Search Criteria |
Gene/Clone | Species | Stage | Anatomy Item | Experimenter |
---|---|---|---|---|
tnni3 | xenopus | embryonic structure |
Too many results?Too few results?
Expression summary for tnni3
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Experiment | Species | Images | Stages | Anatomy | Assay |
Brade T et al. (2007) Assay
Paper |
laevis |
1 image |
NF stage 28 | cardiac mesoderm, heart primordium | in situ hybridization |
Inui M et al. (2009) Assay
Paper |
laevis |
1 image |
NF stage 29 and 30 | cardiac mesoderm, heart primordium | in situ hybridization |
Gessert S et al. (2008) Assay
Paper |
laevis |
4 images |
NF stage 24 to NF stage 29 and 30 | cardiac mesoderm, heart primordium | in situ hybridization |
Lavery DL et al. (2009) Assay
Paper |
xenopus |
3 images |
NF stage 32 | heart primordium | in situ hybridization |
Lavery DL et al. (2009) Assay
Paper |
laevis |
1 image |
NF stage 32 | heart primordium | in situ hybridization |
Gessert S and Kühl M (2009) Assay
Paper |
laevis |
1 image |
NF stage 29 and 30 to NF stage 31 | endocardial tube | in situ hybridization |
Paper |
laevis |
1 image |
NF stage 28 | heart primordium | in situ hybridization |
Paper |
laevis |
1 image |
NF stage 33 and 34 to NF stage 40 | heart primordium | in situ hybridization |
In vitro organogenesis from undifferentiated cells in Xenopus.
Paper |
laevis |
2 images |
NF stage 37 and 38 | cardiac mesoderm | in situ hybridization |
The slow isoform of Xenopus troponin I is expressed in developing skeletal muscle but not in the heart.
Paper |
laevis |
1 image |
NF stage 29 and 30 | cardiac mesoderm | in situ hybridization |
A role for GATA-4/5/6 in the regulation of Nkx2.5 expression with implications for patterning of the precardiac field.
Paper |
xenopus |
1 image |
NF stage 35 and 36 | heart primordium | in situ hybridization |
Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis.
Paper |
laevis |
1 image |
NF stage 29 and 30 | cardiac mesoderm, heart primordium | in situ hybridization |
Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis.
Paper |
laevis |
1 image |
NF stage 29 and 30 | cardiac mesoderm, heart primordium | in situ hybridization |
Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis.
Paper |
laevis |
1 image |
NF stage 29 and 30 | cardiac mesoderm, heart primordium | in situ hybridization |
Retinoic acid can block differentiation of the myocardium after heart specification.
Paper |
laevis |
1 image |
NF stage 33 and 34 | stomodeal-hypophyseal primordium | in situ hybridization |
Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm.
Paper |
laevis |
1 image |
NF stage 28 to NF stage 29 and 30 | cardiac mesoderm | in situ hybridization |
Cleaver OB et al. (1996) Assay
Paper |
laevis |
2 images |
NF stage 26 to NF stage 33 and 34 | cardiac mesoderm, heart primordium | in situ hybridization |
Haworth KE et al. (2008) Assay
Paper |
laevis |
1 image |
NF stage 35 and 36 to NF stage 37 and 38 | cardiac mesoderm | in situ hybridization |
Li Y et al. (2008) Assay
Paper |
laevis |
2 images |
NF stage 35 and 36 | cardiac mesoderm | in situ hybridization |
Cardiac troponin I is a heart-specific marker in the Xenopus embryo: expression during abnormal heart morphogenesis.
Paper |
laevis |
1 image |
NF stage 28 to NF stage 29 and 30 | cardiac mesoderm | in situ hybridization |
Drysdale TA et al. (1994) Assay
Paper |
laevis |
1 image |
NF stage 28 to NF stage 29 and 30 | cardiac mesoderm | in situ hybridization |
Fox (forkhead) genes are involved in the dorso-ventral patterning of the Xenopus mesoderm.
Paper |
laevis |
1 image |
NF stage 40 | lateral plate mesoderm | in situ hybridization |
Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5.
Paper |
laevis |
1 image |
NF stage 26 to NF stage 41 | heart primordium | in situ hybridization |
Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory...
Paper |
laevis |
1 image |
NF stage 28 to NF stage 29 and 30 | heart primordium | in situ hybridization |
Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory...
Paper |
laevis |
1 image |
NF stage 29 and 30 | heart primordium | in situ hybridization |
Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory...
Paper |
laevis |
1 image |
NF stage 29 and 30 | heart primordium | in situ hybridization |
A crucial role of a high mobility group protein HMGA2 in cardiogenesis.
Paper |
laevis |
1 image |
NF stage 41 | cardiac mesoderm, heart primordium | in situ hybridization |
Warkman AS and Atkinson BG (2002) Assay
Paper |
laevis |
1 image |
NF stage 29 and 30 | cardiac mesoderm | in situ hybridization |
Prolonged FGF signaling is necessary for lung and liver induction in Xenopus.
Paper |
laevis |
1 image |
NF stage 35 and 36 | heart primordium | in situ hybridization |
Prolonged FGF signaling is necessary for lung and liver induction in Xenopus.
Paper |
laevis |
1 image |
NF stage 35 and 36 | heart primordium | in situ hybridization |
The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis.
Paper |
laevis |
1 image |
NF stage 28 | heart primordium | in situ hybridization |
A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis.
Paper |
laevis |
1 image |
NF stage 32 | cardiac mesoderm | in situ hybridization |
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