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DAVID LOMBARD, MD, PHD
MD, PHD
Molecular Genetic Pathology (Pathology) Physician
NPI: 1649508458Individual
Specialties, Licenses & Credentials
Molecular Genetic Pathology (Pathology) PhysicianPrimary
Pathology — Molecular Genetic Pathology
Code: 207ZP0007X
ME155101(FL)
Research & Publications (20)
Novel non-sense GCH1 mutation in a South African family diagnosed with dopa-responsive dystonia.
PMID 19566901·Eur J Neurol·2010
8-other
A broad-spectrum sunscreen prevents cumulative damage from repeated exposure to sub-erythemal solar ultraviolet radiation representative of temperate latitudes.
PMID 19522775·J Eur Acad Dermatol Venereol·2010
8-other
A South African family with the mitochondrial A1555G mutation on haplogroup L0d.
PMID 19285484·Biochem Biophys Res Commun·2009
8-other
Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease.
PMID 18514563·Parkinsonism Relat Disord·2009
8-other
Calorie restriction alters mitochondrial protein acetylation.
PMID 19594485·Aging Cell·2009
7-preclinical
The sirtuin SIRT6 deacetylates H3 K56Ac in vivo to promote genomic stability.
PMID 19597350·Cell Cycle·2009
7-preclinical
A role for the NAD-dependent deacetylase Sirt1 in the regulation of autophagy.
PMID 18296641·Proc Natl Acad Sci U S A·2008
7-preclinical
Mice lacking histone deacetylase 6 have hyperacetylated tubulin but are viable and develop normally.
PMID 18180281·Mol Cell Biol·2008
7-preclinical
Mammalian Sir2 homolog SIRT3 regulates global mitochondrial lysine acetylation.
PMID 17923681·Mol Cell Biol·2007
7-preclinical
Genomic instability and aging-like phenotype in the absence of mammalian SIRT6.
PMID 16439206·Cell·2006
7-preclinical
Biological effects of simulated ultraviolet daylight: a new approach to investigate daily photoprotection.
PMID 16606411·Photodermatol Photoimmunol Photomed·2006
8-other
H2AX prevents DNA breaks from progressing to chromosome breaks and translocations.
PMID 16427010·Mol Cell·2006
7-preclinical
Mammalian SIRT1 limits replicative life span in response to chronic genotoxic stress.
PMID 16054100·Cell Metab·2005
7-preclinical
Telomere shortening exposes functions for the mouse Werner and Bloom syndrome genes.
PMID 15367665·Mol Cell Biol·2004
7-preclinical
Essential role of limiting telomeres in the pathogenesis of Werner syndrome.
PMID 15235603·Nat Genet·2004
7-preclinical
Defective DNA repair and increased genomic instability in Artemis-deficient murine cells.
PMID 12615897·J Exp Med·2003
7-preclinical
Leaky Scid phenotype associated with defective V(D)J coding end processing in Artemis-deficient mice.
PMID 12504013·Mol Cell·2002
7-preclinical
Analysis of the role of RecQ helicases in RNAi in mammals.
PMID 11883931·Biochem Biophys Res Commun·2002
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
- 1295 NW 14TH ST
MIAMI, FL 33125 - Phone
- (305) 243-1111
Quick Facts
- NPI
- 1649508458
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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