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Artigo de periodico
Pathogenic TERT promoter variants in telomere diseases (2019)
Gutierrez-Rodrigues, Fernanda ; Donaires, Flávia Sacilotto ; Santos, André Luiz Pinto ; Vicente, Alana; Dillon, Laura W.; Clé, Diego Villa ; Santana, Bárbara Amélia Aparecida ; Pirooznia, Mehdi; Ibanez, Maria del Pilar F.; Townsley, Danielle M.; Kajigaya, Sachiko; Hourigan, Christopher S.; Cooper, James N.; Calado, Rodrigo Tocantins ; Young, Neal S.
Fonte: Genetics in Medicine. Unidade: FMRP
Assuntos: MEDULA ÓSSEA, TELÔMERO, FIBROSE PULMONAR
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ABNT
GUTIERREZ-RODRIGUES, Fernanda et al. Pathogenic TERT promoter variants in telomere diseases. Genetics in Medicine, v. 21, n. 7, p. 1594-1602, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41436-018-0385-x. Acesso em: 20 abr. 2024.
APA
Gutierrez-Rodrigues, F., Donaires, F. S., Santos, A. L. P., Vicente, A., Dillon, L. W., Clé, D. V., et al. (2019). Pathogenic TERT promoter variants in telomere diseases. Genetics in Medicine, 21( 7), 1594-1602. doi:10.1038/s41436-018-0385-x
NLM
Gutierrez-Rodrigues F, Donaires FS, Santos ALP, Vicente A, Dillon LW, Clé DV, Santana BAA, Pirooznia M, Ibanez M del PF, Townsley DM, Kajigaya S, Hourigan CS, Cooper JN, Calado RT, Young NS. Pathogenic TERT promoter variants in telomere diseases [Internet]. Genetics in Medicine. 2019 ; 21( 7): 1594-1602.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1038/s41436-018-0385-x
Vancouver
Gutierrez-Rodrigues F, Donaires FS, Santos ALP, Vicente A, Dillon LW, Clé DV, Santana BAA, Pirooznia M, Ibanez M del PF, Townsley DM, Kajigaya S, Hourigan CS, Cooper JN, Calado RT, Young NS. Pathogenic TERT promoter variants in telomere diseases [Internet]. Genetics in Medicine. 2019 ; 21( 7): 1594-1602.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1038/s41436-018-0385-x
Artigo de periodico
A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation (2019)
Gutierrez-Rodrigues, Fernanda ; Masri, Nohad; Chouery, Eliane; Diamond, Carrie; Jalkh, Nadine; Vicente, Alana; Kajigaya, Sachiko; Abillama, Fayez; Bejjani, Noha; Serhal, Wassim; Calado, Rodrigo Tocantins ; Young, Neal S.; Farhat, Hussein; Coussa, Marie Louise
Fonte: Human Genetics. Unidade: FMRP
Assuntos: HEMATOLOGIA, TELÔMERO, FENÓTIPOS, GENÉTICA
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ABNT
GUTIERREZ-RODRIGUES, Fernanda et al. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation. Human Genetics, v. 138, n. 11-12, p. 1323-1330, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00439-019-02076-8. Acesso em: 20 abr. 2024.
APA
Gutierrez-Rodrigues, F., Masri, N., Chouery, E., Diamond, C., Jalkh, N., Vicente, A., et al. (2019). A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation. Human Genetics, 138( 11-12), 1323-1330. doi:10.1007/s00439-019-02076-8
NLM
Gutierrez-Rodrigues F, Masri N, Chouery E, Diamond C, Jalkh N, Vicente A, Kajigaya S, Abillama F, Bejjani N, Serhal W, Calado RT, Young NS, Farhat H, Coussa ML. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation [Internet]. Human Genetics. 2019 ; 138( 11-12): 1323-1330.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1007/s00439-019-02076-8
Vancouver
Gutierrez-Rodrigues F, Masri N, Chouery E, Diamond C, Jalkh N, Vicente A, Kajigaya S, Abillama F, Bejjani N, Serhal W, Calado RT, Young NS, Farhat H, Coussa ML. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation [Internet]. Human Genetics. 2019 ; 138( 11-12): 1323-1330.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1007/s00439-019-02076-8
Artigo de periodico
Telomerase enzyme deficiency promotes metabolic dysfunction in murine hepatocytes upon dietary stress (2018)
Paiva, Raquel de Melo Alves; Kajigaya, Sachiko; Feng, Xingmin; Chen, Jichun; Desierto, Marie J.; Wong, Susan; Townsley, Danielle M.; Donaires, Flávia Sacilotto; Bertola, Adeline; Gao, Bin; Young, Neal S.; Calado, Rodrigo Tocantins
Fonte: Liver International. Unidade: FMRP
Assuntos: FÍGADO GORDUROSO, METABOLISMO ENERGÉTICO, TELÔMERO, INIBIDORES DE ENZIMAS, ANIMAIS DE LABORATÓRIO
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ABNT
PAIVA, Raquel de Melo Alves et al. Telomerase enzyme deficiency promotes metabolic dysfunction in murine hepatocytes upon dietary stress. Liver International, v. 38, n. 1, p. 144-154, 2018Tradução . . Disponível em: https://doi.org/10.1111/liv.13529. Acesso em: 20 abr. 2024.
