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Results 1 to 25 of 703

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Large intron 14 rearrangement in APC results in splice defect and attenuated FAPTUOHY, Thérèse M. F; DONE, Michelle W; LEWANDOWSKI, Michelle S et al.Human genetics. 2010, Vol 127, Num 3, pp 359-369, issn 0340-6717, 11 p.Article

TopHat : discovering splice junctions with RNA-SeqTRAPNELL, Cole; PACHTER, Lior; SALZBERG, Steven L et al.Bioinformatics (Oxford. Print). 2009, Vol 25, Num 9, pp 1105-1111, issn 1367-4803, 7 p.Article

A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1HACKMANN, Karl; MARKOFF, Arseni; FENG QIAN et al.Human molecular genetics (Print). 2005, Vol 14, Num 21, pp 3249-3262, issn 0964-6906, 14 p.Article

ARH: predicting splice variants from genome-wide data with modified entropyRASCHE, Axel; HERWIG, Ralf.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 1, pp 84-90, issn 1367-4803, 7 p.Article

New implosive connector technology for high voltage conductorsPASINI, C.IEE conference publication. 2006, pp 192-196, issn 0537-9989, isbn 0-86341-613-6, 1Vol, 5 p.Conference Paper

Novel L1CAM Splice Site Mutation in a Young Male With L1 SyndromeREHNBERG, Malin; JONASSON, Jon; GUNNARSSON, Cecilia et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 439-441, issn 1552-4825, 3 p.Article

SSgo1, a Major Splice Variant of Sgo1, Functions in Centriole Cohesion Where It Is Regulated by PIk1XIAOXING WANG; YALI YANG; QING DUAN et al.Developmental cell. 2008, Vol 14, Num 3, pp 331-341, issn 1534-5807, 11 p.Article

Ontogenomic study of the relationship between number of gene splice variants and GO categorizationKAHN, Ari B; ZEEBERG, Barry R; RYAN, Michael C et al.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 16, pp 1945-1949, issn 1367-4803, 5 p.Article

Coevolution of genomic intron number and splice sitesIRIMIA, Manuel; PENNY, David; ROY, Scott W et al.Trends in genetics (Regular ed.). 2007, Vol 23, Num 7, pp 321-325, issn 0168-9525, 5 p.Article

A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis familyMINTCHEV, Nikolay; ZAMBA-PAPANICOLAOU, Eleni; KLEOPA, Kleopas A et al.Neurology. 2009, Vol 72, Num 1, pp 28-32, issn 0028-3878, 5 p.Article

A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type IIKIM, J.-W; NAM, S. H; JANG, K.-T et al.Human genetics. 2004, Vol 115, Num 3, pp 248-254, issn 0340-6717, 7 p.Article

ABMapper: a suffix array-based tool for multi-location searching and splice-junction mappingLOU, Shao-Ke; BING NI; LO, Leung-Yau et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 3, pp 421-422, issn 1367-4803, 2 p.Article

PIk1-Dependent and -Independent Roles of an ODF2 Splice Variant, hCenexin1, at the Centrosome of Somatic CellsSOUNG, Nak-Kyun; PARK, Jung-Eun; YU, Li-Rong et al.Developmental cell. 2009, Vol 16, Num 4, pp 539-550, issn 1534-5807, 12 p.Article

Chimerization of multiple antibody classes using splice overlap extension PCRJONES, Martina L; BARNARD, Ross T.BioTechniques. 2005, Vol 38, Num 2, pp 181-182, issn 0736-6205, 2 p.Article

Environmental qualification of heat shrinkable splices using the degradation factor methodALLMAN, M. J; SMITH, D. L.IEEE transactions on energy conversion. 1989, Vol 4, Num 1, pp 68-73, issn 0885-8969, 6 p.Conference Paper

CNS malformations in knobloch syndrome with splice mutation in COL18A1 geneKEREN, Boris; SUZUKI, Oscar T; GDRARD-BLANLUCT, Marion et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 13, pp 1514-1518, issn 1552-4825, 5 p.Article

An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPPBELLONE, E; BALESTRA, P; RIBIZZI, G et al.Journal of neurology, neurosurgery and psychiatry. 2006, Vol 77, Num 4, pp 538-540, issn 0022-3050, 3 p.Article

Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variantsMUKHOPADHYAY, Arijit; NIKOPOULOS, Konstantinos; VAN DER VELDE-VISSER, Saskia D et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 8, pp 3565-3572, issn 0146-0404, 8 p.Article

FOXP2: novel exons, splice variants, and CAG repeat length stabilityBRUCE, Heather A; MARGOLIS, Russell L.Human genetics. 2002, Vol 111, Num 2, pp 136-144, issn 0340-6717Article

The USH1C216G → A splice-site mutation results in a 35-base-pair deletionLENTZ, Jennifer; SAVAS, Sevtap; NG, San-San et al.Human genetics. 2005, Vol 116, Num 3, pp 225-227, issn 0340-6717, 3 p.Article

PCR isolation and cloning of novel splice variant mRNAs from known drug target genesPEI JIN; FU, Glenn K; WILSON, Amy D et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 4, pp 566-571, issn 0888-7543, 6 p.Article

Contribution aux méthodes d'étalonnage en réflectométrie optique dans le domaine temporel. Mesure précise des faibles réflectances = Contribution to calibration methods concerning Optical Time Domain Reflectometry. Accurate measurement of low reflectancesDucos, Lionel; Facq, P.1994, 125 p.Thesis

A new 3D high resolution servo microdisplacement stage applied to the low-loss splices of single-mode fibresYUNJIANG RAO; SHANGLIAN HUANG.Measurement science & technology (Print). 1991, Vol 2, Num 9, pp 876-878, issn 0957-0233Article

Stripping-free mechanical splicerABE, Y; HIROTA, H; ASAKAWA, S et al.Electronics letters. 2012, Vol 48, Num 11, pp 641-642, issn 0013-5194, 2 p.Article

Development of single-mode four-fiber ribbon splicer with accurate splice loss estimationONODERA, T; TAYA, H; YAMADA, T et al.Optics letters. 1990, Vol 15, Num 23, pp 1406-1408, issn 0146-9592Article

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