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Artigo de periodico
Pan-cancer analysis reveals that CTC1-STN1-TEN1 (CST) complex may have a key position in oncology (2022)
Santos, Gabriel Arantes dos; Viana, Nayara I; Pimenta, Ruan; Camargo, Juliana Alves de; Guimaraes, Vanessa R; Romao, Poliana; Candido, Patricia; Ghazarian, Vitoria; Reis, Sabrina T; Leite, Katia Ramos Moreira ; Srougi, Miguel
Source: Cancer genetics. Unidade: FM
Subjects: TELÔMERO, CROMOSSOMOS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Gabriel Arantes dos et al. Pan-cancer analysis reveals that CTC1-STN1-TEN1 (CST) complex may have a key position in oncology. Cancer genetics, v. 262, p. 80-90, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.cancergen.2022.01.006. Acesso em: 03 jun. 2024.
APA
Santos, G. A. dos, Viana, N. I., Pimenta, R., Camargo, J. A. de, Guimaraes, V. R., Romao, P., et al. (2022). Pan-cancer analysis reveals that CTC1-STN1-TEN1 (CST) complex may have a key position in oncology. Cancer genetics, 262, 80-90. doi:10.1016/j.cancergen.2022.01.006
NLM
Santos GA dos, Viana NI, Pimenta R, Camargo JA de, Guimaraes VR, Romao P, Candido P, Ghazarian V, Reis ST, Leite KRM, Srougi M. Pan-cancer analysis reveals that CTC1-STN1-TEN1 (CST) complex may have a key position in oncology [Internet]. Cancer genetics. 2022 ; 262 80-90.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.cancergen.2022.01.006
Vancouver
Santos GA dos, Viana NI, Pimenta R, Camargo JA de, Guimaraes VR, Romao P, Candido P, Ghazarian V, Reis ST, Leite KRM, Srougi M. Pan-cancer analysis reveals that CTC1-STN1-TEN1 (CST) complex may have a key position in oncology [Internet]. Cancer genetics. 2022 ; 262 80-90.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.cancergen.2022.01.006
Artigo de periodico-carta/editorial
Stem cell factor receptor gene mutation [Carta]: achalasia, mastocytosis and gastrointestinal stromal tumors (2020)
Tustumi, Francisco; Szor, Daniel Jose; Sallum, Rubens Antonio Aissar; Cecconello, Ivan
Source: Cancer genetics. Unidade: FM
Subjects: ACALÁSIA ESOFÁGICA, NEOPLASIAS DO TECIDO CONJUNTIVO, MASTÓCITOS, MUTAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TUSTUMI, Francisco et al. Stem cell factor receptor gene mutation [Carta]: achalasia, mastocytosis and gastrointestinal stromal tumors. Cancer genetics. New York: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.cancergen.2019.11.006. Acesso em: 03 jun. 2024. , 2020
APA
Tustumi, F., Szor, D. J., Sallum, R. A. A., & Cecconello, I. (2020). Stem cell factor receptor gene mutation [Carta]: achalasia, mastocytosis and gastrointestinal stromal tumors. Cancer genetics. New York: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.cancergen.2019.11.006
NLM
Tustumi F, Szor DJ, Sallum RAA, Cecconello I. Stem cell factor receptor gene mutation [Carta]: achalasia, mastocytosis and gastrointestinal stromal tumors [Internet]. Cancer genetics. 2020 ; 241 66-66.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.cancergen.2019.11.006
Vancouver
Tustumi F, Szor DJ, Sallum RAA, Cecconello I. Stem cell factor receptor gene mutation [Carta]: achalasia, mastocytosis and gastrointestinal stromal tumors [Internet]. Cancer genetics. 2020 ; 241 66-66.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.cancergen.2019.11.006
Artigo de periodico
Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia (2018)
Silva, Marcela Cavalcante de Andrade; Rocha, Vanderson; Velloso, Elvira Deolinda Rodrigues Pereira
Source: Cancer genetics. Unidade: FM
Subjects: TROMBOCITOPENIA, LEUCEMIA, DOENÇAS GENÉTICAS, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Marcela Cavalcante de Andrade e ROCHA, Vanderson e VELLOSO, Elvira Deolinda Rodrigues Pereira. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia. Cancer genetics, v. 222, p. 32-37, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cancergen.2018.01.002. Acesso em: 03 jun. 2024.
APA
Silva, M. C. de A., Rocha, V., & Velloso, E. D. R. P. (2018). Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia. Cancer genetics, 222, 32-37. doi:10.1016/j.cancergen.2018.01.002
NLM
Silva MC de A, Rocha V, Velloso EDRP. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia [Internet]. Cancer genetics. 2018 ; 222 32-37.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.cancergen.2018.01.002
Vancouver
Silva MC de A, Rocha V, Velloso EDRP. Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia [Internet]. Cancer genetics. 2018 ; 222 32-37.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.cancergen.2018.01.002

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