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FIB/SEM technology and high-throughput 3D reconstruction of dendritic spines and synapses in GFP-labeled adult-generated neurons.

Frontiers in neuroanatomy

Bosch C, Martínez A, Masachs N, Teixeira CM, Fernaud I, Ulloa F, Pérez-Martínez E, Lois C, Comella JX, DeFelipe J, Merchán-Pérez A, Soriano E.
PMID: 26052271
Front Neuroanat. 2015 May 21;9:60. doi: 10.3389/fnana.2015.00060. eCollection 2015.

The fine analysis of synaptic contacts is usually performed using transmission electron microscopy (TEM) and its combination with neuronal labeling techniques. However, the complex 3D architecture of neuronal samples calls for their reconstruction from serial sections. Here we show...

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Bosch C, Martínez A, Masachs N, et al. FIB/SEM technology and high-throughput 3D reconstruction of dendritic spines and synapses in GFP-labeled adult-generated neurons. Front Neuroanat. 2015;9:60doi: 10.3389/fnana.2015.00060.
Bosch, C., Martínez, A., Masachs, N., Teixeira, C. M., Fernaud, I., Ulloa, F., Pérez-Martínez, E., Lois, C., Comella, J. X., DeFelipe, J., Merchán-Pérez, A., & Soriano, E. (2015). FIB/SEM technology and high-throughput 3D reconstruction of dendritic spines and synapses in GFP-labeled adult-generated neurons. Frontiers in neuroanatomy, 960. https://doi.org/10.3389/fnana.2015.00060
Bosch, Carles, et al. "FIB/SEM technology and high-throughput 3D reconstruction of dendritic spines and synapses in GFP-labeled adult-generated neurons." Frontiers in neuroanatomy vol. 9 (2015): 60. doi: https://doi.org/10.3389/fnana.2015.00060
Bosch C, Martínez A, Masachs N, Teixeira CM, Fernaud I, Ulloa F, Pérez-Martínez E, Lois C, Comella JX, DeFelipe J, Merchán-Pérez A, Soriano E. FIB/SEM technology and high-throughput 3D reconstruction of dendritic spines and synapses in GFP-labeled adult-generated neurons. Front Neuroanat. 2015 May 21;9:60. doi: 10.3389/fnana.2015.00060. eCollection 2015. PMID: 26052271; PMCID: PMC4440362.
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Dissociation of 70 S E. coli ribosomes induced by a ribosomal factor (DF). Electrophoretic studies of the ribosomal particles.

FEBS letters

J Talens, Kalousek F, Bosch L.
PMID: 11945527
FEBS Lett. 1970 Dec 23;12(1):4-8. doi: 10.1016/0014-5793(70)80580-4.

The dissociation of purified 70 S.E. coli ribosomes, induced by the dissociation factor DF, has been studied by submitting the reaction mixtures to electrophoresis on polyacrylamide gels. The electrophoretic analysis of the ribosome mixtures revealed a heterogeneity which escaped...

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J Talens, Kalousek F, Bosch L. Dissociation of 70 S E. coli ribosomes induced by a ribosomal factor (DF). Electrophoretic studies of the ribosomal particles. FEBS Lett. 1970;12(1):4-8doi: 10.1016/0014-5793(70)80580-4.
J Talens, Kalousek, F., & Bosch, L. (1970). Dissociation of 70 S E. coli ribosomes induced by a ribosomal factor (DF). Electrophoretic studies of the ribosomal particles. FEBS letters, 12(1), 4-8. https://doi.org/10.1016/0014-5793(70)80580-4
J Talens, et al. "Dissociation of 70 S E. coli ribosomes induced by a ribosomal factor (DF). Electrophoretic studies of the ribosomal particles." FEBS letters vol. 12,1 (1970): 4-8. doi: https://doi.org/10.1016/0014-5793(70)80580-4
J Talens, Kalousek F, Bosch L. Dissociation of 70 S E. coli ribosomes induced by a ribosomal factor (DF). Electrophoretic studies of the ribosomal particles. FEBS Lett. 1970 Dec 23;12(1):4-8. doi: 10.1016/0014-5793(70)80580-4. PMID: 11945527.
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Generation and intermolecular reactions of 2-indolylacyl radicals.

Organic letters

Bennasar ML, Roca T, Griera R, Bosch J.
PMID: 11405689
Org Lett. 2001 May 31;3(11):1697-700. doi: 10.1021/ol0100576.

The generation of 2-indolylacyl radicals from the corresponding phenyl selenoesters, aldehydes, and alpha-keto carboxylic acids and the scope of their participation in intermolecular addition reactions to carbon-carbon double bonds have been studied. Whereas the phenyl selenoester method has provided...

