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Items: 1 to 20 of 43

1.

Abnormal development of zebrafish after knockout and knockdown of ribosomal protein L10a.

Palasin K, Uechi T, Yoshihama M, Srisowanna N, Choijookhuu N, Hishikawa Y, Kenmochi N, Chotigeat W.

Sci Rep. 2019 Dec 2;9(1):18130. doi: 10.1038/s41598-019-54544-w.

2.

Zebrafish Models of Diamond-Blackfan Anemia: A Tool for Understanding the Disease Pathogenesis and Drug Discovery.

Uechi T, Kenmochi N.

Pharmaceuticals (Basel). 2019 Oct 9;12(4). pii: E151. doi: 10.3390/ph12040151. Review.

3.

Age- and α-Synuclein-Dependent Degeneration of Dopamine and Noradrenaline Neurons in the Annual Killifish Nothobranchius furzeri.

Matsui H, Kenmochi N, Namikawa K.

Cell Rep. 2019 Feb 12;26(7):1727-1733.e6. doi: 10.1016/j.celrep.2019.01.015.

4.

RNAcentral: a hub of information for non-coding RNA sequences.

The RNAcentral Consortium.

Nucleic Acids Res. 2019 Jan 8;47(D1):D1250-D1251. doi: 10.1093/nar/gky1206. No abstract available.

5.

RNAcentral: a hub of information for non-coding RNA sequences.

The RNAcentral Consortium .

Nucleic Acids Res. 2019 Jan 8;47(D1):D221-D229. doi: 10.1093/nar/gky1034. Erratum in: Nucleic Acids Res. 2019 Jan 8;47(D1):D1250-D1251.

6.

De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome.

Toki T, Yoshida K, Wang R, Nakamura S, Maekawa T, Goi K, Katoh MC, Mizuno S, Sugiyama F, Kanezaki R, Uechi T, Nakajima Y, Sato Y, Okuno Y, Sato-Otsubo A, Shiozawa Y, Kataoka K, Shiraishi Y, Sanada M, Chiba K, Tanaka H, Terui K, Sato T, Kamio T, Sakaguchi H, Ohga S, Kuramitsu M, Hamaguchi I, Ohara A, Kanno H, Miyano S, Kojima S, Ishiguro A, Sugita K, Kenmochi N, Takahashi S, Eto K, Ogawa S, Ito E.

Am J Hum Genet. 2018 Sep 6;103(3):440-447. doi: 10.1016/j.ajhg.2018.07.020. Epub 2018 Aug 23.

7.

Identification of zebrafish steroid sulfatase and comparative analysis of the enzymatic properties with human steroid sulfatase.

Kurogi K, Yoshihama M, Williams FE, Kenmochi N, Sakakibara Y, Suiko M, Liu MC.

J Steroid Biochem Mol Biol. 2019 Jan;185:110-117. doi: 10.1016/j.jsbmb.2018.08.004. Epub 2018 Aug 14.

PMID:
30118815
8.

The Role of scaRNAs in Adjusting Alternative mRNA Splicing in Heart Development.

Nagasawa C, Ogren A, Kibiryeva N, Marshall J, O'Brien JE, Kenmochi N, Bittel DC.

J Cardiovasc Dev Dis. 2018 May 8;5(2). pii: E26. doi: 10.3390/jcdd5020026. Review.

9.

Cross talk between TP53 and c-Myc in the pathophysiology of Diamond-Blackfan anemia: Evidence from RPL11-deficient in vivo and in vitro models.

Chakraborty A, Uechi T, Nakajima Y, Gazda HT, O'Donohue MF, Gleizes PE, Kenmochi N.

Biochem Biophys Res Commun. 2018 Jan 8;495(2):1839-1845. doi: 10.1016/j.bbrc.2017.12.019. Epub 2017 Dec 7.

PMID:
29225165
10.

Identification and characterization of 5α-cyprinol-sulfating cytosolic sulfotransferases (Sults) in the zebrafish (Danio rerio).

Kurogi K, Yoshihama M, Horton A, Schiefer IT, Krasowski MD, Hagey LR, Williams FE, Sakakibara Y, Kenmochi N, Suiko M, Liu MC.

J Steroid Biochem Mol Biol. 2017 Nov;174:120-127. doi: 10.1016/j.jsbmb.2017.08.005. Epub 2017 Aug 12.

11.

Characterization of human telomere RNA G-quadruplex structures in vitro and in living cells using 19F NMR spectroscopy.

