نتایج جستجو برای: spliced variants

تعداد نتایج: 114651  

2017
Anouk C. M. Platteel Juliane Liepe Willem van Eden Michele Mishto Alice J. A. M. Sijts

Efficient and safe induction of CD8+ T cell responses is a desired characteristic of vaccines against intracellular pathogens. To achieve this, a new generation of safe vaccines is being developed accommodating single, dominant antigens of pathogens of interest. In particular, the selection of such antigens is challenging, since due to HLA polymorphism the ligand specificities and immunodominan...

Journal: :Cancer discovery 2015
Elena Sotillo David M Barrett Kathryn L Black Asen Bagashev Derek Oldridge Glendon Wu Robyn Sussman Claudia Lanauze Marco Ruella Matthew R Gazzara Nicole M Martinez Colleen T Harrington Elaine Y Chung Jessica Perazzelli Ted J Hofmann Shannon L Maude Pichai Raman Alejandro Barrera Saar Gill Simon F Lacey Jan J Melenhorst David Allman Elad Jacoby Terry Fry Crystal Mackall Yoseph Barash Kristen W Lynch John M Maris Stephan A Grupp Andrei Thomas-Tikhonenko

UNLABELLED The CD19 antigen, expressed on most B-cell acute lymphoblastic leukemias (B-ALL), can be targeted with chimeric antigen receptor-armed T cells (CART-19), but relapses with epitope loss occur in 10% to 20% of pediatric responders. We detected hemizygous deletions spanning the CD19 locus and de novo frameshift and missense mutations in exon 2 of CD19 in some relapse samples. However, w...

Journal: :Bioinformation 2007
Luv Kashyap Mohammad Tabish

Cadherins are calcium-dependent, homophilic, cell-cell adhesion receptors that regulate morphogenesis, pattern formation and cell migration. The C. elegans Genome Sequencing Consortium has reported 12 genes from C. elegansgenome encoding members of the cadherin superfamily. Alternative splicing of eukaryotic pre-mRNAs is a mechanism for generating potentially many transcript isoforms from a sin...

2014
Alessandra Perfetti Simona Greco Pasquale Fasanaro Enrico Bugiardini Rosanna Cardani Jose M. Garcia. Manteiga Michela Riba Davide Cittaro Elia Stupka Giovanni Meola Fabio Martelli

Myotonic dystrophy type 2 (DM2) is a genetic, autosomal dominant disease due to expansion of tetraplet (CCTG) repetitions in the first intron of the ZNF9/CNBP gene. DM2 is a multisystemic disorder affecting the skeletal muscle, the heart, the eye and the endocrine system. According to the proposed pathological mechanism, the expanded tetraplets have an RNA toxic effect, disrupting the splicing ...

Journal: :The Japanese journal of veterinary research 2004
Yuka Namiki Yasuhiro Kon Nobuya Sasaki Takashi Agui Daiji Endoh

In MRL/MpJ mice, there is a genetic mutation of exonuclease 1 (Exo1), in which the exon 9 is sometimes deleted. In the present study, to check the generation of the spliced exons, exon 8-intron 8-exon 9 (pCX/Ex/EIE/B and pCX/Ex/EIE/M) plasmids were temporally transfected in vitro into BALB 3T3 cells, and RT-PCR using appropriate primer pair was carried out 1 day after transfection. In these con...

2011
L. Didierlaurent P. J. Racine L. Houzet C. Chamontin B. Berkhout M. Mougel

HIV-1 particles contain RNA species other than the unspliced viral RNA genome. For instance, viral spliced RNAs and host 7SL and U6 RNAs are natural components that are non-randomly incorporated. To understand the mechanism of packaging selectivity, we analyzed the content of a large panel of HIV-1 variants mutated either in the 5'UTR structures of the viral RNA or in the Gag-nucleocapsid prote...

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