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1,664 Possible Causes for (Inosine, 1, Dehydrogenase, Gene, IMP, Monophosphate)

  • Malnutrition

    The aim of this study is to evaluate the effect of low-level laser on the saliva of children aged 1 to 5 years with energy-protein malnutrition.[ncbi.nlm.nih.gov] Inosine monophosphate dehydrogenase (IMPDH) regulates intracellular fat accumulation, pre-adipicytes maturation, and is a target of mycophenolic acid (MPA) used as a standard[ncbi.nlm.nih.gov] Abstract Urea cycle disorders (UCDs) most often involve inherited deficiencies in genes that code for enzymes normally used by the urea cycle to breakdown nitrogen.[ncbi.nlm.nih.gov] We concluded that severe ketoacidosis associated with rapid-onset hyperglycemia due to autoimmune type 1 diabetes (AT1D) had occurred shortly before death.[ncbi.nlm.nih.gov] AFB 1 -lysine concentrations in this population ranged between 0.2 and 59.2 pg/mg albumin, with a median value of 2.6 pg/mg albumin.[ncbi.nlm.nih.gov] Development and validation of KASP assays for genes underpinning key economic traits in bread wheat. 2016.[cimmyt.org]

  • Legionella Pneumophila

    Genome information T number T00199 Org code lpn Aliases LEGPH, 272624 Full name Legionella pneumophila subsp. pneumophila Philadelphia 1 (serogroup 1) Definition Legionella[genome.jp] (IMP) or guanosine monophosphate (GMP) in the purine salvage pathway.[ncbi.nlm.nih.gov] Accordingly, DNA was extracted from the bronchoalveolar lavage fluid and used for the PCR-based cloning of the bacterial 16S rRNA gene.[ncbi.nlm.nih.gov] Lp infection increased extracellular lactate dehydrogenase levels and decreased the number of living cells.[ncbi.nlm.nih.gov] Upon translocation into U937 cells, RavN was almost exclusively found in the cytosolic fraction together with the marker protein glyceraldehyde 3-phosphate dehydrogenase ([journals.plos.org] OBJECTIVE: To investigate the potential source of a case of Legionnaires' disease caused by an unusual serotype of Legionella pneumophila serogroup 1 (Lp1) in regional Victoria[ncbi.nlm.nih.gov]

  • Xanthinuria

    We performed an allopurinol loading test and diagnosed classical type 1 xanthinuria.[ncbi.nlm.nih.gov] […] reductase 17 19,543,274 19,580,929 RGD:10402751 G Gmps guanine monophosphate synthase 2 154,555,967 154,590,662 RGD:10402751 G Gucy1a2 guanylate cyclase 1 soluble subunit[rgd.mcw.edu] Genomic DNA was screened for point mutations and imbalances in the XDH gene by sequencing and microarray typing.[ncbi.nlm.nih.gov] Abstract Xanthinuria due to xanthine dehydrogenase (XDH) deficiency is a rare genetic disorder characterized by hypouricemia and the accumulation of xanthine in the urine.[ncbi.nlm.nih.gov] […] acid Pemetrexed Pralatrexate Many others Others Precursors: Adenine Adenosine AMP ADP ATP Cytosine Cytidine CMP CDP CTP Guanine Guanosine GMP GDP GTP Hypoxanthine Inosine IMP[en.wikipedia.org] The duodenal mucosa from the subject had no xanthine dehydrogenase protein while the mRNA level was not reduced.[ncbi.nlm.nih.gov]

