The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
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Citations
Cites
The packing of α-helices: simple coiled-coils
Crick, F. H. C. (1953) · Acta Crystallographica · doi:10.1107/s0365110x53001964 · Cited by 1,578
The DNA sequence of human chromosome 22
Dunham, I., Hunt, A. R., Collins, J. E., Bruskiewich, R., Beare, D. M., Clamp, M., Smink, L. J., Ainscough, R., Almeida, J. P., Babbage, A., et al. (1999) · Nature · doi:10.1038/990031 · Cited by 1,157
Myosins: a diverse superfamily
Sellers, J. R. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(00)00005-7 · Cited by 848
Dominguez, R., Freyzon, Y., Trybus, K. M., & Cohen, C. (1998) · Cell · doi:10.1016/s0092-8674(00)81598-6 · Cited by 640
The Fourier transform of a coiled-coil
Crick, F. H. C. (1953) · Acta Crystallographica · doi:10.1107/s0365110x53001952 · Cited by 313
Harrington, W. F., & Rodgers, M. E. (1984) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.53.070184.000343 · Cited by 287
Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes.
Simons, M., Wang, M., McBride, O. W., Kawamoto, S., Yamakawa, K., Gdula, D., Adelstein, R. S., & Weir, L. (1991) · Circulation Research · doi:10.1161/01.res.69.2.530 · Cited by 272
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
Kelley, M. J., Jawien, W., Ortel, T. L., & Korczak, J. F. (2000) · Nature Genetics · doi:10.1038/79069 · Cited by 264
Kawamoto, S., & Adelstein, R. S. (1991) · The Journal of cell biology · doi:10.1083/jcb.112.5.915 · Cited by 214
Genetic Causes of Hearing Loss
Willems, P. J. (2000) · New England Journal of Medicine · doi:10.1056/nejm200004133421506 · Cited by 198
Sáez, C. G., Myers, J. C., Shows, T. B., & Leinwand, L. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.3.1164 · Cited by 121
Toothaker, L., Gonzalez, D., Tung, N., Lemons, R. S., Beau, M. M. L., Arnaout, M., Clayton, L., & Tenen, D. G. (1991) · Blood · doi:10.1182/blood.v78.7.1826.1826 · Cited by 70
The Gene for May-Hegglin Anomaly Localizes to a <1-Mb Region on Chromosome 22q12.3-13.1
Martignetti, J. A., Heath, K. E., Harris, J. M., Bizzaro, N., Savoia, A., Balduini, C. L., & Desnick, R. J. (2000) · The American Journal of Human Genetics · doi:10.1086/302873 · Cited by 45
Localisation of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11–q13
Cusano, R., Gangarossa, S., Forabosco, P., Caridi, G., Ghiggeri, G. M., Russo, G. M., Iolascon, A., Ravazzolo, R., & Seri, M. (2000) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200533 · Cited by 10
Cited by
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
Hirokawa, N., Niwa, S., & Tanaka, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.039 · Cited by 1,138
Identification and Characterization of Nucleolin as a c-myc G-quadruplex-binding Protein
González, V., Guo, K., Hurley, L., & Sun, D. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.018028 · Cited by 321
Mertk drives myosin II redistribution during retinal pigment epithelial phagocytosis
Strick, D. J., Feng, W., & Vollrath, D. (2009) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.08-3058 · Cited by 81
Kamnev, A., Lacouture, C., Fusaro, M., & Dupré, L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.750537 · Cited by 38
Metadata
- Authors
- Syndrome Consortium, T. M.-H.
- Venue
- Nature Genetics
- Published
- 2000-09
- Volume
- 26
- Issue
- 1
- Pages
- 103-105
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2413578523
- Cited by
- 448
- References
- 14
- FWCI
- 9.60
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
