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A Review of The Society for Assisted Reproductive Technology Embryo Grading System and Proposed Modification.

International journal of fertility & sterility

Hossain A, Phelps J, Agarwal A, Sanz E, Mahadevan M.
PMID: 27441045
Int J Fertil Steril. 2016 Jul-Sep;10(2):141-7. doi: 10.22074/ijfs.2016.4956. Epub 2016 Jun 01.

The Society for Assisted Reproductive Technology (SART) method of embryo grad- ing is unique, simple, and widely practiced, and its use has been mandatory for SART membership programs since 2010. Developed by SART in 2006, the current embryo grading...

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Hossain A, Phelps J, Agarwal A, et al. A Review of The Society for Assisted Reproductive Technology Embryo Grading System and Proposed Modification. Int J Fertil Steril. 2016;10(2):141-7doi: 10.22074/ijfs.2016.4956.
Hossain, A., Phelps, J., Agarwal, A., Sanz, E., & Mahadevan, M. (2016). A Review of The Society for Assisted Reproductive Technology Embryo Grading System and Proposed Modification. International journal of fertility & sterility, 10(2), 141-7. https://doi.org/10.22074/ijfs.2016.4956
Hossain, Amjad, et al. "A Review of The Society for Assisted Reproductive Technology Embryo Grading System and Proposed Modification." International journal of fertility & sterility vol. 10,2 (2016): 141-7. doi: https://doi.org/10.22074/ijfs.2016.4956
Hossain A, Phelps J, Agarwal A, Sanz E, Mahadevan M. A Review of The Society for Assisted Reproductive Technology Embryo Grading System and Proposed Modification. Int J Fertil Steril. 2016 Jul-Sep;10(2):141-7. doi: 10.22074/ijfs.2016.4956. Epub 2016 Jun 01. PMID: 27441045; PMCID: PMC4948064.
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Adsorption of probe molecules in pillared interlayered clays: experiment and computer simulation.

The Journal of chemical physics

Gallardo A, Guil JM, Lomba E, Almarza NG, Khatib SJ, Cabrillo C, Sanz A, Pires J.
PMID: 24929408
J Chem Phys. 2014 Jun 14;140(22):224701. doi: 10.1063/1.4880962.

In this paper we investigate the adsorption of various probe molecules in order to characterize the porous structure of a series of pillared interlayered clays (PILC). To that aim, volumetric and microcalorimetric adsorption experiments were performed on various Zr...

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Gallardo A, Guil JM, Lomba E, et al. Adsorption of probe molecules in pillared interlayered clays: experiment and computer simulation. J Chem Phys. 2014;140(22):224701doi: 10.1063/1.4880962.
Gallardo, A., Guil, J. M., Lomba, E., Almarza, N. G., Khatib, S. J., Cabrillo, C., Sanz, A., & Pires, J. (2014). Adsorption of probe molecules in pillared interlayered clays: experiment and computer simulation. The Journal of chemical physics, 140(22), 224701. https://doi.org/10.1063/1.4880962
Gallardo, A, et al. "Adsorption of probe molecules in pillared interlayered clays: experiment and computer simulation." The Journal of chemical physics vol. 140,22 (2014): 224701. doi: https://doi.org/10.1063/1.4880962
Gallardo A, Guil JM, Lomba E, Almarza NG, Khatib SJ, Cabrillo C, Sanz A, Pires J. Adsorption of probe molecules in pillared interlayered clays: experiment and computer simulation. J Chem Phys. 2014 Jun 14;140(22):224701. doi: 10.1063/1.4880962. PMID: 24929408.
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Proton cascade in a molecular solid: H/D exchange on mobile and immobile water.

Angewandte Chemie (International ed. in English)

Capelli SC, Falvello LR, Forcén-Vázquez E, McIntyre GJ, Palacio F, Sanz S, Tomás M.
PMID: 24307020
Angew Chem Int Ed Engl. 2013 Dec 09;52(50):13463-7. doi: 10.1002/anie.201307994. Epub 2013 Nov 07.

No abstract available.

