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87 Possible Causes for 4 Nitrophenylphosphate, phosphohydrolase

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  • Glycogen Storage Disease due to Glucose-6-Phosphat Transport Defect

    The activity of glucose-6-phosphate phosphohydrolase was assayed in a liver specimen biopsied from a patient according to Nordlie and Arion's method.[jstage.jst.go.jp] […] phosphate specific transport system that shuttles G6P from the cytoplasm to the lumen of the endoplasmic reticulum (a G6P translocase), and (2) an enzyme, glucose-6-phosphate phosphohydrolase[en.wikibooks.org] Recently, it was postulated that the G6Pase system contains a phosphate translocase which mediates the efflux of phosphate, in addition to a G6P translocase and a non-specific phosphohydrolase[link.springer.com]

    Missing: 4 Nitrophenylphosphate
  • PTEN Hamartoma Tumor Syndrome

    * Young Adult Substances FOXP3 protein, human Forkhead Transcription Factors Nuclear Proteins PHLPP1 protein, human Phosphoprotein Phosphatases PTEN Phosphohydrolase PTEN[ncbi.nlm.nih.gov] Indexing Status Subject indexing assigned by CRD MeSH Hamartoma Syndrome, Multiples; PTEN Phosphohydrolase Language Published English Country of organisation United States[crd.york.ac.uk] Adolescent — Adult — Aged — Child — Female — Hamartoma Syndrome, Multiple/genetics/pathology — Humans — Hyperplasia/pathology — Male — Middle Aged — Mutation/genetics — PTEN Phosphohydrolase[archive-ouverte.unige.ch]

    Missing: 4 Nitrophenylphosphate
  • Desmoplastic Medulloblastoma

    Medulloblastoma/therapy Mutation Neoplasm Recurrence, Local/genetics Neoplasm Recurrence, Local/pathology Neoplasm Recurrence, Local/therapy Neurosurgical Procedures PTEN Phosphohydrolase[ncbi.nlm.nih.gov] Protein alpha Subunits, Gs Humans Immunotherapy In Situ Hybridization, Fluorescence Male Medulloblastoma Mutation Neoplasm Recurrence, Local Neurosurgical Procedures PTEN Phosphohydrolase[scholars.duke.edu] Receptors Patched-1 Receptor Radiotherapy Receptors, Cell Surface Substances Chromogranins PTCH protein, human Patched Receptors Patched-1 Receptor Receptors, Cell Surface PTEN Phosphohydrolase[ncbi.nlm.nih.gov]

    Missing: 4 Nitrophenylphosphate
  • Neurocutaneous Melanocytosis

    View in: PubMed subject areas Apoptosis Benzimidazoles Blotting, Western Brain Neoplasms Cell Proliferation Child Child, Preschool Fluorescent Antibody Technique GTP Phosphohydrolases[profiles.uchicago.edu] . , , , , , , Source MeSH Adolescent Cell Proliferation Child Child, Preschool DNA Mutational Analysis Female GTP Phosphohydrolases Genotype Humans Infant Male Melanocytes[unboundmedicine.com]

    Missing: 4 Nitrophenylphosphate
  • Hypophosphatasia

    TNSALP is a cell-surface homodimeric phosphohydrolase that is richly expressed in the skeleton, liver, kidney and developing teeth.[ncbi.nlm.nih.gov] TNSALP is a cell-surface homodimeric phosphohydrolase richly expressed in the skeleton, liver, kidney, and developing teeth.[ncbi.nlm.nih.gov] Consequently, cell-surface deficiency of TNSALP phosphohydrolase activity leads to extracellular accumulation of inorganic pyrophosphate, a natural substrate of TNSALP and[ncbi.nlm.nih.gov]

    Missing: 4 Nitrophenylphosphate
  • Autosomal Dominant Optic Atrophy

    Gov't MeSH terms Adult Asian Continental Ancestry Group Base Sequence Exons Female Fibroblasts/metabolism Fibroblasts/pathology GTP Phosphohydrolases/genetics* GTP Phosphohydrolases[ncbi.nlm.nih.gov] RNA, Messenger/metabolism Retinal Ganglion Cells/metabolism Retinal Ganglion Cells/pathology Sequence Deletion Skin/metabolism Skin/pathology Substances RNA, Messenger GTP Phosphohydrolases[ncbi.nlm.nih.gov]

    Missing: 4 Nitrophenylphosphate
  • Juvenile Polyposis Syndrome

    […] deficiency PTEN Phosphohydrolase/genetics* Phenotype Young Adult Substances BMPR1A protein, human Bone Morphogenetic Protein Receptors, Type I PTEN Phosphohydrolase PTEN[ncbi.nlm.nih.gov] […] surgery Male Monitoring, Physiologic Neoplastic Syndromes, Hereditary/genetics* Neoplastic Syndromes, Hereditary/pathology Neoplastic Syndromes, Hereditary/surgery PTEN Phosphohydrolase[ncbi.nlm.nih.gov]

    Missing: 4 Nitrophenylphosphate
  • Glycogen Storage Disease Type 1

    […] phosphate specific transport system that shuttles G6P from the cytoplasm to the lumen of the endoplasmic reticulum (a G6P translocase), and (2) an enzyme, glucose-6-phosphate phosphohydrolase[en.wikibooks.org] […] fructose-1,6-bisphosphatase 1 fructose-1,6-bisphosphatase, Liver fructose-1,6-diphosphatase FBP1 FBP 611570 3606 fructose-bisphosphatase 2 D-fructose-1,6-bisphosphate 1-phosphohydrolase[ukgtn.nhs.uk]

    Missing: 4 Nitrophenylphosphate
  • Metabolic Myopathy

    3 enolase 3 (beta, muscle) enolase 3, (beta, muscle) enolase, beta enolase, muscle-specific ENO3 MSE 131370 3354 fructose-bisphosphatase 2 D-fructose-1,6-bisphosphate 1-phosphohydrolase[ukgtn.nhs.uk]

    Missing: 4 Nitrophenylphosphate
  • Thiamine

    In other organisms, ThTP can be hydrolyzed by unspecific phosphohydrolases.[ncbi.nlm.nih.gov]

    Missing: 4 Nitrophenylphosphate

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