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1141por Bychkovsky, Brittany L., Lo, Min-Tzu, Yussuf, Amal, Horton, Carrie, Hemyari, Parichehr, LaDuca, Holly, Garber, Judy E., Scheib, Rochelle, Rana, Huma Q.“…METHODS: Females with BC and cancer of ≥ 1 other site (multiple primary cancers, MPC) who underwent MGPT through Ambry Genetics from March 2012 to December 2016 were included if they had testing of at least 21 genes of interest (ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, and TP53). …”
Publicado 2023
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1142por Young, E L, Feng, B J, Stark, A W, Damiola, F, Durand, G, Forey, N, Francy, T C, Gammon, A, Kohlmann, W K, Kaphingst, K A, McKay-Chopin, S, Nguyen-Dumont, T, Oliver, J, Paquette, A M, Pertesi, M, Robinot, N, Rosenthal, J S, Vallee, M, Voegele, C, Hopper, J L, Southey, M C, Andrulis, I L, John, E M, Hashibe, M, Gertz, J, Le Calvez-Kelm, F, Lesueur, F, Goldgar, D E, Tavtigian, S V“…METHODS: We evaluated rare missense substitutions identified from a mutation screen of ATM, CHEK2, MRE11A, RAD50, NBN, RAD51, RINT1, XRCC2 and BARD1 in 1297 cases of early-onset breast cancer and 1121 controls via scores from Align-Grantham Variation Grantham Deviation (GVGD), combined annotation dependent depletion (CADD), multivariate analysis of protein polymorphism (MAPP) and PolyPhen-2. …”
Publicado 2016
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1143“…LaPlante, Merck: Grant Investigator, Grant recipient; Pfizer: Grant Investigator, Grant recipient; Cempra: Scientific Advisor, Consulting fee; The Medicines Company: Grant Investigator, Grant recipient; Allergan: Scientific Advisor, Consulting fee; Bard/ Davol: Scientific Advisor, Consulting fee; Ocean Spray: Grant Investigator and Scientific Advisor, Consulting fee and Grant recipient; Zavante: Scientific Advisor, Consulting fee; Achaogen: Scientific Advisor, Consulting fee…”
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1144por Maksimenko, J., Irmejs, A., Trofimovičs, G., Bērziņa, D., Skuja, E., Purkalne, G., Miklaševičs, E., Gardovskis, J.“…In a 26-gene panel, the following breast and/or ovarian cancer susceptibility genes were included: ATM, BARD1, BLM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, FAM175A, MEN1, MLH1, MRE11A, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, RAD50, RAD51C, RAD51D, STK11, TP53, and XRCC2. …”
Publicado 2018
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1145“…The most accurate gene signatures for each platin are: cisplatin: BARD1, BCL2, BCL2L1, CDKN2C, FAAP24, FEN1, MAP3K1, MAPK13, MAPK3, NFKB1, NFKB2, SLC22A5, SLC31A2, TLR4, and TWIST1; carboplatin: AKT1, EIF3K, ERCC1, GNGT1, GSR, MTHFR, NEDD4L, NLRP1, NRAS, RAF1, SGK1, TIGD1, TP53, VEGFB, and VEGFC; and oxaliplatin: BRAF, FCGR2A, IGF1, MSH2, NAGK, NFE2L2, NQO1, PANK3, SLC47A1, SLCO1B1, and UGT1A1. …”
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1146por Li, Wenhui, Shao, Di, Li, Lei, Wu, Ming, Ma, Shuiqing, Tan, Xianjie, Zhong, Sen, Guo, Fengming, Wang, Zhe, Ye, Mingzhi“…All patients were tested using a 21-gene panel that included BRCA1, BRCA2, CHEK2, PALB2, BRIP1, TP53, PTEN, STK11, CDH1, ATM, BARD1, MLH1, MRE11A, MSH2, MSH6, MUTYH, NBN, PMS1, PMS2, RAD50, and RAD51C. …”
Publicado 2019
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1147por Bodily, Weston R., Shirts, Brian H., Walsh, Tom, Gulsuner, Suleyman, King, Mary-Claire, Parker, Alyssa, Roosan, Moom, Piccolo, Stephen R.“…Additionally, somatic-mutation signatures of tumors with germline or somatic events in ATR (n = 16) and BARD1 (n = 8) showed high similarity to tumors from BRCA1/BRCA2 carriers. …”
