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Correction for Szul et al., "Carbon Fate and Flux in .

mSystems

Szul MJ, Dearth SP, Campagna SR, Zinser ER.
PMID: 30944884
mSystems. 2019 Apr 02;4(2). doi: 10.1128/mSystems.00204-19. eCollection 2019.

[This corrects the article DOI: 10.1128/mSystems.00254-18.].

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Szul MJ, Dearth SP, Campagna SR, et al. Correction for Szul et al., "Carbon Fate and Flux in . mSystems. 2019;4(2)doi: 10.1128/mSystems.00204-19.
Szul, M. J., Dearth, S. P., Campagna, S. R., & Zinser, E. R. (2019). Correction for Szul et al., "Carbon Fate and Flux in . mSystems, 4(2), . https://doi.org/10.1128/mSystems.00204-19
Szul, Martin J, et al. "Correction for Szul et al., "Carbon Fate and Flux in ." mSystems vol. 4,2 (2019). doi: https://doi.org/10.1128/mSystems.00204-19
Szul MJ, Dearth SP, Campagna SR, Zinser ER. Correction for Szul et al., "Carbon Fate and Flux in . mSystems. 2019 Apr 02;4(2). doi: 10.1128/mSystems.00204-19. eCollection 2019. PMID: 30944884; PMCID: PMC6445866.
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The Type of Forage Substrate Preparation Included as Substrate in a RUSITEC System Affects the Ruminal Microbiota and Fermentation Characteristics.

Frontiers in microbiology

Duarte AC, Holman DB, Alexander TW, Durmic Z, Vercoe PE, Chaves AV.
PMID: 28473826
Front Microbiol. 2017 Apr 20;8:704. doi: 10.3389/fmicb.2017.00704. eCollection 2017.

No abstract available.

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Duarte AC, Holman DB, Alexander TW, et al. The Type of Forage Substrate Preparation Included as Substrate in a RUSITEC System Affects the Ruminal Microbiota and Fermentation Characteristics. Front Microbiol. 2017;8:704doi: 10.3389/fmicb.2017.00704.
Duarte, A. C., Holman, D. B., Alexander, T. W., Durmic, Z., Vercoe, P. E., & Chaves, A. V. (2017). The Type of Forage Substrate Preparation Included as Substrate in a RUSITEC System Affects the Ruminal Microbiota and Fermentation Characteristics. Frontiers in microbiology, 8704. https://doi.org/10.3389/fmicb.2017.00704
Duarte, Andrea C, et al. "The Type of Forage Substrate Preparation Included as Substrate in a RUSITEC System Affects the Ruminal Microbiota and Fermentation Characteristics." Frontiers in microbiology vol. 8 (2017): 704. doi: https://doi.org/10.3389/fmicb.2017.00704
Duarte AC, Holman DB, Alexander TW, Durmic Z, Vercoe PE, Chaves AV. The Type of Forage Substrate Preparation Included as Substrate in a RUSITEC System Affects the Ruminal Microbiota and Fermentation Characteristics. Front Microbiol. 2017 Apr 20;8:704. doi: 10.3389/fmicb.2017.00704. eCollection 2017. PMID: 28473826; PMCID: PMC5397515.
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Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis - a very rare condition.

Revista brasileira de hematologia e hemoterapia

Duarte S, Pereira SC, Rodrigues É, Pereira A.
PMID: 28577655
Rev Bras Hematol Hemoter. 2017 Apr - Jun;39(2):167-169. doi: 10.1016/j.bjhh.2017.02.004. Epub 2017 Mar 11.

No abstract available.

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Duarte S, Pereira SC, Rodrigues É, et al. Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis - a very rare condition. Rev Bras Hematol Hemoter. 2017;39(2):167-169doi: 10.1016/j.bjhh.2017.02.004.
Duarte, S., Pereira, S. C., Rodrigues, �. �., & Pereira, A. (2017). Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis - a very rare condition. Revista brasileira de hematologia e hemoterapia, 39(2), 167-169. https://doi.org/10.1016/j.bjhh.2017.02.004
Duarte, Sara, et al. "Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis - a very rare condition." Revista brasileira de hematologia e hemoterapia vol. 39,2 (2017): 167-169. doi: https://doi.org/10.1016/j.bjhh.2017.02.004
Duarte S, Pereira SC, Rodrigues É, Pereira A. Concomitant chronic myeloid leukemia and monoclonal B cell lymphocytosis - a very rare condition. Rev Bras Hematol Hemoter. 2017 Apr - Jun;39(2):167-169. doi: 10.1016/j.bjhh.2017.02.004. Epub 2017 Mar 11. PMID: 28577655; PMCID: PMC5457473.
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Intrafamilial heterogeneity in hereditary diffuse leukoencephalopathy with axonal spheroids.

