Frameshift mutation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Frameshift mutation" in English language version.

refsWebsite

Global rank English rank

34nih.gov

4^th place

19doi.org

2^nd place

4harvard.edu

18^th place

17^th place

2patents.google.com

1,182^nd place

725^th place

2handle.net

102^nd place

76^th place

2semanticscholar.org

11^th place

8^th place

1nature.com

234^th place

397^th place

1archive.org

6^th place

1unil.ch

9,112^th place

7,304^th place

1web.archive.org

1^st place

1cancer.gov

1,684^th place

1,350^th place

1umich.edu

459^th place

360^th place

1genome.gov

9,308^th place

8,899^th place

archive.org

Cox, Michael; Nelson, David R.; Lehninger, Albert L (2008). Lehninger principles of biochemistry. San Francisco: W.H. Freeman. ISBN 978-0-7167-7108-1.

cancer.gov

"Cancer Genomics". National Cancer Institute at the National Institute of Health. Archived from the original on 18 March 2013. Retrieved 24 March 2013.

doi.org

Negoro S, Ohki T, Shibata N, Mizuno N, Wakitani Y, Tsurukame J, Matsumoto K, Kawamoto I, Takeo M, Higuchi Y (November 2005). "X-ray crystallographic analysis of 6-aminohexanoate-dimer hydrolase: molecular basis for the birth of a nylon oligomer-degrading enzyme". J Biol Chem. 280 (47): 39644–52. doi:10.1074/jbc.m505946200. PMID 16162506.
Zhang, J (August 2004). "Host RNA polymerase II makes minimal contributions to retroviral frame-shift mutations". The Journal of General Virology. 85 (Pt 8): 2389–95. doi:10.1099/vir.0.80081-0. PMID 15269381.
Sagher, Daphna; Turkington, Edith; Acharya, Sonia; Strauss, Bernard (July 1994). "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. PMID 8028006.
Johnson, Neil P.; Walter A. Baase; Peter H. von Hippel (March 2004). "Low-energy circular dichroism of 2-aminopurine dinucleotide as a probe of local conformation of DNA and RNA". Proc Natl Acad Sci U S A. 101 (10): 3426–31. Bibcode:2004PNAS..101.3426J. doi:10.1073/pnas.0400591101. PMC 373478. PMID 14993592.
Baase, Walter A.; Davis Jose; Benjamin C. Ponedel; Peter H. von Hippel; Neil P. Johnson (2009). "DNA models of trinucleotide frameshift deletions: the formation of loops and bulges at the primer–template junction". Nucleic Acids Research. 37 (5): 1682–9. doi:10.1093/nar/gkn1042. PMC 2655659. PMID 19155277.
Hu, J; Ng, PC (9 February 2012). "Predicting the effects of frameshifting indels". Genome Biology. 13 (2): R9. doi:10.1186/gb-2012-13-2-r9. PMC 3334572. PMID 22322200.
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. doi:10.1016/j.ajhg.2009.06.022. PMC 2725244. PMID 19679224.
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". Proc Natl Acad Sci U S A. 108 (44): 18032–7. Bibcode:2011PNAS..10818032W. doi:10.1073/pnas.1115052108. PMC 3207658. PMID 22006311.
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". Proc Natl Acad Sci U S A. 107 (28): 12629–33. Bibcode:2010PNAS..10712629W. doi:10.1073/pnas.1007983107. PMC 2906584. PMID 20616022.
Harfe, BD; Jinks-Robertson, S (July 1999). "Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae". Molecular and Cellular Biology. 19 (7): 4766–73. doi:10.1128/MCB.19.7.4766. PMC 84275. PMID 10373526.
Davies, J E; Rubinsztein, D C (2006). "Polyalanine and polyserine frameshift products in Huntington's disease". Journal of Medical Genetics. 43 (11): 893–896. doi:10.1136/jmg.2006.044222. PMC 2563184. PMID 16801344.
Schmoldt, A; Benthe, HF; Haberland, G (1 September 1975). "Digitoxin metabolism by rat liver microsomes". Biochemical Pharmacology. 24 (17): 1639–41. doi:10.1016/0006-2952(75)90094-5. hdl:10033/333424. PMID 10.
Xu, XiaoLin; Zhu, KaiChang; Liu, Feng; Wang, Yue; Shen, JianGuo; Jin, Jizhong; Wang, Zhong; Chen, Lin; Li, Jiadong; Xu, Min (May 2013). "Identification of somatic mutations in human prostate cancer by RNA-Seq". Gene. 519 (2): 343–7. doi:10.1016/j.gene.2013.01.046. PMID 23434521.
Ogura Y, Bonen DK, 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 (May 31, 2001). "A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease" (PDF). Nature. 411 (6837): 603–6. Bibcode:2001Natur.411..603O. doi:10.1038/35079114. hdl:2027.42/62856. PMID 11385577. S2CID 205017657.
Farrell PM, Rosenstein BJ, White TB, Accurso FJ, Castellani C, Cutting GR, Durie PR, Legrys VA, Massie J, Parad RB, Rock MJ, Campbell PW (2008). "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. PMC 2810958. PMID 18639722.
Myerowitz, R (1997). "Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene". Human Mutation. 9 (3): 195–208. doi:10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. PMID 9090523.
Truong, Hoa T; Dudding, Tracy; Blanchard, Christopher L.; Elsea, Sarah H (2010). "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. PMC 2964533. PMID 20932317.
Chung WK, Kitner C, Maron BJ (June 2011). "Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death". Cardiol Young. 21 (3): 345–8. doi:10.1017/S1047951110001927. PMID 21262074. S2CID 46682245.
Hu, Hailiang; Gatti, Richard A (2008). "New approaches to treatment of primary immunodeficiencies: fixing mutations with chemicals". Current Opinion in Allergy and Clinical Immunology. 8 (6): 540–6. doi:10.1097/ACI.0b013e328314b63b. PMC 2686128. PMID 18978469.

