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Artigo de periodico
Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers (2015)
Hernández-Ramirez, Laura C.; Gabrovska, Plamena; Dénes, Judit; Stals, Karen; Trivellin, Giampaolo; Tilley, Daniel; Ferraú, Francesco; Evanson, Jane; Ellard, Sian; Grossman, Ashley B.; Roncaroli, Federico; Gadelha, Mônica R.; Korbonits, Márta; Castro, Margaret de
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Subjects: GLÂNDULA PITUITÁRIA, ADENOMA, MUTAÇÃO GENÉTICA, HIDROCARBONETOS
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ABNT
HERNÁNDEZ-RAMIREZ, Laura C. et al. Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers. Journal of Clinical Endocrinology and Metabolism, v. 100, n. 9, p. E1242-E1254, 2015Tradução . . Disponível em: https://doi.org/10.1210/jc.2015-1869. Acesso em: 01 jun. 2024.
APA
Hernández-Ramirez, L. C., Gabrovska, P., Dénes, J., Stals, K., Trivellin, G., Tilley, D., et al. (2015). Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers. Journal of Clinical Endocrinology and Metabolism, 100( 9), E1242-E1254. doi:10.1210/jc.2015-1869
NLM
Hernández-Ramirez LC, Gabrovska P, Dénes J, Stals K, Trivellin G, Tilley D, Ferraú F, Evanson J, Ellard S, Grossman AB, Roncaroli F, Gadelha MR, Korbonits M, Castro M de. Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers [Internet]. Journal of Clinical Endocrinology and Metabolism. 2015 ; 100( 9): E1242-E1254.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1210/jc.2015-1869
Vancouver
Hernández-Ramirez LC, Gabrovska P, Dénes J, Stals K, Trivellin G, Tilley D, Ferraú F, Evanson J, Ellard S, Grossman AB, Roncaroli F, Gadelha MR, Korbonits M, Castro M de. Landscape of familial isolated and young-onset pituitary adenomas: prospective diagnosis in AIP mutation carriers [Internet]. Journal of Clinical Endocrinology and Metabolism. 2015 ; 100( 9): E1242-E1254.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1210/jc.2015-1869
Artigo de periodico
Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: relevance for molecular diagnosis (2015)
Mueller, Geoffrey A.; Pedersen, Lars; Glesner, Jill; Edwards, Lori L.; Zakzuk, Josefina; London, Robert E.; Arruda, Luisa Karla de Paula; Chapman, Martin D.; Caraballo, Luis; Pomés, Anna
Source: Journal of Allergy and Clinical Immunology. Unidade: FMRP
Subjects: BARATAS, HELMINTHES, ÁCAROS, GLUTATIONA TRANSFERASE, ALERGIA E IMUNOLOGIA, ALÉRGENOS
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MUELLER, Geoffrey A. et al. Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: relevance for molecular diagnosis. Journal of Allergy and Clinical Immunology, v. 136, n. 5, p. 1369-1377, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2015.03.015. Acesso em: 01 jun. 2024.
APA
Mueller, G. A., Pedersen, L., Glesner, J., Edwards, L. L., Zakzuk, J., London, R. E., et al. (2015). Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: relevance for molecular diagnosis. Journal of Allergy and Clinical Immunology, 136( 5), 1369-1377. doi:10.1016/j.jaci.2015.03.015
NLM
Mueller GA, Pedersen L, Glesner J, Edwards LL, Zakzuk J, London RE, Arruda LK de P, Chapman MD, Caraballo L, Pomés A. Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: relevance for molecular diagnosis [Internet]. Journal of Allergy and Clinical Immunology. 2015 ; 136( 5): 1369-1377.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.jaci.2015.03.015
Vancouver
Mueller GA, Pedersen L, Glesner J, Edwards LL, Zakzuk J, London RE, Arruda LK de P, Chapman MD, Caraballo L, Pomés A. Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: relevance for molecular diagnosis [Internet]. Journal of Allergy and Clinical Immunology. 2015 ; 136( 5): 1369-1377.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.jaci.2015.03.015
Artigo de periodico
Characterisation of divergent flavivirus NS3 and NS5 protein sequences detected in Rhipicephalus microplus ticks from Brazil (2014)
Maruyama, Sandra Regina; Castro-Jorge, Luiza Antunes de; Ribeiro, José Marcos Chaves; Gardinassi, Luiz Gustavo; Garcia, Gustavo Rocha; Brandão, Lucinda Giampietro; Rodrigues, Aline Rezende; Okada, Marcos Ituo; Abrão, Emiliana Pereira; Ferreira, Beatriz Rossetti; Fonseca, Benedito Antonio Lopes da; Santos, Isabel Kinney Ferreira de Miranda
Source: Memórias do Instituto Oswaldo Cruz. Unidades: EERP, FMRP
Subjects: FLAVIVIRUS (ISOLAMENTO E PURIFICAÇÃO), REAÇÃO EM CADEIA POR POLIMERASE, RNA VIRAL, RHIPICEPHALUS SANGUINEUS
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ABNT
MARUYAMA, Sandra Regina et al. Characterisation of divergent flavivirus NS3 and NS5 protein sequences detected in Rhipicephalus microplus ticks from Brazil. Memórias do Instituto Oswaldo Cruz, v. 109, n. 1, p. 38-50, 2014Tradução . . Disponível em: https://doi.org/10.1590/0074-0276130166. Acesso em: 01 jun. 2024.
