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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2020 | 1 |
2021 | 2 |
2024 | 0 |
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In-frame deletion of SPECC1L microtubule association domain results in gain-of-function phenotypes affecting embryonic tissue movement and fusion events.
Hum Mol Genet. 2021 Dec 17;31(1):18-31. doi: 10.1093/hmg/ddab211.
Hum Mol Genet. 2021.
PMID: 34302166
Free PMC article.
SPECC1L-deficient primary mouse embryonic palatal mesenchyme cells show speed and directionality defects.
Goering JP, Isai DG, Hall EG, Wilson NR, Kosa E, Wenger LW, Umar Z, Yousaf A, Czirok A, Saadi I.
Goering JP, et al.
Sci Rep. 2021 Jan 14;11(1):1452. doi: 10.1038/s41598-021-81123-9.
Sci Rep. 2021.
PMID: 33446878
Free PMC article.
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SPECC1L regulates palate development downstream of IRF6.
Hall EG, Wenger LW, Wilson NR, Undurty-Akella SS, Standley J, Augustine-Akpan EA, Kousa YA, Acevedo DS, Goering JP, Pitstick L, Natsume N, Paroya SM, Busch TD, Ito M, Mori A, Imura H, Schultz-Rogers LE, Klee EW, Babovic-Vuksanovic D, Kroc SA, Adeyemo WL, Eshete MA, Bjork BC, Suzuki S, Murray JC, Schutte BC, Butali A, Saadi I.
Hall EG, et al.
Hum Mol Genet. 2020 Mar 27;29(5):845-858. doi: 10.1093/hmg/ddaa002.
Hum Mol Genet. 2020.
PMID: 31943082
Free PMC article.
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