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A suppressor locus for MODY3-diabetes.

Scientific reports

Garcia-Gonzalez MA, Carette C, Bagattin A, Chiral M, Makinistoglu MP, Garbay S, Prévost G, Madaras C, Hérault Y, Leibovici M, Pontoglio M.
PMID: 27667715
Sci Rep. 2016 Sep 26;6:33087. doi: 10.1038/srep33087.

Maturity Onset Diabetes of the Young type 3 (MODY3), linked to mutations in the transcription factor HNF1A, is the most prevalent form of monogenic diabetes mellitus. HNF1alpha-deficiency leads to defective insulin secretion via a molecular mechanism that is still...

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Garcia-Gonzalez MA, Carette C, Bagattin A, et al. A suppressor locus for MODY3-diabetes. Sci Rep. 2016;6:33087doi: 10.1038/srep33087.
Garcia-Gonzalez, M. A., Carette, C., Bagattin, A., Chiral, M., Makinistoglu, M. P., Garbay, S., Prévost, G., Madaras, C., Hérault, Y., Leibovici, M., & Pontoglio, M. (2016). A suppressor locus for MODY3-diabetes. Scientific reports, 633087. https://doi.org/10.1038/srep33087
Garcia-Gonzalez, Miguel A, et al. "A suppressor locus for MODY3-diabetes." Scientific reports vol. 6 (2016): 33087. doi: https://doi.org/10.1038/srep33087
Garcia-Gonzalez MA, Carette C, Bagattin A, Chiral M, Makinistoglu MP, Garbay S, Prévost G, Madaras C, Hérault Y, Leibovici M, Pontoglio M. A suppressor locus for MODY3-diabetes. Sci Rep. 2016 Sep 26;6:33087. doi: 10.1038/srep33087. PMID: 27667715; PMCID: PMC5036084.
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Morphological Properties of Mass-Spring Networks for Optimal Locomotion Learning.

Frontiers in neurorobotics

Urbain G, Degrave J, Carette B, Dambre J, Wyffels F.
PMID: 28396634
Front Neurorobot. 2017 Mar 27;11:16. doi: 10.3389/fnbot.2017.00016. eCollection 2017.

Robots have proven very useful in automating industrial processes. Their rigid components and powerful actuators, however, render them unsafe or unfit to work in normal human environments such as schools or hospitals. Robots made of compliant, softer materials may...

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Urbain G, Degrave J, Carette B, et al. Morphological Properties of Mass-Spring Networks for Optimal Locomotion Learning. Front Neurorobot. 2017;11:16doi: 10.3389/fnbot.2017.00016.
Urbain, G., Degrave, J., Carette, B., Dambre, J., & Wyffels, F. (2017). Morphological Properties of Mass-Spring Networks for Optimal Locomotion Learning. Frontiers in neurorobotics, 1116. https://doi.org/10.3389/fnbot.2017.00016
Urbain, Gabriel, et al. "Morphological Properties of Mass-Spring Networks for Optimal Locomotion Learning." Frontiers in neurorobotics vol. 11 (2017): 16. doi: https://doi.org/10.3389/fnbot.2017.00016
Urbain G, Degrave J, Carette B, Dambre J, Wyffels F. Morphological Properties of Mass-Spring Networks for Optimal Locomotion Learning. Front Neurorobot. 2017 Mar 27;11:16. doi: 10.3389/fnbot.2017.00016. eCollection 2017. PMID: 28396634; PMCID: PMC5366341.
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The Authors Respond.

Epidemiology (Cambridge, Mass.)

Garn JV, Brumback BA, Freeman MC.
PMID: 28045711
Epidemiology. 2017 May;28(3):e27. doi: 10.1097/EDE.0000000000000615.

No abstract available.

