ERCC4 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ERCC4" in Japanese language version.

refsWebsite

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doi.org (Global: 2^nd place; Japanese: 6^th place)

“Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease”. DNA Repair 10 (7): 781–91. (Jul 2011). doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
“Molecular cloning of a human DNA repair gene”. Nature 310 (5976): 425–9. (1984). Bibcode: 1984Natur.310..425W. doi:10.1038/310425a0. PMID 6462228.
“Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening”. Mutagenesis 4 (5): 349–54. (Sep 1989). doi:10.1093/mutage/4.5.349. PMID 2687628.
“ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs”. Molecular and Cellular Biology 16 (11): 6553–62. (Nov 1996). doi:10.1128/mcb.16.11.6553. PMC 231657. PMID 8887684.
Manandhar, Mandira; Boulware, Karen S.; Wood, Richard D. (2015-09-15). “The ERCC1 and ERCC4 (XPF) genes and gene products”. Gene 569 (2): 153–161. doi:10.1016/j.gene.2015.06.026. ISSN 1879-0038. PMC 4536074. PMID 26074087.
“A relationship between a DNA-repair/recombination nuclease family and archaeal helicases”. Trends in Biochemical Sciences 24 (3): 95–7. (Mar 1999). doi:10.1016/s0968-0004(99)01355-9. PMID 10203755.
“The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif”. The EMBO Journal 21 (8): 2045–53. (Apr 2002). doi:10.1093/emboj/21.8.2045. PMC 125967. PMID 11953324.
“Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair”. Nucleic Acids Research 29 (4): 872–9. (Feb 2001). doi:10.1093/nar/29.4.872. PMC 29621. PMID 11160918.
“Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease”. Cell 86 (5): 811–22. (Sep 1996). doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827.
“Specific cleavage of model recombination and repair intermediates by the yeast Rad1-Rad10 DNA endonuclease”. Science 265 (5181): 2082–5. (Sep 1994). Bibcode: 1994Sci...265.2082B. doi:10.1126/science.8091230. PMID 8091230.
“The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair.”. Structure 13 (12): 1849–1858. (December 2005). doi:10.1016/j.str.2005.08.014. hdl:1874/14818. ISSN 1633-8413. PMID 16338413.
“The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex.”. J Biol Chem 290 (33): 20541–20555. (August 2015). doi:10.1074/jbc.M114.635169. ISSN 1083-351X. PMC 4536458. PMID 26085086.
“Radiation-induced lethality and mutation in a repair-deficient CHO cell line”. International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine 43 (2): 207–13. (Feb 1983). doi:10.1080/09553008314550241. PMID 6600735.
“ERCC1-XPF endonuclease facilitates DNA double-strand break repair”. Molecular and Cellular Biology 28 (16): 5082–92. (Aug 2008). doi:10.1128/MCB.00293-08. PMC 2519706. PMID 18541667.
“Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1”. Proceedings of the National Academy of Sciences of the United States of America 94 (24): 13122–7. (Nov 1997). Bibcode: 1997PNAS...9413122S. doi:10.1073/pnas.94.24.13122. PMC 24273. PMID 9371810.
“The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells”. Nucleic Acids Research 36 (1): 1–9. (Jan 2008). doi:10.1093/nar/gkm888. PMC 2248766. PMID 17962301.
“Alternative-NHEJ is a mechanistically distinct pathway of mammalian chromosome break repair”. PLOS Genetics 4 (6): e1000110. (Jun 2008). doi:10.1371/journal.pgen.1000110. PMC 2430616. PMID 18584027.
“ERCC1-XPF endonuclease facilitates DNA double-strand break repair”. Molecular and Cellular Biology 28 (16): 5082–92. (Aug 2008). doi:10.1128/MCB.00293-08. PMC 2519706. PMID 18541667.
“The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells”. The EMBO Journal 20 (22): 6540–9. (Nov 2001). doi:10.1093/emboj/20.22.6540. PMC 125716. PMID 11707424.
“Mammalian nucleotide excision repair proteins and interstrand crosslink repair”. Environmental and Molecular Mutagenesis 51 (6): 520–6. (Jul 2010). doi:10.1002/em.20569. PMC 3017513. PMID 20658645.
“Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1”. Proceedings of the National Academy of Sciences of the United States of America 94 (24): 13122–7. (Nov 1997). Bibcode: 1997PNAS...9413122S. doi:10.1073/pnas.94.24.13122. PMC 24273. PMID 9371810.
“XPF-ERCC1 acts in Unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4”. Molecular Cell 54 (3): 460–71. (May 2014). doi:10.1016/j.molcel.2014.03.015. PMC 5067070. PMID 24726325.
“Multiple roles of ERCC1-XPF in mammalian interstrand crosslink repair”. Environmental and Molecular Mutagenesis 51 (6): 567–81. (Jul 2010). doi:10.1002/em.20583. PMID 20658648.
“Advances in understanding the complex mechanisms of DNA interstrand cross-link repair”. Cold Spring Harbor Perspectives in Biology 5 (10): a012732. (Oct 2013). doi:10.1101/cshperspect.a012732. PMC 4123742. PMID 24086043.
“Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia”. American Journal of Human Genetics 92 (5): 807–19. (May 2013). doi:10.1016/j.ajhg.2013.04.007. PMC 3644632. PMID 23623389.
“A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis”. Nature 444 (7122): 1038–43. (Dec 2006). Bibcode: 2006Natur.444.1038N. doi:10.1038/nature05456. PMID 17183314.
“Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia”. American Journal of Human Genetics 92 (5): 800–6. (May 2013). doi:10.1016/j.ajhg.2013.04.002. PMC 3644630. PMID 23623386.
“Deficient expression of DNA repair enzymes in early progression to sporadic colon cancer”. Genome Integr 3 (1): 3. (2012). doi:10.1186/2041-9414-3-3. PMC 3351028. PMID 22494821.
“Quantification of crypt and stem cell evolution in the normal and neoplastic human colon”. Cell Rep 8 (4): 940–7. (2014). doi:10.1016/j.celrep.2014.07.019. PMC 4471679. PMID 25127143.
“The DNA damage response: ten years after”. Mol. Cell 28 (5): 739–45. (2007). doi:10.1016/j.molcel.2007.11.015. PMID 18082599.
“Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease”. DNA Repair (Amst.) 10 (7): 781–91. (2011). doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
“Combined genetic and nutritional risk models of triple negative breast cancer”. Nutr Cancer 66 (6): 955–63. (2014). doi:10.1080/01635581.2014.932397. PMID 25023197.

