cytosine and carnitine

cytosine has been researched along with carnitine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chang, YS; Hwang, SJ; Jin, DK; Lee, JE; Paik, KH; Park, WS; Shim, JW; Strauss, AW; Yoon, HR	1
Deng, L; Gong, QM; Kong, XF; La, DD; Li, HW; Peng, CH; Shen, BY; Shi, Q; Yu, YY; Zhang, XX; Zhu-Ge, CD	1

Other Studies

2 other study(ies) available for cytosine and carnitine

Article	Year
A case of mitochondrial trifunctional protein deficiency diagnosed by acylcarnitine profile and DNA analysis in a dried blood spot of a 4-day-old boy. Journal of inherited metabolic disease, 2003, Volume: 26, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Cytosine; DNA Mutational Analysis; Fatal Outcome; Guanine; Humans; Infant, Newborn; Male; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation; Protein Isoforms	2003
No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives. Journal of gastroenterology and hepatology, 2007, Volume: 22, Issue:12 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adult; Carnitine; Cytosine; Family; Fatty Liver; Female; Guanine; Humans; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Mass Spectrometry; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation; Polymorphism, Restriction Fragment Length; Pregnancy; Pregnancy Complications; Protein Subunits; Sequence Analysis, DNA	2007

Article

Year

A case of mitochondrial trifunctional protein deficiency diagnosed by acylcarnitine profile and DNA analysis in a dried blood spot of a 4-day-old boy.

Journal of inherited metabolic disease, 2003, Volume: 26, Issue:4

Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Cytosine; DNA Mutational Analysis; Fatal Outcome; Guanine; Humans; Infant, Newborn; Male; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation; Protein Isoforms

2003

No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.

Journal of gastroenterology and hepatology, 2007, Volume: 22, Issue:12

Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adult; Carnitine; Cytosine; Family; Fatty Liver; Female; Guanine; Humans; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Mass Spectrometry; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation; Polymorphism, Restriction Fragment Length; Pregnancy; Pregnancy Complications; Protein Subunits; Sequence Analysis, DNA

2007