Neurology. Clinical practice

Lopes C, Duarte S, Santos E, Reis C, Pinto M.
PMID: 32042490
Neurol Clin Pract. 2019 Dec;9(6):500-502. doi: 10.1212/CPJ.0000000000000647.

No abstract available.

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Lopes C, Duarte S, Santos E, et al. Intrafamilial heterogeneity in hereditary diffuse leukoencephalopathy with axonal spheroids. Neurol Clin Pract. 2019;9(6):500-502doi: 10.1212/CPJ.0000000000000647.
Lopes, C., Duarte, S., Santos, E., Reis, C., & Pinto, M. (2019). Intrafamilial heterogeneity in hereditary diffuse leukoencephalopathy with axonal spheroids. Neurology. Clinical practice, 9(6), 500-502. https://doi.org/10.1212/CPJ.0000000000000647
Lopes, Carolina, et al. "Intrafamilial heterogeneity in hereditary diffuse leukoencephalopathy with axonal spheroids." Neurology. Clinical practice vol. 9,6 (2019): 500-502. doi: https://doi.org/10.1212/CPJ.0000000000000647
Lopes C, Duarte S, Santos E, Reis C, Pinto M. Intrafamilial heterogeneity in hereditary diffuse leukoencephalopathy with axonal spheroids. Neurol Clin Pract. 2019 Dec;9(6):500-502. doi: 10.1212/CPJ.0000000000000647. PMID: 32042490; PMCID: PMC6927449.
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CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome.

Genetics and molecular biology

Santos LOD, Bispo AVS, Barros JV, Laranjeira RSM, Pinto RDN, Silva JA, Duarte AR, Araújo J, Sandrin-Garcia P, Crovella S, Bezerra MAC, Belmont TFM, Cavalcanti MDS, Santos N.
PMID: 30508004
Genet Mol Biol. 2018 Oct-Dec;41(4):727-734. doi: 10.1590/1678-4685-GMB-2017-0312. Epub 2018 Nov 29.

Turner syndrome (TS) is characterized by a set of clinical conditions, including autoimmune/inflammatory diseases and infectious conditions, that can compromise a patient's quality of life. Here we assessed polymorphisms in CTLA-4 +49A/G (rs231775), PTPN22 +1858G/A (rs2476601), and MBL2 -550...

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Santos LOD, Bispo AVS, Barros JV, et al. CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome. Genet Mol Biol. 2018;41(4):727-734doi: 10.1590/1678-4685-GMB-2017-0312.
Santos, L. O. D., Bispo, A. V. S., Barros, J. V., Laranjeira, R. S. M., Pinto, R. D. N., Silva, J. A., Duarte, A. R., Araújo, J., Sandrin-Garcia, P., Crovella, S., Bezerra, M. A. C., Belmont, T. F. M., Cavalcanti, M. D. S., & Santos, N. (2018). CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome. Genetics and molecular biology, 41(4), 727-734. https://doi.org/10.1590/1678-4685-GMB-2017-0312
Santos, Luana Oliveira Dos, et al. "CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome." Genetics and molecular biology vol. 41,4 (2018): 727-734. doi: https://doi.org/10.1590/1678-4685-GMB-2017-0312
Santos LOD, Bispo AVS, Barros JV, Laranjeira RSM, Pinto RDN, Silva JA, Duarte AR, Araújo J, Sandrin-Garcia P, Crovella S, Bezerra MAC, Belmont TFM, Cavalcanti MDS, Santos N. CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome. Genet Mol Biol. 2018 Oct-Dec;41(4):727-734. doi: 10.1590/1678-4685-GMB-2017-0312. Epub 2018 Nov 29. PMID: 30508004; PMCID: PMC6415610.
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Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice.

