Welcome to the California Institute for Regenerative Medicine

Right Column

Summaries of Review for Applications to RFA 07-05

The following is a listing of all applications reviewed under RFA 07-05 for CIRM New Cell Lines Awards. Applications are ordered by application number and include the score (between 0 and 100, with 100 being the best) and a funding recommendation (indicated by the color key below) made by the Grants Working Group (GWG) during the review meeting on April 10-11, 2008. A link to the Public Abstract (provided by applicant), and Public Review Report are available for each application by clicking on the respective application number.

     = Recommended for funding          = Not Recommended for funding. Recommended to be available for funding only if the ICOC makes a programmatic determination to fund this application          = Not Recommended for funding

 

Application Number Title Scientific Score
RL1-00630-1 Derivation of hESC Lines with Disease Lesions 77
RL1-00631-1 Generating pluripotent cell lines from human neurons. 59
RL1-00632-1 Induction of iPS Cells Using Transient Episomal Expression Vectors: Validation of Toxicity Testing in iPS-Derived Hepatocytes.  
RL1-00633-1 High-fidelity derivation of new stem cell lines 67
RL1-00634-1 Safe, efficient creation of human induced pluripotent stem cells without the use of retroviruses 80
RL1-00635-1 Derivation of human embryonic stem cell lines from human blastocysts: analysis of genetic stability and ethnic diversity 55
RL1-00636-1 Generation of Pluripotent Cell Lines from Human Embryos 82
RL1-00637-1 Induced Pluripotent Stem Cell Lines from Retinal Pigment Epithelial Cells 57
RL1-00638-1 Human Germ-Line Stem Cells As Source for Pluripotent Stem Cells  
RL1-00639-1 Induced Pluripotent Stem Cells for Cardiovascular Diagnostics 73
RL1-00640-1 Isolation and Characterization of A Novel Stem Cell Line from Amniotic Fluid and their Potential for Regenerative Medicine Applications 56
RL1-00641-1 Generation and Testing of Induced Pluripotent Stem Cell Lines for Understanding Human Oligodendrocyte Development and Disease  
RL1-00642-1 Derivation of New ICM-stage hESCs 58
RL1-00644-1 Protein transduction of transcription factors: a non-genetic approach to generate new pluripotent cell lines from human skin. 73
RL1-00645-1 Clinically Relevant iPS Cell Lines  
RL1-00646-1 Derivation of hESC lines from multi-pronuclei zygotes  
RL1-00647-1 Establishing Noonan and Leopard syndrome patient-specific iPS cell lines 55
RL1-00648-1 Optimization of Human Embryonic Stem Cell Derivation Techniques and Production/Distribution of GMP-Grade Lines 82
RL1-00649-1 Development of Induced Pluripotent Stem Cells for Modeling Human Disease 69
RL1-00650-1 Establishment of Frontotemporal Dementia Patient-Specific Induced Pluripotent Stem (iPS) Cell Lines with Defined Genetic Mutations 85
RL1-00652-1 GENERATION OF PLURIPOTENT STEM CELL LINES FROM SPERMATOGONIAL STEM CELLS APPLICABLE TO REGENERATIVE MEDICINE  
RL1-00653-1 Derivation of New iPS Cell Lines and Development of a Novel Stem Cell Platform for Parkinson's Research and Therapeutic Applications  
RL1-00654-1 Comparison of New Lines from Multiple Sources  
RL1-00655-1 Large-Scale Reprogramming of Human Somatic Cells to a Pluripotent Stem Cell-Like State  
RL1-00656-1 Generation of human ESC lines using SCNT 57
RL1-00657-1 Creating the next generation of human iPS cells with global screens for and use of novel pluripotency factors 56
RL1-00658-1 Placental Derived Stem Cells  
RL1-00659-1 Establishment of Human Embryonic Stem Cells Modeling Human Disease by Somatic Cell Nuclear Transfer  
RL1-00660-1 Induction of pluripotent stem cells by small RNA-guided transcriptional activation 71
RL1-00661-1 Derivation of hES Cells in Novel Key Regulators of Cell Survival and Growth  
RL1-00662-1 Derivation and analysis of pluripotent stem cell lines with inherited TGF-b mediated disorders from donated IVF embryos and reprogrammed adult skin fibroblasts 79
RL1-00663-1 Creating stem cells for treatment of neurological disease: a novel microRNA-based method for safe, efficient induction of pluripotence in patient-specific cells  
RL1-00665-1 Derivation of scalable clinical grade human embryonic stem cells under current Good Manufacturing Practice conditions using conventional and single blastomere biopsy protocols 57
RL1-00666-1 Pluripotent human stem cells for creation of disease-specific and genotypically diverse 3-D liver tissues for drug discovery and patient therapies  
RL1-00667-1 NEW TECHNOLOGY FOR THE DERIVATION OF HUMAN PLURIPOTENT STEM CELL LINES FOR CLINICAL USE 85
RL1-00668-1 Derivation of Novel Late Onset Disease-Specific Stem Cell Lines Using Highly Accurate Single Cell Genotyping Technology  
RL1-00669-1 Somatic cell age and memory in the generation of iPS cells 78
RL1-00670-1 Derivation and comparative analysis of human pluripotent ESCs, iPSCs and SSCs: Convergence to an embryonic phenotype 82
RL1-00671-1 Derivation of clinical grade HLA-homozygous human stem cell lines using parthenogenetic activation of oocytes  
RL1-00672-1 In vitro and in vivo characterization of human neuronal precursor cells  
RL1-00674-1 Derivation of new human pluripotent stem cells using small molecules  
RL1-00675-1 Generation of human embryonic stem cell lines, under defined conditions, modeling normal & diseased states from material stored at the {REDACTED} embryo bank 61
RL1-00677-1 Derivation of new induced pluripotent stem (iPS) cells to build neurological disease models 63
RL1-00678-1 New Cell Lines for Huntington's Disease 69
RL1-00679-1 Establishment of human embryonic stem cell lines using re-constructed human embryos derived from polyspermic eggs  
RL1-00680-1 MicroRNA (miRNA)-induced Pluripotent Stem Cells (mirPS)  
RL1-00681-1 Generation of clinical grade human iPS cells 74
RL1-00682-1 Derivation of Parkinson's Disease Coded-Stem Cells (PD-SCs) 67
RL1-00683-1 Generating Pluripotent Stem Cells from Skin of Patients with Multiple Sclerosis and Parkinson's Disease  
RL1-00684-1 Generation of an Engineered Insulin Reporter hES Cell Line to Facilitate Cell-Based Assays for Diabetes Research