Mutación por desplazamiento del marco de lectura (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Mutación por desplazamiento del marco de lectura" in Spanish language version.

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17doi.org

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9nih.gov

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3archive.org

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3issn.org

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2google.com

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1cancer.gov

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archive.org

Cox, Michael; Nelson, David R.; Lehninger, Albert L (2008). Lehninger principles of biochemistry. San Francisco: W.H. Freeman. ISBN 0-7167-7108-X.
Harfe, BD; Jinks-Robertson, S (julio de 1999). «Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae.». Molecular and Cellular Biology 19 (7): 4766-73. PMID 10373526. Consultado el 20 de marzo de 2013.
Iannuzzi, MC; Collins, FS; Hon, CT; Hidaka, N; Strong, T; Becker, L; Drumm, ML; White, MB et al. (febrero de 1991). «Two frameshift mutations in the cystic fibrosis gene.». American Journal of Human Genetics 48 (2): 227-31. PMID 1990834. Consultado el 21 de marzo de 2013. |autor1= y |apellido= redundantes (ayuda);

cancer.gov

«Cancer Genomics». National Cancer Institute at the National Institute of Health. Archivado desde el original el 18 de marzo de 2013. Consultado el 24 de marzo de 2013.

doi.org

dx.doi.org

Zhang, J (agosto de 2004). «Host RNA polymerase II makes minimal contributions to retroviral frame-shift mutations.». The Journal of general virology 85 (Pt 8): 2389-95. PMID 15269381. doi:10.1099/vir.0.80081-0. |fechaacceso= requiere |url= (ayuda)
Sagher, Daphna; Acharya, Sonia; Strauss, Bernard. «Production of UV-induced Frameshift Mutations in Vitro by DNA Polymerases Deficient in 3′ → 5′ Exonuclease Activity». Journal of Molecular Biology 240 (3): 226-242. doi:10.1006/jmbi.1994.1437. |autor1= y |apellido= redundantes (ayuda)
Johnson, Neil P.; Walter A. Baase, Peter H. von Hippel, Low-energy circular dichroism of 2-aminopurine dinucleotide as a probe of local conformation of DNA and RNA, doi:10.1073/pnas.0400591101, «PNAS 2004 101:3426-3431; published online before print March 1, 2004» .
Baase, Walter A.; Davis Jose , Benjamin C. Ponedel , Peter H. von Hippel , and Neil P. Johnson, «DNA models of trinucleotide frameshift deletions: the formation of loops and bulges at the primer–template junction», Nucleic Acids Research 37 (5): 1682-1689, doi:10.1093/nar/gkn1042, «Nucleic Acids Research Advance Access published on April 1, 2009» .
Hu, J; Ng, PC (9 de febrero de 2012). «Predicting the effects of frameshifting indels.». Genome Biology 13 (2): R9. PMID 22322200. doi:10.1186/gb-2012-13-2-r9.
Tucker, Tracy; Marra, Marco; Friedman, Jan M. (2009). «Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine». The American Journal of Human Genetics 85 (2): 142-154. ISSN 0002-9297. PMC 2725244. PMID 19679224. doi:10.1016/j.ajhg.2009.06.022.
Walsh, T.; Casadei, S.; Lee, M. K.; Pennil, C. C.; Nord, A. S.; Thornton, A. M.; Roeb, W.; Agnew, K. J.; Stray, S. M.; Wickramanayake, A.; Norquist, B.; Pennington, K. P.; Garcia, R. L.; King, M.-C.; Swisher, E. M. (2011). «From the Cover: Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing». Proceedings of the National Academy of Sciences 108 (44): 18032-18037. ISSN 0027-8424. doi:10.1073/pnas.1115052108.
