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Alternative splicing

A Flanking Gene Problem Leads to the Discovery of a Gprc5b Splice Variant Predominantly Expressed in C57Bl/6J Mouse Brain and in Maturing Neurons

Bethany H. Cool, Guy C-K. Chan, [ ... ], Qubai Hu

Isoform-Specific Regulation and Localization of the Coxsackie and Adenovirus Receptor in Human Airway Epithelia

Katherine J. D. A. Excoffon, Nicholas D. Gansemer, [ ... ], Joseph Zabner

Endothelial Cell Processing and Alternatively Spliced Transcripts of Factor VIII: Potential Implications for Coagulation Cascades and Pulmonary Hypertension

Claire L. Shovlin, Gillian Angus, [ ... ], Francesco A. Mauri

Alternative Splicing of the Angiogenesis Associated Extra-Domain B of Fibronectin Regulates the Accessibility of the B-C Loop of the Type III Repeat 8

Elisa Ventura, Francesca Sassi, [ ... ], Luciano Zardi

SRRM2, a Potential Blood Biomarker Revealing High Alternative Splicing in Parkinson's Disease

Lina A. Shehadeh, Kristine Yu, [ ... ], Spyridon Papapetropoulos

Expression Map of the Human Exome in CD34+ Cells and Blood Cells: Increased Alternative Splicing in Cell Motility and Immune Response Genes

Sylvie Tondeur, Céline Pangault, [ ... ], John De Vos

Alternative Splicing and Extensive RNA Editing of Human TPH2 Transcripts

Maik Grohmann, Paul Hammer, [ ... ], Diego J. Walther

A Statistical Method for the Detection of Alternative Splicing Using RNA-Seq

Liguo Wang, Yuanxin Xi, [ ... ], Wei Li

Genome-Wide Analysis of Immune Activation in Human T and B Cells Reveals Distinct Classes of Alternatively Spliced Genes

Yevgeniy A. Grigoryev, Sunil M. Kurian, [ ... ], Daniel R. Salomon

Alternative Splicing and Transcriptome Profiling of Experimental Autoimmune Encephalomyelitis Using Genome-Wide Exon Arrays

Alan Gillett, Klio Maratou, [ ... ], Tomas Olsson

A Unique, Consistent Identifier for Alternatively Spliced Transcript Variants

Alberto Riva, Graziano Pesole

Alternative Splicing of TCF7L2 Gene in Omental and Subcutaneous Adipose Tissue and Risk of Type 2 Diabetes

Ludmila Prokunina-Olsson, Lee M. Kaplan, Eric E. Schadt, Francis S. Collins

No Evidence for Mutations of CTCFL/BORIS in Silver-Russell Syndrome Patients with IGF2/H19 Imprinting Control Region 1 Hypomethylation

Jeremiah Bernier-Latmani, Alessandra Baumer, Phillip Shaw

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