Littérature scientifique sur le sujet « PCR-free »
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Articles de revues sur le sujet "PCR-free"
Hou, Chih-Sheng Johnson, Nebojsa Milovic, Michel Godin, Peter R. Russo, Raj Chakrabarti et Scott R. Manalis. « Label-Free Microelectronic PCR Quantification ». Analytical Chemistry 78, no 8 (avril 2006) : 2526–31. http://dx.doi.org/10.1021/ac0520689.
Texte intégralLee, Sang Hun, Jihwan Song, Byungrae Cho, SoonGweon Hong, Ori Hoxha, Taewook Kang, Dongchoul Kim et Luke P. Lee. « Bubble-free rapid microfluidic PCR ». Biosensors and Bioelectronics 126 (février 2019) : 725–33. http://dx.doi.org/10.1016/j.bios.2018.10.005.
Texte intégralErdeniz, Naz, Uffe H. Mortensen et Rodney Rothstein. « Cloning-Free PCR-Based Allele Replacement Methods ». Genome Research 7, no 12 (1 décembre 1997) : 1174–83. http://dx.doi.org/10.1101/gr.7.12.1174.
Texte intégralShao, Zhenyu, Yuexing Liu, Han Xiao et Genxi Li. « PCR-free electrochemical assay of telomerase activity ». Electrochemistry Communications 10, no 10 (octobre 2008) : 1502–4. http://dx.doi.org/10.1016/j.elecom.2008.07.051.
Texte intégralChen, Yuchao, et Tae Seok Seo. « PCR-free digital minisatellite tandem repeat genotyping ». ELECTROPHORESIS 32, no 12 (30 mai 2011) : 1456–64. http://dx.doi.org/10.1002/elps.201100073.
Texte intégralJafari, Hamed Mazhab, Karim Abdelhalim, Leyla Soleymani, Edward H. Sargent, Shana O. Kelley et Roman Genov. « Nanostructured CMOS Wireless Ultra-Wideband Label-Free PCR-Free DNA Analysis SoC ». IEEE Journal of Solid-State Circuits 49, no 5 (mai 2014) : 1223–41. http://dx.doi.org/10.1109/jssc.2014.2312571.
Texte intégralBrouard, D., O. Ratelle, J. Perreault, D. Boudreau et M. St-Louis. « PCR-free blood group genotyping using a nanobiosensor ». Vox Sanguinis 108, no 2 (3 décembre 2014) : 197–204. http://dx.doi.org/10.1111/vox.12207.
Texte intégralSenchyna, Fiona, Rajiv L. Gaur, Saurabh Gombar, Cynthia Y. Truong, Lee F. Schroeder et Niaz Banaei. « Clostridium difficile PCR Cycle Threshold Predicts Free Toxin ». Journal of Clinical Microbiology 55, no 9 (14 juin 2017) : 2651–60. http://dx.doi.org/10.1128/jcm.00563-17.
Texte intégralKraytsberg, Yevgenya, et Konstantin Khrapko. « Single-molecule PCR : an artifact-free PCR approach for the analysis of somatic mutations ». Expert Review of Molecular Diagnostics 5, no 5 (septembre 2005) : 809–15. http://dx.doi.org/10.1586/14737159.5.5.809.
Texte intégralHsieh, Shen-Yuan, Mohammad A. Tariq, Andrea Telatin, Rebecca Ansorge, Evelien M. Adriaenssens, George M. Savva, Catherine Booth, Tom Wileman, Lesley Hoyles et Simon R. Carding. « Comparison of PCR versus PCR-Free DNA Library Preparation for Characterising the Human Faecal Virome ». Viruses 13, no 10 (18 octobre 2021) : 2093. http://dx.doi.org/10.3390/v13102093.
Texte intégralThèses sur le sujet "PCR-free"
White, James David dvm. « Real-Time Quantitative PCR of tet (C), in 2 Swine Populations : Antibiotic Free versus Conventionally Reared ». The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1437046111.
Texte intégralSillence, Kelly. « Cell-free fetal DNA (cffDNA) enrichment for non-invasive prenatal testing (NIPT) : a comparison of molecular techniques ». Thesis, University of Plymouth, 2016. http://hdl.handle.net/10026.1/5319.
Texte intégralMiran, Tara. « Enrichment of minority DNA in admixes of DNA samples : potential use in non-invasive prenatal diagnosis (NIPD) of Down syndrome ». Thesis, University of Plymouth, 2012. http://hdl.handle.net/10026.1/1190.