ensembl.org (Global: 1,626^th place; Japanese: 2,625^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000113456 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000022248 - Ensembl, May 2017

handle.net (Global: 102^nd place; Japanese: 78^th place)

hdl.handle.net

“Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease”. Cell 86 (5): 811–22. (Sep 1996). doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827.
“The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair.”. Structure 13 (12): 1849–1858. (December 2005). doi:10.1016/j.str.2005.08.014. hdl:1874/14818. ISSN 1633-8413. PMID 16338413.

harvard.edu (Global: 18^th place; Japanese: 107^th place)

ui.adsabs.harvard.edu

“Molecular cloning of a human DNA repair gene”. Nature 310 (5976): 425–9. (1984). Bibcode: 1984Natur.310..425W. doi:10.1038/310425a0. PMID 6462228.
“Specific cleavage of model recombination and repair intermediates by the yeast Rad1-Rad10 DNA endonuclease”. Science 265 (5181): 2082–5. (Sep 1994). Bibcode: 1994Sci...265.2082B. doi:10.1126/science.8091230. PMID 8091230.
“Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1”. Proceedings of the National Academy of Sciences of the United States of America 94 (24): 13122–7. (Nov 1997). Bibcode: 1997PNAS...9413122S. doi:10.1073/pnas.94.24.13122. PMC 24273. PMID 9371810.
“Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1”. Proceedings of the National Academy of Sciences of the United States of America 94 (24): 13122–7. (Nov 1997). Bibcode: 1997PNAS...9413122S. doi:10.1073/pnas.94.24.13122. PMC 24273. PMID 9371810.
“A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis”. Nature 444 (7122): 1038–43. (Dec 2006). Bibcode: 2006Natur.444.1038N. doi:10.1038/nature05456. PMID 17183314.

