课题基金 / 基金详情

CONTROL OF HEMOGLOBIN SYNTHESIS

CONTROL OF HEMOGLOBIN SYNTHESIS
血红蛋白合成的控制
批准号:
3336314
负责人:
JOSEPH DESIMONE
金额:
$6.88万
依托单位国家:
美国
项目类别:
财政年份:
1978
资助国家:
美国
项目状态:
已结题
起止时间:
1978-07-01 至 1986-06-30

项目摘要

项目成果

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中文摘要
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英文摘要
The major objective of the research project is to determine the mechanisms of control responsible for the production of fetal hemoglobin (HbF) and adult hemoglobin (HbA) in the baboon, Papio cynocephalus. This species was chosen because it provides an excellent experimental model for elucidation for HbF synthesis. The specific aims of the project are: 1. To determine the factors underlying the switch from adult hemoglobin synthesis to fetal hemoglobin synthesis following acute hypoxic stress in vivo, 2. To determine the minimal amount of hypoxic stress required to induce F-cell synthesis, 3. To detemine the erythrocyte precursor cell stages which can respond to hypoxic stress by synthesizing HbF, 4. To determine the factors underlying the switch from HbA synthesis to HbF synthesis which occurs during erythroid cell culture. 5. To determine the factors underlying the switch from HbF synthesis to HbA synthesis which occurs during fetal and neonatal development.
期刊论文(11)
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会议论文
Changes in the gamma chain heterogeneity of hemoglobin F of the baboon (Papio cynocephalus) postnatally and after partial switching to hemoglobin F production by various stimuli.
狒狒(Papio cynocephalus)出生后以及在各种刺激下部分转换为血红蛋白 F 产生后,血红蛋白 F 的 γ 链异质性发生变化。
DOI: --
发表时间: 1983
期刊: The Journal of biological chemistry
影响因子: --
作者: [Schroeder,WA, DeSimone,J, Shelton,JB, Shelton,JR, Espinueva,Z, Hall,L, Zwiers,D]
通讯作者: Zwiers,D
Is increase of fetal hemoglobin due to erythropoietic stress the result of DNA hypomethylation?
红细胞生成应激导致胎儿血红蛋白增加是 DNA 低甲基化的结果吗?
DOI: --
发表时间: 1983
期刊: Transactions of the Association of American Physicians
影响因子: --
作者: [DeSimone,J, Schimenti,JC, Duncan,CH, Heller,P]
通讯作者: Heller,P
On the mechanism of Hb F elevations in the baboon by erythropoietic stress and pharmacologic manipulation.
红细胞生成应激和药物操作导致狒狒 Hb F 升高的机制。
DOI: --
发表时间: 1986
期刊: Blood
影响因子: 20.3
作者: [Lavelle,D, DeSimone,J, Heller,P, Zwiers,D, Hall,L]
通讯作者: Hall,L
Speciation in the baboon and its relation to gamma-chain heterogeneity and to the response to induction of HbF by 5-azacytidine.
狒狒的物种形成及其与 γ 链异质性的关系以及与 5-氮杂胞苷诱导 HbF 的反应的关系。
DOI: --
发表时间: 1984
期刊: Blood
影响因子: 20.3
作者: [DeSimone,J, Schroeder,WA, Shelton,JB, Shelton,JR, Espinueva,Z, Huynh,V, Hall,L, Zwiers,D]
通讯作者: Zwiers,D
7
    A Novel, Non-Cytotoxic, Epigenetic Therapeutic for Sickle Cell Disease
    • 批准号:
      9755493
    • 项目类别:
    • 资助金额:
      $75.0万
    • 财政年份:
      2017
    • 负责人:
      JOSEPH DESIMONE
    • 依托单位:
    Improving HbF induction by inhibiting epigenetic target enzymes
    Improving HbF induction by inhibiting epigenetic target enzymes
    Chicago Comprehensive Sickle Cell Center: Basic & Translational Research Program
    海外基金