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Artigo de periodico
Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord (2015)
Wang, Yuxuan; Springer, Simeon; Zhang, Ming; McMahon, K. Wyatt; Kinde, Isaac; Dobbyn, Lisa; Ptak, Janine; Brem, Henry; Chaichana, Kaisorn; Gallia, Gary L.; Gokaslan, Ziya L.; Groves, Mari L.; Jallo, George I.; Lim, Michael; Olivi, Alessandro; Quinones-Hinojosa, Alfredo; Rigamonti, Daniele; Riggins, Greg J.; Sciubba, Daniel M.; Weingart, Jon D.; Wolinsky, Jean-Paul; Ye, Xiaobu; Oba-Shinjo, Sueli Mieko; Marie, Suely K. N.; Holdhoff, Matthias; Agrawal, Nishant; Diaz Jr., Luis A.; Papadopoulos, Nickolas; Kinzler, Kenneth W.; Vogelstein, Bert; Bettegowa, Chetan
Fonte: Proceedings of the National Academy of Sciences of the United States of America. Unidade: FM
Assuntos: DNA, NEOPLASIAS DA MEDULA ESPINHAL, BIOMARCADORES, LÍQUIDO CEFALORRAQUIDIANO, NEOPLASIAS CEREBRAIS
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ABNT
WANG, Yuxuan et al. Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord. Proceedings of the National Academy of Sciences of the United States of America, v. 112, n. 31, p. 9704-9709, 2015Tradução . . Disponível em: https://doi.org/10.1073/pnas.1511694112. Acesso em: 03 nov. 2025.
APA
Wang, Y., Springer, S., Zhang, M., McMahon, K. W., Kinde, I., Dobbyn, L., et al. (2015). Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord. Proceedings of the National Academy of Sciences of the United States of America, 112( 31), 9704-9709. doi:10.1073/pnas.1511694112
NLM
Wang Y, Springer S, Zhang M, McMahon KW, Kinde I, Dobbyn L, Ptak J, Brem H, Chaichana K, Gallia GL, Gokaslan ZL, Groves ML, Jallo GI, Lim M, Olivi A, Quinones-Hinojosa A, Rigamonti D, Riggins GJ, Sciubba DM, Weingart JD, Wolinsky J-P, Ye X, Oba-Shinjo SM, Marie SKN, Holdhoff M, Agrawal N, Diaz Jr. LA, Papadopoulos N, Kinzler KW, Vogelstein B, Bettegowa C. Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord [Internet]. Proceedings of the National Academy of Sciences of the United States of America. 2015 ; 112( 31): 9704-9709.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1073/pnas.1511694112
Vancouver
Wang Y, Springer S, Zhang M, McMahon KW, Kinde I, Dobbyn L, Ptak J, Brem H, Chaichana K, Gallia GL, Gokaslan ZL, Groves ML, Jallo GI, Lim M, Olivi A, Quinones-Hinojosa A, Rigamonti D, Riggins GJ, Sciubba DM, Weingart JD, Wolinsky J-P, Ye X, Oba-Shinjo SM, Marie SKN, Holdhoff M, Agrawal N, Diaz Jr. LA, Papadopoulos N, Kinzler KW, Vogelstein B, Bettegowa C. Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord [Internet]. Proceedings of the National Academy of Sciences of the United States of America. 2015 ; 112( 31): 9704-9709.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1073/pnas.1511694112
Artigo de periodico
Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS (2013)
Agrawal, Nishant; Jiao, Yuchen; Sausen, Mark; Leary, Rebecca; Bettegowda, Chetan; Roberts, Nicholas J; Bhan, Sheetal; Ho, Allen S; Khan, Zubair; Bishop, Justin; Westra, William H; Wood, Laura D; Hruban, Ralph H; Tufano, Ralph P; Robinson, Bruce; Dralle, Henning; Toledo, Sergio Pereira Almeida; Toledo, Rodrigo A; Morris, Luc G T; Ghossein, Ronald A; Fagin, James A; Chan, Timothy A; Velculescu, Victor E; Vogelstein, Bert; Kinzler, Kenneth W; Papadopoulos, Nickolas; Nelkin, Barry D; Ball, Douglas W
Fonte: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Assuntos: NEOPLASIAS DA TIREOIDE (QUIMIOTERAPIA;RADIOTERAPIA), CARCINOMA MEDULAR, MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO, DOENÇAS HEREDITÁRIAS, REAÇÃO EM CADEIA POR POLIMERASE
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ABNT
AGRAWAL, Nishant et al. Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS. The Journal of Clinical Endocrinology & Metabolism, v. 98, n. 2, p. E364-E369, 2013Tradução . . Disponível em: https://doi.org/10.1210/jc.2012-2703. Acesso em: 03 nov. 2025.
