Page last updated: 2024-08-23

s-adenosylmethionine and Diseases, Metabolic

s-adenosylmethionine has been researched along with Diseases, Metabolic in 27 studies

Research

Studies (27)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (3.70)18.2507
2000's4 (14.81)29.6817
2010's16 (59.26)24.3611
2020's6 (22.22)2.80

Authors

AuthorsStudies
He, X; Li, Q; Liu, H; Miao, J; Wan, K; Wang, D; Yuan, Z; Zhang, J; Zhu, J; Zou, L1
Adam, T; Bekárek, V; Friedecká, J; Friedecký, D; Hlídková, E; Ivanovová, E; Kvasnička, A; Piskláková, B; Prídavok, M1
Becker, S; Beuchel, C; Ceglarek, U; Dittrich, J; Isermann, B; Kirsten, H; Kovacs, P; Loeffler, M; Scholz, M; Stumvoll, M; Teren, A; Thiery, J; Tönjes, A1
Baud, O; Benoist, JF; Bower, A; Imbard, A; Pichard, S; Rigal, O; Schiff, M1
Burger, D; Gerber, V; Mach, N; Nuoffer, JM; Ramseyer, A; Thomas, S; van der Kolk, JH1
Abbey, D; Bennett, MJ; Brown, C; Hand, NJ; Kim, HI; Lee, JJ; Lu, W; Rabinowitz, JD; Rader, DJ; Raffler, J; Saleheen, D1
Antone, U; Dambrova, M; Kuka, J; Liepinsh, E; Makarova, E; Makrecka-Kuka, M; Pugovics, O; Sevostjanovs, E; Vilks, K; Volska, K1
Cusmano-Ozog, K; McGuire, PJ; Tarasenko, TN1
Castro, H; Kopecky, J; Kuda, O; Palou, A; Picó, C; Pomar, CA; Rombaldova, M; Sánchez, J1
Celis-Morales, C; Muilwijk, M; Peters, RJG; van Valkengoed, IGM; Vaz, FM1
Gao, X; Gu, X; Han, F; Han, L; Ji, W; Qiu, W; Wang, Y; Ye, J; Zhang, H1
Adams, SH; Knotts, TA; McCoin, CS1
Chen, XX; Fu, W; Li, XW; Liu, J; Zhang, WQ1
Carter, RJ; Fung, E; Hodges, SD; Mantik, KB; Snyder, FF1
Besley, GT; Fleming, G; Henderson, MJ; Patterson, A; Till, J; Walter, JH1
Johnson, DW; Liu, A; Pasquali, M1
Espinoza, L; Holden, KR; Pollard, LM; Schroer, RJ; Spector, EB; Williams, NR; Wood, TC1
Chace, DH; De Jesús, VR; Hannon, WH; Lim, TH; Mei, JV1
Abdenur, JE; Abdulrahman, M; Adair, O; Åhlman, H; Al Nuaimi, SA; Allen, JJ; Antonozzi, I; Archer, S; Au, S; Auray-Blais, C; Baker, M; Bamforth, F; Beckmann, K; Berberich, SL; Bermejo, MS; Binard, R; Boemer, F; Bonham, J; Breen, NN; Bryant, SC; Caggana, M; Caldwell, SG; Cameron, CA; Camilot, M; Campbell, C; Carducci, C; Cariappa, R; Carlisle, C; Caruso, U; Cassanello, M; Castilla, AM; Chakraborty, P; Chandrasekar, R; Cheillan, D; Chien, YH; Childs, TA; Chrastina, P; Colandre, ME; Corso, G; Currier, R; Cyr, D; Czuczy, N; D'Apolito, O; Davis, T; de Juan, JA; de Sain-Van der Velden, MG; Delgado Pecellin, C; Di Gangi, IM; Di Stefano, CM; Domingos, MT; Dotsikas, Y; Downing, M; Downs, SM; Dy, B; Dymerski, M; Eaton, R; Eckerd, BM; El