Gotowa bibliografia na temat „Single nucleotide polymorphisms”
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Artykuły w czasopismach na temat "Single nucleotide polymorphisms"
Shaw, Greg. "Polymorphism and single nucleotide polymorphisms (SNPs)". BJU International 112, nr 5 (7.08.2013): 664–65. http://dx.doi.org/10.1111/bju.12298.
Pełny tekst źródłaDong, Chunming, Joseph R. Nevins i Pascal J. Goldschmidt-Clermont. "ABCA1 Single Nucleotide Polymorphisms". Circulation Research 88, nr 9 (11.05.2001): 855–57. http://dx.doi.org/10.1161/hh0901.091208.
Pełny tekst źródłaMeyer, Nuala J. "Beyond Single-Nucleotide Polymorphisms". Clinics in Chest Medicine 35, nr 4 (grudzień 2014): 673–84. http://dx.doi.org/10.1016/j.ccm.2014.08.006.
Pełny tekst źródłaPandav, Surinder Singh, Partha Chakma, Alka Khera, Neera Chugh, Parul Chawla Gupta, Faisal Thattaruthody, Natasha Gautam Seth i in. "Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population". European Journal of Ophthalmology 29, nr 4 (6.09.2018): 431–36. http://dx.doi.org/10.1177/1120672118795405.
Pełny tekst źródłaZhu, Y. L., Q. J. Song, D. L. Hyten, C. P. Van Tassell, L. K. Matukumalli, D. R. Grimm, S. M. Hyatt, E. W. Fickus, N. D. Young i P. B. Cregan. "Single-Nucleotide Polymorphisms in Soybean". Genetics 163, nr 3 (1.03.2003): 1123–34. http://dx.doi.org/10.1093/genetics/163.3.1123.
Pełny tekst źródłaWang, Ting, Yuting Liang, Hong Li, Haibo Li, Quanze He, Ying Xue, Cong Shen i in. "Single Nucleotide Polymorphisms and Osteoarthritis". Medicine 95, nr 7 (luty 2016): e2811. http://dx.doi.org/10.1097/md.0000000000002811.
Pełny tekst źródłaKarthikeyan, Ramalingam, Manohar Murugan, SyedWali Peeran, MareiHamad Al Mugrabi, Khaled Awidat i Omar Basheer. "Single nucleotide polymorphisms and periodontitis". Dentistry and Medical Research 2, nr 1 (2014): 3. http://dx.doi.org/10.4103/2348-1471.131556.
Pełny tekst źródłaThomas, Sandy. "Shares in single nucleotide polymorphisms". Expert Opinion on Therapeutic Patents 9, nr 7 (lipiec 1999): 811–12. http://dx.doi.org/10.1517/13543776.9.7.811.
Pełny tekst źródłaPhillips, C., M. Lareu, A. Salas, M. Fondevila, G. Berniell Lee, A. Carracedo, N. Morling, P. Schneider i D. Syndercombe Court. "Population specific single nucleotide polymorphisms". International Congress Series 1261 (kwiecień 2004): 233–35. http://dx.doi.org/10.1016/j.ics.2003.12.041.
Pełny tekst źródłaRieder, Mark J., i Deborah A. Nickerson. "Hypertension and single nucleotide polymorphisms". Current Hypertension Reports 2, nr 1 (luty 2000): 44–49. http://dx.doi.org/10.1007/s11906-000-0057-4.
Pełny tekst źródłaRozprawy doktorskie na temat "Single nucleotide polymorphisms"
Sauer, Sascha. "Technology development for genotyping single nucleotide polymorphisms". [S.l.] : [s.n.], 2001. http://www.diss.fu-berlin.de/2002/102/index.html.
Pełny tekst źródłaLau, Chi Chiu. "Hepatitis B virus and single nucleotide polymorphisms". HKBU Institutional Repository, 2007. http://repository.hkbu.edu.hk/etd_ra/810.
Pełny tekst źródłaSchwonbeck, Susanne. "Analyse von Single-Nucleotide-Polymorphisms an Glas-Oberflächen". [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=974115568.
