. 2000 Mar 15;20(6):2255–2265. doi: 10.1523/JNEUROSCI.20-06-02255.2000

Table 1.

Putative thyroid hormone-responsive genes identified by differential display (Experiment I)

cDNA fragment^1-a	Match in GenBank	DNA identity %	GenBank accession no.	Reference	mRNA localization in GD16 fetus
2A	Cl-13/	97.7	X52817	Wieczorek and Hughes, 1991	Cortex, hippocampus, hypothalamus,
	NSP/	85.6	L10333	Roebroek et al., 1993	diencephalon, midbrain, medulla, spinal cord,
	s-rex_b	98.4	U17604	Baka et al., 1996	trigeminal ganglion
18C	Oct-1	99.0	U17013	J. N. Buskin, unpublished data	Cortex, hippocampus, diencephalon, midbrain, retina, liver
6C	None	N/A	AF133273 ^1-b		Cortex, hippocampus, diencephalon, midbrain, spinal cord, liver
15A	None	N/A	AF133274 ^1-b		Cortex, retina, liver
4C	None	N/A	AF133275 ^1-b		Cortex, midbrain, liver
5C	None	N/A	AF133276 ^1-b		Cortex, midbrain, liver
17C	BC1	98.0	M16113	DeChiara and Brosius, 1987	All tissues
17CB	Ribosomal protein L31	91.9	X04809	Tanaka et al., 1987	Cortex, hippocampus, midbrain, liver
18AL^1-c		N/A			Global expression
18AS^1-c		N/A			Global expression
14C^1-c		N/A			Global expression

^F1-a

RNAimage primers used to generate cDNA fragments: number indicates H-AP forward arbitrary primer (1–8), letter indicates H-T₁₁M reverse primer (H-T₁₁A, H-T₁₁C, or H-T₁₁G), and a prefix of 1 indicates upregulation by thyroid hormone. For example, fragment 18C is upregulated by thyroid hormone and was generated using H-AP8 and H-T₁₁C primers.

^F1-b

Submitted to GenBank at the time of manuscript submission.

^F1-c

Fragments not sequenced. Global expression pattern revealed by in situ hybridization suggested that these fragments were falsely identified differential display products.