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Connection

Shannon Conley to Peripherins

This is a "connection" page, showing publications Shannon Conley has written about Peripherins.
Connection Strength

5.868
  1. Prph2 initiates outer segment morphogenesis but maturation requires Prph2/Rom1 oligomerization. Hum Mol Genet. 2019 02 01; 28(3):459-475.
    View in: PubMed
    Score: 0.636
  2. The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis. Adv Exp Med Biol. 2019; 1185:495-499.
    View in: PubMed
    Score: 0.632
  3. Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa. Hum Mol Genet. 2017 02 01; 26(3):509-518.
    View in: PubMed
    Score: 0.553
  4. Gene therapy for PRPH2-associated ocular disease: challenges and prospects. Cold Spring Harb Perspect Med. 2014 Aug 28; 4(11):a017376.
    View in: PubMed
    Score: 0.468
  5. Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS. Hum Mol Genet. 2014 Jun 15; 23(12):3102-14.
    View in: PubMed
    Score: 0.449
  6. Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Invest Ophthalmol Vis Sci. 2022 07 08; 63(8):19.
    View in: PubMed
    Score: 0.202
  7. Prph2 disease mutations lead to structural and functional defects in the RPE. FASEB J. 2022 05; 36(5):e22284.
    View in: PubMed
    Score: 0.199
  8. Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration. Int J Mol Sci. 2020 Oct 29; 21(21).
    View in: PubMed
    Score: 0.179
  9. ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal disease. Hum Mol Genet. 2020 09 29; 29(16):2708-2722.
    View in: PubMed
    Score: 0.178
  10. Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival. Proc Natl Acad Sci U S A. 2020 08 25; 117(34):20615-20624.
    View in: PubMed
    Score: 0.177
  11. Novel molecular mechanisms for Prph2-associated pattern dystrophy. FASEB J. 2020 01; 34(1):1211-1230.
    View in: PubMed
    Score: 0.168
  12. Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation. Hum Mol Genet. 2018 10 15; 27(20):3507-3518.
    View in: PubMed
    Score: 0.156
  13. The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function. Hum Mol Genet. 2016 08 15; 25(16):3500-3514.
    View in: PubMed
    Score: 0.133
  14. Role of RDS and Rhodopsin in Cngb1-Related Retinal Degeneration. Invest Ophthalmol Vis Sci. 2016 Mar; 57(3):787-97.
    View in: PubMed
    Score: 0.130
  15. PRPH2/RDS and ROM-1: Historical context, current views and future considerations. Prog Retin Eye Res. 2016 05; 52:47-63.
    View in: PubMed
    Score: 0.128
  16. RDS Functional Domains and Dysfunction in Disease. Adv Exp Med Biol. 2016; 854:217-22.
    View in: PubMed
    Score: 0.128
  17. Retinal Degeneration Slow (RDS) Glycosylation Plays a Role in Cone Function and in the Regulation of RDS·ROM-1 Protein Complex Formation. J Biol Chem. 2015 Nov 13; 290(46):27901-13.
    View in: PubMed
    Score: 0.126
  18. SNAREs Interact with Retinal Degeneration Slow and Rod Outer Segment Membrane Protein-1 during Conventional and Unconventional Outer Segment Targeting. PLoS One. 2015; 10(9):e0138508.
    View in: PubMed
    Score: 0.126
  19. The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse. Hum Mol Genet. 2014 Dec 01; 23(23):6260-74.
    View in: PubMed
    Score: 0.116
  20. Initiation of rod outer segment disc formation requires RDS. PLoS One. 2014; 9(6):e98939.
    View in: PubMed
    Score: 0.115
  21. Rim formation is not a prerequisite for distribution of cone photoreceptor outer segment proteins. FASEB J. 2014 Aug; 28(8):3468-79.
    View in: PubMed
    Score: 0.114
  22. Overexpression of retinal degeneration slow (RDS) protein adversely affects rods in the rd7 model of enhanced S-cone syndrome. PLoS One. 2013; 8(5):e63321.
    View in: PubMed
    Score: 0.107
  23. Mislocalization of oligomerization-incompetent RDS is associated with mislocalization of cone opsins and cone transducin. Adv Exp Med Biol. 2012; 723:657-62.
    View in: PubMed
    Score: 0.097
  24. Biochemical analysis of phenotypic diversity associated with mutations in codon 244 of the retinal degeneration slow gene. Biochemistry. 2010 Feb 09; 49(5):905-11.
    View in: PubMed
    Score: 0.085
  25. RDS in cones does not interact with the beta subunit of the cyclic nucleotide gated channel. Adv Exp Med Biol. 2010; 664:63-70.
    View in: PubMed
    Score: 0.085
  26. Focus on molecules: RDS. Exp Eye Res. 2009 Sep; 89(3):278-9.
    View in: PubMed
    Score: 0.081
  27. Late-onset cone photoreceptor degeneration induced by R172W mutation in Rds and partial rescue by gene supplementation. Invest Ophthalmol Vis Sci. 2007 Dec; 48(12):5397-407.
    View in: PubMed
    Score: 0.073
  28. ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims. Elife. 2023 Nov 22; 12.
    View in: PubMed
    Score: 0.055
  29. Structural characterization of the second intra-discal loop of the photoreceptor tetraspanin RDS. FEBS J. 2013 Jan; 280(1):127-38.
    View in: PubMed
    Score: 0.026
  30. Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS. Hum Mol Genet. 2010 Dec 15; 19(24):4799-812.
    View in: PubMed
    Score: 0.022
  31. A 350 bp region of the proximal promoter of Rds drives cell-type specific gene expression. Exp Eye Res. 2010 Aug; 91(2):186-94.
    View in: PubMed
    Score: 0.022
  32. The function of oligomerization-incompetent RDS in rods. Adv Exp Med Biol. 2010; 664:39-46.
    View in: PubMed
    Score: 0.021
  33. Gene therapy in the Retinal Degeneration Slow model of retinitis pigmentosa. Adv Exp Med Biol. 2010; 664:611-9.
    View in: PubMed
    Score: 0.021
  34. Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa. FASEB J. 2010 Apr; 24(4):1178-91.
    View in: PubMed
    Score: 0.021
  35. A partial structural and functional rescue of a retinitis pigmentosa model with compacted DNA nanoparticles. PLoS One. 2009; 4(4):e5290.
    View in: PubMed
    Score: 0.020
  36. Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus cones. Hum Mol Genet. 2009 Mar 01; 18(5):797-808.
    View in: PubMed
    Score: 0.020
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.

THIS IS A DEVELOPMENT VERSION OF PROFILES. PLEASE GO TO THE PRODUCTION ENVIRONMENT FOR UPDATES