インデル (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "インデル" in Japanese language version.

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genome.cshlp.org

Mills, R. E. (9 August 2006). “An initial map of insertion and deletion (INDEL) variation in the human genome”. Genome Research 16 (9): 1182–1190. doi:10.1101/gr.4565806.

doi.org

Mills, R. E. (9 August 2006). “An initial map of insertion and deletion (INDEL) variation in the human genome”. Genome Research 16 (9): 1182–1190. doi:10.1101/gr.4565806.
Mullaney, J. M.; Mills, R. E.; Pittard, W. S.; Devine, S. E. (21 September 2010). “Small insertions and deletions (INDELs) in human genomes”. Human Molecular Genetics 19 (R2): R131–R136. doi:10.1093/hmg/ddq400.
Kondrashov AS, Rogozin IB (February 2004). “Context of deletions and insertions in human coding sequences”. Hum. Mutat. 23 (2): 177–85. doi:10.1002/humu.10312. PMID 14722921.
Ogurtsov AY, Sunyaev S, Kondrashov AS (August 2004). “Indel-based evolutionary distance and mouse-human divergence”. Genome Res. 14 (8): 1610–6. doi:10.1101/gr.2450504. PMC 509270. PMID 15289479.
Gregory TR (January 2004). “Insertion-deletion biases and the evolution of genome size”. Gene 324 (7): 15–34. doi:10.1016/j.gene.2003.09.030. PMID 14693368.
Halangoda A, Still JG, Hill KA, Sommer SS (2001). “Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity”. Environ. Mol. Mutagen. 37 (4): 311–23. doi:10.1002/em.1038. PMID 11424181.
Sachin apurwa; Wilson MD; Rubio JM; Post RJ (March 2004). “A molecular marker for the identification of Simulium squamosum (Diptera: Simuliidae)”. Ann Trop Med Parasitol 98 (2): 197–208. doi:10.1179/000349804225003118. PMID 15035730.
Gonzalez KD; Hill KA; Li K et al. (January 2007). “Somatic microindels: analysis in mouse soma and comparison with the human germline”. Hum. Mutat. 28 (1): 69–80. doi:10.1002/humu.20416. PMID 16977595.
Jing Hu1 & Pauline C Ng (2012). “Predicting the effects of frameshifting indels”. Genome Biology 13 (2): R9. doi:10.1186/gb-2012-13-2-r9. PMC 3334572.
Kaneko T, Tahara S, Matsuo M (May 1996). “Non-linear accumulation of 8-hydroxy-2'-deoxyguanosine, a marker of oxidized DNA damage, during aging”. Mutat. Res. 316 (5–6): 277–85. doi:10.1016/S0921-8734(96)90010-7. PMID 8649461.
Hill KA, Wang J, Farwell KD, Sommer SS (January 2003). “Spontaneous tandem-base mutations (TBM) show dramatic tissue, age, pattern and spectrum specificity”. Mutat. Res. 534 (1–2): 173–86. doi:10.1016/S1383-5718(02)00277-2. PMID 12504766.
Victoria L. Buettner, Kathleen A. Hill, Asanga Halangoda,Steve S. Sommer (1999). “Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age”. Environmental and molecular mutagenesis 33 (4): 320-324. doi:10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S. PMID 10398380.
Väli U, Brandström M, Johansson M, Ellegren H (2008). “Insertion-deletion polymorphisms (indels) as genetic markers in natural populations”. BMC Genetic 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (2008). Volff, Jean-Nicolas. ed. “Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene”. PLoS ONE 3 (1): e1386. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira, F.; Carneiro, J.; Matthiesen, R.; van Asch, B.; Pinto, N.; Gusmao, L.; Amorim, A. (4 October 2010). “Identification of species by multiplex analysis of variable-length sequences”. Nucleic Acids Research 38 (22): e203–e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Nakamura, H; Muro, T; Imamura, S; Yuasa, I (March 2009). “Forensic species identification based on size variation of mitochondrial DNA hypervariable regions.”. International journal of legal medicine 123 (2): 177–84. doi:10.1007/s00414-008-0306-7. PMID 19052767.
