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STEVEN CURRAN, M.D.
M.D.
Family Medicine Physician
NPI: 1871688861IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
G64923(CA)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1987
Research & Publications (20)
Lifespan regulation by evolutionarily conserved genes essential for viability.
PMID 17411345·PLoS Genet·2007
7-preclinical
Endorectal MRI of prostatic and periprostatic cystic lesions and their mimics.
PMID 17449785·AJR Am J Roentgenol·2007
8-other
Oxygen transport and cell viability in an annular flow bioreactor: comparison of laminar Couette and Taylor-vortex flow regimes.
PMID 15696514·Biotechnol Bioeng·2005
4-observational
Process evaluation of a store-based environmental obesity intervention on two American Indian Reservations.
PMID 15872001·Health Educ Res·2005
8-other
The role of Hot13p and redox chemistry in the mitochondrial TIM22 import pathway.
PMID 15294910·J Biol Chem·2004
8-other
Defective mitochondrial protein translocation precludes normal Caenorhabditis elegans development.
PMID 15485840·J Biol Chem·2004
7-preclinical
The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins.
PMID 12221072·J Cell Biol·2002
8-other
The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier.
PMID 11867522·EMBO J·2002
8-other
"The psychiatrist will be with you in a day or two". Unnecessary delays in assessing the mentally ill in police custody in Scotland.
PMID 11394334·Scott Med J·2001
8-other
Massive visceral pentastomiasis caused by Porocephalus crotali in a dog.
PMID 19176495·Vet Pathol·2009
5-case
A soma-to-germline transformation in long-lived Caenorhabditis elegans mutants.
PMID 19506556·Nature·2009
7-preclinical
A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.
PMID 19116236·J Clin Endocrinol Metab·2009
8-other
Allelic depletion of grem1 attenuates diabetic kidney disease.
PMID 19401426·Diabetes·2009
7-preclinical
A common variant in DRD3 receptor is associated with autism spectrum disorder.
PMID 19058789·Biol Psychiatry·2009
8-other
Drug-associated linear IgA disease mimicking toxic epidermal necrolysis.
PMID 19077099·Clin Exp Dermatol·2009
5-case
Isolation of lactobacilli with probiotic properties from the human stomach.
PMID 19241519·Lett Appl Microbiol·2008
8-other
The role of HLA-DQ8 beta57 polymorphism in the anti-gluten T-cell response in coeliac disease.
PMID 19037317·Nature·2008
7-preclinical
Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.
PMID 19125863·Genes Brain Behav·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 46690 MOHAVE DR
FREMONT, CA 94539 - Phone
- (510) 248-1065
Quick Facts
- NPI
- 1871688861
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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