Literature DB >> 20450910

Focus on molecules: nuclear hormone receptor Nr2e3: impact on retinal development and disease.

Nissa Mollema1, Neena B Haider.   

Abstract

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Year:  2010        PMID： 20450910     DOI： 10.1016/j.exer.2010.04.013

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN： 0014-4835            Impact factor:   3.467


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  8 in total

1.  Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.

Authors:  Debarshi Mustafi; Brian M Kevany; Christel Genoud; Kiichiro Okano; Artur V Cideciyan; Alexander Sumaroka; Alejandro J Roman; Samuel G Jacobson; Andreas Engel; Mark D Adams; Krzysztof Palczewski
Journal:  FASEB J       Date:  2011-06-09       Impact factor: 5.191

2.  FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.

Authors:  Leah A Owen; Margaux A Morrison; Jeeyun Ahn; Se Joon Woo; Hajime Sato; Rosann Robinson; Denise J Morgan; Fani Zacharaki; Marina Simeonova; Hironori Uehara; Usha Chakravarthy; Ruth E Hogg; Balamurali K Ambati; Maria Kotoula; Wolfgang Baehr; Neena B Haider; Giuliana Silvestri; Joan W Miller; Evangelia E Tsironi; Lindsay A Farrer; Ivana K Kim; Kyu Hyung Park; Margaret M DeAngelis
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-05-08       Impact factor: 4.799

3.  Expanded clinical spectrum of enhanced S-cone syndrome.

Authors:  Suzanne Yzer; Irene Barbazetto; Rando Allikmets; Mary J van Schooneveld; Arthur Bergen; Stephen H Tsang; Samuel G Jacobson; Lawrence A Yannuzzi
Journal:  JAMA Ophthalmol       Date:  2013-10       Impact factor: 7.389

4.  Photoreceptor cells display a daily rhythm in the orphan receptor Esrrβ.

Authors:  Stefanie Kunst; Tanja Wolloscheck; Markus Grether; Patricia Trunsch; Uwe Wolfrum; Rainer Spessert
Journal:  Mol Vis       Date:  2015-02-19       Impact factor: 2.367

5.  Multimodal Regulation Orchestrates Normal and Complex Disease States in the Retina.

Authors:  A M Olivares; A S Jelcick; J Reinecke; B Leehy; A Haider; M A Morrison; L Cheng; D F Chen; M M DeAngelis; N B Haider
Journal:  Sci Rep       Date:  2017-04-06       Impact factor: 4.379

6.  Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization.

Authors:  Matteo Di Scipio; Erika Tavares; Shriya Deshmukh; Isabelle Audo; Kit Green-Sanderson; Yuliya Zubak; Fayçal Zine-Eddine; Alexander Pearson; Anjali Vig; Chen Yu Tang; Antonio Mollica; Jonathan Karas; Anupreet Tumber; Caberry W Yu; Gail Billingsley; Michael D Wilson; Christina Zeitz; Elise Héon; Ajoy Vincent
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-08-03       Impact factor: 4.799

7.  Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients.

Authors:  Saoud Al-Khuzaei; Suzanne Broadgate; Stephanie Halford; Jasleen K Jolly; Morag Shanks; Penny Clouston; Susan M Downes
Journal:  Genes (Basel)       Date:  2020-10-29       Impact factor: 4.096

8.  Modifier genes as therapeutics: the nuclear hormone receptor Rev Erb alpha (Nr1d1) rescues Nr2e3 associated retinal disease.

Authors:  Nelly M Cruz; Yang Yuan; Barrett D Leehy; Rinku Baid; Uday Kompella; Margaret M DeAngelis; Pascal Escher; Neena B Haider
Journal:  PLoS One       Date:  2014-01-31       Impact factor: 3.240
  8 in total

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