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. 2022 Apr 19;5:372. doi: 10.1038/s42003-022-03268-1

Table 2.

Weights and significance of covariance between the expression of individual genes of interest and [11C]flumazenil signal.

Gene PLS rank/15,633 PLS gene weight (Z-score) pFDR
GABRB2 22 6.91 1.45 × 10−9
GABRD 227 5.64 3.95 × 10−7
GABRG3 392 5.11 3.97 × 10−6
GABRA1 401 5.07 4.67 × 10−6
GABRG2 597 4.67 2.31 × 10−-5
GABRA4 2101 2.94 6.43 × 10−3
GAD1 2405 2.70 0.0117
VIP 2566 2.60 0.0150
CCK 3050 2.26 0.0311
PVALB 3059 2.26 0.0315
GABRA3 12,482 −2.09 0.0436
GABRG1 12,816 −2.29 0.0293
CALB1 13,166 −2.50 0.0190
NOS1 13,727 −2.91 6.70 × 10−3
CALB2 15,393 −5.09 4.34 × 10−6

Statistically significant results (pFDR < 0.05) shown only. PLS weight and pFDR shown to third significant figure. PLS, partial least squares regression analysis. CALB1, calbindin, CALB2, calretinin, CCK, cholecystokinin, GABRA1/3/4, GABAAR receptor subunits α1/3/4, GABRB2, GABAAR receptor subunit β2, GABRD, GABAAR receptor subunit δ, GABRG1-3, GABAAR receptor subunits γ1-3, GAD1, GABA-synthesising enzyme GAD67, NOS1, neuronal nitric oxide synthase, PVALB, parvalbumin, VIP, vasoactive intestinal peptide.