Publications scientifiques
Les équipes de recherches de l'IGBMC publient régulièrement des articles qui font avancer les connaissances dans divers domaines de recherche. Vous trouverez sur cette page l'ensemble des publications dans lesquels les travaux de nos scientifiques sont cités.
Publications
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2009
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Inhibition of the Peptidyl-Prolyl-Isomerase Pin1 Enhances the Responses of Acute Myeloid Leukemia Cells to Retinoic Acid via Stabilization of RARα and PML-RARα
- Maurizio Gianni
- Andrea Boldetti
- Valeria Guarnaccia
- Alessandro Rambaldi
- Edoardo Parrella
- Ivan Raska
- Cecile Rochette-Egly
- Giannino del Sal
- Alessandra Rustighi
- Mineko Terao
- Enrico Garattini
Cancer Research ; Volume: 69 ; Page: 1016-1026
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A set of baculovirus transfer vectors for screening of affinity tags and parallel expression strategies
- Wassim Abdulrahman
- Muriel Uhring
- Isabelle Kolb-Cheynel
- Jean-Marie Garnier
- Dino Moras
- Natacha Rochel
- Didier Busso
- Arnaud Poterszman
Analytical Biochemistry ; Volume: 385 ; Page: 383-385
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Early mouse caudal development relies on crosstalk between retinoic acid, Shh and Fgf signalling pathways.
- Vanessa Ribes
- Isabelle Le Roux
- Muriel Rhinn
- Brigitte Schuhbaur
- Pascal Dollé
Development (Cambridge, England) ; Volume: 136 ; Page: 665-76
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A single-codon mutation converts HPV16 E6 oncoprotein into a potential tumor suppressor, which induces p53-dependent senescence of HPV-positive HeLa cervical cancer cells
- T Ristriani
- Sadek Fournane
- Georges Orfanoudakis
- Gilles Trave
- Murielle Masson
Oncogene ; Volume: 28 ; Page: 762-772
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Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasia.
- Stéphanie Pannier
- Vincent Couloigner
- Nadia Messaddeq
- Monique Elmaleh-Bergès
- Arnold Munnich
- Raymond Romand
- Laurence Legeai-Mallet
BBA - Biochimica et Biophysica Acta ; Volume: 1792 ; Page: 140-7
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Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
- David Parry
- Alan J. Mighell
- Walid El-Sayed
- Roger C. Shore
- Ismail K. Jalili
- Hélène Dollfus
- Agnes Bloch-Zupan
- Roman Carlos
- Ian M. Carr
- Louise M. Downey
- Katharine M. Blain
- David C. Mansfield
- Mehdi Shahrabi
- Mansour Heidari
- Parissa Aref
- Mohsen Abbasi
- Michel Michaelides
- Anthony T. Moore
- Jennifer Kirkham
- Chris F. Inglehearn
American Journal of Human Genetics ; Volume: 84 ; Page: 266-73
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Oral cobalamin (vitamin B12) treatment. An update
- E. Andrès
- N. Dali-Youcef
- T. Vogel
- K. Serraj
- J. Zimmer
International Journal of Laboratory Hematology ; Volume: 31 ; Page: 1-8
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HMGB4, a Novel Member of the HMGB Family, Is Preferentially Expressed in the Mouse Testis and Localizes to the Basal Pole of Elongating Spermatids.
- Raffaella Catena
- Emmanuelle Escoffier
- Cécile Caron
- Saadi Khochbin
- Igor Martianov
- Irwin Davidson
Biology of Reproduction ; Volume: 80 ; Page: 358-66
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A structural view of translation initiation in bacteria.
- Angelita Simonetti
- Stefano Marzi
- L. Jenner
- Alexander Myasnikov
- Pascale Romby
- Gulnara Yusupova
- Bruno Klaholz
- Marat Yusupov
Cellular and Molecular Life Sciences ; Volume: 66 ; Page: 423-36
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Induction of thymic stromal lymphopoietin expression in keratinocytes is necessary for generating an atopic dermatitis upon application of the active vitamin D3 analogue MC903 on mouse skin.
- Mei Li
- Pierre Hener
- Zhikun Zhang
- Krishna P. Ganti
- Daniel Metzger
- Pierre Chambon
Journal of Investigative Dermatology ; Volume: 129 ; Page: 498-502
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Page 388 sur 682