  • Treponema Denticola

    In this study we investigated the ability of T. denticola to bind the complement regulatory proteins factor H and factor H-like protein 1 (FHL-1).[ncbi.nlm.nih.gov] Glycosaminoglycan metabolism Terpenoid backbone biosynthesis Sterol biosynthesis Other terpenoid biosynthesis Nucleotide and amino acid metabolism Purine metabolism M00048 Inosine monophosphate[genome.jp] To understand the possible evolution of this protein, we analyzed the sequence of the msp gene in 17 T. denticola positive clinical samples.[ncbi.nlm.nih.gov] A gene matching the 3-oxo-5alpha-steroid 4-dehydrogenase family protein (gene ID: 2739284; locus tag: TDE2697) has been identified in T. denticola ATCC 35405.[ncbi.nlm.nih.gov] Southern blot analysis demonstrated that T. denticola ATCC 35405 expresses the lrrA gene, but the gene was not identified in T. denticola ATCC 33520.[ncbi.nlm.nih.gov] […] denticola cultures are capable of metabolising cholesterol, progesterone, 4-androstenedione and testosterone by means of 5alpha-reductase, 3beta-and 17beta-hydroxysteroid dehydrogenase[ncbi.nlm.nih.gov]

  • Toxoplasma Gondii

    Han Y 1 , Zhou A 2 , Lu G 1 , Zhao G 3 , Sha W 1 , Wang L 4 , Guo J 1 , Zhou J 1 , Zhou H 1 , Cong H 1 , He S 1 .[ncbi.nlm.nih.gov] KEYWORDS: Apicomplexan; Differentiation; Inosine monophosphate dehydrogenase; Mycophenolic acid; Tissue cyst; Toxoplasma[ncbi.nlm.nih.gov] […] of how an intracellular T. gondii can manipulate host genes to avoid host defense.[ncbi.nlm.nih.gov] This study was mainly focused on an estradiol regulatory factor-Hydroxysteroid dehydrogenase (HSD) gene in T. gondii.[ncbi.nlm.nih.gov] Author information 1 Department of Virology, Postgraduate Institute of Medical Education & Research, Chandigarh, India. 160 012.[ncbi.nlm.nih.gov] Deficiency of insulin production accounts for the occurrence of type-1 diabetes mellitus (T1D).[ncbi.nlm.nih.gov]

    Missing: IMP
  • Retinitis Pigmentosa 32

    Epub 2018 Mar 1 doi: 10.1111/aos.13680.[ncbi.nlm.nih.gov] Research article Biochemical Journal Aug 09, 2005, 390 (1) 41-47; DOI: 10.1042/BJ20042051 Abstract Two mutations of IMPDH1 (inosine 5′-monophosphate dehydrogenase type I),[biochemj.org] Gene ID: 641433, updated on 8-Apr-2017 Go to complete Gene record for RP32 Go to Variation Viewer for RP32 variants Associated conditions Description Tests retinitis pigmentosa[ncbi.nlm.nih.gov] […] region of the gene, which was not screened.[jmg.bmj.com] January 01, 1999 ; 52 (1) Articles Joseph J. Higgins , D. Holmes Morton , Joseph M.[n.neurology.org] All Filters Sort By Relevance Relevance Price - Low to High Price - High to Low Years of Experience Recommendation Gender Male Doctor Female Doctor Consultation Fee Free 1-[practo.com]

  • Antimetabolite

    S1 - 1st & 2nd Medical Students S2 - 3rd & 4th Medical Students L1 - PGY1 & PGY2 L2 - PGY3 L3 - PGY4 L4 - PGY5 L5 - Fellow L6 - 1-3 years in practice L7 - 3-10 years in practice[step1.medbullets.com] Purine antagonist: 6-Mercaptopurine • Mechanism of action: • 6-MP inhibit the conversion of inosine monophosphate to adenine and guanine nucleotides that are building blocks[slideshare.net] However, other cellular target enzymes, including thymidylate synthase, inosinate dehydrogenase, cytidine-5'-triphosphate synthetase, and other enzymes from the de novo nucleotide[ncbi.nlm.nih.gov] We also observed that p53 status influenced correlations between ENT1 transporter gene RNA levels and sensitivity to the drugs tiazafurin, AZQ and 3-deazauridine.[ncbi.nlm.nih.gov] […] were evaluated for methylenetetrahydrofolate reductase (MTHFR) gene C667T, thymidilate synthase (TS) gene 5' UTR variable number of tandem repeats (VNTR), dihydroprymidine dehydrogenase[ncbi.nlm.nih.gov] Structure rendered from 2h31.pdb . 16.3.6 Synthesis of AMP from IMP The synthesis of AMP from IMP occurs in two steps.[watcut.uwaterloo.ca]

