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DAVID VALENZUELA, MD

MD

Diagnostic Radiology Physician

NPI: 1184937021Individual

Specialties, Licenses & Credentials

Student in an Organized Health Care Education/Training Program

Student in an Organized Health Care Education/Training Program

Code: 390200000X

Diagnostic Radiology PhysicianPrimary

Radiology — Diagnostic Radiology

Code: 2085R0202X

51673(AZ)

CMS Specialties

PrimaryDIAGNOSTIC RADIOLOGY

Education

UNIVERSITY OF SOUTHERN CALIFORNIA KECK SCHOOL OF MEDICINE

Class of 2010

Research & Publications (20)

Connective tissue growth factor (CTGF) inactivation leads to defects in islet cell lineage allocation and beta-cell proliferation during embryogenesis.
PMID 19131512·Mol Endocrinol·2009
7-preclinical
During muscle atrophy, thick, but not thin, filament components are degraded by MuRF1-dependent ubiquitylation.
PMID 19506036·J Cell Biol·2009
7-preclinical
RORgamma-expressing Th17 cells induce murine chronic intestinal inflammation via redundant effects of IL-17A and IL-17F.
PMID 18992745·Gastroenterology·2009
7-preclinical
Angiomodulin is a specific marker of vasculature and regulates vascular endothelial growth factor-A-dependent neoangiogenesis.
PMID 19542015·Circ Res·2009
7-preclinical
Alternatively activated macrophage-derived RELM-{alpha} is a negative regulator of type 2 inflammation in the lung.
PMID 19349464·J Exp Med·2009
7-preclinical
VelociMouse: fully ES cell-derived F0-generation mice obtained from the injection of ES cells into eight-cell-stage embryos.
PMID 19266341·Methods Mol Biol·2009
7-preclinical
Generation and functional characterization of mice with a conditional BMP7 allele.
PMID 19247966·Int J Dev Biol·2009
7-preclinical
Unique functions of the type II interleukin 4 receptor identified in mice lacking the interleukin 13 receptor alpha1 chain.
PMID 18066066·Nat Immunol·2008
7-preclinical
Puromycin-sensitive aminopeptidase limits MHC class I presentation in dendritic cells but does not affect CD8 T cell responses during viral infections.
PMID 18209067·J Immunol·2008
7-preclinical
The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome.
PMID 18353862·Development·2008
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
2323 W Rose Garden Ln
Phoenix, AZ 85027

Locations (2)

Practice Location

2323 W Rose Garden Ln, Phoenix, AZ
(602) 521-6252

Practice Location

3501 N SCOTTSDALE RD STE 130, SCOTTSDALE, AZ
(480) 425-5000

Quick Facts

NPI
1184937021
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
2
Years in Practice
16
Publications
20

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