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Garn JV, Brumback BA, Freeman MC. The Authors Respond. Epidemiology. 2017;28(3):e27doi: 10.1097/EDE.0000000000000615.
Garn, J. V., Brumback, B. A., & Freeman, M. C. (2017). The Authors Respond. Epidemiology (Cambridge, Mass.), 28(3), e27. https://doi.org/10.1097/EDE.0000000000000615
Garn, Joshua V, et al. "The Authors Respond." Epidemiology (Cambridge, Mass.) vol. 28,3 (2017): e27. doi: https://doi.org/10.1097/EDE.0000000000000615
Garn JV, Brumback BA, Freeman MC. The Authors Respond. Epidemiology. 2017 May;28(3):e27. doi: 10.1097/EDE.0000000000000615. PMID: 28045711; PMCID: PMC5378614.
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Anionogenic mixed valency in KxBa1-xO2-δ.

Inorganic chemistry

Giriyapura S, Zhang B, de Groot RA, de Wijs GA, Caretta A, van Loosdrecht PH, Kockelmann W, Palstra TT, Blake GR.
PMID: 24328297
Inorg Chem. 2014 Jan 06;53(1):496-502. doi: 10.1021/ic402493q. Epub 2013 Dec 11.

We have synthesized members of an isostructural solid solution series KxBa1-xO2-δ (x < 0.41, δ < 0.11) containing mixed-valent dioxygen anions. Synthesis in liquid ammonia solution allows a continuous range of compounds to be prepared. X-ray and neutron diffraction...

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Giriyapura S, Zhang B, de Groot RA, et al. Anionogenic mixed valency in KxBa1-xO2-δ. Inorg Chem. 2013;53(1):496-502doi: 10.1021/ic402493q.
Giriyapura, S., Zhang, B., de Groot, R. A., de Wijs, G. A., Caretta, A., van Loosdrecht, P. H., Kockelmann, W., Palstra, T. T., & Blake, G. R. (2014). Anionogenic mixed valency in KxBa1-xO2-δ. Inorganic chemistry, 53(1), 496-502. https://doi.org/10.1021/ic402493q
Giriyapura, Shivakumara, et al. "Anionogenic mixed valency in KxBa1-xO2-δ." Inorganic chemistry vol. 53,1 (2014): 496-502. doi: https://doi.org/10.1021/ic402493q
Giriyapura S, Zhang B, de Groot RA, de Wijs GA, Caretta A, van Loosdrecht PH, Kockelmann W, Palstra TT, Blake GR. Anionogenic mixed valency in KxBa1-xO2-δ. Inorg Chem. 2014 Jan 06;53(1):496-502. doi: 10.1021/ic402493q. Epub 2013 Dec 11. PMID: 24328297.
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Resonance Effects in Photoemission Time Delays.

Physical review letters

Sabbar M, Heuser S, Boge R, Lucchini M, Carette T, Lindroth E, Gallmann L, Cirelli C, Keller U.
PMID: 26451550
Phys Rev Lett. 2015 Sep 25;115(13):133001. doi: 10.1103/PhysRevLett.115.133001. Epub 2015 Sep 23.

We present measurements of single-photon ionization time delays between the outermost valence electrons of argon and neon using a coincidence detection technique that allows for the simultaneous measurement of both species under identical conditions. The analysis of the measured...

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Sabbar M, Heuser S, Boge R, et al. Resonance Effects in Photoemission Time Delays. Phys Rev Lett. 2015;115(13):133001doi: 10.1103/PhysRevLett.115.133001.
Sabbar, M., Heuser, S., Boge, R., Lucchini, M., Carette, T., Lindroth, E., Gallmann, L., Cirelli, C., & Keller, U. (2015). Resonance Effects in Photoemission Time Delays. Physical review letters, 115(13), 133001. https://doi.org/10.1103/PhysRevLett.115.133001
Sabbar, M, et al. "Resonance Effects in Photoemission Time Delays." Physical review letters vol. 115,13 (2015): 133001. doi: https://doi.org/10.1103/PhysRevLett.115.133001
Sabbar M, Heuser S, Boge R, Lucchini M, Carette T, Lindroth E, Gallmann L, Cirelli C, Keller U. Resonance Effects in Photoemission Time Delays. Phys Rev Lett. 2015 Sep 25;115(13):133001. doi: 10.1103/PhysRevLett.115.133001. Epub 2015 Sep 23. PMID: 26451550.
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Erratum: Figure Correction: Probiotics as Complementary Treatment for Metabolic Disorders.

