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2015


125 publication(s):

Note: when necessary, only the first 15 authors are displayed.

International refereed journal articles

1 - 
Intérêt du dosage de l’immunoglobuline monoclonale complète lors du diagnostic ou du suivi des patients présentant un myélome à immunoglobuline complète : l’électrophorèse des protéines sériques et l’immonofixation ne seraient-elles pas suffisantes ? [Heavy/light chain specific immunoglobulin ratios provides no additional information than serum proteins electrophoresis and immunofixation for the diagnosis and the follow-up of intact immunoglobulin multiple myeloma patients]
M. -P. Beaumont-Epinette, Caroline Moreau, S. Besnard, F. Latute, N. Collet, M. Sebillot, B. Grosbois, C. Bendavid, L. Guenet, O Decaux
Pathologie Biologie, 2015, 63 (4-5), pp.215-221.
DOI : https://doi.org/10.1016/j.patbio.2015.06.001
Pubmed : 26319969
 Reprint request: Subject to availability
2 - 
A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome
Marie Abitbol, Christophe Hitte, Philippe Bossé, Nicolas Blanchard-Gutton, Anne Thomas, Lionel Martignat, Stéphane Blot, Laurent Tiret
PLoS ONE, 2015, 10 (9), pp.e0137019.
DOI : https://doi.org/10.1371/journal.pone.0137019
Pubmed : 26327126
PDF file
 Reprint request: Subject to availability
3 - 
CD9, a key actor in the dissemination of lymphoblastic leukemia, modulating CXCR4-mediated migration via RAC1 signaling
Marie-Pierre Arnaud, Audrey Vallée, Guillaume Robert, Jacinthe Bonneau, Christine Leroy, Nadine Varin-Blank, Anne-Gaelle Rio, Marie-Bérengère Troadec, Marie-Dominique Galibert, Virginie Gandemer
Blood, 2015, 126 (15), pp.1802-1812.
DOI : https://doi.org/10.1182/blood-2015-02-628560
Pubmed : 26320102
 Reprint request: Subject to availability
4 - 
From the core to beyond the margin: a genomic picture of glioblastoma intratumor heterogeneity
Marc Aubry, Marie de Tayrac, Amandine Etcheverry, Anne Clavreul, Stéphan Saikali, Philippe Menei, Jean Mosser
Oncotarget, 2015, 6 (14), pp.12094-12109.
DOI : https://doi.org/10.18632/oncotarget.3297
Pubmed : 25940437
 Reprint request: Subject to availability
5 - 
Identification and characterization of cichlid TAAR genes and comparison with other teleost TAAR repertoires
Naoual Azzouzi, Frédérique Barloy-Hubler, Francis Galibert
BMC Genomics, 2015, 16 (1), pp.335.
DOI : https://doi.org/10.1186/s12864-015-1478-4
Pubmed : 25900688
PDF file
 Reprint request: Subject to availability
6 - 
GNPAT variant associated with severe iron overload in HFE hemochromatosis
Edouard Bardou-Jacquet, Marie De Tayrac, Jean Mosser, Yves Deugnier
Hepatology, 2015, 62 (6), pp.1917-1918.
DOI : https://doi.org/10.1002/hep.27854
Pubmed : 25891252
 Reprint request: Subject to availability
7 - 
Annexin A2 is required for the early steps of cytokinesis.
Christelle Benaud, Gaëlle Le Dez, Sevtlana Mironov, Federico Galli, David Reboutier, Claude Prigent
Annexin A2 is required for the early steps of cytokinesis. EMBO Reports, 2015, 16 (4), pp.481-9.
DOI : https://doi.org/10.15252/embr.201440015
Pubmed : 25712672
 Reprint request: Subject to availability
8 - 
Hypogonadism associated with Cyp19a1 (Aromatase) posttranscriptional upregulation in Celf1 knockout mice
Gaëlla Boulanger, Marie Cibois, Justine Viet, Alexis Fostier, Stéphane Deschamps, Sylvain Pastezeur, Catherine Massart, Bernhard Gschloessl, Carole Gautier-Courteille, Luc Paillard
Molecular and Cellular Biology, 2015, 35 (18), pp.3244--3253.
DOI : https://doi.org/10.1128/MCB.00074-15
Pubmed : 26169831
 Reprint request: Subject to availability
9 - 
Hidden Mutations in CdLS - Limitations of Sanger Sequencing in Molecular Diagnostics
Diana Braunholz, Carolin Obieglo, Ilaria Parenti, Jelena Pozojevic, Juliane Eckhold, Benedikt Reiz, Ingrid Braenne, Kerstin S. Wendt, Erwan Watrin, Julia Vodopiutz, Harald Rieder, Gabriele Gillessen-Kaesbach, Frank J. Kaiser
Human Mutation, 2015, 36 (1), pp.26-29.
DOI : https://doi.org/10.1002/humu.22685
Pubmed : 25196272
 Reprint request: Subject to availability
10 - 
Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization
Frederic Brioude, Irène Netchine, Françoise Praz, Marilyne Le Jule, Claire Calmel, Didier Lacombe, Patrick Edery, Martin Catala, Sylvie Odent, Bertrand Isidor, Stanislas Lyonnet, Sabine Sigaudy, Bruno Leheup, Séverine Audebert-Bellanger, Lydie Burglen et al.
Human Mutation, 2015, 36 (9), pp.894--902.
DOI : https://doi.org/10.1002/humu.22824
Pubmed : 26077438
 Reprint request: Subject to availability


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