NICOLAS CHARLET BERGUERAND

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Article dans une revue (64)

‘Non-coding’ GGC repeats are translated into toxic polyglycine proteins in neuromuscular diseases Nicolas Charlet-Berguerand,Manon Boivin Nature Genetics, 2026, 58 (3), pp.475-476. ⟨10.1038/s41588-026-02517-x⟩ Article dans une revue hal-05590272v1
GGC repeat expansions within new open reading frames are translated into toxic polyglycine proteins in oculopharyngodistal myopathy Manon Boivin,Jiaxi Yu,Nobuyuki Eura,Léa Schmitt,David Pietriet al. Nature Genetics, 2026, 58 (3), pp.517-529. ⟨10.1038/s41588-026-02507-z⟩ Article dans une revue hal-05585702v1
An unexpected polyglycine route to spinocerebellar ataxia Nicolas Charlet-Berguerand Nature Genetics, 2024, 56 (6), pp.1039-1041. ⟨10.1038/s41588-024-01770-2⟩ Article dans une revue hal-04984007v1
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest Ozlem Okutman,Manon Boivin,Jean Muller,Nicolas Charlet-Berguerand,Stephane Viville Human Reproduction, 2023, 38 (2), pp.306-314. ⟨10.1093/humrep/deac259⟩ Article dans une revue hal-04433444v1
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes Marcello Scala,Nathalie Drouot,Suzanna C. Maclennan,Marja W. Wessels,Magdalena Krygieret al. Human Mutation, 2022, 43 (9), pp.1299-1313. ⟨10.1002/humu.24414⟩ Article dans une revue hal-04219176v1
Trinucleotide CGG Repeat Diseases: An Expanding Field of Polyglycine Proteins? Manon Boivin,Nicolas Charlet-Berguerand Frontiers in Genetics, 2022, 13, pp.843014. ⟨10.3389/fgene.2022.843014⟩ Article dans une revue hal-04076612v1
Evidence for a fragile X messenger ribonucleoprotein 1 ( FMR1 ) mRNA gain‐of‐function toxicity mechanism contributing to the pathogenesis of fragile X‐associated premature ovarian insufficiency Roseanne Rosario,Hazel L. Stewart,Nila Roy Choudhury,Gracjan Michlewski,Nicolas Charlet-Berguerandet al. FASEB Journal, 2022, 36 (11), pp.e22612. ⟨10.1096/fj.202200468RR⟩ Article dans une revue hal-03850426v1
PolyGA targets the ER stress-adaptive response by impairing GRP75 function at the MAM in C9ORF72-ALS/FTD Federica Pilotto,Alexander Schmitz,Niran Maharjan,Rim Diab,Adolfo Odriozolaet al. Acta Neuropathologica, 2022, 144 (5), pp.939-966. ⟨10.1007/s00401-022-02494-5⟩ Article dans une revue hal-03850427v1
CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model Jiaxi Yu,Tongling Liufu,Yilei Zheng,Jin Xu,Lingchao Menget al. Proceedings of the National Academy of Sciences of the United States of America, 2022, 119 (41), ⟨10.1073/pnas.2208649119⟩ Article dans une revue hal-04220480v1
Neuropathology of FMR1 -premutation carriers presenting with dementia and neuropsychiatric symptoms Anke Dijkstra,Saif Haify,Niek Verwey,Niels Prins,Esmay van Der Toornet al. Brain Communications, 2021, 3 (1), pp.fcab007. ⟨10.1093/braincomms/fcab007⟩ Article dans une revue hal-03339489v1
Expression of expanded FMR1-CGG repeats alters mitochondrial miRNAs and modulates mitochondrial functions and cell death in cellular model of FXTAS Dhruv Gohel,Lakshmi Sripada,Paresh Prajapati,Fatema Currim,Milton Royet al. Free Radical Biology and Medicine, 2021, 165, pp.100-110. ⟨10.1016/j.freeradbiomed.2021.01.038⟩ Article dans une revue hal-03339492v1
Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases Manon Boivin,Jianwen Deng,Véronique Pfister,Erwan Grandgirard,Mustapha Oulad-Abdelghaniet al. Neuron, 2021, 109 (11), pp.1825-1835.e5. ⟨10.1016/j.neuron.2021.03.038⟩ Article dans une revue hal-03339485v1
