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CHRISTINA RAMAN, M.D.
M.D.
Pediatrics Physician
NPI: 1699917294Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
15103(NV)
Research & Publications (20)
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
PMID 19409525·Am J Hum Genet·2009
8-other
Increased numbers of thymic and peripheral CD4+ CD25+Foxp3+ cells in the absence of CD5 signaling.
PMID 19609976·Eur J Immunol·2009
7-preclinical
Subcellular localization of transporters along the rat blood-brain barrier and blood-cerebral-spinal fluid barrier by in vivo biotinylation.
PMID 18619525·Neuroscience·2008
7-preclinical
Expression of the thyroid hormone transporters monocarboxylate transporter-8 (SLC16A2) and organic ion transporter-14 (SLCO1C1) at the blood-brain barrier.
PMID 18687783·Endocrinology·2008
7-preclinical
Lithium prevents and ameliorates experimental autoimmune encephalomyelitis.
PMID 18566399·J Immunol·2008
7-preclinical
CD5 plays an inhibitory role in the suppressive function of murine CD4(+) CD25(+) T(reg) cells.
PMID 18573278·Immunol Lett·2008
7-preclinical
Structural insights into the evolutionary paths of oxylipin biosynthetic enzymes.
PMID 18716621·Nature·2008
7-preclinical
Macromolecule release from monodisperse PLG microspheres: control of release rates and investigation of release mechanism.
PMID 17455338·J Pharm Sci·2007
8-other
MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II.
PMID 17666408·Hum Mol Genet·2007
8-other
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
PMID 17994018·Nat Genet·2007
8-other
A new mutation within the porphobilinogen deaminase gene leading to a truncated protein as a cause of acute intermittent porphyria in an extended Indian family.
PMID 18070416·Folia Biol (Praha)·2007
8-other
De Novo mutation found in the porphobilinogen deaminase gene in Slovak acute intermittent porphyria patient: molecular biochemical study.
PMID 17298218·Physiol Res·2006
5-case
CD5-CK2 binding/activation-deficient mice are resistant to experimental autoimmune encephalomyelitis: protection is associated with diminished populations of IL-17-expressing T cells in the central nervous system.
PMID 17142752·J Immunol·2006
7-preclinical
Analogies and surprising differences between recombinant nitric oxide synthase-like proteins from Staphylococcus aureus and Bacillus anthracis in their interactions with l-arginine analogs and iron ligands.
PMID 17084900·J Inorg Biochem·2006
8-other
Dynamics of NO rebinding to the heme domain of NO synthase-like proteins from bacterial pathogens.
PMID 16690332·Nitric Oxide·2006
8-other
Structural basis of hereditary coproporphyria.
PMID 16176984·Proc Natl Acad Sci U S A·2005
4-observational
Critical requirement of CD11b (Mac-1) on T cells and accessory cells for development of experimental autoimmune encephalomyelitis.
PMID 16272284·J Immunol·2005
7-preclinical
Requirement of the Fc receptor common gamma-chain for gamma delta T cell-mediated promotion of murine experimental autoimmune encephalomyelitis.
PMID 16278814·Eur J Immunol·2005
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 6350 MAE ANNE AVE STE 3
RENO, NV 89523 - Phone
- (775) 624-6350
Quick Facts
- NPI
- 1699917294
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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