APA
Agrawal, N., Jiao, Y., Sausen, M., Leary, R., Bettegowda, C., Roberts, N. J., et al. (2013). Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS. The Journal of Clinical Endocrinology & Metabolism, 98( 2), E364-E369. doi:10.1210/jc.2012-2703
NLM
Agrawal N, Jiao Y, Sausen M, Leary R, Bettegowda C, Roberts NJ, Bhan S, Ho AS, Khan Z, Bishop J, Westra WH, Wood LD, Hruban RH, Tufano RP, Robinson B, Dralle H, Toledo SPA, Toledo RA, Morris LGT, Ghossein RA, Fagin JA, Chan TA, Velculescu VE, Vogelstein B, Kinzler KW, Papadopoulos N, Nelkin BD, Ball DW. Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2013 ; 98( 2): E364-E369.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1210/jc.2012-2703
Vancouver
Agrawal N, Jiao Y, Sausen M, Leary R, Bettegowda C, Roberts NJ, Bhan S, Ho AS, Khan Z, Bishop J, Westra WH, Wood LD, Hruban RH, Tufano RP, Robinson B, Dralle H, Toledo SPA, Toledo RA, Morris LGT, Ghossein RA, Fagin JA, Chan TA, Velculescu VE, Vogelstein B, Kinzler KW, Papadopoulos N, Nelkin BD, Ball DW. Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2013 ; 98( 2): E364-E369.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1210/jc.2012-2703
Artigo de periodico
Exomic sequencing of four rare central nervous system tumor types (2013)
Bettegowda, Chetan; Agrawal, Nishant; Jiao, Yuchen; Wang, Yuxuan; Wood, Laura D; Rodriguez, Fausto J; Hruban, Ralph H; Gallia, Gary L; Binder, Zev A; Riggins, Calle J; Salmasi, Vafi; Riggins, Gregory J; Reitman, Zachary J; Rasheed, Ahmed; Keir, Stephen; Shinjo, Sueli Mieko Oba; Marie, Suely Kazue Nagahashi; McLendon, Roger; Jallo, George; Vogelstein, Bert; Bigner, Darell; Yan, Hai; Kinzler, Kenneth W; Papadopoulos, Nickolas
Fonte: Oncotarget. Unidade: FM
Assuntos: NEOPLASIAS DO SISTEMA NERVOSO (GENÉTICA;MORTALIDADE), SEQUENCIAMENTO GENÉTICO, NEOPLASIAS CEREBRAIS (GENÉTICA;MORTALIDADE), CRIANÇAS, MUTAÇÃO GENÉTICA, NEUROCIRURGIA, RESUMOS (EVENTOS)
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ABNT
BETTEGOWDA, Chetan et al. Exomic sequencing of four rare central nervous system tumor types. Oncotarget, v. 4, n. 4, p. 572-583, 2013Tradução . . Disponível em: http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path%5B%5D=964&path%5B%5D=1267. Acesso em: 03 nov. 2025.
