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3821por Buchwald, Zachary S., Tian, Sibo, Rossi, Michael, Smith, Geoffrey H., Switchenko, Jeffrey, Hauenstein, Jennifer E., Moreno, Carlos S., Press, Robert H., Prabhu, Roshan S., Zhong, Jim, Saxe, Debra F., Neill, Stewart G., Olson, Jeffrey J., Crocker, Ian R., Curran, Walter J., Shu, Hui-Kuo G.“…Results were confirmed on The Cancer Genome Atlas (TCGA) glioblastoma dataset. 25 (44.6%) patients had MGMT hyper-methylated tumors, 6 (10.7%) were IDH1 mutated. Median follow-up was 36.4 months. …”
Publicado 2020
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3822por Ramakrishnan, Valya, Xu, Beibei, Akers, Johnny, Nguyen, Thien, Ma, Jun, Dhawan, Sanjay, Ning, Jianfang, Mao, Ying, Hua, Wei, Kokkoli, Efrosini, Furnari, Frank, Carter, Bob S., Chen, Clark C.“…All specimens harbored unmethylated O(6)-methylguanine-DNA methyltransferase promoters (umMGMT) and wild-type isocitrate dehydrogenase (wtIDH). The most altered miRNA, miR-603, was characterized. …”
Publicado 2020
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3823por Mori, Kanji, Shofuda, Tomoko, Mano, Masayuki, Kodama, Yoshinori, Kinoshita, Manabu, Arita, Hideyuki, Moriuchi, Shusuke, Uda, Takehiro, Taki, Takuyu, Fukai, Junya, Nonaka, Masahiro, Ishibashi, Kenichi, Sakamoto, Daisuke, Izumoto, Shuichi, Nishida, Namiko, Okita, Yoshiko, Nakajima, Yoshikazu, Takano, Koji, Hashimoto, Naoya, Tsuyuguchi, Naohiro, Okuda, Takeshi, Achiha, Takamune, Hayashi, Nobuhide, Dehara, Makoto, Kanemura, Yonehiro“…Proportion of methylated MGMT promoter was 43.3% (65 patients), and mutated IDH was 5.4% (8 patients). Median overall survival after recurrence (mSAR) was 8.2 months. …”
Publicado 2019
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3824por Basch, Corey H., Hillyer, Grace Clarke, Erwin, Zoe Meleo-, Mohlman, Jan, Cosgrove, Alison, Quinones, NasiaEnlace del recurso
Publicado 2020
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3825“…Chi-square test results showed that Piezo1 expression was significantly related to age (P=0.00), WHO grade (P=0.00), Histopathology (P=0.00), IDH1 mutation (P=0.00) and chemotherapy (P=0.00). …”
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3826por Elhadi, Muhammed, Msherghi, Ahmed, Alkeelani, Mohammed, Alsuyihili, Ali, Khaled, Ala, Buzreg, Anis, Boughididah, Tariq, Abukhashem, Mohamed, Alhashimi, Ayiman, Khel, Samer, Gaffaz, Rawanda, Ben Saleim, Najah, Bahroun, Sumayyah, Elharb, Abdelmunam, Eisay, Mohamed, Alnafati, Nafati, Almiqlash, Bushray, Biala, Marwa, Alghanai, EsraEnlace del recurso
Publicado 2020
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3827por Kong, Lin, Wu, Jinsong, Gao, Jing, Qiu, Xianxin, Yang, Jing, Hu, Jiyi, Hu, Weixu, Mao, Ying, Lu, Jiade J.“…Univariate analyses revealed that age (>50 vs ≤50 years), World Health Organization grade (3 vs 4), and Karnofsky performance status (>80 vs ≤80) were significant prognosticators for OS, and IDH mutation and World Health Organization grade were significant for predicting PFS. …”
Publicado 2020
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3828por Kudryavtseva, Anna V., Kalinin, Dmitry V., Pavlov, Vladislav S., Savvateeva, Maria V., Fedorova, Maria S., Pudova, Elena A., Kobelyatskaya, Anastasiya A., Golovyuk, Alexander L., Guvatova, Zulfiya G., Razmakhaev, George S., Demidova, Tatiana B., Simanovsky, Sergey A., Slavnova, Elena N., Poloznikov, Andrey А., Polyakov, Andrey P., Melnikova, Nataliya V., Dmitriev, Alexey A., Krasnov, George S., Snezhkina, Anastasiya V.“…In a patient, we found a novel variant of the IDH2 gene that was predicted as pathogenic by a series of algorithms used (such as SIFT, PolyPhen2, FATHMM, MutationTaster, and LRT). …”
Publicado 2020
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3829por Shah, Kalpit, Gagliano, Teresa, Garland, Lisa, O’Hanlon, Timothy, Bortolotti, Daria, Gentili, Valentina, Rizzo, Roberta, Giamas, Georgios, Dean, Michael“…For example, we found evidence for an inadvertent AR-antagonist-mediated switch in IDH1 and PL2G2A isoform expression, which is associated with a decrease in overall survival of patients. …”
Publicado 2020
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3830por Fryk, Jesse J., Tong, Steven, Marshall, Caroline, Rajkhowa, Arjun, Buising, Kirsty, MacIsaac, Christopher, Walsham, Nicola, Thevarajan, IraniEnlace del recurso
Publicado 2021
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3831“…The expression of SLC39A1 is significantly correlated with clinical pathological parameters such as Grade, IDH mutation status, and 1p19q codeletion status. …”
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3832por Umehara, Toru, Kinoshita, Manabu, Sasaki, Takahiro, Arita, Hideyuki, Yoshioka, Ema, Shofuda, Tomoko, Kodama, Yoshinori, Hirayama, Ryuichi, Kijima, Noriyuki, Kagawa, Naoki, Okita, Yoshiko, Takano, Koji, Uda, Takehiro, Fukai, Junya, Sakamoto, Daisuke, Mori, Kanji, Kanemura, Yonehiro“…Method: We included all cases of IDH wild-type pGBM available of preoperative MRI (T1WI, T2WI, and Gd-T1WI) from the databases of Kansai Molecular Diagnosis Network for CNS tumors (KN) and The Cancer Genome Atlas (TCGA). …”