Pełny tekst źródłaSchwonbeck, Susanne. "Analyse von Single Nucleotide Polymorphisms an Glas-Oberflächen". Phd thesis, Universität Potsdam, 2004. http://opus.kobv.de/ubp/volltexte/2005/221/.
Pełny tekst źródłaDie Versuche am faseroptischen Affinitätssensor zeigten, dass DNA-DNA-Hybride sowohl von Oligonukleotiden als auch von PCR-Produkten ein typisches Dissoziationsverhalten aufweisen, wobei fehlgepaarte Hybride eine signifikant schnellere Dissoziation zeigen als perfekt passende Hybride. Dieser Geschwindigkeitsunterschied lässt sich durch den Vergleich der jeweiligen kinetischen Geschwindigkeitskonstanten kD quantitativ erfassen.
Da die Kopplung des Analyten an der Chipoberfläche sowie die Hybridisierungs- und Dissoziationsparameter essentiell für die Methodenentwicklung war, wurden die Parameter für ein optimales Spotting und die Immobilisierung von PCR-Produkten ermittelt. Getestet wurden die affine Kopplung von biotinylierten PCR-Produkten an Streptavidin-, Avidin- und NeutrAvidin-Oberflächen sowie die kovalente Bindung von phosphorylierten Amplifikaten mit der EDC/Methylimidazol-Methode. Die besten Ergebnisse sowohl in Spotform und -homogenität als auch im Signal/Rausch-Verhältnis wurden an NeutrAvidin-Oberflächen erreicht.
Für die Etablierung der Mikroarray-Genotypisierungsmethode durch kinetische Analyse nach einem Hybridisierungsexperiment wurden Sondenlänge, Puffersystem, Spotting-Konzentration des Analyten sowie Temperatur optimiert. Das Analysensystem erlaubte es, PCR-Produkte mit einer Konzentration von 250 ng/µl in einem HEPES-EDTA-NaCl-Puffer auf mit NeutrAvidin beschichtete Glasträger zu spotten. In den anschließenden Hybridisierungs- und Dissoziationsexperimenten bei 30 °C konnte die Diskriminierung von homocygoter Wildtyp- und homocygoter Mutanten- sowie heterocygoter DNA am Beispiel von Oligonukleotid-Hybriden erreicht werden.
In einer Gruppe von 24 homocygoten Patienten wurde ein Polymorphismus im SULT1A1-Gen analysiert. Sowohl durch kinetische Auswertung als auch mit der Analyse der Fluoreszenzintensität wurde der Genotyp der Proben identifiziert. Die Ergebnisse wurden mit dem Referenzverfahren, der Restriktionschnittstellenanalyse (PCR-RFLP) validiert. Lediglich ein Genotyp wurde falsch bestimmt, die Genauigkeit lag bei 96%.
In einer Gruppe von 44 Patienten wurde der Genotyp eines SNP in der Adiponectin-Promotor-Region untersucht. Nach Vergleich der Analysenergebnisse mit denen eines Referenzverfahrens konnten lediglich 14 der untersuchten Genotypen bestätigt werden. Ursache für die unzureichende Genauigkeit der Methode war vor allem das schlechte Signal/Rausch-Verhältnis.
Zusammenfassend kann gesagt werden, dass das in dieser Arbeit entwickelte Analysesystem für die Genotypisierung von Einzelpunktmutationen geeignet ist, homocygote Patientenproben zuverlässig zu analysieren. Prinzipiell ist das auch bei heterocygoter DNA möglich. Da nach aktuellem Kenntnisstand eine SNP-Analysemethode an immobilisierten PCR-Produkten noch nicht veröffentlicht wurde, stellt das hier entwickelte Verfahren eine Alternative zu bisher bekannten Mikroarray-Verfahren dar. Als besonders vorteilhaft erweist sich der reverse Ansatz der Methode.
