E-LIB Suche - Ergebnisse für: Orhan, Elise

1

A New Mouse Model for Complete Congenital Stationary Night ..:

Orhan, Elise ; Neuillé, Marion ; de Sousa Dias, Miguel...
International Journal of Molecular Sciences. 22 (2021) 9 - p. 4424 , 2021

Link: https://doi.org/10.3390/..

2

Functional expression of complement factor I following AAV-..:

Dreismann, Anna K. ; McClements, Michelle E. ; Barnard, Alun R....
Gene Therapy. 28 (2021) 5 - p. 265-276 , 2021

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

3

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:

Zeitz, Christina ; Méjécase, Cécile ; Michiels, Christelle...
International Journal of Molecular Sciences. 22 (2021) 15 - p. 7875 , 2021

Link: https://doi.org/10.3390/..

4

WDR34, a candidate gene for non‐syndromic rod‐cone dystroph:

Solaguren‐Beascoa, Maria ; Bujakowska, Kinga M. ; Méjécase, Cécile...
Clinical Genetics. 99 (2020) 2 - p. 298-302 , 2020

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

5

Genotypic and Phenotypic Characterization of P23H Line 1 Ra..:

Orhan, Elise ; Dalkara, Deniz ; Neuillé, Marion...
PLOS ONE. 10 (2015) 5 - p. e0127319 , 2015

Link: https://doi.org/10.1371/..

6

LRIT3 is essential to localize TRPM1 to the dendritic tips ..:

Neuillé, Marion ; Morgans, Catherine W. ; Cao, Yan...
European Journal of Neuroscience. 42 (2015) 3 - p. 1966-1975 , 2015

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

7

Lrit3 Deficient Mouse (nob6): A Novel Model of Complete Con..:

Neuillé, Marion ; El Shamieh, Said ; Orhan, Elise...
PLoS ONE. 9 (2014) 3 - p. e90342 , 2014

Link: https://doi.org/10.1371/..

8

The familial dementia gene revisited: a missense mutation r..:

Audo, Isabelle ; Bujakowska, Kinga ; Orhan, Elise...
Human Molecular Genetics. 23 (2013) 2 - p. 491-501 , 2013

Link: https://doi.org/10.1093/..

9

RP1 and autosomal dominant rod-cone dystrophy: Novel mutati..:

Audo, Isabelle ; Mohand-Saïd, Saddek ; Dhaenens, Claire-Marie...
Human Mutation. 33 (2011) 1 - p. 73-80 , 2011

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

10

A New Mouse Model for Complete Congenital Stationary Night ..:

Orhan, Elise ; Neuillé, Marion ; de Sousa Dias, Miguel...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22094424. , 2021

Link: https://hal.sorbonne-uni..

11

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:

Zeitz, Christina ; Méjécase, Cécile ; Michiels, Christelle...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22157875. , 2021

Link: https://inserm.hal.scien..

12

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:

Zeitz, Christina ; Méjécase, Cécile ; Michiels, Christelle...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22157875. , 2021

Link: https://inserm.hal.scien..

13

Functional expression of complement factor I following AAV-..:

Dreismann, Anna K ; McClements, Michelle E ; Barnard, Alun R...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149295/. , 2021

Link: http://www.ncbi.nlm.nih...

14

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:

Zeitz, Christina ; Méjécase, Cécile ; Michiels, Christelle...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22157875. , 2021

Link: https://inserm.hal.scien..

15

A New Mouse Model for Complete Congenital Stationary Night ..:

Orhan, Elise ; Neuillé, Marion ; de Sousa Dias, Miguel...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122890/. , 2021

Link: http://www.ncbi.nlm.nih...