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Items: 1 to 50 of 69

1.

Development of a laser amplification system for the multi-pass Thomson scattering system for GAMMA 10/PDX.

Yoshikawa M, Kohagura J, Chikatsu M, Shima Y, Sakamoto M, Nakashima Y, Ezumi N, Minami R, Yasuhara R, Yamada I, Funaba H, Minami T, Kenmochi N.

Rev Sci Instrum. 2018 Oct;89(10):10C102. doi: 10.1063/1.5032224.

PMID:
30399870
2.

Coherence-imaging spectroscopy for 2D distribution of ion temperature and flow velocity in a laboratory magnetosphere.

Nakamura K, Nishiura M, Takahashi N, Yoshida Z, Kenmochi N, Sugata T, Katsura S, Howard J.

Rev Sci Instrum. 2018 Oct;89(10):10D133. doi: 10.1063/1.5037124.

PMID:
30399835
3.

Nd:YAG laser Thomson scattering diagnostics for a laboratory magnetosphere.

Kenmochi N, Nishiura M, Yoshida Z, Yamada I, Funaba H, Sugata T, Nakamura K, Katsura S.

Rev Sci Instrum. 2018 Oct;89(10):10C101. doi: 10.1063/1.5037473.

PMID:
30399734
4.

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.

PMID:
30146126
5.

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
6.

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.

7.

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
8.

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.

9.

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.

10.

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.

11.

Calibrations of the LHD Thomson scattering system.

Yamada I, Funaba H, Yasuhara R, Hayashi H, Kenmochi N, Minami T, Yoshikawa M, Ohta K, Lee JH, Lee SH.

Rev Sci Instrum. 2016 Nov;87(11):11E531.

PMID:
27910483
12.

Development of beam emission spectroscopy for turbulence transport study in Heliotron J.

Kobayashi S, Ohshima S, Matsuda H, Lu XX, Kokubu D, Ida K, Kobayashi T, Yoshinuma M, Kado S, Oishi T, Nagasaki K, Okada H, Minami T, Yamamoto S, Nakamura Y, Ishizawa A, Kenmochi N, Otani Y, Konoshima S, Mizuuchi T.

Rev Sci Instrum. 2016 Nov;87(11):11E519.

PMID:
27910398
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.

Highly time-resolved evaluation technique of instantaneous amplitude and phase difference using analytic signals for multi-channel diagnostics.

Ohshima S, Kobayashi S, Yamamoto S, Nagasaki K, Mizuuchi T, Kado S, Okada H, Minami T, Lee HY, Zang L, Kenmochi N, Kasajima K, Ohtani Y, Shi N, Nagae Y, Konoshima S, Sano F.

Rev Sci Instrum. 2014 Nov;85(11):11E814. doi: 10.1063/1.4891102.

PMID:
25430379
18.

First measurement of time evolution of electron temperature profiles with Nd:YAG Thomson scattering system on Heliotron J.

Kenmochi N, Minami T, Takahashi C, Tei S, Mizuuchi T, Kobayashi S, Nagasaki K, Nakamura Y, Okada H, Kado S, Yamamoto S, Ohshima S, Konoshima S, Shi N, Zang L, Ohtani Y, Kasajima K, Sano F.

Rev Sci Instrum. 2014 Nov;85(11):11D819. doi: 10.1063/1.4890255.

PMID:
25430232
19.

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
20.

A novel electron density reconstruction method for asymmetrical toroidal plasmas.

Shi N, Ohshima S, Tanaka K, Minami T, Nagasaki K, Yamamoto S, Ohtani Y, Zang L, Mizuuchi T, Okada H, Kado S, Kobayashi S, Konoshima S, Kenmochi N, Sano F.

Rev Sci Instrum. 2014 May;85(5):053506. doi: 10.1063/1.4872379.

PMID:
24880368
21.

[Regulation of ribosome function and disease].

Tuneoka M, Kenmochi N.

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

PMID:
24796026
22.

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
23.

[Ribosomopathies--defective ribosome biogenesis and diseases].

Kenmochi N.

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

PMID:
24392590
24.

snOPY: a small nucleolar RNA orthological gene database.

Yoshihama M, Nakao A, Kenmochi N.

BMC Res Notes. 2013 Oct 23;6:426. doi: 10.1186/1756-0500-6-426.

25.

Dissecting the protein-RNA interface: the role of protein surface shapes and RNA secondary structures in protein-RNA recognition.

Iwakiri J, Tateishi H, Chakraborty A, Patil P, Kenmochi N.

Nucleic Acids Res. 2012 Apr;40(8):3299-306. doi: 10.1093/nar/gkr1225. Epub 2011 Dec 22.

26.

Guarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathway.

Chakraborty A, Uechi T, Kenmochi N.

Wiley Interdiscip Rev RNA. 2011 Jul-Aug;2(4):507-22. doi: 10.1002/wrna.73. Epub 2011 Jan 20. Review.

PMID:
21957040
27.

Loss of ribosomal RNA modification causes developmental defects in zebrafish.

Higa-Nakamine S, Suzuki T, Uechi T, Chakraborty A, Nakajima Y, Nakamura M, Hirano N, Suzuki T, Kenmochi N.

Nucleic Acids Res. 2012 Jan;40(1):391-8. doi: 10.1093/nar/gkr700. Epub 2011 Sep 8.

28.

Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.

Torihara H, Uechi T, Chakraborty A, Shinya M, Sakai N, Kenmochi N.

Br J Haematol. 2011 Mar;152(5):648-54. doi: 10.1111/j.1365-2141.2010.08535.x. Epub 2011 Jan 12.

PMID:
21223253
29.

The NPC motif of aquaporin-11, unlike the NPA motif of known aquaporins, is essential for full expression of molecular function.