Der hier vorgestellte Ansatz ist eine kostengünstigere und weniger hoch
dimensionierte Lösung für Fragestellungen beispielsweise in der Ernährungswissenschaft,
bei denen meist eine mittlere Anzahl Patienten auf nur einige wenige SNPs
zu untersuchen ist. Wenn es gelingt, durch die Weiterentwicklung der Hardware
bzw. weiterer Optimierung, eine Verbesserung des Signal/Rausch-Verhältnisses
und damit die Diskriminierung von heterocygoter DNA zu erreichen, kann
diese Methode zukünftig bei der Analyse von mittelgroßen Patientengruppen
alternativ zu anderen Genotypisierungsmethoden verwendet werden.
The aim of this thesis was the development of a SNP genotyping method
involving PCR products immobilised on microarrays. For the analysis a fibre
optic affinity biosensor and a flow-through biochip scanner were used.
Fluorescent probes were hybridized with the immobilised PCR products. In
order to start the dissociation process the surface was rinsed with buffer
and the fluorescence intensity was measured.
Two different cases were studied: First, the full-matched DNA hybrid
(wildtyp single strand with complementary wildtype single strand), second
the mis-matched hybrid (wildtype single strand and mutant single strand).
After determinating the reaction rates (kD) as kinetic parameter the kD
values of both cases were compared. The experiments showed a significant
difference in the kD value of the full- and the mis-match hybrids.
Therefore, mutant and wildtype DNA were discriminated by kinetic analysis
of the dissociation process and analysis of the fluorescence intensity.
To set up the complete analysis process the reaction parameters like
coupling of the PCR products had to be optimised. Both affininty coupled
(streptavidin, neutravidin, avidin - biotin) and covalent methods
(EDC/methylimidazol) were carried out. Best results in spot homogeinity and
spot appearance were obtained with coupling of biotinylated PCR products on
neutravidin coated chip surfaces. Additionally, the length of the probe,
the spotting concentration, the spotting buffer and the reaction
temperature were optimised. In the optimised analysis PCR products (250
µg/µl) were spotted onto neutravidin coated surfaces. The hybridisation
and dissociation processes were carried out at 30°C. A HEPES-EDTA-NaCl
buffer was used for spotting, diluting of the fluorescent probe and rinsing
the microarray surface. A fluorescent probe was used with 13 nucleotides in
length. The mis- or full-matching base indicating the polymorphism was
located in the center position of the probe.
The analysis system was tested with the genomic DNA of a group of 24
homocygote individuals with a SNP in the SULT1A1 gene region. The
hybridisation and dissociation processes were carried out and the reaction
rates were determinated. Subsequently after the analysis in the
flow-through biochip scanner the fluorescence intensity of the
spots were measured. The results showed very good comparability with
results of a PCR-RFLP analysis (one false genotype). Additionally, a group
of 44 heterocygote DNA samples with one SNP in the adiponectin promotor
region were also genotyped. Compared to a reference method only 14
genotypes were correctly determined. This was mostly due to a low
signal-noise-ratio and needs to be further investigated.
Besides the problem in analysing heterocygote DNA samples the developed
analysis system is very useful for genotyping SNP in homocygote DNA
samples. The successful analysis of heterocygote sample is principally
possible and with further investigations/optimisation, a better analysis
should be possible.
The most important advantage of the developed method is the reverse
approach of binding PCR products at the surface instead of
oligonucleotides. This allows the parallel genotyping of several
individuals. Other advantages include low costs and medium sized dimensions
in terms of throughput.
Reeves, Emma. "Functional consequences of single nucleotide polymorphisms in ERAAP". Thesis, University of Southampton, 2011. https://eprints.soton.ac.uk/375582/.
Pełny tekst źródłaDallin, Joshua Jeffrey. "Analytical Comparison of Bovine Parentage Single Nucleotide Polymorphisms". DigitalCommons@USU, 2015. https://digitalcommons.usu.edu/etd/4450.
Pełny tekst źródłaBarbati, E. "SINGLE NUCLEOTIDE POLYMORPHISMS AND MICRORNAS AFFECTING PTX3 PRODUCTION". Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/168370.
Pełny tekst źródłaFreeman, Julia Carol. "Single Nucleotide Polymorphisms Linked to Essential Hypertension in Kasigau, Kenya". TopSCHOLAR®, 2013. http://digitalcommons.wku.edu/theses/1316.
