User profiles for A. Vielle

Anne Vielle

Cellsight program, University of Colorado, depart. of ophtalmology
Verified email at cuanschutz.edu
Cited by 3040

An assessment of histone-modification antibody quality

…, YB Schwartz, GA Shanower, A Vielle… - Nature structural & …, 2011 - nature.com
We have tested the specificity and utility of more than 200 antibodies raised against 57 different
histone modifications in Drosophila melanogaster, Caenorhabditis elegans and human …

Integrative Analysis of the Caenorhabditis elegans Genome by the modENCODE Project

…, M Morris, RK Auerbach, X Feng, J Leng, A Vielle… - Science, 2010 - science.org
We systematically generated large-scale data sets to improve genome annotation for the
nematode Caenorhabditis elegans, a key model organism. These data sets include …

[HTML][HTML] Comparative analysis of metazoan chromatin organization

…, B Qin, YB Schwartz, N Shoresh, P Stempor, A Vielle… - Nature, 2014 - nature.com
Genome function is dynamically regulated in part by chromatin, which consists of the histones,
non-histone proteins and RNA molecules that package DNA. Studies in Caenorhabditis …

Broad chromosomal domains of histone modification patterns in C. elegans

T Liu, A Rechtsteiner, TA Egelhofer, A Vielle… - Genome …, 2011 - genome.cshlp.org
Chromatin immunoprecipitation identifies specific interactions between genomic DNA and
proteins, advancing our understanding of gene-level and chromosome-level regulation. …

[HTML][HTML] Organoids for the study of retinal development and developmental abnormalities

A Vielle, YK Park, C Secora… - Frontiers in Cellular …, 2021 - frontiersin.org
The cumulative knowledge of retina development has been instrumental in the generation of
retinal organoid systems from pluripotent stem cells; and these three-dimensional organoid …

RNAs in the spliceosome: Insight from cryoEM structures

L Zhang, A Vielle, S Espinosa… - Wiley Interdisciplinary …, 2019 - Wiley Online Library
Pre‐mRNA splicing is catalyzed by the spliceosome, a multimegadalton RNA–protein
complex. The spliceosome undergoes dramatic compositional and conformational changes …

[HTML][HTML] Molecular epidemiology of DFNB1 deafness in France

AF Roux, N Pallares-Ruiz, A Vielle, V Faugère… - BMC medical …, 2004 - Springer
Background Mutations in the GJB2 gene have been established as a major cause of inherited
non syndromic deafness in different populations. A high number of sequence variations …

Molecular and in silico analyses of the full‐length isoform of usherin identify new pathogenic alleles in Usher type II patients

…, C Blanchet, C Hamel, S Ben Salah, A Vielle… - Human …, 2007 - Wiley Online Library
The usherin gene (USH2A) has been screened for mutations causing Usher syndrome type
II (USH2). Two protein isoforms have been identified: a short isoform of 1,546 amino acids …

Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a …

…, S Le Guedard, N Pallares-Ruiz, A Vielle… - Journal of medical …, 2006 - jmg.bmj.com
Background: Usher syndrome, a devastating recessive disorder which combines hearing
loss with retinitis pigmentosa, is clinically and genetically heterogeneous. Usher syndrome …

[HTML][HTML] H4K20me1 Contributes to Downregulation of X-Linked Genes for C. elegans Dosage Compensation

A Vielle, J Lang, Y Dong, S Ercan, C Kotwaliwale… - 2012 - journals.plos.org
The Caenorhabditis elegans dosage compensation complex (DCC) equalizes X-chromosome
gene dosage between XO males and XX hermaphrodites by two-fold repression of X-…