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	921.	[Left dominant arrhythmogenic cardiomyopathy caused by a novel nonsense mutation in desmoplakin]. [electronic resource] by Navarro-Manchón, Josep Fernández, Elena Igual, Begoña Asimaki, Angeliki Syrris, Petros Osca, Joaquín Salvador, Antonio Zorio, Esther Producer: 20111006 In: Revista espanola de cardiologia vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	922.	Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation. [electronic resource] by Umegaki, N Nakano, H Tamai, K Mitsuhashi, Y Akasaka, E Sawamura, D Katayama, I Producer: 20110914 In: The British journal of dermatology vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	923.	Therapeutics based on stop codon readthrough. [electronic resource] by Keeling, Kim M Xue, Xiaojiao Gunn, Gwen Bedwell, David M Producer: 20150514 In: Annual review of genomics and human genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	924.	Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay. [electronic resource] by Haga, Rie Miki, Yasuo Funamizu, Yukihisa Kon, Tomoya Suzuki, Chieko Ueno, Tatsuya Nishijima, Haruo Arai, Akira Tomiyama, Masahiko Shimazaki, Haruo Takiyama, Yoshihisa Baba, Masayuki Producer: 20121016 In: Clinical neurology and neurosurgery vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	925.	A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16). [electronic resource] by Pattnaik, Bikash R Shahi, Pawan K Marino, Meghan J Liu, Xinying York, Nathaniel Brar, Simran Chiang, John Pillers, De-Ann M Traboulsi, Elias I Producer: 20160322 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	926.	Cattle genome-wide analysis reveals genetic signatures in trypanotolerant N'Dama. [electronic resource] by Kim, Soo-Jin Ka, Sojeong Ha, Jung-Woo Kim, Jaemin Yoo, DongAhn Kim, Kwondo Lee, Hak-Kyo Lim, Dajeong Cho, Seoae Hanotte, Olivier Mwai, Okeyo Ally Dessie, Tadelle Kemp, Stephen Oh, Sung Jong Kim, Heebal Producer: 20171225 In: BMC genomics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	927.	GM2 gangliosidosis AB variant: novel mutation from India - a case report with a review. [electronic resource] by Sheth, Jayesh Datar, Chaitanya Mistri, Mehul Bhavsar, Riddhi Sheth, Frenny Shah, Krati Producer: 20171122 In: BMC pediatrics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	928.	Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population. [electronic resource] by Jagannathan, Sujatha Bradley, Robert K Producer: 20171215 In: Genome research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	929.	Roles of Epstein-Barr virus BGLF3.5 gene and two upstream open reading frames in lytic viral replication in HEK293 cells. [electronic resource] by Watanabe, Takahiro Fuse, Kenshiro Takano, Takahiro Narita, Yohei Goshima, Fumi Kimura, Hiroshi Murata, Takayuki Producer: 20151012 In: Virology vol. 483 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	930.	Protein Mis-Termination Initiates Genetic Diseases, Cancers, and Restricts Bacterial Genome Expansion. [electronic resource] by Wong, Tit-Yee Schwartzbach, Steve D Producer: 20160413 In: Journal of environmental science and health. Part C, Environmental carcinogenesis & ecotoxicology reviews vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	931.	A frameshift variant in the COL5A1 gene in a cat with Ehlers-Danlos syndrome. [electronic resource] by Spycher, M Bauer, A Jagannathan, V Frizzi, M De Lucia, M Leeb, T Producer: 20181211 In: Animal genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	932.	Global coagulation tests to assess the value of the presurgical treatment in a patient with congenital factor XI deficiency and inhibitor. [electronic resource] by Biguzzi, Eugenia Siboni, Simona M Clerici, Marigrazia Padovan, Lidia Scalambrino, Erica Chantarangkul, Veena Novembrino, Cristina Tripodi, Armando Producer: 20201207 In: International journal of laboratory hematology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	933.	Efficient ZFN-Mediated Stop Codon Integration into the CCR5 Locus in Hematopoietic Stem Cells: A Possible Source for Intrabone Marrow Cell Transplantation. [electronic resource] by Chattong, Supreecha Chaikomon, Kamontip Chaiya, Theerasak Tangkosakul, Thitirat Palavutitotai, Nattawan Anusornvongchai, Thitinun Manotham, Krissanapong Producer: 20190722 In: AIDS research and human retroviruses vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	934.	Corneal confocal microscopy and familial amyloidotic polyneuropathy. [electronic resource] by Bouaich, K Dufrane, R Youssfi, A Slim, E Ehongo, A Producer: 20200916 In: Journal francais d'ophtalmologie vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	935.	Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report. [electronic resource] by Ouchkat, Fatima Regragui, Wafaa Smaili, Imane Naciri Darai, Hajar Bouslam, Naima Rahmani, Mounia Melhaoui, Adyl Arkha, Yasser El Fahime, Elmostafa Bouhouche, Ahmed Producer: 20200504 In: BMC medical genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	936.	Gp4 is a nuclease required for morphogenesis of T4-like bacteriophages. [electronic resource] by Benler, Sean Hung, Shr-Hau Vander Griend, Jacob A Peters, Gregory A Rohwer, Forest Segall, Anca M Producer: 20200930 In: Virology vol. 543 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	937.	UGA suppression by tRNACmCATrp occurs in diverse virus RNAs due to a limited influence of the codon context. [electronic resource] by Urban, C Zerfass, K Fingerhut, C Beier, H Producer: 19961125 In: Nucleic acids research vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	938.	An exonic mutation of the GH-1 gene causing familial isolated growth hormone deficiency type II. [electronic resource] by Takahashi, I Takahashi, T Komatsu, M Sato, T Takada, G Producer: 20021212 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	939.	Stop making nonSense: the C. elegans smg genes. [electronic resource] by Mango, S E Producer: 20011214 In: Trends in genetics : TIG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	940.	Identification of a new beta-thalassemia nonsense mutation [codon 59 (AAG-->TAG)]. [electronic resource] by Patterson, Margie Walker, Lynda Chui, David H K Cohen, Alan R Waye, John S Producer: 20040402 In: Hemoglobin vol. 27 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 5852 results.