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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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2017 | 3 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
2023 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 55773
7 results
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FAM91A1-TBC1D23 complex structure reveals human genetic variations susceptible for PCH.
Proc Natl Acad Sci U S A. 2023 Nov 7;120(45):e2309910120. doi: 10.1073/pnas.2309910120. Epub 2023 Oct 30.
Proc Natl Acad Sci U S A. 2023.
PMID: 37903274
Free PMC article.
TBC1 domain family member 23 interacts with Ras-related protein Rab-11A to promote poor prognosis of non-small-cell lung cancer via β1-integrin.
Zhang Y, Su H, Wudu M, Ren H, Xu Y, Zhang Q, Jiang J, Wang Q, Jiang X, Zhang B, Liu Z, Zou Z, Qiu X.
Zhang Y, et al.
J Cell Mol Med. 2021 Sep;25(18):8821-8835. doi: 10.1111/jcmm.16841. Epub 2021 Aug 7.
J Cell Mol Med. 2021.
PMID: 34363324
Free PMC article.
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Structure of TBC1D23 N-terminus reveals a novel role for rhodanese domain.
Liu D, Yang F, Liu Z, Wang J, Huang W, Meng W, Billadeau DD, Sun Q, Mo X, Jia D.
Liu D, et al.
PLoS Biol. 2020 May 26;18(5):e3000746. doi: 10.1371/journal.pbio.3000746. eCollection 2020 May.
PLoS Biol. 2020.
PMID: 32453802
Free PMC article.
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Structural and functional studies of TBC1D23 C-terminal domain provide a link between endosomal trafficking and PCH.
Huang W, Liu Z, Yang F, Zhou H, Yong X, Yang X, Zhou Y, Xue L, Zhang Y, Liu D, Meng W, Zhang W, Zhang X, Shen X, Sun Q, Li L, Ma C, Wei Y, Billadeau DD, Mo X, Jia D.
Huang W, et al.
Proc Natl Acad Sci U S A. 2019 Nov 5;116(45):22598-22608. doi: 10.1073/pnas.1909316116. Epub 2019 Oct 17.
Proc Natl Acad Sci U S A. 2019.
PMID: 31624125
Free PMC article.
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TBC1D23 is a bridging factor for endosomal vesicle capture by golgins at the trans-Golgi.
Shin JJH, Gillingham AK, Begum F, Chadwick J, Munro S.
Shin JJH, et al.
Nat Cell Biol. 2017 Dec;19(12):1424-1432. doi: 10.1038/ncb3627. Epub 2017 Oct 30.
Nat Cell Biol. 2017.
PMID: 29084197
Free PMC article.
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Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development.
Ivanova EL, Mau-Them FT, Riazuddin S, Kahrizi K, Laugel V, Schaefer E, de Saint Martin A, Runge K, Iqbal Z, Spitz MA, Laura M, Drouot N, Gérard B, Deleuze JF, de Brouwer APM, Razzaq A, Dollfus H, Assir MZ, Nitchké P, Hinckelmann MV, Ropers H, Riazuddin S, Najmabadi H, van Bokhoven H, Chelly J.
Ivanova EL, et al.
Am J Hum Genet. 2017 Sep 7;101(3):428-440. doi: 10.1016/j.ajhg.2017.07.010. Epub 2017 Aug 17.
Am J Hum Genet. 2017.
PMID: 28823707
Free PMC article.
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Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia.
Marin-Valencia I, Gerondopoulos A, Zaki MS, Ben-Omran T, Almureikhi M, Demir E, Guemez-Gamboa A, Gregor A, Issa MY, Appelhof B, Roosing S, Musaev D, Rosti B, Wirth S, Stanley V, Baas F, Barr FA, Gleeson JG.
Marin-Valencia I, et al.
Am J Hum Genet. 2017 Sep 7;101(3):441-450. doi: 10.1016/j.ajhg.2017.07.015. Epub 2017 Aug 17.
Am J Hum Genet. 2017.
PMID: 28823706
Free PMC article.
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