Diabetes & metabolism journal

Le Barz M, Anhê FF, Varin TV, Desjardins Y, Levy E, Roy D, Urdaci MC, Marette A.
PMID: 26566505
Diabetes Metab J. 2015 Oct;39(5):448-9. doi: 10.4093/dmj.2015.39.5.448. Epub 2015 Oct 22.

[This corrects the article on p. 291 in vol. 39, PMID: 26301190.].

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Le Barz M, Anhê FF, Varin TV, et al. Erratum: Figure Correction: Probiotics as Complementary Treatment for Metabolic Disorders. Diabetes Metab J. 2015;39(5):448-9doi: 10.4093/dmj.2015.39.5.448.
Le Barz, M., Anhê, F. F., Varin, T. V., Desjardins, Y., Levy, E., Roy, D., Urdaci, M. C., & Marette, A. (2015). Erratum: Figure Correction: Probiotics as Complementary Treatment for Metabolic Disorders. Diabetes & metabolism journal, 39(5), 448-9. https://doi.org/10.4093/dmj.2015.39.5.448
Le Barz, Mélanie, et al. "Erratum: Figure Correction: Probiotics as Complementary Treatment for Metabolic Disorders." Diabetes & metabolism journal vol. 39,5 (2015): 448-9. doi: https://doi.org/10.4093/dmj.2015.39.5.448
Le Barz M, Anhê FF, Varin TV, Desjardins Y, Levy E, Roy D, Urdaci MC, Marette A. Erratum: Figure Correction: Probiotics as Complementary Treatment for Metabolic Disorders. Diabetes Metab J. 2015 Oct;39(5):448-9. doi: 10.4093/dmj.2015.39.5.448. Epub 2015 Oct 22. PMID: 26566505; PMCID: PMC4641977.
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Photoinduced alkyl group exchange of ethylzinc alkoxides: X-ray crystal structure of an iodomethylzinc methoxide.

Chemical communications (Cambridge, England)

Charette A, Beauchemin A, Francoeur S, Bélanger-Gariépy F, Enright GD.
PMID: 12120544
Chem Commun (Camb). 2002 Mar 07;(5):466-7. doi: 10.1039/b110736d.

Irradiation of a solution of ethyl zinc alkoxides and CH2I2 leads to clean formation of iodomethylzinc alkoxides; these intermediates are important species generated in stereoselective cyclopropanation processes; no alkyl group exchange is observed in the absence of irradiation; the...

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Charette A, Beauchemin A, Francoeur S, et al. Photoinduced alkyl group exchange of ethylzinc alkoxides: X-ray crystal structure of an iodomethylzinc methoxide. Chem Commun (Camb). 2002;(5):466-7doi: 10.1039/b110736d.
Charette, A., Beauchemin, A., Francoeur, S., Bélanger-Gariépy, F., & Enright, G. D. (2002). Photoinduced alkyl group exchange of ethylzinc alkoxides: X-ray crystal structure of an iodomethylzinc methoxide. Chemical communications (Cambridge, England), (5), 466-7. https://doi.org/10.1039/b110736d
Charette, André, et al. "Photoinduced alkyl group exchange of ethylzinc alkoxides: X-ray crystal structure of an iodomethylzinc methoxide." Chemical communications (Cambridge, England) vol. ,5 (2002): 466-7. doi: https://doi.org/10.1039/b110736d
Charette A, Beauchemin A, Francoeur S, Bélanger-Gariépy F, Enright GD. Photoinduced alkyl group exchange of ethylzinc alkoxides: X-ray crystal structure of an iodomethylzinc methoxide. Chem Commun (Camb). 2002 Mar 07;(5):466-7. doi: 10.1039/b110736d. PMID: 12120544.
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[Professor Paul Lebeau].

