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Stille Mutation (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Stille Mutation" in German language version.

Last modified:

Ref.Un. Ref.Website
Global rank German rank
1514doi.org
2nd place
3rd place
1413nih.gov
5th place
7th place
11sciencemag.org
1,019th place
763rd place

doi.org (Global: 2nd place; German: 3rd place)

  • S. Teng, T. Madej, A. Panchenko, E. Alexov: Modeling effects of human single nucleotide polymorphisms on protein-protein interactions. In: Biophysical Journal. Band 96, Nummer 6, März 2009, S. 2178–2188, doi:10.1016/j.bpj.2008.12.3904, PMID 19289044, PMC 2717281 (freier Volltext).
  • J. V. Chamary, J. L. Parmley, L. D. Hurst: Hearing silence: non-neutral evolution at synonymous sites in mammals. In: Nature Reviews Genetics. Band 7, Nummer 2, Februar 2006, S. 98–108, doi:10.1038/nrg1770, PMID 16418745.
  • Patrick Goymer: Synonymous mutations break their silence. In: Nature Reviews Genetics. 8, 2007, S. 92, doi:10.1038/nrg2056.
  • T. Zhou, E. A. Ko, W. Gu, I. Lim, H. Bang, J. H. Ko: Non-silent story on synonymous sites in voltage-gated ion channel genes. In: PLOS ONE. Band 7, Nummer 10, 2012, S. e48541, doi:10.1371/journal.pone.0048541, PMID 23119053, PMC 3485311 (freier Volltext).
  • S. A. Shabalina, A. Y. Ogurtsov, N. A. Spiridonov: A periodic pattern of mRNA secondary structure created by the genetic code. In: Nucleic acids research. Band 34, Nummer 8, 2006, S. 2428–2437, doi:10.1093/nar/gkl287, PMID 16682450, PMC 1458515 (freier Volltext).
  • Czech A, Fedyunin I, Zhang G, Ignatova Z: Silent mutations in sight: co-variations in tRNA abundance as a key to unravel consequences of silent mutations. In: Mol Biosyst. 6. Jahrgang, Nr. 10, Oktober 2010, S. 1767–72, doi:10.1039/c004796c, PMID 20617253 (englisch).
  • Komar AA: Genetics. SNPs, silent but not invisible. In: Science. 315. Jahrgang, Nr. 5811, Januar 2007, S. 466–7, doi:10.1126/science.1138239, PMID 17185559 (englisch, sciencemag.org).
  • Komar AA: Silent SNPs: impact on gene function and phenotype. In: Pharmacogenomics. 8. Jahrgang, Nr. 8, August 2007, S. 1075–80, doi:10.2217/14622416.8.8.1075, PMID 17716239 (englisch).
  • Z. Zhang, M. A. Miteva, L. Wang, E. Alexov: Analyzing effects of naturally occurring missense mutations. In: Computational and mathematical methods in medicine. Band 2012, 2012, S. 805827, doi:10.1155/2012/805827, PMID 22577471, PMC 3346971 (freier Volltext).
  • C. Kimchi-Sarfaty, J. M. Oh, I.-W. Kim, Z. E. Sauna, A. M. Calcagno, S. V. Ambudkar, M. M. Gottesman,: A "Silent" Polymorphism in the MDR1 Gene Changes Substrate Specificity. In: Science. 315. Jahrgang, Nr. 5811, 26. Januar 2007, S. 525–8, doi:10.1126/science.1135308, PMID 17185560 (englisch).
  • Angov E: Codon usage: nature's roadmap to expression and folding of proteins. In: Biotechnol J. 6. Jahrgang, Nr. 6, Juni 2011, S. 650–9, doi:10.1002/biot.201000332, PMID 21567958, PMC 3166658 (freier Volltext) – (englisch).
  • R. Bartoszewski, J. Króliczewski, A. Piotrowski, A. J. Jasiecka, S. Bartoszewska, B. Vecchio-Pagan, L. Fu, A. Sobolewska, S. Matalon, G. R. Cutting, S. M. Rowe, J. F. Collawn: Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator. In: Cellular & molecular biology letters. Band 21, 2016, S. 23, doi:10.1186/s11658-016-0025-x, PMID 28536625, PMC 5415761 (freier Volltext).
  • Maria J. Berry, Laila Banu, Yoyi Chen et al.: Recognition of UGA as a selenocysteine codon in Type I deiodinase requires sequences in the 3′ untranslated region. In: Nature. Band 353, Nr. 6341, 1991, S. 273–276, doi:10.1038/353273a0 (englisch).
  • S. Mueller, J. R. Coleman, E. Wimmer: Putting synthesis into biology: a viral view of genetic engineering through de novo gene and genome synthesis. In: Chemistry & biology. Band 16, Nummer 3, März 2009, S. 337–347, doi:10.1016/j.chembiol.2009.03.002, PMID 19318214, PMC 2728443 (freier Volltext).