Texte intégralBatista, Ribrio Ivan Tavares Pereira. « Efeito do ácido linoléico conjugado TRANS-10, CIS-12 na regulação do acúmulo de lípides e expressão gênica em embriões produzidos in vitro ». Universidade Federal de Juiz de Fora (UFJF), 2010. https://repositorio.ufjf.br/jspui/handle/ufjf/2507.
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FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais
A suplementação do ácido linoléico conjugado trans-10, cis-10 no meio de cultivo, representa uma importante alternativa para aumento da sobrevivência dos embriões após a criopreservação. No entanto este isômero de CLA no cultivo in vitro sem antioxidante pode aumentar a taxa apoptótica. O objetivo do presente estudo foi avaliar o efeito da adição CLA trans-10, cis-12 no cultivo in vitro de embriões sem antioxidante. Zigotos bovinos (n = 1.694) foram divididos em dois tratamentos: (T1) grupo controle, zigotos cultivados no meio CR2aa suplementado com soro fetal (n = 815); (T2) zigotos cultivados no meio CR2aa suplementado com soro fetal mais 100 µM CLA trans-10, cis-12. Os embriões foram avaliados quanto a desenvolvimento, quantidade de lípides e criotolerância. Transcritos dos RNA mensageiros (RNAm) dos genes selecionados foram mensurados pelo Real Time PCR. Suplementação de CLA trans-10, cis-12 não afeta significativamente a taxa de blastocisto (31,8% e 34,1% T1 e T2, respectivamente, p = 0,20) e nível dos RNAm dos genes relacionados com stress celular, apoptose e síntese de novo de ácido graxo. Quantidade de lípides e transcritos do RNAm do gene 1-acilglicerol-3-fosfato oaciltransferase 1 enzima relacionado a síntese de triglicérides foram significativamente reduzidos nos embriões cultivados na presença de CLA trans-10, cis-12 em comparação com o grupo controle. Teve aumento significativo na taxa de re-expansão dos blastocistos cultivados na presença de CLA trans-10, cis-12, após o descongelamento (34.4 e 56.3% para T1 e T2, respectivamente p = 0,002). Essa diferença não persistiu na taxa de eclosão (14,0% e 16,5% para T1 e T2, respectivamente, P = 0,62). Esses resultados mostram que o CLA trans-10, cis-12 reduz o acúmulo de lípides nos embriões pela redução nos níveis dos transcritos do gene 1-acilglicerol-3-fosfato o-aciltransferase 1 sem afetar a qualidade do embrião. Adicionalmente, este ácido graxo aumenta a taxa de re-expansão, no entanto, não melhora a taxa de eclosão.
Supplementation of conjugated linoleic acid trans-10, cis-10 in the culture medium, represents an important alternative to increasing the survival of embryos after cryopreservation. However the addition of culture media with CLA trans-10, cis-12 without antioxidant may increase the apoptotic rate. The aim of this study was to evaluate the effect of adding CLA trans-10, cis-12 in vitro culture of embryos without antioxidant. Bovine zygotes (n = 1,694) were divided into two treatments: (T1) control group, zygotes cultured in CR2aa medium supplemented with fetal calf serum (n = 815), (T2) zygotes cultured in CR2aa medium supplemented with fetal calf serum plus 100 µM CLA trans-10, cis-12. Embryos were evaluated for development, amount of lipids and cryotolerance. Transcripts of messenger RNA (mRNA) of selected genes were measured by real time PCR. Supplementation of CLA trans-10, cis-12 did not significantly affect the blastocyst rate (31.8% and 34.1% T1 and T2, respectively, p = 0,20) and the mRNA level of genes related to cell stress, apoptosis and de novo synthesis of fatty acid . Lipids and transcripts of the mRNA of the gene 1-acilglicerol-3-phosphate o-acyltransferase 1 enzyme related to the synthesis of triglycerides were significantly reduced in embryos cultured in the presence of CLA trans-10, cis-12 in comparison the control group. Had increased rate re-expansion of blastocysts cultured in the presence of CLA trans-10, cis-12, after thawing (34.4 and 56.3% for T1 and T2, respectively p = 0,002). This difference did not persist in the hatching rate (14.0 and 16.5% for T1 and T2, respectively, P = 0,62). These results show that the CLA trans-10, cis-12 reduces the accumulation of lipids in the embryos by reducing the levels of gene transcripts acilglicerol-1-3-phosphate oacyltransferase 1 without affecting the quality of the embryo. Additionally, this fatty acid increases the rate re-expansion, but does not improve the hatching rate.