Produits pharmaceutiques

MORETTE A.
PMID: 14424069
Prod Pharm. 1960 Jan;15:33-4.

No abstract available.

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MORETTE A. [Professor Paul Lebeau]. Prod Pharm. 1960;15:33-4
MORETTE, A. (1960). [Professor Paul Lebeau]. Produits pharmaceutiques, 1533-4.
MORETTE, A. "[Professor Paul Lebeau]." Produits pharmaceutiques vol. 15 (1960): 33-4.
MORETTE A. [Professor Paul Lebeau]. Prod Pharm. 1960 Jan;15:33-4. French. PMID: 14424069.
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Ovule number per flower in a world of unpredictable pollination.

American journal of botany

Burd M, Ashman TL, Campbell DR, Dudash MR, Johnston MO, Knight TM, Mazer SJ, Mitchell RJ, Steets JA, Vamosi JC.
PMID: 21628266
Am J Bot. 2009 Jun;96(6):1159-67. doi: 10.3732/ajb.0800183.

The number of ovules per flower varies over several orders of magnitude among angiosperms. Here we consider evidence that stochastic uncertainty in pollen receipt and ovule fertilization has been a selective factor in the evolution of ovule number per...

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Burd M, Ashman TL, Campbell DR, et al. Ovule number per flower in a world of unpredictable pollination. Am J Bot. 2009;96(6):1159-67doi: 10.3732/ajb.0800183.
Burd, M., Ashman, T. L., Campbell, D. R., Dudash, M. R., Johnston, M. O., Knight, T. M., Mazer, S. J., Mitchell, R. J., Steets, J. A., & Vamosi, J. C. (2009). Ovule number per flower in a world of unpredictable pollination. American journal of botany, 96(6), 1159-67. https://doi.org/10.3732/ajb.0800183
Burd, Martin, et al. "Ovule number per flower in a world of unpredictable pollination." American journal of botany vol. 96,6 (2009): 1159-67. doi: https://doi.org/10.3732/ajb.0800183
Burd M, Ashman TL, Campbell DR, Dudash MR, Johnston MO, Knight TM, Mazer SJ, Mitchell RJ, Steets JA, Vamosi JC. Ovule number per flower in a world of unpredictable pollination. Am J Bot. 2009 Jun;96(6):1159-67. doi: 10.3732/ajb.0800183. PMID: 21628266.
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Performances of a polymer-cholesteric-liquidcrystal output-coupler in Nd-doped fiber lasers.

Optics express

Meziane B, Li C, Carette P, Warenghem M, Mitov M.
PMID: 19451951
Opt Express. 2002 Sep 09;10(18):965-71. doi: 10.1364/oe.10.000965.

The performances and characteristics of a polymer-cholestericliquid-crystal reflector, used as an output coupler in a Nd-doped fiber laser, are presented. We show that a judicious combination of a linear polarizer and a quarter wave plate with the cholesteric coupler...

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Meziane B, Li C, Carette P, et al. Performances of a polymer-cholesteric-liquidcrystal output-coupler in Nd-doped fiber lasers. Opt Express. 2002;10(18):965-71doi: 10.1364/oe.10.000965.
Meziane, B., Li, C., Carette, P., Warenghem, M., & Mitov, M. (2002). Performances of a polymer-cholesteric-liquidcrystal output-coupler in Nd-doped fiber lasers. Optics express, 10(18), 965-71. https://doi.org/10.1364/oe.10.000965
Meziane, Belkacem, et al. "Performances of a polymer-cholesteric-liquidcrystal output-coupler in Nd-doped fiber lasers." Optics express vol. 10,18 (2002): 965-71. doi: https://doi.org/10.1364/oe.10.000965
Meziane B, Li C, Carette P, Warenghem M, Mitov M. Performances of a polymer-cholesteric-liquidcrystal output-coupler in Nd-doped fiber lasers. Opt Express. 2002 Sep 09;10(18):965-71. doi: 10.1364/oe.10.000965. PMID: 19451951.
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Acacetin and chrysin, two polyphenolic compounds, alleviate telomeric position effect in human cells.