APA
Maruyama, S. R., Castro-Jorge, L. A. de, Ribeiro, J. M. C., Gardinassi, L. G., Garcia, G. R., Brandão, L. G., et al. (2014). Characterisation of divergent flavivirus NS3 and NS5 protein sequences detected in Rhipicephalus microplus ticks from Brazil. Memórias do Instituto Oswaldo Cruz, 109( 1), 38-50. doi:10.1590/0074-0276130166
NLM
Maruyama SR, Castro-Jorge LA de, Ribeiro JMC, Gardinassi LG, Garcia GR, Brandão LG, Rodrigues AR, Okada MI, Abrão EP, Ferreira BR, Fonseca BAL da, Santos IKF de M. Characterisation of divergent flavivirus NS3 and NS5 protein sequences detected in Rhipicephalus microplus ticks from Brazil [Internet]. Memórias do Instituto Oswaldo Cruz. 2014 ; 109( 1): 38-50.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1590/0074-0276130166
Vancouver
Maruyama SR, Castro-Jorge LA de, Ribeiro JMC, Gardinassi LG, Garcia GR, Brandão LG, Rodrigues AR, Okada MI, Abrão EP, Ferreira BR, Fonseca BAL da, Santos IKF de M. Characterisation of divergent flavivirus NS3 and NS5 protein sequences detected in Rhipicephalus microplus ticks from Brazil [Internet]. Memórias do Instituto Oswaldo Cruz. 2014 ; 109( 1): 38-50.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1590/0074-0276130166
Artigo de periodico
A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome (2014)
Ueda, Yasutaka; Calado, Rodrigo Tocantins; Norberg, Anna; Kajigaya, Sachiko; Ross, Göran; Hellstrom-Lindberg, Eva; Young, Neal S
Source: BMC Medical Genetics. Unidade: FMRP
Subjects: DOENÇAS HEMATOLÓGICAS (GENÉTICA), PROTEÍNAS NUCLEARES (METABOLISMO), NUCLEOTÍDEOS
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ABNT
UEDA, Yasutaka et al. A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome. BMC Medical Genetics, v. 15, 2014Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-15-68. Acesso em: 01 jun. 2024.
APA
Ueda, Y., Calado, R. T., Norberg, A., Kajigaya, S., Ross, G., Hellstrom-Lindberg, E., & Young, N. S. (2014). A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome. BMC Medical Genetics, 15. doi:10.1186/1471-2350-15-68
NLM
Ueda Y, Calado RT, Norberg A, Kajigaya S, Ross G, Hellstrom-Lindberg E, Young NS. A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome [Internet]. BMC Medical Genetics. 2014 ; 15[citado 2024 jun. 01 ] Available from: https://doi.org/10.1186/1471-2350-15-68
Vancouver
Ueda Y, Calado RT, Norberg A, Kajigaya S, Ross G, Hellstrom-Lindberg E, Young NS. A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome [Internet]. BMC Medical Genetics. 2014 ; 15[citado 2024 jun. 01 ] Available from: https://doi.org/10.1186/1471-2350-15-68
Trabalho de evento-resumo
Telomere elongation and hematologic improvement in humans treated with androgens: a prospective clinical trial of danazol in telomeropathies (2014)
Dumitriu, Bagdan; Townsley, Danielle M.; Chen, Christina; Calado, Rodrigo Tocantins; Scheinberg, Phillip; Young, Neal S.
