Retinitis pigmentosa GTPase regulator (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Retinitis pigmentosa GTPase regulator" in English language version.

refsWebsite

Global rank English rank

24nih.gov

4^th place

12doi.org

2^nd place

2ensembl.org

1,626^th place

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2semanticscholar.org

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1handle.net

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1harvard.edu

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1uzh.ch

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doi.org

Meindl A, Dry K, Herrmann K, Manson F, Ciccodicola A, Edgar A, Carvalho MR, Achatz H, Hellebrand H, Lennon A, Migliaccio C, Porter K, Zrenner E, Bird A, Jay M, Lorenz B, Wittwer B, D'Urso M, Meitinger T, Wright A (May 1996). "A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)". Nature Genetics. 13 (1): 35–42. doi:10.1038/ng0596-35. PMID 8673101. S2CID 31695757.
Roepman R, van Duijnhoven G, Rosenberg T, Pinckers AJ, Bleeker-Wagemakers LM, Bergen AA, Post J, Beck A, Reinhardt R, Ropers HH, Cremers FP, Berger W (Jul 1996). "Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1". Human Molecular Genetics. 5 (7): 1035–41. doi:10.1093/hmg/5.7.1035. hdl:2066/22748. PMID 8817343.
Murga-Zamalloa CA, Atkins SJ, Peranen J, Swaroop A, Khanna H (Sep 2010). "Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration". Human Molecular Genetics. 19 (18): 3591–8. doi:10.1093/hmg/ddq275. PMC 2928130. PMID 20631154.
Khanna H (October 2015). "Photoreceptor Sensory Cilium: Traversing the Ciliary Gate". Cells. 4 (4): 674–86. doi:10.3390/cells4040674. PMC 4695852. PMID 26501325.
Churchill JD, Bowne SJ, Sullivan LS, Lewis RA, Wheaton DK, Birch DG, et al. (February 2013). "Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa". Investigative Ophthalmology & Visual Science. 54 (2): 1411–6. doi:10.1167/iovs.12-11541. PMC 3597192. PMID 23372056.
Glomset JA, Farnsworth CC (1994). "Role of protein modification reactions in programming interactions between ras-related GTPases and cell membranes". Annual Review of Cell Biology. 10: 181–205. doi:10.1146/annurev.cb.10.110194.001145. PMID 7888176.
Linari M, Ueffing M, Manson F, Wright A, Meitinger T, Becker J (Feb 1999). "The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase". Proceedings of the National Academy of Sciences of the United States of America. 96 (4): 1315–20. Bibcode:1999PNAS...96.1315L. doi:10.1073/pnas.96.4.1315. PMC 15460. PMID 9990021.
Roepman R, Bernoud-Hubac N, Schick DE, Maugeri A, Berger W, Ropers HH, Cremers FP, Ferreira PA (Sep 2000). "The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors". Human Molecular Genetics. 9 (14): 2095–105. doi:10.1093/hmg/9.14.2095. PMID 10958648.
Rao KN, Zhang W, Li L, Ronquillo C, Baehr W, Khanna H (May 2016). "Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR". Human Molecular Genetics. 25 (10): 2005–2012. doi:10.1093/hmg/ddw075. PMC 5062589. PMID 26936822.
Wang J, Deretic D (January 2014). "Molecular complexes that direct rhodopsin transport to primary cilia". Progress in Retinal and Eye Research. 38: 1–19. doi:10.1016/j.preteyeres.2013.08.004. PMC 3883129. PMID 24135424.
Moritz OL, Tam BM, Hurd LL, Peränen J, Deretic D, Papermaster DS (August 2001). "Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods". Molecular Biology of the Cell. 12 (8): 2341–51. doi:10.1091/mbc.12.8.2341. PMC 58598. PMID 11514620.
Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, et al. (April 2007). "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss" (PDF). Human Genetics. 121 (2): 203–11. doi:10.1007/s00439-006-0304-0. PMID 17171570. S2CID 22632047.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000156313 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000031174 – Ensembl, May 2017

handle.net

hdl.handle.net

Roepman R, van Duijnhoven G, Rosenberg T, Pinckers AJ, Bleeker-Wagemakers LM, Bergen AA, Post J, Beck A, Reinhardt R, Ropers HH, Cremers FP, Berger W (Jul 1996). "Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1". Human Molecular Genetics. 5 (7): 1035–41. doi:10.1093/hmg/5.7.1035. hdl:2066/22748. PMID 8817343.

