-Alfred L George Researcher Activity Profile

Research Author Detailed Information 

Alfred L George Publication Rate By Year

Alfred L George has published 5 paper(s) in 2006, 15 paper(s) in 2007, 7 paper(s) in 2008, for a total of 27 research publications in total.

Alfred L Al George Author Information

LAST NAME: george

FIRST NAME: Alfred L

INITIALS: al

AFFILIATION:

Papers

Alfred L George's Publication Record

1. Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome. Year Published: 2006
Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37027-0275, USA.
2. Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy. Year Published: 2006
Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, Tennessee 37232-0275, USA.
3. Impaired inactivation gate stabilization predicts increased persistent current for an epilepsy-associated SCN1A mutation. Year Published: 2006
Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, Tennessee 37232-0275, USA.
4. PiggyBac Transposon-mediated Gene Transfer in Human Cells. Year Published: 2006
1Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
5. Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome. Year Published: 2007
Department of Biochemistry, Center for Structural Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-8725, USA.
6. Improved DNA sequencing quality and efficiency using an optimized fast cycle sequencing protocol. Year Published: 2007
Vanderbilt University, Nashville, TN 37232, USA.
7. Antiviral effect of orally administered (-)-beta-D-2-aminopurine dioxolane in woodchucks with chronic woodchuck hepatitis virus infection. Year Published: 2007
Gastrointestinal Unit, Department of Clinical Sciences, College of Veterinary Medicine, Room C-2005 VMC, Cornell University, Ithaca, NY 14853, USA. sm119@cornell.edu
8. Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption. Year Published: 2007
Department of Medicine, Vanderbilt University, Nashville, Tenn 37232-0275, USA. saba.sile@vanderbilt.edu
9. Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome. Year Published: 2007
Department of Biochemistry, Center for Structural Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-8725, USA.
10. Functional BSND variants in essential hypertension. Year Published: 2007
Department of Medicine, Vanderbilt University, Nashville, Tennessee 37232-0275, USA. saba.sile@vanderbilt.edu
11. Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function. Year Published: 2007
Department of Physiology and Cellular Biophysics, Clyde and Helen Wu Center for Molecular Cardiology, College of Physicians and Surgeons of Columbia University, P&S 9-401 box 22, 630 W 168 St, New York, NY 10032, USA. sel2004@columbia.edu
12. Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption. Year Published: 2007
Department of Medicine, Vanderbilt University, Nashville, Tenn 37232-0275, USA. saba.sile@vanderbilt.edu
13. Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function. Year Published: 2007
Department of Physiology and Cellular Biophysics, Clyde and Helen Wu Center for Molecular Cardiology, College of Physicians and Surgeons of Columbia University, P&S 9-401 box 22, 630 W 168 St, New York, NY 10032, USA. sel2004@columbia.edu
14. Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome. Year Published: 2007
Department of Biochemistry, Center for Structural Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-8725, USA.
15. Strategy for encoding and comparison of gene expression signatures. Year Published: 2008
Department of Medicine, Garland Avenue, Vanderbilt University, Nashville, Tennessee 37232-0275,USA. yajun.yi@vanderbilt.edu.
16. Antiviral effect of orally administered (-)-beta-D-2-aminopurine dioxolane in woodchucks with chronic woodchuck hepatitis virus infection. Year Published: 2007
Gastrointestinal Unit, Department of Clinical Sciences, College of Veterinary Medicine, Room C-2005 VMC, Cornell University, Ithaca, NY 14853, USA. sm119@cornell.edu
17. Preparation, functional characterization, and NMR studies of human KCNE1, a voltage-gated potassium channel accessory subunit associated with deafness and long QT syndrome. Year Published: 2007
Department of Biochemistry, Center for Structural Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-8725, USA.
18. Strategy for encoding and comparison of gene expression signatures. Year Published: 2008
Department of Medicine, Garland Avenue, Vanderbilt University, Nashville, Tennessee 37232-0275,USA. yajun.yi@vanderbilt.edu.
19. Structural models for the KCNQ1 voltage-gated potassium channel. Year Published: 2007
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37232-8725, USA.
20. Functional BSND variants in essential hypertension. Year Published: 2007
Department of Medicine, Vanderbilt University, Nashville, Tennessee 37232-0275, USA. saba.sile@vanderbilt.edu
21. Strategy for encoding and comparison of gene expression signatures. Year Published: 2008
Department of Medicine, Vanderbilt University, Nashville, Tennessee 37232-0275, USA.
22. Structural models for the KCNQ1 voltage-gated potassium channel. Year Published: 2007
Department of Biochemistry, Vanderbilt University, Nashville, Tennessee 37232-8725, USA.
23. Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia. Year Published: 2008
Department of Medicine, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.
24. Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted rats. Year Published: 2008
Department of Pharmacobiology, Faculty of Pharmacy, University of Bari, via Orabona no 4, 70120 Bari, Italy. dtricarico@farmbiol.uniba.it
25. Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome. Year Published: 2008
Section of Cardiology, Department of Lung, Blood and Heart, University of Pavia, Pavia, Italy.
26. Fibrocystin/polyductin modulates renal tubular formation by regulating polycystin-2 expression and function. Year Published: 2008
Division of Genetic Medicine, Department of Medicine and Cell and Developmental Biology, Vanderbilt University, 539 LH, 2215 Garland Avenue, Nashville, TN 37232, USA.
27. PiggyBac transposon-mediated gene transfer in human cells. Year Published: 2006
1Division of Genetic Medicine, Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.