Walsh, T.; Lee, M. K.; Casadei, S.; Thornton, A. M.; Stray, S. M.; Pennil, C.; Nord, A. S.; Mandell, J. B.; Swisher, E. M.; King, M.-C. (2010). «Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing». Proceedings of the National Academy of Sciences 107 (28): 12629-12633. ISSN 0027-8424. doi:10.1073/pnas.1007983107.
Davies, J E; Rubinsztein, D C. «Polyalanine and polyserine frameshift products in Huntington's disease». Journal of Medical Genetics 43 (11): 893-896. doi:10.1136/jmg.2006.044222.
Schmoldt, A; Haberland, G (1 de septiembre de 1975). «Digitoxin metabolism by rat liver microsomes.». Biochemical pharmacology 24 (17): 1639-41. doi:10.1093/hmg/ddq151. |autor1= y |apellido= redundantes (ayuda); |fechaacceso= requiere |url= (ayuda)
Xu, XiaoLin; Liu, Feng; Wang, Yue; Shen, JianGuo; Jin, Jizhong; Wang, Zhong; Chen, Lin; Li, Jiadong et al.. «Identification of somatic mutations in human prostate cancer by RNA-Seq». Gene. doi:10.1016/j.gene.2013.01.046. |autor1= y |apellido= redundantes (ayuda); |fechaacceso= requiere |url= (ayuda)
Ogura, Y; Inohara, N; Nicolae, DL; Chen, FF; Ramos, R; Britton, H; Moran, T; Karaliuskas, R; Duerr, RH; Achkar, JP; Brant, SR; Bayless, TM; Kirschner, BS; Hanauer, SB; Nuñez, G; Cho, JH (31 de mayo de 2001). «A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.». Nature 411 (6837): 603-6. PMID 11385577. doi:10.1038/35079114. |autor1= y |apellido= redundantes (ayuda)
Farrell, Philip M.; White, Terry B.; Accurso, Frank J.; Castellani, Carlo; Cutting, Garry R.; Durie, Peter R.; LeGrys, Vicky A.; Massie, John; Parad, Richard B.; Rock, Michael J.; Campbell, Preston W. «Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report». The Journal of Pediatrics 153 (2): S4-S14. doi:10.1016/j.jpeds.2008.05.005. |autor1= y |apellido= redundantes (ayuda); |fechaacceso= requiere |url= (ayuda)
Myerowitz, R (1997). «Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.». Human Mutation 9 (3): 195-208. PMID 9090523. doi:10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. |fechaacceso= requiere |url= (ayuda)
Truong, Hoa T; Blanchard, Christopher L.; Elsea, Sarah H. «Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature». BMC Medical Genetics 11 (1): 142. doi:10.1186/1471-2350-11-142. |autor1= y |apellido= redundantes (ayuda)
Chung WK, Kitner C, Maron BJ (junio de 2011). «Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death». Cardiol Young 21 (3): 345-8. PMID 21262074. doi:10.1017/S1047951110001927.
Hu, Hailiang; Gatti, Richard A. «New approaches to treatment of primary immunodeficiencies: fixing mutations with chemicals». Current Opinion in Allergy and Clinical Immunology 8 (6): 540-546. doi:10.1097/ACI.0b013e328314b63b.

genome.gov

«Learning About Tay-Sachs Disease». National Human Genome Research Institute. Consultado el 24 de marzo de 2013.

google.com

US Patent 5,958,684 (September 28, 1999) "Diagnosis of Neurodegenerative Disease" by Leeuwen et al
European Patent [1] (December 10, 2003) "Use of coding microsatellite region frameshift mutation-derived peptides for treating cancer" by Bork et al