Ikeda M, Andoo A, Shimono M, Takamatsu N, Taki A, Muta K, Matsushita W, Uechi T, Matsuzaki T, Kenmochi N, Takata K, Sasaki S, Ito K, Ishibashi K.

J Biol Chem. 2011 Feb 4;286(5):3342-50. doi: 10.1074/jbc.M110.180968. Epub 2010 Nov 30.

30.

[Analysis of RNA modification in zebrafish].

Higa S, Kenmochi N.

Tanpakushitsu Kakusan Koso. 2009 Dec;54(16 Suppl):2092-7. Review. Japanese. No abstract available.

PMID:
21089623
31.

Loss of ribosomal protein L11 affects zebrafish embryonic development through a p53-dependent apoptotic response.

Chakraborty A, Uechi T, Higa S, Torihara H, Kenmochi N.

PLoS One. 2009;4(1):e4152. doi: 10.1371/journal.pone.0004152. Epub 2009 Jan 8.

32.

Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia.

Uechi T, Nakajima Y, Chakraborty A, Torihara H, Higa S, Kenmochi N.

Hum Mol Genet. 2008 Oct 15;17(20):3204-11. doi: 10.1093/hmg/ddn216. Epub 2008 Jul 24.

PMID:
18653748
33.

The ribosomal protein genes and Minute loci of Drosophila melanogaster.

Marygold SJ, Roote J, Reuter G, Lambertsson A, Ashburner M, Millburn GH, Harrison PM, Yu Z, Kenmochi N, Kaufman TC, Leevers SJ, Cook KR.

Genome Biol. 2007;8(10):R216.

34.

The evolution of spliceosomal introns in alveolates.

Nguyen HD, Yoshihama M, Kenmochi N.

Mol Biol Evol. 2007 May;24(5):1093-6. Epub 2007 Mar 1.

PMID:
17331959
35.

Intron dynamics in ribosomal protein genes.

Yoshihama M, Nguyen HD, Kenmochi N.

PLoS One. 2007 Jan 3;2(1):e141.

36.

Ribosomal protein gene knockdown causes developmental defects in zebrafish.

Uechi T, Nakajima Y, Nakao A, Torihara H, Chakraborty A, Inoue K, Kenmochi N.

PLoS One. 2006 Dec 20;1:e37.

37.

Improving the thermal stability of lactate oxidase by directed evolution.

Minagawa H, Yoshida Y, Kenmochi N, Furuichi M, Shimada J, Kaneko H.

Cell Mol Life Sci. 2007 Jan;64(1):77-81.

PMID:
17131051
38.

Phase distribution of spliceosomal introns: implications for intron origin.

Nguyen HD, Yoshihama M, Kenmochi N.

BMC Evol Biol. 2006 Sep 8;6:69.

39.

Analysis of ribosomal protein gene structures: implications for intron evolution.

Yoshihama M, Nakao A, Nguyen HD, Kenmochi N.

PLoS Genet. 2006 Mar;2(3):e25. Epub 2006 Mar 3.

40.

Characteristics and clustering of human ribosomal protein genes.

Ishii K, Washio T, Uechi T, Yoshihama M, Kenmochi N, Tomita M.

BMC Genomics. 2006 Feb 28;7:37.

41.

New maximum likelihood estimators for eukaryotic intron evolution.

Nguyen HD, Yoshihama M, Kenmochi N.

PLoS Comput Biol. 2005 Dec;1(7):e79. Epub 2005 Dec 30. Erratum in: PLoS Comput Biol. 2006 Mar;2(3):e28.

42.

A novel nucleolar protein interacts with ribosomal protein S19.

Maeda N, Toku S, Kenmochi N, Tanaka T.

Biochem Biophys Res Commun. 2006 Jan 6;339(1):41-6. Epub 2005 Nov 8.

PMID:
16289379
43.

RPG: the Ribosomal Protein Gene database.

Nakao A, Yoshihama M, Kenmochi N.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D168-70.

44.

[Ribosomapathy: possible roles of ribosomal defects in human disease].

Kenmochi N.

Tanpakushitsu Kakusan Koso. 2003 Mar;48(4 Suppl):508-16. Review. Japanese. No abstract available.

PMID:
12696161
45.

Functional second genes generated by retrotransposition of the X-linked ribosomal protein genes.

Uechi T, Maeda N, Tanaka T, Kenmochi N.

Nucleic Acids Res. 2002 Dec 15;30(24):5369-75.

46.

Location of 2(')-O-methyl nucleotides in 26S rRNA and methylation guide snoRNAs in Caenorhabditis elegans.

Higa S, Maeda N, Kenmochi N, Tanaka T.

Biochem Biophys Res Commun. 2002 Oct 11;297(5):1344-9.

PMID:
12372436
47.

The human ribosomal protein genes: sequencing and comparative analysis of 73 genes.

Yoshihama M, Uechi T, Asakawa S, Kawasaki K, Kato S, Higa S, Maeda N, Minoshima S, Tanaka T, Shimizu N, Kenmochi N.

Genome Res. 2002 Mar;12(3):379-90.

48.

The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders.

Kenmochi N, Suzuki T, Uechi T, Magoori M, Kuniba M, Higa S, Watanabe K, Tanaka T.

Genomics. 2001 Sep;77(1-2):65-70.

PMID:
11543634
49.
50.

Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6.

Ion A, Crosby AH, Kremer H, Kenmochi N, Van Reen M, Fenske C, Van Der Burgt I, Brunner HG, Montgomery K, Kucherlapati RS, Patton MA, Page C, Mariman E, Jeffery S.

J Med Genet. 2000 Nov;37(11):884-6. No abstract available.

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