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Mohamad Navab Selected Research
Atherosclerosis (Atheroma)
02/2008
The effect of apolipoprotein mimetic peptides in inflammatory disorders other than atherosclerosis.
06/2007
Adenovirus-mediated expression of human paraoxonase 3 protects against the progression of atherosclerosis in apolipoprotein E-deficient mice.
12/2006
Adenovirus mediated expression of human paraoxonase 2 protects against the development of atherosclerosis in apolipoprotein E-deficient mice.
10/2006
Paraoxonase-2 deficiency aggravates atherosclerosis in mice despite lower apolipoprotein-B-containing lipoproteins: anti-atherogenic role for paraoxonase-2.
10/2006
Apolipoprotein A-I mimetic peptides and their role in atherosclerosis prevention.
08/2006
Proinflammatory high-density lipoprotein as a biomarker for atherosclerosis in patients with systemic lupus erythematosus and rheumatoid arthritis.
10/2005
Increased atherosclerosis in mice lacking apolipoprotein A-I attributable to both impaired reverse cholesterol transport and increased inflammation.
09/2005
Oral small peptides render HDL antiinflammatory in mice and monkeys and reduce atherosclerosis in ApoE null mice.
09/2005
An oral apoJ peptide renders HDL antiinflammatory in mice and monkeys and dramatically reduces atherosclerosis in apolipoprotein E-null mice.
01/2005
The paraoxonase gene family and atherosclerosis.
12/2004
Human apolipoprotein A-I and A-I mimetic peptides: potential for atherosclerosis reversal.
06/2004
The oxidation hypothesis of atherogenesis: the role of oxidized phospholipids and HDL.
10/2003
Oral synthetic phospholipid (DMPC) raises high-density lipoprotein cholesterol levels, improves high-density lipoprotein function, and markedly reduces atherosclerosis in apolipoprotein E-null mice.
09/2003
Human apolipoprotein AI mimetic peptides for the treatment of atherosclerosis.
04/2003
Increased low-density lipoprotein oxidation and impaired high-density lipoprotein antioxidant defense are associated with increased macrophage homing and atherosclerosis in dyslipidemic obese mice: LCAT gene transfer decreases atherosclerosis.
01/2002
Oral administration of an Apo A-I mimetic Peptide synthesized from D-amino acids dramatically reduces atherosclerosis in mice independent of plasma cholesterol.
Articles by Research Topic
Disease
16
Atherosclerosis (Atheroma)
02/2008 - 01/2002
4
Inflammation
04/2008 - 05/2005
2
Human Influenza (Influenza)
11/2004 - 08/2002
2
Infection
11/2004 - 08/2002
1
Leprosy (Hansen's Disease)
08/2008
1
Experimental Arthritis
05/2008
1
Stroke (Strokes)
03/2007
1
Rheumatoid Arthritis
08/2006
1
Systemic Lupus Erythematosus (Libman-Sacks Disease)
08/2006
1
Acute-Phase Reaction
08/2006
1
Coronary Disease (Coronary Heart Disease)
08/2002
1
Coronary Artery Disease (Coronary Atherosclerosis)
06/2002
Drug/Important Bio-Agent (IBA)
9
Apolipoprotein A-I (Apolipoprotein A1)
IBA
05/2008 - 01/2002
7
Apolipoproteins
IBA
02/2008 - 06/2002
6
Peptides
IBA
04/2008 - 09/2003
6
Lipoproteins (Lipoprotein)
IBA
04/2008 - 04/2003
5
Aryldialkylphosphatase (Paraoxonase)
IBA
06/2007 - 06/2002
2
Phospholipids
IBA
08/2008 - 06/2004
2
HDL Cholesterol
IBA
03/2007 - 10/2003
2
Cholesterol
IBA
10/2005 - 01/2002
1
Pravastatin (Pravachol)
FDA Link
Generic
05/2008
1
Messenger RNA (mRNA)
IBA
01/2008
1
LDL Receptors (LDL Receptor)
IBA
01/2008
1
Sterol Regulatory Element Binding Protein 1
IBA
01/2008
1
HDL Lipoproteins
IBA
08/2006
1
Apolipoproteins E (ApoE)
IBA
09/2005
1
Dimyristoylphosphatidylcholine (DMPC)
IBA
10/2003
1
Lipids
IBA
08/2002
1
Amino Acids
FDA Link
01/2002