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Pediatric Hematology Research Training Program

Pediatric Hematology Research Training Program
儿科血液学研究培训计划
批准号:
10590576
负责人:
STELLA T CHOU
金额:
$44.83万
依托单位国家:
美国
项目类别:
财政年份:
1976
资助国家:
美国
项目状态:
未结题
起止时间:
1976-07-01 至 2027-06-30

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中文摘要
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英文摘要
PROJECT SUMMARY The primary objective of the Pediatric Hematology Research Training Program has been to train individuals – mostly pediatric hematology/oncology fellows – for academic or industrial careers in pediatric-related, benign hematology. Pediatric benign hematology is a highly underserved area of research. Our Division, supported by this T32, has excelled at attracting, training, and retaining young, talented individuals to this field who have risen to leadership roles in pediatric benign hematology research. In this renewal, we propose to expand the scope of our T32, increasing our slots from 4 to 6 postdoctoral slots per year to pursue a new, more ambitious vision. The Specific Aims of this renewal are as follows: (1) This T32 renewal will offer a wide range of research training opportunities of particular import to pediatrics in hemoglobinopathies and other anemias, hemostasis/ thrombosis, megakaryocyte/platelet biology, transfusion medicine, stem cell development, bone marrow failure, and now, vasculogenesis. (2) It will support a wide pool of potential trainees. Besides the pediatric hematology/oncology fellows pool we will include: i. non-hematology pediatric fellows interested in pursuing research in benign hematology, and ii. candidates from a proposed sickle cell disease (SCD) subspecialty training program offering state-of-the-art research training related to SCD. (3) Training will continue to involve a “team” approach of a primary mentor plus advisory faculty with key ancillary skills (e.g., bioinformatics or gene therapy). (4) The T32 infrastructure will continue to carefully monitor individual trainee progress and oversee mentorship towards reaching the appropriate next career milestones using a novel “stepwise oversight” committee designed to transition pediatric hematology/oncology fellows from their clinical year(s) to their early assistant professor years. (5) Our program will continue to emphasize acquisition of skills critical for successful academic careers. Preparation of manuscripts, presentations and grant submissions, detailed bioethical training, laboratory or investigator leadership skills, and specific training in optimizing authentication of key reagents, in designing the laboratory and/or clinical study, and in rigorous data analysis. Thetraining faculty is comprised of a closely-knit group of productive, well-funded, pediatric benign hematology physicians and scientists with strong records as mentors, supplemented by additional trainers that bring in skills key for the success of our trainees. Our program has been successful in the research training of minority students, and this effort remains a priority that the proposed inclusion of trainees pursuing a SCD subspecialty fellowship should further enhance. Despite a national trend away from subspecialty research training in pediatrics, this T32 mechanism has enabled our Program to train outstanding candidates for academic careers to become national and international leaders in many areas of benign pediatric hematology. We believe that the expanded vision we propose for our T32 renewal shows the program’s continued vigor, and its ability to evolve and maintain relevance in our field of benign pediatric hematology.
期刊论文(23)
专著(0)
科研奖励(0)
会议论文
Comparison of idarubicin to daunomycin in a randomized multidrug treatment of childhood acute lymphoblastic leukemia at first bone marrow relapse: a report from the Children's Cancer Group.
伊达比星与道诺霉素在首次骨髓复发儿童急性淋巴细胞白血病随机多药治疗中的比较:来自儿童癌症小组的报告。
DOI: 10.1002/(sici)1096-911x(199612)27:6
发表时间: 1996
期刊: Medical and pediatric oncology.
影响因子: --
作者: [Feig,SA, Ames,MM, Sather,HN, Steinherz,L, Reid,JM, Trigg,M, Pendergrass,TW, Warkentin,P, Gerber,M, Leonard,M, Bleyer,WA, Harris,RE]
通讯作者: Harris,RE
Generation of 2 isogenic clones from a patient with Trisomy 21 and a GATA1 mutation.
来自21三体患者和GATA1突变的患者的2个同源克隆产生。
DOI: 10.1016/j.scr.2023.103098
发表时间: 2023-06
期刊: STEM CELL RESEARCH
影响因子: 1.2
作者: [Takasaki, Kaoru, Kumar, Sara S., Gagne, Alyssa, French, Deborah L., Chou, Stella T.]
通讯作者: Chou, Stella T.
Variant RHD alleles and Rh immunization in patients with sickle cell disease.
镰状细胞病患者的变异 RHD 等位基因和 Rh 免疫。
DOI: 10.1111/bjh.18774
发表时间: 2023
期刊: British journal of haematology
影响因子: 6.5
作者: [Takasaki,Kaoru, Friedman,DavidF, Uter,Stacey, Vege,Sunitha, Westhoff,ConnieM, Chou,StellaT]
通讯作者: Chou,StellaT
Generation of CHOPi-008-B, a euploid iPSC line from a patient with Trisomy 21 and a GATA1 mutation.
生成 CHOPi-008-B,这是来自 21 三体和 GATA1 突变患者的整倍体 iPSC 系。
DOI: 10.1016/j.scr.2023.103198
发表时间: 2023
期刊: Stem cell research
影响因子: 1.2
作者: [Takasaki,Kaoru, Kumar,SaraS, Gagne,Alyssa, French,DeborahL, Chou,StellaT]
通讯作者: Chou,StellaT
11
    Understanding the complexity of gene dosage imbalance in Down syndrome
    • 批准号:
      9894132
    • 项目类别:
    • 资助金额:
      $335.22万
    • 财政年份:
      2019
    • 负责人:
      STELLA T CHOU
    • 依托单位:
    RH genotype matched red cell transfusions for patients with sickle cell disease
    • 批准号:
      10470880
    • 项目类别:
    • 资助金额:
      $83.48万
    • 财政年份:
      2019
    • 负责人:
      STELLA T CHOU
    • 依托单位:
    RH genotype matched red cell transfusions for patients with sickle cell disease
    • 批准号:
      10259737
    • 项目类别:
    • 资助金额:
      $83.48万
    • 财政年份:
      2019
    • 负责人:
      STELLA T CHOU
    • 依托单位:
    Improving transfusion therapy for patients with sickle cell disease with pluripotent stem cell-derived red cells
    • 批准号:
      10181018
    • 项目类别:
    • 资助金额:
      $126.42万
    • 财政年份:
      2016
    • 负责人:
      STELLA T CHOU
    • 依托单位:
    海外基金