APA
Paiva, R. de M. A., Kajigaya, S., Feng, X., Chen, J., Desierto, M. J., Wong, S., et al. (2018). Telomerase enzyme deficiency promotes metabolic dysfunction in murine hepatocytes upon dietary stress. Liver International, 38( 1), 144-154. doi:10.1111/liv.13529
NLM
Paiva R de MA, Kajigaya S, Feng X, Chen J, Desierto MJ, Wong S, Townsley DM, Donaires FS, Bertola A, Gao B, Young NS, Calado RT. Telomerase enzyme deficiency promotes metabolic dysfunction in murine hepatocytes upon dietary stress [Internet]. Liver International. 2018 ; 38( 1): 144-154.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1111/liv.13529
Vancouver
Paiva R de MA, Kajigaya S, Feng X, Chen J, Desierto MJ, Wong S, Townsley DM, Donaires FS, Bertola A, Gao B, Young NS, Calado RT. Telomerase enzyme deficiency promotes metabolic dysfunction in murine hepatocytes upon dietary stress [Internet]. Liver International. 2018 ; 38( 1): 144-154.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1111/liv.13529
Artigo de periodico
Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms (2018)
Marsh, Judith C. W. ; Gutierrez-Rodrigues, Fernanda ; Cooper, James; Jiang, Jie; Gandhi, Shreyans; Kajigaya, Sachiko; Feng, Xingmin; Ibanez, Maria del Pilar F.; Donaires, Flávia Sacilotto ; Silva, João Paulo Lopes da ; Li, Zejuan; Das, Soma; Ibanez, Maria; Smith, Alexander E.; Lea, Nicholas; Best, Steven; Ireland, Robin; Kulasekararaj, Austin G.; McLornan, Donal P.; Pagliuca, Anthony ; Callebaut, Isabelle ; Young, Neal S.; Calado, Rodrigo Tocantins ; Townsley, Danielle M.; Mufti, Ghulam J.
Fonte: Blood Advances. Unidade: FMRP
Assuntos: NEOPLASIAS, MEDULA ÓSSEA, TELÔMERO, DOENÇAS
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ABNT
MARSH, Judith C. W. et al. Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms. Blood Advances, v. 2, n. 1, p. 36-48, 2018Tradução . . Disponível em: https://doi.org/10.1182/bloodadvances.2017008110. Acesso em: 20 abr. 2024.
