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The Complete Genome Sequence of Escherichia coli K-12

k-12

Plunkett G, Perna NT.
GSID: QuiXuX72_fgJ
FR Blattner, G Plunkett III, CA Bloch, NT Perna… - science, 1997 - science.org

… coli K-12 was the earliest organism to be suggested as a candidate for whole genome … one of the isoleucine-valine biosynthesis pathways in all K-12 isolates (9). Finally, almost all … It will be interesting to compare strain...

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Blattner, F. R., Plunkett III, G., Bloch, C. A., Perna, N. T., Burland, V., Riley, M., ... & Shao, Y. (1997). The complete genome sequence of Escherichia coli K-12. science, 277(5331), 1453-1462.
Blattner, Frederick R., et al. "The complete genome sequence of Escherichia coli K-12." science 277.5331 (1997): 1453-1462.
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[On 2 cases of primary granuloma gangraenescens localized in the nasal sinus].

Archivii italiani di laringologia

Alinei D, Galli V.
PMID: 5633647
Arch Ital Laringol. 1967 Jan-Feb;75(1):53-64.

No abstract available.

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Alinei D, Galli V. Su due casi di granuloma gangraenescens primitivi a sede naso sinusale. [On 2 cases of primary granuloma gangraenescens localized in the nasal sinus]. Arch Ital Laringol. 1967;75(1):53-64
Alinei, D., & Galli, V. (1967). Su due casi di granuloma gangraenescens primitivi a sede naso sinusale. [On 2 cases of primary granuloma gangraenescens localized in the nasal sinus]. Archivii italiani di laringologia, 75(1), 53-64.
Alinei, D, and Galli, V. "Su due casi di granuloma gangraenescens primitivi a sede naso sinusale." [On 2 cases of primary granuloma gangraenescens localized in the nasal sinus]. Archivii italiani di laringologia vol. 75,1 (1967): 53-64.
Alinei D, Galli V. Su due casi di granuloma gangraenescens primitivi a sede naso sinusale. [On 2 cases of primary granuloma gangraenescens localized in the nasal sinus]. Arch Ital Laringol. 1967 Jan-Feb;75(1):53-64. Italian. PMID: 5633647.
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Experimental evidence of twin fast metastable H(2(2)S) atoms from dissociation of cold H2 induced by electrons.

Physical review letters

Robert J, Zappa F, de Carvalho CR, Jalbert G, Nascimento RF, Trimeche A, Dulieu O, Medina A, Carvalho C, Faria NV.
PMID: 24237516
Phys Rev Lett. 2013 Nov 01;111(18):183203. doi: 10.1103/PhysRevLett.111.183203. Epub 2013 Oct 30.

We report the direct detection of two metastable H(2^{2}S) atoms coming from the dissociation of a single cold H(2) molecule, in coincidence measurements. The molecular dissociation was induced by electron impact in order to avoid limitations by the selection...

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Robert J, Zappa F, de Carvalho CR, et al. Experimental evidence of twin fast metastable H(2(2)S) atoms from dissociation of cold H2 induced by electrons. Phys Rev Lett. 2013;111(18):183203doi: 10.1103/PhysRevLett.111.183203.
Robert, J., Zappa, F., de Carvalho, C. R., Jalbert, G., Nascimento, R. F., Trimeche, A., Dulieu, O., Medina, A., Carvalho, C., & Faria, N. V. (2013). Experimental evidence of twin fast metastable H(2(2)S) atoms from dissociation of cold H2 induced by electrons. Physical review letters, 111(18), 183203. https://doi.org/10.1103/PhysRevLett.111.183203
Robert, J, et al. "Experimental evidence of twin fast metastable H(2(2)S) atoms from dissociation of cold H2 induced by electrons." Physical review letters vol. 111,18 (2013): 183203. doi: https://doi.org/10.1103/PhysRevLett.111.183203
Robert J, Zappa F, de Carvalho CR, Jalbert G, Nascimento RF, Trimeche A, Dulieu O, Medina A, Carvalho C, Faria NV. Experimental evidence of twin fast metastable H(2(2)S) atoms from dissociation of cold H2 induced by electrons. Phys Rev Lett. 2013 Nov 01;111(18):183203. doi: 10.1103/PhysRevLett.111.183203. Epub 2013 Oct 30. PMID: 24237516.
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Exploration of the barriers of reporting nursing errors in intensive care units: A qualitative study.

