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methylmalonic acid and Disease Models, Animal

methylmalonic acid has been researched along with Disease Models, Animal in 20 studies

Methylmalonic Acid: A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.
methylmalonic acid : A dicarboxylic acid that is malonic acid in which one of the methylene hydrogens is substituted by a methyl group.

Disease Models, Animal: Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases.

Research Excerpts

ExcerptRelevanceReference
"In vivo characteristics of isatins [(18)F]-2 and [(18)F]-3 were studied and compared by μPET to previously described 1-[4-(2-[(18)F]fluoroethyl)benzyl]-5-(2-methoxymethylpyrrolidin-1-ylsulfonyl)isatin ([(18)F]-1) and to 2-(5-[(18)F]fluoropentyl)-2-methyl-malonic acid ([(18)F]ML-10) used as a reference radiotracer in a rat stroke model."3.83In Vivo Evaluation of Radiofluorinated Caspase-3/7 Inhibitors as Radiotracers for Apoptosis Imaging and Comparison with [18F]ML-10 in a Stroke Model in the Rat. ( Barré, L; Delamare, J; Dhilly, M; Fraser, BH; Greguric, I; Krause-Heuer, AM; Matesic, L; Médoc, M; Sobrio, F; Toutain, J; Touzani, O, 2016)
"Methylmalonic acidemias are inherited metabolic disorders characterized by methylmalonate (MMA) accumulation and neurologic dysfunction, including seizures."3.78Prostaglandin E(2) potentiates methylmalonate-induced seizures. ( Banderó, CR; Bortoluzzi, VT; Bueno, LM; Gomes, AT; Jesse, AC; Mello, CF; Oliveira, MS; Rambo, LM; Salvadori, MG, 2012)
" The body weight of the mice fed on a B12-deficient diet for 90 days was slightly lower than that of the control mice administrated CN-B12, and the urinary excretion of methylmalonic acid (MMA) was increased."3.72Breeding severely vitamin B12-deficient mice as model animals. ( Arai, K; Funada, U; Kawata, T; Kuwamori, M; Maekawa, A; Matsushita, M; Sanai, T; Tadokoro, T; Tanaka, N; Wada, M; Yamada, H; Yamamoto, Y, 2004)
"Hyperhomocysteinemia adversely affects fundamental aspects of fetal development, adulthood, and aging, but the role of elevated homocysteine levels in these birth defects and adult diseases remains unclear."3.71Genetic and molecular control of folate-homocysteine metabolism in mutant mice. ( Bale, A; Balling, R; Christensen, B; Colmenares, C; Ernest, S; Gilfix, BM; Hosack, A; Mamer, OA; McGrath, J; Nadeau, JH; Rodier, M; Rosenblatt, DS; Sankoff, D, 2002)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19901 (5.00)18.7374
1990's1 (5.00)18.2507
2000's11 (55.00)29.6817
2010's6 (30.00)24.3611
2020's1 (5.00)2.80

