Scientific publications
Publications
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2017
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1α,20S-Dihydroxyvitamin D3 Interacts with Vitamin D Receptor: Crystal Structure and Route of Chemical Synthesis
- Zongtao Lin
- Hao Chen
- Anna Belorusova
- John Bollinger
- Edith Tang
- Zorica Janjetovic
- Tae-Kang Kim
- Zhongzhi Wu
- Duane Miller
- Andrzef Slominski
- Arnold Postlethwaite
- Robert Tuckey
- Natacha Rochel-Guiberteau
- Wei Li
Scientific Reports ; Volume: 7 ; Page: 10193
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Homozygous truncating variants in TBC1D23 cause pontocerebellar hypoplasia and alter cortical development
- Ekaterina Ivanova
- F Mau-Them
- Saima Riazuddin
- Kimia Kahrizi
- Vincent Laugel
- Elise Schaefer
- A de Saint Martin
- Karen Runge
- Zafar Iqbal
- Marie-Aude Spitz
- Mary Laura
- Nathalie Drouot
- Bénédicte Gerard
- Jean-François Deleuze
- Arjan de Brouwer
- Attia Razzaq
- Helene Dollfus
- Muhammad Assir
- Patrick Nitchké
- Maria-Victoria Hinckelmann Rivas
- ...
American Journal of Human Genetics ; Volume: 101 ; Page: 428-440
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Fragile X syndrome
- Randi Hagerman
- Elizabeth Berry-Kravis
- Heather Hazlett
- Donald Bailey
- Herve Moine
- R Kooy
- Flora Tassone
- Ilse Gantois
- Nahum Sonenberg
- Jean-Louis Mandel
- Paul Hagerman
Nature reviews Disease primers ; Volume: 3
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LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo
- Joanna Jachowicz
- Xinyang Bing
- Julien Pontabry
- Ana Bošković
- Oliver j. Rando
- Maria-Elena Torres-Padilla
Nature Genetics ; Volume: 49 ; Page: 1502--1510
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Epimetheus - a multi-profile normalizer for epigenomic sequencing data
- Mohamed Ashick Mohamed Saleem
- Marco Antonio Mendoza Parra
- Pierre Cholley
- Matthias Blum
- Hinrich Gronemeyer
BMC Bioinformatics ; Volume: 18
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GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
- Konrad Platzer
- Hongjie Yuan
- Hannah Schutz
- Alexander Winschel
- Wenjuan Chen
- Chun Hu
- Hirofumi Kusumoto
- Henrike Heyne
- Katherine Helbig
- Sha Tang
- Marcia Willing
- Brad Tinkle
- Darius Adams
- Christel Depienne
- Boris Keren
- Cyril Mignot
- Eirik Frengen
- Petter Strømme
- Saskia Biskup
- Dennis Döcker
- ...
Journal of Medical Genetics ; Volume: 54 ; Page: 460-470
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WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.
- Mara Cavallin
- Maria A Rujano
- Nathalie Bednarek
- Daniel Medina-Cano
- Antoinette Bernabe Gelot
- Séverine Drunat
- Camille Maillard
- Meriem Garfa-Traore
- Christine Bole
- Patrick Nitschke
- Claire Beneteau
- Thomas Besnard
- Benjamin Cogné
- Marion Eveillard
- Alice Kuster
- Karine Poirier
- Alain Verloes
- Jelena Martinovic
- Laurent Bidat
- Marlène Rio
- ...
Brain - A Journal of Neurology ; Volume: 140 ; Page: 2597-2609
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Dual role of DR5 in death and survival signaling leads to TRAIL resistance in cancer cells
- Yelyzaveta Shlyakhtina
- Valeria Pavet-Portal
- Hinrich Gronemeyer
Cell Death and Disease ; Volume: 8
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MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression
- Lise-Marie Donnio
- Baptiste Bidon
- Satoru Hashimoto
- Melanie May
- Alexey Epanchintsev
- Colm Ryan
- William Allen
- Anna Hackett
- Jozef Gecz
- Cindy Skinner
- Roger Stevenson
- Arjan de Brouwer
- Charles Coutton
- Christine Francannet
- Pierre-Simon Jouk
- Charles Schwartz
- Jean-Marc Egly
Human Molecular Genetics ; Volume: 26 ; Page: 2062-2075
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SECIS-binding protein 2 interacts with the SMN complex and the methylosome for selenoprotein mRNP assembly and translation
- Anne-Sophie Gribling-Burrer
- Michael Leichter
- Laurence Wurth
- Alexandra Huttin
- Florence Schlotter
- Nathalie Troffer-Charlier
- Vincent Cura
- Martine Barkats
- Jean Cavarelli
- Séverine Massenet
- Christine Allmang
Nucleic Acids Research ; Volume: 45 ; Page: 5399-5413
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