harvard.edu

ui.adsabs.harvard.edu

Linari M, Ueffing M, Manson F, Wright A, Meitinger T, Becker J (Feb 1999). "The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase". Proceedings of the National Academy of Sciences of the United States of America. 96 (4): 1315–20. Bibcode:1999PNAS...96.1315L. doi:10.1073/pnas.96.4.1315. PMC 15460. PMID 9990021.

nih.gov

pubmed.ncbi.nlm.nih.gov

Meindl A, Dry K, Herrmann K, Manson F, Ciccodicola A, Edgar A, Carvalho MR, Achatz H, Hellebrand H, Lennon A, Migliaccio C, Porter K, Zrenner E, Bird A, Jay M, Lorenz B, Wittwer B, D'Urso M, Meitinger T, Wright A (May 1996). "A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)". Nature Genetics. 13 (1): 35–42. doi:10.1038/ng0596-35. PMID 8673101. S2CID 31695757.
Roepman R, van Duijnhoven G, Rosenberg T, Pinckers AJ, Bleeker-Wagemakers LM, Bergen AA, Post J, Beck A, Reinhardt R, Ropers HH, Cremers FP, Berger W (Jul 1996). "Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1". Human Molecular Genetics. 5 (7): 1035–41. doi:10.1093/hmg/5.7.1035. hdl:2066/22748. PMID 8817343.
Murga-Zamalloa CA, Atkins SJ, Peranen J, Swaroop A, Khanna H (Sep 2010). "Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration". Human Molecular Genetics. 19 (18): 3591–8. doi:10.1093/hmg/ddq275. PMC 2928130. PMID 20631154.
Khanna H (October 2015). "Photoreceptor Sensory Cilium: Traversing the Ciliary Gate". Cells. 4 (4): 674–86. doi:10.3390/cells4040674. PMC 4695852. PMID 26501325.
Churchill JD, Bowne SJ, Sullivan LS, Lewis RA, Wheaton DK, Birch DG, et al. (February 2013). "Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa". Investigative Ophthalmology & Visual Science. 54 (2): 1411–6. doi:10.1167/iovs.12-11541. PMC 3597192. PMID 23372056.
Glomset JA, Farnsworth CC (1994). "Role of protein modification reactions in programming interactions between ras-related GTPases and cell membranes". Annual Review of Cell Biology. 10: 181–205. doi:10.1146/annurev.cb.10.110194.001145. PMID 7888176.
Linari M, Ueffing M, Manson F, Wright A, Meitinger T, Becker J (Feb 1999). "The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase". Proceedings of the National Academy of Sciences of the United States of America. 96 (4): 1315–20. Bibcode:1999PNAS...96.1315L. doi:10.1073/pnas.96.4.1315. PMC 15460. PMID 9990021.
Murga-Zamalloa CA, Desai NJ, Hildebrandt F, Khanna H (July 2010). "Interaction of ciliary disease protein retinitis pigmentosa GTPase regulator with nephronophthisis-associated proteins in mammalian retinas". Molecular Vision. 16: 1373–81. PMC 2905641. PMID 20664800.
Roepman R, Bernoud-Hubac N, Schick DE, Maugeri A, Berger W, Ropers HH, Cremers FP, Ferreira PA (Sep 2000). "The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors". Human Molecular Genetics. 9 (14): 2095–105. doi:10.1093/hmg/9.14.2095. PMID 10958648.
Rao KN, Zhang W, Li L, Ronquillo C, Baehr W, Khanna H (May 2016). "Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR". Human Molecular Genetics. 25 (10): 2005–2012. doi:10.1093/hmg/ddw075. PMC 5062589. PMID 26936822.
Wang J, Deretic D (January 2014). "Molecular complexes that direct rhodopsin transport to primary cilia". Progress in Retinal and Eye Research. 38: 1–19. doi:10.1016/j.preteyeres.2013.08.004. PMC 3883129. PMID 24135424.
