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Literature DB >> 15928072

Biography of Mark T. Keating.

Regina Nuzzo.

Abstract

Mesh：

Year: 2005 PMID： 15928072 PMCID： PMC1149450 DOI： 10.1073/pnas.0503300102

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

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References

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13 in total

1. Heart regeneration in zebrafish.

Authors: Kenneth D Poss; Lindsay G Wilson; Mark T Keating
Journal: Science Date: 2002-12-13 Impact factor: 47.728

2. Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.

Authors: Igor Splawski; Katherine W Timothy; Niels Decher; Pradeep Kumar; Frank B Sachse; Alan H Beggs; Michael C Sanguinetti; Mark T Keating
Journal: Proc Natl Acad Sci U S A Date: 2005-04-29 Impact factor: 11.205

3. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.

Authors: M Keating; D Atkinson; C Dunn; K Timothy; G M Vincent; M Leppert
Journal: Science Date: 1991-05-03 Impact factor: 47.728

4. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

Authors: A K Ewart; C A Morris; D Atkinson; W Jin; K Sternes; P Spallone; A D Stock; M Leppert; M T Keating
Journal: Nat Genet Date: 1993-09 Impact factor: 38.330

5. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.

Authors: Igor Splawski; Katherine W Timothy; Leah M Sharpe; Niels Decher; Pradeep Kumar; Raffaella Bloise; Carlo Napolitano; Peter J Schwartz; Robert M Joseph; Karen Condouris; Helen Tager-Flusberg; Silvia G Priori; Michael C Sanguinetti; Mark T Keating
Journal: Cell Date: 2004-10-01 Impact factor: 41.582

Biography of Mark T. Keating.

1. Heart regeneration in zebrafish.

2. Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.

3. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.

4. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

5. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.

6. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.

Review 7. A new form of long QT syndrome associated with syndactyly.

8. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.

9. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.

10. A proliferation gradient between proximal and msxb-expressing distal blastema directs zebrafish fin regeneration.