genome.gov

"Learning About Tay-Sachs Disease". National Human Genome Research Institute. Retrieved 24 March 2013.

handle.net

hdl.handle.net

Schmoldt, A; Benthe, HF; Haberland, G (1 September 1975). "Digitoxin metabolism by rat liver microsomes". Biochemical Pharmacology. 24 (17): 1639–41. doi:10.1016/0006-2952(75)90094-5. hdl:10033/333424. PMID 10.
Ogura Y, Bonen DK, 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 (May 31, 2001). "A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease" (PDF). Nature. 411 (6837): 603–6. Bibcode:2001Natur.411..603O. doi:10.1038/35079114. hdl:2027.42/62856. PMID 11385577. S2CID 205017657.

harvard.edu

ui.adsabs.harvard.edu

Johnson, Neil P.; Walter A. Baase; Peter H. von Hippel (March 2004). "Low-energy circular dichroism of 2-aminopurine dinucleotide as a probe of local conformation of DNA and RNA". Proc Natl Acad Sci U S A. 101 (10): 3426–31. Bibcode:2004PNAS..101.3426J. doi:10.1073/pnas.0400591101. PMC 373478. PMID 14993592.
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". Proc Natl Acad Sci U S A. 108 (44): 18032–7. Bibcode:2011PNAS..10818032W. doi:10.1073/pnas.1115052108. PMC 3207658. PMID 22006311.
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". Proc Natl Acad Sci U S A. 107 (28): 12629–33. Bibcode:2010PNAS..10712629W. doi:10.1073/pnas.1007983107. PMC 2906584. PMID 20616022.
Ogura Y, Bonen DK, 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 (May 31, 2001). "A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease" (PDF). Nature. 411 (6837): 603–6. Bibcode:2001Natur.411..603O. doi:10.1038/35079114. hdl:2027.42/62856. PMID 11385577. S2CID 205017657.

nature.com

"DNA Is Constantly Changing through the Process of Mutation". Nature. Retrieved 17 May 2019.