Publicado 2020
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1148por Michalak, Agata, Cichoż-Lach, Halina, Guz, Małgorzata, Kozicka, Joanna, Cybulski, Marek, Jeleniewicz, Witold, Stepulak, Andrzej“…Model for end-stage liver disease (MELD) score in ALC group and NAFLD fibrosis score together with BARD score were calculated in NAFLD patients. Receiver operating characteristic (ROC) curves and area under the curve (AUC) values were applied to assess the sensitivity and specificity of examined markers and to evaluate proposed cut-offs of measured indices in the course of ALC and NAFLD. …”
Publicado 2020
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1149por Ren, Megan, Orozco, Anali, Shao, Kang, Albanez, Anaseidy, Ortiz, Jeremy, Cao, Boyang, Wang, Lusheng, Barreda, Lilian, Alvarez, Christian S., Garland, Lisa, Wu, Dongjing, Chung, Charles C., Wang, Jiahui, Frone, Megan, Ralon, Sergio, Argueta, Victor, Orozco, Roberto, Gharzouzi, Eduardo, Dean, Michael“…Pathogenic variants were also detected in the moderate penetrance genes ATM, BARD1, CHEK2, and MSH6. The high ratio of BRCA1/BRCA2 mutations is due to two potential founder mutations: BRCA1 c.212 + 1G > A splice mutation (15 cases) and BRCA1 c.799delT (9 cases). …”
Publicado 2021
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1150por Wessman, Sandra, Fuentes, Beatriz Bohorquez, Törngren, Therese, Kvist, Anders, Kokaraki, Georgia, Menkens, Hanna, Hjerpe, Elisabet, Hugo, Ythalo, Petta, Tirzah Braz, Borg, Åke, Carlson, Joseph W.“…Mutations were identified in TP53, BRCA1, BRCA2, as well as additional homologous recombination repair pathway genes BARD1, ATR, CHEK2, PALB2, RAD51D, RAD50, SLX4, FANCA, RAD51C, and RAD54L. …”
Publicado 2021
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1151por Yoo, Hae Won, Jin, Hyun Young, Yon, Dong Keon, Effenberger, Maria, Shin, Youn Ho, Kim, So Young, Yang, Jee Myung, Kim, Min Seo, Koyanagi, Ai, Jacob, Louis, Smith, Lee, Yoo, In Kyung, Shin, Jae Il, Lee, Seung Won“…These associations are more evident as liver fibrosis advanced (based on the BARD scoring system). Similar patterns were observed in several sensitivity analyses including the full-unmatched cohort. …”
Publicado 2021
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1152por Emelyanova, Marina, Pudova, Elena, Khomich, Darya, Krasnov, George, Popova, Anna, Abramov, Ivan, Mikhailovich, Vladimir, Filipenko, Maxim, Menshikova, Sofia, Tjulandin, Sergey, Pokataev, Ilya“…METHODS: We performed targeted DNA sequencing of 30 genes (ABRAXAS1, ATM, ATR, BARD1, BLM, BRCA1, BRCA2, BRIP1, CDKN2A, CHEK1, CHEK2, FANCC, FANCF, FANCG, FANCI, FANCL, FANCM, MRE11A, NBN, PALB2, PTEN, RAD50, RAD51C, RAD51D, RAD52, RAD54B, RBBP8, RINT1, SLX4, and XRCC2) for 543 PC patients. …”
Publicado 2022
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1153por Shaji, Namitha, Singhai, Abhishek, Sarawagi, Radha, Pakhare, Abhijit P, Mishra, V N, Joshi, Rajnish“…Five non-invasive scores such as aspartate aminotransferase/alanine aminotransferase (AST/ALT) ratio, aspartate aminotransferase to platelet ratio index (APRI) score, fibrosis-4 (FIB-4) index, BARD score, and NAFLD fibrosis score were determined in all of the participants. …”
Publicado 2022
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1154por Cianci, Nicole, Subhani, Mohsan, Hill, Trevor, Khanna, Amardeep, Zheng, Dong, Sheth, Abhishek, Crooks, Colin, Aithal, Guruprasad P“…The non-invasive scoring system that performed best at predicting all-cause mortality was NAFLD fibrosis score (NFS) [pHR 3.07 (1.62-5.83)], followed by fibrosis-4 index [pHR 3.06 (1.54-6.07)], BARD [pHR 2.87 (1.27-6.46)], and AST to platelet ratio index [pHR 1.90 (1.32-2.73)]. …”
