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Experimental histopathological study on retinal and renal cellular response to intravitreous antiangiogenic drugs.

International journal of ophthalmology

Fortes Filho JB, Maia M, Tartarella MB, Meyer FS, Fortes BG, Kliemann LM.
PMID: 24967187
Int J Ophthalmol. 2014 Jun 18;7(3):437-40. doi: 10.3980/j.issn.2222-3959.2014.03.09. eCollection 2014.

AIM: To evaluate histopathological retinal and renal response after one single dose of intravitreous injection of antiangiogenic drugs ranibizumab and bevacizumab in rats.METHODS: Experimental study in 60d of life adults Wistar rats. Ten animals were included. Group 1 included...

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Fortes Filho JB, Maia M, Tartarella MB, et al. Experimental histopathological study on retinal and renal cellular response to intravitreous antiangiogenic drugs. Int J Ophthalmol. 2014;7(3):437-40doi: 10.3980/j.issn.2222-3959.2014.03.09.
Fortes Filho, J. B., Maia, M., Tartarella, M. B., Meyer, F. S., Fortes, B. G., & Kliemann, L. M. (2014). Experimental histopathological study on retinal and renal cellular response to intravitreous antiangiogenic drugs. International journal of ophthalmology, 7(3), 437-40. https://doi.org/10.3980/j.issn.2222-3959.2014.03.09
Fortes Filho, João Borges, et al. "Experimental histopathological study on retinal and renal cellular response to intravitreous antiangiogenic drugs." International journal of ophthalmology vol. 7,3 (2014): 437-40. doi: https://doi.org/10.3980/j.issn.2222-3959.2014.03.09
Fortes Filho JB, Maia M, Tartarella MB, Meyer FS, Fortes BG, Kliemann LM. Experimental histopathological study on retinal and renal cellular response to intravitreous antiangiogenic drugs. Int J Ophthalmol. 2014 Jun 18;7(3):437-40. doi: 10.3980/j.issn.2222-3959.2014.03.09. eCollection 2014. PMID: 24967187; PMCID: PMC4067655.
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Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates.

Chemical communications (Cambridge, England)

Chauvier C, Godou T, Cantat T.
PMID: 29022015
Chem Commun (Camb). 2017 Oct 24;53(85):11697-11700. doi: 10.1039/c7cc05212j.

The silylation of O-H bonds is a useful methodology in organic synthesis and materials science. While this transformation is commonly achieved by reacting alcohols with reactive chlorosilanes or hydrosilanes, we show herein for the first time that silylformates HCO

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Chauvier C, Godou T, Cantat T. Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates. Chem Commun (Camb). 2017;53(85):11697-11700doi: 10.1039/c7cc05212j.
Chauvier, C., Godou, T., & Cantat, T. (2017). Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates. Chemical communications (Cambridge, England), 53(85), 11697-11700. https://doi.org/10.1039/c7cc05212j
Chauvier, Clément, et al. "Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates." Chemical communications (Cambridge, England) vol. 53,85 (2017): 11697-11700. doi: https://doi.org/10.1039/c7cc05212j
Chauvier C, Godou T, Cantat T. Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates. Chem Commun (Camb). 2017 Oct 24;53(85):11697-11700. doi: 10.1039/c7cc05212j. PMID: 29022015.
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Comparison of uterine and tubal pathology identified by transvaginal sonography, hysterosalpingography, and hysteroscopy in female patients with infertility.

Fertility research and practice

Phillips CH, Benson CB, Ginsburg ES, Frates MC.
PMID: 28620525
Fertil Res Pract. 2015 Dec 23;1:20. doi: 10.1186/s40738-015-0012-3. eCollection 2015.

BACKGROUND: The causes of female infertility are multifactorial and necessitate comprehensive evaluation including physical examination, hormonal testing, and imaging. Given the associated psychological and financial stress that imaging can cause, infertility patients benefit from a structured and streamlined evaluation....