Mougy, F; Elvers, B; Eroh, S; Espada, M; Espinoza, VC; Evans, C; Fawbush, S; Fijolek, KF; Fisher, L; Franzson, L; Frazier, DM; Garcia, LR; García-Blanco, MI; Gavrilov, D; Gerace, R; Giordano, G; Greed, LC; Greenberg, CR; Grier, R; Grycki, E; Gu, X; Gulamali-Majid, F; Hadachi, SM; Hagar, AF; Han, L; Hannon, WH; Haslip, C; Hassan, FA; He, M; Hietala, A; Himstedt, L; Hoffman, GL; Hoffman, W; Hoggatt, P; Hopkins, PV; Hougaard, DM; Hughes, K; Hunt, PR; Hwu, WL; Hynes, J; Ibarra-González, I; Ingham, CA; Irazabal, YG; Ivanova, M; Jacox, WB; John, C; Johnson, JP; Jones, AL; Jónsson, JJ; Juan-Fita, MJ; Karg, E; Kasper, D; Katakouzinos, D; Khneisser, I; Klopper, B; Knoll, D; Kobayashi, H; Kohlmueller, D; Koneski, R; Kouapei, R; Kozich, V; Kremensky, I; la Marca, G; Lavochkin, M; Lee, SY; Lehotay, DC; Lemes, A; Lepage, J; Lesko, B; Lewis, B; Lim, C; Linard, S; Lindner, M; Lloyd-Puryear, MA; Lorey, F; Loukas, YL; Luedtke, J; Maffitt, N; Magee, JF; Manning, A; Manos, S; Marie, S; Marquardt, G; Martin, SJ; Matern, D; Mayfield Gibson, SK; Mayne, P; McCallister, TD; McCann, M; McClure, J; McGill, JJ; McHugh, D; McKeever, CD; McNeilly, B; Mellado, JM; Morrissey, MA; Moutsatsou, P; Mulcahy, EA; Nikoloudis, D; Norgaard-Pedersen, B; Oglesbee, D; Ojodu, J; Oltarzewski, M; Ombrone, D; Papakonstantinou, V; Park, HD; Pasquali, M; Pasquini, E; Pass, KA; Patel, P; Peterson, C; Pettersen, RD; Pino, GB; Pitt, JJ; Poh, S; Pollak, A; Porter, C; Poston, PA; Price, RW; Queijo, C; Quesada, J; Ramos, AC; Ramos, DE; Randell, E; Ranieri, E; Raymond, K; Reddic, JE; Reoyo, SP; Reuben, A; Ricciardi, C; Rinaldo, P; Rivera, JD; Roberts, A; Rocha, H; Roche, G; Rueda, I; Ruiz, C; Ruoppolo, M; Rutledge, SL; Ryu, E; Saban, C; Sahai, I; Santiago-Borrero, P; Schenone, A; Schoos, R; Schweitzer, B; Scott, P; Seashore, MR; Seeterlin, MA; Sesser, DE; Sevier, DW; Shone, SM; Sica, YC; Sinclair, G; Skrinska, VA; Stanley, EL; Strovel, ET; Sunny, S; Takats, Z; Tanyalcin, T; Teofoli, F; Thompson, JR; Tomashitis, K; Torres, J; Torres, R; Tortorelli, S; Turi, S; Turner, K; Tzanakos, N; Valiente, AG; Vallance, H; Vela-Amieva, M; Vilarinho, L; Vincent, MF; von Döbeln, U; Vorster, BC; Watson, MS; Webster, D; Weiss, S; Wilcken, B; Wiley, V; Williams, SK; Willis, SA; Woontner, M; Wright, K; Yahyaoui, R; Yamaguchi, S; Yssel, M; Zakowicz, WM1
Heales, S; Malone, M; Pryce, JW; Sebire, NJ; Weber, MA1
Amoroso, A; Boniotto, M; Braida, L; Casetta, B; Crovella, S; de Vonderweid, U; Luchesi, A1
Kožich, V; Stabler, S1
Gao, Y; Martin, NI; van Haren, MJ1
Alberto, JM; Battaglia-Hsu, SF; Coelho, D; Dreumont, N; Gauchotte, G; Ghemrawi, R; Guéant, JL; Hergalant, S; Houlgatte, R; Jung, M; Mosca, P; Ndiongue, M; Paoli, J; Quadros, EV; Robert, A; Sequeira, JM; Umoret, R1
Andrianov, AIu; Batotsyrenov, BV; Shikalova, IA; Shilov, VV; Vasil'ev, SA1
Ballhausen, D; Blom, HJ; Dionisi-Vici, C; Dobbelaere, D; Douillard, C; Freisinger, P; Grünert, SC; Haas, D; Hoffmann, GF; Kahrizi, K; Kölker, S; la Marca, G; Lindner, M; Makhseed, N; Staufner, C; Straub, BK1
Bottiglieri, T; Hyland, K1

