Genetically Engineered Mouse Facility
Genetically Engineered Mouse Facility
批准号:
7695935
负责人:
WILLIAM H. KLEIN
金额:
$34.35万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-28 至 2013-06-30
关键词:
AdultAdvertisingAnimal ModelAnimalsArchivesBacterial Artificial ChromosomesCancer CenterCancer Center Support GrantComplexCryopreservationDNADerivation procedureDetectionDevelopmentEmbryoFacultyFeesFundingGene TargetingGenerationsGenesGeneticGenetic EngineeringGenetic VariationGenetically Engineered MouseGenomicsGoldGreen Fluorescent ProteinsGrowthHumanImmunologyInjection of therapeutic agentLacZ GenesLeadMalignant NeoplasmsMethodsMissionModelingMusMutationNorthern BlottingNumbersPhenocopyPhenotypePliabilityPoint MutationProceduresProcessed GenesRangeReagentReproductive ImmunologyResearch PersonnelResourcesServicesSourceStandards of Weights and MeasuresTP53 geneTechnical ExpertiseTechniquesTestingTimeTissuesTrainingTransgenic MiceTransgenic OrganismsTumor Suppressor GenesUniversity of Texas M D Anderson Cancer CenterblastocystcDNA Libraryembryo tissueembryonic stem cellgerm free conditionin vivomembermouse genomemouse modelpathogenplasmid DNAprogramstumorvector
中文摘要
转基因小鼠已成为癌症动物模型的“黄金标准”。它们广泛存在于
用于模拟具有肿瘤抑制基因特定点突变的人类癌症,以及组织特异性
突变在体细胞组织中的表达。通过在一种动物身上结合几种突变,现在是
有可能复制以前难以在动物模型中复制的人类癌症。这个
基因工程老鼠设施(GEMF)为癌症中心成员提供了宝贵的资源。它
产生转基因和基因靶向的小鼠,进行胚胎再衍生以产生无病原体
小鼠,并提供冷冻保存服务以存档动物模型。鼠标资源工具
(MRF),作为GEMF的一部分,为构建发育、成虫和
胚胎组织、基因组DNA和cdna文库以及袋式过滤器。MRF也有一个很小的殖民地
Cre和LacZ转基因小鼠对小鼠产生条件性缺失至关重要。因此,GEMF
为教职员工提供独特的机会来开发复杂的动物模型来研究各种癌症
有问题。GEMF在生成和维护老鼠模型方面非常成功。在
在过去的五年里,GEMF为MDACC调查人员制作了300多个项目的动物模型
并已冷冻保存了120多个小鼠品系。A>;实现了1000%的利用率
鼠标资源通过MRF。首席设施协调员开发了新的、更有效的方法
产生供该设施使用的胚胎。她负责培训教职员工,以及
为许多不同项目的研究人员提供遗传和技术方面的专业知识。除
作为设施协调员,GEMF由7名训练有素的技术人员组成。在过去的五年中,GEMF
已经为96个不同的用户提供了服务,他们代表了20个赞助节目中的19个;97%的调查人员
提供服务的是MDACC教职员工。为了更好地满足我们调查人员的需求并增加所需的能力,
南校区最近增加了卫星设施。这一扩展将使GEMF能够发展
更多型号,并提供额外的服务。全球环境管理基金目前的资金来源有多种,包括
53%由CCSG提供,45%通过用户费用收回,其余部分由MDACC提供。
英文摘要
Genetically engineered mice have become the "gold standard" for animal models in cancer. They are widely
used to mimic human cancers with specific point mutations in tumor suppressor genes, as well as tissuespecific
expression of mutations in somatic tissues. By combining several mutations in one animal, it is now
possible to phenocopy human cancers that were difficult to reproduce previously in animal models. The
Genetically Engineered Mouse Facility (GEMF) provides valuable resources to Cancer Center members. It
generates transgenic and gene-targeted mice, performs embryo rederivations to generate pathogen-free
mice, and provides cryopreservation services to archive animal models. The Mouse Resource Facility
(MRF), as part of the GEMF, provides vectors for construct development, northern blots of adult and
embryonic tissues, genomic DNA and cDNA libraries, and BAG filter sets. The MRF also has a small colony
of Cre and lacZ transgenic mice essential for generating conditional deletions in mice. The GEMF thus
provides unique opportunities to faculty to develop sophisticated animal models to study a variety of cancer
problems. The GEMF has been extremely successful in generating and maintaining mouse models. In the
last five years, the GEMF has generated animal models for more than 300 projects for MDACC investigators
and has cryopreserved more than 120 mouse lines. A >1000% increase has been achieved in utilization of
mouse resources through the MRF. The lead facility coordinator has developed new, more efficient methods
of generating embryos for use by the facility. She is responsible for training faculty and their staff, and
provides genetic and technical expertise to many investigators in many different programs. In addition to the
facility coordinator, the GEMF is staffed by 7 highly-trained technicians. In the past five years, the GEMF
has served 96 different users who represent 19 of the 20 sponsored programs; 97% of the investigators
served are MDACC faculty. To better serve the needs of our investigators and add needed capacity, a small
