Pages that link to "Q44674034"

The following pages link to Targeted disruption of the mouse 3-phosphoglycerate dehydrogenase gene causes severe neurodevelopmental defects and results in embryonic lethality (Q44674034):

Displaying 47 items.

• Phosphoserine aminotransferase deficiency: a novel disorder of the serine biosynthesis pathway (Q24682720) (← links)
• Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway (Q28246648) (← links)
• Strain-specific modifier genes governing craniofacial phenotypes (Q30457692) (← links)
• Proteome alteration of U251 human astrocytoma cell after inhibiting retinoic acid synthesis (Q33393710) (← links)
• A detailed genome-wide reconstruction of mouse metabolism based on human Recon 1. (Q33722800) (← links)
• D-amino acids in the central nervous system in health and disease (Q33988102) (← links)
• Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDH. (Q34000892) (← links)
• Effects of L-serine ingestion on human sleep (Q34135776) (← links)
• Mouse genetics suggests cell-context dependency for Myc-regulated metabolic enzymes during tumorigenesis (Q34205937) (← links)
• Brain-specific Phgdh deletion reveals a pivotal role for L-serine biosynthesis in controlling the level of D-serine, an N-methyl-D-aspartate receptor co-agonist, in adult brain. (Q34438746) (← links)
• Treatment with amino acids in serine deficiency disorders (Q34536482) (← links)
• L-serine synthesis in the central nervous system: a review on serine deficiency disorders (Q35016184) (← links)
• Gene expression profiling reveals putative HOXA10 downstream targets in the periimplantation mouse uterus (Q35023831) (← links)
• Ganglioside biochemistry (Q35361488) (← links)
• Glycolytic flux controls D-serine synthesis through glyceraldehyde-3-phosphate dehydrogenase in astrocytes (Q35567073) (← links)
• L-Serine Deficiency Elicits Intracellular Accumulation of Cytotoxic Deoxysphingolipids and Lipid Body Formation (Q35860803) (← links)
• Cancer's sweet tooth for serine (Q35861498) (← links)
• The importance of serine metabolism in cancer (Q37145927) (← links)
• A world of sphingolipids and glycolipids in the brain--novel functions of simple lipids modified with glucose (Q38002318) (← links)
• Serine biosynthesis by photorespiratory and non-photorespiratory pathways: an interesting interplay with unknown regulatory networks. (Q38063938) (← links)
• On the phenotypic spectrum of serine biosynthesis defects (Q38767340) (← links)
• Serine biosynthesis and transport defects (Q38830566) (← links)
• Identification of LncRNAs/mRNAs related to endometrium function regulated by Homeobox A10 in Ishikawa cells (Q38901594) (← links)
• Serine and one-carbon metabolism in cancer (Q38955873) (← links)
• One-Carbon Metabolism in Health and Disease (Q38957946) (← links)
• Amino acid synthesis deficiencies (Q39400023) (← links)
• Novel mutations in 3-phosphoglycerate dehydrogenase (PHGDH) are distributed throughout the protein and result in altered enzyme kinetics (Q39880829) (← links)
• Adaptive response to l-serine deficiency is mediated by p38 MAPK activation via 1-deoxysphinganine in normal fibroblasts (Q39881905) (← links)
• Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH. (Q40046496) (← links)
• A novel role of L-serine (L-Ser) for the expression of nuclear factor of activated T cells (NFAT)2 in receptor activator of nuclear factor kappa B ligand (RANKL)-induced osteoclastogenesis in vitro (Q40238894) (← links)
• Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination. (Q40871094) (← links)
• Inactivation of the 3-phosphoglycerate dehydrogenase gene in mice: changes in gene expression and associated regulatory networks resulting from serine deficiency (Q41939417) (← links)
• A phenotypic small-molecule screen identifies an orphan ligand-receptor pair that regulates neural stem cell differentiation (Q42579390) (← links)
• D-serine influences synaptogenesis in a p19 cell model (Q43186293) (← links)
• The phosphorylated pathway of serine biosynthesis is essential both for male gametophyte and embryo development and for root growth in Arabidopsis (Q43478090) (← links)
• L-serine deficiency caused by genetic Phgdh deletion leads to robust induction of 4E-BP1 and subsequent repression of translation initiation in the developing central nervous system (Q43763036) (← links)
• Expression of L-serine biosynthetic enzyme 3-phosphoglycerate dehydrogenase (Phgdh) and neutral amino acid transporter ASCT1 following an excitotoxic lesion in the mouse hippocampus (Q46408557) (← links)
• Dietary L-serine modifies free amino acid composition of maternal milk and lowers the body weight of the offspring in mice (Q47173212) (← links)
• Targeting Metabolism for Cancer Therapy. (Q47646742) (← links)
• Transcriptional regulatory control of mammalian nephron progenitors revealed by multi-factor cistromic analysis and genetic studies. (Q48149649) (← links)
• Detection of D-3-phosphoglycerate dehydrogenase autoantibodies in patients with autoimmune hepatitis: Clinical significance evaluation. (Q54358503) (← links)
• Enhanced vulnerability to oxidative stress and induction of inflammatory gene expression in 3-phosphoglycerate dehydrogenase-deficient fibroblasts. (Q55332284) (← links)
• Reduction of stratum corneum ceramides in Neu-Laxova syndrome caused by phosphoglycerate dehydrogenase deficiency (Q57803833) (← links)
• D-3-Phosphoglycerate Dehydrogenase (Q60956684) (← links)
• Deoxysphingolipid precursors indicate abnormal sphingolipid metabolism in individuals with primary and secondary disturbances of serine availability (Q88777219) (← links)
• Metabolism of amino acid neurotransmitters: the synaptic disorder underlying inherited metabolic diseases (Q88991048) (← links)
• Hypoxia tolerance in the Norrin-deficient retina and the chronically hypoxic brain studied at single-cell resolution (Q93110741) (← links)