Authors

AuthorsStudies
Lucienne, M1
Aguilar-Pimentel, JA1
Amarie, OV1
Becker, L1
Calzada-Wack, J1
da Silva-Buttkus, P1
Garrett, L1
Hölter, SM1
Mayer-Kuckuk, P1
Rathkolb, B1
Rozman, J1
Spielmann, N1
Treise, I1
Busch, DH1
Klopstock, T1
Schmidt-Weber, C1
Wolf, E1
Wurst, W1
Forny, M1
Mathis, D2
Fingerhut, R2
Froese, DS2
Gailus-Durner, V1
Fuchs, H1
de Angelis, MH1
Baumgartner, MR2
Médoc, M1
Dhilly, M1
Matesic, L1
Toutain, J1
Krause-Heuer, AM1
Delamare, J1
Fraser, BH1
Touzani, O1
Barré, L1
Greguric, I1
Sobrio, F1
Colín-González, AL1
Paz-Loyola, AL1
Serratos, I1
Seminotti, B1
Ribeiro, CA1
Leipnitz, G1
Souza, DO1
Wajner, M4
Santamaría, A1
Hyafil, F1
Tran-Dinh, A1
Burg, S1
Leygnac, S1
Louedec, L1
Milliner, M1
Ben Azzouna, R1
Reshef, A2
Ben Ami, M1
Meilhac, O1
Le Guludec, D1
Forny, P1
Schumann, A1
Mustedanagic, M1
Wulf, MA1
Nägele, N1
Langhans, CD1
Zhakupova, A1
Heeren, J1
Scheja, L1
Peters, HL2
Hornemann, T1
Thony, B1
Kölker, S1
Burda, P1
Devuyst, O1
Shirvan, A1
Waterhouse, RN1
Grimberg, H1
Levin, G1
Cohen, A1
Ulysse, LG1
Friedman, G1
Antoni, G1
Ziv, I1
Salvadori, MG1
Banderó, CR1
Jesse, AC1
Gomes, AT1
Rambo, LM1
Bueno, LM1
Bortoluzzi, VT1
Oliveira, MS2
Mello, CF2
Buck, NE1
Dashnow, H1
Pitt, JJ1
Wood, LR1
Royes, LF1
Fighera, MR1
Furian, AF1
da Silva, LG1
Malfatti, CR1
Schneider, PH1
Braga, AL1
Das, AM1
Pettenuzzo, LF1
Wyse, AT1
Wannmacher, CM1
Dutra-Filho, CS1
Netto, CA1
Kawata, T2
Funada, U1
Wada, M2
Matsushita, M1
Sanai, T1
Yamada, H1
Kuwamori, M1
Arai, K1
Yamamoto, Y1
Tanaka, N2
Tadokoro, T2
Maekawa, A2
Takada, N1
Ogita, K1
Taguchi, T1
Masumoto, K1
Suita, S1
Vasques, V1
Brinco, F1
Viegas, CM1
Yamada, K1
Mori, K1
Tamai, H1
Tobimatsu, T1
Toraya, T1
Chandler, RJ2
Sloan, J1
Fu, H1
Tsai, M1
Stabler, S1
Allen, R1
Kaestner, KH1
Kazazian, HH1
Venditti, CP2
Scalabrino, G1
Buccellato, FR1
Tredici, G1
Morabito, A1
Lorenzini, EC1
Allen, RH1
Lindenbaum, J1
Ernest, S1
Christensen, B1
Gilfix, BM1
Mamer, OA1
Hosack, A1
Rodier, M1
Colmenares, C1
McGrath, J1
Bale, A1
Balling, R1
Sankoff, D1
Rosenblatt, DS1
Nadeau, JH1
Bailey, LB1
Molloy, A1
Scott, J1
Rice, D1

Reviews

1 review available for methylmalonic acid and Disease Models, Animal

ArticleYear
Regulation of the mitochondrial ATP-synthase in health and disease.
    Molecular genetics and metabolism, 2003, Volume: 79, Issue:2

    Topics: Animals; Brain; Brain Diseases, Metabolic, Inborn; Cells, Cultured; Chickens; Disease; Disease Model

2003

Other Studies

19 other studies available for methylmalonic acid and Disease Models, Animal

ArticleYear
In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduria.
    Biochimica et biophysica acta. Molecular basis of disease, 2020, 03-01, Volume: 1866, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Anxiety; Bone Density; Disease Models, Animal; Female

2020
In Vivo Evaluation of Radiofluorinated Caspase-3/7 Inhibitors as Radiotracers for Apoptosis Imaging and Comparison with [18F]ML-10 in a Stroke Model in the Rat.
    Molecular imaging and biology, 2016, Volume: 18, Issue:1

    Topics: Animals; Apoptosis; Caspase 3; Caspase 7; Caspase Inhibitors; Disease Models, Animal; Isatin; Male;

2016
Toxic synergism between quinolinic acid and organic acids accumulating in glutaric acidemia type I and in disorders of propionate metabolism in rat brain synaptosomes: Relevance for metabolic acidemias.
    Neuroscience, 2015, Nov-12, Volume: 308

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain; Brain Diseases, Metabolic; Disease Models, Ani

2015
Detection of Apoptotic Cells in a Rabbit Model with Atherosclerosis-Like Lesions Using the Positron Emission Tomography Radiotracer [18F]ML-10.
    Molecular imaging, 2015, Volume: 14

    Topics: Animals; Aorta; Atherosclerosis; Disease Models, Animal; Fluorine Radioisotopes; Injections; Male; M