Moritz OL, Tam BM, Hurd LL, Peränen J, Deretic D, Papermaster DS (August 2001). "Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods". Molecular Biology of the Cell. 12 (8): 2341–51. doi:10.1091/mbc.12.8.2341. PMC 58598. PMID 11514620.
Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, et al. (April 2007). "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss" (PDF). Human Genetics. 121 (2): 203–11. doi:10.1007/s00439-006-0304-0. PMID 17171570. S2CID 22632047.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Murga-Zamalloa CA, Atkins SJ, Peranen J, Swaroop A, Khanna H (Sep 2010). "Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration". Human Molecular Genetics. 19 (18): 3591–8. doi:10.1093/hmg/ddq275. PMC 2928130. PMID 20631154.
"Entrez Gene: RPGR retinitis pigmentosa GTPase regulator".
Khanna H (October 2015). "Photoreceptor Sensory Cilium: Traversing the Ciliary Gate". Cells. 4 (4): 674–86. doi:10.3390/cells4040674. PMC 4695852. PMID 26501325.
Churchill JD, Bowne SJ, Sullivan LS, Lewis RA, Wheaton DK, Birch DG, et al. (February 2013). "Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa". Investigative Ophthalmology & Visual Science. 54 (2): 1411–6. doi:10.1167/iovs.12-11541. PMC 3597192. PMID 23372056.
Linari M, Ueffing M, Manson F, Wright A, Meitinger T, Becker J (Feb 1999). "The retinitis pigmentosa GTPase regulator, RPGR, interacts with the delta subunit of rod cyclic GMP phosphodiesterase". Proceedings of the National Academy of Sciences of the United States of America. 96 (4): 1315–20. Bibcode:1999PNAS...96.1315L. doi:10.1073/pnas.96.4.1315. PMC 15460. PMID 9990021.
Murga-Zamalloa CA, Desai NJ, Hildebrandt F, Khanna H (July 2010). "Interaction of ciliary disease protein retinitis pigmentosa GTPase regulator with nephronophthisis-associated proteins in mammalian retinas". Molecular Vision. 16: 1373–81. PMC 2905641. PMID 20664800.
Rao KN, Zhang W, Li L, Ronquillo C, Baehr W, Khanna H (May 2016). "Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR". Human Molecular Genetics. 25 (10): 2005–2012. doi:10.1093/hmg/ddw075. PMC 5062589. PMID 26936822.
Wang J, Deretic D (January 2014). "Molecular complexes that direct rhodopsin transport to primary cilia". Progress in Retinal and Eye Research. 38: 1–19. doi:10.1016/j.preteyeres.2013.08.004. PMC 3883129. PMID 24135424.
Moritz OL, Tam BM, Hurd LL, Peränen J, Deretic D, Papermaster DS (August 2001). "Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods". Molecular Biology of the Cell. 12 (8): 2341–51. doi:10.1091/mbc.12.8.2341. PMC 58598. PMID 11514620.

semanticscholar.org

api.semanticscholar.org

Meindl A, Dry K, Herrmann K, Manson F, Ciccodicola A, Edgar A, Carvalho MR, Achatz H, Hellebrand H, Lennon A, Migliaccio C, Porter K, Zrenner E, Bird A, Jay M, Lorenz B, Wittwer B, D'Urso M, Meitinger T, Wright A (May 1996). "A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)". Nature Genetics. 13 (1): 35–42. doi:10.1038/ng0596-35. PMID 8673101. S2CID 31695757.
Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, et al. (April 2007). "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss" (PDF). Human Genetics. 121 (2): 203–11. doi:10.1007/s00439-006-0304-0. PMID 17171570. S2CID 22632047.

uzh.ch

zora.uzh.ch

Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, et al. (April 2007). "A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss" (PDF). Human Genetics. 121 (2): 203–11. doi:10.1007/s00439-006-0304-0. PMID 17171570. S2CID 22632047.