PubMed for id: 28981

Year	Number of Results
2000	1
2002	2
2003	1
2004	3
2007	1
2011	2
2012	1
2013	1
2014	2
2015	8
2016	3
2017	6
2018	4
2019	1
2020	3
2021	4
2022	6
2023	2
2024	0

1

Expanding the phenotypic spectrum of IFT81: Associated ciliopathy syndrome.

Ashraf T, Vaina C, Giri D, Burren CP, James M, Offiah AC, Overton T, Baptista J, Ellard S, Smithson SF. Ashraf T, et al. Am J Med Genet A. 2020 Oct;182(10):2403-2408. doi: 10.1002/ajmg.a.61781. Epub 2020 Aug 11. Am J Med Genet A. 2020. PMID: 32783357

2

IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration.

Dharmat R, Liu W, Ge Z, Sun Z, Yang L, Li Y, Wang K, Thomas K, Sui R, Chen R. Dharmat R, et al. Invest Ophthalmol Vis Sci. 2017 May 1;58(5):2483-2490. doi: 10.1167/iovs.16-19133. Invest Ophthalmol Vis Sci. 2017. PMID: 28460050 Free PMC article.

3

IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.

Perrault I, Halbritter J, Porath JD, Gérard X, Braun DA, Gee HY, Fathy HM, Saunier S, Cormier-Daire V, Thomas S, Attié-Bitach T, Boddaert N, Taschner M, Schueler M, Lorentzen E, Lifton RP, Lawson JA, Garfa-Traore M, Otto EA, Bastin P, Caillaud C, Kaplan J, Rozet JM, Hildebrandt F. Perrault I, et al. J Med Genet. 2015 Oct;52(10):657-65. doi: 10.1136/jmedgenet-2014-102838. Epub 2015 Aug 14. J Med Genet. 2015. PMID: 26275418 Free PMC article.

4

Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias.

Pettersson M, Vaz R, Hammarsjö A, Eisfeldt J, Carvalho CMB, Hofmeister W, Tham E, Horemuzova E, Voss U, Nishimura G, Klintberg B, Nordgren A, Nilsson D, Grigelioniene G, Lindstrand A. Pettersson M, et al. Hum Mutat. 2018 Oct;39(10):1456-1467. doi: 10.1002/humu.23605. Epub 2018 Aug 22. Hum Mutat. 2018. PMID: 30080953

5

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.

Duran I, Taylor SP, Zhang W, Martin J, Forlenza KN, Spiro RP, Nickerson DA, Bamshad M, Cohn DH, Krakow D. Duran I, et al. Sci Rep. 2016 Sep 26;6:34232. doi: 10.1038/srep34232. Sci Rep. 2016. PMID: 27666822 Free PMC article.

6

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

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

Identification of human CDV-1R and mouse Cdv-1R, two novel proteins with putative signal peptides, especially highly expressed in testis and increased with the male sex maturation.

Peng J, Yu L, Horiuchi M, Zhang P, Huang X, Zhang Y, Li D, Jalil MA, Zhao S. Peng J, et al. Mol Biol Rep. 2002 Dec;29(4):353-62. doi: 10.1023/a:1021232518628. Mol Biol Rep. 2002. PMID: 12549821

9

Genomic organization and mapping of mouse CDV (carnitine deficiency-associated gene expressed in ventricle)-1 and its related CDV-1R gene.

Higashi M, Kobayashi K, Iijima M, Wakana S, Horiuchi M, Yasuda T, Yoshida G, Kanmura Y, Saheki T. Higashi M, et al. Mamm Genome. 2000 Dec;11(12):1053-7. doi: 10.1007/s003350010207. Mamm Genome. 2000. PMID: 11130971

10

RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly.

Nishijima Y, Hagiya Y, Kubo T, Takei R, Katoh Y, Nakayama K. Nishijima Y, et al. Mol Biol Cell. 2017 Jun 15;28(12):1652-1666. doi: 10.1091/mbc.E17-01-0017. Epub 2017 Apr 20. Mol Biol Cell. 2017. PMID: 28428259 Free PMC article.

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