PubMed (GeneRIF) for id: 80173

Year	Number of Results
2007	1
2008	1
2013	1
2021	3
2022	1
2023	2
2024	0

1

Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations.

Fassad MR, Rumman N, Junger K, Patel MP, Thompson J, Goggin P, Ueffing M, Beyer T, Boldt K, Lucas JS, Mitchison HM. Fassad MR, et al. Hum Mol Genet. 2023 Oct 17;32(21):3090-3104. doi: 10.1093/hmg/ddad132. Hum Mol Genet. 2023. PMID: 37555648 Free PMC article.

2

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.

Bakey Z, Cabrera OA, Hoefele J, Antony D, Wu K, Stuck MW, Micha D, Eguether T, Smith AO, van der Wel NN, Wagner M, Strittmatter L, Beales PL, Jonassen JA, Thiffault I, Cadieux-Dion M, Boyes L, Sharif S, Tüysüz B, Dunstheimer D, Niessen HWM, Devine W, Lo CW, Mitchison HM, Schmidts M, Pazour GJ. Bakey Z, et al. PLoS Genet. 2023 Jun 14;19(6):e1010796. doi: 10.1371/journal.pgen.1010796. eCollection 2023 Jun. PLoS Genet. 2023. PMID: 37315079 Free PMC article.

3

Impaired cooperation between IFT74/BBS22-IFT81 and IFT25-IFT27/BBS19 causes Bardet-Biedl syndrome.

Zhou Z, Qiu H, Castro-Araya RF, Takei R, Nakayama K, Katoh Y. Zhou Z, et al. Hum Mol Genet. 2022 May 19;31(10):1681-1693. doi: 10.1093/hmg/ddab354. Hum Mol Genet. 2022. PMID: 34888642

4

Third case of Bardet-Biedl syndrome caused by a biallelic variant predicted to affect splicing of IFT74.

Mardy AH, Hodoglugil U, Yip T, Slavotinek AM. Mardy AH, et al. Clin Genet. 2021 Jul;100(1):93-99. doi: 10.1111/cge.13962. Epub 2021 Mar 27. Clin Genet. 2021. PMID: 33748949

5

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

Lorès P, Kherraf ZE, Amiri-Yekta A, Whitfield M, Daneshipour A, Stouvenel L, Cazin C, Cavarocchi E, Coutton C, Llabador MA, Arnoult C, Thierry-Mieg N, Ferreux L, Patrat C, Hosseini SH, Mustapha SFB, Zouari R, Dulioust E, Ray PF, Touré A. Lorès P, et al. Hum Genet. 2021 Jul;140(7):1031-1043. doi: 10.1007/s00439-021-02270-7. Epub 2021 Mar 10. Hum Genet. 2021. PMID: 33689014

6

Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.

Luo M, Lin Z, Zhu T, Jin M, Meng D, He R, Cao Z, Shen Y, Lu C, Cai R, Zhao Y, Wang X, Li H, Wu S, Zou X, Luo G, Cao L, Huang M, Jiao H, Gao H, Sui R, Zhao C, Ma X, Cao M. Luo M, et al. Genet Med. 2021 Jun;23(6):1041-1049. doi: 10.1038/s41436-021-01106-z. Epub 2021 Feb 2. Genet Med. 2021. PMID: 33531668 Free article.

7

Molecular basis of tubulin transport within the cilium by IFT74 and IFT81.

Bhogaraju S, Cajanek L, Fort C, Blisnick T, Weber K, Taschner M, Mizuno N, Lamla S, Bastin P, Nigg EA, Lorentzen E. Bhogaraju S, et al. Science. 2013 Aug 30;341(6149):1009-12. doi: 10.1126/science.1240985. Science. 2013. PMID: 23990561 Free PMC article.

8

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis.

Xiao S, Sato C, Kawarai T, Goodall EF, Pall HS, Zinman LH, Robertson J, Morrison K, Rogaeva E. Xiao S, et al. Neurobiol Aging. 2008 Aug;29(8):1279-82. doi: 10.1016/j.neurobiolaging.2007.02.022. Epub 2007 Mar 23. Neurobiol Aging. 2008. PMID: 17383054

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