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Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments.
Honsho M, Yagita Y, Kinoshita N, Fujiki Y. Honsho M, et al. Biochim Biophys Acta. 2008 Oct;1783(10):1857-65. doi: 10.1016/j.bbamcr.2008.05.018. Epub 2008 Jun 3. Biochim Biophys Acta. 2008. PMID: 18571506
Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants.
Yanago E, Hiromasa T, Matsumura T, Kinoshita N, Fujiki Y. Yanago E, et al. Biochem Biophys Res Commun. 2002 Apr 26;293(1):225-30. doi: 10.1016/S0006-291X(02)00219-X. Biochem Biophys Res Commun. 2002. PMID: 12054588
Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants.
Fujiki Y, Okumoto K, Kinoshita N, Ghaedi K. Fujiki Y, et al. Biochim Biophys Acta. 2006 Dec;1763(12):1374-81. doi: 10.1016/j.bbamcr.2006.09.012. Epub 2006 Sep 14. Biochim Biophys Acta. 2006. PMID: 17045664 Review.
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.
Matsuzono Y, Kinoshita N, Tamura S, Shimozawa N, Hamasaki M, Ghaedi K, Wanders RJ, Suzuki Y, Kondo N, Fujiki Y. Matsuzono Y, et al. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2116-21. doi: 10.1073/pnas.96.5.2116. Proc Natl Acad Sci U S A. 1999. PMID: 10051604 Free PMC article.
Farnesylated Pex19p is partly, if not all, anchored in the peroxisomal membrane, exposing its N-terminal part to the cytosol. ...
Farnesylated Pex19p is partly, if not all, anchored in the peroxisomal membrane, exposing its N-terminal part to the cytosol. ...
Evidence for early mitogenic stimulation of metabolic flux through phosphoribosyl pyrophosphate into nucleotides in Swiss 3T3 cells.
Ishijima S, Kita K, Kinoshita N, Ishizuka T, Suzuki N, Tatibana M. Ishijima S, et al. J Biochem. 1988 Oct;104(4):570-5. doi: 10.1093/oxfordjournals.jbchem.a122512. J Biochem. 1988. PMID: 2467906
Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.
Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Kondo N, Kinoshita N, Fujiki Y, Tsukamoto T, Osumi T, Imanaka T, Orii T, Beemer F, Mooijer P, Dekker C, Wanders RJ. Shimozawa N, et al. Am J Hum Genet. 1998 Dec;63(6):1898-903. doi: 10.1086/302142. Am J Hum Genet. 1998. PMID: 9837841 Free PMC article. No abstract available.
Unrestricted modification search reveals lysine methylation as major modification induced by tissue formalin fixation and paraffin embedding.
Zhang Y, Muller M, Xu B, Yoshida Y, Horlacher O, Nikitin F, Garessus S, Magdeldin S, Kinoshita N, Fujinaka H, Yaoita E, Hasegawa M, Lisacek F, Yamamoto T. Zhang Y, et al. Proteomics. 2015 Aug;15(15):2568-79. doi: 10.1002/pmic.201400454. Epub 2015 May 3. Proteomics. 2015. PMID: 25825003
Why are they missing? : Bioinformatics characterization of missing human proteins.
Elguoshy A, Magdeldin S, Xu B, Hirao Y, Zhang Y, Kinoshita N, Takisawa Y, Nameta M, Yamamoto K, El-Refy A, El-Fiky F, Yamamoto T. Elguoshy A, et al. J Proteomics. 2016 Oct 21;149:7-14. doi: 10.1016/j.jprot.2016.08.005. Epub 2016 Aug 13. J Proteomics. 2016. PMID: 27535355
Coherently, using both mature protein database and signal peptidome database could be a promising option to identify some missing proteins by targeting their unique N-terminal tryptic peptide from mature protein database and or C-terminus tryptic peptide from signal peptid …
Coherently, using both mature protein database and signal peptidome database could be a promising option to identify some missing proteins b …
Datasets from label-free quantitative proteomic analysis of human glomeruli with sclerotic lesions.
Zhang Y, Xu B, Kinoshita N, Yoshida Y, Tasaki M, Fujinaka H, Magdeldin S, Yaoita E, Yamamoto T. Zhang Y, et al. Data Brief. 2015 May 27;4:180-5. doi: 10.1016/j.dib.2015.05.013. eCollection 2015 Sep. Data Brief. 2015. PMID: 26217785 Free PMC article.
The label-free quantification was performed using the Normalized Spectral Index (SI N ) to assess the relative molar concentration of each protein identified in a sample. ...
The label-free quantification was performed using the Normalized Spectral Index (SI N ) to assess the relative molar concentration of …
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