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Ribonukleasen H (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ribonukleasen H" in German language version.

refsWebsite
Global rank German rank
20doi.org
2nd place
3rd place
19nih.gov
4th place
7th place
1rcsb.org
8,838th place
low place
1zenodo.org
621st place
5,656th place

doi.org

  • M. Figiel, H. Chon, S. M. Cerritelli, M. Cybulska, R. J. Crouch, M. Nowotny: The structural and biochemical characterization of human RNase H2 complex reveals the molecular basis for substrate recognition and Aicardi-Goutières syndrome defects. In: Journal of Biological Chemistry. Band 286, Nummer 12, März 2011, S. 10540–10550, doi:10.1074/jbc.M110.181974, PMID 21177858, PMC 3060507 (freier Volltext).
  • Simon L. Dürr, Olga Bohuszewicz, Dénes Berta, Reynier Suardiaz, Pablo G. Jambrina: The Role of Conserved Residues in the DEDDh Motif: the Proton-Transfer Mechanism of HIV-1 RNase H. In: ACS Catalysis. 16. Juni 2021, S. 7915–7927, doi:10.1021/acscatal.1c01493.
  • S. M. Cerritelli, R. J. Crouch: Ribonuclease H: the enzymes in eukaryotes. In: The FEBS journal. Band 276, Nummer 6, März 2009, S. 1494–1505, doi:10.1111/j.1742-4658.2009.06908.x, PMID 19228196, PMC 2746905 (freier Volltext).
  • M. Figiel, M. Nowotny: Crystal structure of RNase H3-substrate complex reveals parallel evolution of RNA/DNA hybrid recognition. In: Nucleic acids research. Band 42, Nummer 14, August 2014, S. 9285–9294, doi:10.1093/nar/gku615, PMID 25016521, PMC 4132731 (freier Volltext).
  • J. F. Davies, Z. Hostomska, Z. Hostomsky, S. R. Jordan, D. A. Matthews: Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase. In: Science. Band 252, Nummer 5002, April 1991, S. 88–95, doi:10.1126/science.1707186, PMID 1707186.
  • Y. J. Crow, A. Leitch, B. E. Hayward, A. Garner, R. Parmar, E. Griffith, M. Ali, C. Semple, J. Aicardi, R. Babul-Hirji, C. Baumann, P. Baxter, E. Bertini, K. E. Chandler, D. Chitayat, D. Cau, C. Déry, E. Fazzi, C. Goizet, M. D. King, J. Klepper, D. Lacombe, G. Lanzi, H. Lyall, M. L. Martínez-Frías, M. Mathieu, C. McKeown, A. Monier, Y. Oade, O. W. Quarrell, C. D. Rittey, R. C. Rogers, A. Sanchis, J. B. Stephenson, U. Tacke, M. Till, J. L. Tolmie, P. Tomlin, T. Voit, B. Weschke, C. G. Woods, P. Lebon, D. T. Bonthron, C. P. Ponting, A. P. Jackson: Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. In: Nature genetics. Band 38, Nummer 8, August 2006, S. 910–916, doi:10.1038/ng1842, PMID 16845400.
  • T. Tadokoro, S. Kanaya: Ribonuclease H: molecular diversities, substrate binding domains, and catalytic mechanism of the prokaryotic enzymes. In: The FEBS journal. Band 276, Nummer 6, März 2009, S. 1482–1493, doi:10.1111/j.1742-4658.2009.06907.x, PMID 19228197.
  • Amon JD, Koshland D: RNase H enables efficient repair of R-loop induced DNA damage. In: eLife. 5. Jahrgang, Dezember 2016, S. e20533, doi:10.7554/eLife.20533, PMID 27938663, PMC 5215079 (freier Volltext).
  • Lima WF, Murray HM, Damle SS, Hart CE, Hung G, De Hoyos CL, Liang XH, Crooke ST: Viable RNaseH1 knockout mice show RNaseH1 is essential for R loop processing, mitochondrial and liver function. In: Nucleic Acids Research. 44. Jahrgang, Nr. 11, Juni 2016, S. 5299–312, doi:10.1093/nar/gkw350, PMID 27131367, PMC 4914116 (freier Volltext).
