1 - 25 of 56 results for author:"Keating M.T." in Literature citations
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| Activin-betaA signaling is required for zebrafish fin regeneration. Jazwinska A., Badakov R., Keating M.T. Curr. Biol. 17:1390-1395(2007) · Mapped (8) |
| Transcriptional profiling of caudal fin regeneration in zebrafish. Schebesta M., Lien C.L., Engel F.B., Keating M.T. ScientificWorldJournal 6 Suppl 1:38-54(2006) · Mapped (16) |
| Gene expression analysis of zebrafish heart regeneration. Lien C.L., Schebesta M., Makino S., Weber G.J., Keating M.T. |
| CACNA1H mutations in autism spectrum disorders. Splawski I., Yoo D.S., Stotz S.C., Cherry A., Clapham D.E., Keating M.T. J. Biol. Chem. 281:22085-22091(2006) · Mapped (8) |
| Chemical modulation of receptor signaling inhibits regenerative angiogenesis in adult zebrafish. Bayliss P.E., Bellavance K.L., Whitehead G.G., Abrams J.M., Aegerter S., Robbins H.S., Cowan D.B., Keating M.T., O'Reilly T., Wood J.M. et al. Nat. Chem. Biol. 2:265-273(2006) · Mapped (6) |
| fgf20 is essential for initiating zebrafish fin regeneration. Whitehead G.G., Makino S., Lien C.L., Keating M.T. |
| Tissue inhibitor of metalloproteinase 1 regulates matrix metalloproteinase activity during newt limb regeneration. Stevenson T.J., Vinarsky V., Atkinson D.L., Keating M.T., Odelberg S.J. Dev. Dyn. 235:606-616(2006) · UniProtKB (1) |
| Generation and characterization of Sca2 (ataxin-2) knockout mice. Kiehl T.R., Nechiporuk A., Figueroa K.P., Keating M.T., Huynh D.P., Pulst S.M. Biochem. Biophys. Res. Commun. 339:17-24(2006) · Mapped (11) |
| Heat-shock protein 60 is required for blastema formation and maintenance during regeneration. Makino S., Whitehead G.G., Lien C.L., Kim S., Jhawar P., Kono A., Kawata Y., Keating M.T. Proc. Natl. Acad. Sci. U.S.A. 102:14599-14604(2005) · Mapped (3) |
| p38 MAP kinase inhibition enables proliferation of adult mammalian cardiomyocytes. Engel F.B., Schebesta M., Duong M.T., Lu G., Ren S., Madwed J.B., Jiang H., Wang Y., Keating M.T. Genes Dev. 19:1175-1187(2005) · Mapped (6) |
| Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations. Splawski I., Timothy K.W., Decher N., Kumar P., Sachse F.B., Beggs A.H., Sanguinetti M.C., Keating M.T. Proc. Natl. Acad. Sci. U.S.A. 102:8089-8096(2005) · UniProtKB (1) · Mapped (20) |
| 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. Ackerman M.J., Splawski I., Makielski J.C., Tester D.J., Will M.L., Timothy K.W., Keating M.T., Jones G., Chadha M., Burrow C.R. et al. Heart Rhythm 1:600-607(2004) · Mapped (14) |
| Normal newt limb regeneration requires matrix metalloproteinase function. Vinarsky V., Atkinson D.L., Stevenson T.J., Keating M.T., Odelberg S.J. Dev. Biol. 279:86-98(2005) · UniProtKB (4) |
| Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Splawski I., Timothy K.W., Sharpe L.M., Decher N., Kumar P., Bloise R., Napolitano C., Schwartz P.J., Joseph R.M., Condouris K. et al. |
| An intronic mutation causes long QT syndrome. Zhang L., Vincent G.M., Baralle M., Baralle F.E., Anson B.D., Benson D.W., Whiting B., Timothy K.W., Carlquist J., January C.T. et al. J. Am. Coll. Cardiol. 44:1283-1291(2004) · Mapped (14) |
| Germ cell aneuploidy in zebrafish with mutations in the mitotic checkpoint gene mps1. Poss K.D., Nechiporuk A., Stringer K.F., Lee C., Keating M.T. |
| A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. Mohler P.J., Splawski I., Napolitano C., Bottelli G., Sharpe L., Timothy K., Priori S.G., Keating M.T., Bennett V. Proc. Natl. Acad. Sci. U.S.A. 101:9137-9142(2004) · UniProtKB (1) · Mapped (9) |
| Compound mutations: a common cause of severe long-QT syndrome. Westenskow P., Splawski I., Timothy K.W., Keating M.T., Sanguinetti M.C. Circulation 109:1834-1841(2004) · UniProtKB (2) · Mapped (35) |
| Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome. Zareba W., Moss A.J., Sheu G., Kaufman E.S., Priori S., Vincent G.M., Towbin J.A., Benhorin J., Schwartz P.J., Napolitano C. et al. J. Cardiovasc. Electrophysiol. 14:1149-1153(2003) · Mapped (6) |
| GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region. Morris C.A., Mervis C.B., Hobart H.H., Gregg R.G., Bertrand J., Ensing G.J., Sommer A., Moore C.A., Hopkin R.J., Spallone P.A. et al. Am. J. Med. Genet. A 123A:45-59(2003) · Mapped (6) |
| Positional cloning of a temperature-sensitive mutant emmental reveals a role for sly1 during cell proliferation in zebrafish fin regeneration. Nechiporuk A., Poss K.D., Johnson S.L., Keating M.T. |
| Heart regeneration in zebrafish. Poss K.D., Wilson L.G., Keating M.T. Science 298:2188-2190(2002) · UniProtKB (1) |
| Mps1 defines a proximal blastemal proliferative compartment essential for zebrafish fin regeneration. Poss K.D., Nechiporuk A., Hillam A.M., Johnson S.L., Keating M.T. Development 129:5141-5149(2002) · UniProtKB (1) · Mapped (3) |
| Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia. Splawski I., Timothy K.W., Tateyama M., Clancy C.E., Malhotra A., Beggs A.H., Cappuccio F.P., Sagnella G.A., Kass R.S., Keating M.T. |
| 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. Moss A.J., Zareba W., Kaufman E.S., Gartman E., Peterson D.R., Benhorin J., Towbin J.A., Keating M.T., Priori S.G., Schwartz P.J. et al. Circulation 105:794-799(2002) · Mapped (14) |