Taberlet, P.; Coissac, E.; Pompanon, F.; Gielly, L.; Miquel, C.; Valentini, A.; Vermat, T.; Corthier, G. et al. (26 January 2007). “Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding”. Nucleic Acids Research 35 (3): e14–e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
van Hoof A, Frischmeyer PA, Dietz HC, Parker R (2002 Mar 22). “Exosome-mediated recognition and degradation of mRNAs lacking a termination codon”. Science 295 (5563): 2262-2264. doi:10.1126/science.1067272. PMID 11910110.
Scofield DG, Hong X, Lynch M (2007 Apr 24). “Position of the final intron in full-length transcripts: determined by NMD?”. Molecular biology and evolution 24 (4): 896-899. doi:10.1093/molbev/msm010.
Ng PC, Levy S, Huang J, Stockwell TB, Walenz BP, Li K, Axelrod N, Busam DA, Strausberg RL, Venter JC (2008 Aug). “Genetic Variation in an Individual Human Exome”. PLoS Genetics 4 (8): e1000160. doi:10.1371/journal.pgen.1000160. PMC 2493042. PMID 18704161.
Pelak K, Shianna KV, Ge D, Maia JM, Zhu M, Smith JP, Cirulli ET, Fellay J, Dickson SP, Gumbs CE, Heinzen EL, Need AC, Ruzzo EK, Singh A, Campbell CR, Hong LK, Lornsen KA, McKenzie AM, Sobreira NL, Hoover-Fong JE, Milner JD, Ottman R, Haynes BF, Goedert JJ, Goldstein DB (2010 Sep). “The Characterization of Twenty Sequenced Human Genomes”. PLoS Genetics 6 (9): e1001111. doi:10.1371/journal.pgen.1001111. PMC 2936541. PMID 20838461.
Hui Bai, Yinghao Cao, Jianzhang Quan, Li Dong, Zhiyong Li, Yanbin Zhu, Lihuang Zhu, Zhiping Dong (2013). “Identifying the Genome-Wide Sequence Variations and Developing New Molecular Markers for Genetics Research by Re-Sequencing a Landrace Cultivar of Foxtail Millet”. PLoS One 8 (9): e73514. doi:10.1371/journal.pone.0073514.
Zheng, L. Y., Guo, X. S., He, B., Sun, L. J., Peng, Y., Dong, S. S., ... & Jing, H. C. (2011). “Genome-wide patterns of genetic variation in sweet and grain sorghum (Sorghum bicolor)”. Genome Biology 12 (11): R114. doi:10.1186/gb-2011-12-11-r114.
The 1000 Genomes Project Consortium; Durbin, RM; Abecasis, GR; Altshuler, DL; Auton, A; Brooks, LD; Durbin, RM; Gibbs, RA et al. (2010-10-28). “A map of human genome variation from population-scale sequencing”. Nature 467 (7319): 1061–73. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kondrashov AS, Rogozin IB (February 2004). “Context of deletions and insertions in human coding sequences”. Hum. Mutat. 23 (2): 177–85. doi:10.1002/humu.10312. PMID 14722921.
Ogurtsov AY, Sunyaev S, Kondrashov AS (August 2004). “Indel-based evolutionary distance and mouse-human divergence”. Genome Res. 14 (8): 1610–6. doi:10.1101/gr.2450504. PMC 509270. PMID 15289479.
Gregory TR (January 2004). “Insertion-deletion biases and the evolution of genome size”. Gene 324 (7): 15–34. doi:10.1016/j.gene.2003.09.030. PMID 14693368.
Halangoda A, Still JG, Hill KA, Sommer SS (2001). “Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity”. Environ. Mol. Mutagen. 37 (4): 311–23. doi:10.1002/em.1038. PMID 11424181.
Sachin apurwa; Wilson MD; Rubio JM; Post RJ (March 2004). “A molecular marker for the identification of Simulium squamosum (Diptera: Simuliidae)”. Ann Trop Med Parasitol 98 (2): 197–208. doi:10.1179/000349804225003118. PMID 15035730.
