PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
20923787-0	2011	Therapeutic modulation of cerebral L-lysine metabolism in a mouse model for glutaric aciduria type I. Glutaric aciduria type I, an inherited deficiency of glutaryl-coenzyme A dehydrogenase localized in the final common catabolic pathway of L-lysine, L-hydroxylysine and L-tryptophan, leads to accumulation of neurotoxic glutaric and 3-hydroxyglutaric acid, as well as non-toxic glutarylcarnitine.	glutarylcarnitine	378-395	glutaryl-Coenzyme A dehydrogenase	Mus musculus	155-188
33483254-7	2021	We found that GA1 mice with SUGCT deficiency have decreased excretion of urine 3-hydroxyglutaric acid and decreased levels glutarylcarnitine in urine, plasma and kidney.	glutarylcarnitine	123-140	succinyl-CoA glutarate-CoA transferase	Mus musculus	28-33
32567100-3	2020	We show that loss of AASS function in GCDH-deficient HEK-293 cells leads to a ~ 5-fold reduction in the established GA1 clinical biomarker glutarylcarnitine.	glutarylcarnitine	139-156	aminoadipate-semialdehyde synthase	Homo sapiens	21-25
32567100-3	2020	We show that loss of AASS function in GCDH-deficient HEK-293 cells leads to a ~ 5-fold reduction in the established GA1 clinical biomarker glutarylcarnitine.	glutarylcarnitine	139-156	glutaryl-CoA dehydrogenase	Homo sapiens	38-42
32160276-3	2020	Here we show that loss of DHTKD1 in GCDH-deficient HEK-293 cells leads to a 2-fold decrease in the established GA1 clinical biomarker glutarylcarnitine, and demonstrate that OGDH is responsible for this remaining glutarylcarnitine production.	glutarylcarnitine	134-151	dehydrogenase E1 and transketolase domain containing 1	Homo sapiens	26-32
32160276-3	2020	Here we show that loss of DHTKD1 in GCDH-deficient HEK-293 cells leads to a 2-fold decrease in the established GA1 clinical biomarker glutarylcarnitine, and demonstrate that OGDH is responsible for this remaining glutarylcarnitine production.	glutarylcarnitine	134-151	glutaryl-CoA dehydrogenase	Homo sapiens	36-40
32160276-3	2020	Here we show that loss of DHTKD1 in GCDH-deficient HEK-293 cells leads to a 2-fold decrease in the established GA1 clinical biomarker glutarylcarnitine, and demonstrate that OGDH is responsible for this remaining glutarylcarnitine production.	glutarylcarnitine	213-230	dehydrogenase E1 and transketolase domain containing 1	Homo sapiens	26-32
32160276-3	2020	Here we show that loss of DHTKD1 in GCDH-deficient HEK-293 cells leads to a 2-fold decrease in the established GA1 clinical biomarker glutarylcarnitine, and demonstrate that OGDH is responsible for this remaining glutarylcarnitine production.	glutarylcarnitine	213-230	glutaryl-CoA dehydrogenase	Homo sapiens	36-40
32160276-3	2020	Here we show that loss of DHTKD1 in GCDH-deficient HEK-293 cells leads to a 2-fold decrease in the established GA1 clinical biomarker glutarylcarnitine, and demonstrate that OGDH is responsible for this remaining glutarylcarnitine production.	glutarylcarnitine	213-230	oxoglutarate dehydrogenase	Homo sapiens	174-178
28545977-2	2017	GCDH deficiency leads to disruption of l-lysine degradation with characteristic accumulation of glutarylcarnitine and neurotoxic glutaric acid (GA), glutaryl-CoA, 3-hydroxyglutaric acid (3-OHGA).	glutarylcarnitine	96-113	glutaryl-Coenzyme A dehydrogenase	Mus musculus	0-4
22464876-10	2012	Acylcarnitines such as glutarylcarnitine were associated inversely with eGFR (-3.73 mL/min/1.73 m(2) per standard deviation [SD] increase, pooled P = 1.8 x 10(-69)).	glutarylcarnitine	23-40	epidermal growth factor receptor	Homo sapiens	72-76
22464876-10	2012	Acylcarnitines such as glutarylcarnitine were associated inversely with eGFR (-3.73 mL/min/1.73 m(2) per standard deviation [SD] increase, pooled P = 1.8 x 10(-69)).	glutarylcarnitine	23-40	CD59 molecule (CD59 blood group)	Homo sapiens	87-92