  • Coronary Artery Disease

    BACKGROUND: Many studies investigated the association between intercellular adhesion molecule 1 (ICAM-1) gene rs5498 polymorphism and the risk of coronary artery disease ([ncbi.nlm.nih.gov] PPI network were identified based on their degrees: LCK proto‑oncogene, Src family tyrosine kinase (LCK), euchromatic histone lysine methyltransferase 2 (EHMT2), inosine monophosphate[ncbi.nlm.nih.gov] METHODS: Chip data (GSE9820) retrieved from Gene Expression Omnibus (GEO) was re-analyzed, and the selected candidate genes, meeting specific conditions, were up-regulated[ncbi.nlm.nih.gov] Abstract The aim of this study is to investigate the impact of aldehyde dehydrogenase 2 (ALDH2) genotype and alcohol consumption on coronary artery lesions in Chinese patients[ncbi.nlm.nih.gov] Then the differentially expressed genes that gradually up-regulated or down-regulated were enriched by Gene Ontology (GO) functional annotation and Kyoto Encyclopedia of Genes[ncbi.nlm.nih.gov] Abstract T regulatory type 1 (Tr1) cells can promote tolerance and suppress inflammation.[ncbi.nlm.nih.gov]

    Missing: IMP
  • Retinitis pigmentosa, Y-Linked

    -2 III; 6.94 16 AMP-Activated Kinase Beta subunit. 10 aap-1 I;-0.38 42 phosphoinositide 3-kinase AGE-1 AdAPter subunit. 11 aat-1 IV; 4.71 29 putative Amino Acid Transporter[ncbi.nlm.nih.gov] Research article Biochemical Journal Aug 09, 2005, 390 (1) 41-47; DOI: 10.1042/BJ20042051 Abstract Two mutations of IMPDH1 (inosine 5′-monophosphate dehydrogenase type I),[biochemj.org] User Ratings 5.0 out of 5 stars ease 1 of 5 2 of 5 3 of 5 4 of 5 5 of 5 0 / 5 features 1 of 5 2 of 5 3 of 5 4 of 5 5 of 5 0 / 5 design 1 of 5 2 of 5 3 of 5 4 of 5 5 of 5 0[sourceforge.net] ORF cDNA Clones and Custom Clones » Species Summary » Homo sapiens » RPY cDNA ORF clone RPY Summary Gene Symbol RPY Entrez Gene ID 79051 Full Name Retinitis pigmentosa, Y-linked[genscript.com] Clear Turn Off Turn On RPY [Homo sapiens] RPY [Homo sapiens] Gene ID:79051 Gene The post-thrombotic syndrome: incidence and prognostic value of non-invasive ven...[ncbi.nlm.nih.gov] Aarskog syndrome Acanthocytosis Acatalasemia Acetyl-CoA carboxylase deficiency Achondroplasia ACTH deficiency Acute hepatic porphyria Acute intermittent porphyria Acyl-CoA dehydrogenase[easternbiotech.com]

  • Ribavirin

    Average 5.0 of 1 Ratings Thank you for rating![medbullets.com] Its metabolite, ribavirin 5′-phosphate, is an inhibitor of inosine monophosphate (IMP) dehydrogenase.[sigmaaldrich.com] It is generally understood that the inosine triphosphatase-CC genotype does not have a significantly lower reduction by pegylated interferon combined with ribavirin in the[ncbi.nlm.nih.gov] BACKGROUND: This study was carried out to search for mutations in the gene encoding for Non- Structural Protein 5A, specifically in the interferon sensitivity determining[ncbi.nlm.nih.gov] Structure and mechanism of inosine monophosphate dehydrogenase in complex with the immunosuppressant mycophenolic acid. Cell 85 : 921 -930. 22. Smee, D. F., M.[jvi.asm.org] […] record] Record 1 - internal organization data 2003-10-09 Record 1, English Record 1, Subject field(s) Record 1, Abbreviations, English Record 1, Synonyms, English Virazole[btb.termiumplus.gc.ca]