2015
Novel Mouse Models of Methylmalonic Aciduria Recapitulate Phenotypic Traits with a Genetic Dosage Effect.
    The Journal of biological chemistry, 2016, 09-23, Volume: 291, Issue:39

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Biomarkers; Brain; Carnitine; Dietary Protei

2016
Molecular imaging of neurovascular cell death in experimental cerebral stroke by PET.
    Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2008, Volume: 49, Issue:9

    Topics: Animals; Apoptosis; Disease Models, Animal; Male; Methylmalonic Acid; Molecular Probe Techniques; Ne

2008
Prostaglandin E(2) potentiates methylmalonate-induced seizures.
    Epilepsia, 2012, Volume: 53, Issue:1

    Topics: Animals; Celecoxib; Cyclooxygenase 2 Inhibitors; Dinoprostone; Disease Models, Animal; Electrodes, I

2012
Development of transgenic mice containing an introduced stop codon on the human methylmalonyl-CoA mutase locus.
    PloS one, 2012, Volume: 7, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Breeding; Codon, Nonsense; Disease Models, Animal; Fe

2012
Creatine protects against the convulsive behavior and lactate production elicited by the intrastriatal injection of methylmalonate.
    Neuroscience, 2003, Volume: 118, Issue:4

    Topics: Animals; Behavior, Animal; Corpus Striatum; Creatine; Disease Models, Animal; Dizocilpine Maleate; D

2003
Evaluation of the effect of chronic administration of drugs on rat behavior in the water maze task.
    Brain research. Brain research protocols, 2003, Volume: 12, Issue:2

    Topics: Animals; Behavior, Animal; Brain; Brain Diseases, Metabolic; Cognition Disorders; Disease Models, An

2003
Breeding severely vitamin B12-deficient mice as model animals.
    International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 2004, Volume: 74, Issue:1

    Topics: Animals; Body Weight; Diet; Disease Models, Animal; Liver; Male; Maternal Nutritional Physiological

2004
Effect of a valine-rich diet on a rat model of short bowel syndrome.
    Pediatric surgery international, 2005, Volume: 21, Issue:11

    Topics: Adaptation, Physiological; Animals; Disease Models, Animal; Male; Methylmalonic Acid; Rats; Rats, In

2005
Creatine prevents behavioral alterations caused by methylmalonic acid administration into the hippocampus of rats in the open field task.
    Journal of the neurological sciences, 2006, May-15, Volume: 244, Issue:1-2

    Topics: Animals; Avoidance Learning; Brain Diseases, Metabolic, Inborn; Creatine; Disease Models, Animal; En

2006
Testicular injury to rats fed on soybean protein-based vitamin B12-deficient diet can be reduced by methionine supplementation.
    Journal of nutritional science and vitaminology, 2007, Volume: 53, Issue:2

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Analysis of Variance; Animals; Body Weigh

2007
Metabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscle.
    BMC medical genetics, 2007, Oct-15, Volume: 8

    Topics: Adult; Animals; Animals, Newborn; Blotting, Northern; Blotting, Western; Disease Models, Animal; Fem

2007
Adenovirus-mediated gene delivery rescues a neonatal lethal murine model of mut(0) methylmalonic acidemia.
    Human gene therapy, 2008, Volume: 19, Issue:1

    Topics: Adenoviridae; Animals; Animals, Newborn; Disease Models, Animal; Gene Transfer Techniques; Genetic T

2008
Enhanced levels of biochemical markers for cobalamin deficiency in totally gastrectomized rats: uncoupling of the enhancement from the severity of spongy vacuolation in spinal cord.
    Experimental neurology, 1997, Volume: 144, Issue:2

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Anemia, Pernicious; Animals; Bacteria, An

1997
Genetic and molecular control of folate-homocysteine metabolism in mutant mice.
    Mammalian genome : official journal of the International Mammalian Genome Society, 2002, Volume: 13, Issue:5

    Topics: Animals; Blotting, Northern; Disease Models, Animal; Female; Folic Acid; Gene Expression Regulation;

2002
Streptozotocin-induced diabetes is not a model for methylmalonic acidaemia.
    Journal of inherited metabolic disease, 1989, Volume: 12, Issue:4

    Topics: Animals; Chromatography, Gas; Diabetes Mellitus, Experimental; Disease Models, Animal; Male; Malonat

1989