Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS
Ehrich M, Böcker S, Boom D van den (2005)
Nucleic Acids Research 33(4): e38.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
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Autor*in
Ehrich, Mathias;
Böcker, Sebastian;
Boom, Dirk van den
Einrichtung
Abstract / Bemerkung
The completion of the Human Genome Project provides researchers with a reference sequence that covers about 99% of the gene-containing regions and is more than 99.9% accurate. Sequence drafts and completed sequences for several other species are also available to researchers worldwide. The ongoing effort to provide more and more genomic reference information now enables the detection of deviations from this `genetic blueprint'. Comparative sequencing projects will play a major role in elucidating the meaning of the genetic code and in establishing a correlation between genotype and phenotype. As part of this effort, a number of projects will focus on distinct functional aspects, like resequencing of exons or HLA determining regions. Typically these target regions are short in length and their analysis does not require long read length. To find an efficient solution for these applications, we developed a novel method that allows simultaneous analysis of multiple independent target regions (Multiplexed Comparative Sequence Analysis) by employing base-specific cleavage biochemistry and MALDI TOF-MS analysis.
Erscheinungsjahr
2005
Zeitschriftentitel
Nucleic Acids Research
Band
33
Ausgabe
4
Seite(n)
e38
ISSN
1362-4962
eISSN
1362-4962
Page URI
https://pub.uni-bielefeld.de/record/1773690
Zitieren
Ehrich M, Böcker S, Boom D van den. Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research. 2005;33(4):e38.
Ehrich, M., Böcker, S., & Boom, D. van den (2005). Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research, 33(4), e38. https://doi.org/10.1093/nar/gni038
Ehrich, Mathias, Böcker, Sebastian, and Boom, Dirk van den. 2005. “Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS”. Nucleic Acids Research 33 (4): e38.
Ehrich, M., Böcker, S., and Boom, D. van den (2005). Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research 33, e38.
Ehrich, M., Böcker, S., & Boom, D. van den, 2005. Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research, 33(4), p e38.
M. Ehrich, S. Böcker, and D. van den Boom, “Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS”, Nucleic Acids Research, vol. 33, 2005, pp. e38.
Ehrich, M., Böcker, S., Boom, D. van den: Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research. 33, e38 (2005).
Ehrich, Mathias, Böcker, Sebastian, and Boom, Dirk van den. “Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS”. Nucleic Acids Research 33.4 (2005): e38.
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Daten bereitgestellt von European Bioinformatics Institute (EBI)
49 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
The effect of inflammation-related lifestyle exposures and interactions with gene variants on long interspersed nuclear element-1 DNA methylation.
Gogna P, O'Sullivan DE, King WD., Epigenomics 10(6), 2018
PMID: 29888958
Gogna P, O'Sullivan DE, King WD., Epigenomics 10(6), 2018
PMID: 29888958
Polygenic Risk Score associated with specific symptom dimensions in first-episode psychosis.
Sengupta SM, MacDonald K, Fathalli F, Yim A, Lepage M, Iyer S, Malla A, Joober R., Schizophr Res 184(), 2017
PMID: 27916287
Sengupta SM, MacDonald K, Fathalli F, Yim A, Lepage M, Iyer S, Malla A, Joober R., Schizophr Res 184(), 2017
PMID: 27916287
Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells.
Daniele G, Simonetti G, Fusilli C, Iacobucci I, Lonoce A, Palazzo A, Lomiento M, Mammoli F, Marsano RM, Marasco E, Mantovani V, Quentmeier H, Drexler HG, Ding J, Palumbo O, Carella M, Nadarajah N, Perricone M, Ottaviani E, Baldazzi C, Testoni N, Papayannidis C, Ferrari S, Mazza T, Martinelli G, Storlazzi CT., Haematologica 102(7), 2017
PMID: 28411256
Daniele G, Simonetti G, Fusilli C, Iacobucci I, Lonoce A, Palazzo A, Lomiento M, Mammoli F, Marsano RM, Marasco E, Mantovani V, Quentmeier H, Drexler HG, Ding J, Palumbo O, Carella M, Nadarajah N, Perricone M, Ottaviani E, Baldazzi C, Testoni N, Papayannidis C, Ferrari S, Mazza T, Martinelli G, Storlazzi CT., Haematologica 102(7), 2017
PMID: 28411256
Identification of HERC5 and its potential role in NSCLC progression.