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Capelli SC, Falvello LR, Forcén-Vázquez E, et al. Proton cascade in a molecular solid: H/D exchange on mobile and immobile water. Angew Chem Int Ed Engl. 2013;52(50):13463-7doi: 10.1002/anie.201307994.
Capelli, S. C., Falvello, L. R., Forcén-Vázquez, E., McIntyre, G. J., Palacio, F., Sanz, S., & Tomás, M. (2013). Proton cascade in a molecular solid: H/D exchange on mobile and immobile water. Angewandte Chemie (International ed. in English), 52(50), 13463-7. https://doi.org/10.1002/anie.201307994
Capelli, Silvia C, et al. "Proton cascade in a molecular solid: H/D exchange on mobile and immobile water." Angewandte Chemie (International ed. in English) vol. 52,50 (2013): 13463-7. doi: https://doi.org/10.1002/anie.201307994
Capelli SC, Falvello LR, Forcén-Vázquez E, McIntyre GJ, Palacio F, Sanz S, Tomás M. Proton cascade in a molecular solid: H/D exchange on mobile and immobile water. Angew Chem Int Ed Engl. 2013 Dec 09;52(50):13463-7. doi: 10.1002/anie.201307994. Epub 2013 Nov 07. PMID: 24307020.
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Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes.

Beilstein journal of organic chemistry

Sanjuán AM, Martínez A, García-García P, Fernández-Rodríguez MA, Sanz R.
PMID: 24204437
Beilstein J Org Chem. 2013 Oct 29;9:2242-9. doi: 10.3762/bjoc.9.263. eCollection 2013.

The cyclization of o-(alkynyl)-3-(methylbut-2-enyl)benzenes, 1,6-enynes having a condensed aromatic ring at C3-C4 positions, has been studied under the catalysis of cationic gold(I) complexes. The selective 6-endo-dig mode of cyclization observed for the 7-substituted substrates in the presence of water...

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Sanjuán AM, Martínez A, García-García P, et al. Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes. Beilstein J Org Chem. 2013;9:2242-9doi: 10.3762/bjoc.9.263.
Sanjuán, A. M., Martínez, A., García-García, P., Fernández-Rodríguez, M. A., & Sanz, R. (2013). Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes. Beilstein journal of organic chemistry, 92242-9. https://doi.org/10.3762/bjoc.9.263
Sanjuán, Ana M, et al. "Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes." Beilstein journal of organic chemistry vol. 9 (2013): 2242-9. doi: https://doi.org/10.3762/bjoc.9.263
Sanjuán AM, Martínez A, García-García P, Fernández-Rodríguez MA, Sanz R. Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes. Beilstein J Org Chem. 2013 Oct 29;9:2242-9. doi: 10.3762/bjoc.9.263. eCollection 2013. PMID: 24204437; PMCID: PMC3817472.
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Meiotic pairing and alpha-amylase phenotype in a 5B/5R(m) Triticum aestivum - Secale montanum translocation line in common wheat.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Montero M, Sanz J, Jouve N.
PMID: 24240757
Theor Appl Genet. 1986 Nov;73(1):122-8. doi: 10.1007/BF00273728.

A 5BS/5R(m)S translocation chromosome spontaneously recovered from a 'Chinese Spring' - Secale montanum wheat-rye telocentric 5R(m)S addition line has been identified and cytologically studied using C-banding in somatic and meiotic cells. Analysis of the translocated chromosome showed that a...

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Montero M, Sanz J, Jouve N. Meiotic pairing and alpha-amylase phenotype in a 5B/5R(m) Triticum aestivum - Secale montanum translocation line in common wheat. Theor Appl Genet. 1986;73(1):122-8doi: 10.1007/BF00273728.
Montero, M., Sanz, J., & Jouve, N. (1986). Meiotic pairing and alpha-amylase phenotype in a 5B/5R(m) Triticum aestivum - Secale montanum translocation line in common wheat. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 73(1), 122-8. https://doi.org/10.1007/BF00273728
Montero, M, et al. "Meiotic pairing and alpha-amylase phenotype in a 5B/5R(m) Triticum aestivum - Secale montanum translocation line in common wheat." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 73,1 (1986): 122-8. doi: https://doi.org/10.1007/BF00273728
Montero M, Sanz J, Jouve N. Meiotic pairing and alpha-amylase phenotype in a 5B/5R(m) Triticum aestivum - Secale montanum translocation line in common wheat. Theor Appl Genet. 1986 Nov;73(1):122-8. doi: 10.1007/BF00273728. PMID: 24240757.
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Gold(I)-catalyzed cycloisomerizations and alkoxycyclizations of ortho-(alkynyl)styrenes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Sanjuán AM, Rashid MA, García-García P, Martínez-Cuezva A, Fernández-Rodríguez MA, Rodríguez F, Sanz R.
PMID: 25557166
Chemistry. 2015 Feb 09;21(7):3042-52. doi: 10.1002/chem.201405789. Epub 2014 Dec 29.

