Molecular Cytogenetics Shared Resource
Molecular Cytogenetics Shared Resource
批准号:
10022772
负责人:
Shan Zha
金额:
$8.29万
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:
未结题
起止时间:
1997-07-04 至 2025-06-30
关键词:
AddressApplications GrantsAreaBase SequenceBiological AssayCancer Center Support GrantCancer ModelCellsChromosomal translocationChromosome PaintingChromosome StructuresComputer softwareConsultConsultationsCost Effectiveness AnalysisCytogeneticsCytogenetics Shared ResourceDNA DamageDNA Double Strand BreakDNA RepairDNA Repair GeneDNA SequenceDataData AnalysesDefectDevelopmentDoctor of PhilosophyDouble Strand Break RepairEquipmentExperimental DesignsFluorescent in Situ HybridizationFundingFutureGenome StabilityGenomic InstabilityGenomic SegmentGoalsGrantHerbert Irving Comprehensive Cancer CenterHigh-Throughput Nucleotide SequencingHourHumanImageJournalsKaryotype determination procedureKineticsKnowledgeLeadershipMalignant NeoplasmsMicroscopeMolecularMolecular CytogeneticsMorphologyMusMutationNCI Center for Cancer ResearchNatureNeoplasm MetastasisNew YorkOrganismPaperPathway AnalysisPathway interactionsPatternPattern RecognitionPeer ReviewPhenotypePreparationProcessPublicationsRecombinant DNARelapseReproducibilityResearchResearch PersonnelResearch SupportResolutionSamplingSecureServicesSourceSpectral KaryotypingStainsSystemTechniquesTechnologyTimeTissuesTrainingTraining and EducationUnited States National Institutes of HealthVariantanalytical toolbasecancer cellcost effectivedata acquisitiondesignexperiencegenome-wideimaging systeminnovationinstrumentinstrumentationmembermetropolitannew technologynoveloperationpremalignantprogramsprospectiverepairedresponseskillstelomeretool
中文摘要
点击翻译按钮获取中文摘要
英文摘要
MOLECULAR CYTOGENETICS SHARED RESOURCE: PROJECT SUMMARY
The Molecular Cytogenetics Shared Resource (MCSR) provides access to advanced DNA repair and genomic
instability analyses to members of the Herbert Irving Comprehensive Cancer Center (HICCC). The services
include (1) analyses of chromosomal structural, morphological, and rearrangement patterns (including
karyotyping, spectral karyotyping (SKY), chromosome painting, and fluorescence in situ hybridization [FISH]),
(2) analyses of genomic instability at specialized genomic regions (telomere, rDNA), (3) DNA damage responses
and repair pathway analyses (including the kinetics of DNA repair protein foci), (4) development of genome-wide
tools to analyze chromosomal translocation and mutations patterns (including high throughput sequence
platforms), and (5) consultation and completed packages for experimental design, staining, data acquisition, and
processing. Under the leadership of Shan Zha, PhD, an expert in DNA double-strand breaks repair, these
comprehensive and customizable services, together with specialized instruments maintained by the MCSR,
enable investigators at varying skill levels with the knowledge to characterize clonal changes as well as non-
clonal genomic instability in cancer cells and in premalignant tissues from a wide range of organisms. Over the
current project period (2014-2019), MSR has undergone leadership and instrument reorganization. In this
process, the MCSR acquired new equipment and developed new assays, which significantly expanded its ability
to quantitatively study DNA repair mechanisms. The reorganized MCSR is now managed by a dedicated PhD-
level staff and provides convenient, cost-effective, and innovative service to HICCC members. The MCSR
provides services that are not available from commercial sources and not easily accessible within the New York
metropolitan area and are proven to be critically important to the research of many HICCC members, providing
key preliminary data for grant applications and high-impact publications. In addition to providing both basic and
advanced services across different area of DNA repair and genomic instability studies, the MCSR also provides
training to HICCC members in the operation of specialized instruments and in sample preparation and analyses.