Wrage M, Hagmann W, Kemming D, Uzunoglu FG, Riethdorf S, Effenberger K, Westphal M, Lamszus K, Kim SZ, Becker N, Izbicki JR, Sandoval J, Esteller M, Pantel K, Risch A, Wikman H., Int J Cancer 136(10), 2015
PMID: 25353388
Wrage M, Hagmann W, Kemming D, Uzunoglu FG, Riethdorf S, Effenberger K, Westphal M, Lamszus K, Kim SZ, Becker N, Izbicki JR, Sandoval J, Esteller M, Pantel K, Risch A, Wikman H., Int J Cancer 136(10), 2015
PMID: 25353388
Mendelian randomization supports causality between maternal hyperglycemia and epigenetic regulation of leptin gene in newborns.
Allard C, Desgagné V, Patenaude J, Lacroix M, Guillemette L, Battista MC, Doyon M, Ménard J, Ardilouze JL, Perron P, Bouchard L, Hivert MF., Epigenetics 10(4), 2015
PMID: 25800063
Allard C, Desgagné V, Patenaude J, Lacroix M, Guillemette L, Battista MC, Doyon M, Ménard J, Ardilouze JL, Perron P, Bouchard L, Hivert MF., Epigenetics 10(4), 2015
PMID: 25800063
Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults.
Saleh A, Stathopoulou MG, Dadé S, Ndiaye NC, Azimi-Nezhad M, Murray H, Masson C, Lamont J, Fitzgerald P, Visvikis-Siest S., BMC Med Genet 16(), 2015
PMID: 26437765
Saleh A, Stathopoulou MG, Dadé S, Ndiaye NC, Azimi-Nezhad M, Murray H, Masson C, Lamont J, Fitzgerald P, Visvikis-Siest S., BMC Med Genet 16(), 2015
PMID: 26437765
Tracking the progression of speciation: variable patterns of introgression across the genome provide insights on the species delimitation between progenitor-derivative spruces (Picea mariana × P. rubens).
de Lafontaine G, Prunier J, Gérardi S, Bousquet J., Mol Ecol 24(20), 2015
PMID: 26346701
de Lafontaine G, Prunier J, Gérardi S, Bousquet J., Mol Ecol 24(20), 2015
PMID: 26346701
TCF4 gene polymorphism and cognitive performance in patients with first episode psychosis.
Albanna A, Choudhry Z, Harvey PO, Fathalli F, Cassidy C, Sengupta SM, Iyer SN, Rho A, Lepage M, Malla A, Joober R., Schizophr Res 152(1), 2014
PMID: 24275585
Albanna A, Choudhry Z, Harvey PO, Fathalli F, Cassidy C, Sengupta SM, Iyer SN, Rho A, Lepage M, Malla A, Joober R., Schizophr Res 152(1), 2014
PMID: 24275585
Single-nucleotide polymorphism discovery in Leptographium longiclavatum, a mountain pine beetle-associated symbiotic fungus, using whole-genome resequencing.
Ojeda DI, Dhillon B, Tsui CK, Hamelin RC., Mol Ecol Resour 14(2), 2014
PMID: 24152017
Ojeda DI, Dhillon B, Tsui CK, Hamelin RC., Mol Ecol Resour 14(2), 2014
PMID: 24152017
Association of a risk allele of ANK3 with cognitive performance and cortical thickness in patients with first-episode psychosis.
Cassidy C, Buchy L, Bodnar M, Dell'elce J, Choudhry Z, Fathalli F, Sengupta S, Fox R, Malla A, Lepage M, Iyer S, Joober R., J Psychiatry Neurosci 39(1), 2014
PMID: 24016415
Cassidy C, Buchy L, Bodnar M, Dell'elce J, Choudhry Z, Fathalli F, Sengupta S, Fox R, Malla A, Lepage M, Iyer S, Joober R., J Psychiatry Neurosci 39(1), 2014
PMID: 24016415
Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects.
