Search - Inserm - Institut national de la santé et de la recherche médicale Access content directly

Filter your results

11 Results
Author: personID (integer) : 758439
Image document

Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing

Nadège Calmels , Géraldine Greff , Cathy Obringer , Nadine Kempf , Claire Gasnier , et al.
Orphanet Journal of Rare Diseases, 2016, 11 (1), pp.26. ⟨10.1186/s13023-016-0408-0⟩
Journal articles hal-01295286v1

Time-resolved analysis of transcriptional events during SNAI1-triggered epithelial to mesenchymal transition.

Guillaume Vetter , A. Le Béchec , Jean Muller , Arnaud H. Muller , M. Moes , et al.
Biochemical and Biophysical Research Communications, 2009, 385 (4), pp.485-91. ⟨10.1016/j.bbrc.2009.05.025⟩
Journal articles istex inserm-00420101v1
Image document

The economic, medical and psychosocial consequences of whole genome sequencing for the genetic diagnosis of patients with intellectual disability: The DEFIDIAG study protocol

Catherine Lejeune , Charley Robert-Viard , Nicolas Meunier-Beillard , Myriam Alice Borel , Léna Gourvès , et al.
Frontiers in Genetics, 2022, 13, pp.852472. ⟨10.3389/fgene.2022.852472⟩
Journal articles hal-03678712v1

Transcriptome analysis identifies genes with enriched expression in the mouse central extended amygdala.

Jérôme A. J. Becker , Katia Befort , Clara Blad , Dominique Filliol , A. Ghate , et al.
Neuroscience, 2008, 156 (4), pp.950-65. ⟨10.1016/j.neuroscience.2008.07.070⟩
Journal articles inserm-00350728v1
Image document

Identifying single copy orthologs in Metazoa.

Christopher J. Creevey , Jean Muller , Tobias Doerks , Julie D. Thompson , Detlev Arendt , et al.
PLoS Computational Biology, 2011, 7 (12), pp.e1002269. ⟨10.1371/journal.pcbi.1002269⟩
Journal articles inserm-00691543v1
Image document

Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

Chris Balak , Marianne Bénard , Elise Schaefer , Sumaiya Iqbal , Keri Ramsey , et al.
American Journal of Human Genetics, 2019, 105 (3), pp.509-525. ⟨10.1016/j.ajhg.2019.07.010⟩
Journal articles hal-02271087v1
Image document

Reproduction Function in Male Patients With Bardet Biedl Syndrome

Isabelle Koscinski , Manuel Mark , Nadia Messaddeq , Jean Jacques Braun , Catherine Celebi , et al.
Journal of Clinical Endocrinology and Metabolism, 2020, 105 (12), pp.e4417-e4429. ⟨10.1210/clinem/dgaa551⟩
Journal articles hal-03663322v1
Image document

KD4v: comprehensible knowledge discovery system for missense variant

Tien-Dao Luu , Alin Rusu , Vincent Walter , Benjamin Linard , Laetitia Poidevin , et al.
Nucleic Acids Research, 2012, 40 (W1), pp.W71-W75. ⟨10.1093/nar/gks474⟩
Journal articles hal-01636871v1

PLCB3 Loss of Function Reduces Pseudomonas aeruginosa –Dependent IL-8 Release in Cystic Fibrosis

Alessandro Rimessi , Valentino Bezzerri , Francesca Salvatori , Anna Tamanini , Federica Nigro , et al.
American Journal of Respiratory Cell and Molecular Biology, 2018, 59 (4), pp.428-436. ⟨10.1165/rcmb.2017-0267OC⟩
Journal articles hal-03672215v1
Image document

Self-assembly and properties of nano-organized multimaterial films with complex anisotropies

Jean Muller
Theoretical and/or physical chemistry. Université de Strasbourg, 2021. English. ⟨NNT : 2021STRAE031⟩
Theses tel-03560519v1

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 Gaucherot , et al.
Journal of Assisted Reproduction and Genetics, 2017, 34 (5), pp.683-694. ⟨10.1007/s10815-017-0900-z⟩
Journal articles hal-03339528v1