Gonzalez KD; Hill KA; Li K et al. (January 2007). “Somatic microindels: analysis in mouse soma and comparison with the human germline”. Hum. Mutat. 28 (1): 69–80. doi:10.1002/humu.20416. PMID 16977595.
Kaneko T, Tahara S, Matsuo M (May 1996). “Non-linear accumulation of 8-hydroxy-2'-deoxyguanosine, a marker of oxidized DNA damage, during aging”. Mutat. Res. 316 (5–6): 277–85. doi:10.1016/S0921-8734(96)90010-7. PMID 8649461.
Hill KA, Wang J, Farwell KD, Sommer SS (January 2003). “Spontaneous tandem-base mutations (TBM) show dramatic tissue, age, pattern and spectrum specificity”. Mutat. Res. 534 (1–2): 173–86. doi:10.1016/S1383-5718(02)00277-2. PMID 12504766.
Victoria L. Buettner, Kathleen A. Hill, Asanga Halangoda,Steve S. Sommer (1999). “Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age”. Environmental and molecular mutagenesis 33 (4): 320-324. doi:10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S. PMID 10398380.
Väli U, Brandström M, Johansson M, Ellegren H (2008). “Insertion-deletion polymorphisms (indels) as genetic markers in natural populations”. BMC Genetic 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (2008). Volff, Jean-Nicolas. ed. “Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene”. PLoS ONE 3 (1): e1386. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira, F.; Carneiro, J.; Matthiesen, R.; van Asch, B.; Pinto, N.; Gusmao, L.; Amorim, A. (4 October 2010). “Identification of species by multiplex analysis of variable-length sequences”. Nucleic Acids Research 38 (22): e203–e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Nakamura, H; Muro, T; Imamura, S; Yuasa, I (March 2009). “Forensic species identification based on size variation of mitochondrial DNA hypervariable regions.”. International journal of legal medicine 123 (2): 177–84. doi:10.1007/s00414-008-0306-7. PMID 19052767.
Taberlet, P.; Coissac, E.; Pompanon, F.; Gielly, L.; Miquel, C.; Valentini, A.; Vermat, T.; Corthier, G. et al. (26 January 2007). “Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding”. Nucleic Acids Research 35 (3): e14–e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
van Hoof A, Frischmeyer PA, Dietz HC, Parker R (2002 Mar 22). “Exosome-mediated recognition and degradation of mRNAs lacking a termination codon”. Science 295 (5563): 2262-2264. doi:10.1126/science.1067272. PMID 11910110.
Nagy E, Maquat LE (1998 Jun 23). “A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance”. Trends in biochemical sciences 23 (6): 198-199. PMID 9644970.
Ng PC, Levy S, Huang J, Stockwell TB, Walenz BP, Li K, Axelrod N, Busam DA, Strausberg RL, Venter JC (2008 Aug). “Genetic Variation in an Individual Human Exome”. PLoS Genetics 4 (8): e1000160. doi:10.1371/journal.pgen.1000160. PMC 2493042. PMID 18704161.
Pelak K, Shianna KV, Ge D, Maia JM, Zhu M, Smith JP, Cirulli ET, Fellay J, Dickson SP, Gumbs CE, Heinzen EL, Need AC, Ruzzo EK, Singh A, Campbell CR, Hong LK, Lornsen KA, McKenzie AM, Sobreira NL, Hoover-Fong JE, Milner JD, Ottman R, Haynes BF, Goedert JJ, Goldstein DB (2010 Sep). “The Characterization of Twenty Sequenced Human Genomes”. PLoS Genetics 6 (9): e1001111. doi:10.1371/journal.pgen.1001111. PMC 2936541. PMID 20838461.
The 1000 Genomes Project Consortium; Durbin, RM; Abecasis, GR; Altshuler, DL; Auton, A; Brooks, LD; Durbin, RM; Gibbs, RA et al. (2010-10-28). “A map of human genome variation from population-scale sequencing”. Nature 467 (7319): 1061–73. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.