Medicines (Basel, Switzerland)

Direito R, Rocha J, Lima A, Gonçalves MM, Duarte MP, Mateus V, Sousa C, Fernandes A, Pinto R, Boavida Ferreira R, Sepodes B, Figueira ME.
PMID: 31174376
Medicines (Basel). 2019 Jun 06;6(2). doi: 10.3390/medicines6020065.

No abstract available.

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Direito R, Rocha J, Lima A, et al. Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice. Medicines (Basel). 2019;6(2)doi: 10.3390/medicines6020065.
Direito, R., Rocha, J., Lima, A., Gonçalves, M. M., Duarte, M. P., Mateus, V., Sousa, C., Fernandes, A., Pinto, R., Boavida Ferreira, R., Sepodes, B., & Figueira, M. E. (2019). Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice. Medicines (Basel, Switzerland), 6(2), . https://doi.org/10.3390/medicines6020065
Direito, Rosa, et al. "Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice." Medicines (Basel, Switzerland) vol. 6,2 (2019). doi: https://doi.org/10.3390/medicines6020065
Direito R, Rocha J, Lima A, Gonçalves MM, Duarte MP, Mateus V, Sousa C, Fernandes A, Pinto R, Boavida Ferreira R, Sepodes B, Figueira ME. Reduction of Inflammation and Colon Injury by a Spearmint Phenolic Extract in Experimental Bowel Disease in Mice. Medicines (Basel). 2019 Jun 06;6(2). doi: 10.3390/medicines6020065. PMID: 31174376; PMCID: PMC6630206.
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Birth defects surveillance: experiences in Argentina and Colombia.

Journal of community genetics

Groisman B, Liascovich R, Bidondo MP, Barbero P, Duarte S, Tellechea AL, Holguín J, Rodríguez C, Hurtado-Villa P, Caicedo N, Botta G, Zarante I.
PMID: 30607893
J Community Genet. 2019 Jul;10(3):385-393. doi: 10.1007/s12687-018-00403-6. Epub 2019 Jan 03.

Birth defects (BDs) are structural or functional anomalies, sporadic or hereditary, of prenatal origin. Public health surveillance is defined as the ongoing systematic collection, analysis, and interpretation of outcome-specific data for use in the planning, implementation, and evaluation of...

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Groisman B, Liascovich R, Bidondo MP, et al. Birth defects surveillance: experiences in Argentina and Colombia. J Community Genet. 2019;10(3):385-393doi: 10.1007/s12687-018-00403-6.
Groisman, B., Liascovich, R., Bidondo, M. P., Barbero, P., Duarte, S., Tellechea, A. L., Holguín, J., Rodríguez, C., Hurtado-Villa, P., Caicedo, N., Botta, G., & Zarante, I. (2019). Birth defects surveillance: experiences in Argentina and Colombia. Journal of community genetics, 10(3), 385-393. https://doi.org/10.1007/s12687-018-00403-6
Groisman, Boris, et al. "Birth defects surveillance: experiences in Argentina and Colombia." Journal of community genetics vol. 10,3 (2019): 385-393. doi: https://doi.org/10.1007/s12687-018-00403-6
Groisman B, Liascovich R, Bidondo MP, Barbero P, Duarte S, Tellechea AL, Holguín J, Rodríguez C, Hurtado-Villa P, Caicedo N, Botta G, Zarante I. Birth defects surveillance: experiences in Argentina and Colombia. J Community Genet. 2019 Jul;10(3):385-393. doi: 10.1007/s12687-018-00403-6. Epub 2019 Jan 03. PMID: 30607893; PMCID: PMC6591326.
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Can Luminol Be a Fluorophore?.

Journal of fluorescence

Barroso MF, Silva RJA, Moreira SF, Rodrigues SS, Gonçalves HMR, Duarte AJ.
PMID: 30887388
J Fluoresc. 2019 Mar;29(2):343-346. doi: 10.1007/s10895-019-02362-8. Epub 2019 Mar 18.

