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324 Possible Causes for biosynthesis, myo inositol

  • Tuberculosis

    Additionally, Mannosyl-phosphatidyl- myo -inositol-based glycolipids (PIM) and related lipoglycans such as lipomannan (LM) and lipoarabinomannan (LAM) are also abundantly[doi.org] Defective mycolic acid biosynthesis in a mutant of Mycobacterium sme gmatis . J. Gen. Microbiol. 137 , 2197–2200. PubMed Google Scholar 67.[doi.org] Biosynthesis of D-arabinose in mycobacteria –a novel bacterial pathway with implications for antimycobacterial therapy.[dx.doi.org]

  • Rhizomelic Chondrodysplasia Punctata

    MR spectroscopy of the brain showed that normal-appearing white matter was characterized by increased levels of mobile lipids and myo-inositol, reduced levels of choline,[ncbi.nlm.nih.gov] The regulation in the biosynthesis of plasmalogens also takes place at this step using a feedback mechanism to stimulate or inhibit the biosynthesis.[ncbi.nlm.nih.gov] The signals from myo -inositol (Ins) and glycine (Gly), choline (Cho), creatine and phosphocreatine (tCr), and N -acetylaspartate (NAA) were integrated.[ajnr.org]

  • Mevalonate Kinase Deficiency

    Deficiency of mevaldate reductase Deficiency of mevalonate kinase Deficiency of monodehydroascorbate reductase Deficiency of monooxygenase Deficiency of mutase Deficiency of myo-inositol[icd9data.com] […] disorder mevalonate kinase (MK) deficiency, which includes the hyperimmunoglobulin D with periodic fever syndrome, MK becomes the rate-limiting enzyme in the isoprenoid biosynthesis[ncbi.nlm.nih.gov] , further suggesting an impairment of non-sterol isoprenoid biosynthesis in MKD.[ncbi.nlm.nih.gov]

  • Chondrodysplasia Punctata

    The signals from myo -inositol (Ins) and glycine (Gly), choline (Cho), creatine and phosphocreatine (tCr), and N -acetylaspartate (NAA) were integrated.[ajnr.org] […] dehydrocholesterol (42.2 micromol/l, controls 1) and 7-dehydrocholesterol (25.5 micromol/l, controls 1) recognised with GC/MS suggested an endogenous defect of cholesterol biosynthesis[ncbi.nlm.nih.gov] The regulation in the biosynthesis of plasmalogens also takes place at this step using a feedback mechanism to stimulate or inhibit the biosynthesis.[ncbi.nlm.nih.gov]

  • Molybdenum Cofactor Deficiency Complementation Group B

    Mycothiol, 1- O -(2′-[ N -acetyl- l -cysteinyl]amido-2′-deoxy-alpha- d -glucopyranosyl)- d - myo -inositol, is the factor of NAD/factor-dependent formaldehyde dehydrogenase[mic.microbiologyresearch.org] […] inhibition and Moco biosynthesis.[pnas.org] The interacting partners are mog (molybdopterin biosynthesis protein), moaA1 (molybdenum cofactor biosynthesis protein A moaA1), moaA2 (molybdenum cofactor biosynthesis protein[journals.plos.org]

  • Polycystic Ovary Syndrome

    A) or myo inositol and folic acid only (Group B), continuously for 6 months.[ncbi.nlm.nih.gov] Pathway analysis results indicated that these aberrantly expressed mRNAs were related to several specific signaling pathways, including insulin resistance, steroid hormone biosynthesis[ncbi.nlm.nih.gov] Bisphenol A impairs follicle growth, inhibits steroidogenesis, and down-regulates rate-limiting enzymes in the estradiol biosynthesis pathway.[doi.org]

  • Chondrodysplasia with Joint Dislocations Type gPAPP

    )P3 Myo-inositol Pathway Diagram Inositol Phosphate Metabolism, Ins(1,3,4,5)P4 Ins(1,3,4)P3 Myo-inositol Pathway antibodies Inositol Phosphate Metabolism, Ins(1,3,4,5)P4 Ins[mybiosource.com] Pathway: Polyol metabolism; myo-inositol biosynthesis; myo-inositol from D-glucose 6-phosphate: step 2/2.[abcam.com] The underlying etiology of RCDP is a deficiency in the biosynthesis of ether phospholipids, of which plasmalogens are the most abundant form in nervous tissue and myelin;[readbyqxmd.com]

  • Rhizomelic Chondrodysplasia Punctata Type 2

    The signals from myo -inositol (Ins) and glycine (Gly), choline (Cho), creatine and phosphocreatine (tCr), and N -acetylaspartate (NAA) were integrated.[ajnr.org] The reported girl's abnormal formation of myelin is probably related to the inadequacy of plasmalogen biosynthesis, which is likely to be due to deficient DHAPAT activity.[ncbi.nlm.nih.gov] The underlying molecular defect is mutation in the PEX7 gene resulting in abnormal peroxisome biosynthesis.[casereports.bmj.com]

  • Disorder of Purine Metabolism

    Progesterone Propentofylline PMAT Decynium-22 Enzyme ( inhibitors ) XO Allopurinol Amflutizole Benzbromarone Caffeic acid Cinnamaldehyde Cinnamomum osmophloeum Febuxostat Myo-inositol[en.wikipedia.org] […] on bacteria, but not in human cells inhibit the reduction of dihydrofolate to tetrahydrofolate. limit the amount of tetra available and will slow down purine biosynthesis[quizlet.com] An important purine compound is adenosine triphosphate (ATP), which is used to transfer chemical energy for processes such as biosynthesis and transport.[medicine.jrank.org]

  • Aromatic L-Amino Acid Decarboxylase Deficiency

    Deficiency of mevaldate reductase Deficiency of mevalonate kinase Deficiency of monodehydroascorbate reductase Deficiency of monooxygenase Deficiency of mutase Deficiency of myo-inositol[icd9data.com] Abstract Aromatic L-amino acid decarboxylase (EC. 4.1.1.28) deficiency is a newly described inborn error of metabolism that affects serotonin and dopamine biosynthesis.[ncbi.nlm.nih.gov] Women's Medical University, Tokyo, Japan. [email protected] Abstract Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare inborn error of neurotransmitter biosynthesis[ncbi.nlm.nih.gov]

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