ncbi.nlm.nih.gov

Kondrashov AS, Rogozin IB (February 2004). “Context of deletions and insertions in human coding sequences”. Hum. Mutat. 23 (2): 177–85. doi:10.1002/humu.10312. PMID 14722921.
Ogurtsov AY, Sunyaev S, Kondrashov AS (August 2004). “Indel-based evolutionary distance and mouse-human divergence”. Genome Res. 14 (8): 1610–6. doi:10.1101/gr.2450504. PMC 509270. PMID 15289479.
Halangoda A, Still JG, Hill KA, Sommer SS (2001). “Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity”. Environ. Mol. Mutagen. 37 (4): 311–23. doi:10.1002/em.1038. PMID 11424181.
Jing Hu1 & Pauline C Ng (2012). “Predicting the effects of frameshifting indels”. Genome Biology 13 (2): R9. doi:10.1186/gb-2012-13-2-r9. PMC 3334572.
Victoria L. Buettner, Kathleen A. Hill, Asanga Halangoda,Steve S. Sommer (1999). “Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age”. Environmental and molecular mutagenesis 33 (4): 320-324. doi:10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S. PMID 10398380.
Väli U, Brandström M, Johansson M, Ellegren H (2008). “Insertion-deletion polymorphisms (indels) as genetic markers in natural populations”. BMC Genetic 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (2008). Volff, Jean-Nicolas. ed. “Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene”. PLoS ONE 3 (1): e1386. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira, F.; Carneiro, J.; Matthiesen, R.; van Asch, B.; Pinto, N.; Gusmao, L.; Amorim, A. (4 October 2010). “Identification of species by multiplex analysis of variable-length sequences”. Nucleic Acids Research 38 (22): e203–e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Taberlet, P.; Coissac, E.; Pompanon, F.; Gielly, L.; Miquel, C.; Valentini, A.; Vermat, T.; Corthier, G. et al. (26 January 2007). “Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding”. Nucleic Acids Research 35 (3): e14–e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
Nagy E, Maquat LE (1998 Jun 23). “A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance”. Trends in biochemical sciences 23 (6): 198-199. PMID 9644970.
Hui Bai, Yinghao Cao, Jianzhang Quan, Li Dong, Zhiyong Li, Yanbin Zhu, Lihuang Zhu, Zhiping Dong (2013). “Identifying the Genome-Wide Sequence Variations and Developing New Molecular Markers for Genetics Research by Re-Sequencing a Landrace Cultivar of Foxtail Millet”. PLoS One 8 (9): e73514. doi:10.1371/journal.pone.0073514.
Zheng, L. Y., Guo, X. S., He, B., Sun, L. J., Peng, Y., Dong, S. S., ... & Jing, H. C. (2011). “Genome-wide patterns of genetic variation in sweet and grain sorghum (Sorghum bicolor)”. Genome Biology 12 (11): R114. doi:10.1186/gb-2011-12-11-r114.
The 1000 Genomes Project Consortium; Durbin, RM; Abecasis, GR; Altshuler, DL; Auton, A; Brooks, LD; Durbin, RM; Gibbs, RA et al. (2010-10-28). “A map of human genome variation from population-scale sequencing”. Nature 467 (7319): 1061–73. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.

