Create issue ticket

2,735 Possible Causes for (NAD(P), ), dehydrogenase, formation,, glutamate, glutamate, using

Did you mean: (NAD(P), ), dehydrogenase, formication, glutamate, glutamate, using

  • Hyperammonemia

    RESULTS: The number of patients who developed hyperammonemia during VPA-based therapy was 20 (9.9%) using the 200 μg/dL cutoff value and 30 (14.9%) using the 170 μg/dL cutoff[ncbi.nlm.nih.gov] His hyperammonemia was found on celiac angiography to be due to the formation of a spontaneous portacaval shunt.[ncbi.nlm.nih.gov] […] second most common cause of hyperinsulinemic hypoglycemia of infancy, and it is caused by activating mutations in GLUD1, the gene that encodes mitochondrial enzyme glutamate dehydrogenase[ncbi.nlm.nih.gov] ( p ) h nicotinamide adenine dinucleotide (phosphate); ass argininosuccinate synthetase; asl argininosuccinate lyase; arg1 arginase 1; ornt1 ornithine transporter; oat ornithine[current-oncology.com] OBJECTIVE: The aim of this research letter was to describe the use of N-carbamoyl-L-glutamate as first-line treatment of hyperammonemia in a 4-month-old female patient with[ncbi.nlm.nih.gov] After an extensive workup, he was found to have hyperammonemia and encephalopathy due to formation of a spontaneous splenorenal shunt.[ncbi.nlm.nih.gov] The genetic diagnosis revealed that the patient carried a heterozygous, de novo missense mutation (N410I, c.1401A T) in the glutamate dehydrogenase 1 gene (GLUD1).[ncbi.nlm.nih.gov]

    Missing: )
  • Aldehyde

    Using a multiple reaction-monitoring mass spectrometry analysis, we found that multiple ALDH isozymes were generally abundant in NSCLC cells compared with their levels in[ncbi.nlm.nih.gov] Efficient catalytic greenhouse gas-free hydrogen and aldehyde formation from aqueous alcohol solutions Author affiliations * Corresponding authors a Department of Chemistry[pubs.rsc.org] These enzymes include alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH), which play a significant role in the metabolism of many biological substances and exist[ncbi.nlm.nih.gov] Can use ferredoxin or methylviologen but not NAD(P) as electron acceptor. Please wait a moment until the data is sorted.[brenda-enzymes.org] Head and neck CSC (CD44 hi /ALDH hi ) exhibited higher glutaminase, glutamate, and sphere levels than CD44 lo /ALDH lo cells.[ncbi.nlm.nih.gov] IHC was performed using an immunoperoxidase method with a primary polyclonal rabbit anti-ALDH1A1 antibody.[ncbi.nlm.nih.gov] Thus, this anion provides a useful method for the synthesis of α-hydroxy and α-keto acids, particularly in cases where cyanohydrin formation is difficult.[doi.org]

    Missing: )
  • Ketamine

    To prevent ketamine from being improperly used and evolving into an epidemic, a thorough survey on the prevalence and characteristics of illicit ketamine use is imperative[ncbi.nlm.nih.gov] Ketamine (100 microM) reversed DAMGO (mu) and spiradoline (kappa) inhibition of formation of cyclic adenosine monophosphate.[ncbi.nlm.nih.gov] CASE SUMMARY: A 2-year-old girl with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and stable hypertrophic cardiomyopathy was admitted to the pediatric intensive care[ncbi.nlm.nih.gov] This review focuses on the use of glutamate receptor modulators for depression in bipolar disorder. 1.[ncbi.nlm.nih.gov] In addition, no significant effect was observed on lactate dehydrogenase (LDH) release (indicating necrotic cell death) in ketamine-treated (10μM) rat cultures ( Wang et al[doi.org] Ketamine (100 [micro sign]M) reversed DAMGO ([micro sign]) and spiradoline ([small kappa, Greek]) inhibition of formation of cyclic adenosine monophosphate.[doi.org] Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.[dovepress.com]

