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	3821.	A novel somatic mutation of SIN3A detected in breast cancer by whole-exome sequencing enhances cell proliferation through ERα expression. [electronic resource] by Watanabe, Kenji Yamamoto, Shigeru Sakaguti, Syuiti Isayama, Keishiro Oka, Masaaki Nagano, Hiroaki Mizukami, Yoichi Producer: 20191024 In: Scientific reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3822.	Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway. [electronic resource] by Andreoletti, Gaia Shakhnovich, Valentina Christenson, Kathy Coelho, Tracy Haggarty, Rachel Afzal, Nadeem A Batra, Akshay Petersen, Britt-Sabina Mort, Matthew Beattie, R Mark Ennis, Sarah Producer: 20190715 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3823.	Pathway level alterations rather than mutations in single genes predict response to HER2-targeted therapies in the neo-ALTTO trial. [electronic resource] by Shi, W Jiang, T Nuciforo, P Hatzis, C Holmes, E Harbeck, N Sotiriou, C Peña, L Loi, S Rosa, D D Chia, S Wardley, A Ueno, T Rossari, J Eidtmann, H Armour, A Piccart-Gebhart, M Rimm, D L Baselga, J Pusztai, L Producer: 20180501 In: Annals of oncology : official journal of the European Society for Medical Oncology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3824.	Prediction of breast cancer risk based on flow-variant analysis of circulating peripheral blood B cells. [electronic resource] by Syeda, Mahrukh M Upadhyay, Kinnari Loke, Johnny Pearlman, Alexander Klugman, Susan Shao, Yongzhao Ostrer, Harry Producer: 20180504 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3825.	Prevalence of four Mendelian disorders associated with autism in 2392 affected families. [electronic resource] by Saskin, Avi Fulginiti, Vanessa Birch, Ashley H Trakadis, Yannis Producer: 20180118 In: Journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3826.	Alternative Lengthening of Telomeres and Loss of DAXX/ATRX Expression Predicts Metastatic Disease and Poor Survival in Patients with Pancreatic Neuroendocrine Tumors. [electronic resource] by Singhi, Aatur D Liu, Ta-Chiang Roncaioli, Justin L Cao, Dengfeng Zeh, Herbert J Zureikat, Amer H Tsung, Allan Marsh, J Wallis Lee, Kenneth K Hogg, Melissa E Bahary, Nathan Brand, Randall E McGrath, Kevin M Slivka, Adam Cressman, Kristi L Fuhrer, Kimberly O'Sullivan, Roderick J Producer: 20180206 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3827.	The implication of FLT3 amplification for FLT targeted therapeutics in solid tumors. [electronic resource] by Lim, Sung Hee Kim, Sun-Young Kim, Kyung Jang, Hyojin Ahn, Soomin Kim, Kyoung-Mee Kim, Nayoung K D Park, Woongyang Lee, Su Jin Kim, Seung Tae Park, Se Hoon Park, Joon Oh Park, Young Suk Lee, Se-Hoon Lim, Ho Yeong Park, Keunchil Kang, Won Ki Lee, Jeeyun Producer: 20180305 In: Oncotarget vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3828.	Lack of APC somatic mutation is associated with early-onset colorectal cancer in African Americans. [electronic resource] by Xicola, Rosa M Manojlovic, Zarko Augustus, Gaius J Kupfer, Sonia S Emmadi, Rajyasree Alagiozian-Angelova, Victoria Triche, Tim Salhia, Bodour Carpten, John Llor, Xavier Ellis, Nathan A Producer: 20190613 In: Carcinogenesis vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3829.	A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis. [electronic resource] by Vahidnezhad, Hassan Youssefian, Leila Saeidian, Amir Hossein Mansoori, Behzad Jazayeri, Ali Azizpour, Arghavan Hesari, Kambriz Kamyab Yousefi, Mehdi Zeinali, Sirous Jouanguy, Emmanuelle Casanova, Jean-Laurent Uitto, Jouni Producer: 20200507 In: The Journal of investigative dermatology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3830.	Potential Role of Ocular Microbiome, Host Genotype, Tear Cytokines, and Environmental Factors in Corneal Infiltrative Events in Contact Lens Wearers. [electronic resource] by Chao, Cecilia Akileswaran, Lakshmi Cooke Bailey, Jessica N Willcox, Mark Van Gelder, Russell Lakkis, Carol Stapleton, Fiona Richdale, Kathryn Producer: 20190524 In: Investigative ophthalmology & visual science vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3831.	