nih.gov

pubmed.ncbi.nlm.nih.gov

Zimmerman PA, Buckler-White A, 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 (January 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. 3 (1): 23–36. PMC 2230106. PMID 9132277.
Negoro S, Ohki T, Shibata N, Mizuno N, Wakitani Y, Tsurukame J, Matsumoto K, Kawamoto I, Takeo M, Higuchi Y (November 2005). "X-ray crystallographic analysis of 6-aminohexanoate-dimer hydrolase: molecular basis for the birth of a nylon oligomer-degrading enzyme". J Biol Chem. 280 (47): 39644–52. doi:10.1074/jbc.m505946200. PMID 16162506.
Zhang, J (August 2004). "Host RNA polymerase II makes minimal contributions to retroviral frame-shift mutations". The Journal of General Virology. 85 (Pt 8): 2389–95. doi:10.1099/vir.0.80081-0. PMID 15269381.
Sagher, Daphna; Turkington, Edith; Acharya, Sonia; Strauss, Bernard (July 1994). "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. PMID 8028006.
Johnson, Neil P.; Walter A. Baase; Peter H. von Hippel (March 2004). "Low-energy circular dichroism of 2-aminopurine dinucleotide as a probe of local conformation of DNA and RNA". Proc Natl Acad Sci U S A. 101 (10): 3426–31. Bibcode:2004PNAS..101.3426J. doi:10.1073/pnas.0400591101. PMC 373478. PMID 14993592.
Baase, Walter A.; Davis Jose; Benjamin C. Ponedel; Peter H. von Hippel; Neil P. Johnson (2009). "DNA models of trinucleotide frameshift deletions: the formation of loops and bulges at the primer–template junction". Nucleic Acids Research. 37 (5): 1682–9. doi:10.1093/nar/gkn1042. PMC 2655659. PMID 19155277.
Hu, J; Ng, PC (9 February 2012). "Predicting the effects of frameshifting indels". Genome Biology. 13 (2): R9. doi:10.1186/gb-2012-13-2-r9. PMC 3334572. PMID 22322200.
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. doi:10.1016/j.ajhg.2009.06.022. PMC 2725244. PMID 19679224.
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". Proc Natl Acad Sci U S A. 108 (44): 18032–7. Bibcode:2011PNAS..10818032W. doi:10.1073/pnas.1115052108. PMC 3207658. PMID 22006311.
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". Proc Natl Acad Sci U S A. 107 (28): 12629–33. Bibcode:2010PNAS..10712629W. doi:10.1073/pnas.1007983107. PMC 2906584. PMID 20616022.
Harfe, BD; Jinks-Robertson, S (July 1999). "Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae". Molecular and Cellular Biology. 19 (7): 4766–73. doi:10.1128/MCB.19.7.4766. PMC 84275. PMID 10373526.
Davies, J E; Rubinsztein, D C (2006). "Polyalanine and polyserine frameshift products in Huntington's disease". Journal of Medical Genetics. 43 (11): 893–896. doi:10.1136/jmg.2006.044222. PMC 2563184. PMID 16801344.
Schmoldt, A; Benthe, HF; Haberland, G (1 September 1975). "Digitoxin metabolism by rat liver microsomes". Biochemical Pharmacology. 24 (17): 1639–41. doi:10.1016/0006-2952(75)90094-5. hdl:10033/333424. PMID 10.
Xu, XiaoLin; Zhu, KaiChang; Liu, Feng; Wang, Yue; Shen, JianGuo; Jin, Jizhong; Wang, Zhong; Chen, Lin; Li, Jiadong; Xu, Min (May 2013). "Identification of somatic mutations in human prostate cancer by RNA-Seq". Gene. 519 (2): 343–7. doi:10.1016/j.gene.2013.01.046. PMID 23434521.
Ogura Y, Bonen DK, 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 (May 31, 2001). "A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease" (PDF). Nature. 411 (6837): 603–6. Bibcode:2001Natur.411..603O. doi:10.1038/35079114. hdl:2027.42/62856. PMID 11385577. S2CID 205017657.
Farrell PM, Rosenstein BJ, White TB, Accurso FJ, Castellani C, Cutting GR, Durie PR, Legrys VA, Massie J, Parad RB, Rock MJ, Campbell PW (2008). "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. PMC 2810958. PMID 18639722.
Iannuzzi, MC; Stern, RC; Collins, FS; Hon, CT; Hidaka, N; Strong, T; Becker, L; Drumm, ML; White, MB; Gerrard, B (February 1991). "Two frameshift mutations in the cystic fibrosis gene". American Journal of Human Genetics. 48 (2): 227–31. PMC 1683026. PMID 1990834.
Myerowitz, R (1997). "Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene". Human Mutation. 9 (3): 195–208. doi:10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. PMID 9090523.
Truong, Hoa T; Dudding, Tracy; Blanchard, Christopher L.; Elsea, Sarah H (2010). "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. PMC 2964533. PMID 20932317.
Chung WK, Kitner C, Maron BJ (June 2011). "Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death". Cardiol Young. 21 (3): 345–8. doi:10.1017/S1047951110001927. PMID 21262074. S2CID 46682245.
Hu, Hailiang; Gatti, Richard A (2008). "New approaches to treatment of primary immunodeficiencies: fixing mutations with chemicals". Current Opinion in Allergy and Clinical Immunology. 8 (6): 540–6. doi:10.1097/ACI.0b013e328314b63b. PMC 2686128. PMID 18978469.

