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PETER BROSS, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1295298628IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Education
OTHER
Class of 2019
Research & Publications (20)
Role of flavinylation in a mild variant of multiple acyl-CoA dehydrogenation deficiency: a molecular rationale for the effects of riboflavin supplementation.
PMID 19088074·J Biol Chem·2009
8-other
Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress.
PMID 19476632·Proteome Sci·2009
8-other
Drug-diagnostic codevelopment strategies: FDA and industry dialog at the 4th FDA/DIA/PhRMA/PWG/BIO Pharmacogenomics Workshop.
PMID 19102722·Pharmacogenomics·2009
8-other
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia.
PMID 19423133·J Neurol Sci·2009
8-other
Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy.
PMID 18571143·Am J Hum Genet·2008
8-other
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level.
PMID 18523805·Hum Genet·2008
4-observational
Mitochondrial fatty acid oxidation defects--remaining challenges.
PMID 18836889·J Inherit Metab Dis·2008
8-other
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13).
PMID 18378094·Neuroscience·2008
8-other
The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.
PMID 18400758·J Biol Chem·2008
8-other
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential.
PMID 17072495·J Hum Genet·2007
8-other
A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia.
PMID 17420924·J Neurol·2007
8-other
Reduced heat shock response in human mononuclear cells during aging and its association with polymorphisms in HSP70 genes.
PMID 17009593·Cell Stress Chaperones·2006
4-observational
Heat-shock protein 70 genes and human longevity: a view from Denmark.
PMID 16804002·Ann N Y Acad Sci·2006
4-observational
Measuring therapeutic response in chronic graft-versus-host disease: National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: IV. Response Criteria Working Group report.
PMID 16503494·Biol Blood Marrow Transplant·2006
6-review
Down-regulation of Hsp60 expression by RNAi impairs folding of medium-chain acyl-CoA dehydrogenase wild-type and disease-associated proteins.
PMID 15927499·Mol Genet Metab·2005
8-other
Differential degradation of variant medium-chain acyl-CoA dehydrogenase by the protein quality control proteases Lon and ClpXP.
PMID 15978546·Biochem Biophys Res Commun·2005
8-other
Protein misfolding, aggregation, and degradation in disease.
PMID 16170215·Mol Biotechnol·2005
6-review
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation.
PMID 15819894·FEBS J·2005
7-preclinical
Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships.
PMID 14728674·Eur J Biochem·2004
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1 COOPER PLZ
CAMDEN, NJ 08103 - Phone
- (800) 826-6737
Quick Facts
- NPI
- 1295298628
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 7
- Publications
- 20
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