In addition, consulting services are available to investigators to assist in the design of the most cost-effective
analyses and provide controls needed to validate the assay and the data. The MCSR is committed to
incorporating novel experimental portfolios and the use of analytic tools, providing state-of-the-art genomic
stability services, and promoting accessibility of services through training and consulting in support of highly
collaborative and innovative research ongoing at the HICCC. During the current project period, the MCSR was
utilized by 21 HICCC members, supported key data for seven peer-reviewed publications, including four papers
in high-impact journals (e.g., Nature, Molecular Cell), and currently supports research for five NIH-funded
projects, four from NCI.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
The role of DNA-PKcs in DNA repair, lymphocyte development, RNA metabolism and tumor suppression
-
批准号:10539944
-
项目类别:
-
资助金额:$59.75万
-
财政年份:2022
-
负责人:Shan Zha
-
依托单位:
The role of DNA-PKcs in DNA repair, lymphocyte development, RNA metabolism and tumor suppression
-
批准号:10651884
-
项目类别:
-
资助金额:$56.57万
-
财政年份:2022
-
负责人:Shan Zha
-
依托单位:
The non-catalytic function of PARP2 in DNA repair and cancer therapy
-
批准号:10641934
-
项目类别:
-
资助金额:$57.98万
-
财政年份:2022
-
负责人:Shan Zha
-
依托单位:
The non-catalytic function of PARP2 in DNA repair and cancer therapy
-
批准号:10540084
-
项目类别:
-
资助金额:$59.71万
-
财政年份:2022
-
负责人:Shan Zha
-
依托单位:
The catalytic and non-catalytic functions of PARP1 in cancer biology
-
批准号:10377548
-
项目类别:
-
资助金额:$35.87万
-
财政年份:2018
-
负责人:Shan Zha
-
依托单位:
The catalytic and non-catalytic functions of PARP1 in cancer biology
-
批准号:9886208
-
项目类别:
-
资助金额:$36.6万
-
财政年份:2018
-
负责人:Shan Zha
-
依托单位:
The structural function of ATR in development, oncogenesis and cancer therapy
-
批准号:9886205
-
项目类别:
-
资助金额:$42.18万
-
财政年份:2017
-
负责人:Shan Zha
-
依托单位:
Project 3 Zha
-
批准号:10614967
-
项目类别:
-
资助金额:$35.23万
-
财政年份:2014
-
负责人:Shan Zha
-
依托单位:
DNA-PKCS Phosphorylation in DNA Repair and Chromosomal Translocations
-
批准号:8975763
-
项目类别:
-
资助金额:$36.6万
-
财政年份:2014
-
负责人:Shan Zha
-
依托单位:
Project 3 Zha
-
批准号:10394196
-
项目类别:
-
资助金额:$35.23万
-
财政年份:2014
-
负责人:Shan Zha
-
依托单位:
The Role of ATM in Suppression of Lymphomas
-
批准号:8606350
-
项目类别:
-
资助金额:$32.2万
-
财政年份:2011
-
负责人:Shan Zha
-
依托单位:
The Role of ATM in Suppression of Lymphomas
-
批准号:10083198
-
项目类别:
-
资助金额:$38.0万
-
财政年份:2011
-
负责人:Shan Zha
-
依托单位:
The Role of ATM in Suppression of Lymphomas
-
批准号:8790429
-
项目类别:
-
资助金额:$33.2万
-
财政年份:2011
-
负责人:Shan Zha
-
依托单位:
The Role of ATM in Suppression of Lymphomas
-
批准号:8214501
-
项目类别:
-
资助金额:$33.2万
-
财政年份:2011
-
负责人:Shan Zha
-
依托单位:
The Role of ATM in Suppression of Lymphomas
-
批准号:8444717
-
项目类别:
-
资助金额:$31.21万
-
财政年份:2011
-
负责人:Shan Zha
-
依托单位:
The Role of ATM in Suppression of Lymphomas
-
批准号:8085529
-
项目类别:
-
资助金额:$33.29万
-
财政年份:2011
-
负责人:Shan Zha
-
依托单位:
Molecular Cytogenetics Shared Resource
-
批准号:10469548
-
项目类别:
-
资助金额:$8.29万
-
财政年份:1997
-
负责人:Shan Zha
-
依托单位:
Molecular Cytogenetics Shared Resource
-
批准号:10245185
-
项目类别:
-
资助金额:$8.29万
-
财政年份:1997
-
负责人:Shan Zha
-
依托单位:
Molecular Cytogenetics Shared Resource
-
批准号:10661678
-
项目类别:
-
资助金额:$8.29万
-
财政年份:1997
-
负责人:Shan Zha
-
依托单位:
The Role of CTIP in Lymphocyte Development and Lymphomagenesis
-
批准号:8608847
-
项目类别:
-
资助金额:$36.43万
-
财政年份:--
-
负责人:Shan Zha
-
依托单位: