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SLC25A38 is a member of the mitochondrial carrier family. Zusätzlich bieten wir Ihnen SLC25A38 Antikörper (22) und SLC25A38 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
the biochemical and molecular characterization of yeast Hem25p and human SLC25A38, providing evidence that they are mitochondrial carriers for glycine. In particular, the hem25Delta mutant manifests a defect in the biosynthesis of delta-aminolevulinic acid and displays reduced levels of downstream heme and mitochondrial cytochromes.
Given the tolerability of glycine and folate in humans, this study points to a potential novel treatment for SLC25A38 congenital sideroblastic anemia
This study findings reveal a novel role for appoptosin in neurological disorders with tau neuropathology, linking caspase-3 (zeige CASP3 ELISA Kits)-mediated tau cleavage to synaptic dysfunction and behavioral/motor defects.
Letter/Case Report: novel frameshift mutation in SLC25A38 causing congenital sideroblastic anaemia.
Several missense mutations are found in SLC25A38 in a Chinese population with congenital sideroblastic anemia.
Compares and contrasts all the known human SLC25A (zeige SLC25A25 ELISA Kits)* genes and includes functional information.
Mutations in the SLC25A38 gene cause severe, non-syndromic, microcytic/hypochromic sideroblastic anemia in many populations.
Twelve CSA (zeige ERCC8 ELISA Kits) probands had biallelic mutations in SLC25A38
This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia.
solute carrier family 25, member 38
, solute carrier family 25 member 38