Source: Abstracts & Program. Conference titles: Annual Meeting and Exposition of American Society of Hematology (ASH). Unidade: FMRP
Subjects: HEMATOLOGIA, ANDRÓGENOS, ONCOLOGIA, CÉLULAS
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ABNT
DUMITRIU, Bagdan et al. Telomere elongation and hematologic improvement in humans treated with androgens: a prospective clinical trial of danazol in telomeropathies. 2014, Anais.. San Francisco: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2014. . Acesso em: 01 jun. 2024.
APA
Dumitriu, B., Townsley, D. M., Chen, C., Calado, R. T., Scheinberg, P., & Young, N. S. (2014). Telomere elongation and hematologic improvement in humans treated with androgens: a prospective clinical trial of danazol in telomeropathies. In Abstracts & Program. San Francisco: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Dumitriu B, Townsley DM, Chen C, Calado RT, Scheinberg P, Young NS. Telomere elongation and hematologic improvement in humans treated with androgens: a prospective clinical trial of danazol in telomeropathies. Abstracts & Program. 2014 ;[citado 2024 jun. 01 ]
Vancouver
Dumitriu B, Townsley DM, Chen C, Calado RT, Scheinberg P, Young NS. Telomere elongation and hematologic improvement in humans treated with androgens: a prospective clinical trial of danazol in telomeropathies. Abstracts & Program. 2014 ;[citado 2024 jun. 01 ]
Artigo de periodico
Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: provisional core sets of domains and instruments for use in clinical trials (2014)
Saketkoo, Lesley Ann; Mittoo, Shikha; Huscher, Dörte; Khanna, Dinesh; Dellaripa, Paul F.; Distler, Oliver; Flaherty, Kevin R.; Frankel, Sid; Oddis, Chester V.; Denton, Christopher P.; Fischer, Aryeh; Kowal-Bielecka, Otylia M.; LeSage, Daphne; Merkel, Peter A.; Phillips, Kristine; Pittrow, David; Swigris, Jeffrey; Antoniou, Katerina; Baughman, Robert P.; Castelino, Flavia V.; Christmann, Romy B.; Christopher-Stine, Lisa; Collard, Harold R.; Cottin, Vincent; Danoff, Sonye; Highland, Kristin B.; Hummers, Laura; Shah, Ami A.; Kim, Dong Soon; Lynch, David A.; Miller, Frederick W.; Proudman, Susanna M.; Richeldi, Luca; Ryu, Jay H.; Sandorfi, Nora; Sarver, Catherine; Wells, Athol U.; Strand, Vibeke; Matteson, Eric L.; Brown, Kevin K.; Seibold, James R.; Carvalho, Carlos Roberto Ribeiro De; Kairalla, Ronaldo Adib; Martinez, José Antônio Baddini
Source: Thorax. Unidades: FM, FMRP
Subjects: DOENÇAS DO TECIDO CONJUNTIVO, FIBROSE PULMONAR, DOENÇAS PULMONARES INTERSTICIAIS, ENSAIO CLÍNICO CONTROLADO RANDOMIZADO
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SAKETKOO, Lesley Ann et al. Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: provisional core sets of domains and instruments for use in clinical trials. Thorax, v. 69, n. 5, p. 428-436, 2014Tradução . . Disponível em: https://doi.org/10.1136/thoraxjnl-2013-204202. Acesso em: 01 jun. 2024.