Bao HL, Ishizuka T, Sakamoto T, Fujimoto K, Uechi T, Kenmochi N, Xu Y.

Nucleic Acids Res. 2017 May 19;45(9):5501-5511. doi: 10.1093/nar/gkx109.

12.

TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophy.

Ikeda T, Nakahara A, Nagano R, Utoyama M, Obara M, Moritake H, Uechi T, Mitsui J, Ishiura H, Yoshimura J, Doi K, Kenmochi N, Morishita S, Nishino I, Tsuji S, Nunoi H.

J Hum Genet. 2017 Apr;62(4):473-480. doi: 10.1038/jhg.2016.149. Epub 2016 Dec 8.

PMID:
27928163
13.

Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.

Ikeda F, Yoshida K, Toki T, Uechi T, Ishida S, Nakajima Y, Sasahara Y, Okuno Y, Kanezaki R, Terui K, Kamio T, Kobayashi A, Fujita T, Sato-Otsubo A, Shiraishi Y, Tanaka H, Chiba K, Muramatsu H, Kanno H, Ohga S, Ohara A, Kojima S, Kenmochi N, Miyano S, Ogawa S, Ito E.

Haematologica. 2017 Mar;102(3):e93-e96. doi: 10.3324/haematol.2016.153932. Epub 2016 Dec 1. No abstract available.

14.

RNAcentral: a comprehensive database of non-coding RNA sequences.

The RNAcentral Consortium, Petrov AI, Kay SJE, Kalvari I, Howe KL, Gray KA, Bruford EA, Kersey PJ, Cochrane G, Finn RD, Bateman A, Kozomara A, Griffiths-Jones S, Frankish A, Zwieb CW, Lau BY, Williams KP, Chan PP, Lowe TM, Cannone JJ, Gutell R, Machnicka MA, Bujnicki JM, Yoshihama M, Kenmochi N, Chai B, Cole JR, Szymanski M, Karlowski WM, Wood V, Huala E, Berardini TZ, Zhao Y, Chen R, Zhu W, Paraskevopoulou MD, Vlachos IS, Hatzigeorgiou AG, Ma L, Zhang Z, Puetz J, Stadler PF, McDonald D, Basu S, Fey P, Engel SR, Cherry JM, Volders PJ, Mestdagh P, Wower J, Clark MB, Quek XC, Dinger ME.

Nucleic Acids Res. 2017 Jan 4;45(D1):D128-D134. doi: 10.1093/nar/gkw1008. Epub 2016 Oct 28.

15.

scaRNAs regulate splicing and vertebrate heart development.

Patil P, Kibiryeva N, Uechi T, Marshall J, O'Brien JE Jr, Artman M, Kenmochi N, Bittel DC.

Biochim Biophys Acta. 2015 Aug;1852(8):1619-29. doi: 10.1016/j.bbadis.2015.04.016. Epub 2015 Apr 23.

16.
17.

Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.

Wang R, Yoshida K, Toki T, Sawada T, Uechi T, Okuno Y, Sato-Otsubo A, Kudo K, Kamimaki I, Kanezaki R, Shiraishi Y, Chiba K, Tanaka H, Terui K, Sato T, Iribe Y, Ohga S, Kuramitsu M, Hamaguchi I, Ohara A, Hara J, Goi K, Matsubara K, Koike K, Ishiguro A, Okamoto Y, Watanabe K, Kanno H, Kojima S, Miyano S, Kenmochi N, Ogawa S, Ito E.

Br J Haematol. 2015 Mar;168(6):854-64. doi: 10.1111/bjh.13229. Epub 2014 Nov 25.

PMID:
25424902
18.

[Regulation of ribosome function and disease].

Tuneoka M, Kenmochi N.

Seikagaku. 2013 Oct;85(10):837-8. Japanese. No abstract available.

PMID:
24796026
19.

Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish.

Yadav GV, Chakraborty A, Uechi T, Kenmochi N.

Int J Biochem Cell Biol. 2014 Apr;49:1-7. doi: 10.1016/j.biocel.2014.01.006. Epub 2014 Jan 11. Erratum in: Int J Biochem Cell Biol. 2014 Oct;55:350.

PMID:
24417973
20.

[Ribosomopathies--defective ribosome biogenesis and diseases].

Kenmochi N.

Seikagaku. 2013 Oct;85(10):909-15. Review. Japanese. No abstract available.

PMID:
24392590

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