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	441.	Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations. [electronic resource] by Bourdet, Karine Vallette, Sophie Deladoëy, Johnny Van Vliet, Guy Producer: 20170403 In: Hormone research in paediatrics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	442.	Enhancement of Transcription by a Splicing-Competent Intron Is Dependent on Promoter Directionality. [electronic resource] by Agarwal, Neha Ansari, Athar Producer: 20170512 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	443.	Noncanonical registers and base pairs in human 5' splice-site selection. [electronic resource] by Tan, Jiazi Ho, Jia Xin Jessie Zhong, Zhensheng Luo, Shufang Chen, Gang Roca, Xavier Producer: 20170605 In: Nucleic acids research vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	444.	Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni. [electronic resource] by Boroni, Mariana Sammeth, Michael Gava, Sandra Grossi Jorge, Natasha Andressa Nogueira Macedo, Andréa Mara Machado, Carlos Renato Mourão, Marina Moraes Franco, Glória Regina Producer: 20191029 In: Scientific reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	445.	Global Co-transcriptional Splicing in Arabidopsis and the Correlation with Splicing Regulation in Mature RNAs. [electronic resource] by Li, Shaofang Wang, Yuan Zhao, Yonghui Zhao, Xinjie Chen, Xuemei Gong, Zhizhong Producer: 20201120 In: Molecular plant vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	446.	A computational scan for U12-dependent introns in the human genome sequence. [electronic resource] by Levine, A Durbin, R Producer: 20011025 In: Nucleic acids research vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	447.	Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome. [electronic resource] by Arnaud, Lionel Salachas, François Lucien, Nicole Maisonobe, Thierry Le Pennec, Pierre-Yves Babinet, Jérôme Cartron, Jean-Pierre Producer: 20090316 In: Transfusion vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	448.	Alternative RNA splicing regulation in the testis. [electronic resource] by Elliott, David J Grellscheid, Sushma N Producer: 20070619 In: Reproduction (Cambridge, England) vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	449.	A conserved element that stabilizes the group II intron active site. [electronic resource] by Fedorova, Olga Pyle, Anna Marie Producer: 20080616 In: RNA (New York, N.Y.) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	450.	Dual-specificity splice sites function alternatively as 5' and 3' splice sites. [electronic resource] by Zhang, Chaolin Hastings, Michelle L Krainer, Adrian R Zhang, Michael Q Producer: 20071127 In: Proceedings of the National Academy of Sciences of the United States of America vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	451.	Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy. [electronic resource] by Kimura, Shigemi Ikezawa, Makoto Ozasa, Shiro Ito, Kaori Ueno, Hiroe Yoshioka, Kowashi Ijiri, Saki Nomura, Keiko Nakamura, Kyoko Matuskura, Makoto Miike, Teruhisa Producer: 20071105 In: Journal of child neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	452.	Successful treatment with narrow-band UVB therapy for a case of generalized Hailey-Hailey disease with a novel splice-site mutation in ATP2C1 gene. [electronic resource] by Mizuno, Kana Hamada, Takahiro Hashimoto, Takashi Okamoto, Hiroyuki Producer: 20150408 In: Dermatologic therapy vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	453.	Two novel mutations affecting the same splice site of PKD1 correlate with different phenotypes in ADPKD. [electronic resource] by Yu, Chaowen Li, Jing Yuan, Zhaojian Liu, Shan Zou, Lin Producer: 20150209 In: Renal failure vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	454.	Survey of Programs Used to Detect Alternative Splicing Isoforms from Deep Sequencing Data In Silico. [electronic resource] by Min, Feng Wang, Sumei Zhang, Li Producer: 20160711 In: BioMed research international vol. 2015 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	455.	Multiple tandem splicing silencer elements suppress aberrant splicing within the long exon 26 of the human Apolipoprotein B gene. [electronic resource] by Srirangalingam, Umasuthan Akker, Scott A Norman, Dennis Navaratnam, Naveenan Chew, Shern L Khoo, Bernard Producer: 20130729 In: BMC molecular biology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	456.	Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26. [electronic resource] by Meregalli, Mirella Maciotta, Simona Angeloni, Valentina Torrente, Yvan Producer: 20170427 In: BMC medical genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	457.	Delayed vitreous haemorrhage after paediatric cataract surgery in Lowe syndrome. [electronic resource] by Mikhail, M Modabber, M Koenekoop, R K Braverman, N Khan, A Producer: 20170324 In: Eye (London, England) vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	458.	Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia. [electronic resource] by Zhang, Tingting Wu, Jing Zhao, Xiaoxue Hou, Feifei Ma, Tengfei Wang, Huijuan Zhang, Xu Zhang, Xiangyu Producer: 20191212 In: Archives of oral biology vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	459.	Enigmatic rhodopsin mutation creates an exceptionally strong splice acceptor site. [electronic resource] by Riedmayr, Lisa M Böhm, Sybille Biel, Martin Becirovic, Elvir Producer: 20201019 In: Human molecular genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	460.	SnapShot: Splicing Alterations in Cancer. [electronic resource] by Rahman, Mohammad Alinoor Krainer, Adrian R Abdel-Wahab, Omar Producer: 20200721 In: Cell vol. 180 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 3387 results.