  • Arudchandran A, Cerritelli S, Narimatsu S, Itaya M, Shin DY, Shimada Y, Crouch RJ: The absence of ribonuclease H1 or H2 alters the sensitivity of Saccharomyces cerevisiae to hydroxyurea, caffeine and ethyl methanesulphonate: implications for roles of RNases H in DNA replication and repair. In: Genes to Cells. 5. Jahrgang, Nr. 10, 2000, S. 789–802, doi:10.1046/j.1365-2443.2000.00373.x, PMID 11029655 (zenodo.org [PDF]).
  • Cerritelli SM, Frolova EG, Feng C, Grinberg A, Love PE, Crouch RJ: Failure to produce mitochondrial DNA results in embryonic lethality in Rnaseh1 null mice. In: Molecular Cell. 11. Jahrgang, Nr. 3, 2003, S. 807–15, doi:10.1016/s1097-2765(03)00088-1, PMID 12667461.
  • Reyes A, Melchionda L, Nasca A, Carrara F, Lamantea E, Zanolini A, Lamperti C, Fang M, Zhang J, Ronchi D, Bonato S, Fagiolari G, Moggio M, Ghezzi D, Zeviani M: RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy. In: American Journal of Human Genetics. 97. Jahrgang, Nr. 1, Juli 2015, S. 186–93, doi:10.1016/j.ajhg.2015.05.013, PMID 26094573, PMC 4572567 (freier Volltext).
  • Thomas Hollis, Nadine M. Shaban: Ribonucleases. Hrsg.: Allen W. Nicholson (= Nucleic Acids and Molecular Biology). Springer Berlin Heidelberg, 2011, ISBN 978-3-642-21077-8, S. 299–317, doi:10.1007/978-3-642-21078-5_12.
  • Chon H, Vassilev A, DePamphilis ML, Zhao Y, Zhang J, Burgers PM, Crouch RJ, Cerritelli SM: Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex. In: Nucleic Acids Research. 37. Jahrgang, Nr. 1, Januar 2009, S. 96–110, doi:10.1093/nar/gkn913, PMID 19015152, PMC 2615623 (freier Volltext).
  • Reijns MA, Jackson AP: Ribonuclease H2 in health and disease. In: Biochemical Society Transactions. 42. Jahrgang, Nr. 4, August 2014, S. 717–25, doi:10.1042/BST20140079, PMID 25109948.
  • Chon H, Vassilev A, DePamphilis ML, Zhao Y, Zhang J, Burgers PM, Crouch RJ, Cerritelli SM: Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex. In: Nucleic Acids Research. 37. Jahrgang, Nr. 1, Januar 2009, S. 96–110, doi:10.1093/nar/gkn913, PMID 19015152, PMC 2615623 (freier Volltext) – (englisch).
  • Wahba L, Amon JD, Koshland D, Vuica-Ross M: RNase H and multiple RNA biogenesis factors cooperate to prevent RNA:DNA hybrids from generating genome instability. In: Molecular Cell. 44. Jahrgang, Nr. 6, Dezember 2011, S. 978–88, doi:10.1016/j.molcel.2011.10.017, PMID 22195970, PMC 3271842 (freier Volltext).
  • Kim N, Huang SN, Williams JS, Li YC, Clark AB, Cho JE, Kunkel TA, Pommier Y, Jinks-Robertson S: Mutagenic processing of ribonucleotides in DNA by yeast topoisomerase I. In: Science. 332. Jahrgang, Nr. 6037, Juni 2011, S. 1561–4, doi:10.1126/science.1205016, PMID 21700875, PMC 3380281 (freier Volltext).
  • Ohtani N, Haruki M, Morikawa M, Crouch RJ, Itaya M, Kanaya S: Identification of the genes encoding Mn2+-dependent RNase HII and Mg2+-dependent RNase HIII from Bacillus subtilis: classification of RNases H into three families. In: Biochemistry. 38. Jahrgang, Nr. 2, Januar 1999, S. 605–18, doi:10.1021/bi982207z, PMID 9888800.
  • Kochiwa H, Tomita M, Kanai A: Evolution of ribonuclease H genes in prokaryotes to avoid inheritance of redundant genes. In: BMC Evolutionary Biology. 7. Jahrgang, Juli 2007, S. 128, doi:10.1186/1471-2148-7-128, PMID 17663799, PMC 1950709 (freier Volltext).

