Results
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5681.
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X-linked high myopia associated with cone dysfunction. [electronic resource] by
- Young, Terri L
- Deeb, Samir S
- Ronan, Shawn M
- Dewan, Andrew T
- Alvear, Alison B
- Scavello, Genaro S
- Paluru, Prasuna C
- Brott, Marcia S
- Hayashi, Takaaki
- Holleschau, Ann M
- Benegas, Nancy
- Schwartz, Marianne
- Atwood, Larry D
- Oetting, William S
- Rosenberg, Thomas
- Motulsky, Arno G
- King, Richard A
Producer: 20040720
In:
Archives of ophthalmology (Chicago, Ill. : 1960) vol. 122
Availability: No items available.
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5682.
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Targeted ablation of the Pde6h gene in mice reveals cross-species differences in cone and rod phototransduction protein isoform inventory. [electronic resource] by
- Brennenstuhl, Christina
- Tanimoto, Naoyuki
- Burkard, Markus
- Wagner, Rebecca
- Bolz, Sylvia
- Trifunovic, Dragana
- Kabagema-Bilan, Clement
- Paquet-Durand, Francois
- Beck, Susanne C
- Huber, Gesine
- Seeliger, Mathias W
- Ruth, Peter
- Wissinger, Bernd
- Lukowski, Robert
Producer: 20150619
In:
The Journal of biological chemistry vol. 290
Availability: No items available.
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5683.
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Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia. [electronic resource] by
- Schön, Christian
- Asteriti, Sabrina
- Koch, Susanne
- Sothilingam, Vithiyanjali
- Garcia Garrido, Marina
- Tanimoto, Naoyuki
- Herms, Jochen
- Seeliger, Mathias W
- Cangiano, Lorenzo
- Biel, Martin
- Michalakis, Stylianos
Producer: 20161215
In:
Human molecular genetics vol. 25
Availability: No items available.
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5684.
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5685.
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5686.
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5687.
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5688.
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5689.
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Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase. [electronic resource] by
- Gregory-Evans, K
- Kelsell, R E
- Gregory-Evans, C Y
- Downes, S M
- Fitzke, F W
- Holder, G E
- Simunovic, M
- Mollon, J D
- Taylor, R
- Hunt, D M
- Bird, A C
- Moore, A T
Producer: 20000128
In:
Ophthalmology vol. 107
Availability: No items available.
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5690.
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5691.
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Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A). [electronic resource] by
- Jiang, Li
- Katz, Bradley J
- Yang, Zhenglin
- Zhao, Yu
- Faulkner, Nathan
- Hu, Jianbin
- Baird, Jennifer
- Baehr, Wolfgang
- Creel, Donnell J
- Zhang, Kang
Producer: 20051103
In:
Molecular vision vol. 11
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5692.
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5693.
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5694.
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5695.
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5696.
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Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia. [electronic resource] by
- Azam, Maleeha
- Collin, Rob W J
- Shah, Syed Tahir Abbas
- Shah, Aftab Ali
- Khan, Muhammad Imran
- Hussain, Alamdar
- Sadeque, Ahmed
- Strom, Tim M
- Thiadens, Alberta A H J
- Roosing, Susanne
- den Hollander, Anneke I
- Cremers, Frans P M
- Qamar, Raheel
Producer: 20100825
In:
Molecular vision vol. 16
Availability: No items available.
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5697.
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5698.
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5699.
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5700.
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