Journal of the Intensive Care Society

Peyrovi H, Nikbakht Nasrabadi A, Valiee S.
PMID: 28979494
J Intensive Care Soc. 2016 Aug;17(3):215-221. doi: 10.1177/1751143716638370. Epub 2016 Mar 15.

AIM: The aim of this study was to explore the barriers to reporting nursing errors in intensive care units in Iranian hospitals.METHODS: A descriptive qualitative analysis design was used. The data were collected through in-depth semi-structured interviews with a...

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Peyrovi H, Nikbakht Nasrabadi A, Valiee S. Exploration of the barriers of reporting nursing errors in intensive care units: A qualitative study. J Intensive Care Soc. 2016;17(3):215-221doi: 10.1177/1751143716638370.
Peyrovi, H., Nikbakht Nasrabadi, A., & Valiee, S. (2016). Exploration of the barriers of reporting nursing errors in intensive care units: A qualitative study. Journal of the Intensive Care Society, 17(3), 215-221. https://doi.org/10.1177/1751143716638370
Peyrovi, Hamid, et al. "Exploration of the barriers of reporting nursing errors in intensive care units: A qualitative study." Journal of the Intensive Care Society vol. 17,3 (2016): 215-221. doi: https://doi.org/10.1177/1751143716638370
Peyrovi H, Nikbakht Nasrabadi A, Valiee S. Exploration of the barriers of reporting nursing errors in intensive care units: A qualitative study. J Intensive Care Soc. 2016 Aug;17(3):215-221. doi: 10.1177/1751143716638370. Epub 2016 Mar 15. PMID: 28979494; PMCID: PMC5606520.
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Crystal structure and biochemical characterization of the recombinant ThBgl, a GH1 β-glucosidase overexpressed in Trichoderma harzianum under biomass degradation conditions.

Biotechnology for biofuels

Santos CA, Zanphorlin LM, Crucello A, Tonoli CCC, Ruller R, Horta MAC, Murakami MT, de Souza AP.
PMID: 27006690
Biotechnol Biofuels. 2016 Mar 22;9:71. doi: 10.1186/s13068-016-0487-0. eCollection 2016.

BACKGROUND: The conversion of biomass-derived sugars via enzymatic hydrolysis for biofuel production is a challenge. Therefore, the search for microorganisms and key enzymes that increase the efficiency of the saccharification of cellulosic substrates remains an important and high-priority area...

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Santos CA, Zanphorlin LM, Crucello A, et al. Crystal structure and biochemical characterization of the recombinant ThBgl, a GH1 β-glucosidase overexpressed in Trichoderma harzianum under biomass degradation conditions. Biotechnol Biofuels. 2016;9:71doi: 10.1186/s13068-016-0487-0.
Santos, C. A., Zanphorlin, L. M., Crucello, A., Tonoli, C. C. C., Ruller, R., Horta, M. A. C., Murakami, M. T., & de Souza, A. P. (2016). Crystal structure and biochemical characterization of the recombinant ThBgl, a GH1 β-glucosidase overexpressed in Trichoderma harzianum under biomass degradation conditions. Biotechnology for biofuels, 971. https://doi.org/10.1186/s13068-016-0487-0
Santos, Clelton A, et al. "Crystal structure and biochemical characterization of the recombinant ThBgl, a GH1 β-glucosidase overexpressed in Trichoderma harzianum under biomass degradation conditions." Biotechnology for biofuels vol. 9 (2016): 71. doi: https://doi.org/10.1186/s13068-016-0487-0
Santos CA, Zanphorlin LM, Crucello A, Tonoli CCC, Ruller R, Horta MAC, Murakami MT, de Souza AP. Crystal structure and biochemical characterization of the recombinant ThBgl, a GH1 β-glucosidase overexpressed in Trichoderma harzianum under biomass degradation conditions. Biotechnol Biofuels. 2016 Mar 22;9:71. doi: 10.1186/s13068-016-0487-0. eCollection 2016. PMID: 27006690; PMCID: PMC4802607.
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Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: .

Frontiers in physiology

Gillis E, Kumar AA, Luyckx I, Preuss C, Cannaerts E, van de Beek G, Wieschendorf B, Alaerts M, Bolar N, Vandeweyer G, Meester J, Wünnemann F, Gould RA, Zhurayev R, Zerbino D, Mohamed SA, Mital S, Mertens L, Björck HM, Franco-Cereceda A, McCallion AS, Van Laer L, Verhagen JMA, van de Laar IMBH, Wessels MW, Messas E, Goudot G, Nemcikova M, Krebsova A, Kempers M, Salemink S, Duijnhouwer T, Jeunemaitre X, Albuisson J, Eriksson P, Andelfinger G, Dietz HC, Verstraeten A, Loeys BL.
PMID: 28974934
Front Physiol. 2017 Sep 25;8:730. doi: 10.3389/fphys.2017.00730. eCollection 2017.