De Marco P, Merello E, Consales A, Piatelli G, Cama A, Kibar Z, Capra V., J Mol Neurosci 49(3), 2013
PMID: 22892949
De Marco P, Merello E, Consales A, Piatelli G, Cama A, Kibar Z, Capra V., J Mol Neurosci 49(3), 2013
PMID: 22892949
Genetic evidence for the association of the hypothalamic-pituitary-adrenal (HPA) axis with ADHD and methylphenidate treatment response.
Fortier MÈ, Sengupta SM, Grizenko N, Choudhry Z, Thakur G, Joober R., Neuromolecular Med 15(1), 2013
PMID: 23055001
Fortier MÈ, Sengupta SM, Grizenko N, Choudhry Z, Thakur G, Joober R., Neuromolecular Med 15(1), 2013
PMID: 23055001
Associations of vascular endothelial growth factor (VEGF) with adhesion and inflammation molecules in a healthy population.
Azimi-Nezhad M, Stathopoulou MG, Bonnefond A, Rancier M, Saleh A, Lamont J, Fitzgerald P, Ndiaye NC, Visvikis-Siest S., Cytokine 61(2), 2013
PMID: 23201487
Azimi-Nezhad M, Stathopoulou MG, Bonnefond A, Rancier M, Saleh A, Lamont J, Fitzgerald P, Ndiaye NC, Visvikis-Siest S., Cytokine 61(2), 2013
PMID: 23201487
A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C.
Stathopoulou MG, Bonnefond A, Ndiaye NC, Azimi-Nezhad M, El Shamieh S, Saleh A, Rancier M, Siest G, Lamont J, Fitzgerald P, Visvikis-Siest S., J Lipid Res 54(2), 2013
PMID: 23204297
Stathopoulou MG, Bonnefond A, Ndiaye NC, Azimi-Nezhad M, El Shamieh S, Saleh A, Rancier M, Siest G, Lamont J, Fitzgerald P, Visvikis-Siest S., J Lipid Res 54(2), 2013
PMID: 23204297
Vimentin DNA methylation predicts survival in breast cancer.
Ulirsch J, Fan C, Knafl G, Wu MJ, Coleman B, Perou CM, Swift-Scanlan T., Breast Cancer Res Treat 137(2), 2013
PMID: 23239149
Ulirsch J, Fan C, Knafl G, Wu MJ, Coleman B, Perou CM, Swift-Scanlan T., Breast Cancer Res Treat 137(2), 2013
PMID: 23239149
Association between obesity-related gene FTO and ADHD.
Choudhry Z, Sengupta SM, Grizenko N, Thakur GA, Fortier ME, Schmitz N, Joober R., Obesity (Silver Spring) 21(12), 2013
PMID: 23512716
Choudhry Z, Sengupta SM, Grizenko N, Thakur GA, Fortier ME, Schmitz N, Joober R., Obesity (Silver Spring) 21(12), 2013
PMID: 23512716
Inherited common variants in mitochondrial DNA and invasive serous epithelial ovarian cancer risk.
Earp MA, Brooks-Wilson A, Cook L, Le N., BMC Res Notes 6(), 2013
PMID: 24148579
Earp MA, Brooks-Wilson A, Cook L, Le N., BMC Res Notes 6(), 2013
PMID: 24148579
Differential methylation relative to breast cancer subtype and matched normal tissue reveals distinct patterns.
Bardowell SA, Parker J, Fan C, Crandell J, Perou CM, Swift-Scanlan T., Breast Cancer Res Treat 142(2), 2013
PMID: 24212716
Bardowell SA, Parker J, Fan C, Crandell J, Perou CM, Swift-Scanlan T., Breast Cancer Res Treat 142(2), 2013
PMID: 24212716
FZD6 is a novel gene for human neural tube defects.
De Marco P, Merello E, Rossi A, Piatelli G, Cama A, Kibar Z, Capra V., Hum Mutat 33(2), 2012
PMID: 22045688
De Marco P, Merello E, Rossi A, Piatelli G, Cama A, Kibar Z, Capra V., Hum Mutat 33(2), 2012
PMID: 22045688
Differential association between the norepinephrine transporter gene and ADHD: role of sex and subtype.