In this work, we report a new chemiluminescence system using bis-(2,4,6-trichlorophenyl) oxalate (TCPO) with hydrogen peroxide and luminol as fluorophore. The intense chemiluminescence reaction here described was fully investigated and it was determined that this fluorescent system has two...

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Barroso MF, Silva RJA, Moreira SF, et al. Can Luminol Be a Fluorophore?. J Fluoresc. 2019;29(2):343-346doi: 10.1007/s10895-019-02362-8.
Barroso, M. F., Silva, R. J. A., Moreira, S. F., Rodrigues, S. S., Gonçalves, H. M. R., & Duarte, A. J. (2019). Can Luminol Be a Fluorophore?. Journal of fluorescence, 29(2), 343-346. https://doi.org/10.1007/s10895-019-02362-8
Barroso, M Fátima, et al. "Can Luminol Be a Fluorophore?." Journal of fluorescence vol. 29,2 (2019): 343-346. doi: https://doi.org/10.1007/s10895-019-02362-8
Barroso MF, Silva RJA, Moreira SF, Rodrigues SS, Gonçalves HMR, Duarte AJ. Can Luminol Be a Fluorophore?. J Fluoresc. 2019 Mar;29(2):343-346. doi: 10.1007/s10895-019-02362-8. Epub 2019 Mar 18. PMID: 30887388.
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Granulomatosis with polyangiitis - the incomplete puzzle.

Acta reumatologica portuguesa

Duarte AC, Cordeiro A, Gonçalves P, Santos MJ.
PMID: 34962242
Acta Reumatol Port. 2021 Oct-Dec;46(4):350-354.

Granulomatous with polyangiitis (GPA) is a necrotizing granulomatous vasculitis that mostly affects small-sized vessels. The disease can affect many organs, although renal and respiratory tract involvement are the most frequent and distinguishing features. Musculoskeletal manifestations have been reported in...

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Duarte AC, Cordeiro A, Gonçalves P, et al. Granulomatosis with polyangiitis – the incomplete puzzle. Granulomatosis with polyangiitis - the incomplete puzzle. Acta Reumatol Port. 2021;46(4):350-354
Duarte, A. C., Cordeiro, A., Gonçalves, P., & Santos, M. J. (2021). Granulomatosis with polyangiitis – the incomplete puzzle. Granulomatosis with polyangiitis - the incomplete puzzle. Acta reumatologica portuguesa, 46(4), 350-354.
Duarte, Ana Catarina, et al. "Granulomatosis with polyangiitis – the incomplete puzzle." Granulomatosis with polyangiitis - the incomplete puzzle. Acta reumatologica portuguesa vol. 46,4 (2021): 350-354.
Duarte AC, Cordeiro A, Gonçalves P, Santos MJ. Granulomatosis with polyangiitis – the incomplete puzzle. Granulomatosis with polyangiitis - the incomplete puzzle. Acta Reumatol Port. 2021 Oct-Dec;46(4):350-354. PMID: 34962242.
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Suspected microplastics in Atlantic horse mackerel fish (Trachurus trachurus) captured in Portugal.

Marine pollution bulletin

Prata JC, da Costa JP, Duarte AC, Rocha-Santos T.
PMID: 34953263
Mar Pollut Bull. 2021 Dec 22;174:113249. doi: 10.1016/j.marpolbul.2021.113249. Epub 2021 Dec 22.

Microplastics have been found in fish, but most studies have focused on the digestive system without considering additional organs. Herein, the objective was to assess the presence of microplastics in internal organs (gills, guts, kidney, heart) of the Atlantic...

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Prata JC, da Costa JP, Duarte AC, et al. Suspected microplastics in Atlantic horse mackerel fish (Trachurus trachurus) captured in Portugal. Mar Pollut Bull. 2021;174:113249doi: 10.1016/j.marpolbul.2021.113249.
Prata, J. C., da Costa, J. P., Duarte, A. C., & Rocha-Santos, T. (2021). Suspected microplastics in Atlantic horse mackerel fish (Trachurus trachurus) captured in Portugal. Marine pollution bulletin, 174113249. https://doi.org/10.1016/j.marpolbul.2021.113249
Prata, Joana C, et al. "Suspected microplastics in Atlantic horse mackerel fish (Trachurus trachurus) captured in Portugal." Marine pollution bulletin vol. 174 (2021): 113249. doi: https://doi.org/10.1016/j.marpolbul.2021.113249
Prata JC, da Costa JP, Duarte AC, Rocha-Santos T. Suspected microplastics in Atlantic horse mackerel fish (Trachurus trachurus) captured in Portugal. Mar Pollut Bull. 2021 Dec 22;174:113249. doi: 10.1016/j.marpolbul.2021.113249. Epub 2021 Dec 22. PMID: 34953263.
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Gabra2 is a genetic modifier of Dravet syndrome in mice.