Reviews

5 review(s) available for s-adenosylmethionine and Diseases, Metabolic

ArticleYear
An atlas of genome-wide gene expression and metabolite associations and possible mediation effects towards body mass index.
    Journal of molecular medicine (Berlin, Germany), 2023, Volume: 101, Issue:10

    Topics: Amino Acids; Body Mass Index; Chromatography, Liquid; Humans; Leukocytes, Mononuclear; Metabolic Diseases; Metabolomics; Obesity; Tandem Mass Spectrometry; Transcriptome

2023
Acylcarnitines--old actors auditioning for new roles in metabolic physiology.
    Nature reviews. Endocrinology, 2015, Volume: 11, Issue:10

    Topics: Carnitine; Humans; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Metabolic Diseases; Metabolic Networks and Pathways; Metabolism

2015
Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
    The Journal of nutrition, 2020, 10-01, Volume: 150, Issue:Suppl 1

    Topics: Amino Acids, Sulfur; Animals; Brain Diseases; Cysteine; Glutathione; Homocysteine; Homocystinuria; Humans; Hydrogen Sulfide; Liver; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Methylation; S-Adenosylmethionine; Sulfites; Sulfur; Sulfur Compounds

2020
Nicotinamide N-methyl transferase (NNMT): An emerging therapeutic target.
    Drug discovery today, 2021, Volume: 26, Issue:11

    Topics: Enzyme Inhibitors; Humans; Metabolic Diseases; Neoplasms; Neurodegenerative Diseases; Niacinamide; Nicotinamide N-Methyltransferase; S-Adenosylmethionine

2021
S-adenosylmethionine levels in psychiatric and neurological disorders: a review.
    Acta neurologica Scandinavica. Supplementum, 1994, Volume: 154

    Topics: Administration, Oral; Adolescent; Adult; Age Factors; Aged; AIDS Dementia Complex; Alzheimer Disease; Brain; Catecholamines; Child; Child, Preschool; Depressive Disorder; DNA; Female; Humans; Injections, Intravenous; Liver; Male; Metabolic Diseases; Methylation; Middle Aged; Nervous System Diseases; Phospholipids; RNA; S-Adenosylmethionine; Spinal Cord Diseases

1994

Trials

1 trial(s) available for s-adenosylmethionine and Diseases, Metabolic

ArticleYear
The Association of Acylcarnitines and Amino Acids With Age in Dutch and South-Asian Surinamese Living in Amsterdam.
    The Journal of clinical endocrinology and metabolism, 2018, 10-01, Volume: 103, Issue:10

    Topics: Adolescent; Adult; Age Factors; Aged; Amino Acids; Asian People; Biomarkers; Carnitine; Cohort Studies; Cross-Sectional Studies; Ethnicity; Female; Follow-Up Studies; Humans; Male; Metabolic Diseases; Middle Aged; Netherlands; Prevalence; Prognosis; Suriname; White People; Young Adult

2018

Other Studies

21 other study(ies) available for s-adenosylmethionine and Diseases, Metabolic

ArticleYear
Untargeted metabolomic analysis of urine samples for diagnosis of inherited metabolic disorders.
    Functional & integrative genomics, 2021, Volume: 21, Issue:5-6

    Topics: Amino Acids; Biomarkers; Carnitine; Child; Humans; Mass Spectrometry; Metabolic Diseases; Metabolomics; Nucleosides

2021
Rapid and efficient LC-MS/MS diagnosis of inherited metabolic disorders: a semi-automated workflow for analysis of organic acids, acylglycines, and acylcarnitines in urine.
    Clinical chemistry and laboratory medicine, 2023, 10-26, Volume: 61, Issue:11

    Topics: Child; Chromatography, Liquid; Humans; Metabolic Diseases; Organic Chemicals; Tandem Mass Spectrometry; Workflow

2023
Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
    Scientific reports, 2019, Oct-01, Volume: 9, Issue:1

