PUBLICATIONS of MMG

Veuillez utiliser l'outil ci-dessous pour consulter nos publications par mots clés et/ou par équipe et/ou par année.

Suivez les liens pour consulter les publications sur le site de PubMed.



Rechercher une publication





Résultats : 4196  publications trouvées.

Balducci, E.  et al. 2019

Extracellular vesicles from T cells overexpress miR-146b-5p in HIV-1 infection and repress endothelial activation

- issue: - volume: 9 - pages: .

Balducci, E.  et al. 2019

Extracellular vesicles from T cells overexpress miR-146b-5p in HIV-1 infection and repress endothelial activation

Human immunodeficiency virus type 1 (HIV-1) infection promotes a generalized activation of host responses that involves not only CD4 T cells, but also cells of the microenvironment, which are not...
- issue: - volume: 9 - pages: .

El-Bazzal, L.  et al. 2019

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1

- issue: 14 - volume: 28 - pages: 2378-2394.

El-Bazzal, L.  et al. 2019

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1

Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases, resembling Charcot-Marie-Tooth syndromes, but characterized by an exclusive involvement of the motor part of the...
Hum. Mol. Genet. - issue: 14 - volume: 28 - pages: 2378-2394.

El-Bazzal, L.  et al. 2019

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1

Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases, resembling Charcot-Marie-Tooth syndromes, but characterized by an exclusive involvement of the motor part of the...
- issue: 14 - volume: 28 - pages: 2378-2394.

El-Bazzal, L.  et al. 2019

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1

Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases, resembling Charcot-Marie-Tooth syndromes, but characterized by an exclusive involvement of the motor part of the...
Hum. Mol. Genet. - issue: 14 - volume: 28 - pages: 2378-2394.

Kermezli, Y.  et al. 2019

A comprehensive catalog of LncRNAs expressed in T-cell acute lymphoblastic leukemia

- issue: 8 - volume: 60 - pages: 2002-2014.

Kermezli, Y.  et al. 2019

A comprehensive catalog of LncRNAs expressed in T-cell acute lymphoblastic leukemia

Several studies have demonstrated that LncRNAs can play major roles in cancer development. The creation of a catalog of LncRNAs expressed in T cell acute lymphoblastic leukemia (T-ALL) is thus of...
- issue: 8 - volume: 60 - pages: 2002-2014.

Piard, J.  et al. 2019

The phenotypic spectrum of WWOX-related Epileptic Encephalopathy: 20 additional cases and review of the literature

- issue: 1 - volume: 27 - pages: 246-247.

Piard, J.  et al. 2019

Epileptic encephalopathy due to BRAT1 pathogenic variants: report of eight new patients

- issue: 1 - volume: 27 - pages: 263.

Yauy, K.  et al. 2019

Evaluation of missense and splicing in silico predictions tools and implementation of an efficient SNV prioritization NGS pipeline for molecular diagnosis of Myopathies and Muscular Dystrophies

- issue: 1 - volume: 27 - pages: 339.

Pujol, P.  et al. 2019

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations

- issue: 1 - volume: 27 - pages: 562-563.

Faivre, L.  et al. 2019

Description Osteo-Oto-Hepato-Enteric (O2HE) syndrome, a new recessive autosomal syndrome secondary to loss of function mutations in the UNC45A gene

- issue: 1 - volume: 27 - pages: 795-796.

Greco, A.  et al. 2019

Molecular Inverse Comorbidity between Alzheimer's Disease and Lung Cancer: New Insights from Matrix Factorization

- issue: 13 - volume: 20 - pages: .

Benoit, S.  et al. 2019

Self-report questionnaire vs. clinical evaluation form in the French National Registry on facioscapulohumeral dystrophy: a statistical comparison

- issue: 1, SI - volume: 26 - pages: 325.

Piard, J.  et al. 2019

The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (vol 21, pg 1308, 2018)

- issue: 7 - volume: 21 - pages: 1667.

Pareyson, D.  et al. 2019

A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)

- issue: 1 - volume: 86 - pages: 55-67.

Amodru, V.  et al. 2019

LARGE ADRENAL INCIDENTALOMAS REQUIRE A DEDICATED DIAGNOSTIC PROCEDURE.

Objective: The management of large nonsecreting adrenal tumors (at least 4 cm) is still a matter of debate as it is unclear whether imaging, especially (18)F-fluorodeoxyglucose (FDG), can be used to...
Endocr Pract - issue: 7 - volume: 25 - pages: 669-677.

Piard, J.  et al. 2019

The phenotypic spectrum of WWOX-related Epileptic Encephalopathy: 20 additional cases and review of the literature

- issue: 1 - volume: 27 - pages: 246-247.

Piard, J.  et al. 2019

Epileptic encephalopathy due to BRAT1 pathogenic variants: report of eight new patients

- issue: 1 - volume: 27 - pages: 263.