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SHMT1 encodes the cellular form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. Additionally we are shipping serine Hydroxymethyltransferase 1 (Soluble) Antibodies (64) and serine Hydroxymethyltransferase 1 (Soluble) Proteins (14) and many more products for this protein.
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SHMT1 C1420T polymorphism contributes to the risk of non-Hodgkin.
we identified SHMT1 as a target gene of miR (show MLXIP ELISA Kits)-198. In conclusion, miR (show MLXIP ELISA Kits)-198 suppressed proliferation of lung adenocarcinoma cells both in vitro and in vivo by directly targeting SHMT1.
an association between MTRR (show MTRR ELISA Kits) 66 and SHMT1 1420 polymorphisms and spaceflight-induced vision changes
our meta-analysis suggested that the SHMT1 C1420T polymorphism was associated with decreased risk of breast cancer.
SHMT1 knockdown in lung cancer cells leads to cell cycle arrest and to p53 (show TP53 ELISA Kits)-dependent apoptosis.
In this meta-analysis, SHMT1 C1420T polymorphism did not have a significant association with the risk of cancer overall.
SHMT1 exists in solution as a tetramer, both in the absence and presence of PLP (show PLP1 ELISA Kits), while SHMT2 (show SHMT2 ELISA Kits) undergoes a dimer-to-tetramer transition.
found evidence for association of SHMT1 C1420T polymorphism with significantly reduced risk of breast cancer in Asians
SHMT1 C1420T polymorphism is not associated with overall cancer development.
serine hydroxymethyltransfarase C1420T reduces risk for both acute lymphoblastic leukemia and acute myeloid leukemia (show BCL11A ELISA Kits) and influences disease progression in acute lymphoblastic leukemia
Shmt1 and dietary folate deficiency influence metabolic markers of homocysteine remethylation in mice.
SHMT1 and TYMS (show TYMS ELISA Kits) localization to the nucleus is essential to prevent uracil accumulation in DNA
Data show that Shmt1 hemizygosity was associated with increased risk for intestinal cancer in Apc (show APC ELISA Kits)(min)(/+) mice through a gene-by-diet interaction.
These results provide evidence that disruption of Shmt1 expression causes NTDs by impairing thymidylate biosynthesis and shows that changes in the expression of genes that encode folate-dependent enzymes may be key determinates of NTD risk.
Shmt1 (SHMT1), but not Srr (show SRR ELISA Kits), is likely to be one of the genetic components regulating prepulse inhibition in mice and possibly relevant to human schizophrenia.
mitochondrial SHMT-derived one-carbon units are essential for folate-mediated one-carbon metabolism in the cytoplasm
SHMT1 and SHMT2 (show SHMT2 ELISA Kits) are functionally redundant in nuclear de novo thymidylate biosynthesis
we have expressed, characterized, and determined the crystal structures of rabbit cytosolic serine hydroxymethyltransferase T254A and T254C mutant forms, in the absence and presence of substrates.
SHM1 and SHM2 operate in a redundant manner in one-carbon metabolism of nonphotorespiring cells with a high demand of one-carbon units.
The senescence is initiated in shm1-1 under photorespiratory conditions. Transcription of the senescence marker SAG12 is enhanced in shm1-1.
Structural modeling of SHM1, SHM2, and SHM4 presented features that may explain the activity differences between the mitochondrial and cytosolic isozymes.
The characterization and expression of SHMT1 in A. thaliana. [SHMT1]
SHM1 expression is required for mitochondrial serine hydroxymethyltransferase (show SHMT2 ELISA Kits) activity and proper function of the C2 cycle during growth in ambient air.
SHMT1 interacts with GLU1 and this interaction is necessary for photorespiratory serine hydroxymethyltransferase (SHMT) activity.
This gene encodes the cellular form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing of this gene results in 2 transcript variants encoding 2 different isoforms. Additional transcript variants have been described, but their biological validity has not been determined.
serine hydroxymethyltransferase, cytosolic
, serine hydroxymethyltransferase 1 (soluble)
, glycine hydroxymethyltransferase
, serine methylase
, cytoplasmic serine hydroxymethyltransferase
, cytosolic serine hydroxymethyltransferase
, serine hydroxymethyl transferase
, serine hydroxymethyltransferase 2 (mitochondrial)