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Bennasar ML, Roca T, Griera R, et al. Generation and intermolecular reactions of 2-indolylacyl radicals. Org Lett. 2001;3(11):1697-700doi: 10.1021/ol0100576.
Bennasar, M. L., Roca, T., Griera, R., & Bosch, J. (2001). Generation and intermolecular reactions of 2-indolylacyl radicals. Organic letters, 3(11), 1697-700. https://doi.org/10.1021/ol0100576
Bennasar, M L, et al. "Generation and intermolecular reactions of 2-indolylacyl radicals." Organic letters vol. 3,11 (2001): 1697-700. doi: https://doi.org/10.1021/ol0100576
Bennasar ML, Roca T, Griera R, Bosch J. Generation and intermolecular reactions of 2-indolylacyl radicals. Org Lett. 2001 May 31;3(11):1697-700. doi: 10.1021/ol0100576. PMID: 11405689.
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Electrophilic Oxidative Additions upon 1,4-Dihydropyridines.

The Journal of organic chemistry

Lavilla R, Coll O, Kumar R, Bosch J.
PMID: 11672145
J Org Chem. 1998 Apr 17;63(8):2728-2730. doi: 10.1021/jo971947v.

No abstract available.

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Lavilla R, Coll O, Kumar R, et al. Electrophilic Oxidative Additions upon 1,4-Dihydropyridines. J Org Chem. 1998;63(8):2728-2730doi: 10.1021/jo971947v.
Lavilla, R., Coll, O., Kumar, R., & Bosch, J. (1998). Electrophilic Oxidative Additions upon 1,4-Dihydropyridines. The Journal of organic chemistry, 63(8), 2728-2730. https://doi.org/10.1021/jo971947v
Lavilla, Rodolfo, et al. "Electrophilic Oxidative Additions upon 1,4-Dihydropyridines." The Journal of organic chemistry vol. 63,8 (1998): 2728-2730. doi: https://doi.org/10.1021/jo971947v
Lavilla R, Coll O, Kumar R, Bosch J. Electrophilic Oxidative Additions upon 1,4-Dihydropyridines. J Org Chem. 1998 Apr 17;63(8):2728-2730. doi: 10.1021/jo971947v. PMID: 11672145.
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One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions.

Inorganic chemistry

Bosch E, Barnes CL.
PMID: 11978124
Inorg Chem. 2002 May 06;41(9):2543-7. doi: 10.1021/ic010795q.

The self-assembly of coordination networks from reaction of 2,4,6-trimesityl-1,3,5-triazine and silver(I) trifluoroacetate is described. A one-dimensional linear polymer is formed from solutions deficient in silver while a two-dimensional, graphite-like sheet is formed from solutions containing 3 equiv of silver...

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Bosch E, Barnes CL. One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions. Inorg Chem. 2002;41(9):2543-7doi: 10.1021/ic010795q.
Bosch, E., & Barnes, C. L. (2002). One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions. Inorganic chemistry, 41(9), 2543-7. https://doi.org/10.1021/ic010795q
Bosch, Eric, and Barnes, Charles L. "One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions." Inorganic chemistry vol. 41,9 (2002): 2543-7. doi: https://doi.org/10.1021/ic010795q
Bosch E, Barnes CL. One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions. Inorg Chem. 2002 May 06;41(9):2543-7. doi: 10.1021/ic010795q. PMID: 11978124.
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Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis.

The Journal of organic chemistry

Amat M, Hadida S, Pshenichnyi G, Bosch J.
PMID: 11671699
J Org Chem. 1997 May 16;62(10):3158-3175. doi: 10.1021/jo962169u.

Palladium(0)-catalyzed coupling of (1-(benzenesulfonyl)-2-indolyl)zinc chloride (1) and (1-(tert-butyldimethylsilyl)-3-indolyl)zinc chloride (6) with diversely substituted (alkyl, methoxy, methoxycarbonyl, nitro, hydroxy) 2-halopyridines gives the corresponding 2- and 3-(2-pyridyl)indoles [4 and 7 (or 8), respectively] in excellent yields. A series of other 3-(heteroaryl)indoles...