nih.gov

ncbi.nlm.nih.gov

  • M. Figiel, H. Chon, S. M. Cerritelli, M. Cybulska, R. J. Crouch, M. Nowotny: The structural and biochemical characterization of human RNase H2 complex reveals the molecular basis for substrate recognition and Aicardi-Goutières syndrome defects. In: Journal of Biological Chemistry. Band 286, Nummer 12, März 2011, S. 10540–10550, doi:10.1074/jbc.M110.181974, PMID 21177858, PMC 3060507 (freier Volltext).
  • S. M. Cerritelli, R. J. Crouch: Ribonuclease H: the enzymes in eukaryotes. In: The FEBS journal. Band 276, Nummer 6, März 2009, S. 1494–1505, doi:10.1111/j.1742-4658.2009.06908.x, PMID 19228196, PMC 2746905 (freier Volltext).
  • M. Figiel, M. Nowotny: Crystal structure of RNase H3-substrate complex reveals parallel evolution of RNA/DNA hybrid recognition. In: Nucleic acids research. Band 42, Nummer 14, August 2014, S. 9285–9294, doi:10.1093/nar/gku615, PMID 25016521, PMC 4132731 (freier Volltext).
  • J. F. Davies, Z. Hostomska, Z. Hostomsky, S. R. Jordan, D. A. Matthews: Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase. In: Science. Band 252, Nummer 5002, April 1991, S. 88–95, doi:10.1126/science.1707186, PMID 1707186.
  • J. Hansen, T. Schulze, W. Mellert, K. Moelling: Identification and characterization of HIV-specific RNase H by monoclonal antibody. In: The EMBO Journal. Band 7, Nummer 1, Januar 1988, S. 239–243, PMID 2452083, PMC 454263 (freier Volltext).
  • Y. J. Crow, A. Leitch, B. E. Hayward, A. Garner, R. Parmar, E. Griffith, M. Ali, C. Semple, J. Aicardi, R. Babul-Hirji, C. Baumann, P. Baxter, E. Bertini, K. E. Chandler, D. Chitayat, D. Cau, C. Déry, E. Fazzi, C. Goizet, M. D. King, J. Klepper, D. Lacombe, G. Lanzi, H. Lyall, M. L. Martínez-Frías, M. Mathieu, C. McKeown, A. Monier, Y. Oade, O. W. Quarrell, C. D. Rittey, R. C. Rogers, A. Sanchis, J. B. Stephenson, U. Tacke, M. Till, J. L. Tolmie, P. Tomlin, T. Voit, B. Weschke, C. G. Woods, P. Lebon, D. T. Bonthron, C. P. Ponting, A. P. Jackson: Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. In: Nature genetics. Band 38, Nummer 8, August 2006, S. 910–916, doi:10.1038/ng1842, PMID 16845400.
  • T. Tadokoro, S. Kanaya: Ribonuclease H: molecular diversities, substrate binding domains, and catalytic mechanism of the prokaryotic enzymes. In: The FEBS journal. Band 276, Nummer 6, März 2009, S. 1482–1493, doi:10.1111/j.1742-4658.2009.06907.x, PMID 19228197.
  • Amon JD, Koshland D: RNase H enables efficient repair of R-loop induced DNA damage. In: eLife. 5. Jahrgang, Dezember 2016, S. e20533, doi:10.7554/eLife.20533, PMID 27938663, PMC 5215079 (freier Volltext).
  • Lima WF, Murray HM, Damle SS, Hart CE, Hung G, De Hoyos CL, Liang XH, Crooke ST: Viable RNaseH1 knockout mice show RNaseH1 is essential for R loop processing, mitochondrial and liver function. In: Nucleic Acids Research. 44. Jahrgang, Nr. 11, Juni 2016, S. 5299–312, doi:10.1093/nar/gkw350, PMID 27131367, PMC 4914116 (freier Volltext).
  • Arudchandran A, Cerritelli S, Narimatsu S, Itaya M, Shin DY, Shimada Y, Crouch RJ: The absence of ribonuclease H1 or H2 alters the sensitivity of Saccharomyces cerevisiae to hydroxyurea, caffeine and ethyl methanesulphonate: implications for roles of RNases H in DNA replication and repair. In: Genes to Cells. 5. Jahrgang, Nr. 10, 2000, S. 789–802, doi:10.1046/j.1365-2443.2000.00373.x, PMID 11029655 (zenodo.org [PDF]).