Gul, Fatma. « Development Of An Oligonucleotide Based Sandwich Array Platform For The Detection Of Transgenic Elements From Plant Sources Using Label-free Pcr Products ». Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/12612659/index.pdf.
Texte intégralHerrmann, Simon [Verfasser], et Matthias [Akademischer Betreuer] Ebert. « Multiplex-PCR and deep sequencing for mutation detection in circulating cell-free DNA of colorectal cancer patients / Simon Herrmann ; Betreuer : Matthias Ebert ». Heidelberg : Universitätsbibliothek Heidelberg, 2021. http://d-nb.info/1234987856/34.
Texte intégralBerg, Emily Katherine. « Thermodynamics of λ-PCR Primer Design and Effective Ribosome Binding Sites ». Thesis, Virginia Tech, 2019. http://hdl.handle.net/10919/89900.
Texte intégralMaster of Science
Recombinant DNA technology has been used to genetically enhance organisms to produce greater amounts of a product already made by the organism or to make an organism synthesize a new product. Genes are commonly modified in organisms using cloning practices which typically involves inserting a target gene into a plasmid and transforming the plasmid into the organism of interest. A new cloning process developed in the Senger lab, λ-PCR, improves the cloning process compared to other methods due to its use of relatively inexpensive materials and high efficiency. A primary goal of this study was to develop a procedure for λ-PCR primer design that allows for accurate use of the cloning method. Additionally, this study investigated the use of synthetic ribosome binding sites to control and improve expression of proteins cloned into an organism. Ribosome binding sites are sequences located upstream of the gene that increase the molecule’s affinity for the rRNA sequence on the ribosome, bind to the ribosome just upstream of the beginning of the gene, and initiate expression of the gene. Tools have been developed that create synthetic ribosome binding sites designed to produce specific amounts of protein. For example, the tools can increase or decrease expression of a gene depending on the application. These tools, the Salis Lab RBS Calculator and NUPACK, were used to design and evaluate the effects of the synthetic ribosome binding sites. Additionally, a new method was created to design synthetic ribosome binding sites since the methods used during the design process yielded inaccuracies. Each strain of E. coli contained the same gene, a cyan fluorescent protein (CFP), but had different RBS sequences located upstream of the gene. Expression of CFP was controlled via induction, meaning the addition of a particular molecule, IPTG in this system, triggered expression of CFP. Each of the CFP strains were tested with a variety of v conditions in order to find the conditions most suitable for protein expression; the variables tested include: induction time, IPTG (inducer) concentration, and temperature. Media was also tested for the cell-free systems, meaning the strains were grown overnight for 18 hours and lysed, a process where the cell membrane is broken in order to utilize the cell’s components for protein expression; the cell lysate was resuspended in new media for the experiments. ANOVA and multiple linear regression revealed IPTG concentration, induction time, and media to be significant factors impacting protein expression. This analysis also showed each CFP strain did not perform as the RBS Calculator predicted. Modeling each strain’s CFP expression using the RBS-rRNA binding strengths and secondary structures present in the RBS allowed for the creation of a new model for predicting and designing RBS sequences.
Tanniche, Imen. « New Methods of DNA Assembly, Gene Regulation with a Synthetic sRNA, and Cyanobacterium Phenotype Monitoring with Raman Spectroscopy ». Diss., Virginia Tech, 2019. http://hdl.handle.net/10919/100954.
Texte intégralDoctor of Philosophy
Periyannan, Rajeswari Prem Kumar. « Droplet microfluidics for single cell and nucleic acid analysis ». Doctoral thesis, KTH, Proteomik och nanobioteknologi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-192668.
Texte intégralQC 20160926
Wuttig, Daniela. « Identifizierung metastasierungsassoziierter molekularer Faktoren durch genomweite Expressionsanalysen an pulmonalen Metastasen und Primärtumoren des klarzelligen Nierenzellkarzinoms ». Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-63743.