    Missing: (NAD(P) )
  • 2-Hydroxyglutaric Aciduria

    We also used mass spectrometric methods to measure the levels of 2HG in plasma and serum.[ncbi.nlm.nih.gov] Formation of labelled 2-ketoglutaric acid (2-KG), citric acid and L-2-HG was determined by GC-MS.[ncbi.nlm.nih.gov] […] mutations in the d-2-hydroxyglutarate dehydrogenase gene cause d-2-hydroxyglutaric aciduria.[ncbi.nlm.nih.gov] (P)-binding domain of L2HGDH protein.[ncbi.nlm.nih.gov] The multiplet at 2.10-2.50 ppm might have been created by elevated glutamate and glutamine or l-2-hydroxyglutaric acid itself, which has a similar chemical structure to glutamate[ncbi.nlm.nih.gov] The formation of L: -2-hydroxyglutarate results from a side-activity of mitochondrial L: -malate dehydrogenase, the enzyme that interconverts oxaloacetate and L: -malate,[ncbi.nlm.nih.gov] Enzyme activities were quantified using LC-MS/MS.[ncbi.nlm.nih.gov]

    Missing: )
  • Pyruvate Carboxylase Deficiency

    This is a compassionate use study to allow patients already taking triheptanoin (C7) through previous studies to continue to receive the supplement.[clinicaltrials.gov] Researchers suggest that the loss of pyruvate carboxylase function in the nervous system, particularly the role of the enzyme in myelin formation and neurotransmitter production[en.wikipedia.org] However, pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase activities in liver tissues were within normal limits.[ncbi.nlm.nih.gov] IPERLATTACIDEMIE con AUMENTATO RAPPORTO L/P • deficit di Piruvico Carbossilasi (PC) - deficit di Biotinidasi Glucosio • deficit del ciclo di Krebs NAD β OHbutirrico • deficit[slideshare.net] Glutamine content was greatly reduced in all brain regions, while glutamic acid and proline contents were elevated.[ncbi.nlm.nih.gov] […] complex deficiency Phosphoenolpyruvate carboxykinase deficiency 2-Ketoglutarate dehydrogenase deficiency Dihydrolipoamide dehydrogenase deficiency Fumarase deficiency Lab[emedicine.medscape.com] US: multicystic changes bilaterally US: minimal ventricular dilatation US: bilateral cysts MRI: severe cortical atrophy MRI: intraventricular retrocerebral subdural hemorrhagia[ncbi.nlm.nih.gov]

    Missing: )
  • Sarcosinemia

    The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.[orpha.net] Format Definition A metabolic disorder characterized by an increased concentration of sarcosine in plasma and an increased excretion of sarcosine in urine.[uniprot.org] Sarcosine is a key intermediate in 1-carbon metabolism and under normal circumstances is converted to glycine by the enzyme sarcosine dehydrogenase.[ncbi.nlm.nih.gov] BioCyc Guanidinoacetate N-methyltransferase 743 ChemSpider 5-AMINO-LEVULINATE BioCyc Aminomethyltransferase, mitochondrial 740 ChemSpider 3-P-SERINE BioCyc SMILES [H][[email protected]@[smpdb.ca] […] α-ketoglutarate Histidine Carnosinemia · Histidinemia · Urocanic aciduria Proline Hyperprolinemia · Prolidase deficiency Glutamate / glutamine SSADHD G propionyl-CoA succinyl-CoA[wiki30.com] Copyright 1984 by the American Academy of Pediatrics Log in using your username and password Log in through your institution You may be able to gain access using your login[pediatrics.aappublications.org] The formation and degradation of sarcosine occur in liver and kidney tissue.[ommbid.mhmedical.com]

    Missing: )
  • Connective Tissue Disease

    What tests to doctors use to diagnose connective tissue diseases?[medicinenet.com] However, formatting rules can vary widely between applications and fields of interest or study.[worldcat.org] […] deficiency with mild methylmalonic acidemia Methylmalonic semialdehyde dehydrogenase (see also Branched-chain amino acid metabolism, above) ALDH6A1 (14q24.1) Biochemical[merck.com] Long term use of immunesuppressants and corticosteroids has been associated with increased risk of infections.[symptoma.com] Latent lupus and incomplete lupus are alternative terms that have been used to describe this condition. Psoriatic arthritis is also a collagen vascular disease.[en.wikipedia.org] Collagen vascular disease is a somewhat antiquated term used to describe diseases of the connective tissues that typically include diseases that can be (but are not necessarily[medicinenet.com] : Benign Treatment: None needed Pyridoxine dependency with seizures (266100) Not determined Specific gene not determined (5q31.2-q31.3) Biochemical profile: Elevated CSF glutamate[merck.com]

