Alternative splicing

Alternative splicing a regulated gene expression process that allows a single genetic sequence to code for multiple proteins. Here is that latest research.

September 10, 2020
Review
Open Access

The biological function and clinical significance of SF3B1 mutations in cancer

Biomarker Research
Zhixia ZhouPeifeng Li
September 11, 2020
Open Access

Identification of Key mRNAs and lncRNAs in Neonatal Sepsis by Gene Expression Profiling

Computational and Mathematical Methods in Medicine
Lin BuXiao-Min Li
September 16, 2020
Review

RNA structures in alternative splicing and back-splicing

Wiley Interdisciplinary Reviews. RNA
Bingbing XuYongfeng Jin
September 11, 2020
Case Report
Open Access

A Novel SPAST/SPG4 Splice-Site Variant in a Family with Dominant Hereditary Spastic Paraplegia

Case Reports in Neurological Medicine
Nathaniel M RobbinsTanya M Bardakjian
September 16, 2020
Open Access

Global analysis of SBP gene family in Brachypodium distachyon reveals its association with spike development

Scientific Reports
Rajiv K TripathiJaswinder Singh
September 16, 2020

NPC1 silent variant induces skipping of exon 11 (p.V562V) and unfolded protein response was found in a specific Niemann-Pick type C patient

Molecular Genetics & Genomic Medicine
Marisa EncarnaçãoSandra Alves
September 17, 2020
Open Access

Mouse Ataxin-2 Expansion Downregulates CamKII and Other Calcium Signaling Factors, Impairing Granule-Purkinje Neuron Synaptic Strength

International Journal of Molecular Sciences
Aleksandar ArsovićGeorg Auburger
September 15, 2020

Shark: fishing relevant reads in an RNA-Seq sample

Bioinformatics
Luca DentiPaola Bonizzoni
September 16, 2020
Open Access

A customized scaffolds approach for the detection and phasing of complex variants by next-generation sequencing

Scientific Reports
Qiandong ZengPatricia M Okamoto
September 11, 2020
Preprint
Open Access

An extended catalogue of tandem alternative splice sites in human tissue transcriptomes

BioRxiv : the Preprint Server for Biology
A. MironovDmitri Pervouchine
September 10, 2020

Histone H3K9 and H3K14 acetylation at the promoter of the LGALS9 gene are associated with mRNA levels in cervical cancer cells

FEBS Open Bio
Erick Armenta-CastroVerónica Vallejo-Ruiz
September 11, 2020
Open Access

The Expression and Potential Role of Tubulin Alpha 1b in Wilms' Tumor

BioMed Research International
Qiong-Qian XuJia-Bo Chen
September 12, 2020

Effects of Alternative Splicing Events on Acute Myeloid Leukemia

DNA and Cell Biology
Si-Liang ChenYang Liang
September 10, 2020
Review
Open Access

Targeting Alternative Splicing as a Potential Therapy for Episodic Ataxia Type 2

Biomedicines
Fanny JaudonLorenzo A Cingolani
September 12, 2020
Open Access

Splicing Enhancers at Intron-Exon Borders Participate in Acceptor Splice Sites Recognition

International Journal of Molecular Sciences
Tatiana KováčováLucie Grodecká

Sign up to follow this feed and discover related papers.

Related Feeds

Archaeal RNA Polymerase

Archaeal RNA polymerases are most similar to eukaryotic RNA polymerase II but require the support of only two archaeal general transcription factors, TBP (TATA-box binding protein) and TFB (archaeal homologue of the eukaryotic general transcription factor TFIIB) to initiate basal transcription. Here is the latest research on archaeal RNA polymerases.

CREs: Gene & Cell Therapy

Gene and cell therapy advances have shown promising outcomes for several diseases. The role of cis-regulatory elements (CREs) is crucial in the design of gene therapy vectors. Here is the latest research on CREs in gene and cell therapy.

CRISPR & Single Cell Analyses

CRISPR-Cas system enables the editing of genes to create or correct mutations. This feed focuses on CRISPR-Cas applications relevant to single cell analyses. Here is the latest research.

CRISPR & Staphylococcus

CRISPR-Cas system enables the editing of genes to create or correct mutations. Staphylococci are associated with life-threatening infections in hospitals, as well as the community. Here is the latest research on how CRISPR-Cas system can be used for treatment of Staphylococcal infections.

CRISPR (general)

Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). CRISPR-Cas system enables the editing of genes to create or correct mutations. Discover the latest research on CRISPR here.

CRISPR Genome Editing & Therapy

CRISPR-Cas system enables the editing of genes to create or correct mutations. This feed focuses on the application of this system for gene editing and therapy in human diseases.

CRISPR Ribonucleases Deactivation

CRISPR-Cas system enables the editing of genes to create or correct mutations. This feed focuses on mechanisms that underlie deactivation of CRISPR ribonucleases. Here is the latest research.

CRISPR Screens in Drug Resistance

CRISPR-Cas system enables the editing of genes to create or correct mutations. This feed focuses on the application of CRISPR-Cas system in high-throughput genome-wide screens to identify genes that may confer drug resistance.

CRISPR Screens in Virology

This feed focuses on the application of CRISPR-Cas system in high-throughput genome-wide screens to identify genes that affect virus-host interactions. Here is the latest research.

CRISPR for Genome Editing

Genome editing technologies enable the editing of genes to create or correct mutations. Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). Here is the latest research on the use of CRISPR-Cas system in gene editing.

© 2020 Meta ULC. All rights reserved
/feed-previews/alternative-splicing/74162fec-4777-4430-b61a-12f563c8cd7c