Sengupta SM, Grizenko N, Thakur GA, Bellingham J, DeGuzman R, Robinson S, TerStepanian M, Poloskia A, Shaheen SM, Fortier ME, Choudhry Z, Joober R., J Psychiatry Neurosci 37(2), 2012
PMID: 22297068
Sengupta SM, Grizenko N, Thakur GA, Bellingham J, DeGuzman R, Robinson S, TerStepanian M, Poloskia A, Shaheen SM, Fortier ME, Choudhry Z, Joober R., J Psychiatry Neurosci 37(2), 2012
PMID: 22297068
Ribo-polymerase chain reaction--a facile method for the preparation of chimeric RNA/DNA applied to DNA sequencing.
Mauger F, Bauer K, Semhoun J, Myers TW, Gelfand DH, Gut IG., Hum Mutat 33(6), 2012
PMID: 22354560
Mauger F, Bauer K, Semhoun J, Myers TW, Gelfand DH, Gut IG., Hum Mutat 33(6), 2012
PMID: 22354560
LPHN3 and attention-deficit/hyperactivity disorder: interaction with maternal stress during pregnancy.
Choudhry Z, Sengupta SM, Grizenko N, Fortier ME, Thakur GA, Bellingham J, Joober R., J Child Psychol Psychiatry 53(8), 2012
PMID: 22486528
Choudhry Z, Sengupta SM, Grizenko N, Fortier ME, Thakur GA, Bellingham J, Joober R., J Child Psychol Psychiatry 53(8), 2012
PMID: 22486528
In hepatocellular carcinoma miR-519d is up-regulated by p53 and DNA hypomethylation and targets CDKN1A/p21, PTEN, AKT3 and TIMP2.
Fornari F, Milazzo M, Chieco P, Negrini M, Marasco E, Capranico G, Mantovani V, Marinello J, Sabbioni S, Callegari E, Cescon M, Ravaioli M, Croce CM, Bolondi L, Gramantieri L., J Pathol 227(3), 2012
PMID: 22262409
Fornari F, Milazzo M, Chieco P, Negrini M, Marasco E, Capranico G, Mantovani V, Marinello J, Sabbioni S, Callegari E, Cescon M, Ravaioli M, Croce CM, Bolondi L, Gramantieri L., J Pathol 227(3), 2012
PMID: 22262409
Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.
Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SL., Am J Med Genet B Neuropsychiatr Genet 159B(5), 2012
PMID: 22573456
Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SL., Am J Med Genet B Neuropsychiatr Genet 159B(5), 2012
PMID: 22573456
BRCA2 variants and cardiovascular disease in a multi-ethnic study.
Zbuk K, Xie C, Young R, Heydarpour M, Pare G, Davis AD, Miller R, Lanktree MB, Saleheen D, Danesh J, Yusuf S, Engert JC, Hegele RA, Anand SS., BMC Med Genet 13(), 2012
PMID: 22809218
Zbuk K, Xie C, Young R, Heydarpour M, Pare G, Davis AD, Miller R, Lanktree MB, Saleheen D, Danesh J, Yusuf S, Engert JC, Hegele RA, Anand SS., BMC Med Genet 13(), 2012
PMID: 22809218
Refining psychiatric phenotypes for response to treatment: contribution of LPHN3 in ADHD.
Labbe A, Liu A, Atherton J, Gizenko N, Fortier MÈ, Sengupta SM, Ridha J., Am J Med Genet B Neuropsychiatr Genet 159B(7), 2012
PMID: 22851411
Labbe A, Liu A, Atherton J, Gizenko N, Fortier MÈ, Sengupta SM, Ridha J., Am J Med Genet B Neuropsychiatr Genet 159B(7), 2012
PMID: 22851411
Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer.
Olkhov-Mitsel E, Van der Kwast T, Kron KJ, Ozcelik H, Briollais L, Massey C, Recker F, Kwiatkowski M, Fleshner NE, Diamandis EP, Zlotta AR, Bapat B., Epigenetics 7(9), 2012
PMID: 22874102
Olkhov-Mitsel E, Van der Kwast T, Kron KJ, Ozcelik H, Briollais L, Massey C, Recker F, Kwiatkowski M, Fleshner NE, Diamandis EP, Zlotta AR, Bapat B., Epigenetics 7(9), 2012
PMID: 22874102
Comprehensive phenotype/genotype analyses of the norepinephrine transporter gene (SLC6A2) in ADHD: relation to maternal smoking during pregnancy.