Molecular therapy. Nucleic acids

Boussouar A, Barette C, Nadon R, Saint-Léger A, Broucqsault N, Ottaviani A, Firozhoussen A, Lu Y, Lafanechère L, Gilson E, Magdinier F, Ye J.
PMID: 23962900
Mol Ther Nucleic Acids. 2013 Aug 20;2:e116. doi: 10.1038/mtna.2013.42.

We took advantage of the ability of human telomeres to silence neighboring genes (telomere position effect or TPE) to design a high-throughput screening assay for drugs altering telomeres. We identified, for the first time, that two dietary flavones, acacetin...

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Boussouar A, Barette C, Nadon R, et al. Acacetin and chrysin, two polyphenolic compounds, alleviate telomeric position effect in human cells. Mol Ther Nucleic Acids. 2013;2:e116doi: 10.1038/mtna.2013.42.
Boussouar, A., Barette, C., Nadon, R., Saint-Léger, A., Broucqsault, N., Ottaviani, A., Firozhoussen, A., Lu, Y., Lafanechère, L., Gilson, E., Magdinier, F., & Ye, J. (2013). Acacetin and chrysin, two polyphenolic compounds, alleviate telomeric position effect in human cells. Molecular therapy. Nucleic acids, 2e116. https://doi.org/10.1038/mtna.2013.42
Boussouar, Amina, et al. "Acacetin and chrysin, two polyphenolic compounds, alleviate telomeric position effect in human cells." Molecular therapy. Nucleic acids vol. 2 (2013): e116. doi: https://doi.org/10.1038/mtna.2013.42
Boussouar A, Barette C, Nadon R, Saint-Léger A, Broucqsault N, Ottaviani A, Firozhoussen A, Lu Y, Lafanechère L, Gilson E, Magdinier F, Ye J. Acacetin and chrysin, two polyphenolic compounds, alleviate telomeric position effect in human cells. Mol Ther Nucleic Acids. 2013 Aug 20;2:e116. doi: 10.1038/mtna.2013.42. PMID: 23962900; PMCID: PMC3759739.
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Design of a photowritten cavity neodymium-doped fiber laser tunable around an absorption molecular line.

Applied optics

Martinelli G, Douay M, Pureur D, Bernage P, Niay P, Henninot JF, Li C, Carette P, Bayon JF, Boj S.
PMID: 21060353
Appl Opt. 1995 Aug 20;34(24):5338-42. doi: 10.1364/AO.34.005338.

Experiments have shown that it is possible to realize laser cavities photowritten within rare-earth-doped silicate fibers. Experimental results on a particular application, namely, the detection of gas traces by identification of one of the gas's absorption lines, are presented....

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Martinelli G, Douay M, Pureur D, et al. Design of a photowritten cavity neodymium-doped fiber laser tunable around an absorption molecular line. Appl Opt. 1995;34(24):5338-42doi: 10.1364/AO.34.005338.
Martinelli, G., Douay, M., Pureur, D., Bernage, P., Niay, P., Henninot, J. F., Li, C., Carette, P., Bayon, J. F., & Boj, S. (1995). Design of a photowritten cavity neodymium-doped fiber laser tunable around an absorption molecular line. Applied optics, 34(24), 5338-42. https://doi.org/10.1364/AO.34.005338
Martinelli, G, et al. "Design of a photowritten cavity neodymium-doped fiber laser tunable around an absorption molecular line." Applied optics vol. 34,24 (1995): 5338-42. doi: https://doi.org/10.1364/AO.34.005338
Martinelli G, Douay M, Pureur D, Bernage P, Niay P, Henninot JF, Li C, Carette P, Bayon JF, Boj S. Design of a photowritten cavity neodymium-doped fiber laser tunable around an absorption molecular line. Appl Opt. 1995 Aug 20;34(24):5338-42. doi: 10.1364/AO.34.005338. PMID: 21060353.
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Showing 1 to 12 of 233 entries