APA
Saketkoo, L. A., Mittoo, S., Huscher, D., Khanna, D., Dellaripa, P. F., Distler, O., et al. (2014). Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: provisional core sets of domains and instruments for use in clinical trials. Thorax, 69( 5), 428-436. doi:10.1136/thoraxjnl-2013-204202
NLM
Saketkoo LA, Mittoo S, Huscher D, Khanna D, Dellaripa PF, Distler O, Flaherty KR, Frankel S, Oddis CV, Denton CP, Fischer A, Kowal-Bielecka OM, LeSage D, Merkel PA, Phillips K, Pittrow D, Swigris J, Antoniou K, Baughman RP, Castelino FV, Christmann RB, Christopher-Stine L, Collard HR, Cottin V, Danoff S, Highland KB, Hummers L, Shah AA, Kim DS, Lynch DA, Miller FW, Proudman SM, Richeldi L, Ryu JH, Sandorfi N, Sarver C, Wells AU, Strand V, Matteson EL, Brown KK, Seibold JR, Carvalho CRRD, Kairalla RA, Martinez JAB. Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: provisional core sets of domains and instruments for use in clinical trials [Internet]. Thorax. 2014 ; 69( 5): 428-436.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1136/thoraxjnl-2013-204202
Vancouver
Saketkoo LA, Mittoo S, Huscher D, Khanna D, Dellaripa PF, Distler O, Flaherty KR, Frankel S, Oddis CV, Denton CP, Fischer A, Kowal-Bielecka OM, LeSage D, Merkel PA, Phillips K, Pittrow D, Swigris J, Antoniou K, Baughman RP, Castelino FV, Christmann RB, Christopher-Stine L, Collard HR, Cottin V, Danoff S, Highland KB, Hummers L, Shah AA, Kim DS, Lynch DA, Miller FW, Proudman SM, Richeldi L, Ryu JH, Sandorfi N, Sarver C, Wells AU, Strand V, Matteson EL, Brown KK, Seibold JR, Carvalho CRRD, Kairalla RA, Martinez JAB. Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: provisional core sets of domains and instruments for use in clinical trials [Internet]. Thorax. 2014 ; 69( 5): 428-436.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1136/thoraxjnl-2013-204202
Artigo de periodico
Telomere dynamics in mice and humans (2013)
Calado, Rodrigo Tocantins; Dumitriu, Bogdan
Source: Seminars in Hematology. Unidade: FMRP
Subjects: ENVELHECIMENTO, NEOPLASIAS (GENÉTICA;METABOLISMO), FENÓTIPOS
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ABNT
CALADO, Rodrigo Tocantins e DUMITRIU, Bogdan. Telomere dynamics in mice and humans. Seminars in Hematology, v. 50, n. 2, p. 165\2013174, 2013Tradução . . Disponível em: https://doi.org/10.1053/j.seminhematol.2013.03.030. Acesso em: 01 jun. 2024.
APA
Calado, R. T., & Dumitriu, B. (2013). Telomere dynamics in mice and humans. Seminars in Hematology, 50( 2), 165\2013174. doi:10.1053/j.seminhematol.2013.03.030
NLM
Calado RT, Dumitriu B. Telomere dynamics in mice and humans [Internet]. Seminars in Hematology. 2013 ; 50( 2): 165\2013174.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1053/j.seminhematol.2013.03.030
Vancouver
Calado RT, Dumitriu B. Telomere dynamics in mice and humans [Internet]. Seminars in Hematology. 2013 ; 50( 2): 165\2013174.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1053/j.seminhematol.2013.03.030
Artigo de periodico
Quantification of bold fMRI parameters to infer cerebrovascular reactivity of the middle cerebral artery (2013)
Mazzetto-Betti, Kelley C.; Leoni, Renata F.; Pontes Neto, Octávio Marques; Sturzbecher, Marcio J.; Santos, Antônio Carlos dos; Leite, João Pereira; Silva, Afonso C.; Araújo, Dráulio Barros de
Source: Journal of Magnetic Resonance Imaging. Unidade: FMRP
Subjects: ARTÉRIAS CEREBRAIS, ESTIMULAÇÃO CEREBRAL, IMAGEM POR RESSONÂNCIA MAGNÉTICA
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ABNT
MAZZETTO-BETTI, Kelley C. et al. Quantification of bold fMRI parameters to infer cerebrovascular reactivity of the middle cerebral artery. Journal of Magnetic Resonance Imaging, v. 38, n. 5, p. 1203-1209, 2013Tradução . . Disponível em: https://doi.org/10.1002/jmri.23943. Acesso em: 01 jun. 2024.
