E-LIB Suche - Ergebnisse für: le Meur, Alice

1

Design, baseline characteristics, and 18-24 months follow-u..:

Wijburg, Frits ; Parker, Samantha ; Drevot, Philippe...
Molecular Genetics and Metabolism. 126 (2019) 2 - p. S153 , 2019

Link: https://doi.org/10.1016/..

2

Five years of clinical data in a direct to CNS gene therapy..:

Olivier, Sophie ; Le Meur, Alice ; Deiva, Kumaran
Molecular Genetics and Metabolism. 123 (2018) 2 - p. S110 , 2018

Link: https://doi.org/10.1016/..

3

AAVrh10-SGSH intracerebral gene therapy corrects the defect..:

Parker, Samantha ; Hocquemiller, Michaël ; le Meur, Alice
Molecular Genetics and Metabolism. 114 (2015) 2 - p. S90 , 2015

Link: https://doi.org/10.1016/..

4

Gold nanoparticles designed for combining dual modality ima..:

Alric, Christophe ; Serduc, Raphaël ; Mandon, Céline...
Gold Bulletin. 41 (2008) 2 - p. 90-97 , 2008

Link: https://doi.org/10.1007/..

5

Gadolinium Chelate Coated Gold Nanoparticles As Contrast Ag..:

Alric, Christophe ; Taleb, Jacqueline ; Le Duc, Géraldine...
Journal of the American Chemical Society. 130 (2008) 18 - p. 5908-5915 , 2008

Link: https://doi.org/10.1021/..

6

Recurrence of an early postzygotic rescue of an inherited u..:

Blanluet, Maud ; Chantot‐Bastaraud, Sandra ; Chambon, Pascal...
American Journal of Medical Genetics Part A. 185 (2021) 10 - p. 3057-3061 , 2021

Link: https://doi.org/10.1002/..

7

Rare genetic susceptibility variants assessment in autism s..:

Husson, Thomas ; Lecoquierre, François ; Cassinari, Kevin...
Translational Psychiatry. 10 (2020) 1 - p. , 2020

Link: https://doi.org/10.1038/..

8

De novo TBR1 variants cause a neurocognitive phenotype with..:

CAUSES Study ; Nambot, Sophie ; Faivre, Laurence...
European Journal of Human Genetics. 28 (2020) 6 - p. 770-782 , 2020

Link: https://doi.org/10.1038/..

9

A Simple, Universal, and Cost-Efficient Digital PCR Method ..:

Cassinari, Kévin ; Quenez, Olivier ; Joly-Hélas, Géraldine...
Clinical Chemistry. 65 (2019) 9 - p. 1153-1160 , 2019

Link: https://doi.org/10.1373/..

10

Defects in mitophagy promote redox‐driven metabolic syndrom..:

Seillier, Marion ; Pouyet, Laurent ; N'Guessan, Prudence...
EMBO Molecular Medicine. 7 (2015) 6 - p. 802-818 , 2015

Link: https://doi.org/10.15252..

11

Mutations in NMNAT1 cause Leber congenital amaurosis with e..:

Perrault, Isabelle ; Hanein, Sylvain ; Zanlonghi, Xavier...
Nature Genetics. 44 (2012) 9 - p. 975-977 , 2012

Link: https://doi.org/10.1038/..

12

Transcriptome profiling uncovers metabolic and regulatory p..:

Buitink, Julia ; Leger, Jean J. ; Guisle, Isabelle...
The Plant Journal. 47 (2006) 5 - p. 735-750 , 2006

Link: https://doi.org/10.1111/..

13

Molecular characterization of a 14q deletion in a boy with ..:

Le Meur, Nathalie ; Goldenberg, Alice ; Michel‐Adde, Christine...
American Journal of Medical Genetics Part A. 134A (2005) 4 - p. 439-442 , 2005

Link: https://doi.org/10.1002/..

14

La continuité pédagogique pour les élèves notifiés ULIS:

Cochet, Alice ; Le Meur, Teva
dumas-03396191. , 2021

Link: https://dumas.ccsd.cnrs...

15

Rare genetic susceptibility variants assessment in autism s..:

Husson, Thomas ; Lecoquierre, François ; Cassinari, Kevin...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41398-020-0760-7. , 2020

Link: https://normandie-univ.h..