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2015

Articles

21 - 

90 Focus on a clear message: conserved RNA binding proteins function in mRNA control in eye lens development and their deficiency causes cataract

Archana D. Siddam, Carole Gautier-Courteille, Atul Kakrana, Vincent Legagneux, Christine A. Dang et al.

Journal of Biomolecular Structure and Dynamics, 2015, 33 (1), pp.58-59.

DOI : https://doi.org/10.1080/07391102.2015.1032707

Pubmed : 26103300

 

22 - 

Complete Genome Sequence of Noninvasive Streptococcus pyogenes M/emm28 Strain STAB10015, Isolated from a Child with Perianal Dermatitis in French Brittany

Suzane De Andrade Barboza, Alexandra Meygret, Pascal Vincent, Séverine Moullec, Nicolas Soriano et al.

Genome Announcements, 2015, 3 (4), pp.e00806-15.

DOI : https://doi.org/10.1128/genomeA.00806-15

Pubmed : 26184948

 

23 - 

X-linked retinitis pigmentosa 2 is a novel maternal-effect gene required for left-right asymmetry in zebrafish

Thomas Desvignes, Thuy Thao Vi Nguyen, Frank Chesnel, Aurélien Bouleau, Christian Fauvel et al.

Biology of Reproduction, 2015, 93 (2), pp.42.

DOI : https://doi.org/10.1095/biolreprod.115.130575

Pubmed : 26134862

 

24 - 

Long-term side effects of radiotherapy for pediatric localized neuroblastoma

Anne Ducassou, Marion Gambart, Caroline Munzer, Laetitia Padovani, Christian Carrie et al.

Strahlentherapie und Onkologie, 2015, 191 (7), pp.604--612.

DOI : https://doi.org/10.1007/s00066-015-0837-z

Pubmed : 25896312

 

25 - 

Oral Gram-negative anaerobic bacilli as a reservoir of β-lactam resistance genes facilitating infections with multiresistant bacteria

Clarisse Dupin, Zohreh Tamanai-Shacoori, Elodie Ehrmann, Anais Dupont, Frédérique Barloy-Hubler et al.

International Journal of Antimicrobial Agents, 2015, 45 (2), pp.99-105.

DOI : https://doi.org/10.1016/j.ijantimicag.2014.10.003

Pubmed : 25465519

 

26 - 

New insights into genotype-phenotype correlation for GLI3 mutations

Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, Martine Le Merrer, Géraldine Goudefroye et al.

European Journal of Human Genetics, 2015, 23 (1), pp.92-102.

DOI : https://doi.org/10.1038/ejhg.2014.62

Pubmed : 24736735

 

27 - 

SNPs at miR-155 binding sites of TYRP1 explain discrepancy between mRNA and protein and refine TYRP1 prognostic value in melanoma

P. El Hajj, D. Gilot, M. Migault, A. Theunis, L. C. Van Kempen et al.

British Journal of Cancer, 2015, 113 (1), pp.91--98.

DOI : https://doi.org/10.1038/bjc.2015.194

Pubmed : 26068396

 

28 - 

Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1.

Laïla El Khattabi, Fabien Guimiot, Eva Pipiras, Joris Andrieux, Clarisse Baumann et al.

Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1. European Journal of Human Genetics, 2015, 23 (8), pp.1010-1018.

DOI : https://doi.org/10.1038/ejhg.2014.230

Pubmed : 25351778

 

29 - 

Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review

Laïla El Khattabi, Sylvie Jaillard, Joris Andrieux, Laurent Pasquier, Laurence Perrin et al.

American Journal of Medical Genetics Part A, 2015, 167 (6), pp.1252--1261.

DOI : https://doi.org/10.1002/ajmg.a.36932

Pubmed : 25847481

 

30 - 

Efficacy of Azacitidine (AZA) in Autoimmune and Inflammatory Disorders (AID) Associated with Myelodysplastic Syndromes (MDS) and Chronic Myelomonocytic Leukemia (CMML)

Jean-Baptiste Fraison, Arsène Mekinian, Eric Grignano, Jean-Emmanuel Kahn, Jean-Benoît Arlet et al.

Blood, 2015, 126 (23), pp.1695.