    Topics: Amino Acids; Carnitine; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intensive Care Units, Neonatal; Male; Maple Syrup Urine Disease; Metabolic Diseases; Neonatal Screening; Paris; Phenylketonurias; Propionic Acidemia

2019
Serum acylcarnitine profile in endurance horses with and without metabolic dysfunction.
    Veterinary journal (London, England : 1997), 2020, Volume: 255

    Topics: Animals; Carnitine; Fatty Acids; Female; Horses; Male; Metabolic Diseases; Mitochondria; Oxidation-Reduction; Physical Endurance; Running; Tandem Mass Spectrometry

2020
Fine Mapping and Functional Analysis Reveal a Role of SLC22A1 in Acylcarnitine Transport.
    American journal of human genetics, 2017, Oct-05, Volume: 101, Issue:4

    Topics: Alleles; Alternative Splicing; Animals; Biological Transport; Carnitine; Cells, Cultured; Cohort Studies; CRISPR-Cas Systems; Female; Gene Expression Regulation; Genome-Wide Association Study; High-Throughput Nucleotide Sequencing; Humans; Liver; Male; Metabolic Diseases; Metabolomics; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Knockout; Organic Cation Transporter 1; Polymorphism, Single Nucleotide; Tissue Distribution

2017
Plasma acylcarnitine concentrations reflect the acylcarnitine profile in cardiac tissues.
    Scientific reports, 2017, 12-13, Volume: 7, Issue:1

    Topics: Animals; Blood Glucose; Carnitine; Glucose Tolerance Test; Insulin; Liver; Male; Metabolic Diseases; Mice; Muscle, Skeletal; Myocardium; Random Allocation; Rats, Wistar; Running

2017
Tissue acylcarnitine status in a mouse model of mitochondrial β-oxidation deficiency during metabolic decompensation due to influenza virus infection.
    Molecular genetics and metabolism, 2018, Volume: 125, Issue:1-2

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Animals; Cardiomyopathies; Carnitine; Congenital Bone Marrow Failure Syndromes; Disease Models, Animal; Fatty Acids; Female; Humans; Hypoglycemia; Lipid Metabolism, Inborn Errors; Lipid Peroxidation; Liver; Liver Failure; Metabolic Diseases; Mice; Mitochondrial Diseases; Muscle, Skeletal; Muscular Diseases; Myocardium; Oxidation-Reduction

2018
Alterations in plasma acylcarnitine and amino acid profiles may indicate poor nutrition during the suckling period due to maternal intake of an unbalanced diet and may predict later metabolic dysfunction.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019, Volume: 33, Issue:1

    Topics: Amino Acids; Animals; Animals, Suckling; Carnitine; Diet; Female; Lactation; Lipid Metabolism; Liver; Male; Maternal Nutritional Physiological Phenomena; Metabolic Diseases; Models, Animal; Multivariate Analysis; Nutritional Status; Pregnancy; Prenatal Exposure Delayed Effects; Rats

2019
Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry.
    Journal of clinical laboratory analysis, 2015, Volume: 29, Issue:2

    Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carboxylic Acids; Carnitine; Child; Child, Preschool; China; Fatty Acids; Female; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Metabolic Diseases; Middle Aged; Oxidation-Reduction; Phenylketonurias; Tandem Mass Spectrometry

2015
Metabolomic Research on Newborn Infants With Intrauterine Growth Restriction.
    Medicine, 2016, Volume: 95, Issue:17

    Topics: Amino Acids; Carnitine; Female; Fetal Growth Retardation; Gestational Age; Humans; Infant, Newborn; Intensive Care Units, Neonatal; Male; Metabolic Diseases; Metabolomics; Neonatal Screening; Reference Values; Research

2016
Application of metabolomic principles to disorders of nucleotide metabolism reveals new metabolic perturbations.
    Nucleosides, nucleotides & nucleic acids, 2008, Volume: 27, Issue:6

    Topics: Adenine Phosphoribosyltransferase; Adenosine Deaminase; Amino Acids; Carnitine; Dihydropyrimidine Dehydrogenase Deficiency; Dihydrouracil Dehydrogenase (NADP); Genetic Diseases, Inborn; Humans; Hypoxanthine Phosphoribosyltransferase; Metabolic Diseases; Ninhydrin; Nucleotides

2008
Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort study.
    Journal of inherited metabolic disease, 2009, Volume: 32, Issue:1

