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Human Polyclonal MTHFD1 Primary Antibody für IHC, IHC (p) - ABIN4335962
Tyleckova, Hrabakova, Mairychova, Halada, Radova, Dzubak, Hajduch, Gadher, Kovarova: Cancer cell response to anthracyclines effects: mysteries of the hidden proteins associated with these drugs. in International journal of molecular sciences 2013
Human Polyclonal MTHFD1 Primary Antibody für ELISA, WB - ABIN451607
Dorszewska, Florczak, Rozycka, Kempisty, Jaroszewska-Kolecka, Chojnacka, Trzeciak, Kozubski: Oxidative DNA damage and level of thiols as related to polymorphisms of MTHFR, MTR, MTHFD1 in Alzheimer's and Parkinson's diseases. in Acta neurobiologiae experimentalis 2007
Human Polyclonal MTHFD1 Primary Antibody für ICC, IF - ABIN4335960
Germain, Chatel-Chaix, Gagné, Bonneil, Thibault, Pradezynski, de Chassey, Meyniel-Schicklin, Lotteau, Baril, Lamarre: Elucidating novel hepatitis C virus-host interactions using combined mass spectrometry and functional genomics approaches. in Molecular & cellular proteomics : MCP 2014
MTHFR (zeige MTHFR Antikörper) 1298CC was significantly associated with AE risk. The MTHFR (zeige MTHFR Antikörper) haplotypes 677C-1298C/677T-1298A and 677T-1298C conferred risk in a progressive manner. MTHFD1 1958G>A was not associated with disease susceptibility. Children with the rs2236225 GA and the rs1801131 CC genotypes were at an increased risk as compared to the reference genotype of rs2236225 GG and rs1801131
Our study suggests no significant genetic association of MTHFR (zeige MTHFR Antikörper) (rs1801131, rs1801133) and MTHFD1 (rs8006686) polymorphisms in South Indian Pseudoexfoliation syndrome patients.
The AA and GA genotypes of MTHFD1 G1958A, TT and GT genotypes of eNOS (zeige NOS3 Antikörper) G894T and the AA and GA genotypes of ACE (zeige ACE Antikörper) A2350G are risk factors for congenital heart defects.
2 common and functional MTHFD1 polymorphisms (rs2236225 and rs1076991) modulate the risk associations of plasma serine and glycine with acute myocardial infarction in patients with stable angina pectoris.
MTHFD1 1958AA genotype is linked to a significantly reduced cancer risk. The 1958GG genotype is associated to PBMCs DNA hypomethylation as compared to the A allele carriership that may exert a protective effect for cancer risk by preserving from DNA hypomethylation
Results propose that MTHFD1 synthetase deficiency does not contribute to tumor initiation in the normal colon, but it limits tumor growth by reducing purine pools and altering expression of genes involved in cell proliferation and inflammation.
B vitamin treatments modify the risk of myocardial infarction associated with a MTHFD1 polymorphism in patients with stable angina pectoris.
Paternal, rather than a maternal, transmission bias of MTHFD1 G1958A variant for neural tube defects susceptibility in the offspring.
impairments in MTHFD1 activity compromise both homocysteine remethylation and de novo thymidylate biosynthesis, and provide evidence that MTHFD1-associated disruptions in de novo thymidylate biosynthesis lead to genome instability that may underlie folate-associated immunodeficiency and birth defects
G1958A (MTHFD1) polymorphisms showed no association with ischemic heart disease in patients from Yucatan, Mexico
Study evaluated cognitive function in Mthfd1(gt/+) male and female mice using a behavioral battery composed of eight different tests, found that these mice display impaired cue-conditioned learning, while other behaviors remain intact.
Study observed decreased tumor growth in mice with reduced MTHFD1-synthetase activity, a model for the decreased metabolic activity of the human R653Q variant. These results propose that synthetase deficiency does not contribute to tumor initiation in the normal colon, but it limits tumor growth by reducing purine pools and altering expression of genes involved in cell proliferation and inflammation.
Moderately higher folate intake and MTHFD1-synthetase deficiency in pregnant mice result in a lower methylation potential in maternal liver and embryos and a greater incidence of defects in embryos.
Deficiency of the MTHFD1 10-formyltetrahydrofolate synthetase activity in embryos is associated with increased incidence of congenital heart defects
methylenetetrahydrofolate dehydrogenase 1 (MTHFD1), an enzyme that generates methylenetetrahydrofolate from formate, ATP, and NADPH (zeige FDXR Antikörper), functions in the nucleus to support de novo thymidylate biosynthesis.
Mthfd1gt/+ mice exhibited attentional dysfunction and a blunted affective response to committing an error. They also showed decreased expression levels for genes encoding choline dehydrogenase (zeige CHDH Antikörper) and the alpha 7 nicotinic cholinergic receptor (zeige CHRFAM7A Antikörper).
Data suggest that decreased MTHFD1 activity (here, insertional mutant heterozygotes) has greater impact on one-carbon metabolism compared with folate-deficient diet; no interaction was observed between MTHFD1 genotype and folate deficiency.
Data suggest that heterozygosity in a lethal Mthfd1 mutation impairs folate status in pregnant mice (i.e., impairs fetal growth) but does not significantly affect homocysteine metabolism (i.e., does not cause neural tube defects).
Mthfd1 is a modifier of chemically induced intestinal carcinogenesis.
MTHFD1 has a role in production of monofunctional 10-formyltetrahydrofolate synthetase in mammalian mitochondria
Data suggest that upregulation of 10-formyltetrahydrofolate dehydrogenase (FDH (zeige ALDH1L1 Antikörper)) involving CEBPalpha helps relieve embryonic oxidative stress induced (zeige SQSTM1 Antikörper) by ethanol exposure.
This gene encodes a protein that possesses three distinct enzymatic activities, 5,10-methylenetetrahydrofolate dehydrogenase, 5,10-methenyltetrahydrofolate cyclohydrolase and 10-formyltetrahydrofolate synthetase. Each of these activities catalyzes one of three sequential reactions in the interconversion of 1-carbon derivatives of tetrahydrofolate, which are substrates for methionine, thymidylate, and de novo purine syntheses. The trifunctional enzymatic activities are conferred by two major domains, an aminoterminal portion containing the dehydrogenase and cyclohydrolase activities and a larger synthetase domain.
5,10-methylenetetrahydrofolate dehydrogenase, 5,10-methylenetetrahydrofolate cyclohydrolase, 10-formyltetrahydrofolate synthetase
, C-1-tetrahydrofolate synthase, cytoplasmic
, C1-THF synthase
, cytoplasmic C-1-tetrahydrofolate synthase
, C1-tetrahydrofolate synthase
, methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase
, methylenetetrahydrofolate dehydrogenase 1
, methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
, c-1-tetrahydrofolate synthase, cytoplasmic
, formyltetrahydrofolate synthetase
, methenyltetrahydrofolate cyclohydrolase
, mthfd1 protein
, methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
, c-1-tetrahydrofolate synthase, cytoplasmic-like
, LOW QUALITY PROTEIN: C-1-tetrahydrofolate synthase, cytoplasmic