APA
Marsh, J. C. W., Gutierrez-Rodrigues, F., Cooper, J., Jiang, J., Gandhi, S., Kajigaya, S., et al. (2018). Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms. Blood Advances, 2( 1), 36-48. doi:10.1182/bloodadvances.2017008110
NLM
Marsh JCW, Gutierrez-Rodrigues F, Cooper J, Jiang J, Gandhi S, Kajigaya S, Feng X, Ibanez M del PF, Donaires FS, Silva JPL da, Li Z, Das S, Ibanez M, Smith AE, Lea N, Best S, Ireland R, Kulasekararaj AG, McLornan DP, Pagliuca A, Callebaut I, Young NS, Calado RT, Townsley DM, Mufti GJ. Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms [Internet]. Blood Advances. 2018 ; 2( 1): 36-48.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1182/bloodadvances.2017008110
Vancouver
Marsh JCW, Gutierrez-Rodrigues F, Cooper J, Jiang J, Gandhi S, Kajigaya S, Feng X, Ibanez M del PF, Donaires FS, Silva JPL da, Li Z, Das S, Ibanez M, Smith AE, Lea N, Best S, Ireland R, Kulasekararaj AG, McLornan DP, Pagliuca A, Callebaut I, Young NS, Calado RT, Townsley DM, Mufti GJ. Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms [Internet]. Blood Advances. 2018 ; 2( 1): 36-48.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1182/bloodadvances.2017008110
Artigo de periodico
Danazol treatment for telomere diseases (2016)
Townsley, Danielle M.; Dumitriu, Bogdan; Liu, Delong; Biancotto, Angélique; Weinstein, Barbara; Chen, Christina; Hardy, Nathan; Mihalek, Andrew D.; Lingala, Shilpa; Kim, Yun Ju; Yao, Jianhua; Jones, Elizabeth; Gochuico, Bernadette R.; Heller, Theo; Wu, Colin O.; Calado, Rodrigo Tocantins; Scheinberg, Phillip; Young, Neal S.
Fonte: New England Journal of Medicine. Unidade: FMRP
Assuntos: DOENÇAS DA MEDULA ÓSSEA, CIRROSE HEPÁTICA, FIBROSE PULMONAR, ESTRÓGENOS, TELÔMERO
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ABNT
TOWNSLEY, Danielle M. et al. Danazol treatment for telomere diseases. New England Journal of Medicine, v. 374, n. 20, p. 1922-1931, 2016Tradução . . Disponível em: https://doi.org/10.1056/NEJMoa1515319. Acesso em: 20 abr. 2024.
APA
Townsley, D. M., Dumitriu, B., Liu, D., Biancotto, A., Weinstein, B., Chen, C., et al. (2016). Danazol treatment for telomere diseases. New England Journal of Medicine, 374( 20), 1922-1931. doi:10.1056/NEJMoa1515319
NLM
Townsley DM, Dumitriu B, Liu D, Biancotto A, Weinstein B, Chen C, Hardy N, Mihalek AD, Lingala S, Kim YJ, Yao J, Jones E, Gochuico BR, Heller T, Wu CO, Calado RT, Scheinberg P, Young NS. Danazol treatment for telomere diseases [Internet]. New England Journal of Medicine. 2016 ; 374( 20): 1922-1931.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1056/NEJMoa1515319
Vancouver
Townsley DM, Dumitriu B, Liu D, Biancotto A, Weinstein B, Chen C, Hardy N, Mihalek AD, Lingala S, Kim YJ, Yao J, Jones E, Gochuico BR, Heller T, Wu CO, Calado RT, Scheinberg P, Young NS. Danazol treatment for telomere diseases [Internet]. New England Journal of Medicine. 2016 ; 374( 20): 1922-1931.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1056/NEJMoa1515319
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.
Fonte: Abstracts & Program. Nome do evento: Annual Meeting and Exposition of American Society of Hematology (ASH). Unidade: FMRP
Assuntos: 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: 20 abr. 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 abr. 20 ]
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 abr. 20 ]
Artigo de periodico
Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas (2014)
Zhang, Yuwei; Calado, Rodrigo do Tocantins; Rao, Makadev; Hong, Julie A.; Meeker, Alan K.; Dumitriu, Bogdan; Atay, Scott; McCormick, Peter J.; Garfield, Susan H.; Wangsa, Danny; Padilla-Nash, Hesed M.; Burkett, Sandra; Zhang, Mary; Kunst, Tricia F.; Peterson, Nathan R.; Xi, Sichuan; Inchauste, Suzanne; Altorki, Nasser K.; Casson, Alan G.; Beer, David G.; Harris, Curtis C.; Ried, Thomas; Young, Neal S.; Schrump, David S.
Fonte: PLOS ONE. Unidade: FMRP
Assuntos: CARCINOMA (GENÉTICA), NEOPLASIAS GÁSTRICAS (GENÉTICA)
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ABNT
ZHANG, Yuwei et al. Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas. PLOS ONE, v. 9, n. 7, p. e101010-1 - e101010-15, 2014Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0101010. Acesso em: 20 abr. 2024.
