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sarcosine and Electron Transport Chain Deficiencies, Mitochondrial

sarcosine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 6 studies

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Research Excerpts

ExcerptRelevanceReference
"Sarcosinemia is an autosomal recessive metabolic trait manifested by relatively high concentrations of sarcosine in blood and urine."1.38Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia. ( Abu-Horvitz, A; Anikster, Y; Auray-Blais, C; Bar-joseph, I; Benarrosh, A; Dekel, M; Dushnitzky, M; Garnotel, R; Gillery, P; Goldstein, N; Hofliger, N; Marek-Yagel, D; Pode-Shakked, B; Pras, E; Reznik-Wolf, H; Rienstein, S; Zlotnik, J, 2012)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's5 (83.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Thygesen, C1
Metaxas, A1
Larsen, MR1
Finsen, B1
Pundir, CS1
Deswal, R1
Kumar, P1
de Andrade, RB1
Gemelli, T1
Rojas, DB1
Dutra-Filho, CS1
Wannmacher, CM1
Pfeffer, G1
Majamaa, K2
Turnbull, DM1
Thorburn, D2
Chinnery, PF1
Bar-joseph, I1
Pras, E1
Reznik-Wolf, H1
Marek-Yagel, D1
Abu-Horvitz, A1
Dushnitzky, M1
Goldstein, N1
Rienstein, S1
Dekel, M1
Pode-Shakked, B1
Zlotnik, J1
Benarrosh, A1
Gillery, P1
Hofliger, N1
Auray-Blais, C1
Garnotel, R1
Anikster, Y1
Chinnery, P1
Turnbull, D1

Reviews

3 reviews available for sarcosine and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
Quantitative analysis of sarcosine with special emphasis on biosensors: a review.
    Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals, 2019, Volume: 24, Issue:5

    Topics: Alzheimer Disease; Amino Acid Metabolism, Inborn Errors; Biomarkers; Biosensing Techniques; Colorect

2019
Treatment for mitochondrial disorders.
    The Cochrane database of systematic reviews, 2012, Apr-18, Issue:4

    Topics: Creatine; Dichloroacetic Acid; Humans; Mitochondrial Diseases; Randomized Controlled Trials as Topic

2012
Treatment for mitochondrial disorders.
    The Cochrane database of systematic reviews, 2006, Jan-25, Issue:1

    Topics: Creatine; Dichloroacetic Acid; Humans; Mitochondrial Diseases; Sarcosine; Ubiquinone

2006

Other Studies

3 other studies available for sarcosine and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
Age-Dependent Changes in the Sarkosyl-Insoluble Proteome of APPSWE/PS1ΔE9 Transgenic Mice Implicate Dysfunctional Mitochondria in the Pathogenesis of Alzheimer's Disease.
    Journal of Alzheimer's disease : JAD, 2018, Volume: 64, Issue:4

    Topics: Aging; Alzheimer Disease; Amyloid beta-Protein Precursor; Animals; Brain; Disease Models, Animal; Ge

2018
Chemically induced acute model of sarcosinemia in wistar rats.
    Metabolic brain disease, 2016, Volume: 31, Issue:2

    Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Animals; Animals, Newborn; Brain; Disease Model

2016
Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia.
    Human genetics, 2012, Volume: 131, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; DNA; DNA Primers; Female; Humans; Male; Mitochondrial Diseases

2012