ncbi.nlm.nih.gov

Zimmerman PA, Buckler-White A, 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 (January 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. 3 (1): 23–36. PMC 2230106. PMID 9132277.
Johnson, Neil P.; Walter A. Baase; Peter H. von Hippel (March 2004). "Low-energy circular dichroism of 2-aminopurine dinucleotide as a probe of local conformation of DNA and RNA". Proc Natl Acad Sci U S A. 101 (10): 3426–31. Bibcode:2004PNAS..101.3426J. doi:10.1073/pnas.0400591101. PMC 373478. PMID 14993592.
Baase, Walter A.; Davis Jose; Benjamin C. Ponedel; Peter H. von Hippel; Neil P. Johnson (2009). "DNA models of trinucleotide frameshift deletions: the formation of loops and bulges at the primer–template junction". Nucleic Acids Research. 37 (5): 1682–9. doi:10.1093/nar/gkn1042. PMC 2655659. PMID 19155277.
Hu, J; Ng, PC (9 February 2012). "Predicting the effects of frameshifting indels". Genome Biology. 13 (2): R9. doi:10.1186/gb-2012-13-2-r9. PMC 3334572. PMID 22322200.
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. doi:10.1016/j.ajhg.2009.06.022. PMC 2725244. PMID 19679224.
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". Proc Natl Acad Sci U S A. 108 (44): 18032–7. Bibcode:2011PNAS..10818032W. doi:10.1073/pnas.1115052108. PMC 3207658. PMID 22006311.
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". Proc Natl Acad Sci U S A. 107 (28): 12629–33. Bibcode:2010PNAS..10712629W. doi:10.1073/pnas.1007983107. PMC 2906584. PMID 20616022.
Harfe, BD; Jinks-Robertson, S (July 1999). "Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae". Molecular and Cellular Biology. 19 (7): 4766–73. doi:10.1128/MCB.19.7.4766. PMC 84275. PMID 10373526.
Davies, J E; Rubinsztein, D C (2006). "Polyalanine and polyserine frameshift products in Huntington's disease". Journal of Medical Genetics. 43 (11): 893–896. doi:10.1136/jmg.2006.044222. PMC 2563184. PMID 16801344.
Farrell PM, Rosenstein BJ, White TB, Accurso FJ, Castellani C, Cutting GR, Durie PR, Legrys VA, Massie J, Parad RB, Rock MJ, Campbell PW (2008). "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. PMC 2810958. PMID 18639722.
Iannuzzi, MC; Stern, RC; Collins, FS; Hon, CT; Hidaka, N; Strong, T; Becker, L; Drumm, ML; White, MB; Gerrard, B (February 1991). "Two frameshift mutations in the cystic fibrosis gene". American Journal of Human Genetics. 48 (2): 227–31. PMC 1683026. PMID 1990834.
Truong, Hoa T; Dudding, Tracy; Blanchard, Christopher L.; Elsea, Sarah H (2010). "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. PMC 2964533. PMID 20932317.
Hu, Hailiang; Gatti, Richard A (2008). "New approaches to treatment of primary immunodeficiencies: fixing mutations with chemicals". Current Opinion in Allergy and Clinical Immunology. 8 (6): 540–6. doi:10.1097/ACI.0b013e328314b63b. PMC 2686128. PMID 18978469.

patents.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

semanticscholar.org

api.semanticscholar.org

Ogura Y, Bonen DK, 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 (May 31, 2001). "A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease" (PDF). Nature. 411 (6837): 603–6. Bibcode:2001Natur.411..603O. doi:10.1038/35079114. hdl:2027.42/62856. PMID 11385577. S2CID 205017657.
Chung WK, Kitner C, Maron BJ (June 2011). "Novel frameshift mutation in Troponin C ( TNNC1) associated with hypertrophic cardiomyopathy and sudden death". Cardiol Young. 21 (3): 345–8. doi:10.1017/S1047951110001927. PMID 21262074. S2CID 46682245.

umich.edu

deepblue.lib.umich.edu

Ogura Y, Bonen DK, 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 (May 31, 2001). "A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease" (PDF). Nature. 411 (6837): 603–6. Bibcode:2001Natur.411..603O. doi:10.1038/35079114. hdl:2027.42/62856. PMID 11385577. S2CID 205017657.

unil.ch

serval.unil.ch

Schmoldt, A; Benthe, HF; Haberland, G (1 September 1975). "Digitoxin metabolism by rat liver microsomes". Biochemical Pharmacology. 24 (17): 1639–41. doi:10.1016/0006-2952(75)90094-5. hdl:10033/333424. PMID 10.

web.archive.org

"Cancer Genomics". National Cancer Institute at the National Institute of Health. Archived from the original on 18 March 2013. Retrieved 24 March 2013.