Pełny tekst źródłaChen-Cheng, Charles. "JAMALAH--a system for the detection of single nucleotide polymorphisms". Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/40606.
Pełny tekst źródłaIncludes bibliographical references (leaves 70-75).
by Charles Chen-Cheng.
M.Eng.
Perla, Sravan K. "Epigenetic Regulation of the Human Angiotensinogen by Single Nucleotide Polymorphisms". University of Toledo Health Science Campus / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=mco1544800350207546.
Pełny tekst źródłaKsiążki na temat "Single nucleotide polymorphisms"
Kwok, Pui-Yan. Single Nucleotide Polymorphisms. New Jersey: Humana Press, 2002. http://dx.doi.org/10.1385/1592593275.
Pełny tekst źródłaSauna, Zuben E., i Chava Kimchi-Sarfaty, red. Single Nucleotide Polymorphisms. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1.
Pełny tekst źródłaKomar, Anton A., red. Single Nucleotide Polymorphisms. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-411-1.
Pełny tekst źródłaSingle nucleotide polymorphisms: Methods and protocols. Wyd. 2. New York: Humana, 2009.
Znajdź pełny tekst źródłaLiu, Zhanjiang. Next generation sequencing and whole genome selection in aquaculture. Ames, Iowa: Wiley-Blackwell, 2011.
Znajdź pełny tekst źródła1955-, Carracedo Ángel, red. Forensic DNA typing protocols. Totowa, N.J: Humana Press, 2005.
Znajdź pełny tekst źródła1956-, Kwok Pui-Yan, red. Single nucleotide polymorphisms: Methods and protocols. Totowa, N.J: Humana Press, 2003.
Znajdź pełny tekst źródłaKomar, Anton A. Single Nucleotide Polymorphisms: Methods and Protocols. Humana Press, 2012.
Znajdź pełny tekst źródłaKwok, Pui-Yan. Single Nucleotide Polymorphisms: Methods and Protocols (Methods in Molecular Biology). Humana Press, 2002.
Znajdź pełny tekst źródłaSauna, Zuben E., i Chava Kimchi-Sarfaty. Single Nucleotide Polymorphisms: Human Variation and a Coming Revolution in Biology and Medicine. Springer International Publishing AG, 2022.
Znajdź pełny tekst źródłaCzęści książek na temat "Single nucleotide polymorphisms"
Hettiarachchi, Gaya, i Anton A. Komar. "GWAS to Identify SNPs Associated with Common Diseases and Individual Risk: Genome Wide Association Studies (GWAS) to Identify SNPs Associated with Common Diseases and Individual Risk". W Single Nucleotide Polymorphisms, 51–76. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_4.
Pełny tekst źródłaPeña-Llopis, Samuel. "SNPs and Personalized Medicine: Scrutinizing Pathogenic Synonymous Mutations for Precision Oncology". W Single Nucleotide Polymorphisms, 185–95. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_9.
Pełny tekst źródłaOoi, Brandon N. S., Ashley J. W. Lim, Samuel S. Chong i Caroline G. L. Lee. "Using Genome Wide Studies to Generate and Test Hypotheses that Provide Mechanistic Details of How Synonymous Codons Affect Protein Structure and Function: Functional SNPs in the Age of Precision Medicine". W Single Nucleotide Polymorphisms, 171–83. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_8.
Pełny tekst źródłaPhan, Lon. "SNPs Classification and Terminology: dbSNP Reference SNP (rs) Gene and Consequence Annotation". W Single Nucleotide Polymorphisms, 3–12. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_1.
Pełny tekst źródłaLin, Brian C., Katarzyna I. Jankowska, Douglas Meyer i Upendra K. Katneni. "Methods to Evaluate the Effects of Synonymous Variants". W Single Nucleotide Polymorphisms, 133–68. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_7.
Pełny tekst źródłaHerreros, Eduardo, Xander Janssens, Daniele Pepe i Kim De Keersmaecker. "SNPs Ability to Influence Disease Risk: Breaking the Silence on Synonymous Mutations in Cancer". W Single Nucleotide Polymorphisms, 77–96. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_5.
