Back to Search
GEORGE BANKS, MD
MD
Neurology Physician
NPI: 1720449655IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD201485(OR)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 2016
Research & Publications (20)
Acetylcholine binding protein of mollusks is unlikely to act as a regulator of cholinergic neurotransmission at neurite-neurite synaptic sites in vivo.
PMID 19395478·FASEB J·2009
7-preclinical
Truncated dystrophins can influence neuromuscular synapse structure.
PMID 19171194·Mol Cell Neurosci·2009
7-preclinical
Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin.
PMID 18799475·Hum Mol Genet·2008
7-preclinical
Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain.
PMID 17588958·Hum Mol Genet·2007
7-preclinical
Neuromuscular synapses mediate motor axon branching and motoneuron survival during the embryonic period of programmed cell death.
PMID 12710958·Dev Biol·2003
7-preclinical
Elucidating the molecular mechanisms that underlie the target control of motoneuron death.
PMID 12141443·Int J Dev Biol·2002
6-review
Hormone-mediated dephosphorylation of specific histone H1 isoforms.
PMID 11479299·J Biol Chem·2001
7-preclinical
Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice.
PMID 19593442·PLoS One·2009
7-preclinical
Detection of respiratory viruses with a multiplex polymerase chain reaction assay (MultiCode-PLx Respiratory Virus Panel) in patients with hematologic malignancies.
PMID 19373660·Leuk Lymphoma·2009
8-other
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.
PMID 19351902·Proc Natl Acad Sci U S A·2009
7-preclinical
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies.
PMID 19186250·Curr Top Dev Biol·2008
6-review
TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander.
PMID 18592312·Mamm Genome·2008
6-review
Global changes in and characterization of specific sites of phosphorylation in mouse and human histone H1 Isoforms upon CDK inhibitor treatment using mass spectrometry.
PMID 18416567·J Proteome Res·2008
7-preclinical
Cytoplasmic dynein could be key to understanding neurodegeneration.
PMID 18373888·Genome Biol·2008
6-review
rAAV6-microdystrophin rescues aberrant Golgi complex organization in mdx skeletal muscles.
PMID 17714427·Traffic·2007
7-preclinical
MultiCode-PLx system for multiplexed detection of seventeen respiratory viruses.
PMID 17596361·J Clin Microbiol·2007
4-observational
Large-scale pathways-based association study in amyotrophic lateral sclerosis.
PMID 17439985·Brain·2007
8-other
Relevance of motoneuron specification and programmed cell death in embryos to therapy of ALS.
PMID 16425251·Birth Defects Res C Embryo Today·2005
6-review
Glycinergic and GABAergic synaptic activity differentially regulate motoneuron survival and skeletal muscle innervation.
PMID 15689563·J Neurosci·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3181 SW SAM JACKSON PARK RD # L-579
PORTLAND, OR 97239 - Phone
- (503) 494-8652
Quick Facts
- NPI
- 1720449655
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 10
- Publications
- 20
Are you this provider?
Claim Your Profile