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TRENTON GRIMM MD
MD
Internal Medicine Physician
NPI: 1255746509IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
125.064986(IL)
Education
SOUTHERN ILLINOIS UNIVERSITY SCHOOL OF MEDICINE
Class of 2014
Research & Publications (20)
Inhibition of NF-kappaB activation and MMP-9 secretion by plasma of human volunteers after ingestion of maritime pine bark extract (Pycnogenol).
PMID 16441890·J Inflamm (Lond)·2006
8-other
Single and multiple dose pharmacokinetics of maritime pine bark extract (pycnogenol) after oral administration to healthy volunteers.
PMID 16887024·BMC Clin Pharmacol·2006
4-observational
Antioxidant activity and inhibition of matrix metalloproteinases by metabolites of maritime pine bark extract (pycnogenol).
PMID 14990359·Free Radic Biol Med·2004
8-other
Simian immunodeficiency viruses from multiple lineages infect human macrophages: implications for cross-species transmission.
PMID 12640192·J Acquir Immune Defic Syndr·2003
7-preclinical
[Nikolaus Friedreich, the first Heidelberg "neurologist"].
PMID 11507658·Fortschr Neurol Psychiatr·2001
8-other
Congenital heart disease is a feature of severe infantile spinal muscular atrophy.
PMID 18662980·J Med Genet·2008
8-other
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.
PMID 18371931·Am J Hum Genet·2008
7-preclinical
Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy.
PMID 18348272·Am J Med Genet A·2008
5-case
PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.
PMID 19061984·Am J Hum Genet·2008
8-other
Determination of water-extractable nonstructural carbohydrates, including inulin, in grass samples with high-performance anion exchange chromatography and pulsed amperometric detection.
PMID 18698790·J Agric Food Chem·2008
8-other
A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.
PMID 17212350·Muscle Nerve·2007
8-other
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
PMID 17437276·Hum Mutat·2007
8-other
Severe periorbital edema secondary to imatinib mesylate for chronic myelogenous leukemia.
PMID 17620589·Arch Ophthalmol·2007
5-case
The BRCT domain of mammalian Pes1 is crucial for nucleolar localization and rRNA processing.
PMID 17189298·Nucleic Acids Res·2007
8-other
Interdependence of Pes1, Bop1, and WDR12 controls nucleolar localization and assembly of the PeBoW complex required for maturation of the 60S ribosomal subunit.
PMID 17353269·Mol Cell Biol·2007
7-preclinical
Modelling germline mosaicism and different new mutation rates simultaneously for appropriate risk calculations in families with Duchenne muscular dystrophy.
PMID 16626333·Ann Hum Genet·2006
8-other
Expression of calcitonin receptor-like receptor in human vascular tumours.
PMID 17021138·J Clin Pathol·2006
8-other
Mast cells and neutrophils proteolytically activate chemokine precursor CTAP-III and are subject to counterregulation by PF-4 through inhibition of chymase and cathepsin G.
PMID 16317101·Blood·2006
8-other
Dominant-negative Pes1 mutants inhibit ribosomal RNA processing and cell proliferation via incorporation into the PeBoW-complex.
PMID 16738141·Nucleic Acids Res·2006
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
- 701 N 1ST ST
SPRINGFIELD, IL 62702 - Phone
- (217) 545-0182
Quick Facts
- NPI
- 1255746509
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 12
- Publications
- 20
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