Publicado 2022
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1155por Guinot, Jose Luis, Casanova, Juan, Gonzalez-Perez, Victor, Santos, Miguel Angel, De los Dolores, Victor, Tortajada, Maria Isabel, Guardino, Carmen, Crispin, Vicente, Rubio-Briones, Jose, Arribas, Leoncio“…MATERIAL AND METHODS: Between 2007 and 2016, 706 patients were treated with real-time technique using Bard-ProLink™ system. 145 Gy was administered to the prostate with exclusive BT and 108 Gy after 46 Gy of external radiotherapy (EBRT). …”
Publicado 2022
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1156por Ramírez-Manent, J. I., Altisench Jané, B., Arroyo Bote, S., López Roig, C., González San Miguel, H., López-González, A. A.“…The risk of developing non-alcoholic fatty liver and liver fibrosis was much higher in men than in women, with an OR of 4.06 (95% CI: 3.66–4.50) for the former and an OR of 2.10 (95% CI: 1.95–2.26) for the BARD index. CONCLUSIONS: The highest risk groups were observed in male subjects with a history of smoking and blue-collar workers and, as such, should be considered for cardiovascular risk screening programs.…”
Publicado 2022
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1157por van der Merwe, Nerina C., Ntaita, Kholiwe S., Stofberg, Hanri, Combrink, Herkulaas MvE., Oosthuizen, Jaco, Kotze, Maritha J.“…Detection of actionable variants in established non-BRCA1/2 risk genes contributed 29% to the total percentage (14/48), distributed amongst ATM, CHEK2, BARD1, BRIP1, PALB2 and TP53. Experimental WES using a virtually constructed multi-cancer NGS panel in 16 genetically unresolved cases (and four controls) revealed novel protein truncating variants in the basal cell carcinoma gene PTCH1 (c.4187delG) and the signal transmission and transduction gene KIT (c.930delA) involved in crucial cellular processes. …”
Publicado 2022
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1158“…GO functional enrichment analysis showed that the DEGs were mainly enriched in the DNA replication process at the biological level, and the top DEGs were CACYBP, PCNA, MCM6, SMC1A, DTL, GINS4, MCM2, CDT1, RRM2, BRCA1, RFC5, MCM4, GINS3, GINS1, MCM10, CDC7, CDAN1, BRIP1, GINS2, CDK1, NFIB, and BARD1. The expression of CDC7 and PCNA was significantly different in high-risk MM and standard-risk MM as determined by RT-qPCR. …”
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1159por Barreto, Talita Lemos Neves, de Carvalho Filho, Roberto José, Shigueoka, David Carlos, Fonseca, Fernando Luiz Affonso, Ferreira, Ariel Cordeiro, Kochi, Cristiane, Aranda, Carolina Sanchez, Sarni, Roseli Oselka Saccardo“…The following were calculated: Homeostasis Model Assessment—Insulin Resistance, Homeostasis Model Assessment—Adiponectin (HOMA-AD), Matsuda index, aspartate aminotransferase (AST): platelet ratio index, nonalcoholic fatty liver disease fibrosis score and BARD score. Liver ultrasonography and transient liver elastography by FibroScan(®) were performed. …”
Publicado 2023
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1160por Van Den Bruck, J, Woermann, J, Sultan, A, Filipovic, K, Scheurlen, C, Erlhoefer, S, Dittrich, S, Schipper, J, Steven, D, Lueker, J“…Using an automated waveform comparison algorithm (Bard® LabSystem™ PRO software; Boston Scientific, MA, USA), the resulting QRS complexes were matched with the clinical PVC, and with the gold standard. …”
Publicado 2023
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