
Scientific publications
Publications
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2024
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Correction: Efficient pathway for men fertility preservation in testicular cancer or lymphoma: a cross-sectional study of national 2018 data (vol 33, 35, 2023)
- Segolene Prades
- Sarah-Lyne Jos
- Jacqueline Saias-Magnan
- Louis Bujan
- Florence Eustache
- Oxana Blagosklonov
- Eric Lechevallier
- Florence Brugnon
- Vanessa Loup-Cabaniols
- Dorian Bosquet
- Marie Prades
- Berengere Ducrocq
- Celine Chalas
- Sandrine Giscard-d'Estaing
- Anne Mayeur
- Isabelle Koscinsky
- Francoise Schmitt
- Aline Papaxanthos-Roche
- Marius Teletin
- Emmanuelle Thibault
- ...
Basic and clinical andrology ; Volume: 34 ; Page: 5
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A high-light therapy restores the circadian clock and corrects the pathological syndrome generated in restricted-fed mice
- Manohar Damara
- Nisha Misra
- Pierre Chambon
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 121
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Acutely Modifying Phosphatidylinositol Phosphates on Endolysosomes Using Chemically Inducible Dimerization Systems
- Wei Sheng Yap
- Peter K Kim
- Maxime Boutry
Bio-protocol ; Volume: 14
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Repurposing myoglobin into a carbene transferase for a [2,3]-sigmatropic Sommelet-Hauser rearrangement
- Manon Pujol
- Lison Degeilh
- Thibault Sauty de Chalon
- Marius Réglier
- A. Jalila Simaan
- Christophe Decroos
Journal of Inorganic Biochemistry ; Volume: 260 ; Page: 112688
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2023
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How much do we know about the function of mammalian genes?
- Lydia Teboul
- Yann Hérault
- Sara Wells
- Guillaume Pavlovic
BMC Biology ; Volume: 21
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Bi-allelic variants in WDR47 lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans
- Efil Bayam
- Peggy Tilly
- Stephan Collins
- José Rivera Alvarez
- Meghna Kannan
- Lucile Tonneau
- Bruno Rinaldi
- Romain Lecat
- Noémie Schwaller
- Sateesh Maddirevula
- Fabiola Monteiro
- João Paulo Kitajima
- Fernando Kok
- Mitsuhiro Kato
- Ahlam Hamed
- Mustafa Salih
- Saeed Al Tala
- Mais Hashem
- Hiroko Tada
- Hirotomo Saitsu
- ...
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Pathogenic DPAGT1 variants in limb‐girdle congenital myasthenic syndrome (LG‐CMS) associated with tubular aggregates and ORAI1 hypoglycosylation
- Laura Vanden Brande
- Stéphanie Bauché
- Laura Pérez-Guàrdia
- Damien Sternberg
- Andreea Seferian
- Edoardo Malfatti
- Roberto Silva-Rojas
- Clémence Labasse
- Frédéric Chevessier
- Pierre Carlier
- Bruno Eymard
- Norma Romero
- Jocelyn Laporte
- Laurent Servais
- Teresa Gidaro
- Johann Böhm
Neuropathology and Applied Neurobiology ; Volume: 50
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RlmQ: a newly discovered rRNA modification enzyme bridging RNA modification and virulence traits in Staphylococcus aureus
- Roberto Alexander Bahena Ceron
- Chloé Teixeira
- José Refugio Jaramillo Ponce
- Philippe Wolff
- Florence Couzon
- Pauline François
- Bruno P. Klaholz
- François Vandenesch
- Pascale Romby
- Karen Moreau
- Stefano Marzi
RNA ; Volume: 30 ; Page: 200-212
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Evolution of the Ikaros family transcription factors: From a deuterostome ancestor to humans
- Philippe Kastner
- Adina Aukenova
- Susan Chan
Biochemical and Biophysical Research Communications ; Volume: 694
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