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Stille Mutation (German Wikipedia)

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

refsWebsite
Global rank German rank
13doi.org
2nd place
3rd place
13nih.gov
4th place
7th place
1sciencemag.org
857th place
511th place

doi.org

  • 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.
  • 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 (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.
  • 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.
  • 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).
  • 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).
  • 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

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.
  • 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 (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.
  • 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.
  • 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).
  • 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