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Cited by in F6Publishing
For: Postlethwait JH, Navajas Acedo J, Piotrowski T. Evolutionary Origin and Nomenclature of Vertebrate Wnt11-Family Genes. Zebrafish 2019;16:469-76. [PMID: 31295059 DOI: 10.1089/zeb.2019.1760] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Van Itallie ES, Field CM, Mitchison TJ, Kirschner MW. Dorsal lip maturation and initial archenteron extension depend on Wnt11 family ligands. Dev Biol 2023;493:67-79. [PMID: 36334838 DOI: 10.1016/j.ydbio.2022.10.013] [Reference Citation Analysis]
2 Watson CJ, Tang WJ, Rojas MF, Fiedler IAK, Morfin Montes de Oca E, Cronrath AR, Callies LK, Swearer AA, Ahmed AR, Sethuraman V, Addish S, Farr GH, Gómez AE, Rai J, Monstad-rios AT, Gardiner EM, Karasik D, Maves L, Busse B, Hsu Y, Kwon RY. wnt16 regulates spine and muscle morphogenesis through parallel signals from notochord and dermomyotome. PLoS Genet 2022;18:e1010496. [DOI: 10.1371/journal.pgen.1010496] [Reference Citation Analysis]
3 Jimenez E, Slevin CC, Song W, Chen Z, Frederickson SC, Gildea D, Wu W, Elkahloun AG, Ovcharenko I, Burgess SM. A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish. Cell Genomics 2022;2:100170. [DOI: 10.1016/j.xgen.2022.100170] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Heilig AK, Nakamura R, Shimada A, Hashimoto Y, Nakamura Y, Wittbrodt J, Takeda H, Kawanishi T. Wnt11 acts on dermomyotome cells to guide epaxial myotome morphogenesis. Elife 2022;11:e71845. [PMID: 35522214 DOI: 10.7554/eLife.71845] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Van Itallie ES, Field CM, Mitchison TJ, Kirschner MW. Wnt11 family dependent morphogenesis during frog gastrulation is marked by the cleavage furrow protein anillin.. [DOI: 10.1101/2022.01.07.475368] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Xia ZJ, Zeng XI, Tambe M, Ng BG, Dong PDS, Freeze HH. A Dominant Heterozygous Mutation in COG4 Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling. Front Cell Dev Biol 2021;9:720688. [PMID: 34595172 DOI: 10.3389/fcell.2021.720688] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
7 Watson CJ, Tang WJ, Rojas MF, Fiedler IA, de Oca EMM, Cronrath AR, Callies LK, Swearer AA, Ahmed AR, Sethuraman V, Addish S, Farr GH, Gomez AE, Rai J, Monstad-rios AT, Gardiner EM, Karasik D, Maves L, Busse B, Hsu Y, Kwon RY. wnt16 regulates spine and muscle morphogenesis through parallel signals from notochord and dermomyotome.. [DOI: 10.1101/2021.08.12.456120] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Xia Z, Zeng XI, Tambe M, Ng BG, Dong PDS, Freeze HH. A single heterozygous mutation in COG4 disrupts zebrafish early development via Wnt signaling.. [DOI: 10.1101/2021.05.23.443307] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
9 Navajas Acedo J, Voas MG, Alexander R, Woolley T, Unruh JR, Li H, Moens C, Piotrowski T. PCP and Wnt pathway components act in parallel during zebrafish mechanosensory hair cell orientation. Nat Commun 2019;10:3993. [PMID: 31488837 DOI: 10.1038/s41467-019-12005-y] [Cited by in Crossref: 29] [Cited by in F6Publishing: 28] [Article Influence: 7.3] [Reference Citation Analysis]