APA
Zhang, Y., Calado, R. do T., Rao, M., Hong, J. A., Meeker, A. K., Dumitriu, B., et al. (2014). Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas. PLOS ONE, 9( 7), e101010-1 - e101010-15. doi:10.1371/journal.pone.0101010
NLM
Zhang Y, Calado R do T, Rao M, Hong JA, Meeker AK, Dumitriu B, Atay S, McCormick PJ, Garfield SH, Wangsa D, Padilla-Nash HM, Burkett S, Zhang M, Kunst TF, Peterson NR, Xi S, Inchauste S, Altorki NK, Casson AG, Beer DG, Harris CC, Ried T, Young NS, Schrump DS. Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas [Internet]. PLOS ONE. 2014 ; 9( 7): e101010-1 - e101010-15.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1371/journal.pone.0101010
Vancouver
Zhang Y, Calado R do T, Rao M, Hong JA, Meeker AK, Dumitriu B, Atay S, McCormick PJ, Garfield SH, Wangsa D, Padilla-Nash HM, Burkett S, Zhang M, Kunst TF, Peterson NR, Xi S, Inchauste S, Altorki NK, Casson AG, Beer DG, Harris CC, Ried T, Young NS, Schrump DS. Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas [Internet]. PLOS ONE. 2014 ; 9( 7): e101010-1 - e101010-15.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1371/journal.pone.0101010
Artigo de periodico-carta/editorial
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta] (2013)
Aalbers, Anna M.; Calado, Rodrigo Tocantins; Young, Neal S.; Zwaan, C. Michel; Kajigaya, Sachiko; Baruchel, André; Geleijns, Karin; Haas, Valerie de; Kaspers, Gertjan J. L.; Reinhardt, Dirk; Trka, Jan; Kuijpers, Taco W.; Pieters, Rob; Velden, Vincent H. J. van der; Heuvel-Eibrink, Marry M. van den
Fonte: British Journal of Haematology. Unidade: FMRP
Assuntos: LEUCEMIA MIELOIDE AGUDA, MUTAÇÃO GENÉTICA, CRIANÇAS
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ABNT
AALBERS, Anna M. et al. Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]. British Journal of Haematology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/bjh.12134. Acesso em: 20 abr. 2024. , 2013
APA
Aalbers, A. M., Calado, R. T., Young, N. S., Zwaan, C. M., Kajigaya, S., Baruchel, A., et al. (2013). Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta]. British Journal of Haematology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/bjh.12134
NLM
Aalbers AM, Calado RT, Young NS, Zwaan CM, Kajigaya S, Baruchel A, Geleijns K, Haas V de, Kaspers GJL, Reinhardt D, Trka J, Kuijpers TW, Pieters R, Velden VHJ van der, Heuvel-Eibrink MM van den. Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta] [Internet]. British Journal of Haematology. 2013 ; 160( 4): 559-561.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1111/bjh.12134
Vancouver
Aalbers AM, Calado RT, Young NS, Zwaan CM, Kajigaya S, Baruchel A, Geleijns K, Haas V de, Kaspers GJL, Reinhardt D, Trka J, Kuijpers TW, Pieters R, Velden VHJ van der, Heuvel-Eibrink MM van den. Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia. [Carta] [Internet]. British Journal of Haematology. 2013 ; 160( 4): 559-561.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1111/bjh.12134
Artigo de periodico
Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs (2013)
Winkler, Thomas; Hong, So Gun; Decker, Jake E.; Morgan, Mary J.; Wu, Chuafeng; Hughes, William M.; Yang, Yanqin; Wangsa, Danny; Padilla-Nash, Hesed M.; Ried, Thomas; Young, Neal S.; Dunbar, Cynthia E.; Calado, Rodrigo Tocantins
Fonte: Journal of Clinical Investigation. Unidade: FMRP
Assuntos: ANEMIA, DIFERENCIAÇÃO CELULAR, FIBROBLASTOS (CITOLOGIA), CÉLULAS-TRONCO, LEUCÓCITOS
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ABNT
WINKLER, Thomas et al. Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs. Journal of Clinical Investigation, v. 123, n. 5, p. 1952-1963, 2013Tradução . . Disponível em: https://doi.org/10.1172/JCI67146. Acesso em: 20 abr. 2024.
