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RANDALL HILDEBRAND, MD
MD
Orthopaedic Surgery Physician
NPI: 1770547416IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
0423683(KS)
Education
JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE
Class of 1990
Research & Publications (20)
Lidocaine protects from myocardial damage due to ischemia and reperfusion in mice by its antiapoptotic effects.
PMID 19352171·Anesthesiology·2009
4-observational
Independent protective roles for macrophage Abcg1 and Apoe in the atherosclerotic lesion development.
PMID 19217108·Atherosclerosis·2009
7-preclinical
Scavenger receptor class B type I-mediated uptake of serum cholesterol is essential for optimal adrenal glucocorticoid production.
PMID 19179307·J Lipid Res·2009
7-preclinical
Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosis.
PMID 19095997·Arterioscler Thromb Vasc Biol·2009
7-preclinical
Absence of HDL cholesteryl ester uptake in mice via SR-BI impairs an adequate adrenal glucocorticoid-mediated stress response to fasting.
PMID 18204096·J Lipid Res·2008
7-preclinical
Combined deletion of macrophage ABCA1 and ABCG1 leads to massive lipid accumulation in tissue macrophages and distinct atherosclerosis at relatively low plasma cholesterol levels.
PMID 18006857·Arterioscler Thromb Vasc Biol·2008
7-preclinical
Scavenger receptor BI facilitates the metabolism of VLDL lipoproteins in vivo.
PMID 17954936·J Lipid Res·2008
7-preclinical
Hepatic cell-specific ATP-binding cassette (ABC) transporter profiling identifies putative novel candidates for lipid homeostasis in mice.
PMID 17727861·Atherosclerosis·2008
7-preclinical
Increased oxidative stress in scavenger receptor BI knockout mice with dysfunctional HDL.
PMID 17717299·Arterioscler Thromb Vasc Biol·2007
7-preclinical
Robert Willis (1799-1878): the works of William Harvey, M. D., London 1847. A bibliographical note.
PMID 17564162·Sudhoffs Arch·2007
8-other
Bone marrow-derived multidrug resistance protein ABCB4 protects against atherosclerotic lesion development in LDL receptor knockout mice.
PMID 17560559·Cardiovasc Res·2007
7-preclinical
Expression of human OSBP-related protein 1L in macrophages enhances atherosclerotic lesion development in LDL receptor-deficient mice.
PMID 17478758·Arterioscler Thromb Vasc Biol·2007
7-preclinical
Important role for bone marrow-derived cholesteryl ester transfer protein in lipoprotein cholesterol redistribution and atherosclerotic lesion development in LDL receptor knockout mice.
PMID 17293475·Circ Res·2007
4-observational
Macrophage phospholipid transfer protein contributes significantly to total plasma phospholipid transfer activity and its deficiency leads to diminished atherosclerotic lesion development.
PMID 17170377·Arterioscler Thromb Vasc Biol·2007
7-preclinical
High-density lipoproteins and their constituent, sphingosine-1-phosphate, directly protect the heart against ischemia/reperfusion injury in vivo via the S1P3 lysophospholipid receptor.
PMID 16982942·Circulation·2006
7-preclinical
Both hepatic and extrahepatic ABCA1 have discrete and essential functions in the maintenance of plasma high-density lipoprotein cholesterol levels in vivo.
PMID 16940190·Circulation·2006
7-preclinical
Macrophage ABCG1 deletion disrupts lipid homeostasis in alveolar macrophages and moderately influences atherosclerotic lesion development in LDL receptor-deficient mice.
PMID 16857950·Arterioscler Thromb Vasc Biol·2006
7-preclinical
Macrophage ATP-binding cassette transporter A1 overexpression inhibits atherosclerotic lesion progression in low-density lipoprotein receptor knockout mice.
PMID 16456089·Arterioscler Thromb Vasc Biol·2006
7-preclinical
Attic perfection in anatomy: Bernhard Siegfried Albinus (1697-1770) and Samuel Thomas Soemmerring (1755-1830).
PMID 16320834·Ann Anat·2005
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
- 1514 K 96 HIGHWAY
GREAT BEND, KS 67530 - Phone
- (620) 792-4383
Quick Facts
- NPI
- 1770547416
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 36
- Publications
- 20
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