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MEREDITH KOVACH, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1467147983Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (19)
Leveraging natural diversity: back through the bottleneck.
PMID 18313975·Curr Opin Plant Biol·2008
6-review
Quantification methodology for peripheral quantitative computed tomography (PQCT) data using public domain software.
PMID 15133952·Biomed Sci Instrum·2004
4-observational
Site-specific photo-cross-linking between lambda integrase and its DNA recombination target.
PMID 11827961·J Biol Chem·2002
8-other
Atrazine and increased male production by Daphnia: the importance of combining field and laboratory approaches.
PMID 18522478·Environ Toxicol Chem·2008
7-preclinical
RecA and RadA proteins of Brucella abortus do not perform overlapping protective DNA repair functions following oxidative burst.
PMID 16816190·J Bacteriol·2006
8-other
The Brucella abortus Cu,Zn superoxide dismutase is required for optimal resistance to oxidative killing by murine macrophages and wild-type virulence in experimentally infected mice.
PMID 15845493·Infect Immun·2005
7-preclinical
Magnetic resonance imaging of pulmonary lesions in guinea pigs infected with Mycobacterium tuberculosis.
PMID 15385500·Infect Immun·2004
7-preclinical
Role of catalase in the virulence of Brucella melitensis in pregnant goats.
PMID 15288933·Vet Microbiol·2004
7-preclinical
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.
PMID 15034582·Nat Genet·2004
8-other
HL-1 myocytes exhibit PKC and K(ATP) channel-dependent delta opioid preconditioning.
PMID 14559445·J Surg Res·2003
7-preclinical
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes.
PMID 12921793·Neuromuscul Disord·2003
4-observational
Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: delineation of the clinical features and review of the literature.
PMID 11920834·Am J Med Genet·2002
5-case
Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy.
PMID 11891683·Am J Med Genet·2002
5-case
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.
PMID 11749051·Mol Genet Metab·2001
8-other
Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.
PMID 11426460·Am J Med Genet·2001
5-case
An immortalized myocyte cell line, HL-1, expresses a functional delta -opioid receptor.
PMID 11112994·J Mol Cell Cardiol·2000
8-other
The Brucella abortus Lon functions as a generalized stress response protease and is required for wild-type virulence in BALB/c mice.
PMID 10672180·Mol Microbiol·2000
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
- 200 HENRY CLAY AVE
NEW ORLEANS, LA 70118 - Phone
- (504) 896-9511
Quick Facts
- NPI
- 1467147983
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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