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DIEGO VALENZUELA, MD

MD

Nephrology Physician

NPI: 1609526987Individual

Specialties, Licenses & Credentials

Internal Medicine Physician

Internal Medicine

Code: 207R00000X

1609526987(IL)
Critical Care Medicine (Internal Medicine) Physician

Internal Medicine — Critical Care Medicine

Code: 207RC0200X

036.175197(IL)
Student in an Organized Health Care Education/Training Program

Student in an Organized Health Care Education/Training Program

Code: 390200000X

Nephrology PhysicianPrimary

Internal Medicine — Nephrology

Code: 207RN0300X

036.175197(IL)

Research & Publications (20)

High-throughput engineering of the mouse genome coupled with high-resolution expression analysis.
PMID 12730667·Nat Biotechnol·2003
7-preclinical
Generation and functional characterization of mice with a conditional BMP7 allele.
PMID 19247966·Int J Dev Biol·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
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
Angiomodulin is a specific marker of vasculature and regulates vascular endothelial growth factor-A-dependent neoangiogenesis.
PMID 19542015·Circ Res·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
RORgamma-expressing Th17 cells induce murine chronic intestinal inflammation via redundant effects of IL-17A and IL-17F.
PMID 18992745·Gastroenterology·2009
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.

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Contact & Hours

Address
5841 S MARYLAND AVE
CHICAGO, IL 60637

Quick Facts

NPI
1609526987
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
4
Locations
1
Publications
20

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