Indenes and related polycyclic structures have been efficiently synthesized by gold(I)-catalyzed cycloisomerizations of appropriate ortho-(alkynyl)styrenes. Disubstitution at the terminal position of the olefin was demonstrated to be essential to obtain products originating from a formal 5-endo-dig cyclization. Interestingly, a...

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Sanjuán AM, Rashid MA, García-García P, et al. Gold(I)-catalyzed cycloisomerizations and alkoxycyclizations of ortho-(alkynyl)styrenes. Chemistry. 2014;21(7):3042-52doi: 10.1002/chem.201405789.
Sanjuán, A. M., Rashid, M. A., García-García, P., Martínez-Cuezva, A., Fernández-Rodríguez, M. A., Rodríguez, F., & Sanz, R. (2015). Gold(I)-catalyzed cycloisomerizations and alkoxycyclizations of ortho-(alkynyl)styrenes. Chemistry (Weinheim an der Bergstrasse, Germany), 21(7), 3042-52. https://doi.org/10.1002/chem.201405789
Sanjuán, Ana M, et al. "Gold(I)-catalyzed cycloisomerizations and alkoxycyclizations of ortho-(alkynyl)styrenes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,7 (2015): 3042-52. doi: https://doi.org/10.1002/chem.201405789
Sanjuán AM, Rashid MA, García-García P, Martínez-Cuezva A, Fernández-Rodríguez MA, Rodríguez F, Sanz R. Gold(I)-catalyzed cycloisomerizations and alkoxycyclizations of ortho-(alkynyl)styrenes. Chemistry. 2015 Feb 09;21(7):3042-52. doi: 10.1002/chem.201405789. Epub 2014 Dec 29. PMID: 25557166.
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Origin of constant loss in ionic conductors.

Physical review letters

León C, Rivera A, Várez A, Sanz J, Santamaria J, Ngai KL.
PMID: 11178063
Phys Rev Lett. 2001 Feb 12;86(7):1279-82. doi: 10.1103/PhysRevLett.86.1279.

We have analyzed the constant loss contribution to the ac conductivity in the frequency range 10 Hz-1 MHz and temperatures down to 8 K, for two Li ionic conductors, one crystalline (Li(0.18)La(0.61)TiO(3)) and the other glassy (61SiO(2);35Li(2)O.3Al(2)O3.P(2)O(5)). As temperature...

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León C, Rivera A, Várez A, et al. Origin of constant loss in ionic conductors. Phys Rev Lett. 2001;86(7):1279-82doi: 10.1103/PhysRevLett.86.1279.
León, C., Rivera, A., Várez, A., Sanz, J., Santamaria, J., & Ngai, K. L. (2001). Origin of constant loss in ionic conductors. Physical review letters, 86(7), 1279-82. https://doi.org/10.1103/PhysRevLett.86.1279
León, C, et al. "Origin of constant loss in ionic conductors." Physical review letters vol. 86,7 (2001): 1279-82. doi: https://doi.org/10.1103/PhysRevLett.86.1279
León C, Rivera A, Várez A, Sanz J, Santamaria J, Ngai KL. Origin of constant loss in ionic conductors. Phys Rev Lett. 2001 Feb 12;86(7):1279-82. doi: 10.1103/PhysRevLett.86.1279. PMID: 11178063.
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An Efficient and Simple Entry to N-Substituted beta-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines.

The Journal of organic chemistry

Fustero S, Navarro A, Díaz D, de La Torre MG, Asensio A, Sanz F, González ML.
PMID: 11667864
J Org Chem. 1996 Dec 13;61(25):8849-8859. doi: 10.1021/jo961037y.

Reaction of azaenolates of 2-alkyl-oxa(thia)zolines 6 with imidoyl chlorides 7 as electrophiles to furnish masked N-substituted beta-enamino acid derivatives 1-2 in 70-90% yield is described. Alternative routes are discussed. Compounds 1-2 generally appear in one tautomeric form, imino or...

