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Mutacja przesuwająca ramkę odczytu (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Mutacja przesuwająca ramkę odczytu" in Polish language version.

refsWebsite
Global rank Polish rank
8nih.gov
4th place
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8doi.org
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1web.archive.org
1st place
1st place
1cancer.gov
1,684th place
2,913th place
1genome.gov
9,308th place
low place

cancer.gov

  • Cancer Genomics. National Cancer Institute at the National Institute of Health. [dostęp 2013-10-10]. [zarchiwizowane z tego adresu (2013-03-18)].

doi.org

  • A. Schmoldt, H. F. Benthe, G. Haberland. Digitoxin metabolism by rat liver microsomes.. „Biochemical pharmacology”. 24 (17), s. 1639–41, 1975. DOI: 10.1093/hmg/ddq151. 
  • Xiao Lin Xu, Kai Chang Zhu, Feng Liu, Yue Wang, Jian Guo Shen, Jizhong Jin, Zhong Wang, Lin Chen, Jiadong Li, Min Xu. Identification of somatic mutations in human prostate cancer by RNA-Seq. „Gene”. DOI: 10.1016/j.gene.2013.01.046. 
  • Y. Ogura, D. K. Bonen, N. Inohara, D. L. Nicolae, F. F. Chen, R. Ramos, H. Britton, T. Moran, R. Karaliuskas, R. H. Duerr, J. P. Achkar, S. R. Brant, T. M. Bayless, B. S. Kirschner, S. B. Hanauer, G. Nuñez, J. H. Cho. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.. „Nature”. 411 (6837), s. 603–6, 2001. DOI: 10.1038/35079114. PMID: 11385577. 
  • Philip Farrell, Beryl J. Rosenstein, Terry B. White, Frank J. Accurso, Carlo Castellani, Garry R. Cutting, Peter R. Durie, Vicky A. LeGrys, John Massie, Richard B. Parad, Michael J. Rock, Preston W. Campbell. Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report. „The Journal of Pediatrics”. 153 (2). s. S4–S14. DOI: 10.1016/j.jpeds.2008.05.005. 
  • R. Myerowitz. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.. „Human Mutation”. 9 (3), s. 195–208, 1997. DOI: 10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. PMID: 9090523. 
  • W. K. Chung, C. Kitner, B. J. Maron BJ. Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death. „Cardiology in the Young”. 21 (3), s. 345–8, 2011. DOI: 10.1017/S1047951110001927. PMID: 21262074. 
  • R. Anistoroaei, A. K. Krogh, K. Christensen. A frameshift mutation in the LYST gene is responsible for the Aleutian color and the associated Chédiak-Higashi syndrome in American mink.. „Animal Genetics”. 44 (2), s. 178-183, 2013. DOI: 10.1111/j.1365-2052.2012.02391.x.. PMID: 22762706. 
  • Louise M. Downs, Berit Wallin-Håkansson, Mike Boursnell, Stefan Marklund, Åke Hedhammar, Katarina Truvé, Louise Hübinette, Kerstin Lindblad-Toh, Tomas Bergström, Cathryn S. Mellersh1. A Frameshift Mutation in Golden Retriever Dogs with Progressive Retinal Atrophy Endorses SLC4A3 as a Candidate Gene for Human Retinal Degenerations. „PLoS One”. 6 (6), s. 178-183, 2011. DOI: 10.1371/journal.pone.0021452. PMID: 21738669. PMCID: PMC3124514. 

genome.gov

nih.gov

ncbi.nlm.nih.gov

  • P. A. Zimmerman, A. Buckler-White, G. Alkhatib, T. Spalding, J. Kubofcik, C. Combadiere, D. Weissman, O. Cohen, A. Rubbert, G. Lam, M. Vaccarezza, P. E. Kennedy, V. Kumaraswami, J. V. Giorgi, R. Detels, J. Hunter, M. Chopek, E. A. Berger, A. S. Fauci, T. B. Nutman, P. M. Murphy. Inherited resistance to HIV-1 conferred by an inactivating mutation in CC chemokine receptor 5: studies in populations with contrasting clinical phenotypes, defined racial background, and quantified risk. „Molecular medicine (Cambridge, Mass.)”. 3 (1), s. 23–36, 1997. PMID: 9132277. 
  • Y. Ogura, D. K. Bonen, N. Inohara, D. L. Nicolae, F. F. Chen, R. Ramos, H. Britton, T. Moran, R. Karaliuskas, R. H. Duerr, J. P. Achkar, S. R. Brant, T. M. Bayless, B. S. Kirschner, S. B. Hanauer, G. Nuñez, J. H. Cho. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.. „Nature”. 411 (6837), s. 603–6, 2001. DOI: 10.1038/35079114. PMID: 11385577. 
  • Vermeire S. NOD2/CARD15: relevance in clinical practice. „Best Pract Res Clin Gastroenterol”. 18, s. 569-75, 2004. PMID: 15157828. 
  • M. C. Iannuzzi, R. C. Stern, F. S. Collins, C. T. Hon, N. Hidaka, T. Strong, L. Becker, M. L. Drumm, M. B. White, B. Gerrard. Two frameshift mutations in the cystic fibrosis gene.. „American Journal of Human Genetics”. 48 (2), s. 227–31, 1991. PMID: 1990834. 
  • R. Myerowitz. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.. „Human Mutation”. 9 (3), s. 195–208, 1997. DOI: 10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. PMID: 9090523. 
  • W. K. Chung, C. Kitner, B. J. Maron BJ. Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death. „Cardiology in the Young”. 21 (3), s. 345–8, 2011. DOI: 10.1017/S1047951110001927. PMID: 21262074. 
  • R. Anistoroaei, A. K. Krogh, K. Christensen. A frameshift mutation in the LYST gene is responsible for the Aleutian color and the associated Chédiak-Higashi syndrome in American mink.. „Animal Genetics”. 44 (2), s. 178-183, 2013. DOI: 10.1111/j.1365-2052.2012.02391.x.. PMID: 22762706. 
  • Louise M. Downs, Berit Wallin-Håkansson, Mike Boursnell, Stefan Marklund, Åke Hedhammar, Katarina Truvé, Louise Hübinette, Kerstin Lindblad-Toh, Tomas Bergström, Cathryn S. Mellersh1. A Frameshift Mutation in Golden Retriever Dogs with Progressive Retinal Atrophy Endorses SLC4A3 as a Candidate Gene for Human Retinal Degenerations. „PLoS One”. 6 (6), s. 178-183, 2011. DOI: 10.1371/journal.pone.0021452. PMID: 21738669. PMCID: PMC3124514. 

web.archive.org

  • Cancer Genomics. National Cancer Institute at the National Institute of Health. [dostęp 2013-10-10]. [zarchiwizowane z tego adresu (2013-03-18)].