Thakur GA, Sengupta SM, Grizenko N, Choudhry Z, Joober R., PLoS One 7(11), 2012
PMID: 23185385
Thakur GA, Sengupta SM, Grizenko N, Choudhry Z, Joober R., PLoS One 7(11), 2012
PMID: 23185385
Contribution of VANGL2 mutations to isolated neural tube defects.
Kibar Z, Salem S, Bosoi CM, Pauwels E, De Marco P, Merello E, Bassuk AG, Capra V, Gros P., Clin Genet 80(1), 2011
PMID: 20738329
Kibar Z, Salem S, Bosoi CM, Pauwels E, De Marco P, Merello E, Bassuk AG, Capra V, Gros P., Clin Genet 80(1), 2011
PMID: 20738329
The galanin receptor 1 gene associates with tobacco craving in smokers seeking cessation treatment.
Lori A, Tang Y, O'Malley S, Picciotto MR, Wu R, Conneely KN, Cubells JF., Neuropsychopharmacology 36(7), 2011
PMID: 21430647
Lori A, Tang Y, O'Malley S, Picciotto MR, Wu R, Conneely KN, Cubells JF., Neuropsychopharmacology 36(7), 2011
PMID: 21430647
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.
Debette S, Visvikis-Siest S, Chen MH, Ndiaye NC, Song C, Destefano A, Safa R, Azimi Nezhad M, Sawyer D, Marteau JB, Xanthakis V, Siest G, Sullivan L, Pfister M, Smith H, Choi SH, Lamont J, Lind L, Yang Q, Fitzgerald P, Ingelsson E, Vasan RS, Seshadri S., Circ Res 109(5), 2011
PMID: 21757650
Debette S, Visvikis-Siest S, Chen MH, Ndiaye NC, Song C, Destefano A, Safa R, Azimi Nezhad M, Sawyer D, Marteau JB, Xanthakis V, Siest G, Sullivan L, Pfister M, Smith H, Choi SH, Lamont J, Lind L, Yang Q, Fitzgerald P, Ingelsson E, Vasan RS, Seshadri S., Circ Res 109(5), 2011
PMID: 21757650
Mass spectrometry tools for the classification and identification of bacteria.
Sauer S, Kliem M., Nat Rev Microbiol 8(1), 2010
PMID: 20010952
Sauer S, Kliem M., Nat Rev Microbiol 8(1), 2010
PMID: 20010952
Mining transcriptome sequences towards identifying adaptive single nucleotide polymorphisms in lake whitefish species pairs (Coregonus spp. Salmonidae).
Renaut S, Nolte AW, Bernatchez L., Mol Ecol 19 Suppl 1(), 2010
PMID: 20331775
Renaut S, Nolte AW, Bernatchez L., Mol Ecol 19 Suppl 1(), 2010
PMID: 20331775
On the origin of species: insights from the ecological genomics of lake whitefish.
Bernatchez L, Renaut S, Whiteley AR, Derome N, Jeukens J, Landry L, Lu G, Nolte AW, Ostbye K, Rogers SM, St-Cyr J., Philos Trans R Soc Lond B Biol Sci 365(1547), 2010
PMID: 20439281
Bernatchez L, Renaut S, Whiteley AR, Derome N, Jeukens J, Landry L, Lu G, Nolte AW, Ostbye K, Rogers SM, St-Cyr J., Philos Trans R Soc Lond B Biol Sci 365(1547), 2010
PMID: 20439281
Robust hepatitis B virus genotyping by mass spectrometry.
Ganova-Raeva L, Ramachandran S, Honisch C, Forbi JC, Zhai X, Khudyakov Y., J Clin Microbiol 48(11), 2010
PMID: 20810764
Ganova-Raeva L, Ramachandran S, Honisch C, Forbi JC, Zhai X, Khudyakov Y., J Clin Microbiol 48(11), 2010
PMID: 20810764
Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene.