issn.org

portal.issn.org

Tucker, Tracy; Marra, Marco; Friedman, Jan M. (2009). «Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine». The American Journal of Human Genetics 85 (2): 142-154. ISSN 0002-9297. PMC 2725244. PMID 19679224. doi:10.1016/j.ajhg.2009.06.022.
Walsh, T.; Casadei, S.; Lee, M. K.; Pennil, C. C.; Nord, A. S.; Thornton, A. M.; Roeb, W.; Agnew, K. J.; Stray, S. M.; Wickramanayake, A.; Norquist, B.; Pennington, K. P.; Garcia, R. L.; King, M.-C.; Swisher, E. M. (2011). «From the Cover: Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing». Proceedings of the National Academy of Sciences 108 (44): 18032-18037. ISSN 0027-8424. doi:10.1073/pnas.1115052108.
Walsh, T.; Lee, M. K.; Casadei, S.; Thornton, A. M.; Stray, S. M.; Pennil, C.; Nord, A. S.; Mandell, J. B.; Swisher, E. M.; King, M.-C. (2010). «Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing». Proceedings of the National Academy of Sciences 107 (28): 12629-12633. ISSN 0027-8424. doi:10.1073/pnas.1007983107.

jbc.org

http://www.jbc.org/content/280/47/39644.full.pdf+html

nih.gov

ncbi.nlm.nih.gov

Zimmerman, PA; Alkhatib, G; Spalding, T; Kubofcik, J; Combadiere, C; Weissman, D; Cohen, O; Rubbert, A; Lam, G; Vaccarezza, M; Kennedy, PE; Kumaraswami, V; Giorgi, JV; Detels, R; Hunter, J; Chopek, M; Berger, EA; Fauci, AS; Nutman, TB; Murphy, PM (enero de 1997). «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): 23-36. PMID 9132277. |autor1= y |apellido= redundantes (ayuda); |fechaacceso= requiere |url= (ayuda)
Zhang, J (agosto de 2004). «Host RNA polymerase II makes minimal contributions to retroviral frame-shift mutations.». The Journal of general virology 85 (Pt 8): 2389-95. PMID 15269381. doi:10.1099/vir.0.80081-0. |fechaacceso= requiere |url= (ayuda)
Hu, J; Ng, PC (9 de febrero de 2012). «Predicting the effects of frameshifting indels.». Genome Biology 13 (2): R9. PMID 22322200. doi:10.1186/gb-2012-13-2-r9.
Tucker, Tracy; Marra, Marco; Friedman, Jan M. (2009). «Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine». The American Journal of Human Genetics 85 (2): 142-154. ISSN 0002-9297. PMC 2725244. PMID 19679224. doi:10.1016/j.ajhg.2009.06.022.
Harfe, BD; Jinks-Robertson, S (julio de 1999). «Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae.». Molecular and Cellular Biology 19 (7): 4766-73. PMID 10373526. Consultado el 20 de marzo de 2013.
Ogura, Y; Inohara, N; Nicolae, DL; Chen, FF; Ramos, R; Britton, H; Moran, T; Karaliuskas, R; Duerr, RH; Achkar, JP; Brant, SR; Bayless, TM; Kirschner, BS; Hanauer, SB; Nuñez, G; Cho, JH (31 de mayo de 2001). «A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.». Nature 411 (6837): 603-6. PMID 11385577. doi:10.1038/35079114. |autor1= y |apellido= redundantes (ayuda)
Iannuzzi, MC; Collins, FS; Hon, CT; Hidaka, N; Strong, T; Becker, L; Drumm, ML; White, MB et al. (febrero de 1991). «Two frameshift mutations in the cystic fibrosis gene.». American Journal of Human Genetics 48 (2): 227-31. PMID 1990834. Consultado el 21 de marzo de 2013. |autor1= y |apellido= redundantes (ayuda);
Myerowitz, R (1997). «Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.». Human Mutation 9 (3): 195-208. PMID 9090523. doi:10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. |fechaacceso= requiere |url= (ayuda)
Chung WK, Kitner C, Maron BJ (junio de 2011). «Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death». Cardiol Young 21 (3): 345-8. PMID 21262074. doi:10.1017/S1047951110001927.

web.archive.org

«Cancer Genomics». National Cancer Institute at the National Institute of Health. Archivado desde el original el 18 de marzo de 2013. Consultado el 24 de marzo de 2013.