    Missing: (NAD(P) )
  • Formiminotransferase Deficiency

    Abstract During the past six years an increasing number of liver-cell adenomas in women were diagnosed, and we undertook a study of possible etiologic faciors, including use[nejm.org] […] the ReadCube Cloud Printing and saving restrictions apply Rental: USD 8.50 Cloud: USD 20.00 Select Complete book Immediate access to all parts of this book Cover-to-cover formats[karger.com] 3 Hydroxy Acyl CoA Dehydrogenase Deficiency Trifunctional Protein Deficiency Very Long Chain AcylCoA Dehydrogenase Deficiency Short Chain AcylCoA Dehydrogenase Deficiency[neolab.gr] […] the bifunctional enzyme glutamate formiminotransferase-cyclodeaminase (FTCD).[ncbi.nlm.nih.gov] […] formiminotransferase deficiency (mesh:C537425) [ctd_resource:D002220C537425] Faceted Search & Find service v1.13.83 as of Jan 18 2016 Alternative Linked Data Documents: iSPARQL ODE Content Formats[bio2rdf.org] Finding useful health information on the Internet can be difficult, but we’re here to help. This page gathers quality information from trusted sources.[diseaseinfosearch.org] […] capacity because methionine is the immediate precursor of S-adenosylmethionine, a potent inhibitor of 5-methyltetrahydrofolate synthesis; methionine serves as a source of formate[jci.org]

    Missing: (NAD(P) )
  • Malignant Neoplasm

    Abstract We investigated the geographical patterns of mortality from eight (males)/ten (females) sites of malignant neoplasm, using cluster analysis with Standardized Mortality[ncbi.nlm.nih.gov] In this study, the plasma fraction containing AIS is shown to inhibit mouse erythroblast formation in vitro.[ncbi.nlm.nih.gov] Age, white blood count, and serum albumin, alkaline phosphatase, and lactate dehydrogenase levels were selected as the best predictors.[ncbi.nlm.nih.gov] Induction in NAD(P)H/quinone oxidoreductase and heme oxygenase-1 was observed in the breast tissue of all patients, indicating the anticancer effect of SFN ( 77 ).[dx.doi.org] Mech Ageing Dev 112:185–196. doi: 10.1016/S0047-6374(99)00087-1 PubMed Google Scholar Lee J, Chan SL, Lane MA, Mattson MP (2002) Phenformin suppresses calcium responses to glutamate[doi.org] […] stratification: The FL International Prognostic Index prognostic model for FL uses five independent predictors of inferior survival: age 60 years, hemoglobin 12 g/dL, serum lactate dehydrogenase[doi.org] PATIENT(S): One hundred eighteen couples undergoing IVF-ICSI using pretreatment frozen sperm. INTERVENTION(S): Treatment follow-up.[ncbi.nlm.nih.gov]

    Missing: )
  • Acamprosate

    Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.[drugs.com] Also, formation of long-lived hydroxyethyl free radicals from ethanol may result in membrane damage due to an increase in lipid peroxidation ( 49 ).[ajp.psychiatryonline.org] J. ( 1984 ) Aldehyde dehydrogenase isozyme deficiency and alcohol sensitivity in four different Chinese populations. Human Heredity 34 , 183 –186. Helzer, J.[academic.oup.com] Four weeks of acamprosate treatment reduced glutamate levels (P 0.025), an effect that was not observed in subjects who did not take acamprosate.[ncbi.nlm.nih.gov] Disulfiram Disulfiram inhibits acetaldehyde dehydrogenase.[aafp.org] These results suggest that acamprosate reduces serum glutamate levels for those who have elevated baseline serum glutamate levels among responders.[ncbi.nlm.nih.gov] It has been used in Europe, the USA and other countries for many years and was recently approved for this indication in Japan.[doi.org]

    Missing: (NAD(P) )