Gene Targeting & Transgenic Shared Resource
Gene Targeting & Transgenic Shared Resource
批准号:
10641712
负责人:
Eugene Yu
金额:
$7.68万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-06-16 至 2024-04-30
关键词:
AccelerationAnimal ModelAreaBacterial Artificial ChromosomesBiophysicsBreedingCRISPR/Cas technologyCancer Center Support GrantCancer ModelCellular StressChargeClinicalClustered Regularly Interspaced Short Palindromic RepeatsCohort AnalysisCommunitiesComplexConsultationsCryopreservationDNA biosynthesisData SetDevelopmentDevelopmental Therapeutics ProgramEducationElectroporationEmbryoEnvironmentFaculty RecruitmentFundingFutureGene TargetingGenerationsGenesGeneticGenetic EngineeringGenetically Engineered MouseGenomicsGenotypeGlycobiologyGoalsHuman GenomeIn VitroIndividualIndustry CollaborationInvestmentsLaboratoriesMalignant NeoplasmsMalignant neoplasm of pancreasMalignant neoplasm of prostateMalignant neoplasm of urinary bladderMammalian OviductsMethodsMissionMusMutationNamesPathogenesisPathway interactionsPeer ReviewPhenotypeProductionReportingResearchResearch PersonnelResource SharingResourcesRunningScientistServicesSourceSpeedTechniquesTechnologyTrainingTransgenic MiceTransgenic OrganismsWorkcost effectivedesign and constructionembryonic stem cellexperiencegenome editingimprovedin vivoinstrumentationknockout genemalignant breast neoplasmmammalian genomemembermouse genomemouse modelmutantneoplasm immunotherapynew technologynovelnucleic acid deliveryprogramstrendtumortumor immunology
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The mission of the Gene Targeting and Transgenic Shared Resource (GeTT) is to ensure that Roswell Park
CCSG members have access to state-of-the-art transgenic mouse technologies, methods and animal models.
With the development of contemporary mammalian genome manipulation technologies, genetically engineered
mice have become a source of new cancer models that have helped elucidate pathways contributing to tumor
development and progression. GeTT has generated over 1,000 novel genetically engineered mouse lines for
CCSG program members. The recent introduction of CRISPR/Cas9 genome editing technologies has
drastically improved the efficiency of generating new mouse models, and enabled some critical new research
by Roswell Park investigators that would not have been otherwise possible. In the reporting period (2013-
2017), the GeTT served a total of 47 Roswell users, of which 42 (89%) were CCSG members. Typically, GeTT
charges its CCSG members ~one-third of what commercial companies would charge to create genetically
engineered mice. The Resource Director and Co-Director provide guidance to investigators from the earliest
planning stages of the project when constructs are designed to advanced stages of the project during
phenotype analysis. Resource technicians perform the specialized ES cell and embryo manipulation methods
to generate the genetically engineered mice. Projects requiring the development of transgenic mouse models
are becoming increasingly relevant to validate findings from in vitro studies and from high-throughput clinical-
based datasets. The Specific Aims of the GeTT are: 1) To ensure that Roswell Park CCSG members, have
access to state-of-the-art transgenic methods, technologies, and mouse models; 2) To serve as a “one-stop”
Shared Resource for consultation, education, training and expert support related to genetic engineering of
mouse models; 3) To work synergistically with other shared resources at Roswell Park to provide the optimized
research environment for CCSG members. The GeTT has significant expertise in providing all the necessary
technologies and services to achieve the objectives of the Aims. The GeTT future plan is to increase the
number of CCSG members utilizing the GeTT by optimizing several new CRISPR-based genome-editing
techniques. GeTT is currently developing new techniques such as Easi-CRISPR and GONAD (Gonadal
oviductal transfer of Nucleic Acid Delivery). In addition GeTT has recently developed a service that offers
mouse colony management to CCSG member labs who do not have previous experience in complex mouse
breeding for cohort analysis.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
CRISPR-mediated engineering and pilot study of mouse mutants of the bitter taste receptor genes
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批准号:10451169
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项目类别:
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资助金额:$18.23万
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财政年份:2022
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负责人:Eugene Yu
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依托单位:
Generation and analysis of new mouse models to determine novel therapeutic targets for Down syndrome-associated cognitive deficits
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批准号:10704099
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项目类别:
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资助金额:$46.07万
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财政年份:2022
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负责人:Eugene Yu
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依托单位:
Generation and analysis of new mouse models to determine novel therapeutic targets for Down syndrome-associated cognitive deficits
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批准号:10518886
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项目类别:
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资助金额:$47.58万
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财政年份:2022
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负责人:Eugene Yu
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依托单位:
Generation and analysis of new mouse models to determine novel therapeutic targets for Down syndrome-associated cognitive deficits
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批准号:10711887
-
项目类别:
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资助金额:$43.8万
-
财政年份:2022
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负责人:Eugene Yu
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依托单位:
Mutational analysis to understand the role of CHML in developmental regression
-
批准号:8877784
-
项目类别:
-
资助金额:$23.69万
-
财政年份:2015
-
负责人:Eugene Yu
-
依托单位:
Mutational analysis to understand the role of CHML in developmental regression
-
批准号:9069905
-
项目类别:
-
资助金额:$23.69万
-
财政年份:2015
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负责人:Eugene Yu
-
依托单位:
Genetic Dissection of Trisomy 21
-
批准号:8066350
-
项目类别:
-
资助金额:$43.22万
-
财政年份:2008
-
负责人:Eugene Yu
-
依托单位:
Genetic Dissection of Trisomy 21
-
批准号:7585303
-
项目类别:
-
资助金额:$42.22万
-
财政年份:2008
-
负责人:Eugene Yu
-
依托单位:
Genetic Dissection of Trisomy 21
-
批准号:8249053
-
项目类别:
-
资助金额:$43.31万
-
财政年份:2008
-
负责人:Eugene Yu
-
依托单位:
Genetic Dissection of Trisomy 21
-
批准号:7781344
-
项目类别:
-
资助金额:$42.78万
-
财政年份:2008
-
负责人:Eugene Yu
-
依托单位:
Gene Targeting & Transgenic Shared Resource
-
批准号:10398050
-
项目类别:
-
资助金额:$8.08万
-
财政年份:1997
-
负责人:Eugene Yu
-
依托单位:
Gene Targeting & Transgenic Shared Resource
-
批准号:9923571
-
项目类别:
-
资助金额:$8.34万
-
财政年份:--
-
负责人:Eugene Yu
-
依托单位:
海外基金