Cobb JE, Zaloumis SG, Scurrah KJ, Harrap SB, Ellis JA., Exp Dermatol 19(11), 2010
PMID: 21073542
Cobb JE, Zaloumis SG, Scurrah KJ, Harrap SB, Ellis JA., Exp Dermatol 19(11), 2010
PMID: 21073542
Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics Study.
Anand SS, Xie C, Paré G, Montpetit A, Rangarajan S, McQueen MJ, Cordell HJ, Keavney B, Yusuf S, Hudson TJ, Engert JC, INTERHEART Investigators., Circ Cardiovasc Genet 2(1), 2009
PMID: 20031563
Anand SS, Xie C, Paré G, Montpetit A, Rangarajan S, McQueen MJ, Cordell HJ, Keavney B, Yusuf S, Hudson TJ, Engert JC, INTERHEART Investigators., Circ Cardiovasc Genet 2(1), 2009
PMID: 20031563
Novel mutations in VANGL1 in neural tube defects.
Kibar Z, Bosoi CM, Kooistra M, Salem S, Finnell RH, De Marco P, Merello E, Bassuk AG, Capra V, Gros P., Hum Mutat 30(7), 2009
PMID: 19319979
Kibar Z, Bosoi CM, Kooistra M, Salem S, Finnell RH, De Marco P, Merello E, Bassuk AG, Capra V, Gros P., Hum Mutat 30(7), 2009
PMID: 19319979
Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levels.
Iatan I, Dastani Z, Do R, Weissglas-Volkov D, Ruel I, Lee JC, Huertas-Vazquez A, Taskinen MR, Prat A, Seidah NG, Pajukanta P, Engert JC, Genest J., Circ Cardiovasc Genet 2(5), 2009
PMID: 20031622
Iatan I, Dastani Z, Do R, Weissglas-Volkov D, Ruel I, Lee JC, Huertas-Vazquez A, Taskinen MR, Prat A, Seidah NG, Pajukanta P, Engert JC, Genest J., Circ Cardiovasc Genet 2(5), 2009
PMID: 20031622
High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays.
Wang J, Lin M, Crenshaw A, Hutchinson A, Hicks B, Yeager M, Berndt S, Huang WY, Hayes RB, Chanock SJ, Jones RC, Ramakrishnan R., BMC Genomics 10(), 2009
PMID: 19943955
Wang J, Lin M, Crenshaw A, Hutchinson A, Hicks B, Yeager M, Berndt S, Huang WY, Hayes RB, Chanock SJ, Jones RC, Ramakrishnan R., BMC Genomics 10(), 2009
PMID: 19943955
Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study.
Do R, Bailey SD, Desbiens K, Belisle A, Montpetit A, Bouchard C, Pérusse L, Vohl MC, Engert JC., Diabetes 57(4), 2008
PMID: 18316358
Do R, Bailey SD, Desbiens K, Belisle A, Montpetit A, Bouchard C, Pérusse L, Vohl MC, Engert JC., Diabetes 57(4), 2008
PMID: 18316358
Simulating multiplexed SNP discovery rates using base-specific cleavage and mass spectrometry.
Böcker S., Bioinformatics 23(2), 2007
PMID: 17237104
Böcker S., Bioinformatics 23(2), 2007
PMID: 17237104
DNA sequencing by MALDI-TOF MS using alkali cleavage of RNA/DNA chimeras.
Mauger F, Bauer K, Calloway CD, Semhoun J, Nishimoto T, Myers TW, Gelfand DH, Gut IG., Nucleic Acids Res 35(8), 2007
PMID: 17426131
Mauger F, Bauer K, Calloway CD, Semhoun J, Nishimoto T, Myers TW, Gelfand DH, Gut IG., Nucleic Acids Res 35(8), 2007
PMID: 17426131
FLAG assay as a novel method for real-time signal generation during PCR: application to detection and genotyping of KRAS codon 12 mutations.
Amicarelli G, Shehi E, Makrigiorgos GM, Adlerstein D., Nucleic Acids Res 35(19), 2007
PMID: 17932053
Amicarelli G, Shehi E, Makrigiorgos GM, Adlerstein D., Nucleic Acids Res 35(19), 2007
PMID: 17932053
Current methods for high-throughput detection of novel DNA polymorphisms.
