| Faculty |
Grant Source |
Title |
| Aguirre |
NIH EY-13132 |
Models of linked Retinitis Pigmentosa |
| |
NIH EY-06855 |
Models of hereditary retinal degeneration |
| |
NIH EY-13729 |
Gene therapy for Lebers congenital amaurosis |
| |
Fdn Fighting Blindness |
Retinal Degeneration Center |
| Atchison |
NIH GM-71830 |
PcG function of YY1 in transduction and development |
| Avadhani |
NIH GM-34883 |
Evolution & function of hepatic mitochondrial P-450 |
| |
NIH CA-22762 |
Mitochondria-to-nucleus stress signaling and cancer |
| |
NIH GM-49683 |
Physiological regulators of Cyto-chrome Oxidase activity |
| Bennett |
NIH EY-17096 |
AAV- mediated gene correction in the retina |
| |
NIH EY-10820 |
Gene therapy for inherited retinal degeneration |
| |
Macula Vision Res |
Generation of animal models for Malattia |
| |
Fdn- |
Rescue of retinal degeneration in animal models using adeno-associated virus (AAV)- Mediated delivery of rod-derived cell viabilitiy factor |
| |
ITMAT |
Gene therapy for autosomal dominant polycycstic kidney disease |
| Brinster |
NIH HD-44445 |
Male germline stem cell culture and genetic modification |
| |
NIH AG-24992
|
Aging of male germline stem cells |
| Cancro |
NIH AI-54488 |
Role of BLyS in peripheral B cell survival and selection |
| Casal |
NIH AR-49817 |
A canine model for human X-linked ectodermal dysplasia |
| |
Irish Wolfhound Society |
Studies on epilepsy and primary ciliary dyskinesia |
| |
APOXIS |
Recombinant EDA-A1 to treat of canine ectodermal dysplasia |
| |
NORD |
A canine model for the Ehlers-Danlos syndrome |
| Dobrinski |
NIH RR-17359 |
Transplantation of testis stem cells in large animals |
| |
NIH HD-44780 |
Transgenic goats produced by germ cell transplantation |
| Felsburg |
NIH AI-43745 |
Gene therapy for canine X-linked SCID |
| Fraser |
NIH NS-29390 |
Gene transfer to and expression in neurons in vivo |
| |
NIH NS-33768 |
Mechanism of latency of herpes simplex virus |
| Haskins. |
NIH DK-25759 |
Animal models of mucopolysaccharidoses |
| |
NIH DK-54481 |
Gene therapy in MPS VII |
| |
NIH DK-66448 |
Retroviral vector-mediated liver gene therapy for MPS I |
| Henthorn |
NIH NS-41989 |
Molecular analysis of a canine CNS developmental defect |
| |
Canine Health Fdn |
Molecular characterization canine cystinuria and carrier test |
| |
NIH HL-18848 |
Etiology and development of congenital heart disease |
| High |
NIH HL-64190 |
Gene therapy for hemophilia |
| |
NIH HL-74124 |
Biological roles of factors X and Xa |
| |
NIH HL-78810 |
Immune responses to AAV-mediated F.IX Gene transfer |
| Hunter |
NIH A1-42334 |
Regulation of the early immune response to Toxoplasma gondii |
| |
NIH AI-62789 |
Expression and function of TLRs on T cells |
| |
NIH AI-71302 |
Role of dendritic cells in resistance to T. gondii |
| Koretzky |
NIH GM-53256 |
Novel substrates of the TCR kinase |
| |
NIH A1-58019 |
Regulation of T cell and mast cell function by DGKzeta |
| |
NIH CA-93615 |
Temporal and spatial organization of signaling complexes in T and B cells |
| |
NIH A1-61039 |
Regulation of PMN activation by SLP-76, PRAM-1 and ADAP |
| Pearce |
NIH A1-32573 |
Schistosome egg induced Th2 responses |
| |
NIH AI-53825 |
Dendritic cell function in schistosomiasis |
| Scott |
NIH AI-35914 |
Il-12 as an immunopotentiator in leishmaniasis |
| |
NIH AI-59396 |
Vaccine development in leishmaniasis |
| Stedman |
NIH NS-42874 |
Surgical approaches to systemic gene transfer |
| |
NIH NS-52476 |
Translational program for molecular therapeutics in DMD |
| |
NIH HL-64190 |
Safety & efficacy of Intravas. Del. of AAV-F.IX to skeletal muscle |
| |
NIH HL-83078 |
Translational studies in heart failure gene therapy |
| Sweeney |
NIH AR-35661 |
Myosin Isozymes in muscle |
| |
NIH AR-48931 |
Structure and function of Myosin V1 |
| |
NIH AR-48868 |
Understanding and preventing disuse atrophy |
| |
Muscular Dystr Assn |
Validation of MR imaging for clinical trails in muscular dystrophy |
| |
NIH AR-51174 |
Integration and control of molecular motors |
| |
NIH AR-52646 |
Modulation of muscle growth for the muscular dystrophies |
| |
NIH AR-48565 |
Mechanisms of Processivity in Molecular Motors |
| |
DOD- |
Duchenne muscular dystrophy translational research |
| Vite |
Ara Parseghian Fndn |
Evaluating treatment strategies for feline NPC disease |
| Wilson |
NIH HL-59407 |
DNA viruses as vectors for cardiovascular diseases |
| |
NIH HL-51746 |
AAV vectors based on new serotypes novel |
| |
NHLBI HHSN2682007 |
Gene therapy resource program |
| |
CFF R881-CR07 |
RDP COMP II |
| |
Glaxo Smith-Kline |
Creation of vector systems for gene therapy |
| Wolfe |
NIH NS-56243 |
Stem cell transplantation for neurogenetic disease |
| |
NIH NS-38690 |
AAV vector gene therapy for the CNS in MPS VII |
| |
NIH DK-63973 |
Gene transfer & NMR studies in alpha -mannosidosis brain |