Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Search results (17)

« Back to Publications

CDIN1-Codanin-1 complex defective in congenital dyserythropoietic anaemia type I is an RNA nuclease.

Brolih S. et al, (2026), Nat Commun

Temporal changes in erythroid progenitors in critically ill patients: a prospective cohort study.

Scott C. et al, (2025), Haematologica, 110, 739 - 743

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.

Pagnamenta AT. et al, (2023), Genome Med, 15

RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.

Martell DJ. et al, (2023), medRxiv

Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level.

Scott C. et al, (2022), Br J Haematol, 198, e10 - e14

The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin.

Truch J. et al, (2022), Nat Commun, 13

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

Scott C. et al, (2021), Haematologica, 106, 2960 - 2970

Genetic and functional insights into CDA-I prevalence and pathogenesis.

Olijnik A-A. et al, (2021), J Med Genet, 58, 185 - 195

An integrated platform to systematically identify causal variants and genes for polygenic human traits

Downes D. et al, (2019)

Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I)

Scott C. et al, (2019)

A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactions.

Brown JM. et al, (2018), Nat Commun, 9

The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeats.

Nguyen DT. et al, (2017), EMBO Rep, 18, 914 - 928

Overexpression of a family of RPEL proteins modifies cell shape.

Favot L. et al, (2005), FEBS Lett, 579, 100 - 104

Effects of the peripherally selective kappa-opioid asimadoline, on substance P and CGRP mRNA expression in chronic arthritis of the rat.

Walker JS. et al, (2000), Neuropeptides, 34, 193 - 202

Capsaicin-sensitive afferents are involved in signalling transneuronal effects between cutaneous sensory nerves.

Scott C. et al, (2000), Neuroscience, 95, 535 - 541

Load More