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MARTIKA PERCY, MD

MD

Student in an Organized Health Care Education/Training Program

NPI: 1225615891Individual

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)

Characterization of an NF-kappaB-regulated, miRNA-146a-mediated down-regulation of complement factor H (CFH) in metal-sulfate-stressed human brain cells.
PMID 19540598·J Inorg Biochem·2009
8-other
Erythrocytosis-associated HIF-2alpha mutations demonstrate a critical role for residues C-terminal to the hydroxylacceptor proline.
PMID 19208626·J Biol Chem·2009
8-other
Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis.
PMID 19006225·Am J Hematol·2009
6-review
Thrombospondins 1 and 2 are necessary for synaptic plasticity and functional recovery after stroke.
PMID 18594557·J Cereb Blood Flow Metab·2008
7-preclinical
Stages of smoking acquisition of young Taiwanese adolescents: self-efficacy and decisional balance.
PMID 18213639·Res Nurs Health·2008
8-other
Familial erythrocytosis: molecular links to red blood cell control.
PMID 18591620·Haematologica·2008
8-other
Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis.
PMID 18378852·Blood·2008
5-case
NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I.
PMID 18820099·J Clin Pathol·2008
5-case
G protein-coupled receptors disrupted in human genetic disease.
PMID 18370233·Methods Mol Biol·2008
6-review
Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.
PMID 18318771·Br J Haematol·2008
6-review
Involvement of ApoE E4 and H63D in sporadic Alzheimer's disease in a folate-supplemented Ontario population.
PMID 18525129·J Alzheimers Dis·2008
8-other
Metal sulfate-mediated induction of pathogenic genes and repression by phenyl butyl nitrone and Feralex-G.
PMID 18185117·Neuroreport·2008
8-other
A gain-of-function mutation in the HIF2A gene in familial erythrocytosis.
PMID 18184961·N Engl J Med·2008
5-case
Mutation of the von Hippel-Lindau gene alters human cardiopulmonary physiology.
PMID 18085246·Adv Exp Med Biol·2008
8-other
Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway.
PMID 18711622·Ulster Med J·2008
6-review
Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell disease.
PMID 17724704·Am J Hematol·2008
8-other
Genetically heterogeneous origins of idiopathic erythrocytosis.
PMID 17454194·Hematology·2007
6-review
A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove.
PMID 17579185·Blood·2007
5-case
Is congenital secondary erythrocytosis/polycythemia caused by activating mutations within the HIF-2 alpha iron-responsive element?
PMID 17881647·Blood·2007
8-other
The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels.
PMID 18055983·Haematologica·2007
4-observational

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
MSC08 4640 1 UNIVERSITY OF NEW MEXICO
ALBUQUERQUE, NM 87131

Location

Practice Location

MSC08 4640 1 UNIVERSITY OF NEW MEXICO, ALBUQUERQUE, NM
(505) 272-4814

Quick Facts

NPI
1225615891
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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