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Phillips CH, Benson CB, Ginsburg ES, et al. Comparison of uterine and tubal pathology identified by transvaginal sonography, hysterosalpingography, and hysteroscopy in female patients with infertility. Fertil Res Pract. 2015;1:20doi: 10.1186/s40738-015-0012-3.
Phillips, C. H., Benson, C. B., Ginsburg, E. S., & Frates, M. C. (2015). Comparison of uterine and tubal pathology identified by transvaginal sonography, hysterosalpingography, and hysteroscopy in female patients with infertility. Fertility research and practice, 120. https://doi.org/10.1186/s40738-015-0012-3
Phillips, Catherine H, et al. "Comparison of uterine and tubal pathology identified by transvaginal sonography, hysterosalpingography, and hysteroscopy in female patients with infertility." Fertility research and practice vol. 1 (2015): 20. doi: https://doi.org/10.1186/s40738-015-0012-3
Phillips CH, Benson CB, Ginsburg ES, Frates MC. Comparison of uterine and tubal pathology identified by transvaginal sonography, hysterosalpingography, and hysteroscopy in female patients with infertility. Fertil Res Pract. 2015 Dec 23;1:20. doi: 10.1186/s40738-015-0012-3. eCollection 2015. PMID: 28620525; PMCID: PMC5424419.
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Temperature-dependent IR and Raman studies of metal-organic frameworks [(CH₃)₂NH₂][M(HCOO)₃], M=Mg and Cd.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Szymborska-Małek K, Trzebiatowska-Gusowska M, Mączka M, Gągor A.
PMID: 26827175
Spectrochim Acta A Mol Biomol Spectrosc. 2016 Apr 15;159:35-41. doi: 10.1016/j.saa.2016.01.031. Epub 2016 Jan 21.

Two metal-organic frameworks of [(CH3)2NH2][M(HCOO)3], where M=Mg and Cd, have been investigated by temperature-dependent IR and Raman methods in order to determine the nature of the phase transition. Our results indicate that phase transition in the Mg-compound is driven...

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Szymborska-Małek K, Trzebiatowska-Gusowska M, Mączka M, et al. Temperature-dependent IR and Raman studies of metal-organic frameworks [(CH₃)₂NH₂][M(HCOO)₃], M=Mg and Cd. Spectrochim Acta A Mol Biomol Spectrosc. 2016;159:35-41doi: 10.1016/j.saa.2016.01.031.
Szymborska-Małek, K., Trzebiatowska-Gusowska, M., Mączka, M., & Gągor, A. (2016). Temperature-dependent IR and Raman studies of metal-organic frameworks [(CH₃)₂NH₂][M(HCOO)₃], M=Mg and Cd. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 15935-41. https://doi.org/10.1016/j.saa.2016.01.031
Szymborska-Małek, K, et al. "Temperature-dependent IR and Raman studies of metal-organic frameworks [(CH₃)₂NH₂][M(HCOO)₃], M=Mg and Cd." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 159 (2016): 35-41. doi: https://doi.org/10.1016/j.saa.2016.01.031
Szymborska-Małek K, Trzebiatowska-Gusowska M, Mączka M, Gągor A. Temperature-dependent IR and Raman studies of metal-organic frameworks [(CH₃)₂NH₂][M(HCOO)₃], M=Mg and Cd. Spectrochim Acta A Mol Biomol Spectrosc. 2016 Apr 15;159:35-41. doi: 10.1016/j.saa.2016.01.031. Epub 2016 Jan 21. PMID: 26827175.
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Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction.

Acta crystallographica. Section E, Crystallographic communications

Fortes AD.
PMID: 26279871
Acta Crystallogr E Crystallogr Commun. 2015 Jun 17;71:799-806. doi: 10.1107/S2056989015011354. eCollection 2015 Jul 01.

Time-of-flight neutron powder diffraction data have been measured from ∼90 mol% deuterated isotopologues of Na2MoO4·2H2O and Na2WO4·2H2O at 295 K to a resolution of sin (θ)/λ = 0.77 Å(-1). The use of neutrons has allowed refinement of structural parameters...

