1) hereditary persistence of fetal hemoglobin
遗传性持续性胎儿血红蛋白增多症
1.
In order to study the molecular pathology of hereditary persistence of fetal hemoglobin (HPFH) in Chinese, PCR based chemical cleavage of mismatch (CCM) method was used for defining the point mutations causing non deletional HPFH.
为进行中国人遗传性持续性胎儿血红蛋白增多症（ＨＰＦＨ）的分子病理学研究，以四种已知非缺失型ＨＰＦＨ突变样品为研究材料，建立了针对二种γ珠蛋白基因（Ｇγ和Ａγ）的点突变筛查技术———化学裂解法（ＣＣＭ）。
2) Hereditary persistent fetal hemoglobinemia
遗传性持续性胎儿血红蛋白
3) Hereditary persistence of fetal haemoglobin
胎儿血红蛋白持续存在综合症
4) hereditary methemoglobinemia
遗传性高铁血红蛋白血症
1.
Identification of a novel compound heterozygous genotype of hereditary methemoglobinemia type I;
1例新的遗传性高铁血红蛋白血症复合杂合子基因型的鉴定
5) HbF keep on syndrome
胎儿血红蛋白持续综合征
1.
Clinical study on HbF keep on syndrome
胎儿血红蛋白持续综合征的实验研究
6) fetal hemoglobin
胎儿血红蛋白
1.
Objective To investigate the role of directly constitutive activation of p38 mitogen-activated protein kinases(p38MAPKs)signaling in γ-globin gene expression and fetal hemoglobin(HbF)induction,and provide direct data for the relationship between phosphorylation of p38 and erythroid differentiation of human K562 erythroleukemia cells.
目的探讨p38丝裂原活化的蛋白激酶(p38MAPKs)信号通路直接持续活化在γ-珠蛋白基因转录激活和胎儿血红蛋白(HbF)合成中的作用,为阐明p38磷酸化与K562细胞红系分化的关系提供直接依据。
2.
Objective To investigate the relationship of β-thalassemia mutations and the single nucleotide polymorphism(SNP) at position -158 of G γ-globin gene to the altered levels of fetal hemoglobin(Hb F) of β-thalassemia heterozygotes.
目的 探讨 β地中海贫血 (简称 β地贫 )杂合子基因突变类型和 Gγ珠蛋白基因启动子 - 15 8位点 (Gγ- 15 8)单核苷酸多态性与胎儿血红蛋白 (fetal hemoglobin,Hb F)水平的关系。
3.
Aim: To investigate the role of sodium butyrate in γ globin gene expression and fetal hemoglobin induction and its mechanisms.
目的:研究丁酸钠对K562细胞系γ珠蛋白基因表达和胎儿血红蛋白合成的诱导作用及机制。
补充资料：持续性胎儿循环
持续性胎儿循环
persistent fetals circulation
见“持续性肺动脉高压症”。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条