nih.gov (Global: 5th place; German: 7th place)

ncbi.nlm.nih.gov

  • S. Teng, T. Madej, A. Panchenko, E. Alexov: Modeling effects of human single nucleotide polymorphisms on protein-protein interactions. In: Biophysical Journal. Band 96, Nummer 6, März 2009, S. 2178–2188, doi:10.1016/j.bpj.2008.12.3904, PMID 19289044, PMC 2717281 (freier Volltext).
  • J. V. Chamary, J. L. Parmley, L. D. Hurst: Hearing silence: non-neutral evolution at synonymous sites in mammals. In: Nature Reviews Genetics. Band 7, Nummer 2, Februar 2006, S. 98–108, doi:10.1038/nrg1770, PMID 16418745.
  • T. Zhou, E. A. Ko, W. Gu, I. Lim, H. Bang, J. H. Ko: Non-silent story on synonymous sites in voltage-gated ion channel genes. In: PLOS ONE. Band 7, Nummer 10, 2012, S. e48541, doi:10.1371/journal.pone.0048541, PMID 23119053, PMC 3485311 (freier Volltext).
  • S. A. Shabalina, A. Y. Ogurtsov, N. A. Spiridonov: A periodic pattern of mRNA secondary structure created by the genetic code. In: Nucleic acids research. Band 34, Nummer 8, 2006, S. 2428–2437, doi:10.1093/nar/gkl287, PMID 16682450, PMC 1458515 (freier Volltext).
  • Czech A, Fedyunin I, Zhang G, Ignatova Z: Silent mutations in sight: co-variations in tRNA abundance as a key to unravel consequences of silent mutations. In: Mol Biosyst. 6. Jahrgang, Nr. 10, Oktober 2010, S. 1767–72, doi:10.1039/c004796c, PMID 20617253 (englisch).
  • Komar AA: Genetics. SNPs, silent but not invisible. In: Science. 315. Jahrgang, Nr. 5811, Januar 2007, S. 466–7, doi:10.1126/science.1138239, PMID 17185559 (englisch, sciencemag.org).
  • Komar AA: Silent SNPs: impact on gene function and phenotype. In: Pharmacogenomics. 8. Jahrgang, Nr. 8, August 2007, S. 1075–80, doi:10.2217/14622416.8.8.1075, PMID 17716239 (englisch).
  • Z. Zhang, M. A. Miteva, L. Wang, E. Alexov: Analyzing effects of naturally occurring missense mutations. In: Computational and mathematical methods in medicine. Band 2012, 2012, S. 805827, doi:10.1155/2012/805827, PMID 22577471, PMC 3346971 (freier Volltext).
  • C. Kimchi-Sarfaty, J. M. Oh, I.-W. Kim, Z. E. Sauna, A. M. Calcagno, S. V. Ambudkar, M. M. Gottesman,: A "Silent" Polymorphism in the MDR1 Gene Changes Substrate Specificity. In: Science. 315. Jahrgang, Nr. 5811, 26. Januar 2007, S. 525–8, doi:10.1126/science.1135308, PMID 17185560 (englisch).
  • Angov E: Codon usage: nature's roadmap to expression and folding of proteins. In: Biotechnol J. 6. Jahrgang, Nr. 6, Juni 2011, S. 650–9, doi:10.1002/biot.201000332, PMID 21567958, PMC 3166658 (freier Volltext) – (englisch).
  • R. Bartoszewski, J. Króliczewski, A. Piotrowski, A. J. Jasiecka, S. Bartoszewska, B. Vecchio-Pagan, L. Fu, A. Sobolewska, S. Matalon, G. R. Cutting, S. M. Rowe, J. F. Collawn: Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator. In: Cellular & molecular biology letters. Band 21, 2016, S. 23, doi:10.1186/s11658-016-0025-x, PMID 28536625, PMC 5415761 (freier Volltext).
  • E. Kotsopoulou, V. N. Kim, A. J. Kingsman, S. M. Kingsman, K. A. Mitrophanous: A Rev-independent human immunodeficiency virus type 1 (HIV-1)-based vector that exploits a codon-optimized HIV-1 gag-pol gene. In: J Virol. (2000), Bd. 74(10), S. 4839–52. PMID 10775623; PMC 112007 (freier Volltext).
  • S. Mueller, J. R. Coleman, E. Wimmer: Putting synthesis into biology: a viral view of genetic engineering through de novo gene and genome synthesis. In: Chemistry & biology. Band 16, Nummer 3, März 2009, S. 337–347, doi:10.1016/j.chembiol.2009.03.002, PMID 19318214, PMC 2728443 (freier Volltext).

sciencemag.org (Global: 1,019th place; German: 763rd place)