ReP USP - Resultado da busca

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.
Source: Genetics in Medicine. Unidade: FMRP
Subjects: MEDULA ÓSSEA, TELÔMERO, FIBROSE PULMONAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] 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
Source: Human Genetics. Unidade: FMRP
Subjects: HEMATOLOGIA, TELÔMERO, FENÓTIPOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] 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
Source: Liver International. Unidade: FMRP
Subjects: FÍGADO GORDUROSO, METABOLISMO ENERGÉTICO, TELÔMERO, INIBIDORES DE ENZIMAS, ANIMAIS DE LABORATÓRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] 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.
Source: Blood Advances. Unidade: FMRP
Subjects: NEOPLASIAS, MEDULA ÓSSEA, TELÔMERO, DOENÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1182/bloodadvances.2017008110
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1186/1471-2350-15-68
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
Source: British Journal of Haematology. Unidade: FMRP
Subjects: LEUCEMIA MIELOIDE AGUDA, MUTAÇÃO GENÉTICA, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1111/bjh.12134
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
Source: Abstracts. Conference titles: Meeting on Telomeres and Telomerase. Unidade: FMRP
Subjects: HEMATOLOGIA, ENZIMOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ]
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 nov. 08 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ] 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 nov. 08 ] 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.
Source: Blood. Conference titles: Annual Meeting of the American Society of Hematology (ASH). Unidade: FMRP
Subjects: LEUCEMIA, CRIANÇAS, MUTAÇÃO GENÉTICA, CÉLULAS SANGUÍNEAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 08 nov. 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 nov. 08 ]
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 nov. 08 ]
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.
Source: Abstracts. Conference titles: Meeting of the Telomeres & Telomerase. Unidade: FMRP
Subjects: 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: 08 nov. 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 nov. 08 ]
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 nov. 08 ]

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Date published

Subjects

Source title

Funding Agencies

Indexado em

Non normalized affiliation

Countries of institutions of collaboration