E-LIB Suche - Ergebnisse für: Collin, Gayle B

1

Current Views on Chr10q26 Contribution to Age-Related Macul..:

, In: Retinal Degenerative Diseases XIX; Advances in Experimental Medicine and Biology,

Gogna, Navdeep ; Hyde, Lillian F. ; Collin, Gayle B.... - p. 27-36 , 2023

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

2

Chromophore supply modulates cone function and survival in ..:

Xue, Yunlu ; Sun, Xiaomei ; Wang, Sean K....
Proceedings of the National Academy of Sciences. 120 (2023) 23 - p. , 2023

Link: https://doi.org/10.1073/..

3

A mouse model of cone photoreceptor function loss (cpfl9) w..:

Naggert, Anna S. E. N. ; Collin, Gayle B. ; Wang, Jieping..
Frontiers in Molecular Neuroscience. 15 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

4

A Dpagt1 Missense Variant Causes Degenerative Retinopathy w..:

Hyde, Lillian F. ; Kong, Yang ; Zhao, Lihong...
International Journal of Molecular Sciences. 23 (2022) 19 - p. 12005 , 2022

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

5

Identification of Arhgef12 and Prkci as genetic modifiers o..:

Weatherly, Sonia M. ; Collin, Gayle B. ; Charette, Jeremy R....
PLOS Genetics. 18 (2022) 6 - p. e1009798 , 2022

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

6

A Splicing Mutation in Slc4a5 Results in Retinal Detachment..:

Collin, Gayle B. ; Shi, Lanying ; Yu, Minzhong...
International Journal of Molecular Sciences. 23 (2022) 4 - p. 2220 , 2022

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

7

Genetic Interaction between Mfrp and Adipor1 Mutations Affe..:

Gogna, Navdeep ; Weatherly, Sonia ; Zhao, Fuxin...
International Journal of Molecular Sciences. 23 (2022) 3 - p. 1615 , 2022

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

8

Mouse Models of Inherited Retinal Degeneration with Photore..:

Collin, Gayle B. ; Gogna, Navdeep ; Chang, Bo...
Cells. 9 (2020) 4 - p. 931 , 2020

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

9

Mouse models of human ocular disease for translational rese..:

Krebs, Mark P. ; Collin, Gayle B. ; Hicks, Wanda L....
PLOS ONE. 12 (2017) 8 - p. e0183837 , 2017

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

10

Pituitary morphovolumetric changes in Alström syndrome:

Citton, Valentina ; Maffei, Pietro ; Marshall, Jan D....
Journal of Neuroradiology. 43 (2016) 3 - p. 195-199 , 2016

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

11

Mutations in CTNNA1 cause butterfly-shaped pigment dystroph..:

Saksens, Nicole T M ; Krebs, Mark P ; Schoenmaker-Koller, Frederieke E...
Nature Genetics. 48 (2015) 2 - p. 144-151 , 2015

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

12

Erratum: The phenotypic and molecular genetic spectrum of A..:

Ozantürk, Ayşegül ; Marshall, Jan D ; Collin, Gayle B...
Journal of Human Genetics. 60 (2015) 1 - p. 51-51 , 2015

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

13

Disruption of murineAdamtsl4results in zonular fiber detach..:

Collin, Gayle B. ; Hubmacher, Dirk ; Charette, Jeremy R....
Human Molecular Genetics. , 2015

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

14

GLUT4 Defects in Adipose Tissue Are Early Signs of Metaboli..:

Favaretto, Francesca ; Milan, Gabriella ; Collin, Gayle B....
PLoS ONE. 9 (2014) 10 - p. e109540 , 2014

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

15

Gene Profiling of Postnatal Mfrprd6 Mutant Eyes Reveals Dif..:

Soundararajan, Ramani ; Won, Jungyeon ; Stearns, Timothy M....
PLoS ONE. 9 (2014) 10 - p. e110299 , 2014

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