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Fustero S, Navarro A, Díaz D, et al. An Efficient and Simple Entry to N-Substituted beta-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines. J Org Chem. 1996;61(25):8849-8859doi: 10.1021/jo961037y.
Fustero, S., Navarro, A., Díaz, D., de La Torre, M. G., Asensio, A., Sanz, F., & González, M. L. (1996). An Efficient and Simple Entry to N-Substituted beta-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines. The Journal of organic chemistry, 61(25), 8849-8859. https://doi.org/10.1021/jo961037y
Fustero, Santos, et al. "An Efficient and Simple Entry to N-Substituted beta-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines." The Journal of organic chemistry vol. 61,25 (1996): 8849-8859. doi: https://doi.org/10.1021/jo961037y
Fustero S, Navarro A, Díaz D, de La Torre MG, Asensio A, Sanz F, González ML. An Efficient and Simple Entry to N-Substituted beta-Enamino Acid Derivatives from 2-Alkyl-2-oxazolines and 2-Alkyl-2-thiazolines. J Org Chem. 1996 Dec 13;61(25):8849-8859. doi: 10.1021/jo961037y. PMID: 11667864.
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Molecular, 1D, and 2D systems built from phenylcyanamido ligands. Syntheses, crystal structures, and characterization of their magnetic properties.

Inorganic chemistry

Escuer A, Sanz N, Vicente R, Mautner FA.
PMID: 12693237
Inorg Chem. 2003 Jan 27;42(2):541-51. doi: 10.1021/ic025931l.

Several MnII compounds with phenylcyanamido ligands have been synthesized and characterized by means of single-crystal X-ray structural determination. The reported compounds show a wide variety of nuclearity from mononuclear and dinuclear systems to 1D chains and 2D networks in...

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Escuer A, Sanz N, Vicente R, et al. Molecular, 1D, and 2D systems built from phenylcyanamido ligands. Syntheses, crystal structures, and characterization of their magnetic properties. Inorg Chem. 2003;42(2):541-51doi: 10.1021/ic025931l.
Escuer, A., Sanz, N., Vicente, R., & Mautner, F. A. (2003). Molecular, 1D, and 2D systems built from phenylcyanamido ligands. Syntheses, crystal structures, and characterization of their magnetic properties. Inorganic chemistry, 42(2), 541-51. https://doi.org/10.1021/ic025931l
Escuer, Albert, et al. "Molecular, 1D, and 2D systems built from phenylcyanamido ligands. Syntheses, crystal structures, and characterization of their magnetic properties." Inorganic chemistry vol. 42,2 (2003): 541-51. doi: https://doi.org/10.1021/ic025931l
Escuer A, Sanz N, Vicente R, Mautner FA. Molecular, 1D, and 2D systems built from phenylcyanamido ligands. Syntheses, crystal structures, and characterization of their magnetic properties. Inorg Chem. 2003 Jan 27;42(2):541-51. doi: 10.1021/ic025931l. PMID: 12693237.
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Synthesis of functionalized pyrrole and indole derivatives through carbometallation of lithiated double bonds.

Chemistry (Weinheim an der Bergstrasse, Germany)

Fañanás FJ, Granados A, Sanz R, Ignacio JM, Barluenga J.
PMID: 11486966
Chemistry. 2001 Jul 02;7(13):2896-907. doi: 10.1002/1521-3765(20010702)7:13<2896::aid-chem2896>3.0.co;2-r.

Bis(2-lithioallyl)amines derived from bis(2-bromoallyl)amines undergo intramolecular carbometallation of a lithiated double bond, giving dilithiated dihydropyrroles. The cyclizations are promoted by N,N,N',N'-tetramethylethylenediamine (TMEDA). Reaction of these intermediates with electrophiles allows the preparation of some new fused and nonfused five-membered functionalized...

