Search filters

List of works by Nitzan Kol

Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy.

scientific article published on March 2017

G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures

scientific article

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.

scientific article published on 18 July 2016

Nm-seq maps 2'-O-methylation sites in human mRNA with base precision.

scientific article published on 15 May 2017

RNA editing by ADAR1 leads to context-dependent transcriptome-wide changes in RNA secondary structure

scientific article published on 13 November 2017

Stem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation

scientific article

The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNA

scientific journal article

Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community

scientific article published on 03 March 2020

Paulina is supported by:

About Paulina

Help