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Fortes AD. Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction. Acta Crystallogr E Crystallogr Commun. 2015;71:799-806doi: 10.1107/S2056989015011354.
Fortes, A. D. (2015). Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction. Acta crystallographica. Section E, Crystallographic communications, 71799-806. https://doi.org/10.1107/S2056989015011354
Fortes, A Dominic. "Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction." Acta crystallographica. Section E, Crystallographic communications vol. 71 (2015): 799-806. doi: https://doi.org/10.1107/S2056989015011354
Fortes AD. Crystal structures of deuterated sodium molybdate dihydrate and sodium tungstate dihydrate from time-of-flight neutron powder diffraction. Acta Crystallogr E Crystallogr Commun. 2015 Jun 17;71:799-806. doi: 10.1107/S2056989015011354. eCollection 2015 Jul 01. PMID: 26279871; PMCID: PMC4518980.
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Erratum to: Determinants of exclusive breastfeeding cessation: identifying an "at risk population" for special support.

European journal of pediatrics

Lindau JF, Mastroeni S, Gaddini A, Di Lallo D, Fiori Nastro P, Patanè M, Girardi P, Fortes C.
PMID: 25446407
Eur J Pediatr. 2015 Apr;174(4):541. doi: 10.1007/s00431-014-2466-4.

No abstract available.

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Lindau JF, Mastroeni S, Gaddini A, et al. Erratum to: Determinants of exclusive breastfeeding cessation: identifying an "at risk population" for special support. Eur J Pediatr. 2015;174(4):541doi: 10.1007/s00431-014-2466-4.
Lindau, J. F., Mastroeni, S., Gaddini, A., Di Lallo, D., Fiori Nastro, P., Patanè, M., Girardi, P., & Fortes, C. (2015). Erratum to: Determinants of exclusive breastfeeding cessation: identifying an "at risk population" for special support. European journal of pediatrics, 174(4), 541. https://doi.org/10.1007/s00431-014-2466-4
Lindau, Juliana F, et al. "Erratum to: Determinants of exclusive breastfeeding cessation: identifying an "at risk population" for special support." European journal of pediatrics vol. 174,4 (2015): 541. doi: https://doi.org/10.1007/s00431-014-2466-4
Lindau JF, Mastroeni S, Gaddini A, Di Lallo D, Fiori Nastro P, Patanè M, Girardi P, Fortes C. Erratum to: Determinants of exclusive breastfeeding cessation: identifying an "at risk population" for special support. Eur J Pediatr. 2015 Apr;174(4):541. doi: 10.1007/s00431-014-2466-4. PMID: 25446407.
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Similarities of the heme environment in vertebrate and non-vertebrate oxygen-binding hemoproteins.

FEBS letters

Wüthrich K, Keller RM, Brunori M, Giacometti G, Huber R, Formanek H.
PMID: 11946476
FEBS Lett. 1972 Mar;21(1):63-66. doi: 10.1016/0014-5793(72)80164-9.

No abstract available.

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Wüthrich K, Keller RM, Brunori M, et al. Similarities of the heme environment in vertebrate and non-vertebrate oxygen-binding hemoproteins. FEBS Lett. 1972;21(1):63-66doi: 10.1016/0014-5793(72)80164-9.
Wüthrich, K., Keller, R. M., Brunori, M., Giacometti, G., Huber, R., & Formanek, H. (1972). Similarities of the heme environment in vertebrate and non-vertebrate oxygen-binding hemoproteins. FEBS letters, 21(1), 63-66. https://doi.org/10.1016/0014-5793(72)80164-9
Wüthrich, K, et al. "Similarities of the heme environment in vertebrate and non-vertebrate oxygen-binding hemoproteins." FEBS letters vol. 21,1 (1972): 63-66. doi: https://doi.org/10.1016/0014-5793(72)80164-9
Wüthrich K, Keller RM, Brunori M, Giacometti G, Huber R, Formanek H. Similarities of the heme environment in vertebrate and non-vertebrate oxygen-binding hemoproteins. FEBS Lett. 1972 Mar;21(1):63-66. doi: 10.1016/0014-5793(72)80164-9. PMID: 11946476.
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Light induced controlled release of fragrances by Norrish type II photofragmentation of alkyl phenyl ketones.

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Levrand B, Herrmann A.
PMID: 12659532
Photochem Photobiol Sci. 2002 Nov;1(11):907-19. doi: 10.1039/b207918f.

The use of alkyl phenyl ketones as delivery systems for the controlled release of fragrances was investigated by photoirradiation of undegassed solutions with a xenon lamp as well as natural sunlight. A large variety of precursor compounds was prepared...

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Levrand B, Herrmann A. Light induced controlled release of fragrances by Norrish type II photofragmentation of alkyl phenyl ketones. Photochem Photobiol Sci. 2002;1(11):907-19doi: 10.1039/b207918f.
Levrand, B., & Herrmann, A. (2002). Light induced controlled release of fragrances by Norrish type II photofragmentation of alkyl phenyl ketones. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 1(11), 907-19. https://doi.org/10.1039/b207918f
Levrand, Barbara, and Herrmann, Andreas. "Light induced controlled release of fragrances by Norrish type II photofragmentation of alkyl phenyl ketones." Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology vol. 1,11 (2002): 907-19. doi: https://doi.org/10.1039/b207918f
Levrand B, Herrmann A. Light induced controlled release of fragrances by Norrish type II photofragmentation of alkyl phenyl ketones. Photochem Photobiol Sci. 2002 Nov;1(11):907-19. doi: 10.1039/b207918f. PMID: 12659532.
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Surface and Texture Characterization of Alumina-Supported Copper and Mixed Copper-Manganese Oxide Catalysts and Their Formate Precursors.

Journal of colloid and interface science

Stoilova DG, Nickolov RN, Cheshkova KT.
PMID: 10882489
J Colloid Interface Sci. 2000 Aug 01;228(1):24-31. doi: 10.1006/jcis.2000.6905.

Alumina-supported copper and copper-manganese oxide catalysts as well as the parent formates were characterized by means of FTIR spectroscopy in situ and nitrogen physisorption. The IR spectroscopic results are discussed on the basis of the deposition scheme proposed recently...

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Stoilova DG, Nickolov RN, Cheshkova KT. Surface and Texture Characterization of Alumina-Supported Copper and Mixed Copper-Manganese Oxide Catalysts and Their Formate Precursors. J Colloid Interface Sci. 2000;228(1):24-31doi: 10.1006/jcis.2000.6905.
Stoilova, D. G., Nickolov, R. N., & Cheshkova, K. T. (2000). Surface and Texture Characterization of Alumina-Supported Copper and Mixed Copper-Manganese Oxide Catalysts and Their Formate Precursors. Journal of colloid and interface science, 228(1), 24-31. https://doi.org/10.1006/jcis.2000.6905
Stoilova, et al. "Surface and Texture Characterization of Alumina-Supported Copper and Mixed Copper-Manganese Oxide Catalysts and Their Formate Precursors." Journal of colloid and interface science vol. 228,1 (2000): 24-31. doi: https://doi.org/10.1006/jcis.2000.6905
Stoilova DG, Nickolov RN, Cheshkova KT. Surface and Texture Characterization of Alumina-Supported Copper and Mixed Copper-Manganese Oxide Catalysts and Their Formate Precursors. J Colloid Interface Sci. 2000 Aug 01;228(1):24-31. doi: 10.1006/jcis.2000.6905. PMID: 10882489.
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Studies on callose and cutin during the expression of competence and determination for organogenic nodule formation from internodes of Humulus lupulus var. Nugget.

Physiologia plantarum

Fortes AM, Testillano PS, Del Carmen Risueño M, Pais MS.
PMID: 12207669
Physiol Plant. 2002 Sep;116(1):113-120. doi: 10.1034/j.1399-3054.2002.1160114.x.

Callose and cutin deposition were followed by staining with Aniline Blue and Nile Red and by immunolocalization using antibodies raised against callose. Along with morphogenesis induction from internodes of Humulus lupulus var. Nugget, a temporal and spatial differential deposition...

