Lab Reagents and Resources
Prediman Krishan Shah, MD, and Behrooz Sharifi, PhD, resources for current animal models developed for atherosclerosis research:
- Mouse Model for Myocardial Infarction
- Aortic Construction: A Technique to Produce Left Ventricular Hypertrophy in Mice
- Mouse Cervical Cardiac Transplantation
- Artery Injury Model for Atherosclerosis
- Directed Vascular Graft Regeneration in Mice Peritoneal Cavity
- Peritoneal Cavity Bone Marrow Transplantation for Gene Therapy and Atherosclerosis
Shah and Sharifi resources for knock-out mouse models:
- Tenascin-C (TNC) KO
- Pleiotrophin (PTN) KO
- GATA3 Gene Conditional (GATA3) KO
- Krüppel-like Factor 14 (KLF14) KO
- Apolipoprotein E / Apolipoprotein A1 (ApoE/ApoA1) KO
- Delta DBL GATA KO (Eosinophils KO)
- Eotaxin 1,2 KO
- C57 BL6-Tg (Marfia)
Shah clinical protocols:
- A Multicenter, Open-label Study to Assess the Long-term Safety, Tolerability, and Efficacy of AMG 145 on LDL-C in Subjects with Severe Familial Hypercholesterolemia (TAUSSIG: Trial Assessing long-term USe of PCSK9 Inhibition in Subject with Genetic LDL Disorders; Protocol 20110271)
- A Double-blind, Randomized, Multicenter Study to Evaluate the Safety and Efficacy of AMG 145, Compared With Ezetimibe, in Hypercholesterolemic Subjects Unable to Tolerate an Effective Dose of a HMG-CoA Reductase Inhibitor Due to Muscle Related Side Effects (Protocol 20120332;GAUSS-3)
- Open-Label Extension Study of EFC12492, R727-CL1112, EFC12732 & LTS11717 Studies to Assess the Long-Term Safety and Efficacy of Alirocumab in Patients with Heterozygous Familial Hypercholesterolemia
- LOWER: Lomitapide Observational Worldwide Evaluation Registry
- A Multicenter, Controlled, Open-Label Extension (OLE) Study to Assess the Long-term Safety and Efficacy of AMG 145 (Protocol 20120138; OSLER-2 Open Label Study of Long-Term Evaluation Against LDL-C Trial)
Kuang-Yuh Chyu, MD, PhD, and Paul Dimayuga, PhD, resources for current animal studies developed for atherosclerosis research:
- Role of Cathelin-Related Anti-Microbial Peptide (CRAMP)-specific CD8+ T cells in atherosclerosis
- Role of CD8+ regulatory T cells in atherosclerosis
- Comparison of 15 ApoB-100 peptide based vaccines
- Role of DC in ApoB-100 peptide vaccine
- Effect of p210 based immunization on AAA and hypertension
- Effect of lipid lowering on immune function in ApoE (-/-) mice
- Screening for efficacy of different formulations of p210 vaccine
- Role of CD8+ T regulatory cells in the protective effect of a peptide vaccine against atherosclerosis
- Effect of immunization with an ApoB-100 peptide, p210, on Kawasaki disease (KD) vasculitis
- Efficacy of immunization with p210-based vaccines in modulating transplant vasculopathy
- Characterization of p210 specific CD8+ T cells in murine and human atherosclerosis
- Development of accelerated atherosclerosis in an SLE model in ApoE (-/-) mice
- Characterization of immune responses to p210 vaccines in murine model of atherosclerosis
- Atherosclerotic mouse model transgenic for Class-I HLA0201
- Discovery and screening of peptide self-antigens in coronary artery disease
Contact the Shah Lab
127 S. San Vicente Blvd.
Advanced Health Sciences Pavilion, 9th Floor
Los Angeles, CA 90048