APA
Winkler, T., Hong, S. G., Decker, J. E., Morgan, M. J., Wu, C., Hughes, W. M., et al. (2013). Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs. Journal of Clinical Investigation, 123( 5), 1952-1963. doi:10.1172/JCI67146
NLM
Winkler T, Hong SG, Decker JE, Morgan MJ, Wu C, Hughes WM, Yang Y, Wangsa D, Padilla-Nash HM, Ried T, Young NS, Dunbar CE, Calado RT. Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs [Internet]. Journal of Clinical Investigation. 2013 ; 123( 5): 1952-1963.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1172/JCI67146
Vancouver
Winkler T, Hong SG, Decker JE, Morgan MJ, Wu C, Hughes WM, Yang Y, Wangsa D, Padilla-Nash HM, Ried T, Young NS, Dunbar CE, Calado RT. Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs [Internet]. Journal of Clinical Investigation. 2013 ; 123( 5): 1952-1963.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1172/JCI67146
Trabalho de evento-resumo
Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis (2013)
Alves-Paiva, Raquel M.; Bertola, Adeline; Chen, Jichun; Townsley, Danielle; Dumitriu, Bogdan; Kajigaya, Sachiko; Young, Neal S.; Gao, Bin; Calado, Rodrigo Tocantins
Fonte: Abstracts. Nome do evento: Meeting on Telomeres and Telomerase. Unidade: FMRP
Assuntos: HEMATOLOGIA, ENZIMOLOGIA
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ABNT
ALVES-PAIVA, Raquel M. et al. Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis. 2013, Anais.. Cold Spring Harbor: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 20 abr. 2024.
APA
Alves-Paiva, R. M., Bertola, A., Chen, J., Townsley, D., Dumitriu, B., Kajigaya, S., et al. (2013). Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis. In Abstracts. Cold Spring Harbor: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Alves-Paiva RM, Bertola A, Chen J, Townsley D, Dumitriu B, Kajigaya S, Young NS, Gao B, Calado RT. Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis. Abstracts. 2013 ;[citado 2024 abr. 20 ]
Vancouver
Alves-Paiva RM, Bertola A, Chen J, Townsley D, Dumitriu B, Kajigaya S, Young NS, Gao B, Calado RT. Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis. Abstracts. 2013 ;[citado 2024 abr. 20 ]
Artigo de periodico
Interphase chromossome flow-fish (2012)
Keyvanfar, Keyvan; Weed, Janson; Swamy, Prashanth; Kajigaya, Sashiko; Calado, Rodrigo Tocantins; Young, Neal S.
Fonte: Blood. Unidade: FMRP
Assuntos: 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: 20 abr. 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 abr. 20 ] 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 abr. 20 ] 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.
Fonte: Blood. Unidade: FMRP
Assuntos: 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: 20 abr. 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 abr. 20 ] 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 abr. 20 ] Available from: https://doi.org/10.1182/blood-2011-10-383182
Trabalho de evento-resumo periodico
Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia (2012)
Aalbers, Anna M.; Calado, Rodrigo Tocantins; Young, Neal S.; Zwaan, Christian M.; Wu, Colin O.; Kajigaya, Sachiko; Coenen, Eva A.; Baruchel, André; Geleijns, Karin; Haas, Valerie de; Kaspers, Gertjan J. L.; Kuijpers, Taco W.; Reinhardt, Dirk; Trka, Jan; Zimmermann, Martin; Pieters, Rob; van der Velden, Vincent H. J.; van den Heuvel-Eibrink, Marry M.
