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Cited by in F6Publishing
For: Takatani T, Shiohama T, Takatani R, Shimojo N. A novel CUL7 mutation in a Japanese patient with 3M syndrome. Hum Genome Var 2018;5:30. [PMID: 30374406 DOI: 10.1038/s41439-018-0029-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Shi L, Du D, Peng Y, Liu J, Long J. The functional analysis of Cullin 7 E3 ubiquitin ligases in cancer. Oncogenesis 2020;9:98. [PMID: 33130829 DOI: 10.1038/s41389-020-00276-w] [Reference Citation Analysis]
2 Hu L, Wang X, Jin T, Han Y, Liu J, Jiang M, Yan S, Fu X, An B, Huang S. Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing. J Clin Lab Anal 2020;34:e23265. [PMID: 32141654 DOI: 10.1002/jcla.23265] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
3 Cruz Walma DA, Chen Z, Bullock AN, Yamada KM. Ubiquitin ligases: guardians of mammalian development. Nat Rev Mol Cell Biol. [DOI: 10.1038/s41580-021-00448-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
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