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. Author manuscript; available in PMC: 2015 May 18.
Published in final edited form as: Neurobiol Dis. 2012 Dec 4;52:84–93. doi: 10.1016/j.nbd.2012.11.014

Table 2.

Twelve molecular transcripts that emerged from the microarray analysis

Gene name GenBank # Region X group S1 cortex
WIF1 NM_007191.1 p = 0.003 Ns*
PP1R7 BF718769 p = 0.02 Ns*
FLJ10955 NM_018282.1 p = 0.03 Ns*
PRO0518 AF090934.1 p = 0.006 p = 0.009
DDX21 NM_004728.1 p = 0.009 p = 0.02
SNW1 NM_012245.1 p = 0.01 p = 0.004
NFYB AI804118 p = 0.02 p = 0.02
HSPC069 AI761110 p = 0.02 p = 0.01
BIRC2 NM_001166.2 p = 0.03 p = 0.01
FBRNP AA528233 p = 0.03 p = 0.001
PTPRK NM_002844.1 p = 0.04 p = 0.01
PLOD2 NM_000935.1 p = 0.04 p = 0.003

mRNA levels of 12 molecules conformed to the fMRI spatial profile of Huntington's disease (columns 1-3). A secondary analysis identified three molecules whose expression deficit was restricted to the posterior caudate (column 4, Ns). These hits are considered to best-tracked fMRI-phenotype.

Group represents healthy vs. control. Region x group is the interaction term, including region (anterior vs. posterior caudate) and group.

*

Ns= Not Significant