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) Daniel Klionsky,Amal Kamal Abdel-Aziz,Sara Abdelfatah,Mahmoud Abdellatif,Asghar Abdoliet al. Autophagy, 2021, 17 (1), pp.1-382. ⟨10.1080/15548627.2020.1797280⟩ Article dans une revue (article de synthèse) inserm-03285572v1
The emerging molecular mechanisms for mitochondrial dysfunctions in FXTAS Dhruv Gohel,Nicolas Charlet Berguerand,Flora Tassone,Rajesh Singh Biochimica et Biophysica Acta - Molecular Basis of Disease, 2020, 1866 (12), pp.165918. ⟨10.1016/j.bbadis.2020.165918⟩ Article dans une revue hal-03339494v1
Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect Özlem Okutman,Cem Demirel,Firat Tülek,Veronique Pfister,Umut Büyüket al. Genes, 2020, 11 (4), pp.382. ⟨10.3390/genes11040382⟩ Article dans une revue hal-03339501v1
Distribution of Parkinson's disease associated RAB39B in mouse brain tissue Yujing Gao,Gabrielle Wilson,Sarah Stephenson,Mustapha Oulad-Abdelghani,Nicolas Charlet-Berguerandet al. Molecular Brain, 2020, 13 (1), ⟨10.1186/s13041-020-00584-7⟩ Article dans une revue hal-03339507v1
Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders Manon Boivin,Véronique Pfister,Angeline Gaucherot,Frank Ruffenach,Luc Negroniet al. EMBO Journal, 2020, 39 (4), pp.e100574. ⟨10.15252/embj.2018100574⟩ Article dans une revue hal-03339509v1
Curcumin Regulates the r(CGG)exp RNA Hairpin Structure and Ameliorate Defects in Fragile X-Associated Tremor Ataxia Syndrome Arun Kumar Verma,Eshan Khan,Subodh Kumar Mishra,Amit Mishra,Nicolas Charlet-Berguerandet al. Frontiers in Neuroscience, 2020, 14, ⟨10.3389/fnins.2020.00295⟩ Article dans une revue hal-03339498v1
De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder Francesca Mattioli,Gaelle Hayot,Nathalie Drouot,Bertrand Isidor,Jérémie Courraudet al. American Journal of Human Genetics, 2020, 106 (4), pp.438-452. ⟨10.1016/j.ajhg.2020.02.013⟩ Article dans une revue hal-03339508v1
FMRpolyG alters mitochondrial transcripts level and respiratory chain complex assembly in Fragile X associated tremor/ataxia syndrome [FXTAS] Dhruv Gohel,Lakshmi Sripada,Paresh Prajapati,Kritarth Singh,Milton Royet al. Biochimica et Biophysica Acta - Molecular Basis of Disease, 2019, 1865 (6), pp.1379-1388. ⟨10.1016/j.bbadis.2019.02.010⟩ Article dans une revue hal-03339512v1
Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers Petra Frick,Chantal Sellier,Ian Mackenzie,Chieh-Yu Cheng,Julie Tahraoui-Borieset al. Acta Neuropathologica Communications, 2018, 6 (1), ⟨10.1186/s40478-018-0579-0⟩ Article dans une revue hal-03339513v1
Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome M. Rebecca Glineburg,Peter Todd,Nicolas Charlet-Berguerand,Chantal Sellier Brain Research, 2018, 1693, pp.43-54. ⟨10.1016/j.brainres.2018.02.006⟩ Article dans une revue hal-03339526v1
Daunorubicin reduces MBNL1 titration by expanded CUG repeat RNA and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy M. Chakraborty,Chantal Sellier,Michel Ney,Pascal Villa,Nicolas Charlet-Berguerandet al. Disease Models & Mechanisms, 2018, ⟨10.1242/dmm.032557⟩ Article dans une revue hal-03339524v1
rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences Chantal Sellier,Estefanía Cerro-Herreros,Markus Blatter,Fernande Freyermuth,Angeline Gaucherotet al. Nature Communications, 2018, 9 (1), ⟨10.1038/s41467-018-04370-x⟩ Article dans une revue hal-03339515v1
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31 Taro Ishiguro,Nozomu Sato,Morio Ueyama,Nobuhiro Fujikake,Chantal Sellieret al. Neuron, 2017, 94 (1), pp.108-124.e7. ⟨10.1016/j.neuron.2017.02.046⟩ Article dans une revue hal-03339530v1
Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome Chantal Sellier,Ronald Buijsen,Fang He,Sam Natla,Laura Junget al. Neuron, 2017, 93 (2), pp.331-347. ⟨10.1016/j.neuron.2016.12.016⟩ Article dans une revue inserm-03375211v1
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family Ozlem Okutman,Jean Muller,Valerie Skory,Jean-Marie Garnier,Angeline Gaucherotet al. Journal of Assisted Reproduction and Genetics, 2017, 34 (5), pp.683-694. ⟨10.1007/s10815-017-0900-z⟩ Article dans une revue hal-03339528v1
The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway Sorana Ciura,Chantal Sellier,Maria-Letizia Campanari,Nicolas Charlet-Berguerand,Edor Kabashi Autophagy, 2016, 12 (8), pp.1406-1408. ⟨10.1080/15548627.2016.1189070⟩ Article dans une revue hal-03339538v1
Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency R. A. Buijsen,J. A. Visser,P. Kramer,E. A. Severijnen,M. Gearinget al. Human Reproduction, 2016, 31 (1), pp.158-68. ⟨10.1093/humrep/dev280⟩ Article dans une revue hal-03680434v1
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy Fernande Freyermuth,Frédérique Rau,Yosuke Kokunai,Thomas Linke,Chantal Sellieret al. Nature Communications, 2016, 7, pp.11067. ⟨10.1038/ncomms11067⟩ Article dans une revue hal-01301863v1
Loss of C9 ORF 72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death Chantal Sellier,Maria‐letizia Campanari,Camille Julie Corbier,Angeline Gaucherot,Isabelle Kolb‐cheynelet al. EMBO Journal, 2016, 35 (12), pp.1276-1297. ⟨10.15252/embj.201593350⟩ Article dans une revue hal-03339546v1
Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction Mouli Chakraborty,Estela Selma-Soriano,Emile Magny,Juan Pablo Couso,Manuel Pérez-Alonsoet al. Disease Models & Mechanisms, 2015, 8 (12), pp.1569-1578. ⟨10.1242/dmm.021428⟩ Article dans une revue hal-03339550v1
Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS Renate Hukema,Ronald A.M. Buijsen,Martijn Schonewille,Chris Raske,Lies-Anne W.F.M. Severijnenet al. Human Molecular Genetics, 2015, 24 (17), pp.4948-4957. ⟨10.1093/hmg/ddv216⟩ Article dans une revue hal-03339552v1
FXTAS: Size does matter! Chantal Sellier,Nicolas Charlet-Berguerand Cell Cycle, 2014, 13 (21), pp.3319-3319. ⟨10.4161/15384101.2014.972920⟩ Article dans une revue hal-03339556v1
FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome Ronald Am Buijsen,Chantal Sellier,Lies-Anne Wfm Severijnen,Mustapha Oulad-Abdelghani,Rob Fm Verhagenet al. Acta Neuropathologica Communications, 2014, 2 (1), ⟨10.1186/s40478-014-0162-2⟩ Article dans une revue hal-03339558v1
N‐ WASP is required for Amphiphysin‐2/ BIN 1‐dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy Sestina Falcone,William Roman,Karim Hnia,Vincent Gache,Nathalie Didieret al. EMBO Molecular Medicine, 2014, 6 (11), pp.1455-1475. ⟨10.15252/emmm.201404436⟩ Article dans une revue hal-03339560v1
Decreased DGCR8 Expression and miRNA Dysregulation in Individuals with 22q11.2 Deletion Syndrome Chantal Sellier,Vicki Hwang,Ravi Dandekar,Blythe Durbin-Johnson,Nicolas Charlet-Berguerandet al. PLoS ONE, 2014, 9 (8), pp.e103884. ⟨10.1371/journal.pone.0103884⟩ Article dans une revue hal-03339564v1
Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2 C. Carpentier,D. Ghanem,F. J. Fernandez-Gomez,F. Jumeau,J. V. Philippeet al. Biochimica et Biophysica Acta - Molecular Basis of Disease, 2014, 1842 (4), pp.654-664. ⟨10.1016/j.bbadis.2014.01.004⟩ Article dans une revue hal-01453196v1
RETRACTED ARTICLE: A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTD Renate Hukema,Fréderike Riemslagh,Shamiram Melhem,Herma van Der Linde,Lies-Anne Wfm Severijnenet al. Acta Neuropathologica Communications, 2014, 2 (1), ⟨10.1186/s40478-014-0166-y⟩ Article dans une revue hal-03339555v1
CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome Peter K. Todd,Seok Yoon Oh,Amy Krans,Fang He,Chantal Sellieret al. Neuron, 2013, 78 (3), pp.440--455. ⟨10.1016/j.neuron.2013.03.026⟩ Article dans une revue hal-04975891v1
The multiple molecular facets of fragile X-associated tremor/ataxia syndrome. Chantal Sellier,Karen Usdin,Chiara Pastori,Veronica J Peschansky,Flora Tassoneet al. Journal of Neurodevelopmental Disorders, 2013, 6 (1), pp.23. ⟨10.1186/1866-1955-6-23⟩ Article dans une revue inserm-01086046v1
Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome Chantal Sellier,Fernande Freyermuth,Ricardos Tabet,Tuan Tran,Fang Heet al. Cell Reports, 2013, 3 (3), pp.869-880. ⟨10.1016/j.celrep.2013.02.004⟩ Article dans une revue hal-03339569v1
Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons Sandra Almeida,Eduardo Gascon,Hélène Tran,Hsin Jung Chou,Tania Gendronet al. Acta Neuropathologica, 2013, 126 (3), pp.385-399. ⟨10.1007/s00401-013-1149-y⟩ Article dans une revue hal-03339567v1
A Small Molecule That Targets r(CGG) exp and Improves Defects in Fragile X-Associated Tremor Ataxia Syndrome Matthew Disney,Biao Liu,Wang-Yong Yang,Chantal Sellier,Tuan Tranet al. ACS Chemical Biology, 2012, 7 (10), pp.1711-1718. ⟨10.1021/cb300135h⟩ Article dans une revue hal-03339570v1
Mis-splicing of Tau exon 10 in myotonic dystrophy type I is reproduced by overexpression of CELF2 but not by MBNL1 silencing C.M. Dhaenens,H. Tran,M.-L. Frandemiche,C. Carpentier,S. Schraen-Maschkeet al. Biochimica et Biophysica Acta - Molecular Basis of Disease, 2011, ⟨10.1016/j.bbadis.2011.03.010⟩ Article dans une revue hal-00694732v1
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy Frédérique Rau,Fernande Freyermuth,Charlotte Fugier,Jean-Philippe Villemin,Marie-Christine Fischeret al. Nature Structural and Molecular Biology, 2011, 18 (7), pp.840-845. ⟨10.1038/nsmb.2067⟩ Article dans une revue istex hal-03339571v1
Analysis of Exonic Regions Involved in Nuclear Localization, Splicing Activity, and Dimerization of Muscleblind-like-1 Isoforms Helene Tran,Nathalie Gourrier,Camille Lemercier-Neuillet,Claire-Marie Dhaenens,Audrey Vautrinet al. Journal of Biological Chemistry, 2011, 286 (18), pp.16435 - 16446. ⟨10.1074/jbc.M110.194928⟩ Article dans une revue hal-01738403v1
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy. Charlotte Fugier,Arnaud F Klein,Caroline Hammer,Stéphane Vassilopoulos,Ylva Ivarssonet al. Nature Medicine, 2011, 17 (6), pp.720-5. ⟨10.1038/nm.2374⟩ Article dans une revue hal-00811986v1
CELF proteins regulate CFTR pre-mRNA splicing: essential role of the divergent domain of ETR-3 Gwendal Dujardin,Emanuele Buratti,Nicolas Charlet-Berguerand,Mafalda Martins de Araujo,Annick Mbopdaet al. Nucleic Acids Research, 2010, 38 (20), pp.7273-7285. ⟨10.1093/nar/gkq573⟩ Article dans une revue hal-03339576v1
Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients Chantal Sellier,Frédérique Rau,Yilei Liu,Flora Tassone,Renate Hukemaet al. EMBO Journal, 2010, 29 (7), pp.1248-1261. ⟨10.1038/emboj.2010.21⟩ Article dans une revue hal-03339578v1
Overexpression of MBNL1 fetal isoforms and modified splicing of Tau in the DM1 brain: two individual consequences of CUG trinucleotide repeats Claire-Marie Dhaenens,Susanna Schraen-Maschke,Ha Tran,Valérie Vingtdeux,Dana Ghanemet al. Experimental Neurology, 2008, 210 (2), pp.467-478. ⟨10.1016/j.expneurol.2007.11.020⟩ Article dans une revue istex hal-00282892v1
Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia. Anika H D M Dam,Isabelle Koscinski,Jan a M Kremer,Celine Moutou,Anne-Sophie Jaegeret al. American Journal of Human Genetics, 2007, 81 (4), pp.813-20. ⟨10.1086/521314⟩ Article dans une revue hal-00188891v1
RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors. Nicolas Charlet-Berguerand,Sascha Feuerhahn,Stephanie E Kong,Howard Ziserman,Joan W Conawayet al. EMBO Journal, 2006, 25 (23), pp.5481-91. ⟨10.1038/sj.emboj.7601403⟩ Article dans une revue hal-00187859v1
ETR-3 and CELF4 protein domains required for RNA binding and splicing activity in vivo G. Singh,Nicolas Charlet-B,Jin Han,Thomas A. Cooper Nucleic Acids Research, 2004, 32 (3), pp.1232-1241. ⟨10.1093/nar/gkh275⟩ Article dans une revue hal-03339598v1
Expression of GFRα1 receptor splicing variants with different biochemical properties is modulated during kidney development Nicolas Charlet-Berguerand,Hervé Le Hir,Mariarosaria Incoronato,Umberto Di Porzio,Yanbin Yuet al. Cellular Signalling, 2004, 16 (12), pp.1425-1434. ⟨10.1016/j.cellsig.2004.05.006⟩ Article dans une revue istex hal-03339582v1
Muscleblind proteins regulate alternative splicing Thai Ho,Nicolas Charlet-B,Michael Poulos,Gopal Singh,Maurice Swansonet al. EMBO Journal, 2004, 23 (15), pp.3103-3112. ⟨10.1038/sj.emboj.7600300⟩ Article dans une revue hal-03339596v1
Targeted delivery of adenoviral vectors by cytotoxic T cells Patricia Yotnda,Barbara Savoldo,Nicolas Charlet-Berguerand,Cliona Rooney,Malcolm Brenner Blood, 2004, 104 (8), pp.2272-2280. ⟨10.1182/blood-2003-11-3803⟩ Article dans une revue hal-03339583v1
Dynamic Antagonism between ETR-3 and PTB Regulates Cell Type-Specific Alternative Splicing Nicolas Charlet-B,Gopal Singh,Thomas Cooper,Penny Logan Molecular Cell, 2002, 9 (3), pp.649-658. ⟨10.1016/s1097-2765(02)00479-3⟩ Article dans une revue hal-03339600v1
Loss of the Muscle-Specific Chloride Channel in Type 1 Myotonic Dystrophy Due to Misregulated Alternative Splicing Nicolas Charlet-B.,Rajesh Savkur,Gopal Singh,Anne Philips,Elizabeth Griceet al. Molecular Cell, 2002, 10 (1), pp.45-53. ⟨10.1016/s1097-2765(02)00572-5⟩ Article dans une revue hal-03339601v1
5′-End RET Splicing: Absence of Variants in Normal Tissues and Intron Retention in Pheochromocytomas Hervé Le Hir,Nicolas Charlet-Berguerand,Vittorio de Franciscis,Claude Thermes Oncology, 2002, 63 (1), pp.84-91. ⟨10.1159/000065725⟩ Article dans une revue hal-03339610v1
The CELF Family of RNA Binding Proteins Is Implicated in Cell-Specific and Developmentally Regulated Alternative Splicing Andrea Ladd,Nicolas Charlet-B.,Thomas Cooper Molecular and Cellular Biology, 2001, 21 (4), pp.1285-1296. ⟨10.1128/MCB.21.4.1285-1296.2001⟩ Article dans une revue hal-03339591v1
Binding of PurH to a Muscle-specific Splicing Enhancer Functionally Correlates with Exon Inclusion in Vivo Kathryn Ryan,Nicolas Charlet-B.,Thomas Cooper Journal of Biological Chemistry, 2000, 275 (27), pp.20618-20626. ⟨10.1074/jbc.M909977199⟩ Article dans une revue hal-03339604v1
Relative Expression of the RET9 and RET51 Isoforms in Human Pheochromocytomas Hervé Le Hir,Nicolas Charlet-Berguerand,Anne-Paule Gimenez-Roqueplo,Massimo Mannelli,Pierre-François Plouinet al. Oncology, 2000, 58 (4), pp.311-318. ⟨10.1159/000012118⟩ Article dans une revue hal-03339608v1
Mechanisms of Transcriptional Activation of the Promoter of the Rainbow Trout Prolactin Gene by GHF1/Pit1 and Glucocorticoid Francesco Argenton,Nicolas Ramoz,Nicolas Charlet,Serena Bernardini,Lorenzo Colomboet al. Biochemical and Biophysical Research Communications, 1996, 224 (1), pp.57-66. ⟨10.1006/bbrc.1996.0984⟩ Article dans une revue istex hal-03339594v1