APA
Mazzetto-Betti, K. C., Leoni, R. F., Pontes Neto, O. M., Sturzbecher, M. J., Santos, A. C. dos, Leite, J. P., et al. (2013). Quantification of bold fMRI parameters to infer cerebrovascular reactivity of the middle cerebral artery. Journal of Magnetic Resonance Imaging, 38( 5), 1203-1209. doi:10.1002/jmri.23943
NLM
Mazzetto-Betti KC, Leoni RF, Pontes Neto OM, Sturzbecher MJ, Santos AC dos, Leite JP, Silva AC, Araújo DB de. Quantification of bold fMRI parameters to infer cerebrovascular reactivity of the middle cerebral artery [Internet]. Journal of Magnetic Resonance Imaging. 2013 ; 38( 5): 1203-1209.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/jmri.23943
Vancouver
Mazzetto-Betti KC, Leoni RF, Pontes Neto OM, Sturzbecher MJ, Santos AC dos, Leite JP, Silva AC, Araújo DB de. Quantification of bold fMRI parameters to infer cerebrovascular reactivity of the middle cerebral artery [Internet]. Journal of Magnetic Resonance Imaging. 2013 ; 38( 5): 1203-1209.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/jmri.23943
Artigo de periodico
Interphase chromossome flow-fish (2012)
Keyvanfar, Keyvan; Weed, Janson; Swamy, Prashanth; Kajigaya, Sashiko; Calado, Rodrigo Tocantins; Young, Neal S.
Source: Blood. Unidade: FMRP
Subjects: CROMOSSOMOS, PEIXES (FLUXO)
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ABNT
KEYVANFAR, Keyvan et al. Interphase chromossome flow-fish. Blood, v. 120, n. 15, p. e54-e59, 2012Tradução . . Disponível em: https://doi.org/10.1182/blood-2012-05-434266. Acesso em: 01 jun. 2024.
APA
Keyvanfar, K., Weed, J., Swamy, P., Kajigaya, S., Calado, R. T., & Young, N. S. (2012). Interphase chromossome flow-fish. Blood, 120( 15), e54-e59. doi:10.1182/blood-2012-05-434266
NLM
Keyvanfar K, Weed J, Swamy P, Kajigaya S, Calado RT, Young NS. Interphase chromossome flow-fish [Internet]. Blood. 2012 ; 120( 15): e54-e59.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1182/blood-2012-05-434266
Vancouver
Keyvanfar K, Weed J, Swamy P, Kajigaya S, Calado RT, Young NS. Interphase chromossome flow-fish [Internet]. Blood. 2012 ; 120( 15): e54-e59.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1182/blood-2012-05-434266
Artigo de periodico
Human telomere disease due to disruption of the CCAAT box of the TERC promoter (2012)
Aalbers, Anna M.; Kajigaya, Sachiko; Heuvek-Eibrink, Marry M. van den; Velden, Vincent H. J. van der; Calado, Rodrigo Tocantins; Young, Neal S.
Source: Blood. Unidade: FMRP
Subjects: CROMOSSOMOS HUMANOS, MUTAÇÃO GENÉTICA
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ABNT
AALBERS, Anna M. et al. Human telomere disease due to disruption of the CCAAT box of the TERC promoter. Blood, v. 119, n. 3, p. 3060-3063, 2012Tradução . . Disponível em: https://doi.org/10.1182/blood-2011-10-383182. Acesso em: 01 jun. 2024.
APA
Aalbers, A. M., Kajigaya, S., Heuvek-Eibrink, M. M. van den, Velden, V. H. J. van der, Calado, R. T., & Young, N. S. (2012). Human telomere disease due to disruption of the CCAAT box of the TERC promoter. Blood, 119( 3), 3060-3063. doi:10.1182/blood-2011-10-383182
NLM
Aalbers AM, Kajigaya S, Heuvek-Eibrink MM van den, Velden VHJ van der, Calado RT, Young NS. Human telomere disease due to disruption of the CCAAT box of the TERC promoter [Internet]. Blood. 2012 ; 119( 3): 3060-3063.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1182/blood-2011-10-383182
Vancouver
Aalbers AM, Kajigaya S, Heuvek-Eibrink MM van den, Velden VHJ van der, Calado RT, Young NS. Human telomere disease due to disruption of the CCAAT box of the TERC promoter [Internet]. Blood. 2012 ; 119( 3): 3060-3063.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1182/blood-2011-10-383182
Artigo de periodico
Age-adjusted recipient pretransplantation telomere length and treatment-related mortality after hematopoietic stem cell transplantation (2012)
Latour, Régis Peffault de; Calado, Rodrigo Tocantins; Busson, Marc; Abrams, Jeffrey; Adoui, Nadir; Robin, Marie; Larghero, Jérome; Dhedin, Nathalie; Xhaard, Alienor; Clave, Emmanuel; Charron, Diminique; Toubert, Antoine; Loiseau, Pascale; Socié, Gérard; young, Neal S.
