Massive computational identification of somatic variants in exonic splicing enhancers using The Cancer Genome Atlas

by Kousuke Tanimoto, Tomoki Muramatsu, Johji Inazawa
Published 2019-12-01

Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations

by Ana Perdomo-Ramirez, Marian de Armas-Ortiz, Elena Ramos-Trujillo, Lorena Suarez-Artiles, Felix Claverie-Martin
Published 2019-01-01

Myelodysplastic Syndrome-Associated SRSF2 Mutations Cause Splicing Changes by Altering Binding Motif Sequences

by So Masaki, So Masaki, Shun Ikeda, Asuka Hata, Yusuke Shiozawa, Ayana Kon, Seishi Ogawa, Kenji Suzuki, Fumihiko Hakuno, Shin-Ichiro Takahashi, Naoyuki Kataoka, Naoyuki Kataoka
Published 2019-04-01

Can the HIV-1 splicing machinery be targeted for drug discovery?

by Dlamini Z, Hull R
Published 2017-03-01

Regulation of RNA Processing in Human Papillomavirus Type 16

by Rush, Margaret
Published 2005

BIOPHYSICAL CHARACTERIZATION OF ASF/SF2’S INTERACTION WITH SPLICE SITE A7 IN THE HIV GENOME

by Kochert, Brent Andrew
Published 2012

Novel sequence variations in LAMA2 and SGCG genes modulating cis-acting regulatory elements and RNA secondary structure

by Olfa Siala, Ikhlass Hadj Salem, Abdelaziz Tlili, Imen Ammar, Hanen Belguith, Faiza Fakhfakh
Published 2010-01-01

A de novo synonymous variant in EFTUD2 disrupts normal splicing and causes mandibulofacial dysostosis with microcephaly: case report

by Arthur Jacob, Jennifer Pasquier, Raphael Carapito, Frédéric Auradé, Anne Molitor, Philippe Froguel, Khalid Fakhro, Najeeb Halabi, Géraldine Viot, Seiamak Bahram, Arash Rafii
Published 2020-09-01