Literature DB >> 26427409

A Chemical Mutagenesis Screen Identifies Mouse Models with ERG Defects.

Jeremy R Charette1, Ivy S Samuels2, Minzhong Yu3, Lisa Stone4, Wanda Hicks5, Lan Ying Shi6, Mark P Krebs7, Jürgen K Naggert8, Patsy M Nishina9, Neal S Peachey10,11,12.   

Abstract

Mouse models provide important resources for many areas of vision research, pertaining to retinal development, retinal function and retinal disease. The Translational Vision Research Models (TVRM) program uses chemical mutagenesis to generate new mouse models for vision research. In this chapter, we report the identification of mouse models for Grm1, Grk1 and Lrit3. Each of these is characterized by a primary defect in the electroretinogram. All are available without restriction to the research community.

Entities:  

Keywords:  Electroretinogram; Mice; Mutagenesis; Photoreceptor; Retina

Mesh：

Substances：

Year:  2016        PMID： 26427409      PMCID： PMC6716159          DOI： 10.1007/978-3-319-17121-0_24

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


  18 in total

1.  Rapid and reproducible deactivation of rhodopsin requires multiple phosphorylation sites.

Authors:  A Mendez; M E Burns; A Roca; J Lem; L W Wu; M I Simon; D A Baylor; J Chen
Journal:  Neuron       Date:  2000-10       Impact factor: 17.173

2.  Translational vision research models program.

Authors:  Jungyeon Won; Lan Ying Shi; Wanda Hicks; Jieping Wang; Juergen K Naggert; Patsy M Nishina
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

3.  Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase.

Authors:  C K Chen; M E Burns; M Spencer; G A Niemi; J Chen; J B Hurley; D A Baylor; M I Simon
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

4.  Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes.

Authors:  N L Hawes; R S Smith; B Chang; M Davisson; J R Heckenlively; S W John
Journal:  Mol Vis       Date:  1999-09-15       Impact factor: 2.367

5.  Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes.

Authors:  Andreas Menke; Philipp Sämann; Stefan Kloiber; Darina Czamara; Susanne Lucae; Johannes Hennings; Angela Heck; Martin A Kohli; Michael Czisch; Bertram Müller-Myhsok; Florian Holsboer; Elisabeth B Binder
Journal:  Psychoneuroendocrinology       Date:  2011-09-29       Impact factor: 4.905

6.  crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1).

Authors:  Valerio Conti; Asadollah Aghaie; Michele Cilli; Natalia Martin; Gianluca Caridi; Luca Musante; Giovanni Candiano; Maura Castagna; Alfonso Fairen; Roberto Ravazzolo; Jean-Louis Guenet; Aldamaria Puliti
Journal:  Int J Mol Med       Date:  2006-10       Impact factor: 4.101

7.  Age-related changes in visual function in cystathionine-beta-synthase mutant mice, a model of hyperhomocysteinemia.

Authors:  Minzhong Yu; Gwen Sturgill-Short; Preethi Ganapathy; Amany Tawfik; Neal S Peachey; Sylvia B Smith
Journal:  Exp Eye Res       Date:  2011-12-16       Impact factor: 3.467

8.  Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.

Authors:  N L Hawes; B Chang; G S Hageman; S Nusinowitz; P M Nishina; B S Schneider; R S Smith; T H Roderick; M T Davisson; J R Heckenlively
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-09       Impact factor: 4.799

9.  Deletion of GRK1 causes retina degeneration through a transducin-independent mechanism.

Authors:  Jie Fan; Keisuke Sakurai; Ching-Kang Chen; Baerbel Rohrer; Bill X Wu; King-Wai Yau; Vladimir Kefalov; Rosalie K Crouch
Journal:  J Neurosci       Date:  2010-02-17       Impact factor: 6.167

10.  The mouse mutants recoil wobbler and nmf373 represent a series of Grm1 mutations.

Authors:  Andrew J Sachs; Jamie K Schwendinger; Andy W Yang; Neena B Haider; Arne M Nystuen
Journal:  Mamm Genome       Date:  2007-10-13       Impact factor: 2.957
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  9 in total

1.  LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.

Authors:  Marion Neuillé; Yan Cao; Romain Caplette; Debbie Guerrero-Given; Connon Thomas; Naomi Kamasawa; José-Alain Sahel; Christian P Hamel; Isabelle Audo; Serge Picaud; Kirill A Martemyanov; Christina Zeitz
Journal:  Invest Ophthalmol Vis Sci       Date:  2017-03-01       Impact factor: 4.799

