe L, Timothy K, Priori SG, Keating MT, Bennett V. A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. Proceedings of the National Academy of Sciences of the United States of America. 101: 9137-42. PMID 15178757 DOI: 10.1073/Pnas.0402546101 |
0.347 |
|
| 2003 |
Zareba W, Moss AJ, Sheu G, Kaufman ES, Priori S, Vincent GM, Towbin JA, Benhorin J, Schwartz PJ, Napolitano C, Hall WJ, Keating MT, Qi M, Robinson J, Andrews ML, et al. Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome. Journal of Cardiovascular Electrophysiology. 14: 1149-53. PMID 14678125 DOI: 10.1046/J.1540-8167.2003.03177.X |
0.367 |
|
| 2003 |
Nechiporuk A, Poss KD, Johnson SL, Keating MT. Positional cloning of a temperature-sensitive mutant emmental reveals a role for sly1 during cell proliferation in zebrafish fin regeneration. Developmental Biology. 258: 291-306. PMID 12798289 DOI: 10.1016/S0012-1606(03)00129-5 |
0.737 |
|
| 2003 |
Poss KD, Keating MT, Nechiporuk A. Tales of regeneration in zebrafish. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 226: 202-10. PMID 12557199 DOI: 10.1002/Dvdy.10220 |
0.716 |
|
| 2002 |
Poss KD, Wilson LG, Keating MT. Heart regeneration in zebrafish. Science (New York, N.Y.). 298: 2188-90. PMID 12481136 DOI: 10.1126/Science.1077857 |
0.609 |
|
| 2002 |
Poss KD, Nechiporuk A, Hillam AM, Johnson SL, Keating MT. Mps1 defines a proximal blastemal proliferative compartment essential for zebrafish fin regeneration. Development (Cambridge, England). 129: 5141-9. PMID 12399306 |
0.735 |
|
| 2002 |
Splawski I, Timothy KW, Tateyama M, Clancy CE, Malhotra A, Beggs AH, Cappuccio FP, Sagnella GA, Kass RS, Keating MT. Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia. Science (New York, N.Y.). 297: 1333-6. PMID 12193783 DOI: 10.1126/Science.1073569 |
0.332 |
|
| 2002 |
Nechiporuk A, Keating MT. A proliferation gradient between proximal and msxb-expressing distal blastema directs zebrafish fin regeneration. Development (Cambridge, England). 129: 2607-17. PMID 12015289 |
0.627 |
|
| 2002 |
Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, et al. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel. Circulation. 105: 794-9. PMID 11854117 DOI: 10.1161/Hc0702.105124 |
0.375 |
|
| 2002 |
Olson TM, Illenberger S, Kishimoto NY, Huttelmaier S, Keating MT, Jockusch BM. Metavinculin mutations alter actin interaction in dilated cardiomyopathy. Circulation. 105: 431-7. PMID 11815424 DOI: 10.1161/Hc0402.102930 |
0.377 |
|
| 2001 |
McGann CJ, Odelberg SJ, Keating MT. Mammalian myotube dedifferentiation induced by newt regeneration extract. Proceedings of the National Academy of Sciences of the United States of America. 98: 13699-704. PMID 11717431 DOI: 10.1073/Pnas.221297398 |
0.376 |
|
| 2001 |
Huang FD, Chen J, Lin M, Keating MT, Sanguinetti MC. Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel. Circulation. 104: 1071-5. PMID 11524404 DOI: 10.1161/Hc3501.093815 |
0.395 |
|
| 2001 |
Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating MT, Towbin JA, Beggs AH, Brink P, Wilde AA, Toivonen L, et al. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation. 103: 89-95. PMID 11136691 DOI: 10.1161/01.Cir.103.1.89 |
0.345 |
|
| 2001 |
Nechiporuk T, Urness LD, Keating MT. ETL, a novel seven-transmembrane receptor that is developmentally regulated in the heart. ETL is a member of the secretin family and belongs to the epidermal growth factor-seven-transmembrane subfamily. The Journal of Biological Chemistry. 276: 4150-7. PMID 11050079 DOI: 10.1074/Jbc.M004814200 |
0.694 |
|
| 2000 |
Odelberg SJ, Kollhoff A, Keating MT. Dedifferentiation of mammalian myotubes induced by msx1. Cell. 103: 1099-109. PMID 11163185 DOI: 10.1016/S0092-8674(00)00212-9 |
0.321 |
|
| 2000 |
