บทความที่มีข้อกำหนดการเข้าถึงสาธารณะ - Elise Orhanดูข้อมูลเพิ่มเติม
มีให้ใช้งานในบางที่: 9
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness
C Zeitz, SG Jacobson, CP Hamel, K Bujakowska, M Neuillé, E Orhan, ...
The American Journal of Human Genetics 92 (1), 67-75, 2013
ข้อกำหนด: National Institute of Health and Medical Research, France
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
I Audo, K Bujakowska, E Orhan, CM Poloschek, S Defoort-Dhellemmes, ...
The American Journal of Human Genetics 90 (2), 321-330, 2012
ข้อกำหนด: US National Institutes of Health
Genotypic and phenotypic characterization of P23H line 1 rat model
E Orhan, D Dalkara, M Neuillé, C Lechauve, C Michiels, S Picaud, ...
PLoS One 10 (5), e0127319, 2015
ข้อกำหนด: US National Institutes of Health
Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)
M Neuillé, S El Shamieh, E Orhan, C Michiels, A Antonio, ME Lancelot, ...
PloS one 9 (3), e90342, 2014
ข้อกำหนด: US National Institutes of Health
LRIT 3 is essential to localize TRPM 1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation
M Neuillé, CW Morgans, Y Cao, E Orhan, C Michiels, JA Sahel, I Audo, ...
European Journal of Neuroscience 42 (3), 1966-1975, 2015
ข้อกำหนด: US National Institutes of Health
WDR34, a candidate gene for non‐syndromic rod‐cone dystrophy
M Solaguren‐Beascoa, KM Bujakowska, C Méjécase, L Emmenegger, ...
Clinical genetics 99 (2), 298-302, 2021
ข้อกำหนด: US National Institutes of Health, National Institute of Health and Medical …
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency
E Orhan, M Neuillé, M de Sousa Dias, T Pugliese, C Michiels, ...
International Journal of Molecular Sciences 22 (9), 4424, 2021
ข้อกำหนด: Agence Nationale de la Recherche
Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy
C Zeitz, C Méjécase, C Michiels, C Condroyer, J Wohlschlegel, ...
International Journal of Molecular Sciences 22 (15), 7875, 2021
ข้อกำหนด: National Institute of Health and Medical Research, France, Agence Nationale …
A CCDC51 frameshift variant as a candidate gene defect for autosomal recessive rod-cone dystrophy
C Zeitz, C Méjécase, S Mohand-Saïd, L Emmengger, A Schalk, M Neuillé, ...
Investigative Ophthalmology & Visual Science 60 (9), 415-415, 2019
ข้อกำหนด: Agence Nationale de la Recherche
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