New methodology of TMB assessment from tissue and liquid biopsy in NSCLC.
Plos One
Křížová, Ľudmila Ľ; Šafaříková, Markéta M; Kalousová, Marta M; Pfeiferová, Lucie L; Kuběna, Aleš Antonín AA; Vočka, Michal M; Ulrych, Jan J; Franková, Věra V; Petruželka, Luboš L; Zima, Tomáš T; Feltl, David D
Publication Date: 2022
Variant appearance in text: IGF1R: 640+20C>T; rs7174918
Microsecond-timescale MD simulation of EGFR minor mutation predicts the structural flexibility of EGFR kinase core that reflects EGFR inhibitor sensitivity.
Npj Precision Oncology
Yoshizawa, Takahiro T; Uchibori, Ken K; Araki, Mitsugu M; Matsumoto, Shigeyuki S; Ma, Biao B; Kanada, Ryo R; Seto, Yosuke Y; Oh-Hara, Tomoko T; Koike, Sumie S; Ariyasu, Ryo R; Kitazono, Satoru S; Ninomiya, Hironori H; Takeuchi, Kengo K; Yanagitani, Noriko N; Takagi, Satoshi S; Kishi, Kazuma K; Fujita, Naoya N; Okuno, Yasushi Y; Nishio, Makoto M; Katayama, Ryohei R
Publication Date: 2021-04-16
Variant appearance in text: IGF1R: 640+20C>T; rs7174918
Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.
Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes.
Plos One
Salem, Joe-Elie JE; Germain, Marine M; Hulot, Jean-Sébastien JS; Voiriot, Pascal P; Lebourgeois, Bruno B; Waldura, Jean J; Tregouet, David-Alexandre DA; Charbit, Beny B; Funck-Brentano, Christian C
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.
Human Molecular Genetics
Verweij, Niek N; Mateo Leach, Irene I; Isaacs, Aaron A; Arking, Dan E DE; Bis, Joshua C JC; Pers, Tune H TH; Van Den Berg, Marten E ME; Lyytikäinen, Leo-Pekka LP; Barnett, Phil P; Wang, Xinchen X; , ; Soliman, Elsayed Z EZ; Van Duijn, Cornelia M CM; Kähönen, Mika M; Van Veldhuisen, Dirk J DJ; Kors, Jan A JA; Raitakari, Olli T OT; Silva, Claudia T CT; Lehtimäki, Terho T; Hillege, Hans L HL; Hirschhorn, Joel N JN; Boyer, Laurie A LA; Van Gilst, Wiek H WH; Alonso, Alvaro A; Sotoodehnia, Nona N; Eijgelsheim, Mark M; De Boer, Rudolf A RA; De Bakker, Paul I W PI; Franke, Lude L; Van Der Harst, Pim P
Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.
Acta Neuropathologica Communications
Shankar, Ganesh M GM; Taylor-Weiner, Amaro A; Lelic, Nina N; Jones, Robert T RT; Kim, James C JC; Francis, Joshua M JM; Abedalthagafi, Malak M; Borges, Lawrence F LF; Coumans, Jean-Valery JV; Curry, William T WT; Nahed, Brian V BV; Shin, John H JH; Paek, Sun Ha SH; Park, Sung-Hye SH; Stewart, Chip C; Lawrence, Michael S MS; Cibulskis, Kristian K; Thorner, Aaron R AR; Van Hummelen, Paul P; Stemmer-Rachamimov, Anat O AO; Batchelor, Tracy T TT; Carter, Scott L SL; Hoang, Mai P MP; Santagata, Sandro S; Louis, David N DN; Barker, Fred G FG; Meyerson, Matthew M; Getz, Gad G; Brastianos, Priscilla K PK; Cahill, Daniel P DP
Genome-wide association study of the child behavior checklist dysregulation profile.
Journal Of The American Academy Of Child And Adolescent Psychiatry
Mick, Eric E; McGough, James J; Loo, Sandra S; Doyle, Alysa E AE; Wozniak, Janet J; Wilens, Timothy E TE; Smalley, Susan S; McCracken, James J; Biederman, Joseph J; Faraone, Stephen V SV