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AMI ORR, MD
MD
Pediatrics Physician
NPI: 1215933742Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
65348(OH)
Research & Publications (20)
Impaired mitochondrial trafficking in Huntington's disease.
PMID 19591925·Biochim Biophys Acta·2010
6-review
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2.
PMID 19576563·Am J Hum Genet·2009
8-other
Enhanced liver regeneration following changes induced by hepatocyte-specific genetic ablation of integrin-linked kinase.
PMID 19575460·Hepatology·2009
7-preclinical
Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data.
PMID 19399176·PLoS One·2009
4-observational
Focal adhesion kinase modulates activation of NF-kappaB by flow in endothelial cells.
PMID 19587216·Am J Physiol Cell Physiol·2009
7-preclinical
The subendothelial extracellular matrix modulates JNK activation by flow.
PMID 19286608·Circ Res·2009
7-preclinical
Analysis of the functions of herpes simplex virus type 1 regulatory protein ICP0 that are critical for lytic infection and derepression of quiescent viral genomes.
PMID 19264778·J Virol·2009
8-other
Adenosine A(2A) receptor mediates microglial process retraction.
PMID 19525944·Nat Neurosci·2009
7-preclinical
Herpes simplex virus type 1 regulatory protein ICP0 aids infection in cells with a preinduced interferon response but does not impede interferon-induced gene induction.
PMID 19264774·J Virol·2009
7-preclinical
Physiological oxidative stress after arousal from hibernation in Arctic ground squirrel.
PMID 19233307·Comp Biochem Physiol A Mol Integr Physiol·2009
7-preclinical
Molecular mechanisms of collagen isotype-specific modulation of smooth muscle cell phenotype.
PMID 19023090·Arterioscler Thromb Vasc Biol·2009
7-preclinical
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
PMID 19412178·Nat Genet·2009
7-preclinical
Herpes simplex virus type 1 ICP0 phosphorylation mutants impair the E3 ubiquitin ligase activity of ICP0 in a cell type-dependent manner.
PMID 18715910·J Virol·2008
7-preclinical
Accumulation of N-terminal mutant huntingtin in mouse and monkey models implicated as a pathogenic mechanism in Huntington's disease.
PMID 18558632·Hum Mol Genet·2008
7-preclinical
STAT-1- and IRF-3-dependent pathways are not essential for repression of ICP0-null mutant herpes simplex virus type 1 in human fibroblasts.
PMID 18579584·J Virol·2008
8-other
A FRET-based method to study protein thiol oxidation in histological preparations.
PMID 18620047·Free Radic Biol Med·2008
7-preclinical
p21-activated kinase signaling regulates oxidant-dependent NF-kappa B activation by flow.
PMID 18669917·Circ Res·2008
4-observational
Liver-specific ablation of integrin-linked kinase in mice results in abnormal histology, enhanced cell proliferation, and hepatomegaly.
PMID 18846549·Hepatology·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1818 CHAPEL DR STE D
FINDLAY, OH 45840 - Phone
- (419) 424-1922
Quick Facts
- NPI
- 1215933742
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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