亚甲基四氢叶酸还原酶缺乏症致脑积水患儿2 例临床及MTHFR 基因变异分析

董慧, 陈哲晖, 马雪, 张尧, 宋金青, 金颖… - 临床儿科 …, 2023 - jcp.xinhuamed.com.cn
Insights into severe 5, 10-methylenetetrahydrofolate reductase deficiency: molecular genetic
… treatment in patients with severe methylenetetrahydrofolate reductase deficiency [J]. JAMA …

使用临床前模型增加单碳代谢产物对创伤性脑损伤结果的影响

SM Joshi, TC Thomas, NM Jadavji - 中国神经再生研究(英文版), 2024 - sjzsyj.com.cn
… with methylenetetrahydrofolate reductase (MTHFR) in the … differs from ordinary HAP in
terms of nutritional risk, severity of … While short-term measures may provide initial insights into

脑性瘫痪遗传途径: 对精准诊断和了解疾病机制的影响

Y Xu, Y Li, SA Richard, Y Sun, C Zhu - 中国神经再生研究(英文版), 2024 - sjzsyj.com.cn
… Ultimately, our goal is to translate these insights into … it from other movement disorders, and
determining the severity of … 5,10-Methylenetetrahydrofolate reductase is an essential enzyme …

[PDF][PDF] 高同型半胱氨酸血症的诊断, 治疗与预防专家共识

李东晓, 张尧, 张宏武, 王琳… - … OF RARE AND …, 2022 - 11871494.s21i.faimallusr.com
5,10-亚甲基四氢叶酸,并在亚甲基四 氢叶酸还原酶(methylenetetrahydrofolate reductase,MTHFR)作用
下转化为 5… 钴胺素参与5-甲基四氢叶酸的再甲基化反应.蛋氨酸在蛋氨酸腺苷转移酶 作用…

[HTML][HTML] Special Article Current Status of Acute Lymphoblastic Leukaemia in Children 兒童急性淋巴細胞白血病現狀

GCF Chan, CH Pui - HK J Paediatr (new series), 2003 - hkjpaed.org
… Because of the remarkable advances made in the field of molecular biology during
recent years, we have a better understanding of the molecular abnormalities that underlie …

維生素B-6 及葉酸與大腸直腸息肉患者的基因多型性, 抗氧化活性及甲基化作用關係的探討

黃怡嘉 - 97 學年度教師研究計畫補助, 2008 - ir.csmu.edu.tw
… 維生素B6 在合成5,10-亞甲基四氫葉 酸時作為絲胺酸羥基甲基轉移酶(serine … ) 的依賴性
輔酶, 而5,10-亞甲基四氫葉酸則是合成核酸所必須,且亞甲基四氫葉酸轉變成的醛基葉酸 (10-formyl-…

电针抑郁大鼠百会和印堂穴后海马基因表达的变化

D Duan, X Yang, Y Tu, L Chen - 中国神经再生研究(英文版), 2014 - sjzsyj.com.cn
… In essence, chronic stress leads to abnormal expression of … factor, methylenetetrahydrofolate
reductase, tyrosine … The 5-HT deficiency theory of depression: perspectives from

2 型糖尿病环境因素与DNA 甲基化的研究进展

汤琳琳, 刘琼, 步世忠, 徐雷艇, 王钦文, 麦一峰… - 遗传, 2013 - chinagene.cn
Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus
fromMethylenetetrahydrofolate reductase gene polymorphism, homocysteine and risk of …

[HTML][HTML] 丁酸和叶酸预防与治疗肠道疾病及其分子基础

李雄彪, 马庆英, 崔云龙 - 世界华人消化杂志, 2006 - wjgnet.com
… A candidate genetic risk factor for vascular disease: a common mutation in
methylenetetrahydrofolate reductase. Nat Genet. 1995;10:111-113. …

高尿酸血症和痛风的遗传学研究进展

郑敏, 麻骏武 - 遗传, 2016 - chinagene.cn
Molecular analysis of two enzyme genes, HPRT1 and PRPS1, causing X-linked inborn errors
of purine metabolism. Nucleos Nucleot Nucl, 2010, 29(4–6): 291–294. [DOI] [28] Alanazi M…