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The protein encoded by MTHFD1L is involved in the synthesis of tetrahydrofolate (THF) in the mitochondrion. 再加上，我们可以发MTHFD1L 试剂盒 (4) 和 MTHFD1L 蛋白 (4)和数多这个蛋白质的别的产品。
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Human Polyclonal MTHFD1L Primary Antibody for ELISA, WB - ABIN4335965
Parle-McDermott, Pangilinan, OBrien, Mills, Magee, Troendle, Sutton, Scott, Kirke, Molloy, Brody: A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency. in Human mutation 2009
study identifies MTHFD1L in the folate cycle as an important metabolic pathway in cancer cells with the potential for therapeutic targeting
Studies reported that the A allele of a polymorphism in a gene involved in folate metabolism, MTHFD1L, showed a genome-wide significant association with late-onset Alzheimer's Disease.
rs6922269 variant at MTHFD1L gene could be an important prognostic factor for cardiovascular mortality in patients after ACS.
MTHFD1L rs6922269 genotype is associated with active vitamin B12 (显示 NDUFB3 抗体) levels at baseline and may be a marker of prognostic risk in patients with established coronary heart disease.
Results indicate that miR (显示 MLXIP 抗体)-9 and MiR (显示 MLXIP 抗体)-197 specifically downregulate MTHFD1L in HEK293 and MCF-7 cells and that SNPrs7646 affects miR (显示 MLXIP 抗体)-197 binding to the MTHFD1L 3' UTR (显示 UTS2R 抗体) causing gene repression in the presence of the allele associated with neural tube defects.
The rs3832406 polymorphism was associated with isolated cleft lip with or without cleft palate.(MTHFD1L)
This study support a role of MTHFD1L gene in late-onset Alzheimer's disease in a Northern Han Chinese population.
No evidence of association between the MTHFD1L marker and susceptibility to Alzheimer's disease is found in a sample from a Spanish population.
Prevalence of minor allele A (adenosine) in rs11754661 single nucleotide polymorphism of MTHFD1L contributes to the risk of Alzheimer's disease in a Han population of mainland China.
mitochondrial C1-tetrahydrofolate synthase (显示 MTHFD1 抗体) gene structure and tissue distribution
Deletion of Mthfd1l causes embryonic lethality and neural tube and craniofacial defects in mice.
Data show that the MTHFD1L enzyme is present in mitochondria from normal embryonic tissues and embryonic fibroblast cell lines, and embryonic mitochondria possess the ability to synthesize formate from glycine.
The protein encoded by this gene is involved in the synthesis of tetrahydrofolate (THF) in the mitochondrion. THF is important in the de novo synthesis of purines and thymidylate and in the regeneration of methionine from homocysteine. Several transcript variants encoding different isoforms have been found for this gene.
, formyltetrahydrofolate synthetase domain containing 1
, monofunctional C1-tetrahydrofolate synthase, mitochondrial
, formyltetrahydrofolate synthetase