Page last updated: 2024-11-08

serine and Electron Transport Chain Deficiencies, Mitochondrial

serine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 3 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ferreira, CR1
Goorden, SMI1
Soldatos, A1
Byers, HM1
Ghauharali-van der Vlugt, JMM1
Beers-Stet, FS1
Groden, C1
van Karnebeek, CD1
Gahl, WA1
Vaz, FM1
Jiang, X1
Vernon, HJ1
Kim, T1
Wayne Leitner, J1
Adochio, R1
Draznin, B1
Chan, SS1
Longley, MJ1
Copeland, WC1

Other Studies

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

ArticleYear
Deoxysphingolipid precursors indicate abnormal sphingolipid metabolism in individuals with primary and secondary disturbances of serine availability.
    Molecular genetics and metabolism, 2018, Volume: 124, Issue:3

    Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Case-Control Studies; Child; Female;

2018
Knockdown of JNK rescues 3T3-L1 adipocytes from insulin resistance induced by mitochondrial dysfunction.
    Biochemical and biophysical research communications, 2009, Jan-23, Volume: 378, Issue:4

    Topics: 3T3-L1 Cells; Adipocytes; Animals; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Deoxyglucose;

2009
Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders.
    Human molecular genetics, 2006, Dec-01, Volume: 15, Issue:23

    Topics: Amino Acid Sequence; Amino Acid Substitution; Catalytic Domain; DNA; DNA Polymerase gamma; DNA-Direc

2006