[This corrects the article on p. 400 in vol. 8, PMID: 28659821.].

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Gillis E, Kumar AA, Luyckx I, et al. Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: . Front Physiol. 2017;8:730doi: 10.3389/fphys.2017.00730.
Gillis, E., Kumar, A. A., Luyckx, I., Preuss, C., Cannaerts, E., van de Beek, G., Wieschendorf, B., Alaerts, M., Bolar, N., Vandeweyer, G., Meester, J., Wünnemann, F., Gould, R. A., Zhurayev, R., Zerbino, D., Mohamed, S. A., Mital, S., Mertens, L., Björck, H. M., Franco-Cereceda, A., McCallion, A. S., Van Laer, L., Verhagen, J. M. A., van de Laar, I. M. B. H., Wessels, M. W., Messas, E., Goudot, G., Nemcikova, M., Krebsova, A., Kempers, M., Salemink, S., Duijnhouwer, T., Jeunemaitre, X., Albuisson, J., Eriksson, P., Andelfinger, G., Dietz, H. C., Verstraeten, A., Loeys, B. L. (2017). Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: . Frontiers in physiology, 8730. https://doi.org/10.3389/fphys.2017.00730
Gillis, Elisabeth, et al. "Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: ." Frontiers in physiology vol. 8 (2017): 730. doi: https://doi.org/10.3389/fphys.2017.00730
Gillis E, Kumar AA, Luyckx I, Preuss C, Cannaerts E, van de Beek G, Wieschendorf B, Alaerts M, Bolar N, Vandeweyer G, Meester J, Wünnemann F, Gould RA, Zhurayev R, Zerbino D, Mohamed SA, Mital S, Mertens L, Björck HM, Franco-Cereceda A, McCallion AS, Van Laer L, Verhagen JMA, van de Laar IMBH, Wessels MW, Messas E, Goudot G, Nemcikova M, Krebsova A, Kempers M, Salemink S, Duijnhouwer T, Jeunemaitre X, Albuisson J, Eriksson P, Andelfinger G, Dietz HC, Verstraeten A, Loeys BL. Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: . Front Physiol. 2017 Sep 25;8:730. doi: 10.3389/fphys.2017.00730. eCollection 2017. PMID: 28974934; PMCID: PMC5622312.
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Data of PCL-b-P(MMA-DMAEMA).

Data in brief

Franco C, Barcelos Antonow M, Beckenkamp A, Buffon A, Ceolin T, Luiza Tebaldi M, Pozza Silveira G, Stanisçuaski Guterres S, Raffin Pohlmann A.
PMID: 28975143
Data Brief. 2017 Sep 19;15:111-126. doi: 10.1016/j.dib.2017.09.010. eCollection 2017 Dec.

The data presented here are related to the research paper entitled "PCL-

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Franco C, Barcelos Antonow M, Beckenkamp A, et al. Data of PCL-b-P(MMA-DMAEMA). Data Brief. 2017;15:111-126doi: 10.1016/j.dib.2017.09.010.
Franco, C., Barcelos Antonow, M., Beckenkamp, A., Buffon, A., Ceolin, T., Luiza Tebaldi, M., Pozza Silveira, G., Stanisçuaski Guterres, S., & Raffin Pohlmann, A. (2017). Data of PCL-b-P(MMA-DMAEMA). Data in brief, 15111-126. https://doi.org/10.1016/j.dib.2017.09.010
Franco, Camila, et al. "Data of PCL-b-P(MMA-DMAEMA)." Data in brief vol. 15 (2017): 111-126. doi: https://doi.org/10.1016/j.dib.2017.09.010
Franco C, Barcelos Antonow M, Beckenkamp A, Buffon A, Ceolin T, Luiza Tebaldi M, Pozza Silveira G, Stanisçuaski Guterres S, Raffin Pohlmann A. Data of PCL-b-P(MMA-DMAEMA). Data Brief. 2017 Sep 19;15:111-126. doi: 10.1016/j.dib.2017.09.010. eCollection 2017 Dec. PMID: 28975143; PMCID: PMC5614757.
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Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family.