APA
Bettegowda, C., Agrawal, N., Jiao, Y., Wang, Y., Wood, L. D., Rodriguez, F. J., et al. (2013). Exomic sequencing of four rare central nervous system tumor types. Oncotarget, 4( 4), 572-583. Recuperado de http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path%5B%5D=964&path%5B%5D=1267
NLM
Bettegowda C, Agrawal N, Jiao Y, Wang Y, Wood LD, Rodriguez FJ, Hruban RH, Gallia GL, Binder ZA, Riggins CJ, Salmasi V, Riggins GJ, Reitman ZJ, Rasheed A, Keir S, Shinjo SMO, Marie SKN, McLendon R, Jallo G, Vogelstein B, Bigner D, Yan H, Kinzler KW, Papadopoulos N. Exomic sequencing of four rare central nervous system tumor types [Internet]. Oncotarget. 2013 ;4( 4): 572-583.[citado 2025 nov. 03 ] Available from: http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path%5B%5D=964&path%5B%5D=1267
Vancouver
Bettegowda C, Agrawal N, Jiao Y, Wang Y, Wood LD, Rodriguez FJ, Hruban RH, Gallia GL, Binder ZA, Riggins CJ, Salmasi V, Riggins GJ, Reitman ZJ, Rasheed A, Keir S, Shinjo SMO, Marie SKN, McLendon R, Jallo G, Vogelstein B, Bigner D, Yan H, Kinzler KW, Papadopoulos N. Exomic sequencing of four rare central nervous system tumor types [Internet]. Oncotarget. 2013 ;4( 4): 572-583.[citado 2025 nov. 03 ] Available from: http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path%5B%5D=964&path%5B%5D=1267
Artigo de periodico
Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers (2013)
Kinde, Isaac; Bettegowda, Chetan; Wang, Yuxuan; Wu, Jian; Agrawal, Nishant; Shih, Ie-Ming; Kurman, Robert; Dao, Fanny; Levine, Douglas A.; Giuntoli, Robert; Roden, Richard; Eshleman, James R.; Carvalho, Jesus Paula; Marie, Suely Kazue Nagahashi; Papadopoulos, Nickolas; Kinzler, Kenneth W.; Vogelstein, Bert; Diaz Jr., Luis A.
Fonte: Science Translational Medicine. Unidade: FM
Assuntos: DNA (AVALIAÇÃO), GENÓTIPOS, NEOPLASIAS OVARIANAS, ENDOMÉTRIO (PATOLOGIA), NEOPLASIAS UTERINAS
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ABNT
KINDE, Isaac et al. Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers. Science Translational Medicine, v. 5, n. 167, p. 167ra4, 2013Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.3004952. Acesso em: 03 nov. 2025.
APA
Kinde, I., Bettegowda, C., Wang, Y., Wu, J., Agrawal, N., Shih, I. -M., et al. (2013). Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers. Science Translational Medicine, 5( 167), 167ra4. doi:10.1126/scitranslmed.3004952
NLM
Kinde I, Bettegowda C, Wang Y, Wu J, Agrawal N, Shih I-M, Kurman R, Dao F, Levine DA, Giuntoli R, Roden R, Eshleman JR, Carvalho JP, Marie SKN, Papadopoulos N, Kinzler KW, Vogelstein B, Diaz Jr. LA. Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers [Internet]. Science Translational Medicine. 2013 ; 5( 167): 167ra4.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1126/scitranslmed.3004952
Vancouver
Kinde I, Bettegowda C, Wang Y, Wu J, Agrawal N, Shih I-M, Kurman R, Dao F, Levine DA, Giuntoli R, Roden R, Eshleman JR, Carvalho JP, Marie SKN, Papadopoulos N, Kinzler KW, Vogelstein B, Diaz Jr. LA. Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers [Internet]. Science Translational Medicine. 2013 ; 5( 167): 167ra4.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1126/scitranslmed.3004952
Artigo de periodico
Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas (2012)
Jiao, Yuchen; Killela, Patrick J.; Reitman, Zachary J.; Rasheed, B. Ahmed; Heaphy, Christopher M.; Wilde, Roeland F. de; Rodriguez, Fausto J.; Rosemberg, Sergio; Oba-Shinjo, Sueli Meiko; Marie, Suely Kazue Nagahashi; Bettegowda, Chetan; Agrawal, Nishant; Lipp, Eric; Pirozzi, Christopher; Lopez, Giselle; He, Yiping; Friedman, Henry; Friedman, Allan H.; Riggins, Gregory J.; Holdhoff, Matthias; Burger, Peter; McLendon, Roger; Bigner, Darell D.; Vogelstein, Bert; Meeker, Alan K.; Kinzler, Kenneth W.; Papadopoulos, Nickolas; DiazJr., Luis A.; Yan, Hai
Fonte: Oncotarget. Unidade: FM
Assuntos: PROGNÓSTICO, MUTAÇÃO GENÉTICA, NEOPLASIAS CEREBRAIS (DIAGNÓSTICO), ASTRÓCITOS (PATOLOGIA)
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ABNT
JIAO, Yuchen et al. Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas. Oncotarget, v. 3, n. 7, p. 709-722, 2012Tradução . . Disponível em: https://doi.org/10.18632/oncotarget.588. Acesso em: 03 nov. 2025.