satellite facility was added recently to the South Campus. This expansion will enable the GEMF to develop
more models and offer additional services. The GEMF is currently funded from multiple sources, including
53% provided by the CCSG and 45% recovered through user fees, with the remainder provided by MDACC.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Manipulating retinal progenitor cells
-
批准号:7799707
-
项目类别:
-
资助金额:$22.87万
-
财政年份:2009
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Manipulating retinal progenitor cells
-
批准号:7660274
-
项目类别:
-
资助金额:$19.25万
-
财政年份:2009
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Regulatory mechanisms of HBV X gene Transcription
-
批准号:7591750
-
项目类别:
-
资助金额:$31.6万
-
财政年份:2005
-
负责人:WILLIAM H. KLEIN
-
依托单位:
GENE ARRAY
-
批准号:6986497
-
项目类别:
-
资助金额:$9.63万
-
财政年份:2004
-
负责人:WILLIAM H. KLEIN
-
依托单位:
IDENTIFICATION OF GENES REGULATING RETINAL GANGLION CELL
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批准号:6498576
-
项目类别:
-
资助金额:$22.5万
-
财政年份:2001
-
负责人:WILLIAM H. KLEIN
-
依托单位:
IDENTIFICATION OF GENES REGULATING RETINAL GANGLION CELL
-
批准号:6291325
-
项目类别:
-
资助金额:$22.5万
-
财政年份:2001
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Brn3 POU domain proteins in retinal development
-
批准号:7483053
-
项目类别:
-
资助金额:$35.68万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
BRN-3 POU DOMAIN PROTEINS IN RETINAL DEVELOPMENT
-
批准号:6383703
-
项目类别:
-
资助金额:$30.0万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Brn3 POU domain proteins in retinal development
-
批准号:7277180
-
项目类别:
-
资助金额:$36.41万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Brn3 POU domain proteins in retinal development
-
批准号:7105291
-
项目类别:
-
资助金额:$37.5万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Optic nerve regeneration: gene networks in retina development
-
批准号:8457115
-
项目类别:
-
资助金额:$37.53万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
BRN-3 POU DOMAIN PROTEINS IN RETINA DEVELOPMENT
-
批准号:2888589
-
项目类别:
-
资助金额:$18.92万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
BRN-3 POU DOMAIN PROTEINS IN RETINAL DEVELOPMENT
-
批准号:6645403
-
项目类别:
-
资助金额:$30.0万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
BRN-3 POU DOMAIN PROTEINS IN RETINAL DEVELOPMENT
-
批准号:6524939
-
项目类别:
-
资助金额:$30.0万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Brn3 POU domain proteins in retinal development
-
批准号:7659493
-
项目类别:
-
资助金额:$36.41万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Optic nerve regeneration: gene networks in retina development
-
批准号:8655857
-
项目类别:
-
资助金额:$38.71万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Optic nerve regeneration: gene networks in retina development
-
批准号:8839246
-
项目类别:
-
资助金额:$38.71万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
BRN-3 POU DOMAIN PROTEINS IN RETINA DEVELOPMENT
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批准号:2398924
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项目类别:
-
资助金额:$18.22万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
BRN-3 POU DOMAIN PROTEINS IN RETINA DEVELOPMENT
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批准号:2711227
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项目类别:
-
资助金额:$18.37万
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财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
Optic nerve regeneration: gene networks in retina development
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批准号:8297656
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项目类别:
-
资助金额:$39.5万
-
财政年份:1997
-
负责人:WILLIAM H. KLEIN
-
依托单位:
国内基金
海外基金
小型类人猿合唱节奏的功能假说——宣
示社会关系(Social bond
advertising) ——验证研究
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批准号:
-
项目类别:省市级项目
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资助金额:10.0万元
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批准年份:2025
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负责人:马海港
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依托单位: