HUGO ID Detailed Result 4141

PMID	Match String	Actual String	Score	Flanking text	Edited by	Edit
12417341	GAPDH	GAPDH	1.9	For internal standard control the expression of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) GAPDH was quantified simultaneously
12417341	GAPDH	GAPDH	1.9	probe sequences (forward forward primer reverse primer and TaqMan probe GAPDH 5_amp_#x2032 -CCT GGA GAA ACC TGC CAA GTA T-3_amp_#x2032 5_amp_#x2032
12417341	GAPDH	GAPDH	1.9	shown as the weight ratio of the target gene to GAPDH
16436205	GAPDH	GAPDH	0.0	mRNA band was normalized to the sum of the L32 GAPDH bands
16436205	GAPDH	GAPDH	0.0	G93A-SOD1 cells demonstrated lower levels of housekeeping messages L32 and GAPDH than did non-transgenic matched cell cultures (Fig Fig 1
16436205	GAPDH	GAPDH	0.0	of non-housekeeping genes such that the ratio of L32 and GAPDH to total mRNA is fundamentally skewed in G93A-SOD1 gial cultures
16436205	GAPDH	GAPDH	0.0	(% % change in TNF_amp_#x003b1 bands without normalization to L32 GAPDH = 1132 _amp_#x000b1 618% in G93A-SOD1 cells vs 242 _amp_#x000b1
16510725	GAPDH	GAPDH	1.6	follows TNF-alpha sense 5'-GACCCAGTGTGGGAAG-3' and antisense 5'-GGTTCAGTGATGT-AGCGA-3' glyceraldehyde-3-phosphate dehydrogenase (GAPDH), GAPDH sense 5'-CCATGGAGAAGGCTGGG-3' and antisense 5'-CAAAA-GTTGTCATGGATGACC-3'
16510725	GAPDH	GAPDH	1.6	The amounts of TNF-alpha and GAPDH cDNA were calculated using linear regression analysis from standard curves
16510725	GAPDH	GAPDH	1.6	linear regression analysis from standard curves for both TNF-alpha and GAPDH and the amount of TNF-alpha cDNA was expressed as a
16510725	GAPDH	GAPDH	1.6	amount of TNF-alpha cDNA was expressed as a percentage of GAPDH
16510725	GAPDH	GAPDH	1.6	TNF-alpha cDNA amount in different samples was normalized against GAPDH cDNA and expressed as a percentage of GAPDH cDNA (**
16510725	GAPDH	GAPDH	1.6	normalized against GAPDH cDNA and expressed as a percentage of GAPDH cDNA (** ** p _lt_ 0.01 *** p _lt_ 0.0005
16510725	GAPDH	GAPDH	1.6	There were no changes in GAPDH cDNA amount among the groups
16510725	GAPDH	GAPDH	1.6	RNA amounts in different samples were normalized against (L32 L32 GAPDH RNA multiplied by 1000 and presented as an arbitrary number
16510725	GAPDH	GAPDH	1.6	1000 and presented as an arbitrary number per (L32 L32 GAPDH RNA (* * p _lt_ 0.5 ** p _lt_ 0.05
16877542	GAPDH	GAPDH	0.0	phox glial fibrillary acidic protein macrophage antigen complex 1 and GAPDH and PCR conditions are presented in Supporting Text
18598679	GAPDH	GAPDH	1.5	and IL-1_amp_#x3b2 mRNA expression were evaluated by semiquantitative RT-PCR using GAPDH gene as internal standard
18598679	GAPDH	GAPDH	1.5	B Ratio of PCR product from IL-1_amp_#x3b2 to that of GAPDH mRNA
18598679	GAPDH	GAPDH	1.5	product from gp91 phox and p47 phox to that of GAPDH mRNA
18598679	GAPDH	GAPDH	1.5	GAPDH was used as an internal control
12417341	glyceraldehyde 3-phosphate dehydrogenase	glyceraldehyde 3 phosphate dehydrogenase	1.0	for internal standard control the expression of glyceraldehyde 3 phosphate dehydrogenase gapdh was quantified simultaneously.
16120782	glyceraldehyde 3-phosphate dehydrogenase	glyceraldehyde 3 phosphate dehydrogenase	1.0	glyceraldehyde 3 phosphate dehydrogenase forward 5' tca cca ggg ctg cca ttt gc 3' and reverse 5' gac tcc acg aca tac tca gc 3' were used as housekeeping control for socs 1 and 3; beta actin forward 5' cac agc ttc ttt gca gct cct t 3' and re
16510725	glyceraldehyde 3-phosphate dehydrogenase	glyceraldehyde 3 phosphate dehydrogenase	1.0	the primers used were as follows: tnf alpha sense 5' gacccagtgtgggaag 3' and antisense 5' ggttcagtgatgt agcga 3'; glyceraldehyde 3 phosphate dehydrogenase gapdh sense 5' ccatggagaaggctggg 3' and antisense 5' caaaa gttgtcatggatgacc 3'.