Pełny tekst źródłaAgashe, Deepa. "Evolutionary Forces That Generate SNPs: The Evolutionary Impacts of Synonymous Mutations". W Single Nucleotide Polymorphisms, 15–36. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_2.
Pełny tekst źródłaRosenberg, Aviv A., Alex M. Bronstein i Ailie Marx. "Recording Silence – Accurate Annotation of the Genetic Sequence Is Required to Better Understand How Synonymous Coding Affects Protein Structure and Disease". W Single Nucleotide Polymorphisms, 37–47. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_3.
Pełny tekst źródłaMauro, Vincent P. "Condon Optimization: Codon Optimization of Therapeutic Proteins: Suggested Criteria for Increased Efficacy and Safety". W Single Nucleotide Polymorphisms, 197–224. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_10.
Pełny tekst źródłaZhang, Yiming, i Zsuzsa Bebok. "An Examination of Mechanisms by which Synonymous Mutations may Alter Protein Levels, Structure and Functions". W Single Nucleotide Polymorphisms, 99–132. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05616-1_6.
Pełny tekst źródłaStreszczenia konferencji na temat "Single nucleotide polymorphisms"
Weiler, Zachary, Tadashi Sato, Amy Nelson, Xiangde Liu, Yoko Gunji, Kai-Christian Muller, Helgo Magnussen, Klaus Rabe, Stephen I. Rennard i Tricia D. LeVan. "Identification Of Single Nucleotide Polymorphisms In MicroRNA 146A". W American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a3526.
Pełny tekst źródłaCOLLINS, A. "LINKAGE DISEQUILIBRIUM MAPPING USING SINGLE NUCLEOTIDE POLYMORPHISMS -WHICH POPULATION?" W Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 1999. http://dx.doi.org/10.1142/9789814447331_0063.
Pełny tekst źródłaNaumov, Denis, Olesya Kotova, Anna Prikhodko, Sergey Zinovyev, Juliy Perelman i Victor Kolosov. "TRPV4 single nucleotide polymorphisms and airway inflammation in asthma". W ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa1821.
Pełny tekst źródłaAlvarez, Alfonso E., Fernando A. L. Marson, Carmem S. Bertuzzo, Juliana C. S. Santiago, Emilio C. E. Baracat, Antonia T. Tresoldi, Mariana T. N. Romaneli i in. "Influence of single nucleotide polymorphisms in post-bronchiolitis wheezing". W ERS International Congress 2016 abstracts. European Respiratory Society, 2016. http://dx.doi.org/10.1183/13993003.congress-2016.pa1599.
Pełny tekst źródłaRonaghi, Mostafa. "High-throughput pyrosequencing for analysis of single-nucleotide polymorphisms". W International Symposium on Biomedical Optics, redaktorzy Darryl J. Bornhop, David A. Dunn, Raymond P. Mariella, Jr., Catherine J. Murphy, Dan V. Nicolau, Shuming Nie, Michelle Palmer i Ramesh Raghavachari. SPIE, 2002. http://dx.doi.org/10.1117/12.472098.
Pełny tekst źródłaRobayo, Verónica. "Single nucleotide polymorphisms influencing obesity in Hispanics and Mexicans". W 1er Congreso Universal de las Ciencias y la Investigación Medwave 2022;. Medwave Estudios Limitada, 2022. http://dx.doi.org/10.5867/medwave.2022.s2.uta024.
Pełny tekst źródłaXu, M., KG Tantisira, A. Murphy i ST Weiss. "Predicting Severe Asthma Exacerbations Using Thousands of Single Nucleotide Polymorphisms." W American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a2208.
Pełny tekst źródłaStigler, William S., Lin Li, Xihong Lin, Yang Zhao, Mark M. Wurfel i David C. Christiani. "MicroRNA Single Nucleotide Polymorphisms And Risk Of ARDS And ALI". W American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a2120.
Pełny tekst źródłaLevine, Arnold J. "Abstract IA-6: Single nucleotide polymorphisms in the p53 pathway". W Abstracts: First AACR International Conference on Frontiers in Basic Cancer Research--Oct 8–11, 2009; Boston MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.fbcr09-ia-6.
