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	341.	Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitz junctional epidermolysis bullosa, and their application for prenatal testing. [electronic resource] by Takizawa, Y Shimizu, H Pulkkinen, L Suzumori, K Kakinuma, H Uitto, J Nishikawa, T Producer: 19990104 In: The Journal of investigative dermatology vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	342.	Gene symbol: SLC7A9. Disease: cystinuria, type non-I. [electronic resource] by Nunes, V Font-Llitjós, M Jiménez-Vidal, M Bisceglia, L Di Perna, M de Sanctis, L Rousaud, F Zelante, L Palacín, M Producer: 20050412 In: Human genetics vol. 116 Availability: No items available. Save to lists Add to cart (remove)
	343.	Familial cancer and ARLTS1. [electronic resource] by Frank, Bernd Klaes, Rüdiger Burwinkel, Barbara Producer: 20050726 In: The New England journal of medicine vol. 353 Availability: No items available. Save to lists Add to cart (remove)
	344.	A comparative genomics analysis of codon reassignments reveals a link with mitochondrial proteome size and a mechanism of genetic code change via suppressor tRNAs. [electronic resource] by Massey, Steven E Garey, James R Producer: 20070919 In: Journal of molecular evolution vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	345.	Molecular analysis in two siblings African patients with severe form of Hunter Syndrome: identification of a novel (p.Y54X) nonsense mutation. [electronic resource] by Mutesa, Léon Muganga, Narcisse Lissens, Willy Boemer, François Schoos, Roland Pierquin, Geneviève Bours, Vincent Producer: 20080319 In: Journal of tropical pediatrics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	346.	Factor VII deficiency: a double heterozygote of an Arg402Stop with a deletion of the C-terminal five amino acids and a Thr359Met. [electronic resource] by Okamoto, Masataka Katsuda, Itsuro Ohshika, Yasuna Maruyama, Fumio Ezaki, Kohji Emi, Nobuhiko Ichihara, Yoshikazu Producer: 20090518 In: European journal of haematology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	347.	De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome. [electronic resource] by Hoischen, Alexander van Bon, Bregje W M Rodríguez-Santiago, Benjamín Gilissen, Christian Vissers, Lisenka E L M de Vries, Petra Janssen, Irene van Lier, Bart Hastings, Rob Smithson, Sarah F Newbury-Ecob, Ruth Kjaergaard, Susanne Goodship, Judith McGowan, Ruth Bartholdi, Deborah Rauch, Anita Peippo, Maarit Cobben, Jan M Wieczorek, Dagmar Gillessen-Kaesbach, Gabriele Veltman, Joris A Brunner, Han G de Vries, Bert B B A Producer: 20111003 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	348.	Gene symbol: ABCA4. Disease: Macular dystrophy. [electronic resource] by Aguirre-Lamban, Jana Riveiro-Alvarez, R Cantalapiedra, D Vallespin, E Avila-Fernandez, A Trujillo-Tiebas, M J Villaverde-Montero, C Ayuso, C Producer: 20101124 In: Human genetics vol. 123 Availability: No items available. Save to lists Add to cart (remove)
	349.	A new homozygous nonsense mutation in LAMA3A underlying laryngo-onycho-cutaneous syndrome. [electronic resource] by Barzegar, M Mozafari, N Kariminejad, A Asadikani, Z Ozoemena, L McGrath, J A Producer: 20140827 In: The British journal of dermatology vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	350.	Retroviral strategy to stabilize viral RNA. [electronic resource] by Quek, Bao Lin Beemon, Karen Producer: 20141201 In: Current opinion in microbiology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	351.	Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergies. [electronic resource] by Has, C Jakob, T He, Y Kiritsi, D Hausser, I Bruckner-Tuderman, L Producer: 20150921 In: The British journal of dermatology vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	352.	Androgen receptor variants: another twist in the plot. [electronic resource] by Macoska, Jill A Producer: 20190920 In: Oncotarget vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	353.	Novel SGCE mutation (p.Glu65*) in a Japanese family with myoclonus-dystonia. [electronic resource] by Koide, Noriko Dateki, Sumito Watanabe, Kiyoko Moriuchi, Hiroyuki Producer: 20180716 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	354.	An [electronic resource] by Flanagan, Sarah E Dũng, Vũ Chí Houghton, Jayne A L De Franco, Elisa Ngoc, Can Thi Bich Damhuis, Annet Ashcroft, Frances M Harries, Lorna W Ellard, Sian Producer: 20180523 In: Journal of clinical research in pediatric endocrinology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	355.	A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene. [electronic resource] by Noushad, Muhammed Bhattacharjee, Shakya Weatherby, Stuart J Whitefield, Peter Producer: 20210531 In: Acta neurologica Belgica vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	356.	Neighboring base identity affects N-ethyl-N-nitrosourea-induced mutagenesis in Escherichia coli. [electronic resource] by Cai, Zhehong Fix, Douglas Producer: 20021220 In: Mutation research vol. 508 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	357.	[Translational control through nonsense suppression]. [electronic resource] by Muramatsu, T Kuchino, Y Producer: 19970408 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	358.	Identification of two novel nonsense mutations in the transglutaminase 1 gene in a Hungarian patient with congenital ichthyosiform erythroderma. [electronic resource] by Becker, K Csikós, M Sárdy, M Szalai, Z S Horváth, A Kárpáti, S Producer: 20040311 In: Experimental dermatology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	359.	Alström syndrome: intrafamilial phenotypic variability in sibs with a novel nonsense mutation of the ALMS1 gene. [electronic resource] by Titomanlio, L De Brasi, D Buoninconti, A Sperandeo, M P Pepe, A Andria, G Sebastio, G Producer: 20040927 In: Clinical genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	360.	Arabidopsis SMG7 protein is required for exit from meiosis. [electronic resource] by Riehs, Nina Akimcheva, Svetlana Puizina, Jasna Bulankova, Petra Idol, Rachel A Siroky, Jiri Schleiffer, Alexander Schweizer, Dieter Shippen, Dorothy E Riha, Karel Producer: 20081222 In: Journal of cell science vol. 121 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.