Source: Blood. Unidade: FMRP
Subjects: TRANSPLANTES, CÉLULAS-TRONCO
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ABNT
LATOUR, Régis Peffault de et al. Age-adjusted recipient pretransplantation telomere length and treatment-related mortality after hematopoietic stem cell transplantation. Blood, v. 120, n. 16, p. 3353-3359, 2012Tradução . . Disponível em: https://doi.org/10.1182/blood-2012-01-403337. Acesso em: 01 jun. 2024.
APA
Latour, R. P. de, Calado, R. T., Busson, M., Abrams, J., Adoui, N., Robin, M., et al. (2012). Age-adjusted recipient pretransplantation telomere length and treatment-related mortality after hematopoietic stem cell transplantation. Blood, 120( 16), 3353-3359. doi:10.1182/blood-2012-01-403337
NLM
Latour RP de, Calado RT, Busson M, Abrams J, Adoui N, Robin M, Larghero J, Dhedin N, Xhaard A, Clave E, Charron D, Toubert A, Loiseau P, Socié G, young NS. Age-adjusted recipient pretransplantation telomere length and treatment-related mortality after hematopoietic stem cell transplantation [Internet]. Blood. 2012 ; 120( 16): 3353-3359.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1182/blood-2012-01-403337
Vancouver
Latour RP de, Calado RT, Busson M, Abrams J, Adoui N, Robin M, Larghero J, Dhedin N, Xhaard A, Clave E, Charron D, Toubert A, Loiseau P, Socié G, young NS. Age-adjusted recipient pretransplantation telomere length and treatment-related mortality after hematopoietic stem cell transplantation [Internet]. Blood. 2012 ; 120( 16): 3353-3359.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1182/blood-2012-01-403337
Trabalho de evento-resumo periodico
Telomere dynamics in pluripotent stem cells derived from patients with telomere diseases (2011)
Winkler, Thomas; Decker, Jake E.; Hong, So Gun; Wu, Chuanfeng; Morgan, Mary J.; Dunbar, Cynthia E.; Young, Neal S.; Calado, Rodrigo Tocantins
Source: Blood. Conference titles: Annual Meeting and Exposition of the American Society of Hematology (ASH). Unidade: FMRP
Subjects: ENZIMAS, CROMOSSOMOS, GENÉTICA
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ABNT
WINKLER, Thomas et al. Telomere dynamics in pluripotent stem cells derived from patients with telomere diseases. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 01 jun. 2024. , 2011
APA
Winkler, T., Decker, J. E., Hong, S. G., Wu, C., Morgan, M. J., Dunbar, C. E., et al. (2011). Telomere dynamics in pluripotent stem cells derived from patients with telomere diseases. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Winkler T, Decker JE, Hong SG, Wu C, Morgan MJ, Dunbar CE, Young NS, Calado RT. Telomere dynamics in pluripotent stem cells derived from patients with telomere diseases. Blood. 2011 ; 118( 21):[citado 2024 jun. 01 ]
Vancouver
Winkler T, Decker JE, Hong SG, Wu C, Morgan MJ, Dunbar CE, Young NS, Calado RT. Telomere dynamics in pluripotent stem cells derived from patients with telomere diseases. Blood. 2011 ; 118( 21):[citado 2024 jun. 01 ]
Artigo de periodico
Constitutional telomerase mutations are genetic risk factors for cirrhosis (2011)
Calado, Rodrigo Tocantins; Brudno, Jennifer; Mehta, Paulomi; Kovacs, Joseph J.; Wu, Colin; Zago, Marco Antonio; Chanock, Stephen J.; Boyer, Thomas D.; Young, Neal S.
Source: Hepatology. Unidade: FMRP
Subjects: CIRROSE HEPÁTICA, LEUCÓCITOS
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ABNT
CALADO, Rodrigo Tocantins et al. Constitutional telomerase mutations are genetic risk factors for cirrhosis. Hepatology, v. 53, n. 5, p. 1600-1607, 2011Tradução . . Disponível em: https://doi.org/10.1002/hep.24173. Acesso em: 01 jun. 2024.
