
Scientific publications
Publications
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2011
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Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor death.
- Marie-Noëlle Delyfer
- Wolfgang Raffelsberger
- David Mercier
- Jean-François Korobelnik
- Alain Gaudric
- David G. Charteris
- Ramin Tadayoni
- Florence Metge
- Georges Caputo
- Pierre-Olivier Barale
- Raymond Ripp
- Jean-Denis Muller
- Olivier Poch
- José-Alain Sahel
- Thierry Léveillard
PLoS ONE ; Volume: 6 ; Page: e28791
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Regenerating I messenger RNA and protein expression in the failing human testis: a potential molecular prognostic marker of seminoma
- Virginie Mauro
- Daniel Chevallier
- Juliette Haudebourg
- Françoise Sénégas-Balas
- Georges Pointis
Human Pathology ; Volume: 42 ; Page: 1841-1848
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A fraction of the transcription factor TAF15 participates in interactions with a subset of the spliceosomal U1 snRNP complex
- Michael Leichter
- Marija Marko
- Vassiliki Ganou
- Meropi Patrinou-Georgoula
- László Tora
- Apostolia Guialis
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ; Volume: 1814 ; Page: 1812-1824
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Collisions between Replication and Transcription Complexes Cause Common Fragile Site Instability at the Longest Human Genes
- Anne Helmrich
- Monica Ballarino
- Laszlo Tora
Molecular Cell ; Volume: 44 ; Page: 966-977
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Identifying single copy orthologs in Metazoa.
- Christopher J. Creevey
- Jean Muller
- Tobias Doerks
- Julie D. Thompson
- Detlev Arendt
- Peer Bork
PLoS Computational Biology ; Volume: 7 ; Page: e1002269
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Identification of evolutionarily conserved exons as regulated targets for the splicing activator tra2β in development.
- Sushma Grellscheid
- Caroline Dalgliesh
- Markus Storbeck
- Andrew Best
- Yilei Liu
- Miriam Jakubik
- Ylva Mende
- Ingrid Ehrmann
- Tomaz Curk
- Kristina Rossbach
- Cyril F Bourgeois
- James Stévenin
- David Grellscheid
- Michael S. Jackson
- Brunhilde Wirth
- David J. Elliott
PLoS Genetics ; Volume: 7 ; Page: e1002390
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Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects
- Agnès Bloch-Zupan
- Xavier Jamet
- Christelle Etard
- Virginie Laugel
- Jean Muller
- Véronique Geoffroy
- Jean-Pierre Strauss
- Valérie Pelletier
- Vincent Marion
- Olivier Poch
- Uwe Strahle
- Corinne Stoetzel
- Hélène Dollfus
American Journal of Human Genetics ; Volume: 89 ; Page: 773-781
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Characterization of PTZ-Induced Seizure Susceptibility in a Down Syndrome Mouse Model That Overexpresses CSTB
- Benoit Martin
- Nathalie Costet
- Jean-Charles Bizot
- Yann Hérault
- Véronique Brault
PLoS ONE ; Volume: 6 ; Page: e27845
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The PHD Finger of Human UHRF1 Reveals a New Subgroup of Unmethylated Histone H3 Tail Readers
- Nada Lallous
- Pierre Legrand
- Alastair McEwen
- Santiago Ramón-Maiques
- Jean-Pierre Samama
- Catherine Birck
PLoS ONE ; Volume: 6 ; Page: e27599
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Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres
- Maartje van Rij
- Marjan de Rademaeker
- Céline Moutou
- Jos Cfm Dreesen
- Martine de Rycke
- Inge Liebaers
- Joep Pm Geraedts
- Christine Em de Die-Smulders
- Stéphane Viville
European Journal of Human Genetics ; Volume: 20 ; Page: 368-375
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