1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1640293&form=6&db=m	Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis.	causal interaction,unassigned	4,0	
1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1770913&form=6&db=m	Adaptation of renal tricarboxylic acid cycle metabolism to various acid-base states: study with [3-13C,5-15N]glutamine.	causal interaction,therapeutic application,unassigned	4,1,0	
1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2283987&form=6&db=m	Biochemical pathways and modulators of renal ammoniagenesis.	causal interaction,unassigned	4,0	
1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2283989&form=6&db=m	Intramitochondrial pH and ammonium production in rat and dog kidney cortex.	causal interaction,therapeutic application,unassigned	4,2,0	
1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2563203&form=6&db=m	Ammoniagenesis by cultured human renal cortical epithelial cells: study with 15N.	causal interaction,unassigned	4,0	
1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2801699&form=6&db=m	Regulation of rat kidney mitochondrial metabolism in acute acidosis.	causal interaction,therapeutic application,unassigned	1,1,0	
1.2.4.2	Acidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7470078&form=6&db=m	Activation of oxoglutarate dehydrogenase in the kidney in response to acute acidosis.	causal interaction,diagnostic usage,ongoing research,therapeutic application	4,1,3,1	
1.2.4.2	Acidosis, Lactic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=184426&form=6&db=m	Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.	causal interaction,unassigned	2,0	
1.2.4.2	Acidosis, Lactic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=413089&form=6&db=m	Deficiency of dihydrolipoyl dehydrogenase (a component of the pyruvate and alpha-ketoglutarate dehydrogenase complexes): a cause of congenital chronic lactic acidosis in infancy.	causal interaction,unassigned	4,0	
1.2.4.2	Acidosis, Lactic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1640293&form=6&db=m	Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis.	causal interaction,unassigned	4,0