Mammalian genome : official journal of the International Mammalian Genome Society

Hawkins NA, Nomura T, Duarte S, Barse L, Williams RW, Homanics GE, Mulligan MK, Contractor A, Kearney JA.
PMID: 34086081
Mamm Genome. 2021 Oct;32(5):350-363. doi: 10.1007/s00335-021-09877-1. Epub 2021 Jun 04.

Pathogenic variants in epilepsy genes result in a spectrum of clinical severity. One source of phenotypic heterogeneity is modifier genes that affect expressivity of a primary pathogenic variant. Mouse epilepsy models also display varying degrees of clinical severity on...

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Hawkins NA, Nomura T, Duarte S, et al. Gabra2 is a genetic modifier of Dravet syndrome in mice. Mamm Genome. 2021;32(5):350-363doi: 10.1007/s00335-021-09877-1.
Hawkins, N. A., Nomura, T., Duarte, S., Barse, L., Williams, R. W., Homanics, G. E., Mulligan, M. K., Contractor, A., & Kearney, J. A. (2021). Gabra2 is a genetic modifier of Dravet syndrome in mice. Mammalian genome : official journal of the International Mammalian Genome Society, 32(5), 350-363. https://doi.org/10.1007/s00335-021-09877-1
Hawkins, Nicole A, et al. "Gabra2 is a genetic modifier of Dravet syndrome in mice." Mammalian genome : official journal of the International Mammalian Genome Society vol. 32,5 (2021): 350-363. doi: https://doi.org/10.1007/s00335-021-09877-1
Hawkins NA, Nomura T, Duarte S, Barse L, Williams RW, Homanics GE, Mulligan MK, Contractor A, Kearney JA. Gabra2 is a genetic modifier of Dravet syndrome in mice. Mamm Genome. 2021 Oct;32(5):350-363. doi: 10.1007/s00335-021-09877-1. Epub 2021 Jun 04. PMID: 34086081; PMCID: PMC8458207.
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Ruptured popliteal artery aneurysm in a patient with a clinical diagnosis of Marfan syndrome.

Jornal vascular brasileiro

Duarte GP, da Cunha JR.
PMID: 34290752
J Vasc Bras. 2020 Oct 16;19:e20200017. doi: 10.1590/1677-5449.200017. eCollection 2020.

The popliteal artery is the main site of occurrence of peripheral aneurysms. Acute presentations constitute a potential threat to limb viability and to life, especially in the event of rupture. Rupture is a rare event, but one that demands...

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Duarte GP, da Cunha JR. Ruptured popliteal artery aneurysm in a patient with a clinical diagnosis of Marfan syndrome. J Vasc Bras. 2020;19:e20200017doi: 10.1590/1677-5449.200017.
Duarte, G. P., & da Cunha, J. R. (2020). Ruptured popliteal artery aneurysm in a patient with a clinical diagnosis of Marfan syndrome. Jornal vascular brasileiro, 19e20200017. https://doi.org/10.1590/1677-5449.200017
Duarte, Gabriel Paiva, and da Cunha, Jorge Ribeiro. "Ruptured popliteal artery aneurysm in a patient with a clinical diagnosis of Marfan syndrome." Jornal vascular brasileiro vol. 19 (2020): e20200017. doi: https://doi.org/10.1590/1677-5449.200017
Duarte GP, da Cunha JR. Ruptured popliteal artery aneurysm in a patient with a clinical diagnosis of Marfan syndrome. J Vasc Bras. 2020 Oct 16;19:e20200017. doi: 10.1590/1677-5449.200017. eCollection 2020. PMID: 34290752; PMCID: PMC8276642.
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