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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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2013 | 1 |
2018 | 1 |
2019 | 2 |
2020 | 2 |
2021 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 91875
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Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability.
J Med Genet. 2021 Apr;58(4):237-246. doi: 10.1136/jmedgenet-2020-106849. Epub 2020 May 21.
J Med Genet. 2021.
PMID: 32439809
Free PMC article.
TTC5 mediates autoregulation of tubulin via mRNA degradation.
Lin Z, Gasic I, Chandrasekaran V, Peters N, Shao S, Mitchison TJ, Hegde RS.
Lin Z, et al.
Science. 2020 Jan 3;367(6473):100-104. doi: 10.1126/science.aaz4352. Epub 2019 Nov 14.
Science. 2020.
PMID: 31727855
Free PMC article.
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Genetics of intellectual disability in consanguineous families.
Hu H, Kahrizi K, Musante L, Fattahi Z, Herwig R, Hosseini M, Oppitz C, Abedini SS, Suckow V, Larti F, Beheshtian M, Lipkowitz B, Akhtarkhavari T, Mehvari S, Otto S, Mohseni M, Arzhangi S, Jamali P, Mojahedi F, Taghdiri M, Papari E, Soltani Banavandi MJ, Akbari S, Tonekaboni SH, Dehghani H, Ebrahimpour MR, Bader I, Davarnia B, Cohen M, Khodaei H, Albrecht B, Azimi S, Zirn B, Bastami M, Wieczorek D, Bahrami G, Keleman K, Vahid LN, Tzschach A, Gärtner J, Gillessen-Kaesbach G, Varaghchi JR, Timmermann B, Pourfatemi F, Jankhah A, Chen W, Nikuei P, Kalscheuer VM, Oladnabi M, Wienker TF, Ropers HH, Najmabadi H.
Hu H, et al.
Mol Psychiatry. 2019 Jul;24(7):1027-1039. doi: 10.1038/s41380-017-0012-2. Epub 2018 Jan 4.
Mol Psychiatry. 2019.
PMID: 29302074
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Human TTC5, a novel tetratricopeptide repeat domain containing gene, activates p53 and inhibits AP-1 pathway.
Xiong Y, Wang L, Deng W, Wang J, Shi T.
Xiong Y, et al.
Mol Biol Rep. 2013 Nov;40(11):6183-8. doi: 10.1007/s11033-013-2729-6. Epub 2013 Oct 4.
Mol Biol Rep. 2013.
PMID: 24091941
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