nih.gov (Global: 4^th place; Japanese: 24^th place)

pubmed.ncbi.nlm.nih.gov

“Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease”. DNA Repair 10 (7): 781–91. (Jul 2011). doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
“Molecular cloning of a human DNA repair gene”. Nature 310 (5976): 425–9. (1984). Bibcode: 1984Natur.310..425W. doi:10.1038/310425a0. PMID 6462228.
“Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening”. Mutagenesis 4 (5): 349–54. (Sep 1989). doi:10.1093/mutage/4.5.349. PMID 2687628.
“ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs”. Molecular and Cellular Biology 16 (11): 6553–62. (Nov 1996). doi:10.1128/mcb.16.11.6553. PMC 231657. PMID 8887684.
Manandhar, Mandira; Boulware, Karen S.; Wood, Richard D. (2015-09-15). “The ERCC1 and ERCC4 (XPF) genes and gene products”. Gene 569 (2): 153–161. doi:10.1016/j.gene.2015.06.026. ISSN 1879-0038. PMC 4536074. PMID 26074087.
“A relationship between a DNA-repair/recombination nuclease family and archaeal helicases”. Trends in Biochemical Sciences 24 (3): 95–7. (Mar 1999). doi:10.1016/s0968-0004(99)01355-9. PMID 10203755.
“The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif”. The EMBO Journal 21 (8): 2045–53. (Apr 2002). doi:10.1093/emboj/21.8.2045. PMC 125967. PMID 11953324.
“Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair”. Nucleic Acids Research 29 (4): 872–9. (Feb 2001). doi:10.1093/nar/29.4.872. PMC 29621. PMID 11160918.
“Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease”. Cell 86 (5): 811–22. (Sep 1996). doi:10.1016/s0092-8674(00)80155-5. hdl:1765/3110. PMID 8797827.
“Specific cleavage of model recombination and repair intermediates by the yeast Rad1-Rad10 DNA endonuclease”. Science 265 (5181): 2082–5. (Sep 1994). Bibcode: 1994Sci...265.2082B. doi:10.1126/science.8091230. PMID 8091230.
“The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair.”. Structure 13 (12): 1849–1858. (December 2005). doi:10.1016/j.str.2005.08.014. hdl:1874/14818. ISSN 1633-8413. PMID 16338413.
“The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex.”. J Biol Chem 290 (33): 20541–20555. (August 2015). doi:10.1074/jbc.M114.635169. ISSN 1083-351X. PMC 4536458. PMID 26085086.
“Radiation-induced lethality and mutation in a repair-deficient CHO cell line”. International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine 43 (2): 207–13. (Feb 1983). doi:10.1080/09553008314550241. PMID 6600735.
“ERCC1-XPF endonuclease facilitates DNA double-strand break repair”. Molecular and Cellular Biology 28 (16): 5082–92. (Aug 2008). doi:10.1128/MCB.00293-08. PMC 2519706. PMID 18541667.
“Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1”. Proceedings of the National Academy of Sciences of the United States of America 94 (24): 13122–7. (Nov 1997). Bibcode: 1997PNAS...9413122S. doi:10.1073/pnas.94.24.13122. PMC 24273. PMID 9371810.
“The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells”. Nucleic Acids Research 36 (1): 1–9. (Jan 2008). doi:10.1093/nar/gkm888. PMC 2248766. PMID 17962301.
“Alternative-NHEJ is a mechanistically distinct pathway of mammalian chromosome break repair”. PLOS Genetics 4 (6): e1000110. (Jun 2008). doi:10.1371/journal.pgen.1000110. PMC 2430616. PMID 18584027.
“ERCC1-XPF endonuclease facilitates DNA double-strand break repair”. Molecular and Cellular Biology 28 (16): 5082–92. (Aug 2008). doi:10.1128/MCB.00293-08. PMC 2519706. PMID 18541667.
“The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells”. The EMBO Journal 20 (22): 6540–9. (Nov 2001). doi:10.1093/emboj/20.22.6540. PMC 125716. PMID 11707424.