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Fañanás FJ, Granados A, Sanz R, et al. Synthesis of functionalized pyrrole and indole derivatives through carbometallation of lithiated double bonds. Chemistry. 2001;7(13):2896-907doi: 10.1002/1521-3765(20010702)7:13<2896::aid-chem2896>3.0.co;2-r.
Fañanás, F. J., Granados, A., Sanz, R., Ignacio, J. M., & Barluenga, J. (2001). Synthesis of functionalized pyrrole and indole derivatives through carbometallation of lithiated double bonds. Chemistry (Weinheim an der Bergstrasse, Germany), 7(13), 2896-907. https://doi.org/10.1002/1521-3765(20010702)7:13<2896::aid-chem2896>3.0.co;2-r
Fañanás, F J, et al. "Synthesis of functionalized pyrrole and indole derivatives through carbometallation of lithiated double bonds." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 7,13 (2001): 2896-907. doi: https://doi.org/10.1002/1521-3765(20010702)7:13<2896::aid-chem2896>3.0.co;2-r
Fañanás FJ, Granados A, Sanz R, Ignacio JM, Barluenga J. Synthesis of functionalized pyrrole and indole derivatives through carbometallation of lithiated double bonds. Chemistry. 2001 Jul 02;7(13):2896-907. doi: 10.1002/1521-3765(20010702)7:13<2896::aid-chem2896>3.0.co;2-r. PMID: 11486966.
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MIPSIM: similarity analysis of molecular interaction potentials.

Bioinformatics (Oxford, England)

Miquel de Càceres, Villà J, Lozano JJ, Sanz F.
PMID: 10980158
Bioinformatics. 2000 Jun;16(6):568-9. doi: 10.1093/bioinformatics/16.6.568.

SUMMARY: MIPSIM is a computational package designed to analyse and compare 3D distributions of molecular interaction potentials (MIP) of series of biomolecules.

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Miquel de Càceres, Villà J, Lozano JJ, et al. MIPSIM: similarity analysis of molecular interaction potentials. Bioinformatics. 2000;16(6):568-9doi: 10.1093/bioinformatics/16.6.568.
Miquel de Càceres, Villà, J., Lozano, J. J., & Sanz, F. (2000). MIPSIM: similarity analysis of molecular interaction potentials. Bioinformatics (Oxford, England), 16(6), 568-9. https://doi.org/10.1093/bioinformatics/16.6.568
Miquel de Càceres, et al. "MIPSIM: similarity analysis of molecular interaction potentials." Bioinformatics (Oxford, England) vol. 16,6 (2000): 568-9. doi: https://doi.org/10.1093/bioinformatics/16.6.568
Miquel de Càceres, Villà J, Lozano JJ, Sanz F. MIPSIM: similarity analysis of molecular interaction potentials. Bioinformatics. 2000 Jun;16(6):568-9. doi: 10.1093/bioinformatics/16.6.568. PMID: 10980158.
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Aluminum Phenylphosphonates: A Fertile Family of Compounds.

Inorganic chemistry

Cabeza A, Aranda MA, Bruque S, Poojary DM, Clearfield A, Sanz J.
PMID: 11670547
Inorg Chem. 1998 Aug 24;37(17):4168-4178. doi: 10.1021/ic9802350.

Six aluminum phenylphosphonates have been synthesized depending upon the synthetic conditions: Al(2)(O(3)PC(6)H(5))(3).2H(2)O (I), Al(2)(O(3)PC(6)H(5))(3) (II), alpha-Al(HO(3)PC(6)H(5))(O(3)PC(6)H(5)).H(2)O (III), beta-Al(HO(3)PC(6)H(5))(O(3)PC(6)H(5)).H(2)O (IV), Al(HO(3)PC(6)H(5))(3).H(2)O (V), and Al(OH)(O(3)PC(6)H(5)) (VI). Thermal analysis, X-ray powder thermodiffractometry, IR spectroscopy, and (27)Al and (31)P MAS NMR data have...

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Cabeza A, Aranda MA, Bruque S, et al. Aluminum Phenylphosphonates: A Fertile Family of Compounds. Inorg Chem. 1998;37(17):4168-4178doi: 10.1021/ic9802350.
Cabeza, A., Aranda, M. A., Bruque, S., Poojary, D. M., Clearfield, A., & Sanz, J. (1998). Aluminum Phenylphosphonates: A Fertile Family of Compounds. Inorganic chemistry, 37(17), 4168-4178. https://doi.org/10.1021/ic9802350
Cabeza, Aurelio, et al. "Aluminum Phenylphosphonates: A Fertile Family of Compounds." Inorganic chemistry vol. 37,17 (1998): 4168-4178. doi: https://doi.org/10.1021/ic9802350
Cabeza A, Aranda MA, Bruque S, Poojary DM, Clearfield A, Sanz J. Aluminum Phenylphosphonates: A Fertile Family of Compounds. Inorg Chem. 1998 Aug 24;37(17):4168-4178. doi: 10.1021/ic9802350. PMID: 11670547.
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