The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Nkx2-5 Pathways and Congenital Heart Disease
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Citations
Cites
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860
Jenni, R., Oechslin, E., Schneider, J., Jost, C. A., & Kaufmann, P. A. (2001) · Heart · doi:10.1136/heart.86.6.666 · Cited by 1,549
Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5
Schott, J.-J., Benson, D. W., Basson, C. T., Pease, W., Silberbach, G. M., Moak, J. P., Maron, B. J., Seidman, C. E., & Seidman, J. G. (1998) · Science · doi:10.1126/science.281.5373.108 · Cited by 1,308
Self-citationRequirement for neuregulin receptor erbB2 in neural and cardiac development
Lee, K.-F., Simon, H., Chen, H., Bates, B., Hung, M.-C., & Hauser, C. (1995) · Nature · doi:10.1038/378394a0 · Cited by 1,290
Self-citationGATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
Garg, V., Kathiriya, I. S., Barnes, R., Schluterman, M. K., King, I. N., Butler, C. A., Rothrock, C. R., Eapen, R. S., Hirayama-Yamada, K., Joo, K., et al. (2003) · Nature · doi:10.1038/nature01827 · Cited by 1,236
Aberrant neural and cardiac development in mice lacking the ErbB4 neuregulin receptor
Gassmann, M., Casagranda, F., Orioli, D., Simon, H., Lai, C., Klein, R., & Lemke, G. (1995) · Nature · doi:10.1038/378390a0 · Cited by 1,148
Lyons, I., Parsons, L. M., Hartley, L., Li, R., Andrews, J. E., Robb, L., & Harvey, R. P. (1995) · Genes & Development · doi:10.1101/gad.9.13.1654 · Cited by 1,141
Bruneau, B. G., Nemer, G., Schmitt, J. P., Charron, F., Robitaille, L., Caron, S., Conner, D. A., Gessler, M., Nemer, M., Seidman, C. E., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00493-7 · Cited by 1,061
Embryonic stem cells alone are able to support fetal development in the mouse
Nagy, A., Gócza, E., Diaz, E. M., Prideaux, V. R., Iványi, E., Markula, M., & Rossant, J. (1990) · Development · doi:10.1242/dev.110.3.815 · Cited by 781
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
Benson, D. W., Silberbach, G. M., Kavanaugh-McHugh, A., Cottrill, C., Zhang, Y., Riggs, S., Smalls, O., Johnson, M. C., Watson, M. S., Seidman, J. G., et al. (1999) · Journal of Clinical Investigation · doi:10.1172/jci8154 · Cited by 690
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Cited by
A census of human transcription factors: function, expression and evolution
Vaquerizas, J. M., Kummerfeld, S. K., Teichmann, S. A., & Luscombe, N. M. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2538 · Cited by 1,573
Postnatal isl1+ cardioblasts enter fully differentiated cardiomyocyte lineages
Laugwitz, K.-L., Moretti, A., Lam, J., Gruber, P., Chen, Y., Woodard, S., Lin, L.-Z., Cai, C.-L., Lu, M. M., Reth, M., et al. (2005) · Nature · doi:10.1038/nature03215 · Cited by 1,304
Self-citationThe developmental genetics of congenital heart disease
Bruneau, B. G. (2008) · Nature · doi:10.1038/nature06801 · Cited by 687
Left ventricular non-compaction cardiomyopathy
Towbin, J. A., Lorts, A., & Jefferies, J. L. (2015) · The Lancet · doi:10.1016/s0140-6736(14)61282-4 · Cited by 522
Prall, O. W. J., Menon, M. K., Solloway, M. J., Watanabe, Y., Zaffran, S., Bajolle, F., Biben, C., McBride, J. J., Robertson, B. R., Chaulet, H., et al. (2007) · Cell · doi:10.1016/j.cell.2007.01.042 · Cited by 517
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Metadata
- Authors
- Pashmforoush, M., Lu, J. T., Chen, H., Amand, T. S., Kondo, R., Pradervand, S., Evans, S. M., Clark, B., Feramisco, J. R., Giles, W., Ho, S. Y., Benson, D. W., Silberbach, M., Shou, W., & Chien, K. R.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2004-04
- Volume
- 117
- Issue
- 3
- Pages
- 373-386
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2016368778
- Cited by
- 440
- References
- 41
- FWCI
- 11.26
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Nkx2-5 Pathways and Congenital Heart Disease. https://app.cochat.ai/papers/10.1016/s0092-8674(04)00405-2
- The paper
- Pashmforoush, M., Lu, J. T., Chen, H., Amand, T. S., Kondo, R., Pradervand, S., Evans, S. M., Clark, B., Feramisco, J. R., Giles, W., Ho, S. Y., Benson, D. W., Silberbach, M., Shou, W., & Chien, K. R. (2004). Nkx2-5 Pathways and Congenital Heart Disease. Cell. https://doi.org/10.1016/s0092-8674(04)00405-2
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