Publicado 2020
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3833por Funakoshi, Yusuke, Hata, Nobuhiro, Kuga, Daisuke, Hatae, Ryusuke, Sangatsuda, Yuhei, Fujioka, Yutaka, Takigawa, Kosuke, Mizoguchi, Masahiro“…Methods: We included 100 patients with IDH-wildtype GBM between September 2006 and February 2018 from our institution. …”
Publicado 2020
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3834“…In addition, patients in the high risk score group in the TCGA dataset were found to be of an advanced age, IDH mutation, and M5 FAB category. These results suggested that the proposed immune related-gene signature may serve as a potential prognostic tool for AML patients.…”
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3835por Dodgshun, Andrew, Fukuoka, Kohei, Edwards, Melissa, Bianchi, Vanessa, Sexton-Oates, Alexandra, Larouche, Valerie, Magimairajan, Vanan, Lindhorst, Scott, Yalon, Michal, Mason, Gary, Crooks, Bruce, Constantini, Shlomi, Massimino, Maura, Chiaravalli, Stefano, Ramdas, Jagadeesh, Mason, Warren, Shamvil, Ashraf, Farah, Roula, Van Damme, An, Opocher, Enrico, Hamid, Syed Ahmer, Ziegler, David, Samuel, David, Cole, Kristina A, Tomboc, Patrick, Stearns, Duncan, Thomas, Gregory, Lossos, Alexander, Sullivan, Michael, Hansford, Jordan R, Jones, David, Mackay, Alan, Jones, Chris, Ramaswamy, Vijay, Hawkins, Cynthia, Bouffet, Eric, Tabori, Uri“…RRD pHGG displayed a methylation pattern corresponding to specific secondary mutations such as IDH1 and H3K27M. Strikingly, RRD pHGG lacking these known secondary mutations largely clustered together with a poorly described group previously labelled Wild type-C. …”
Publicado 2020
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3836por Lazow, Margot A, Schafer, Austin, DeWire-Schottmiller, Mariko D, Lane, Adam, Boué, Daniel R, Osorio, Diana S, Finlay, Jonathan L, Wright, Erin, Rush, Sarah, Hoffman, Lindsey M, Reuss, Jamie, Hummel, Trent R, Salloum, Ralph, de Blank, Peter M, Smiley, Natasha Pillay, Sutton, Mary E, Asher, Anthony, Stevenson, Charles B, Drissi, Rachid, Fouladi, Maryam, Fuller, Christine“…BRAF fusion and BRAF(V600E) status were conserved in 100% and 97% of paired specimens, respectively. No loss or gain of IDH1 mutations or FGFR1, NTRK2, MYB, or MYBL1 rearrangements were detected over time. …”
Publicado 2020
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3837“…Whole oncogene high flux sequencing of the patient tissue showed TP53, PTEN, IDH1 and PTCH1 mutation were existed. Conclusions: Our study showed that SHG140 was an astrocytoma glioma continuous cell line derived from a human adult male, having a strong tumorigenicity in nude mice, which made it wound be a useful model for the study of human glioblastoma multiforme.…”
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3838por Schulte, Jessica D, Buerki, Robin A, Lapointe, Sarah, Molinaro, Annette M, Zhang, Yalan, Villanueva-Meyer, Javier E, Perry, Arie, Phillips, Joanna J, Tihan, Tarik, Bollen, Andrew W, Pekmezci, Melike, Butowski, Nicholas, Oberheim Bush, Nancy Ann, Taylor, Jennie W, Chang, Susan M, Theodosopoulos, Philip, Aghi, Manish K, Hervey-Jumper, Shawn L, Berger, Mitchel S, Solomon, David A, Clarke, Jennifer L“…The overall survival of this adult cohort was 27.6 months, longer than historical averages for both H3 K27M-mutant DMG in children and IDH-wildtype glioblastoma in adults. CONCLUSIONS: Together, these findings indicate that H3 K27M-mutant DMG represents a heterogeneous disease with regard to outcomes, sites of origin, and molecular pathogenesis in adults versus children.…”
Publicado 2020
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3839por Ferguson, Sherise D, Hodges, Tiffany R, Majd, Nazanin K, Alfaro-Munoz, Kristin, Al-Holou, Wajd N, Suki, Dima, de Groot, John F, Fuller, Gregory N, Xue, Lee, Li, Miao, Jacobs, Carmen, Rao, Ganesh, Colen, Rivka R, Xiu, Joanne, Verhaak, Roel, Spetzler, David, Khasraw, Mustafa, Sawaya, Raymond, Long, James P, Heimberger, Amy B“…RESULTS: Univariate analysis revealed 3 pivotal genetic alterations associated with GBM survival: both high tumor mutational burden (P = .0055) and PTEN mutations (P = .0235) negatively impacted survival, whereas IDH1 mutations positively impacted survival (P < .0001). …”
Publicado 2020
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3840“…With the nomogram, an individualized survival chance could be predicted intuitively with specific age, tumor grade, Isocitrate dehydrogenase (IDH) status, and the PROMISE risk score. ROC showed significant discrimination with the area under curves (AUCs) of 0.917 and 0.817 in TCGA and CGGA, respectively. …”
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