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Amat M, Hadida S, Pshenichnyi G, et al. Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis. J Org Chem. 1997;62(10):3158-3175doi: 10.1021/jo962169u.
Amat, M., Hadida, S., Pshenichnyi, G., & Bosch, J. (1997). Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis. The Journal of organic chemistry, 62(10), 3158-3175. https://doi.org/10.1021/jo962169u
Amat, Mercedes, et al. "Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis." The Journal of organic chemistry vol. 62,10 (1997): 3158-3175. doi: https://doi.org/10.1021/jo962169u
Amat M, Hadida S, Pshenichnyi G, Bosch J. Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis. J Org Chem. 1997 May 16;62(10):3158-3175. doi: 10.1021/jo962169u. PMID: 11671699.
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Introduction of heteroatom-based substituents into 1,4-dihydropyridines by means of a halogen-mediated, oxidative protocol: diamination, sulfonylation, sulfinylation, bis-sulfanylation, and halo-phosphonylation processes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Lavilla R, Kumar R, Coll O, Masdeu C, Spada A, Bosch J, Espinosa E, Molins E.
PMID: 10845634
Chemistry. 2000 May 15;6(10):1763-72. doi: 10.1002/(sici)1521-3765(20000515)6:10<1763::aid-chem1763>3.0.co;2-r.

The natural tendency of 1,4-dihydropyridines to undergo "biomimetic" oxidation to afford pyridinium salts can be switched off and, through the use of reagents that interact electrophilically with the enamine moiety present in the heterocyclic system, it is possible to...

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Lavilla R, Kumar R, Coll O, et al. Introduction of heteroatom-based substituents into 1,4-dihydropyridines by means of a halogen-mediated, oxidative protocol: diamination, sulfonylation, sulfinylation, bis-sulfanylation, and halo-phosphonylation processes. Chemistry. 2000;6(10):1763-72doi: 10.1002/(sici)1521-3765(20000515)6:10<1763::aid-chem1763>3.0.co;2-r.
Lavilla, R., Kumar, R., Coll, O., Masdeu, C., Spada, A., Bosch, J., Espinosa, E., & Molins, E. (2000). Introduction of heteroatom-based substituents into 1,4-dihydropyridines by means of a halogen-mediated, oxidative protocol: diamination, sulfonylation, sulfinylation, bis-sulfanylation, and halo-phosphonylation processes. Chemistry (Weinheim an der Bergstrasse, Germany), 6(10), 1763-72. https://doi.org/10.1002/(sici)1521-3765(20000515)6:10<1763::aid-chem1763>3.0.co;2-r
Lavilla, et al. "Introduction of heteroatom-based substituents into 1,4-dihydropyridines by means of a halogen-mediated, oxidative protocol: diamination, sulfonylation, sulfinylation, bis-sulfanylation, and halo-phosphonylation processes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,10 (2000): 1763-72. doi: https://doi.org/10.1002/(sici)1521-3765(20000515)6:10<1763::aid-chem1763>3.0.co;2-r
Lavilla R, Kumar R, Coll O, Masdeu C, Spada A, Bosch J, Espinosa E, Molins E. Introduction of heteroatom-based substituents into 1,4-dihydropyridines by means of a halogen-mediated, oxidative protocol: diamination, sulfonylation, sulfinylation, bis-sulfanylation, and halo-phosphonylation processes. Chemistry. 2000 May 15;6(10):1763-72. doi: 10.1002/(sici)1521-3765(20000515)6:10<1763::aid-chem1763>3.0.co;2-r. PMID: 10845634.
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Oxidative diphosphonylation of 1,4-dihydropyridines and pyridinium salts.

Organic letters

Lavilla R, Spada A, Bosch J.
PMID: 10841472
Org Lett. 2000 Jun 01;2(11):1533-5. doi: 10.1021/ol0057380.

An oxidative double phosphonylation of dihydropyridines 1 and pyridinium salts 2 is achieved through the use of dialkyl phosphites, DDQ, and triethylamine. Acceptable to good yields of 2, 6-diphosphonylated-1,2-dihydropyridines 3 are obtained in a one-pot reaction involving tandem nucleophilic...

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Lavilla R, Spada A, Bosch J. Oxidative diphosphonylation of 1,4-dihydropyridines and pyridinium salts. Org Lett. 2000;2(11):1533-5doi: 10.1021/ol0057380.
Lavilla, R., Spada, A., & Bosch, J. (2000). Oxidative diphosphonylation of 1,4-dihydropyridines and pyridinium salts. Organic letters, 2(11), 1533-5. https://doi.org/10.1021/ol0057380
Lavilla, et al. "Oxidative diphosphonylation of 1,4-dihydropyridines and pyridinium salts." Organic letters vol. 2,11 (2000): 1533-5. doi: https://doi.org/10.1021/ol0057380
Lavilla R, Spada A, Bosch J. Oxidative diphosphonylation of 1,4-dihydropyridines and pyridinium salts. Org Lett. 2000 Jun 01;2(11):1533-5. doi: 10.1021/ol0057380. PMID: 10841472.
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1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride.

