2008
DOI: 10.1016/j.mcn.2008.07.023
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DCC is required for the tangential migration of noradrenergic neurons in locus coeruleus of mouse brain

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Cited by 23 publications
(25 citation statements)
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“…Norepinephrine innervation to the mPFC matures by the second postnatal week in the rodent (Levitt and Moore, 1979). Nevertheless, we cannot completely rule out the potential involvement of the norepinephrine system in the dcc heterozygous phenotypes because norepinephrine neurons in the locus ceruleus express DCC (Shi et al, 2008).…”
Section: Discussionmentioning
confidence: 92%
“…Norepinephrine innervation to the mPFC matures by the second postnatal week in the rodent (Levitt and Moore, 1979). Nevertheless, we cannot completely rule out the potential involvement of the norepinephrine system in the dcc heterozygous phenotypes because norepinephrine neurons in the locus ceruleus express DCC (Shi et al, 2008).…”
Section: Discussionmentioning
confidence: 92%
“…Sections were processed for TH and BrdU double immunostaining (see below) to localize BrdU-positive cells in the LC. X-gal staining and TUNEL staining of frozen sections were performed as described previously (Shi et al, 2008;Zheng et al, 2009). …”
Section: Wnt1-cre En1mentioning
confidence: 99%
“…Whole mount and section in situ hybridization were performed as previously described (Shi et al, 2008;Shi et al, 2010). The following mouse antisense RNA probes were used: c-Ret (Ohsawa et al, 2005), Dbh , Fgf8 (Wassarman et al, 1997), Gbx2 (Liu and Joyner, 2001b), Hes1 (Lee et al, 2005), Hes5 , Ngn1, Ngn2 (Sommer et al, 1996), Otx2 (MartinezBarbera et al, 2001), Phox2a (Tiveron et al, 1996) and Phox2b (Pattyn et al, 1997).…”
Section: In Situ Hybridization and Immunostainingmentioning
confidence: 99%
“…: NM_013864; forward: 5 0 -CTATCTCGGTCTCGCACAG CA-3 0 , reverse: 5 0 -TTCAGAGAGGCCTGACACATC-3 0 ), and then subcloned into pGEM-T vector (Promega, Madison, WI, USA). Digoxygenin-labeled Ndrg2 anti-sense riboprobe was synthesized and used for in situ hybridization on brain sections as described previously (Shi et al 2008). The uniqueness of Ndrg2 probe was confirmed by the NCBI Blast search program (http://www.ncbi.nlm.nih.gov/BLA ST/Blast.cgi), that is, the probe is specific to Ndrg2 gene and has no homologous sequences with other numbers (e.g.…”
Section: In Situ Hybridizationmentioning
confidence: 99%
“…In situ hybridization and immunohistochemistry double labeling Double labeling of in situ hybridization and immunohistochemistry was carried out as described previously (Liu et al , 2010Shi et al 2008) with some modifications. In brief, in situ hybridization of Ndrg2 was first performed as described above but without proteinase K treatment.…”
Section: Brdu Administrationmentioning
confidence: 99%