Poss KD, Shen J, Keating MT. Induction of lef1 during zebrafish fin regeneration. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 219: 282-6. PMID 11002347 DOI: 10.1002/1097-0177(2000)9999:9999<::Aid-Dvdy1045>3.3.Co;2-3 |
0.601 |
|
| 2000 |
Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT. Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation. 102: 1178-85. PMID 10973849 DOI: 10.1161/01.Cir.102.10.1178 |
0.36 |
|
| 2000 |
Poss KD, Shen J, Nechiporuk A, McMahon G, Thisse B, Thisse C, Keating MT. Roles for Fgf signaling during zebrafish fin regeneration. Developmental Biology. 222: 347-58. PMID 10837124 DOI: 10.1006/Dbio.2000.9722 |
0.721 |
|
| 1999 |
Nechiporuk A, Finney JE, Keating MT, Johnson SL. Assessment of polymorphism in zebrafish mapping strains. Genome Research. 9: 1231-8. PMID 10613846 DOI: 10.1101/Gr.9.12.1231 |
0.603 |
|
| 1999 |
Franqueza L, Lin M, Shen J, Splawski I, Keating MT, Sanguinetti MC. Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits. The Journal of Biological Chemistry. 274: 21063-70. PMID 10409658 DOI: 10.1074/Jbc.274.30.21063 |
0.37 |
|
| 1999 |
Wang Z, Tristani-Firouzi M, Xu Q, Lin M, Keating MT, Sanguinetti MC. Functional effects of mutations in KvLQT1 that cause long QT syndrome. Journal of Cardiovascular Electrophysiology. 10: 817-26. PMID 10376919 DOI: 10.1111/J.1540-8167.1999.Tb00262.X |
0.394 |
|
| 1999 |
Abbott GW, Sesti F, Splawski I, Buck ME, Lehmann MH, Timothy KW, Keating MT, Goldstein SA. MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia. Cell. 97: 175-87. PMID 10219239 DOI: 10.1016/S0092-8674(00)80728-X |
0.359 |
|
| 1999 |
Chen J, Zou A, Splawski I, Keating MT, Sanguinetti MC. Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation. The Journal of Biological Chemistry. 274: 10113-8. PMID 10187793 DOI: 10.1074/Jbc.274.15.10113 |
0.377 |
|
| 1999 |
Morris CA, Mervis CB, Robinson BF, Keating MT, Lu X, Meng X, Spallone P, Dennis TR, Stock AD. Long deletions of the Williams syndrome region on chromosome 7 result in more severe mental retardation Genetics in Medicine. 1: 59-59. DOI: 10.1097/00125817-199901000-00071 |
0.316 |
|
| 1998 |
Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes. Human Genetics. 103: 590-9. PMID 9860302 DOI: 10.1007/S004390050874 |
0.36 |
|
| 1998 |
Lu X, Meng X, Morris CA, Keating MT. A novel human gene, WSTF, is deleted in Williams syndrome. Genomics. 54: 241-9. PMID 9828126 DOI: 10.1006/Geno.1998.5578 |
0.381 |
|
| 1998 |
Meng X, Lu X, Morris CA, Keating MT. A novel human gene FKBP6 is deleted in Williams syndrome. Genomics. 52: 130-7. PMID 9782077 DOI: 10.1006/Geno.1998.5412 |
0.37 |
|
| 1998 |
Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Robinson JL, Priori SG, Benhorin J, Locati EH, Towbin JA, Keating MT, Lehmann MH, Hall WJ. Influence of genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group. The New England Journal of Medicine. 339: 960-5. PMID 9753711 DOI: 10.1056/Nejm199810013391404 |
0.388 |
|
| 1998 |
Splawski I, Shen J, Timothy KW, Vincent GM, Lehmann MH, Keating MT. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1. Genomics. 51: 86-97. PMID 9693036 DOI: 10.1006/Geno.1998.5361 |
0.396 |
|
| 1998 |
Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science (New York, N.Y.). 280: 750-2. PMID 9563954 DOI: 10.1126/Science.280.5364.750 |
0.355 |
|
| 1998 |
Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, ... Keating MT, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 392: 293-6. PMID 9521325 DOI: 10.1038/32675 |
0.396 |
|
| 1997 |
Olson TM, Keating MT. Defining the molecular genetic basis of idiopathic dilated cardiomyopathy. Trends in Cardiovascular Medicine. 7: 60-3. PMID 21235865 DOI: 10.1016/S1050-1738(96)00139-9 |
0.372 |
|
| 1997 |
Keating MT. On the trail of genetic culprits in Williams syndrome. Cardiovascular Research. 36: 134-7. PMID 9463625 DOI: 10.1016/S0008-6363(97)00027-8 |
0.393 |
|
| 1997 |
