Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene (CRX) Essential for Maintenance of the Photoreceptor-Reference-Cited by-同舟云学术

Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene (CRX) Essential for Maintenance of the Photoreceptor

Published:1997-11 Issue:4 Volume:91 Page:543-553
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Freund Carol L,Gregory-Evans Cheryl Y,Furukawa Takahisa,Papaioannou Myrto,Looser Jens,Ploder Lynda,Bellingham James,Ng David,Herbrick Jo-Anne S,Duncan Alessandra,Scherer Stephen W,Tsui Lap-Chee,Loutradis-Anagnostou Aphrodite,Jacobson Samuel G,Cepko Constance L,Bhattacharya Shomi S,McInnes Roderick R

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

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1. Transcription factor interactions explain the context-dependent activity of CRX binding sites;PLOS Computational Biology;2024-01-16

2. Photoreceptor differentiation mechanisms underlying cell-type homology among vertebrates;Hikaku seiri seikagaku(Comparative Physiology and Biochemistry);2023-12-15

3. CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids;Stem Cell Research & Therapy;2023-12-05

4. Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms;eLife;2023-11-14

5. Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms;eLife;2023-11-14