Genetics and molecular biology

Duan Y, Lin S, Xie L, Zheng K, Chen S, Song H, Zeng X, Gu X, Wang H, Zhang L, Shao H, Hong W, Zhang L, Duan S.
PMID: 28863211
Genet Mol Biol. 2017 Jul-Sep;40(3):591-596. doi: 10.1590/1678-4685-GMB-2016-0249. Epub 2017 Aug 31.

X-linked intellectual disability (XLID) has been associated with various genes. Diagnosis of XLID, especially for non-syndromic ones (NS-XLID), is often hampered by the heterogeneity of this disease. Here we report the case of a Chinese family in which three...

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Duan Y, Lin S, Xie L, et al. Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family. Genet Mol Biol. 2017;40(3):591-596doi: 10.1590/1678-4685-GMB-2016-0249.
Duan, Y., Lin, S., Xie, L., Zheng, K., Chen, S., Song, H., Zeng, X., Gu, X., Wang, H., Zhang, L., Shao, H., Hong, W., Zhang, L., & Duan, S. (2017). Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family. Genetics and molecular biology, 40(3), 591-596. https://doi.org/10.1590/1678-4685-GMB-2016-0249
Duan, Yongheng, et al. "Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family." Genetics and molecular biology vol. 40,3 (2017): 591-596. doi: https://doi.org/10.1590/1678-4685-GMB-2016-0249
Duan Y, Lin S, Xie L, Zheng K, Chen S, Song H, Zeng X, Gu X, Wang H, Zhang L, Shao H, Hong W, Zhang L, Duan S. Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family. Genet Mol Biol. 2017 Jul-Sep;40(3):591-596. doi: 10.1590/1678-4685-GMB-2016-0249. Epub 2017 Aug 31. PMID: 28863211; PMCID: PMC5596370.
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Novel GMO-Based Vaccines against Tuberculosis: State of the Art and Biosafety Considerations.

Vaccines

Leunda A, Baldo A, Goossens M, Huygen K, Herman P, Romano M.
PMID: 26344627
Vaccines (Basel). 2014 Jun 16;2(2):463-99. doi: 10.3390/vaccines2020463.

Novel efficient vaccines are needed to control tuberculosis (TB), a major cause of morbidity and mortality worldwide. Several TB vaccine candidates are currently in clinical and preclinical development. They fall into two categories, the one of candidates designed as...

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Leunda A, Baldo A, Goossens M, et al. Novel GMO-Based Vaccines against Tuberculosis: State of the Art and Biosafety Considerations. Vaccines (Basel). 2014;2(2):463-99doi: 10.3390/vaccines2020463.
Leunda, A., Baldo, A., Goossens, M., Huygen, K., Herman, P., & Romano, M. (2014). Novel GMO-Based Vaccines against Tuberculosis: State of the Art and Biosafety Considerations. Vaccines, 2(2), 463-99. https://doi.org/10.3390/vaccines2020463
Leunda, Amaya, et al. "Novel GMO-Based Vaccines against Tuberculosis: State of the Art and Biosafety Considerations." Vaccines vol. 2,2 (2014): 463-99. doi: https://doi.org/10.3390/vaccines2020463
Leunda A, Baldo A, Goossens M, Huygen K, Herman P, Romano M. Novel GMO-Based Vaccines against Tuberculosis: State of the Art and Biosafety Considerations. Vaccines (Basel). 2014 Jun 16;2(2):463-99. doi: 10.3390/vaccines2020463. PMID: 26344627; PMCID: PMC4494264.
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Corrigendum: Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis.

Nature chemical biology

Bastard K, Perret A, Mariage A, Bessonnet T, Pinet-Turpault A, Petit JL, Darii E, Bazire P, Vergne-Vaxelaire C, Brewee C, Debard A, Pellouin V, Besnard-Gonnet M, Artiguenave F, Médigue C, Vallenet D, Danchin A, Zaparucha A, Weissenbach J, Salanoubat M, de Berardinis V.
PMID: 28926556
Nat Chem Biol. 2017 Sep 19;13(10):1137. doi: 10.1038/nchembio1017-1137c.

No abstract available.

