共 50 条
- [41] Dual-loss of PBRM1 and RAD51 identifies hyper-sensitive subset patients to immunotherapy in clear cell renal cell carcinomaCANCER IMMUNOLOGY IMMUNOTHERAPY, 2024, 73 (05)Xu, ZiyangJiang, WenbinLiu, LiQiu, YouqiWang, JiahaoDai, SiyuanGuo, JianmingXu, Jiejie
- [42] Exome sequencing identifies a mutation in OFD1 in a male with Joubert syndrome, orofaciodigital spectrum anomalies and complex polydactylyHuman Genome Variation, 3 (1)Ingrid M WentzensenJennifer J JohnstonJohn H PattonJohn M GrahamJulie C SappLeslie G Biesecker
- [43] Evaluation of the role of downregulation of SNF5/INI1 core subunit of SWI/SNF complex in clear cell renal cell carcinoma developmentAMERICAN JOURNAL OF CANCER RESEARCH, 2017, 7 (11): : 2275 - 2289Sarnowska, ElzbietaSzymanski, MichalRusetska, NataliiaLigaj, MarcinJancewicz, IgaCwiek, PawelSkrodzka, MartaLeszczynski, MarcinSzarkowska, JoannaChrzan, AlicjaStachowiak, MalgorzataSteciuk, JaroSlawMaassen, AnnaGalek, LechDemkow, TomaszSiedlecki, Janusz A.Sarnowski, Tomasz J.
- [44] Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinomaPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (12) : 3317 - 3322Dai, WeiZheng, HongCheung, Arthur Kwok LeungTang, Clara Sze-manKo, Josephine Mun YeeWong, Bonnie Wing YanLeong, Merrin Man LongSham, Pak ChungCheung, FlorenceKwong, Dora Lai-WanNgan, Roger Kai CheongNg, Wai TongYau, Chun ChungPan, JianjiPeng, XunTung, StewartZhang, ZengfengJi, MingfangChiang, Alan Kwok-ShingLee, Anne Wing-MuiLee, Victor Ho-funLam, Ka-OnAu, Kwok HungCheng, Hoi ChingYiu, Harry Ho-YinLung, Maria Li
- [45] Re: Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers with Spermatogenic Failure EDITORIAL COMMENTJOURNAL OF UROLOGICAL SURGERY, 2018, 5 (03): : 217 - 217Bakircioglu, Emre
- [46] VHL, PBRM1, and BAP1 mutation variants and response to first-line therapies in patients with metastatic clear-cell renal cell carcinoma (mRCC)MOLECULAR CANCER THERAPEUTICS, 2023, 22 (12)Zhu, JessicaHu, JunxiaoLam, Elaine T.
- [47] Interrogating the Significance of PARP1 Expression and PBRM1 Mutation as Biomarkers for Predicting the Response to Atezolizumab plus Bevacizumab or to Sunitinib in Patients with Clear Cell Renal Cell CarcinomaEUROPEAN UROLOGY, 2022, 82 (03) : 334 - 335Lanillos, JavierSantos, MariaValdivia, CarlosMora, AlbertoRodriguez-Antona, Cristina
- [48] Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfectaHuman Genomics, 9Katre MaasaluTiit NikopensiusSulev KõksMargit NõukasMart KalsEle PransLidiia ZhytnikAndres MetspaluAare Märtson
- [49] Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfectaHUMAN GENOMICS, 2015, 9 : 6Maasalu, KatreNikopensius, TiitKoks, SulevNoukas, MargitKals, MartPrans, EleZhytnik, LidiiaMetspalu, AndresMaertson, Aare
- [50] Whole-exome sequencing identifies the first French MODY 6 family with a new mutation in the NEUROD1 geneDIABETES & METABOLISM, 2020, 46 (05) : 400 - 402Bouillet, B.Crevisy, E.Baillot-Rudoni, S.Gallegarine, D.Jouan, T.Duffourd, Y.Petit, J. M.Verges, B.Callier, P.