Inorganic chemistry

Bosch E, Barnes CL.
PMID: 11399178
Inorg Chem. 2001 Jun 18;40(13):3097-100. doi: 10.1021/ic010058u.

The design, synthesis, and complexation characteristics of the bipyridyl ligand 1,2-bis-(2-pyridylethynyl)benzene are described. The X-ray crystallographic characterization of the 1:1 complexes of 1,2-bis(2-pyridylethynyl)benzene with silver(I) triflate and palladium(II) chloride are described. In the X-ray crystal structure of the silver(I)...

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Bosch E, Barnes CL. 1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride. Inorg Chem. 2001;40(13):3097-100doi: 10.1021/ic010058u.
Bosch, E., & Barnes, C. L. (2001). 1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride. Inorganic chemistry, 40(13), 3097-100. https://doi.org/10.1021/ic010058u
Bosch, E, and Barnes, C L. "1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride." Inorganic chemistry vol. 40,13 (2001): 3097-100. doi: https://doi.org/10.1021/ic010058u
Bosch E, Barnes CL. 1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride. Inorg Chem. 2001 Jun 18;40(13):3097-100. doi: 10.1021/ic010058u. PMID: 11399178.
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Spain. Research chief a victim of the oil spill?.

Science (New York, N.Y.)

Bosch X.
PMID: 12560518
Science. 2003 Jan 31;299(5607):637. doi: 10.1126/science.299.5607.637b.

No abstract available.

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Bosch X. Spain. Research chief a victim of the oil spill?. Science. 2003;299(5607):637doi: 10.1126/science.299.5607.637b.
Bosch, X. (2003). Spain. Research chief a victim of the oil spill?. Science (New York, N.Y.), 299(5607), 637. https://doi.org/10.1126/science.299.5607.637b
Bosch, Xavier. "Spain. Research chief a victim of the oil spill?." Science (New York, N.Y.) vol. 299,5607 (2003): 637. doi: https://doi.org/10.1126/science.299.5607.637b
Bosch X. Spain. Research chief a victim of the oil spill?. Science. 2003 Jan 31;299(5607):637. doi: 10.1126/science.299.5607.637b. PMID: 12560518.
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Josep Piqué interview. Spain's science minister sees future in telecom.

Science (New York, N.Y.)

Bosch X.
PMID: 12560532
Science. 2003 Jan 31;299(5607):653. doi: 10.1126/science.299.5607.653.

No abstract available.

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Bosch X. Josep Piqué interview. Spain's science minister sees future in telecom. Science. 2003;299(5607):653doi: 10.1126/science.299.5607.653.
Bosch, X. (2003). Josep Piqué interview. Spain's science minister sees future in telecom. Science (New York, N.Y.), 299(5607), 653. https://doi.org/10.1126/science.299.5607.653
Bosch, Xavier. "Josep Piqué interview. Spain's science minister sees future in telecom." Science (New York, N.Y.) vol. 299,5607 (2003): 653. doi: https://doi.org/10.1126/science.299.5607.653
Bosch X. Josep Piqué interview. Spain's science minister sees future in telecom. Science. 2003 Jan 31;299(5607):653. doi: 10.1126/science.299.5607.653. PMID: 12560532.
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Scientific advice. Spanish researchers vent anger over handling of oil spill.

Science (New York, N.Y.)

Bohannon J, Bosch X.
PMID: 12543942
Science. 2003 Jan 24;299(5606):490. doi: 10.1126/science.299.5606.490.

No abstract available.

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Bohannon J, Bosch X. Scientific advice. Spanish researchers vent anger over handling of oil spill. Science. 2003;299(5606):490doi: 10.1126/science.299.5606.490.
Bohannon, J., & Bosch, X. (2003). Scientific advice. Spanish researchers vent anger over handling of oil spill. Science (New York, N.Y.), 299(5606), 490. https://doi.org/10.1126/science.299.5606.490
Bohannon, John, and Bosch, Xavier. "Scientific advice. Spanish researchers vent anger over handling of oil spill." Science (New York, N.Y.) vol. 299,5606 (2003): 490. doi: https://doi.org/10.1126/science.299.5606.490
Bohannon J, Bosch X. Scientific advice. Spanish researchers vent anger over handling of oil spill. Science. 2003 Jan 24;299(5606):490. doi: 10.1126/science.299.5606.490. PMID: 12543942.
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Showing 25 to 36 of 851 entries