Pełny tekst źródłaDamkliang, Kasikrit, Pichaya Tandayya, Theerawut Phusantisampan i Unitsa Sangket. "Taverna Workflow and Supporting Service for Single Nucleotide Polymorphisms Analysis". W 2009 International Conference on Information Management and Engineering. IEEE, 2009. http://dx.doi.org/10.1109/icime.2009.38.
Pełny tekst źródłaRaporty organizacyjne na temat "Single nucleotide polymorphisms"
Larcom, Barbara, Rosemarie Ramos, Lisa Lott, J. M. McDonald, Mark True, Michele Tavish, Heidi Beason, Lee Ann Zarzabel, James Watt i Debra Niemeyer. Genetic Risk Conferred from Single Nucleotide Polymorphisms Towards Type II Diabetes Mellitus. Fort Belvoir, VA: Defense Technical Information Center, luty 2013. http://dx.doi.org/10.21236/ada573655.
Pełny tekst źródłaWang, Ying yuan, Ze chang Chen, Lu xin Zhang i Shuang yi Chen. A systematic review and network meta-analysis of single nucleotide polymorphisms associated with breast cancer risk. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, luty 2022. http://dx.doi.org/10.37766/inplasy2022.2.0010.
Pełny tekst źródłaZheng, Jinghui. A comprehensive evaluation of single nucleotide polymorphisms associated with osteosarcoma risk: a protocol for systematic review and network meta analysis. INPLASY - International Platform of Registered Systematic Review Protocols, kwiecień 2020. http://dx.doi.org/10.37766/inplasy2020.4.0141.
Pełny tekst źródłaZheng, Jinghui. A comprehensive assessment of single nucleotide polymorphisms associated with pancreatic cancer risk: a systematic review and network meta-analysis of protocols. INPLASY - International Platform of Registered Systematic Review Protocols, kwiecień 2020. http://dx.doi.org/10.37766/inplasy2020.4.0023.
Pełny tekst źródłaZheng, Jinghui. A comprehensive evaluation of single nucleotide polymorphisms associated with gastric cancer risk: a protocol for systematic review and network meta analysis. INPLASY - International Platform of Registered Systematic Review Protocols, kwiecień 2020. http://dx.doi.org/10.37766/inplasy2020.4.0132.
Pełny tekst źródłaTang, Zhen-yu, Zhuo-miao Ye, Jing-hui Zheng, Feng Jiang i You-ming Tang. A comprehensive evaluation of single nucleotide polymorphisms associated with atrophic gastritis risk: a protocol for systematic review and network meta-analysis. International Platform of Registered Systematic Review and Meta-analysis Protocols, maj 2020. http://dx.doi.org/10.37766/inplasy2020.5.0016.
Pełny tekst źródłaLi, Li-juan, M. Meda, Yuan-yuan Zhao, M. Medb i Jing-hui Zheng. A comprehensive assessment of single nucleotide polymorphisms associated with lung cancer risk: a protocol for systematic review and network meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, maj 2020. http://dx.doi.org/10.37766/inplasy2020.5.0105.
Pełny tekst źródłaLi, Lijuan. A comprehensive assessment of single nucleotide polymorphisms associated with lung cancer risk: a systematic review and network meta-analysis of protocols. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, kwiecień 2022. http://dx.doi.org/10.37766/inplasy2022.4.0018.
Pełny tekst źródłaWang, Ying yuan, Zechang Chen, Luxin Zhang, Shuangyi Chen, Zhuomiao Ye, Tingting Xu i Yingying Zhang c. A systematic review and network meta-analysis: Role of SNPs in predicting breast carcinoma risk. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, luty 2022. http://dx.doi.org/10.37766/inplasy2022.2.0092.
Pełny tekst źródłaKong, Yixuan, Jinghui Zheng, Zhuomiao Ye, Jie Wang, Xiangmei Xu i Xuan Chen. A comprehensive evaluation of association between homocysteine levels and single nucleotide polymorphisms with hypertension risk : A protocol of systematic review and network meta-analysis. International Platform of Registered Systematic Review and Meta-analysis Protocols, maj 2020. http://dx.doi.org/10.37766/inplasy2020.5.0002.
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