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CHARLES VENDITTI, M.D., PH.D
M.D., PH.D
Clinical Biochemical Genetics Physician
NPI: 1376860882Individual
Specialties, Licenses & Credentials
Clinical Biochemical Genetics PhysicianPrimary
Medical Genetics — Clinical Biochemical Genetics
Code: 207SG0202X
MD068165L(PA)
Research & Publications (20)
Transient lipopolysaccharide-induced cytokine responses in the maternal serum and amniotic fluid of the guinea pig.
PMID 19286142·Am J Obstet Gynecol·2009
7-preclinical
Enamel defects and salivary methylmalonate in methylmalonic acidemia.
PMID 19143946·Oral Dis·2009
4-observational
Interruption of the Ras/MEK/ERK signaling cascade enhances Chk1 inhibitor-induced DNA damage in vitro and in vivo in human multiple myeloma cells.
PMID 18614762·Blood·2008
7-preclinical
Vorinostat synergistically potentiates MK-0457 lethality in chronic myelogenous leukemia cells sensitive and resistant to imatinib mesylate.
PMID 18505786·Blood·2008
7-preclinical
Adenovirus-mediated gene delivery rescues a neonatal lethal murine model of mut(0) methylmalonic acidemia.
PMID 18052792·Hum Gene Ther·2008
7-preclinical
Metabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscle.
PMID 17937813·BMC Med Genet·2007
7-preclinical
Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes.
PMID 17470278·BMC Med Genet·2007
7-preclinical
Large punctuational contribution of speciation to evolutionary divergence at the molecular level.
PMID 17023657·Science·2006
7-preclinical
Detecting the node-density artifact in phylogeny reconstruction.
PMID 16969939·Syst Biol·2006
4-observational
Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome.
PMID 16382448·Genes Chromosomes Cancer·2006
8-other
Identification of CT46/HORMAD1, an immunogenic cancer/testis antigen encoding a putative meiosis-related protein.
PMID 15999985·Cancer Immun·2005
7-preclinical
Identification of cancer/testis-antigen genes by massively parallel signature sequencing.
PMID 15905330·Proc Natl Acad Sci U S A·2005
4-observational
Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency.
PMID 15505378·J Inherit Metab Dis·2004
8-other
Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies.
PMID 14708100·Am J Med Genet A·2004
5-case
Patient with trisomy 9p and a hypoplastic left heart with a tricentric chromosome 9.
PMID 14608650·Am J Med Genet A·2003
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9000 ROCKVILLE PIKE NATIONAL INSTITUTES OF HEALTH, BUILDING 49 RM 4A18
BETHESDA, MD 20892 - Phone
- (301) 496-6213
Quick Facts
- NPI
- 1376860882
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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