Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.
Human Genetics
Tollefson, Mallory R MR; Gogal, Rose A RA; Weaver, A Monique AM; Schaefer, Amanda M AM; Marini, Robert J RJ; Azaiez, Hela H; Kolbe, Diana L DL; Wang, Donghong D; Weaver, Amy E AE; Casavant, Thomas L TL; Braun, Terry A TA; Smith, Richard J H RJH; Schnieders, Michael J MJ
Publication Date: 2023-04-22
Variant appearance in text: FGFR3: 1663G>A; Val555Met
A lymphatic-absorbed multi-targeted kinase inhibitor for myelofibrosis therapy.
Nature Communications
Ross, Brian D BD; Jang, Youngsoon Y; Welton, Amanda A; Bonham, Christopher A CA; Palagama, Dilrukshika S W DSW; Heist, Kevin K; Boppisetti, Jagadish J; Imaduwage, Kasun P KP; Robison, Tanner T; King, Leah R LR; Zhang, Edward Z EZ; Amirfazli, Cyrus C; Luker, Kathryn E KE; Lee, Winston Y WY; Luker, Gary D GD; Chenevert, Thomas L TL; Van Dort, Marcian E ME
Molecular landscape of TP53 mutations in breast cancer and their utility for predicting the response to HER-targeted therapy in HER2 amplification-positive and HER2 mutation-positive amplification-negative patients.
Targeted Therapy of Papillary Thyroid Cancer: A Comprehensive Genomic Analysis.
Frontiers In Endocrinology
Hescheler, Daniel A DA; Riemann, Burkhard B; Hartmann, Milan J M MJM; Michel, Maximilian M; Faust, Michael M; Bruns, Christiane J CJ; Alakus, Hakan H; Chiapponi, Costanza C
Identifying therapeutic drug targets using bidirectional effect genes.
Nature Communications
Estrada, Karol K; Froelich, Steven S; Wuster, Arthur A; Bauer, Christopher R CR; Sterling, Teague T; Clark, Wyatt T WT; Ru, Yuanbin Y; Trinidad, Marena M; Nguyen, Hong Phuc HP; Luu, Amanda R AR; Wendt, Daniel J DJ; Yogalingam, Gouri G; Yu, Guoying Karen GK; LeBowitz, Jonathan H JH; Cardon, Lon R LR
Publication Date: 2021-04-13
Variant appearance in text: FGFR3: 1663G>A; Val555Met
Esteban-Villarrubia, Jorge J; Soto-Castillo, Juan José JJ; Pozas, Javier J; San Román-Gil, María M; Orejana-Martín, Inmaculada I; Torres-Jiménez, Javier J; Carrato, Alfredo A; Alonso-Gordoa, Teresa T; Molina-Cerrillo, Javier J
Identification of targeted therapy options for gastric adenocarcinoma by comprehensive analysis of genomic data.
Gastric Cancer : Official Journal Of The International Gastric Cancer Association And The Japanese Gastric Cancer Association
Hescheler, Daniel A DA; Plum, Patrick S PS; Zander, Thomas T; Quaas, Alexander A; Korenkov, Michael M; Gassa, Asmae A; Michel, Maximilian M; Bruns, Christiane J CJ; Alakus, Hakan H
Efficacy of FGFR Inhibitors and Combination Therapies for Acquired Resistance in FGFR2-Fusion Cholangiocarcinoma.
Molecular Cancer Therapeutics
Krook, Melanie A MA; Lenyo, Alexandria A; Wilberding, Max M; Barker, Hannah H; Dantuono, Mikayla M; Bailey, Kelly M KM; Chen, Hui-Zi HZ; Reeser, Julie W JW; Wing, Michele R MR; Miya, Jharna J; Samorodnitsky, Eric E; Smith, Amy M AM; Dao, Thuy T; Martin, Dorrelyn M DM; Ciombor, Kristen K KK; Hays, John J; Freud, Aharon G AG; Roychowdhury, Sameek S
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Journal Of The American Society Of Nephrology : Jasn
van der Ven, Amelie T AT; Connaughton, Dervla M DM; Ityel, Hadas H; Mann, Nina N; Nakayama, Makiko M; Chen, Jing J; Vivante, Asaf A; Hwang, Daw-Yang DY; Schulz, Julian J; Braun, Daniela A DA; Schmidt, Johanna Magdalena JM; Schapiro, David D; Schneider, Ronen R; Warejko, Jillian K JK; Daga, Ankana A; Majmundar, Amar J AJ; Tan, Weizhen W; Jobst-Schwan, Tilman T; Hermle, Tobias T; Widmeier, Eugen E; Ashraf, Shazia S; Amar, Ali A; Hoogstraaten, Charlotte A CA; Hugo, Hannah H; Kitzler, Thomas M TM; Kause, Franziska F; Kolvenbach, Caroline M CM; Dai, Rufeng R; Spaneas, Leslie L; Amann, Kassaundra K; Stein, Deborah R DR; Baum, Michelle A MA; Somers, Michael J G MJG; Rodig, Nancy M NM; Ferguson, Michael A MA; Traum, Avram Z AZ; Daouk, Ghaleb H GH; Bogdanović, Radovan R; Stajić, Natasa N; Soliman, Neveen A NA; Kari, Jameela A JA; El Desoky, Sherif S; Fathy, Hanan M HM; Milosevic, Danko D; Al-Saffar, Muna M; Awad, Hazem S HS; Eid, Loai A LA; Selvin, Aravind A; Senguttuvan, Prabha P; Sanna-Cherchi, Simone S; Rehm, Heidi L HL; MacArthur, Daniel G DG; Lek, Monkol M; Laricchia, Kristen M KM; Wilson, Michael W MW; Mane, Shrikant M SM; Lifton, Richard P RP; Lee, Richard S RS; Bauer, Stuart B SB; Lu, Weining W; Reutter, Heiko M HM; Tasic, Velibor V; Shril, Shirlee S; Hildebrandt, Friedhelm F
Publication Date: 2018-09
Variant appearance in text: FGFR3: 1663G>A; Val555Met
Integrative omics analyses broaden treatment targets in human cancer.
Genome Medicine
Sengupta, Sohini S; Sun, Sam Q SQ; Huang, Kuan-Lin KL; Oh, Clara C; Bailey, Matthew H MH; Varghese, Rajees R; Wyczalkowski, Matthew A MA; Ning, Jie J; Tripathi, Piyush P; McMichael, Joshua F JF; Johnson, Kimberly J KJ; Kandoth, Cyriac C; Welch, John J; Ma, Cynthia C; Wendl, Michael C MC; Payne, Samuel H SH; Fenyö, David D; Townsend, Reid R RR; Dipersio, John F JF; Chen, Feng F; Ding, Li L
Disease Variants of FGFR3 Reveal Molecular Basis for the Recognition and Additional Roles for Cdc37 in Hsp90 Chaperone System.
Structure (London, England : 1993)
Bunney, Tom D TD; Inglis, Alison J AJ; Sanfelice, Domenico D; Farrell, Brendan B; Kerr, Christopher J CJ; Thompson, Gary S GS; Masson, Glenn R GR; Thiyagarajan, Nethaji N; Svergun, Dmitri I DI; Williams, Roger L RL; Breeze, Alexander L AL; Katan, Matilda M