Texte intégralPatients with clear cell renal cell carcinoma (ccRCC) have an extremely poor prognosis due to their high risk of metastases. Currently used clinico-patological parameters are insufficient for reliable prediction of metastatic risk and disease free survival (DFS) after surgical resection of the primary tumor. Molecular markers are strongly needed to improve outcome prediction, and thus to optimize the follow up and treatment schedule for patients with ccRCC. To identify genes which are suitable for the prediction of metastatic risk and DFS, genome-wide expression analyses were performed on pulmonary metastases (n = 24) and primary tumors (n = 24) obtained from patients with ccRCC. Tumor-intrinsic DFS-associated expression patterns were observed by comparing subgroups of metastases, which had developed within different DFS as well as primary tumors, which had caused metastases after different DFS. Furthermore, genes differentially expressed in primary tumors, which caused macroscopic metastases and tumors, which did not were identified. The differential expression of genes with a potential function in metastatic spread, which has in part been identified in independent published microarray studies as well, were validated by quantitative polymerase chain reaction (qPCR). Moreover, an independent prognostic impact on the survival of ccRCC patients was observed for the EDNRB und the PECAM1 gene expression (qPCR; n = 86) as well as for the TSPAN7 protein level (immunohistochemistry on tissue microarrays; n = 106). Primary tumors of patients with favourable clinico-pathological parameters (TNMI/II, G1/2, V0, N0/M0) showed a significantly higher EDNRB und PECAM1 gene expression than those with unfavorable parameters. TSPAN7 was predominantly detected in blood vessels of ccRCC tissues. In patients with favourable clinico-pathological parameters (pT1/2, TNMI/II, N0) a significantly higher number of TSPAN7-positive vessels was observed. Using survival analyses, a significantly longer DFS was observed for patients with a high compared to those with a low EDNRB expression as well as for patients with TSPAN7-positive vessels in both cores compared to no or one of the both cores investigated on tissue microarrays. A significantly longer TSS was observed for patients with a high EDNRB or PECAM1 expression as well as for patients with TSPAN7-positive vessles in both tissue cores investigated. Furthermore, EDNRB was an independent prognostic factor for the DFS of the patients; EDNRB, PECAM and TSPAN7 had an independent prognostic impact on the TSS. Therefore, these molecular markers are suitable to improve the accuracy of outcome prediction based on clinico-pathological parameters in ccRCC. For the prediction of DFS and metastatic risk EDNRB is particularly interesting
Chapitres de livres sur le sujet "PCR-free"
Gudkov, Anatoly T., et Kirill A. Martemyanov. « Direct Expression of PCR Products in Cell-Free Translation Systems ». Dans Cell-Free Translation Systems, 61–66. Berlin, Heidelberg : Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-59379-6_5.
Texte intégralHoffmann, Thomas, Cordula Nemetz, Regina Schweizer, Wolfgang Mutter et Manfred Watzele. « High-Level Cell-Free Protein Expression from PCR-Generated DNA Templates ». Dans Cell-Free Translation Systems, 203–10. Berlin, Heidelberg : Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-59379-6_19.
Texte intégralWadle, Simon, Stefanie Rubenwolf, Michael Lehnert, Bernd Faltin, Manfred Weidmann, Frank Hufert, Roland Zengerle et Felix von Stetten. « Mediator Probe PCR : Detection of Real-Time PCR by Label-Free Probes and a Universal Fluorogenic Reporter ». Dans Methods in Molecular Biology, 55–73. New York, NY : Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0733-5_6.
Texte intégralMiura, Fumihito, et Takashi Ito. « Post-Bisulfite Adaptor Tagging for PCR-Free Whole-Genome Bisulfite Sequencing ». Dans Methods in Molecular Biology, 123–36. New York, NY : Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7481-8_7.
Texte intégralSigalotti, Luca, Alessia Covre, Francesca Colizzi et Elisabetta Fratta. « Quantitative Methylation-Specific PCR : A Simple Method for Studying Epigenetic Modifications of Cell-Free DNA ». Dans Cell-free DNA as Diagnostic Markers, 137–62. New York, NY : Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8973-7_11.
Texte intégralPodlesniy, Petar, et Ramon Trullas. « Biomarkers in Cerebrospinal Fluid : Analysis of Cell-Free Circulating Mitochondrial DNA by Digital PCR ». Dans Methods in Molecular Biology, 111–26. New York, NY : Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7778-9_7.
Texte intégralWatzele, Manfred, C. Nemetz, W. Obermeier, A. Seidl et B. Buchberger. « High-Throughput Expression PCR Used to Systematically Investigate Regulation of Translation Initiation in an E. coli Cell-Free Expression System ». Dans Cell-Free Protein Expression, 25–34. Berlin, Heidelberg : Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-59337-6_4.
Texte intégralWhale, Alexandra S., Ana Fernandez-Gonzalez, Alice Gutteridge et Alison S. Devonshire. « Control Materials and Digital PCR Methods for Evaluation of Circulating Cell-Free DNA Extractions from Plasma ». Dans Methods in Molecular Biology, 45–65. New York, NY : Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7778-9_4.
