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American Journal of Medical Genetics. Part A
|
August 6, 2008
Novel SCN1A frameshift mutation with absence of truncated Nav1.1 protein in severe myoclonic epilepsy of infancy
Erin J McArdle, Jennifer D Kunic, Alfred L George
FEBS Letters
|
October 26, 2005
Functional zinc finger/sleeping beauty transposase chimeras exhibit attenuated overproduction inhibition
Matthew H Wilson, Joseph M Kaminski, Alfred L George
The Journal of Biological Chemistry
|
January 18, 2021
Cryptic prokaryotic promoters explain instability of recombinant neuronal sodium channels in bacteria
Jean-Marc DeKeyser, Christopher H Thompson, Alfred L George
Epilepsia
|
May 16, 2008
Impaired NaV1.2 function and reduced cell surface expression in benign familial neonatal-infantile seizures
Sunita N Misra, Kristopher M Kahlig, Alfred L George
Biotechniques
|
August 19, 2007
Improved DNA sequencing quality and efficiency using an optimized fast cycle sequencing protocol
Adam R Platt, Robert W Woodhall, Alfred L George
Channels (Austin, Tex.)
|
August 12, 2008
Exaggerated Mg2+ inhibition of Kir2.1 as a consequence of reduced PIP2 sensitivity in Andersen syndrome
Leomar Y Ballester, Carlos G Vanoye, Alfred L George
Heart Rhythm
|
April 27, 2005
Congenital long QT syndrome aggravated by salt-wasting nephropathy
Dawood Darbar, Saba Sile, Frank A Fish, et al.
Journal of Cardiovascular Pharmacology
|
October 28, 2011
Nadolol block of Nav1.5 does not explain its efficacy in the long QT syndrome
Alessandra Besana, Dao W Wang, Alfred L George, et al.
Anesthesiology
|
November 26, 2003
Tissue factor and platelet glycoprotein Ib-alpha alleles are associated with age at first coronary bypass operation
Brian S Donahue, Daniel W Byrne, David Gailani, et al.
Genomics
|
February 19, 2005
Coupled analysis of gene expression and chromosomal location
Yajun Yi, Janni Mirosevich, Yu Shyr, et al.
Page
of 30
Search research articles
Search
Showing results (41-50 of 296) with videos related to
Sort By:
Page
of 30
American Journal of Medical Genetics. Part A
|
August 6, 2008
Novel SCN1A frameshift mutation with absence of truncated Nav1.1 protein in severe myoclonic epilepsy of infancy
Erin J McArdle, Jennifer D Kunic, Alfred L George
FEBS Letters
|
October 26, 2005
Functional zinc finger/sleeping beauty transposase chimeras exhibit attenuated overproduction inhibition
Matthew H Wilson, Joseph M Kaminski, Alfred L George
The Journal of Biological Chemistry
|
January 18, 2021
Cryptic prokaryotic promoters explain instability of recombinant neuronal sodium channels in bacteria
Jean-Marc DeKeyser, Christopher H Thompson, Alfred L George
Epilepsia
|
May 16, 2008
Impaired NaV1.2 function and reduced cell surface expression in benign familial neonatal-infantile seizures
Sunita N Misra, Kristopher M Kahlig, Alfred L George
Biotechniques
|
August 19, 2007
Improved DNA sequencing quality and efficiency using an optimized fast cycle sequencing protocol
Adam R Platt, Robert W Woodhall, Alfred L George
Channels (Austin, Tex.)
|
August 12, 2008
Exaggerated Mg2+ inhibition of Kir2.1 as a consequence of reduced PIP2 sensitivity in Andersen syndrome
Leomar Y Ballester, Carlos G Vanoye, Alfred L George
Heart Rhythm
|
April 27, 2005
Congenital long QT syndrome aggravated by salt-wasting nephropathy
Dawood Darbar, Saba Sile, Frank A Fish, et al.
Journal of Cardiovascular Pharmacology
|
October 28, 2011
Nadolol block of Nav1.5 does not explain its efficacy in the long QT syndrome
Alessandra Besana, Dao W Wang, Alfred L George, et al.
Anesthesiology
|
November 26, 2003
Tissue factor and platelet glycoprotein Ib-alpha alleles are associated with age at first coronary bypass operation
Brian S Donahue, Daniel W Byrne, David Gailani, et al.
Genomics
|
February 19, 2005
Coupled analysis of gene expression and chromosomal location
Yajun Yi, Janni Mirosevich, Yu Shyr, et al.
Page
of 30