Chloride channels and endocytosis: ClC-5 makes a Dent

por George, Alfred L.
Publicado em 1998

Inherited Channelopathies Associated with Epilepsy

por George, Alfred L.
Publicado em 2004

Inherited disorders of voltage-gated sodium channels

por George, Alfred L.
Publicado em 2005

Restoring Repolarization in LQT3

por George, Alfred L.
Publicado em 2008

Genetic Modulation of Impaired Cardiac Conduction – Sodium Channel β(4) Subunit Missing in Action

por George, Alfred L.
Publicado em 2009

Common Genetic Variants in Sudden Cardiac Death

por George, Alfred L.
Publicado em 2009

Association of a Common KCNE1 Variant with Heart Failure

por George, Alfred L.
Publicado em 2009

Leaky channels make weak muscles

por George, Alfred L.
Publicado em 2012

Molecular and genetic basis of sudden cardiac death

por George, Alfred L.
Publicado em 2013

Recent Genetic Discoveries Implicating Ion Channels in Human Cardiovascular Diseases

por George, Alfred L.
Publicado em 2013

Use of Contemporary Genetics in Cardiovascular Diagnosis

por George, Alfred L.
Publicado no Circulation (2014)

Mink Subdomains That Mediate Modulation of and Association with Kvlqt1

por Tapper, Andrew R., George, Alfred L.
Publicado em 2000

Functional characterization of recombinant human ClC-4 chloride channels in cultured mammalian cells

por Vanoye, Carlos G, George, Alfred L
Publicado em 2002

Pharmacogenomics in Pregnancy

por Betcher, Hannah K., George, Alfred L.
Publicado no Semin Perinatol (2020)

Independent Versus Coupled Inactivation in Sodium Channels : Role of the Domain 2 S4 Segment

por Mitrovic, Nenad, George, Alfred L., Horn, Richard
Publicado em 1998

Role of Domain 4 in Sodium Channel Slow Inactivation

por Mitrovic, Nenad, George, Alfred L., Horn, Richard
Publicado em 2000

Mechanism of Ion Permeation in Skeletal Muscle Chloride Channels

por Fahlke, Christoph, Dürr, Christine, George, Alfred L.
Publicado em 1997

New Approaches to Establish Genetic Causality

por McNally, Elizabeth M., George, Alfred L.
Publicado no Trends Cardiovasc Med (2015)

A mutation in autosomal dominant myotonia congenita affects pore properties of the muscle chloride channel

por Fahlke, Christoph, Beck, Carol L., George, Alfred L.
Publicado em 1997

Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I

por Green, Donnella S, George, Alfred L, Cannon, Stephen C
Publicado em 1998