2.  A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density.

Authors:  Jeremy R Charette; Sarah E Earp; Brent A Bell; Cheryl L Ackert-Bicknell; Dana A Godfrey; Sujata Rao; Bela Anand-Apte; Patsy M Nishina; Neal S Peachey
Journal:  Mol Vis       Date:  2017-03-18       Impact factor: 2.367

3.  Noninvasive Prenatal Diagnosis Significance of ERG Methylation as a Biomarker in Down's Syndrome.

Authors:  Xiangju Liu; Ming Xue
Journal:  Med Sci Monit       Date:  2017-01-23

4.  Identification of genes required for eye development by high-throughput screening of mouse knockouts.

Authors:  Bret A Moore; Brian C Leonard; Lionel Sebbag; Sydney G Edwards; Ann Cooper; Denise M Imai; Ewan Straiton; Luis Santos; Christopher Reilly; Stephen M Griffey; Lynette Bower; David Clary; Jeremy Mason; Michel J Roux; Hamid Meziane; Yann Herault; Colin McKerlie; Ann M Flenniken; Lauryl M J Nutter; Zorana Berberovic; Celeste Owen; Susan Newbigging; Hibret Adissu; Mohammed Eskandarian; Chih-Wei Hsu; Sowmya Kalaga; Uchechukwu Udensi; Chinwe Asomugha; Ritu Bohat; Juan J Gallegos; John R Seavitt; Jason D Heaney; Arthur L Beaudet; Mary E Dickinson; Monica J Justice; Vivek Philip; Vivek Kumar; Karen L Svenson; Robert E Braun; Sara Wells; Heather Cater; Michelle Stewart; Sharon Clementson-Mobbs; Russell Joynson; Xiang Gao; Tomohiro Suzuki; Shigeharu Wakana; Damian Smedley; J K Seong; Glauco Tocchini-Valentini; Mark Moore; Colin Fletcher; Natasha Karp; Ramiro Ramirez-Solis; Jacqueline K White; Martin Hrabe de Angelis; Wolfgang Wurst; Sara M Thomasy; Paul Flicek; Helen Parkinson; Steve D M Brown; Terrence F Meehan; Patsy M Nishina; Stephen A Murray; Mark P Krebs; Ann-Marie Mallon; K C Kent Lloyd; Christopher J Murphy; Ala Moshiri
Journal:  Commun Biol       Date:  2018-12-21

5.  Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.

Authors:  Rueben G Das; Doreen Becker; Vidhya Jagannathan; Orly Goldstein; Evelyn Santana; Kendall Carlin; Raghavi Sudharsan; Tosso Leeb; Yuji Nishizawa; Mineo Kondo; Gustavo D Aguirre; Keiko Miyadera
Journal:  Sci Rep       Date:  2019-10-02       Impact factor: 4.379

6.  Reduced expression of the nob8 gene does not normalize the distribution or function of mGluR6 in the mouse retina.

Authors:  Junzo Kinoshita; Nazarul Hasan; Brent A Bell; Neal S Peachey
Journal:  Mol Vis       Date:  2019-12-31       Impact factor: 2.367

7.  A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency.

Authors:  Elise Orhan; Marion Neuillé; Miguel de Sousa Dias; Thomas Pugliese; Christelle Michiels; Christel Condroyer; Aline Antonio; José-Alain Sahel; Isabelle Audo; Christina Zeitz
Journal:  Int J Mol Sci       Date:  2021-04-23       Impact factor: 5.923

Review 8.  Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.

Authors:  Gayle B Collin; Navdeep Gogna; Bo Chang; Nattaya Damkham; Jai Pinkney; Lillian F Hyde; Lisa Stone; Jürgen K Naggert; Patsy M Nishina; Mark P Krebs
Journal:  Cells       Date:  2020-04-10       Impact factor: 7.666

9.  Mouse models of human ocular disease for translational research.

Authors:  Mark P Krebs; Gayle B Collin; Wanda L Hicks; Minzhong Yu; Jeremy R Charette; Lan Ying Shi; Jieping Wang; Jürgen K Naggert; Neal S Peachey; Patsy M Nishina
Journal:  PLoS One       Date:  2017-08-31       Impact factor: 3.240
  9 in total

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