“Mammalian nucleotide excision repair proteins and interstrand crosslink repair”. Environmental and Molecular Mutagenesis 51 (6): 520–6. (Jul 2010). doi:10.1002/em.20569. PMC 3017513. PMID 20658645.
“Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1”. Proceedings of the National Academy of Sciences of the United States of America 94 (24): 13122–7. (Nov 1997). Bibcode: 1997PNAS...9413122S. doi:10.1073/pnas.94.24.13122. PMC 24273. PMID 9371810.
“XPF-ERCC1 acts in Unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4”. Molecular Cell 54 (3): 460–71. (May 2014). doi:10.1016/j.molcel.2014.03.015. PMC 5067070. PMID 24726325.
“Multiple roles of ERCC1-XPF in mammalian interstrand crosslink repair”. Environmental and Molecular Mutagenesis 51 (6): 567–81. (Jul 2010). doi:10.1002/em.20583. PMID 20658648.
“Advances in understanding the complex mechanisms of DNA interstrand cross-link repair”. Cold Spring Harbor Perspectives in Biology 5 (10): a012732. (Oct 2013). doi:10.1101/cshperspect.a012732. PMC 4123742. PMID 24086043.
“Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia”. American Journal of Human Genetics 92 (5): 807–19. (May 2013). doi:10.1016/j.ajhg.2013.04.007. PMC 3644632. PMID 23623389.
“A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis”. Nature 444 (7122): 1038–43. (Dec 2006). Bibcode: 2006Natur.444.1038N. doi:10.1038/nature05456. PMID 17183314.
“Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia”. American Journal of Human Genetics 92 (5): 800–6. (May 2013). doi:10.1016/j.ajhg.2013.04.002. PMC 3644630. PMID 23623386.
“Deficient expression of DNA repair enzymes in early progression to sporadic colon cancer”. Genome Integr 3 (1): 3. (2012). doi:10.1186/2041-9414-3-3. PMC 3351028. PMID 22494821.
“Quantification of crypt and stem cell evolution in the normal and neoplastic human colon”. Cell Rep 8 (4): 940–7. (2014). doi:10.1016/j.celrep.2014.07.019. PMC 4471679. PMID 25127143.
“The DNA damage response: ten years after”. Mol. Cell 28 (5): 739–45. (2007). doi:10.1016/j.molcel.2007.11.015. PMID 18082599.
“Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease”. DNA Repair (Amst.) 10 (7): 781–91. (2011). doi:10.1016/j.dnarep.2011.04.026. PMC 3139823. PMID 21612988.
“Combined genetic and nutritional risk models of triple negative breast cancer”. Nutr Cancer 66 (6): 955–63. (2014). doi:10.1080/01635581.2014.932397. PMID 25023197.

pmc.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

Human PubMed Reference:
Mouse PubMed Reference:
“Entrez Gene: ERCC4 excision repair cross-complementing rodent repair deficiency, complementation group 4”. 2023年1月28日閲覧。

wikipedia.org (Global: low place; Japanese: low place)

en.wikipedia.org

GRCh38: Ensembl release 89: ENSG00000113456 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000022248 - Ensembl, May 2017

worldcat.org (Global: 5^th place; Japanese: 19^th place)

search.worldcat.org

Manandhar, Mandira; Boulware, Karen S.; Wood, Richard D. (2015-09-15). “The ERCC1 and ERCC4 (XPF) genes and gene products”. Gene 569 (2): 153–161. doi:10.1016/j.gene.2015.06.026. ISSN 1879-0038. PMC 4536074. PMID 26074087.
“The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair.”. Structure 13 (12): 1849–1858. (December 2005). doi:10.1016/j.str.2005.08.014. hdl:1874/14818. ISSN 1633-8413. PMID 16338413.
“The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex.”. J Biol Chem 290 (33): 20541–20555. (August 2015). doi:10.1074/jbc.M114.635169. ISSN 1083-351X. PMC 4536458. PMID 26085086.