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Bastard K, Perret A, Mariage A, et al. Corrigendum: Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis. Nat Chem Biol. 2017;13(10):1137doi: 10.1038/nchembio1017-1137c.
Bastard, K., Perret, A., Mariage, A., Bessonnet, T., Pinet-Turpault, A., Petit, J. L., Darii, E., Bazire, P., Vergne-Vaxelaire, C., Brewee, C., Debard, A., Pellouin, V., Besnard-Gonnet, M., Artiguenave, F., Médigue, C., Vallenet, D., Danchin, A., Zaparucha, A., Weissenbach, J., Salanoubat, M., & de Berardinis, V. (2017). Corrigendum: Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis. Nature chemical biology, 13(10), 1137. https://doi.org/10.1038/nchembio1017-1137c
Bastard, Karine, et al. "Corrigendum: Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis." Nature chemical biology vol. 13,10 (2017): 1137. doi: https://doi.org/10.1038/nchembio1017-1137c
Bastard K, Perret A, Mariage A, Bessonnet T, Pinet-Turpault A, Petit JL, Darii E, Bazire P, Vergne-Vaxelaire C, Brewee C, Debard A, Pellouin V, Besnard-Gonnet M, Artiguenave F, Médigue C, Vallenet D, Danchin A, Zaparucha A, Weissenbach J, Salanoubat M, de Berardinis V. Corrigendum: Parallel evolution of non-homologous isofunctional enzymes in methionine biosynthesis. Nat Chem Biol. 2017 Sep 19;13(10):1137. doi: 10.1038/nchembio1017-1137c. PMID: 28926556.
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Diabetes Associated Metabolomic Perturbations in NOD Mice.

Metabolomics : Official journal of the Metabolomic Society

Grapov D, Fahrmann J, Hwang J, Poudel A, Jo J, Periwal V, Fiehn O, Hara M.
PMID: 25755629
Metabolomics. 2015 Apr;11(2):425-437. doi: 10.1007/s11306-014-0706-2.

Non-obese diabetic (NOD) mice are a widely-used model oftype1 diabetes (T1D). However, not all animals develop overt diabetes. This study examined the circulating metabolomic profiles of NOD mice progressing or not progressing to T1D. Total beta-cell mass was quantified...

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Grapov D, Fahrmann J, Hwang J, et al. Diabetes Associated Metabolomic Perturbations in NOD Mice. Metabolomics. 2015;11(2):425-437doi: 10.1007/s11306-014-0706-2.
Grapov, D., Fahrmann, J., Hwang, J., Poudel, A., Jo, J., Periwal, V., Fiehn, O., & Hara, M. (2015). Diabetes Associated Metabolomic Perturbations in NOD Mice. Metabolomics : Official journal of the Metabolomic Society, 11(2), 425-437. https://doi.org/10.1007/s11306-014-0706-2
Grapov, Dmitry, et al. "Diabetes Associated Metabolomic Perturbations in NOD Mice." Metabolomics : Official journal of the Metabolomic Society vol. 11,2 (2015): 425-437. doi: https://doi.org/10.1007/s11306-014-0706-2
Grapov D, Fahrmann J, Hwang J, Poudel A, Jo J, Periwal V, Fiehn O, Hara M. Diabetes Associated Metabolomic Perturbations in NOD Mice. Metabolomics. 2015 Apr;11(2):425-437. doi: 10.1007/s11306-014-0706-2. PMID: 25755629; PMCID: PMC4351755.
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sEMG during Whole-Body Vibration Contains Motion Artifacts and Reflex Activity.

Journal of sports science & medicine

Lienhard K, Cabasson A, Meste O, Colson SS.
PMID: 25729290
J Sports Sci Med. 2015 Mar 01;14(1):54-61. eCollection 2015 Mar.

The purpose of this study was to determine whether the excessive spikes observed in the surface electromyography (sEMG) spectrum recorded during whole-body vibration (WBV) exercises contain motion artifacts and/or reflex activity. The occurrence of motion artifacts was tested by...

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Lienhard K, Cabasson A, Meste O, et al. sEMG during Whole-Body Vibration Contains Motion Artifacts and Reflex Activity. J Sports Sci Med. 2015;14(1):54-61
Lienhard, K., Cabasson, A., Meste, O., & Colson, S. S. (2015). sEMG during Whole-Body Vibration Contains Motion Artifacts and Reflex Activity. Journal of sports science & medicine, 14(1), 54-61.
Lienhard, Karin, et al. "sEMG during Whole-Body Vibration Contains Motion Artifacts and Reflex Activity." Journal of sports science & medicine vol. 14,1 (2015): 54-61.
Lienhard K, Cabasson A, Meste O, Colson SS. sEMG during Whole-Body Vibration Contains Motion Artifacts and Reflex Activity. J Sports Sci Med. 2015 Mar 01;14(1):54-61. eCollection 2015 Mar. PMID: 25729290; PMCID: PMC4306783.
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Showing 1 to 12 of 3450 entries