  • Cerritelli SM, Frolova EG, Feng C, Grinberg A, Love PE, Crouch RJ: Failure to produce mitochondrial DNA results in embryonic lethality in Rnaseh1 null mice. In: Molecular Cell. 11. Jahrgang, Nr. 3, 2003, S. 807–15, doi:10.1016/s1097-2765(03)00088-1, PMID 12667461.
  • Reyes A, Melchionda L, Nasca A, Carrara F, Lamantea E, Zanolini A, Lamperti C, Fang M, Zhang J, Ronchi D, Bonato S, Fagiolari G, Moggio M, Ghezzi D, Zeviani M: RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy. In: American Journal of Human Genetics. 97. Jahrgang, Nr. 1, Juli 2015, S. 186–93, doi:10.1016/j.ajhg.2015.05.013, PMID 26094573, PMC 4572567 (freier Volltext).
  • Chon H, Vassilev A, DePamphilis ML, Zhao Y, Zhang J, Burgers PM, Crouch RJ, Cerritelli SM: Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex. In: Nucleic Acids Research. 37. Jahrgang, Nr. 1, Januar 2009, S. 96–110, doi:10.1093/nar/gkn913, PMID 19015152, PMC 2615623 (freier Volltext).
  • Reijns MA, Jackson AP: Ribonuclease H2 in health and disease. In: Biochemical Society Transactions. 42. Jahrgang, Nr. 4, August 2014, S. 717–25, doi:10.1042/BST20140079, PMID 25109948.
  • Chon H, Vassilev A, DePamphilis ML, Zhao Y, Zhang J, Burgers PM, Crouch RJ, Cerritelli SM: Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex. In: Nucleic Acids Research. 37. Jahrgang, Nr. 1, Januar 2009, S. 96–110, doi:10.1093/nar/gkn913, PMID 19015152, PMC 2615623 (freier Volltext) – (englisch).
  • Wahba L, Amon JD, Koshland D, Vuica-Ross M: RNase H and multiple RNA biogenesis factors cooperate to prevent RNA:DNA hybrids from generating genome instability. In: Molecular Cell. 44. Jahrgang, Nr. 6, Dezember 2011, S. 978–88, doi:10.1016/j.molcel.2011.10.017, PMID 22195970, PMC 3271842 (freier Volltext).
  • Kim N, Huang SN, Williams JS, Li YC, Clark AB, Cho JE, Kunkel TA, Pommier Y, Jinks-Robertson S: Mutagenic processing of ribonucleotides in DNA by yeast topoisomerase I. In: Science. 332. Jahrgang, Nr. 6037, Juni 2011, S. 1561–4, doi:10.1126/science.1205016, PMID 21700875, PMC 3380281 (freier Volltext).
  • Ohtani N, Haruki M, Morikawa M, Crouch RJ, Itaya M, Kanaya S: Identification of the genes encoding Mn2+-dependent RNase HII and Mg2+-dependent RNase HIII from Bacillus subtilis: classification of RNases H into three families. In: Biochemistry. 38. Jahrgang, Nr. 2, Januar 1999, S. 605–18, doi:10.1021/bi982207z, PMID 9888800.
  • Kochiwa H, Tomita M, Kanai A: Evolution of ribonuclease H genes in prokaryotes to avoid inheritance of redundant genes. In: BMC Evolutionary Biology. 7. Jahrgang, Juli 2007, S. 128, doi:10.1186/1471-2148-7-128, PMID 17663799, PMC 1950709 (freier Volltext).

rcsb.org

zenodo.org

  • Arudchandran A, Cerritelli S, Narimatsu S, Itaya M, Shin DY, Shimada Y, Crouch RJ: The absence of ribonuclease H1 or H2 alters the sensitivity of Saccharomyces cerevisiae to hydroxyurea, caffeine and ethyl methanesulphonate: implications for roles of RNases H in DNA replication and repair. In: Genes to Cells. 5. Jahrgang, Nr. 10, 2000, S. 789–802, doi:10.1046/j.1365-2443.2000.00373.x, PMID 11029655 (zenodo.org [PDF]).