2009
DOI: 10.1002/dvdy.21889
|View full text |Cite
|
Sign up to set email alerts
|

Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
4
0

Year Published

2010
2010
2020
2020

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 9 publications
(4 citation statements)
references
References 60 publications
(46 reference statements)
0
4
0
Order By: Relevance
“…In vitro fertilization, embryo culture, mRNA and antisense morpholino oligonucleotides (MO, Gene-Tools Inc.) and protein injections were used as previously described [41] . In situ hybridization analyses were carried out as formerly reported [41] . The wrap assay was as described previously [41] .…”
Section: Methods Summarymentioning
confidence: 99%
See 1 more Smart Citation
“…In vitro fertilization, embryo culture, mRNA and antisense morpholino oligonucleotides (MO, Gene-Tools Inc.) and protein injections were used as previously described [41] . In situ hybridization analyses were carried out as formerly reported [41] . The wrap assay was as described previously [41] .…”
Section: Methods Summarymentioning
confidence: 99%
“…In situ hybridization analyses were carried out as formerly reported [41] . The wrap assay was as described previously [41] . Microsurgery was carried out using hair knives.…”
Section: Methods Summarymentioning
confidence: 99%
“…The Hox genes also regulate intrasegmental MN specification and their target muscle connectivity [51]. In the frog, the Hoxc6 gene has also been shown to affect primary neurogenesis [54]. …”
Section: Discussionmentioning
confidence: 99%
“…In Situ Hybridization : For ISH analysis, the msxB probe was used. The antisense RNA probes labeled with digoxigenin (DIG) were synthesized according to Bardine and co‐workers . After rehydration, the tails were treated with proteinase K (0.5 μg mL −1 in PBS‐Tween) for 8 min at room temperature, followed by enzyme inactivation with a solution of TEA 0.1 m and acetic anhydride 0.5 μL mL −1 in PBS‐T for 10 min.…”
Section: Methodsmentioning
confidence: 99%