Peters T, Sedlmeier R., Drug Discov Today Technol 3(2), 2006
PMID: 24980398
Peters T, Sedlmeier R., Drug Discov Today Technol 3(2), 2006
PMID: 24980398
Quantitative assessment of DNA methylation: Potential applications for disease diagnosis, classification, and prognosis in clinical settings.
Brena RM, Huang TH, Plass C., J Mol Med (Berl) 84(5), 2006
PMID: 16416310
Brena RM, Huang TH, Plass C., J Mol Med (Berl) 84(5), 2006
PMID: 16416310
Detection and genotyping of SHV beta-lactamase variants by mass spectrometry after base-specific cleavage of in vitro-generated RNA transcripts.
Stürenburg E, Storm N, Sobottka I, Horstkotte MA, Scherpe S, Aepfelbacher M, Müller S., J Clin Microbiol 44(3), 2006
PMID: 16517875
Stürenburg E, Storm N, Sobottka I, Horstkotte MA, Scherpe S, Aepfelbacher M, Müller S., J Clin Microbiol 44(3), 2006
PMID: 16517875
Microbial identification by mass cataloging.
Zhang Z, Jackson GW, Fox GE, Willson RC., BMC Bioinformatics 7(), 2006
PMID: 16524471
Zhang Z, Jackson GW, Fox GE, Willson RC., BMC Bioinformatics 7(), 2006
PMID: 16524471
DNA analysis by mass spectrometry-past, present and future.
Tost J, Gut IG., J Mass Spectrom 41(8), 2006
PMID: 16921576
Tost J, Gut IG., J Mass Spectrom 41(8), 2006
PMID: 16921576
7 References
Daten bereitgestellt von Europe PubMed Central.
MALDI-TOF mass spectrometry-based SNP genotyping.
Storm N, Darnhofer-Patel B, van den Boom D, Rodi CP., Methods Mol. Biol. 212(), 2003
PMID: 12491915
Storm N, Darnhofer-Patel B, van den Boom D, Rodi CP., Methods Mol. Biol. 212(), 2003
PMID: 12491915
RNase T1 mediated base-specific cleavage and MALDI-TOF MS for high-throughput comparative sequence analysis.
Hartmer R, Storm N, Boecker S, Rodi CP, Hillenkamp F, Jurinke C, van den Boom D., Nucleic Acids Res. 31(9), 2003
PMID: 12711692
Hartmer R, Storm N, Boecker S, Rodi CP, Hillenkamp F, Jurinke C, van den Boom D., Nucleic Acids Res. 31(9), 2003
PMID: 12711692
SNP and mutation discovery using base-specific cleavage and MALDI-TOF mass spectrometry.
Bocker S., Bioinformatics 19 Suppl 1(), 2003
PMID: 12855436
Bocker S., Bioinformatics 19 Suppl 1(), 2003
PMID: 12855436
Chemiluminescent DNA sequencing with multiplex labeling.
Olesen CE, Martin CS, Bronstein I., BioTechniques 15(3), 1993
PMID: 8217162
Olesen CE, Martin CS, Bronstein I., BioTechniques 15(3), 1993
PMID: 8217162
Enzyme-linked fluorescent detection for automated multiplex DNA sequencing.
Cherry JL, Young H, Di Sera LJ, Ferguson FM, Kimball AW, Dunn DM, Gesteland RF, Weiss RB., Genomics 20(1), 1994
PMID: 8020958
Cherry JL, Young H, Di Sera LJ, Ferguson FM, Kimball AW, Dunn DM, Gesteland RF, Weiss RB., Genomics 20(1), 1994
PMID: 8020958
High-throughput MALDI-TOF discovery of genomic sequence polymorphisms.
Stanssens P, Zabeau M, Meersseman G, Remes G, Gansemans Y, Storm N, Hartmer R, Honisch C, Rodi CP, Bocker S, van den Boom D., Genome Res. 14(1), 2004
PMID: 14707174
Stanssens P, Zabeau M, Meersseman G, Remes G, Gansemans Y, Storm N, Hartmer R, Honisch C, Rodi CP, Bocker S, van den Boom D., Genome Res. 14(1), 2004
PMID: 14707174
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