Fonte: Blood. Nome do evento: Annual Meeting of the American Society of Hematology (ASH). Unidade: FMRP
Assuntos: LEUCEMIA, CRIANÇAS, MUTAÇÃO GENÉTICA, CÉLULAS SANGUÍNEAS
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ABNT
AALBERS, Anna M. et al. Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 20 abr. 2024. , 2012
APA
Aalbers, A. M., Calado, R. T., Young, N. S., Zwaan, C. M., Wu, C. O., Kajigaya, S., et al. (2012). Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Aalbers AM, Calado RT, Young NS, Zwaan CM, Wu CO, Kajigaya S, Coenen EA, Baruchel A, Geleijns K, Haas V de, Kaspers GJL, Kuijpers TW, Reinhardt D, Trka J, Zimmermann M, Pieters R, van der Velden VHJ, van den Heuvel-Eibrink MM. Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia. Blood. 2012 ; 120( 21):[citado 2024 abr. 20 ]
Vancouver
Aalbers AM, Calado RT, Young NS, Zwaan CM, Wu CO, Kajigaya S, Coenen EA, Baruchel A, Geleijns K, Haas V de, Kaspers GJL, Kuijpers TW, Reinhardt D, Trka J, Zimmermann M, Pieters R, van der Velden VHJ, van den Heuvel-Eibrink MM. Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia. Blood. 2012 ; 120( 21):[citado 2024 abr. 20 ]
Trabalho de evento-resumo periodico
Androgen treatment mitigates hematopoietic cell telomere attrition in vivo (2012)
Chen, Jichun; Desierto, Marie J.; Dent, James J.; Bachman, Maria J.; Calado, Rodrigo Tocantins; Stratakis, Constantine A.; Young, Neal S.
Fonte: Blood. Nome do evento: Annual Meeting of the American Society of Hematology (ASH). Unidade: FMRP
Assuntos: CÉLULAS SANGUÍNEAS, MEDULA ÓSSEA, HORMÔNIOS SEXUAIS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHEN, Jichun et al. Androgen treatment mitigates hematopoietic cell telomere attrition in vivo. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 20 abr. 2024. , 2012
APA
Chen, J., Desierto, M. J., Dent, J. J., Bachman, M. J., Calado, R. T., Stratakis, C. A., & Young, N. S. (2012). Androgen treatment mitigates hematopoietic cell telomere attrition in vivo. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Chen J, Desierto MJ, Dent JJ, Bachman MJ, Calado RT, Stratakis CA, Young NS. Androgen treatment mitigates hematopoietic cell telomere attrition in vivo. Blood. 2012 ; 120( 21):[citado 2024 abr. 20 ]
Vancouver
Chen J, Desierto MJ, Dent JJ, Bachman MJ, Calado RT, Stratakis CA, Young NS. Androgen treatment mitigates hematopoietic cell telomere attrition in vivo. Blood. 2012 ; 120( 21):[citado 2024 abr. 20 ]
Artigo de periodico
Telomeres in disease (2012)
Calado, Rodrigo Tocantins; Young, Neal S.
Fonte: F1000 Medicine Reports. Unidade: FMRP
Assuntos: GENÉTICA MÉDICA, GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALADO, Rodrigo Tocantins e YOUNG, Neal S. Telomeres in disease. F1000 Medicine Reports, v. 4, 2012Tradução . . Disponível em: https://doi.org/10.3410/M4-8. Acesso em: 20 abr. 2024.
APA
Calado, R. T., & Young, N. S. (2012). Telomeres in disease. F1000 Medicine Reports, 4. doi:10.3410/M4-8
NLM
Calado RT, Young NS. Telomeres in disease [Internet]. F1000 Medicine Reports. 2012 ; 4[citado 2024 abr. 20 ] Available from: https://doi.org/10.3410/M4-8
Vancouver
Calado RT, Young NS. Telomeres in disease [Internet]. F1000 Medicine Reports. 2012 ; 4[citado 2024 abr. 20 ] Available from: https://doi.org/10.3410/M4-8
Trabalho de evento-resumo
Telomere dynamics in iPS cells derived from human patients with telomerase mutations (2011)
Decker, Jake E.; Hong, So Gun; Winkler, Thomas; Wu, Chuanfeng; Dunbar, Cynthia E.; Calado, Rodrigo Tocantins; Young, Neal S.
Fonte: Abstracts. Nome do evento: Meeting of the Telomeres & Telomerase. Unidade: FMRP
Assuntos: CROMOSSOMOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DECKER, Jake E. et al. Telomere dynamics in iPS cells derived from human patients with telomerase mutations. 2011, Anais.. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2011. . Acesso em: 20 abr. 2024.
