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Artykuły w czasopismach na temat "Molecular marker"
Soriano, Jose Miguel. "Molecular Marker Technology for Crop Improvement". Agronomy 10, nr 10 (24.09.2020): 1462. http://dx.doi.org/10.3390/agronomy10101462.
Pełny tekst źródłaBenchimol-Reis, Luciana L. "Molecular Markers in Plant Breeding". Journal of Agricultural Science 15, nr 3 (15.02.2023): 58. http://dx.doi.org/10.5539/jas.v15n3p58.
Pełny tekst źródłaLee, Tong Geon, Reza Shekasteband, Naama Menda, Lukas A. Mueller i Samuel F. Hutton. "Molecular Markers to Select for the j-2–mediated Jointless Pedicel in Tomato". HortScience 53, nr 2 (luty 2018): 153–58. http://dx.doi.org/10.21273/hortsci12628-17.
Pełny tekst źródłaStalker, H. T., i L. G. Mozingo. "Molecular Markers of Arachis and Marker-Assisted Selection". Peanut Science 28, nr 2 (1.01.2001): 117–23. http://dx.doi.org/10.3146/i0095-3679-28-2-13.
Pełny tekst źródłaChiu, Sung Kay, Ming Hua Hsieh i Chi Meng Tzeng. "Unique marker finder algorithm generates molecular diagnostic markers". International Journal of Bioinformatics Research and Applications 7, nr 1 (2011): 24. http://dx.doi.org/10.1504/ijbra.2011.039168.
Pełny tekst źródłaSalava, J., Y. Wang, B. Krška, J. Polák, P. Komínek, R. W. Miller, W. M. Dowler, G. L. Reighard i A. G. Abbott. "Molecular genetic mapping in apricot". Czech Journal of Genetics and Plant Breeding 38, No. 2 (30.07.2012): 65–68. http://dx.doi.org/10.17221/6113-cjgpb.
Pełny tekst źródłaTeneva, A., i M. P. Petrovic. "Application of molecular markers in livestock improvement". Biotehnologija u stocarstvu 26, nr 3-4 (2010): 135–54. http://dx.doi.org/10.2298/bah1004135t.
Pełny tekst źródłaSurma, Marian. "Molecular Marker of Tumours". Journal of Cancer Therapy 07, nr 10 (2016): 675–79. http://dx.doi.org/10.4236/jct.2016.710070.
Pełny tekst źródłaKoepke, John A. "Molecular marker test standardization". Cancer 69, S6 (15.03.1992): 1578–81. http://dx.doi.org/10.1002/1097-0142(19920315)69:6+<1578::aid-cncr2820691312>3.0.co;2-k.
Pełny tekst źródłaKhatoon, Arifa, Sumeet Verma, Gayatri Wadiye i Anuprita Zore. "Molecular markers and their potentials". International Journal of Bioassays 5, nr 01 (1.01.2016): 4706. http://dx.doi.org/10.21746/ijbio.2016.01.003.
Pełny tekst źródłaRozprawy doktorskie na temat "Molecular marker"
Bitalo, Daphne Nyachaki. "Implementation of molecular markers for triticale cultivar identification and marker-assisted selection". Thesis, Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/71670.
Pełny tekst źródłaTriticale is an amphidiploid that consists of wheat (A and B) and rye (R) genomes. This cereal is fast becoming important on a commercial basis and warrants further assessment for the better management and breeding of the hybrid. The assessment of the genetic diversity among the wheat and rye genomes within triticale can be obtained by using molecular markers developed in both donor genomes. Simple sequence repeats markers (SSRs) and amplified fragment length markers (AFLPs) have been previously used to assess the genetic diversity among triticale lines. SSRs are highly polymorphic markers that are abundant and which have been shown to be highly transferable between species in previous studies while AFLP markers are known to generate plenty of data as they cover so many loci. Thus, the aim of this study was to develop a marker system suitable to assess the genetic diversity and relationships of advanced breeding material (and cultivars) of the Stellenbosch University’s Plant Breeding Laboratory (SU-PBL). Therefore, both AFLP and SSR markers were initially analysed using eight triticale cultivars (with known pedigrees) to facilitate cultivar identification. Fourty-two AFLP primer combinations and 86 SSR markers were used to assess the genetic diversity among the Elite triticale cultivars. The AFLP primer combinations generated under average polymorphism information content (PIC) values. Furthermore, these markers generated neighbour-joining (NJ) and unweighted pair group method with arithmetic average (UPGMA) dendograms that displayed relationships that did not correspond with the available pedigree information. Therefore, this marker system was found not to be suitable. A set of 86 SSRs previously identified in both wheat and rye, was used to test the genetic diversity among the eight cultivars. The markers developed in wheat achieved 84% transferability while those developed in rye achieved 79.3% transferability. A subset of SSR markers was able to distinguish the cultivars, and correctly identify them by generating NJ and UPGMA dendograms that exhibited relationships that corroborated the available pedigree data. This panel of markers was therefore chosen as the most suitable for the assessment of the advanced breeding material. The panel of seven SSR markers was optimised for semi-automated analysis and was used to screen and detect the genetic diversity among 306 triticale entries in the F6, Senior and Elite phases of the SU-PBL triticale breeding programme. An average PIC value of 0.65 was detected and moderate genetic variation was observed. NJ and UPGMA dendograms generated showed no clear groupings. However, the panel of markers managed to accurately identify all cultivars within the breeding program. The marker panel developed in this study is being used to routinely distinguish among the advanced breeding material within the SU-PBL triticale breeding programme and as a tool in molecular-assisted backcross.
von, Ruhland Christopher John. "The molecular basis of modern marker chemistry". Thesis, Cardiff University, 2011. http://orca.cf.ac.uk/22318/.