APA
Jiao, Y., Killela, P. J., Reitman, Z. J., Rasheed, B. A., Heaphy, C. M., Wilde, R. F. de, et al. (2012). Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas. Oncotarget, 3( 7), 709-722. doi:10.18632/oncotarget.588
NLM
Jiao Y, Killela PJ, Reitman ZJ, Rasheed BA, Heaphy CM, Wilde RF de, Rodriguez FJ, Rosemberg S, Oba-Shinjo SM, Marie SKN, Bettegowda C, Agrawal N, Lipp E, Pirozzi C, Lopez G, He Y, Friedman H, Friedman AH, Riggins GJ, Holdhoff M, Burger P, McLendon R, Bigner DD, Vogelstein B, Meeker AK, Kinzler KW, Papadopoulos N, DiazJr. LA, Yan H. Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas [Internet]. Oncotarget. 2012 ; 3( 7): 709-722.[citado 2025 nov. 03 ] Available from: https://doi.org/10.18632/oncotarget.588
Vancouver
Jiao Y, Killela PJ, Reitman ZJ, Rasheed BA, Heaphy CM, Wilde RF de, Rodriguez FJ, Rosemberg S, Oba-Shinjo SM, Marie SKN, Bettegowda C, Agrawal N, Lipp E, Pirozzi C, Lopez G, He Y, Friedman H, Friedman AH, Riggins GJ, Holdhoff M, Burger P, McLendon R, Bigner DD, Vogelstein B, Meeker AK, Kinzler KW, Papadopoulos N, DiazJr. LA, Yan H. Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas [Internet]. Oncotarget. 2012 ; 3( 7): 709-722.[citado 2025 nov. 03 ] Available from: https://doi.org/10.18632/oncotarget.588
Artigo de periodico
Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma (2011)
Bettegowda, Chetan; Agrawal, Nishant; Jiao, Yuchen; Sausen, Mark; Wood, Laura D.; Hruban, Ralph H.; Rodriguez, Fausto J.; Cahill, Daniel P.; McLendon, Roger; Riggins, Gregory; Velculescu, Victor E.; Oba-Shinjo, Sueli Mieko; Marie, Suely Kazue Nagahashi; Vogelstein, Bert; Bigner, Darell; Yan, Hai; Papadopoulos, Nickolas; Kinzler, Kenneth W.
Fonte: Science. Unidade: FM
Assuntos: NEOPLASIAS CEREBRAIS (PATOLOGIA), MUTAÇÃO GENÉTICA, NEOPLASIAS DE TECIDO NERVOSO (PATOLOGIA), BIOMARCADORES, GENES
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ABNT
BETTEGOWDA, Chetan et al. Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma. Science, v. 333, p. 1453-1455, 2011Tradução . . Disponível em: https://doi.org/10.1126/science.1210557. Acesso em: 03 nov. 2025.
APA
Bettegowda, C., Agrawal, N., Jiao, Y., Sausen, M., Wood, L. D., Hruban, R. H., et al. (2011). Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma. Science, 333, 1453-1455. doi:10.1126/science.1210557
NLM
Bettegowda C, Agrawal N, Jiao Y, Sausen M, Wood LD, Hruban RH, Rodriguez FJ, Cahill DP, McLendon R, Riggins G, Velculescu VE, Oba-Shinjo SM, Marie SKN, Vogelstein B, Bigner D, Yan H, Papadopoulos N, Kinzler KW. Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma [Internet]. Science. 2011 ; 333 1453-1455.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1126/science.1210557
Vancouver
Bettegowda C, Agrawal N, Jiao Y, Sausen M, Wood LD, Hruban RH, Rodriguez FJ, Cahill DP, McLendon R, Riggins G, Velculescu VE, Oba-Shinjo SM, Marie SKN, Vogelstein B, Bigner D, Yan H, Papadopoulos N, Kinzler KW. Mutations in CIC and FUBP1 Contribute to Human Oligodendroglioma [Internet]. Science. 2011 ; 333 1453-1455.[citado 2025 nov. 03 ] Available from: https://doi.org/10.1126/science.1210557

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