The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II
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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
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
Chomczynski, P., & Sacchi, N. (1987) · Analytical Biochemistry · doi:10.1016/0003-2697(87)90021-2 · Cited by 46,426
Protein Structure Modeling with MODELLER
Eswar, N., Eramian, D., Webb, B., Shen, M.-Y., & Sali, A. (2008) · Methods in Molecular Biology · doi:10.1007/978-1-60327-058-8_8 · Cited by 1,773
BI-DIRECTIONAL PROTEIN TRANSPORT BETWEEN THE ER AND GOLGI
Lee, M. C. S., Miller, E. A., Goldberg, J., Orci, L., & Schekman, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.105307 · Cited by 813
Cai, H., Reinisch, K., & Ferro-Novick, S. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.04.005 · Cited by 685
Dissection of the Mammalian Midbody Proteome Reveals Conserved Cytokinesis Mechanisms
Skop, A. R., Liu, H., Yates, J., Meyer, B. J., & Heald, R. (2004) · Science · doi:10.1126/science.1097931 · Cited by 516
Structure of the Sec23/24–Sar1 pre-budding complex of the COPII vesicle coat
Bi, X., Corpina, R. A., & Goldberg, J. (2002) · Nature · doi:10.1038/nature01040 · Cited by 461
Multicolour imaging of post-Golgi sorting and trafficking in live cells
Keller, P., Toomre, D., Díaz, E., White, J., & Simons, K. (2001) · Nature Cell Biology · doi:10.1038/35055042 · Cited by 398
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
Jones, B., Jones, E. L., Bonney, S. A., Patel, H. N., Mensenkamp, A. R., Eichenbaum-Voline, S., Rudling, M., Myrdal, U., Annesi, G., Naik, S., et al. (2003) · Nature Genetics · doi:10.1038/ng1145 · Cited by 388
SNARE Selectivity of the COPII Coat
Mossessova, E., Bickford, L. C., & Goldberg, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00608-1 · Cited by 373
Cited by
A Systematic Mammalian Genetic Interaction Map Reveals Pathways Underlying Ricin Susceptibility
Bassik, M. C., Kampmann, M., Lebbink, R. J., Wang, S., Hein, M. Y., Poser, I., Weibezahn, J., Horlbeck, M. A., Chen, S., Mann, M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.01.030 · Cited by 365
Garbes, L., Kim, K., Rieß, A., Hoyer-Kuhn, H., Beleggia, F., Bevot, A., Kim, M. J., Huh, Y. H., Kweon, H.-S., Savarirayan, R., et al. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.01.002 · Cited by 173
Ineffective erythropoiesis and regulation of iron status in iron loading anaemias
Camaschella, C., & Nai, A. (2016) · British Journal of Haematology · doi:10.1111/bjh.13820 · Cited by 172
SEC24A deficiency lowers plasma cholesterol through reduced PCSK9 secretion
Chen, X.-W., Wang, H., Bajaj, K., Zhang, P., Meng, Z.-X., Ma, D., Bai, Y., Liu, H.-H., Adams, E., Baines, A., et al. (2013) · eLife · doi:10.7554/elife.00444 · Cited by 115
The ULK1-FBXW5-SEC23B nexus controls autophagy
Jeong, Y.-T., Simoneschi, D., Keegan, S., Melville, D., Adler, N. S., Saraf, A., Florens, L., Washburn, M. P., Cavasotto, C. N., Fenyö, D., et al. (2018) · eLife · doi:10.7554/elife.42253 · Cited by 79
Metadata
- Authors
- Schwarz, K., Iolascon, A., Verissimo, F., Trede, N. S., Horsley, W., Chen, W., Paw, B. H., Hopfner, K.-P., Holzmann, K., Russo, R., Esposito, M. R., Spano, D., De Falco, L., Heinrich, K., Joggerst, B., Rojewski, M. T., Perrotta, S., Denecke, J., Pannicke, U., Delaunay, J., Pepperkok, R., & Heimpel, H.
- Venue
- Nature Genetics
- Published
- 2009-06-28
- Volume
- 41
- Issue
- 8
- Pages
- 936-940
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2169337490
- Cited by
- 284
- References
- 26
- FWCI
- 8.96
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. https://app.cochat.ai/papers/10.1038/ng.405
- The paper
- Schwarz, K., Iolascon, A., Verissimo, F., Trede, N. S., Horsley, W., Chen, W., Paw, B. H., Hopfner, K.-P., Holzmann, K., Russo, R., Esposito, M. R., Spano, D., De Falco, L., Heinrich, K., Joggerst, B., Rojewski, M. T., Perrotta, S., Denecke, J., Pannicke, U., . . . Heimpel, H. (2009). Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nature Genetics. https://doi.org/10.1038/ng.405
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