APA
Decker, J. E., Hong, S. G., Winkler, T., Wu, C., Dunbar, C. E., Calado, R. T., & Young, N. S. (2011). Telomere dynamics in iPS cells derived from human patients with telomerase mutations. In Abstracts. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Decker JE, Hong SG, Winkler T, Wu C, Dunbar CE, Calado RT, Young NS. Telomere dynamics in iPS cells derived from human patients with telomerase mutations. Abstracts. 2011 ;[citado 2024 abr. 20 ]
Vancouver
Decker JE, Hong SG, Winkler T, Wu C, Dunbar CE, Calado RT, Young NS. Telomere dynamics in iPS cells derived from human patients with telomerase mutations. Abstracts. 2011 ;[citado 2024 abr. 20 ]
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
Fonte: Blood. Nome do evento: Annual Meeting and Exposition of the American Society of Hematology (ASH). Unidade: FMRP
Assuntos: ENZIMAS, CROMOSSOMOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 20 abr. 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 abr. 20 ]
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 abr. 20 ]
Trabalho de evento-resumo
A mutation in the CCAAT box of the TERC promoter region causes telomere disease (2011)
Aalbers, Anna M.; Kajigaya, Sachiko; Heuvel, Marry M. van den; Velden, Vincent van der; Zwaan, Michel; Pieters, Rob; Calado, Rodrigo T.; Young, Neal S.
Fonte: Abstracts. Nome do evento: Meeting of the Telomeres & Telomerase. Unidade: FMRP
Assuntos: CROMOSSOMOS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AALBERS, Anna M. et al. A mutation in the CCAAT box of the TERC promoter region causes telomere disease. 2011, Anais.. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2011. . Acesso em: 20 abr. 2024.
APA
Aalbers, A. M., Kajigaya, S., Heuvel, M. M. van den, Velden, V. van der, Zwaan, M., Pieters, R., et al. (2011). A mutation in the CCAAT box of the TERC promoter region causes telomere disease. In Abstracts. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Aalbers AM, Kajigaya S, Heuvel MM van den, Velden V van der, Zwaan M, Pieters R, Calado RT, Young NS. A mutation in the CCAAT box of the TERC promoter region causes telomere disease. Abstracts. 2011 ;[citado 2024 abr. 20 ]
Vancouver
Aalbers AM, Kajigaya S, Heuvel MM van den, Velden V van der, Zwaan M, Pieters R, Calado RT, Young NS. A mutation in the CCAAT box of the TERC promoter region causes telomere disease. Abstracts. 2011 ;[citado 2024 abr. 20 ]
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.
Fonte: Hepatology. Unidade: FMRP
Assuntos: CIRROSE HEPÁTICA, LEUCÓCITOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 20 abr. 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 abr. 20 ] 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 abr. 20 ] Available from: https://doi.org/10.1002/hep.24173
Artigo de periodico
Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia (2009)
Calado, Rodrigo Tocantins; Regal, Joshua A.; Hills, Mark; Yewdell, William T.; Dalmazzo, Leandro F.; Zago, Marco Antonio; Lansdorp, Peter M.; Hogge, Donna; Chanock, Stephen J.; Estey, Elihu H.; Falcao, Roberto Passetto; Young, Neal S.
Fonte: Proceedings of the National Academy of Sciences. Unidade: FMRP
Assuntos: NEOPLASIAS, LEUCEMIA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALADO, Rodrigo Tocantins et al. Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. Proceedings of the National Academy of Sciences, v. 106, n. 4, p. 1187-1192, 2009Tradução . . Disponível em: https://doi.org/10.1073/pnas.0807057106. Acesso em: 20 abr. 2024.
APA
Calado, R. T., Regal, J. A., Hills, M., Yewdell, W. T., Dalmazzo, L. F., Zago, M. A., et al. (2009). Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. Proceedings of the National Academy of Sciences, 106( 4), 1187-1192. doi:10.1073/pnas.0807057106
NLM
Calado RT, Regal JA, Hills M, Yewdell WT, Dalmazzo LF, Zago MA, Lansdorp PM, Hogge D, Chanock SJ, Estey EH, Falcao RP, Young NS. Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia [Internet]. Proceedings of the National Academy of Sciences. 2009 ; 106( 4): 1187-1192.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1073/pnas.0807057106
Vancouver
Calado RT, Regal JA, Hills M, Yewdell WT, Dalmazzo LF, Zago MA, Lansdorp PM, Hogge D, Chanock SJ, Estey EH, Falcao RP, Young NS. Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia [Internet]. Proceedings of the National Academy of Sciences. 2009 ; 106( 4): 1187-1192.[citado 2024 abr. 20 ] Available from: https://doi.org/10.1073/pnas.0807057106

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