Back to Search
CHRISTOPHER ACQUAVIVA, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1831991629Individual
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 (20)
Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.
PMID 19479957·Hum Mutat·2009
6-review
The centrosomal FOP protein is required for cell cycle progression and survival.
PMID 19305129·Cell Cycle·2009
7-preclinical
UbcH10 has a rate-limiting role in G1 phase but might not act in the spindle checkpoint or as part of an autonomous oscillator.
PMID 18559889·J Cell Sci·2008
8-other
JunB breakdown in mid-/late G2 is required for down-regulation of cyclin A2 levels and proper mitosis.
PMID 18391017·Mol Cell Biol·2008
8-other
Carglumic acid: an additional therapy in the treatment of organic acidurias with hyperammonemia?
PMID 18234091·Orphanet J Rare Dis·2008
5-case
Submicroscopic bone marrow involvement in isolated extramedullary relapses in childhood acute lymphoblastic leukemia: a more precise definition of "isolated" and its possible clinical implications, a collaborative study of the Resistant Disease Committee of the International BFM study group.
PMID 17720883·Blood·2007
4-observational
The prognostic significance of CDKN2A, CDKN2B and MTAP inactivation in B-lineage acute lymphoblastic leukemia of childhood. Results of the EORTC studies 58881 and 58951.
PMID 16818274·Haematologica·2006
8-other
Prenatal diagnosis of guanidinoacetate methyltransferase deficiency: increased guanidinoacetate concentrations in amniotic fluid.
PMID 16595836·Clin Chem·2006
8-other
Electron transfer flavoprotein deficiency: functional and molecular aspects.
PMID 16510302·Mol Genet Metab·2006
8-other
A case of pyruvate carboxylase deficiency with atypical clinical and neuroradiological presentation.
PMID 16325442·Mol Genet Metab·2006
5-case
Single-nucleotide polymorphism phylotyping of Escherichia coli.
PMID 16085876·Appl Environ Microbiol·2005
8-other
Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene.
PMID 15643616·Hum Mutat·2005
8-other
The anaphase promoting complex/cyclosome is recruited to centromeres by the spindle assembly checkpoint.
PMID 15322556·Nat Cell Biol·2004
8-other
c-Fos proto-oncoprotein is degraded by the proteasome independently of its own ubiquitinylation in vivo.
PMID 14517309·Mol Cell Biol·2003
8-other
CDKN2A, CDKN2B, and MTAP gene dosage permits precise characterization of mono- and bi-allelic 9p21 deletions in childhood acute lymphoblastic leukemia.
PMID 12661005·Genes Chromosomes Cancer·2003
4-observational
WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour.
PMID 12637656·Nephrol Dial Transplant·2003
5-case
The structural determinants responsible for c-Fos protein proteasomal degradation differ according to the conditions of expression.
PMID 12629509·Oncogene·2003
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
- TIDELANDS HEALTH FAMILY MEDICINE, 4320 HOLMESTOWN ROAD
MYRTLE BEACH, SC 29588 - Phone
- (843) 652-8440
Quick Facts
- NPI
- 1831991629
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile