81 related articles for article (PubMed ID: 24297530)
1. Extracting significant sample-specific cancer mutations using their protein interactions.
Badea L
Pac Symp Biocomput; 2014; ():15-26. PubMed ID: 24297530
[TBL] [Abstract][Full Text] [Related]
2. Frequent mutations in acetylation and ubiquitination sites suggest novel driver mechanisms of cancer.
Narayan S; Bader GD; Reimand J
Genome Med; 2016 May; 8(1):55. PubMed ID: 27175787
[TBL] [Abstract][Full Text] [Related]
3. Discovery of mutated subnetworks associated with clinical data in cancer.
Vandin F; Clay P; Upfal E; Raphael BJ
Pac Symp Biocomput; 2012; ():55-66. PubMed ID: 22174262
[TBL] [Abstract][Full Text] [Related]
4. Identifying mutation specific cancer pathways using a structurally resolved protein interaction network.
Engin HB; Hofree M; Carter H
Pac Symp Biocomput; 2015; 20():84-95. PubMed ID: 25592571
[TBL] [Abstract][Full Text] [Related]
5. Proteogenomic Analysis of Single Amino Acid Polymorphisms in Cancer Research.
Garin-Muga A; Corrales FJ; Segura V
Adv Exp Med Biol; 2016; 926():93-113. PubMed ID: 27686808
[TBL] [Abstract][Full Text] [Related]
6. The molecular pathogenesis of acute myeloid leukemia.
Steffen B; Müller-Tidow C; Schwäble J; Berdel WE; Serve H
Crit Rev Oncol Hematol; 2005 Nov; 56(2):195-221. PubMed ID: 16236521
[TBL] [Abstract][Full Text] [Related]
7. Structure-Based Analysis Reveals Cancer Missense Mutations Target Protein Interaction Interfaces.
Engin HB; Kreisberg JF; Carter H
PLoS One; 2016; 11(4):e0152929. PubMed ID: 27043210
[TBL] [Abstract][Full Text] [Related]
8. A one-mutation mathematical model can explain the age incidence of acute myeloid leukemia with mutated nucleophosmin (NPM1).
Liso A; Castiglione F; Cappuccio A; Stracci F; Schlenk RF; Amadori S; Thiede C; Schnittger S; Valk PJ; Döhner K; Martelli MF; Schaich M; Krauter J; Ganser A; Martelli MP; Bolli N; Löwenberg B; Haferlach T; Ehninger G; Mandelli F; Döhner H; Michor F; Falini B
Haematologica; 2008 Aug; 93(8):1219-26. PubMed ID: 18603563
[TBL] [Abstract][Full Text] [Related]
9. Identifying Driver Interfaces Enriched for Somatic Missense Mutations in Tumors.
Ozturk K; Carter H
Methods Mol Biol; 2019; 1907():51-72. PubMed ID: 30542990
[TBL] [Abstract][Full Text] [Related]
10. Oncogenic Flt3 receptors display different specificity and kinetics of autophosphorylation.
Razumovskaya E; Masson K; Khan R; Bengtsson S; Rönnstrand L
Exp Hematol; 2009 Aug; 37(8):979-89. PubMed ID: 19477218
[TBL] [Abstract][Full Text] [Related]
11. Identification and selective degradation of neopeptide-containing truncated mutant proteins in the tumors with high microsatellite instability.
Kim WK; Park M; Park M; Kim YJ; Shin N; Kim HK; You KT; Kim H
Clin Cancer Res; 2013 Jul; 19(13):3369-82. PubMed ID: 23674496
[TBL] [Abstract][Full Text] [Related]
12. KIT mutations confer a distinct gene expression signature in core binding factor leukaemia.
Lück SC; Russ AC; Du J; Gaidzik V; Schlenk RF; Pollack JR; Döhner K; Döhner H; Bullinger L
Br J Haematol; 2010 Mar; 148(6):925-37. PubMed ID: 20064158
[TBL] [Abstract][Full Text] [Related]
13. Identification of synthetic lethal pairs in biological systems through network information centrality.
Kranthi T; Rao SB; Manimaran P
Mol Biosyst; 2013 Aug; 9(8):2163-7. PubMed ID: 23728082
[TBL] [Abstract][Full Text] [Related]
14. The evolving molecular genetic landscape in acute myeloid leukaemia.
Sanders MA; Valk PJ
Curr Opin Hematol; 2013 Mar; 20(2):79-85. PubMed ID: 23380602
[TBL] [Abstract][Full Text] [Related]
15. A reliability measure of protein-protein interactions and a reliability measure-based search engine.
Park B; Han K
Comput Methods Biomech Biomed Engin; 2010 Feb; 13(1):97-104. PubMed ID: 19657800
[TBL] [Abstract][Full Text] [Related]
16. Probabilistic model of the human protein-protein interaction network.
Rhodes DR; Tomlins SA; Varambally S; Mahavisno V; Barrette T; Kalyana-Sundaram S; Ghosh D; Pandey A; Chinnaiyan AM
Nat Biotechnol; 2005 Aug; 23(8):951-9. PubMed ID: 16082366
[TBL] [Abstract][Full Text] [Related]
17. Combined testing for CCAAT/enhancer-binding protein alpha (CEBPA) mutations and promoter methylation in acute myeloid leukemia demonstrates shared phenotypic features.
Szankasi P; Ho AK; Bahler DW; Efimova O; Kelley TW
Leuk Res; 2011 Feb; 35(2):200-7. PubMed ID: 20970189
[TBL] [Abstract][Full Text] [Related]
18. Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia.
Bentires-Alj M; Paez JG; David FS; Keilhack H; Halmos B; Naoki K; Maris JM; Richardson A; Bardelli A; Sugarbaker DJ; Richards WG; Du J; Girard L; Minna JD; Loh ML; Fisher DE; Velculescu VE; Vogelstein B; Meyerson M; Sellers WR; Neel BG
Cancer Res; 2004 Dec; 64(24):8816-20. PubMed ID: 15604238
[TBL] [Abstract][Full Text] [Related]
19. Rapid and highly specific screening for NPM1 mutations in acute myeloid leukemia.
Oppliger Leibundgut E; Porret NA; Bienz Muggli M; Baumgartner H; Dahlhaus M; Baerlocher GM
Ann Hematol; 2013 Jan; 92(2):173-7. PubMed ID: 23161387
[TBL] [Abstract][Full Text] [Related]
20. Prevalence and clinical characteristics of N-terminally truncated WT1 expression in acute myeloid leukemia.
Ishikawa Y; Kiyoi H; Naoe T
Leuk Res; 2011 May; 35(5):685-8. PubMed ID: 21256590
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
