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PLoS Genetics, ISSN 1553-7390, 10/2014, Volume 10, Issue 10, p. e1004688
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 04/2012, Volume 122, Issue 4, pp. 1416 - 1426
Journal Article
Nature, ISSN 0028-0836, 01/2017, Volume 541, Issue 7636, pp. 233 - 236
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2006, Volume 103, Issue 50, pp. 19206 - 19211
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2016, Volume 12, Issue 5, p. e1006056
Mitochondrial import of pyruvate by the mitochondrial pyruvate carrier (MPC) is a central step which links cytosolic and mitochondrial intermediary metabolism.... 
TRANSPORT | STIMULATED INSULIN-SECRETION | METABOLISM | GLUCONEOGENESIS | GENETICS & HEREDITY | LACTIC-ACIDOSIS | MICE | DIFFERENTIATION | RAT-LIVER MITOCHONDRIA | MASS-SPECTROMETRY | DEHYDROGENASE DEFICIENCY | Pyruvates | Embryonic development | Genetic aspects | Health aspects | Ketogenic diet | Brain | Genotype & phenotype | Phosphorylation | Dehydrogenases | Metabolites | Diet | Funding | Metabolism | Mammals | Labeling | Experiments | Embryos
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e38941
Sphingosine-1-phosphate (S1P), a sphingolipid metabolite that is produced inside the cells, regulates a variety of physiological and pathological responses via... 
IMMUNOMODULATOR FTY720 | ERYTHROCYTES | METABOLISM | PLATELETS | MAST-CELLS | BIOLOGY | RECEPTOR | RELEASE | LYMPHOCYTE EGRESS | SPHINGOSINE 1-PHOSPHATE | BLOOD | Lymphocytes - metabolism | Gene Targeting | Lysophospholipids - metabolism | Endothelial Cells - metabolism | Humans | Mice, Inbred C57BL | Male | Lysophospholipids - blood | Anion Transport Proteins - metabolism | Mice, Knockout | Sphingosine - analogs & derivatives | Animals | Blood Platelets - metabolism | Anion Transport Proteins - deficiency | Erythrocytes - metabolism | Sphingosine - blood | Female | Transcription, Genetic | Mice | Sphingosine - metabolism | Thymus Gland - metabolism | Anion Transport Proteins - genetics | Phosphates | Sphingosine | Physiological aspects | Lipids | Cellular signal transduction | B cells | Endothelium | Motility | Leukocyte migration | Erythrocytes | Biology | Egress | Kinases | Phosphatase | Thymus | Sphingosine 1-phosphate | Blood plasma | Proteins | Genotype & phenotype | Signal transduction | Receptors | Biomedical materials | Red blood cells | Lymphocytes | Rodents | Biocompatibility | Physiology | Chemical synthesis | Pharmaceutical sciences | Concentration gradient | Quantitative analysis | Antigens | Phosphate transporter | Zebrafish | Pharmacology | Mammals | Exports | Endothelial cells | Signaling | Lymphopenia | Osteoclasts | Transduction | Platelets | Transporter | Cell migration | Cancer
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2006, Volume 103, Issue 43, pp. 15927 - 15932
SLC25A19 mutations cause Amish lethal microcephaly (MCPHA), which markedly retards brain development and leads to α-keto-glutaric aciduria. Previous data... 
Yolk sac | Mitochondria | Dehydrogenases | Amniotic fluid | Central nervous system | Mice | Nucleotides | Diphosphates | Embryos | Genetic mutation | Thiamine pyrophosphate deficiency | Development | Mouse model | Mitochondrial transporter | Neural tube defect | development | TRANSPORTER | mouse model | MULTIDISCIPLINARY SCIENCES | thiamine pyrophosphate deficiency | DEOXYNUCLEOTIDE CARRIER | DEFICIENCY | neural tube defect | BIOGENESIS | GENE | mitochondrial transporter | DNA | STRESS | RECONSTITUTION | EMBRYOGENESIS | EXPRESSION | Central Nervous System - metabolism | Thiamine Pyrophosphate - metabolism | Central Nervous System - abnormalities | Mitochondrial Proteins - genetics | Embryo, Mammalian - metabolism | Thiamine Pyrophosphate - deficiency | Embryo Loss - metabolism | Anemia - genetics | Membrane Transport Proteins - deficiency | Membrane Transport Proteins - genetics | Mitochondrial Proteins - metabolism | Anion Transport Proteins - deficiency | Membrane Transport Proteins - metabolism | Embryo Loss - genetics | Ketoglutaric Acids - metabolism | Mitochondrial Proteins - deficiency | Mitochondria - metabolism | Mutation - genetics | Anion Transport Proteins - metabolism | Mice, Knockout | Anemia - congenital | Anemia - metabolism | Animals | Embryo, Mammalian - embryology | Anion Transport Proteins - genetics | Care and treatment | Research | Gene mutations | Microcephaly | Biological Sciences
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Journal Article
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