Literature DB >> 10800709

Isolation of retinal proteins that interact with retinitis pigmentosa GTPase regulator by interaction trap screen in yeast.

R Roepman1, D Schick, P A Ferreira.   

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Year:  2000        PMID： 10800709     DOI： 10.1016/s0076-6879(00)16757-6

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN： 0076-6879            Impact factor:   1.600


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  13 in total

1.  Limited proteolysis differentially modulates the stability and subcellular localization of domains of RPGRIP1 that are distinctly affected by mutations in Leber's congenital amaurosis.

Authors:  Xinrong Lu; Mallikarjuna Guruju; John Oswald; Paulo A Ferreira
Journal:  Hum Mol Genet       Date:  2005-03-30       Impact factor: 6.150

2.  Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations.

Authors:  Ronald Roepman; Stef J F Letteboer; Heleen H Arts; Sylvia E C van Beersum; Xinrong Lu; Elmar Krieger; Paulo A Ferreira; Frans P M Cremers
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-09       Impact factor: 11.205

3.  A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.

Authors:  Debra K Breuer; Beverly M Yashar; Elena Filippova; Suja Hiriyanna; Robert H Lyons; Alan J Mears; Bersabell Asaye; Ceren Acar; Raf Vervoort; Alan F Wright; Maria A Musarella; Patricia Wheeler; Ian MacDonald; Alessandro Iannaccone; David Birch; Dennis R Hoffman; Gerald A Fishman; John R Heckenlively; Samuel G Jacobson; Paul A Sieving; Anand Swaroop
Journal:  Am J Hum Genet       Date:  2002-04-30       Impact factor: 11.025

4.  Identification of novel murine- and human-specific RPGRIP1 splice variants with distinct expression profiles and subcellular localization.

Authors:  Xinrong Lu; Paulo A Ferreira
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-06       Impact factor: 4.799

5.  Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.

Authors:  Erwin van Wijk; Ferry F J Kersten; Aileen Kartono; Dorus A Mans; Kim Brandwijk; Stef J F Letteboer; Theo A Peters; Tina Märker; Xiumin Yan; Cor W R J Cremers; Frans P M Cremers; Uwe Wolfrum; Ronald Roepman; Hannie Kremer
Journal:  Hum Mol Genet       Date:  2008-09-30       Impact factor: 6.150

Review 6.  Aberrant protein trafficking in retinal degenerations: The initial phase of retinal remodeling.

Authors:  Katie L Bales; Alecia K Gross
Journal:  Exp Eye Res       Date:  2015-11-26       Impact factor: 3.467

7.  Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons.

Authors:  H Patil; N Tserentsoodol; A Saha; Y Hao; M Webb; P A Ferreira
Journal:  Cell Death Dis       Date:  2012-07-19       Impact factor: 8.469

8.  Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina.

Authors:  Aiden Eblimit; Thanh-Minh T Nguyen; Yiyun Chen; Julian Esteve-Rudd; Hua Zhong; Stef Letteboer; Jeroen Van Reeuwijk; David L Simons; Qian Ding; Ka Man Wu; Yumei Li; Sylvia Van Beersum; Yalda Moayedi; Huidan Xu; Patrick Pickard; Keqing Wang; Lin Gan; Samuel M Wu; David S Williams; Graeme Mardon; Ronald Roepman; Rui Chen
Journal:  Hum Mol Genet       Date:  2014-11-14       Impact factor: 6.150

9.  The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically.

Authors:  Ferry Fj Kersten; Erwin van Wijk; Lisette Hetterschijt; Katharina Bauβ; Theo A Peters; Mariam G Aslanyan; Bert van der Zwaag; Uwe Wolfrum; Jan Ee Keunen; Ronald Roepman; Hannie Kremer
Journal:  Cilia       Date:  2012-04-25

10.  Structural and functional plasticity of subcellular tethering, targeting and processing of RPGRIP1 by RPGR isoforms.

Authors:  Hemangi Patil; Mallikarjuna R Guruju; Kyoung-In Cho; Haiqing Yi; Andrew Orry; Hyesung Kim; Paulo A Ferreira
Journal:  Biol Open       Date:  2011-12-30       Impact factor: 2.422
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