Texte intégralCortès, Sandra, Fatima-Ezzahra Hibti, Frydman Chiraz et Safia Ezzine. « High-Throughput E. coli Cell-Free Expression : From PCR Product Design to Functional Validation of GPCR ». Dans Methods in Molecular Biology, 261–79. New York, NY : Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9624-7_12.
Texte intégralOchert, A., M. J. Slomka, J. Ellis et C. G. Teo. « Use of Chelex 100TM in the Extraction of Viruses from Diverse Cell-Free Clinical Samples for PCR ». Dans Methods in DNA Amplification, 47–53. Boston, MA : Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2530-1_6.
Texte intégralActes de conférences sur le sujet "PCR-free"
Yi-Shao Liu, Padmapriya P. Banada, Arun K. Bhunia et Rashid Bashir. « Label free detection of PCR amplification ». Dans 2008 IEEE Sensors. IEEE, 2008. http://dx.doi.org/10.1109/icsens.2008.4716498.
Texte intégralSatsanarukkit, Penvipha, Hsiwen Lo et Yu Chong Tai. « A free-standing and flexible parylene PCR device ». Dans 2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS). IEEE, 2012. http://dx.doi.org/10.1109/nems.2012.6196743.
Texte intégralJiang, Li, Zhengda Lu, Matthew Mancuso et David Erickson. « Solar-thermally driven PCR for power-free diagnostics ». Dans CLEO : Applications and Technology. Washington, D.C. : OSA, 2013. http://dx.doi.org/10.1364/cleo_at.2013.ath4n.5.
Texte intégralSatsanarukkit, P., H. Lo, Q. Quach et Y. C. Tai. « ON-CHIP PCR WITH FREE-STANDING PARYLENE CHANNEL ». Dans 2010 Solid-State, Actuators, and Microsystems Workshop. San Diego : Transducer Research Foundation, 2010. http://dx.doi.org/10.31438/trf.hh2010.118.
Texte intégralHuw, Ling-Yuh, Jill Spoerke, Rajesh Patel, Weiqun Liu, Rajiv Raja, Lukas Amler, Garret Hampton, Elizabeth Punnoose et Mark Lackner. « Abstract 3180 : Mutation detection in circulating free DNA using mutant-enriched PCR and digital PCR ». Dans Proceedings : AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011 ; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-3180.
Texte intégralAli, Md Eaqub, Uda Hashim, Md Fazul Bari et Thakra S. Dhahi. « Colorimetric sensor for label free detection of porcine PCR product ». Dans 2010 International Conference on Enabling Science and Nanotechnology (ESciNano). IEEE, 2010. http://dx.doi.org/10.1109/escinano.2010.5700934.
Texte intégralSayers, Michael B., et Tara M. Dalton. « A Novel Contamination Free Two Temperature Continuous Flow Polymerase Chain Reactor ». Dans ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-43055.
Texte intégralZhang, Rong, Jian Qin, Hao Tian, Weihua Si, Taihong Wang et Zewen Liu. « Study on DNA electrochemical behavior for label-free micro PCR application ». Dans 2011 IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS). IEEE, 2011. http://dx.doi.org/10.1109/nems.2011.6017512.
Texte intégralCulha, Mustafa, Omer F. Karatas, Omer Aydin, Mehmet Kahraman, Kemal Keseroğlu, Ismail Sayin et Omer F. Bayrak. « Toward PCR-free mutation detection based on surface-enhanced Raman scattering ». Dans SPIE BiOS : Biomedical Optics, sous la direction de Tuan Vo-Dinh et Joseph R. Lakowicz. SPIE, 2009. http://dx.doi.org/10.1117/12.808267.
Texte intégralDaly, John, et Mark Davies. « A Quantitative Free Convection DNA Amplifier ». Dans ASME/JSME 2007 Thermal Engineering Heat Transfer Summer Conference collocated with the ASME 2007 InterPACK Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ht2007-32381.
Texte intégralRapports d'organisations sur le sujet "PCR-free"
Manulis, Shulamit, Christine D. Smart, Isaac Barash, Guido Sessa et Harvey C. Hoch. Molecular Interactions of Clavibacter michiganensis subsp. michiganensis with Tomato. United States Department of Agriculture, janvier 2011. http://dx.doi.org/10.32747/2011.7697113.bard.
Texte intégralJordan, Ramon L., Abed Gera, Hei-Ti Hsu, Andre Franck et Gad Loebenstein. Detection and Diagnosis of Virus Diseases of Pelargonium. United States Department of Agriculture, juillet 1994. http://dx.doi.org/10.32747/1994.7568793.bard.
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