The genetic landscape of 87 ovarian germ cell tumors. [electronic resource] by Van Nieuwenhuysen, Els Busschaert, Pieter Neven, Patrick Han, Sileny N Moerman, Philippe Liontos, Michalis Papaspirou, Maria Kupryjanczyk, Jolanta Hogdall, Claus Hogdall, Estrid Oaknin, Ana Garcia, Angel Mahner, Sven Trillsch, Fabian Cibula, David Heitz, Florian Concin, Nicole Speiser, Paul Salvesen, Helga Sehouli, Jalid Lambrechts, Diether Vergote, Ignace Producer: 20181109 In: Gynecologic oncology vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3832.	Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy. [electronic resource] by Hayashi, Takaaki Hosono, Katsuhiro Kurata, Kentaro Katagiri, Satoshi Mizobuchi, Kei Ueno, Shinji Kondo, Mineo Nakano, Tadashi Hotta, Yoshihiro Producer: 20200410 In: Documenta ophthalmologica. Advances in ophthalmology vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3833.	A phase II study of ENMD-2076 in advanced soft tissue sarcoma (STS). [electronic resource] by Veitch, Zachary Zer, Alona Loong, Herbert Salah, Samer Masood, Maryam Gupta, Abha Bradbury, Penelope A Hogg, David Wong, Andrew Kandel, Rita Charames, George S Abdul Razak, Albiruni R Producer: 20201021 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3834.	The Angiosarcoma Project: enabling genomic and clinical discoveries in a rare cancer through patient-partnered research. [electronic resource] by Painter, Corrie A Jain, Esha Tomson, Brett N Dunphy, Michael Stoddard, Rachel E Thomas, Beena S Damon, Alyssa L Shah, Shahrayz Kim, Dewey Gómez Tejeda Zañudo, Jorge Hornick, Jason L Chen, Yen-Lin Merriam, Priscilla Raut, Chandrajit P Demetri, George D Van Tine, Brian A Lander, Eric S Golub, Todd R Wagle, Nikhil Producer: 20200421 In: Nature medicine vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3835.	Germline Mutations in FAF1 Are Associated With Hereditary Colorectal Cancer. [electronic resource] by Bonjoch, Laia Franch-Expósito, Sebastià Garre, Pilar Belhadj, Sami Muñoz, Jenifer Arnau-Collell, Coral Díaz-Gay, Marcos Gratacós-Mulleras, Anna Raimondi, Giulia Esteban-Jurado, Clara Soares de Lima, Yasmin Herrera-Pariente, Cristina Cuatrecasas, Miriam Ocaña, Teresa Castells, Antoni Fillat, Cristina Capellá, Gabriel Balaguer, Francesc Caldés, Trinidad Valle, Laura Castellví-Bel, Sergi Producer: 20210331 In: Gastroenterology vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3836.	Human Cytomegalovirus Protein UL94 Targets MITA to Evade the Antiviral Immune Response. [electronic resource] by Zou, Hong-Mei Huang, Zhe-Fu Yang, Yan Luo, Wei-Wei Wang, Su-Yun Luo, Min-Hua Fu, Yu-Zhi Wang, Yan-Yi Producer: 20201118 In: Journal of virology vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3837.	Two novel mutations in ERCC6 cause Cockayne syndrome B in a Chinese family. [electronic resource] by He, Chunxia Sun, Mao Wang, Guoxia Yang, Ying Yao, Libo Wu, Yuanming Producer: 20180305 In: Molecular medicine reports vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3838.	Tet2 loss leads to hypermutagenicity in haematopoietic stem/progenitor cells. [electronic resource] by Pan, Feng Wingo, Thomas S Zhao, Zhigang Gao, Rui Makishima, Hideki Qu, Guangbo Lin, Li Yu, Miao Ortega, Janice R Wang, Jiapeng Nazha, Aziz Chen, Li Yao, Bing Liu, Can Chen, Shi Weeks, Ophelia Ni, Hongyu Phillips, Brittany Lynn Huang, Suming Wang, Jianlong He, Chuan Li, Guo-Min Radivoyevitch, Tomas Aifantis, Iannis Maciejewski, Jaroslaw P Yang, Feng-Chun Jin, Peng Xu, Mingjiang Producer: 20181120 In: Nature communications vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3839.	Feasibility of real-time molecular profiling for patients with newly diagnosed glioblastoma without MGMT promoter hypermethylation-the NCT Neuro Master Match (N2M2) pilot study. [electronic resource] by Pfaff, Elke Kessler, Tobias Balasubramanian, Gnana Prakash Berberich, Anne Schrimpf, Daniel Wick, Antje Debus, Jürgen Unterberg, Andreas Bendszus, Martin Herold-Mende, Christel Capper, David Schenkel, Irini Eisenmenger, Andreas Dettmer, Susan Brors, Benedikt Platten, Michael Pfister, Stefan M von Deimling, Andreas Jones, David T W Wick, Wolfgang Sahm, Felix Producer: 20190118 In: Neuro-oncology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3840.	Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1. [electronic resource] by Li, Sisi Xi, Quansheng Zhang, Xiaoyu Yu, Dong Li, Lin Jiang, Zhenyang Chen, Qiuyun Wang, Qing K Traboulsi, Elias I Producer: 20180521 In: Molecular genetics and genomics : MGG vol. 293 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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