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	161.	A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon Skipping. [electronic resource] by Charbel Issa, Peter Gliem, Martin Yusuf, Imran H Birtel, Johannes Müller, Philipp L Mangold, Elisabeth Downes, Susan M MacLaren, Robert E Betz, Christian Bolz, Hanno J Producer: 20191227 In: Investigative ophthalmology & visual science vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	162.	Prevalence and architecture of posttranscriptionally impaired synonymous mutations in 8,320 genomes across 22 cancer types. [electronic resource] by Teng, Huajing Wei, Wenqing Li, Qinglan Xue, Meiying Shi, Xiaohui Li, Xianfeng Mao, Fengbiao Sun, Zhongsheng Producer: 20200319 In: Nucleic acids research vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	Designing Signal Peptides for Efficient Periplasmic Expression of Human Growth Hormone in [electronic resource] by Jeiranikhameneh, Meisam Moshiri, Farzaneh Keyhan Falasafi, Soheil Zomorodipour, Alireza Producer: 20180705 In: Journal of microbiology and biotechnology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	The Mcm2-7-interacting domain of human mini-chromosome maintenance 10 (Mcm10) protein is important for stable chromatin association and origin firing. [electronic resource] by Izumi, Masako Mizuno, Takeshi Yanagi, Ken-Ichiro Sugimura, Kazuto Okumura, Katsuzumi Imamoto, Naoko Abe, Tomoko Hanaoka, Fumio Producer: 20170825 In: The Journal of biological chemistry vol. 292 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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