    Topics: Amino Acids; Blood Chemical Analysis; Blood Specimen Collection; Carnitine; Cohort Studies; Efficiency; False Negative Reactions; Fetal Blood; Fetal Diseases; Humans; Infant, Newborn; Metabolic Diseases; Mothers; Neonatal Screening; Reference Values; Time Factors

2009
Addition of formic acid improves acetonitrile extraction of dicarboxylic acylcarnitines.
    Clinica chimica acta; international journal of clinical chemistry, 2009, Jun-27, Volume: 404, Issue:2

    Topics: Acetonitriles; Blood Chemical Analysis; Carnitine; Formates; Humans; Metabolic Diseases; Solvents

2009
Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.
    Journal of child neurology, 2010, Volume: 25, Issue:8

    Topics: Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Developmental Disabilities; Female; Humans; Male; Mass Screening; Metabolic Diseases; Multiple Acyl Coenzyme A Dehydrogenase Deficiency

2010
Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry.
    Clinica chimica acta; international journal of clinical chemistry, 2010, May-02, Volume: 411, Issue:9-10

    Topics: Amino Acids; Butanols; Carnitine; Humans; Infant, Newborn; Leucine; Metabolic Diseases; Methionine; Neonatal Screening; Palmitoylcarnitine; Phenylalanine; Quality Control; Tandem Mass Spectrometry

2010
Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2011, Volume: 13, Issue:3

    Topics: Amino Acids; Carnitine; Humans; Infant, Newborn; International Cooperation; Metabolic Diseases; Neonatal Screening; Reference Values; Sensitivity and Specificity; Software; Tandem Mass Spectrometry

2011
Tandem mass spectrometry findings at autopsy for detection of metabolic disease in infant deaths: postmortem changes and confounding factors.
    Journal of clinical pathology, 2011, Volume: 64, Issue:11

    Topics: Autopsy; Bile; Carnitine; Humans; Infant; Infant, Newborn; Liver; Metabolic Diseases; Organ Size; Postmortem Changes; Sudden Infant Death; Tandem Mass Spectrometry

2011
A rapid and quantitative mass spectrometry method for determining the concentration of acylcarnitines and aminoacids in amniotic fluid.
    Prenatal diagnosis, 2001, Volume: 21, Issue:7

    Topics: Amino Acids; Amniotic Fluid; Carnitine; Female; Fetal Diseases; Humans; Mass Spectrometry; Metabolic Diseases; Predictive Value of Tests; Pregnancy; Prenatal Diagnosis; Sensitivity and Specificity

2001
Inherited disorders of cobalamin metabolism disrupt nucleocytoplasmic transport of mRNA through impaired methylation/phosphorylation of ELAVL1/HuR.
    Nucleic acids research, 2018, 09-06, Volume: 46, Issue:15

    Topics: Animals; Biological Transport; Brain; CARD Signaling Adaptor Proteins; Cell Line, Tumor; Cell Nucleus; ELAV-Like Protein 1; Endoplasmic Reticulum Stress; Exportin 1 Protein; Humans; Karyopherins; Metabolic Diseases; Methylation; Mice; Mice, Inbred C57BL; Mice, Knockout; Okadaic Acid; Phosphorylation; Protein Phosphatase 2; Receptors, Cytoplasmic and Nuclear; RNA-Binding Proteins; RNA, Messenger; S-Adenosylmethionine; Sirtuin 1; Vitamin B 12

2018
[Correction of metabolic disorders during treatment of alcohol-induced liver injuries in patients with acute alcoholic intoxication].
    Klinicheskaia meditsina, 2013, Volume: 91, Issue:2

    Topics: Acute Disease; Adult; Alcoholic Intoxication; Comorbidity; Female; Humans; Liver Diseases, Alcoholic; Male; Metabolic Diseases; Middle Aged; S-Adenosylmethionine; Succinates

2013
Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options.
    Journal of inherited metabolic disease, 2016, Volume: 39, Issue:2

    Topics: Adenosine; Adenosine Kinase; Adolescent; Adult; Biomarkers; Child; Child, Preschool; Diet; Female; Humans; Hypoglycemia; Infant; Liver; Liver Diseases; Male; Metabolic Diseases; Methionine; Retrospective Studies; S-Adenosylhomocysteine; S-Adenosylmethionine; Young Adult

2016