2005
DOI: 10.1002/dvdy.20545
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Short‐term lineage analysis of dorsally derived Olig3 cells in the developing spinal cord

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Cited by 41 publications
(34 citation statements)
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“…In situ hybridization was performed as described previously (Ding et al, 2005), using the following digoxygenin (DIG)-labeled RNA probes: mouse netrin-1, Unc5c (formerly Unc5h3), DCC, and chick netrin-1 (Sugimoto et al, 2001;Watanabe et al, 2006). DIG-labeled RNA probes were synthesized by using a DIG RNA-labeling kit (Roche Diagnostics).…”
Section: Methodsmentioning
confidence: 99%
“…In situ hybridization was performed as described previously (Ding et al, 2005), using the following digoxygenin (DIG)-labeled RNA probes: mouse netrin-1, Unc5c (formerly Unc5h3), DCC, and chick netrin-1 (Sugimoto et al, 2001;Watanabe et al, 2006). DIG-labeled RNA probes were synthesized by using a DIG RNA-labeling kit (Roche Diagnostics).…”
Section: Methodsmentioning
confidence: 99%
“…The expression of the murine bHLH gene Olig3 is first detected around embryonic day 9.25 (E9.25) in the dorsal hindbrain and spinal cord (Takebayashi et al, 2002b;Ding et al, 2005;Muller et al, 2005). We used immunohistochemistry to characterize Olig3 + cells on transverse sections of the hindbrain.…”
Section: + Cells In Rhombomeres 4-7mentioning
confidence: 99%
“…The presence of a 725 bp fragment, a 525 bp fragment, or both, indicated animals with tra/tra, +/+, and +/tra genotypes, respectively. Mice carrying the CP2L1 allele in which its exon 2 was flanked by two loxP sites were crossed with Pc36 Creexpressing mice (provided by H. Takebayashi) (Ding et al, 2005) to excise exon 2, leading to a frame-shift mutation that generates a null allele of Cp2l1 (see Fig. S1 in the supplementary material).…”
Section: Mouse Strainsmentioning
confidence: 99%