Splawski I, Tristani-Firouzi M, Lehmann MH, Sanguinetti MC, Keating MT. Mutations in the hminK gene cause long QT syndrome and suppress IKs function. Nature Genetics. 17: 338-40. PMID 9354802 DOI: 10.1038/Ng1197-338 |
0.357 |
|
| 1997 |
Qian N, Frank D, O'Keefe D, Dao D, Zhao L, Yuan L, Wang Q, Keating M, Walsh C, Tycko B. The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Human Molecular Genetics. 6: 2021-9. PMID 9328465 DOI: 10.1093/Hmg/6.12.2021 |
0.352 |
|
| 1997 |
Li DY, Toland AE, Boak BB, Atkinson DL, Ensing GJ, Morris CA, Keating MT. Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis. Human Molecular Genetics. 6: 1021-8. PMID 9215670 DOI: 10.1093/Hmg/6.7.1021 |
0.35 |
|
| 1997 |
Orias M, Bray-Ward P, Curran ME, Keating MT, Desir GV. Genomic localization of the human gene for KCNA10, a cGMP-activated K channel. Genomics. 42: 33-7. PMID 9177773 DOI: 10.1006/Geno.1997.4712 |
0.335 |
|
| 1997 |
Sanguinetti MC, Keating MT. Role of delayed rectifier potassium channels in cardiac repolarization and arrhythmias News in Physiological Sciences. 12: 152-157. DOI: 10.1152/Physiologyonline.1997.12.4.152 |
0.3 |
|
| 1996 |
Keating MT, Sanguinetti MC. Pathophysiology of ion channel mutations. Current Opinion in Genetics & Development. 6: 326-33. PMID 8791523 DOI: 10.1016/S0959-437X(96)80010-4 |
0.311 |
|
| 1996 |
Sanguinetti MC, Curran ME, Spector PS, Keating MT. Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia. Proceedings of the National Academy of Sciences of the United States of America. 93: 2208-12. PMID 8700910 DOI: 10.1073/Pnas.93.5.2208 |
0.396 |
|
| 1996 |
Frangiskakis JM, Ewart AK, Morris CA, Mervis CB, Bertrand J, Robinson BF, Klein BP, Ensing GJ, Everett LA, Green ED, Pröschel C, Gutowski NJ, Noble M, Atkinson DL, Odelberg SJ, ... Keating MT, et al. LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition. Cell. 86: 59-69. PMID 8689688 DOI: 10.1016/S0092-8674(00)80077-X |
0.302 |
|
| 1996 |
Wang Q, Li Z, Shen J, Keating MT. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel. Genomics. 34: 9-16. PMID 8661019 DOI: 10.1006/Geno.1996.0236 |
0.385 |
|
| 1996 |
Dumaine R, Wang Q, Keating MT, Hartmann HA, Schwartz PJ, Brown AM, Kirsch GE. Multiple mechanisms of Na+ channel--linked long-QT syndrome. Circulation Research. 78: 916-24. PMID 8620612 DOI: 10.1161/01.Res.78.5.916 |
0.391 |
|
| 1996 |
Spector PS, Curran ME, Keating MT, Sanguinetti MC. Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides. Circulation Research. 78: 499-503. PMID 8593709 DOI: 10.1161/01.Res.78.3.499 |
0.305 |
|
| 1996 |
Keating MT. The long QT syndrome. A review of recent molecular genetic and physiologic discoveries. Medicine. 75: 1-5. PMID 8569466 DOI: 10.1097/00005792-199601000-00001 |
0.346 |
|
| 1996 |
Olson TM, Keating MT. Mapping a cardiomyopathy locus to chromosome 3p22-p25. The Journal of Clinical Investigation. 97: 528-32. PMID 8567977 DOI: 10.1172/Jci118445 |
0.36 |
|
| 1996 |
Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, ... ... Keating MT, et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genetics. 12: 17-23. PMID 8528244 DOI: 10.1038/Ng0196-17 |
0.418 |
|
| 1996 |
Priori SG, Napolitano C, Locati EH, Cantù F, Stramba-Badiale M, Keating MT, Towbin JA, Colatsky TJ, Chen LSK, Schwartz PJ. Long QT syndrome patients genetically linked to defective genes on chromosomes 11, 7 and 3 present differential response to changes in heart rate Journal of the American College of Cardiology. 27: 171-172. DOI: 10.1016/S0735-1097(96)81534-8 |
0.347 |
|
| 1995 |
Wang Q, Shen J, Li Z, Timothy K, Vincent GM, Priori SG, Schwartz PJ, Keating MT. Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia. Human Molecular Genetics. 4: 1603-7. PMID 8541846 DOI: 10.1093/Hmg/4.9.1603 |
0.392 |
|
| 1995 |
Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantù F, Towbin JA, Keating MT, Hammoude H, Brown AM, Chen LS. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy. Circulation. 92: 3381-6. PMID 8521555 DOI: 10.1161/01.Cir.92.12.3381 |
0.334 |
|
| 1995 |
Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, Moss AJ, Towbin JA, Keating MT. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 80: 805-11. PMID 7889574 DOI: 10.1016/0092-8674(95)90359-3 |
0.412 |
|
| 1995 |
Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell. 80: 795-803. PMID 7889573 DOI: 10.1016/0092-8674(95)90358-5 |
0.422 |
|
| 1995 |
Landes GM, Curran ME, Keating MT. Molecular characterization and refined genomic localization of three human potassium ion channel genes. Cytogenetics and Cell Genetics. 70: 280-4. PMID 7789190 DOI: 10.1159/000134052 |
0.305 |
|
| 1995 |
Keating MT. Genetic approaches to cardiovascular disease. Supravalvular aortic stenosis, Williams syndrome, and long-QT syndrome. Circulation. 92: 142-7. PMID 7788908 DOI: 10.1161/01.Cir.92.1.142 |
0.417 |
|
| 1995 |
Sanguinetti MC, Jiang C, Curran ME, Keating MT. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. Cell. 81: 299-307. PMID 7736582 DOI: 10.1016/0092-8674(95)90340-2 |
0.351 |
|
| 1994 |
Keating M. Elastin and vascular disease. Trends in Cardiovascular Medicine. 4: 165-169. PMID 21244882 DOI: 10.1016/1050-1738(94)90053-1 |
0.327 |
|
| 1994 |
Ewart AK, Jin W, Atkinson D, Morris CA, Keating MT. Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene. The Journal of Clinical Investigation. 93: 1071-7. PMID 8132745 DOI: 10.1172/Jci117057 |
0.38 |
|
| 1994 |
Jiang C, Atkinson D, Towbin JA, Splawski I, Lehmann MH, Li H, Timothy K, Taggart RT, Schwartz PJ, Vincent GM, Moss AJ, Keating MT. Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity Nature Genetics. 8: 141-147. PMID 7842012 DOI: 10.1038/Ng1094-141 |
0.358 |
|
| 1993 |
Ewart AK, Morris CA, Ensing GJ, Loker J, Moore C, Leppert M, Keating M. A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7. Proceedings of the National Academy of Sciences of the United States of America. 90: 3226-3230. PMID 8475063 DOI: 10.1073/Pnas.90.8.3226 |
0.33 |
|
| 1993 |
Curran M, Atkinson D, Timothy K, Vincent GM, Moss AJ, Leppert M, Keating M. Locus heterogeneity of autosomal dominant long QT syndrome. Journal of Clinical Investigation. 92: 799-803. PMID 8102381 DOI: 10.1172/Jci116653 |
0.361 |
|
| 1993 |
Curran ME, Atkinson DL, Ewart AK, Morris CA, Leppert MF, Keating MT. The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis. Cell. 73: 159-68. PMID 8096434 DOI: 10.1016/0092-8674(93)90168-P |
0.336 |
|
| 1992 |
Vincent GM, Timothy KW, Leppert M, Keating M. The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome The New England Journal of Medicine. 327: 846-852. PMID 1508244 DOI: 10.1056/Nejm199209173271204 |
0.341 |
|
| 1992 |
Keating M. Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease. Circulation. 85: 1973-1986. PMID 1350520 DOI: 10.1161/01.Cir.85.6.1973 |
0.351 |
|
| 1992 |
Curran ME, Landes GM, Keating MT. Molecular cloning, characterization, and genomic localization of a human potassium channel gene. Genomics. 12: 729-37. PMID 1349297 DOI: 10.1016/0888-7543(92)90302-9 |
0.329 |
|
| 1991 |
Keating M, Atkinson D, Dunn C, Timothy K, Vincent G, Leppert M. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene Science. 252: 704-706. PMID 1673802 DOI: 10.1126/Science.1673802 |
0.312 |
|
| 1989 |
Coughlin SR, Keating MT. The platelet-derived growth factor system. Cancer Treatment and Research. 47: 169-76. PMID 2576996 DOI: 10.1007/978-1-4613-1599-5_7 |
0.312 |
|
| 1987 |
Williams LT, Escobedo JA, Keating MT, Coughlin SR. The stimulation of paracrine and autocrine mitogenic pathways by the platelet-derived growth factor receptor. Journal of Cellular Physiology. Supplement. 27-30. PMID 2824531 DOI: 10.1002/Jcp.1041330406 |
0.303 |
|
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