APA
Calado, R. T., Brudno, J., Mehta, P., Kovacs, J. J., Wu, C., Zago, M. A., et al. (2011). Constitutional telomerase mutations are genetic risk factors for cirrhosis. Hepatology, 53( 5), 1600-1607. doi:10.1002/hep.24173
NLM
Calado RT, Brudno J, Mehta P, Kovacs JJ, Wu C, Zago MA, Chanock SJ, Boyer TD, Young NS. Constitutional telomerase mutations are genetic risk factors for cirrhosis [Internet]. Hepatology. 2011 ; 53( 5): 1600-1607.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/hep.24173
Vancouver
Calado RT, Brudno J, Mehta P, Kovacs JJ, Wu C, Zago MA, Chanock SJ, Boyer TD, Young NS. Constitutional telomerase mutations are genetic risk factors for cirrhosis [Internet]. Hepatology. 2011 ; 53( 5): 1600-1607.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/hep.24173
Artigo de periodico
Chemokine production and leukocyte recruitment to the lungs of Paracoccidioides brasiliensis-infected mice is modulated by interferon-'gama' (2003)
Souto, Janeusa Trindade de; Aliberti, Júlio C.; Campanelli, Ana Paula; Livonesi, Márcia Cristina; Maffei, Cláudia Maria Leite; Ferreira, Beatriz Rossetti; Travassos, Luiz R.; Martinez, Roberto; Rossi, Marcos Antonio; Silva, João Santana da
Source: American Journal of Pathology. Unidade: FMRP
Subjects: PARACOCCIDIOIDES BRASILIENSIS, CAMUNDONGOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUTO, Janeusa Trindade de et al. Chemokine production and leukocyte recruitment to the lungs of Paracoccidioides brasiliensis-infected mice is modulated by interferon-'gama'. American Journal of Pathology, v. 163, n. 2, p. 583-590, 2003Tradução . . Acesso em: 01 jun. 2024.
APA
Souto, J. T. de, Aliberti, J. C., Campanelli, A. P., Livonesi, M. C., Maffei, C. M. L., Ferreira, B. R., et al. (2003). Chemokine production and leukocyte recruitment to the lungs of Paracoccidioides brasiliensis-infected mice is modulated by interferon-'gama'. American Journal of Pathology, 163( 2), 583-590.
NLM
Souto JT de, Aliberti JC, Campanelli AP, Livonesi MC, Maffei CML, Ferreira BR, Travassos LR, Martinez R, Rossi MA, Silva JS da. Chemokine production and leukocyte recruitment to the lungs of Paracoccidioides brasiliensis-infected mice is modulated by interferon-'gama'. American Journal of Pathology. 2003 ; 163( 2): 583-590.[citado 2024 jun. 01 ]
Vancouver
Souto JT de, Aliberti JC, Campanelli AP, Livonesi MC, Maffei CML, Ferreira BR, Travassos LR, Martinez R, Rossi MA, Silva JS da. Chemokine production and leukocyte recruitment to the lungs of Paracoccidioides brasiliensis-infected mice is modulated by interferon-'gama'. American Journal of Pathology. 2003 ; 163( 2): 583-590.[citado 2024 jun. 01 ]
Artigo de periodico
Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene (2002)
Mendonça, Berenice Bilharinho de; Leite, Maristela V.; Castro, Margaret de; Kino, Tomoshige; Elias, Lucila L. K.; Bachega, Tania A. S.; Arnhold, Ivo J. P.; Chrousos, George P.; Latronico, Ana Claudia
Source: The Journal of Clinical Endocrinology & Metabolism. Unidades: FM, FMRP
Subjects: ENDOCRINOLOGIA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDONÇA, Berenice Bilharinho de et al. Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism, v. 87, n. 4, p. 1805-1809, 2002Tradução . . Acesso em: 01 jun. 2024.
APA
Mendonça, B. B. de, Leite, M. V., Castro, M. de, Kino, T., Elias, L. L. K., Bachega, T. A. S., et al. (2002). Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism, 87( 4), 1805-1809.
NLM
Mendonça BB de, Leite MV, Castro M de, Kino T, Elias LLK, Bachega TAS, Arnhold IJP, Chrousos GP, Latronico AC. Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 4): 1805-1809.[citado 2024 jun. 01 ]
Vancouver
Mendonça BB de, Leite MV, Castro M de, Kino T, Elias LLK, Bachega TAS, Arnhold IJP, Chrousos GP, Latronico AC. Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 4): 1805-1809.[citado 2024 jun. 01 ]

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