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Fortes AM, Testillano PS, Del Carmen Risueño M, et al. Studies on callose and cutin during the expression of competence and determination for organogenic nodule formation from internodes of Humulus lupulus var. Nugget. Physiol Plant. 2002;116(1):113-120doi: 10.1034/j.1399-3054.2002.1160114.x.
Fortes, A. M., Testillano, P. S., Del Carmen Risueño, M., & Pais, M. S. (2002). Studies on callose and cutin during the expression of competence and determination for organogenic nodule formation from internodes of Humulus lupulus var. Nugget. Physiologia plantarum, 116(1), 113-120. https://doi.org/10.1034/j.1399-3054.2002.1160114.x
Fortes, Ana M, et al. "Studies on callose and cutin during the expression of competence and determination for organogenic nodule formation from internodes of Humulus lupulus var. Nugget." Physiologia plantarum vol. 116,1 (2002): 113-120. doi: https://doi.org/10.1034/j.1399-3054.2002.1160114.x
Fortes AM, Testillano PS, Del Carmen Risueño M, Pais MS. Studies on callose and cutin during the expression of competence and determination for organogenic nodule formation from internodes of Humulus lupulus var. Nugget. Physiol Plant. 2002 Sep;116(1):113-120. doi: 10.1034/j.1399-3054.2002.1160114.x. PMID: 12207669.
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The particular sensitivity of silyl ethers of D-glucal toward two Vilsmeier-Haack reagents POCl3.DMF and (CF3SO2)2O.DMF. Their unique and selective conversion to the corresponding C(6)-O-formates.

The Journal of organic chemistry

Lellouche JP, Koeller S.
PMID: 11430084
J Org Chem. 2001 Feb 09;66(3):693-6. doi: 10.1021/jo005540t.

The two electrophilic Vilsmeier-Haack reagents POCl3.DMF 2 or (CF3SO2)2O.DMF 3 mediate the one-step and selective conversion of O-triethylsilyl (O-TES), O-tert-butyldimethylsilyl (O-TBDMS), O-tert-butyldiphenylsilyl (O-TBDPS), and O-triisopropylsilyl (O-TIPS) ethers of D-glucal to the corresponding C(6)-O-formates.

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Lellouche JP, Koeller S. The particular sensitivity of silyl ethers of D-glucal toward two Vilsmeier-Haack reagents POCl3.DMF and (CF3SO2)2O.DMF. Their unique and selective conversion to the corresponding C(6)-O-formates. J Org Chem. 2001;66(3):693-6doi: 10.1021/jo005540t.
Lellouche, J. P., & Koeller, S. (2001). The particular sensitivity of silyl ethers of D-glucal toward two Vilsmeier-Haack reagents POCl3.DMF and (CF3SO2)2O.DMF. Their unique and selective conversion to the corresponding C(6)-O-formates. The Journal of organic chemistry, 66(3), 693-6. https://doi.org/10.1021/jo005540t
Lellouche, J P, and Koeller, S. "The particular sensitivity of silyl ethers of D-glucal toward two Vilsmeier-Haack reagents POCl3.DMF and (CF3SO2)2O.DMF. Their unique and selective conversion to the corresponding C(6)-O-formates." The Journal of organic chemistry vol. 66,3 (2001): 693-6. doi: https://doi.org/10.1021/jo005540t
Lellouche JP, Koeller S. The particular sensitivity of silyl ethers of D-glucal toward two Vilsmeier-Haack reagents POCl3.DMF and (CF3SO2)2O.DMF. Their unique and selective conversion to the corresponding C(6)-O-formates. J Org Chem. 2001 Feb 09;66(3):693-6. doi: 10.1021/jo005540t. PMID: 11430084.
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The concept of culture.

Nature

FORTES M.
PMID: 14780209
Nature. 1950 Oct 28;166(4226):711-3. doi: 10.1038/166711a0.

No abstract available.

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FORTES M. The concept of culture. Nature. 1950;166(4226):711-3doi: 10.1038/166711a0.
FORTES, M. (1950). The concept of culture. Nature, 166(4226), 711-3. https://doi.org/10.1038/166711a0
FORTES, M. "The concept of culture." Nature vol. 166,4226 (1950): 711-3. doi: https://doi.org/10.1038/166711a0
FORTES M. The concept of culture. Nature. 1950 Oct 28;166(4226):711-3. doi: 10.1038/166711a0. PMID: 14780209.
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Showing 13 to 24 of 576 entries