n-acetylneuraminic acid and Edema, Cardiac

n-acetylneuraminic acid has been researched along with Edema, Cardiac in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abu Bakar, N; Brand-Arzamendi, K; Da Silva, A; de Brouwer, A; Drögemöller, B; El-Rass, S; Engelke, U; Hoskings, M; Huijben, K; Karbassi, F; Lefeber, DJ; Lehman, AM; Moreland, J; Ng, R; Pan, X; Philip, AM; Pshezhetsky, AV; Rakic, B; Ross, CJ; Selby, K; Tarailo-Graovac, M; Vallance, H; van Karnebeek, CD; van Scherpenzeel, M; Wasserman, WW; Wen, XY; Wevers, RA; Willems, A; Ye, XC; Yun, J; Zijlstra, F	1

Studies

Abu Bakar, N; Brand-Arzamendi, K; Da Silva, A; de Brouwer, A; Drögemöller, B; El-Rass, S; Engelke, U; Hoskings, M; Huijben, K; Karbassi, F; Lefeber, DJ; Lehman, AM; Moreland, J; Ng, R; Pan, X; Philip, AM; Pshezhetsky, AV; Rakic, B; Ross, CJ; Selby, K; Tarailo-Graovac, M; Vallance, H; van Karnebeek, CD; van Scherpenzeel, M; Wasserman, WW; Wen, XY; Wevers, RA; Willems, A; Ye, XC; Yun, J; Zijlstra, F

Other Studies

1 other study(ies) available for n-acetylneuraminic acid and Edema, Cardiac

Article	Year
Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function. JCI insight, 2018, 12-20, Volume: 3, Issue:24 Topics: Adult; Animals; Disease Models, Animal; Edema, Cardiac; Gene Expression Regulation, Developmental; Gene Knockdown Techniques; Genetic Diseases, Inborn; HEK293 Cells; Hexosamines; Humans; Male; Muscle, Skeletal; Muscular Diseases; Mutation; N-Acetylneuraminic Acid; Oxo-Acid-Lyases; Sialic Acid Storage Disease; Young Adult; Zebrafish	2018

Article

Year

Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function.

JCI insight, 2018, 12-20, Volume: 3, Issue:24

Topics: Adult; Animals; Disease Models, Animal; Edema, Cardiac; Gene Expression Regulation, Developmental; Gene Knockdown Techniques; Genetic Diseases, Inborn; HEK293 Cells; Hexosamines; Humans; Male; Muscle, Skeletal; Muscular Diseases; Mutation; N-Acetylneuraminic Acid; Oxo-Acid-Lyases; Sialic Acid Storage Disease; Young Adult; Zebrafish

2018