pmc.ncbi.nlm.nih.gov

Ogurtsov AY, Sunyaev S, Kondrashov AS (August 2004). “Indel-based evolutionary distance and mouse-human divergence”. Genome Res. 14 (8): 1610–6. doi:10.1101/gr.2450504. PMC 509270. PMID 15289479.
Jing Hu1 & Pauline C Ng (2012). “Predicting the effects of frameshifting indels”. Genome Biology 13 (2): R9. doi:10.1186/gb-2012-13-2-r9. PMC 3334572.
Väli U, Brandström M, Johansson M, Ellegren H (2008). “Insertion-deletion polymorphisms (indels) as genetic markers in natural populations”. BMC Genetic 9: 8. doi:10.1186/1471-2156-9-8. PMC 2266919. PMID 18211670.
Erixon P, Oxelman B (2008). Volff, Jean-Nicolas. ed. “Whole-gene positive selection, elevated synonymous substitution rates, duplication, and indel evolution of the chloroplast clpP1 gene”. PLoS ONE 3 (1): e1386. doi:10.1371/journal.pone.0001386. PMC 2148103. PMID 18167545.
Pereira, F.; Carneiro, J.; Matthiesen, R.; van Asch, B.; Pinto, N.; Gusmao, L.; Amorim, A. (4 October 2010). “Identification of species by multiplex analysis of variable-length sequences”. Nucleic Acids Research 38 (22): e203–e203. doi:10.1093/nar/gkq865. PMC 3001097. PMID 20923781.
Taberlet, P.; Coissac, E.; Pompanon, F.; Gielly, L.; Miquel, C.; Valentini, A.; Vermat, T.; Corthier, G. et al. (26 January 2007). “Power and limitations of the chloroplast trnL (UAA) intron for plant DNA barcoding”. Nucleic Acids Research 35 (3): e14–e14. doi:10.1093/nar/gkl938. PMC 1807943. PMID 17169982.
Ng PC, Levy S, Huang J, Stockwell TB, Walenz BP, Li K, Axelrod N, Busam DA, Strausberg RL, Venter JC (2008 Aug). “Genetic Variation in an Individual Human Exome”. PLoS Genetics 4 (8): e1000160. doi:10.1371/journal.pgen.1000160. PMC 2493042. PMID 18704161.
Pelak K, Shianna KV, Ge D, Maia JM, Zhu M, Smith JP, Cirulli ET, Fellay J, Dickson SP, Gumbs CE, Heinzen EL, Need AC, Ruzzo EK, Singh A, Campbell CR, Hong LK, Lornsen KA, McKenzie AM, Sobreira NL, Hoover-Fong JE, Milner JD, Ottman R, Haynes BF, Goedert JJ, Goldstein DB (2010 Sep). “The Characterization of Twenty Sequenced Human Genomes”. PLoS Genetics 6 (9): e1001111. doi:10.1371/journal.pgen.1001111. PMC 2936541. PMID 20838461.
The 1000 Genomes Project Consortium; Durbin, RM; Abecasis, GR; Altshuler, DL; Auton, A; Brooks, LD; Durbin, RM; Gibbs, RA et al. (2010-10-28). “A map of human genome variation from population-scale sequencing”. Nature 467 (7319): 1061–73. doi:10.1038/nature09534. PMC 3042601. PMID 20981092.

oup.com

academic.oup.com

Mullaney, J. M.; Mills, R. E.; Pittard, W. S.; Devine, S. E. (21 September 2010). “Small insertions and deletions (INDELs) in human genomes”. Human Molecular Genetics 19 (R2): R131–R136. doi:10.1093/hmg/ddq400.
Scofield DG, Hong X, Lynch M (2007 Apr 24). “Position of the final intron in full-length transcripts: determined by NMD?”. Molecular biology and evolution 24 (4): 896-899. doi:10.1093/molbev/msm010.

plos.org

journals.plos.org

Ng PC, Levy S, Huang J, Stockwell TB, Walenz BP, Li K, Axelrod N, Busam DA, Strausberg RL, Venter JC (2008 Aug). “Genetic Variation in an Individual Human Exome”. PLoS Genetics 4 (8): e1000160. doi:10.1371/journal.pgen.1000160. PMC 2493042. PMID 18704161.
Pelak K, Shianna KV, Ge D, Maia JM, Zhu M, Smith JP, Cirulli ET, Fellay J, Dickson SP, Gumbs CE, Heinzen EL, Need AC, Ruzzo EK, Singh A, Campbell CR, Hong LK, Lornsen KA, McKenzie AM, Sobreira NL, Hoover-Fong JE, Milner JD, Ottman R, Haynes BF, Goedert JJ, Goldstein DB (2010 Sep). “The Characterization of Twenty Sequenced Human Genomes”. PLoS Genetics 6 (9): e1001111. doi:10.1371/journal.pgen.1001111. PMC 2936541. PMID 20838461.

sciencedirect.com

Gregory TR (January 2004). “Insertion-deletion biases and the evolution of genome size”. Gene 324 (7): 15–34. doi:10.1016/j.gene.2003.09.030. PMID 14693368.

uth.edu

med.uth.edu

van Hoof A, Frischmeyer PA, Dietz HC, Parker R (2002 Mar 22). “Exosome-mediated recognition and degradation of mRNAs lacking a termination codon”. Science 295 (5563): 2262-2264. doi:10.1126/science.1067272. PMID 11910110.