Pełny tekst źródłaJessup, Russell William. "Molecular tools for marker-assisted breeding of buffelgrass". Texas A&M University, 2005. http://hdl.handle.net/1969.1/2656.
Pełny tekst źródłaOzen, Ilknur. "Neurogenin2, a molecular marker of postnatal hippocampal neurogenesis". Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612424.
Pełny tekst źródłaSantos, Nadine Castelhano. "SARP2 as molecular marker of human sperm morphology". Master's thesis, Universidade de Aveiro, 2011. http://hdl.handle.net/10773/5800.
Pełny tekst źródłaA fosforilação proteica resulta de um equilíbrio entre fosfatases e quinases constituindo o principal regulador da maioria dos mecanismos existentes nos sistemas biológicos. Muitas doenças (cancro, diabetes, doenças neurodegenerativas, infertilidade, etc.) estão associadas à disrupção deste equilíbrio levando a mudanças nas actividades enzimáticas das proteínas fostatase e quinase. A proteína fosfatase 1 (PP1) é a principal fosfatase serina/treonina sendo ubíqua e altamente conservada nos eucariotas. A PP1 controla várias funções, tais como, a divisão celular, a transcrição, a neurotransmissão, a mobilidade dos espermatozóides, entre outras. A fosforilação proteica é uma das formas de os espermatozóides adquirirem funcionalidade, sendo a proteína PP1γ2 a isoforma mais fortemente enriquecida. Assim, no interior do espermatozóide podemos encontrar a PP1γ2 associada ao comprimento total da cauda e à região equatorial da cabeça, sugerindo uma possível função na mobilidade e reacção acrossómica, respectivamente. Existem inúmeras proteínas que interagem com a PP1γ2 que têm vindo a contribuir para a compreensão do seu papel nas funções fisiológicas do espermatozóide. Apesar de existirem outros, nesta tese, o complexo que serviu de ponto de partida foi o complexo SARP2/PP1γ2. Este complexo inclui uma nova proteína derivada de splicing, primeiramente descrita por Browne e os seus colaboradores em 2007, contendo três isoformas. Nesta tese foi usada a isoforma SARP2. O complexo foi encontrado fortemente enriquecido em espermatozóides e esta descoberta levou a estudos futuros com vista a descobrir a sua função fisiológica no espermatozóide. Usando a proteína SARP2 como um possível marcador molecular procurou-se verificar se era possível distinguir os espermatozóides em normais ou anormais. Considerando a actual necessidade em desenvolver novas técnicas de diagnóstico da infertilidade masculina, a descoberta de biomarcadores pode apresentar uma possível via, especialmente devido à perda de valor da avaliação dos parâmetros de um espermograma. No presente trabalho descobriu-se uma localização sub-celular no espermatozóide diferente da descrita anteriormente. O padrão de expressão da SARP2 é muito variável existindo catorze padrões diferentes do padrão normal encontrado. Contudo não foi possível confirmar com total certeza de que tínhamos um putativo marcador molecular. O presente trabalho fornece dados suficientes para que no futuro se possa realizar um plano experimental optimizado, com mais voluntários, representativo da população Portuguesa. Por fim, é necessário complementar o estudo com testes paralelos (fragmentação do DNA, ROS, etc.) que permitam avaliar a normalidade ou não de um espermatozóide em contraponto com a observada no estudo.
Protein phosphorylation, is the result of a balance between phosphatases and kinases being the key regulator for the major mechanisms in biological systems. Many diseases (cancer, diabetes, neurodegenerative conditions, infertility, etc.) are associated to the disruption of this balance leading to changes in the activities of both kinases and phosphatases enzymes. Protein phosphatase 1 (PP1) is a major serine/threonine phosphatase, ubiquitous and conserved in eukaryotes. PP1 controls a variety of functions, such as, cell division, transcription, neurotransmission, sperm motility, among others. Protein phosphorylation is one of the ways by which spermatozoa acquire functionality; being PP1γ2 a sperm enriched protein. Moreover, within spermatozoa PP1γ2 is present along the entire length of the tail and equatorial region of the head, suggesting a role in sperm motility and acrossome reaction, respectively. There are several interacting proteins of PP1γ2 which are leading to a revelation of its role in sperm functions. Although there are others, in this thesis, the complex that was the leading point of the study was the new complex SARP2/PP1γ2. This complex includes a new spliced protein firstly described by Browne and co-workers in 2007, which has three different isoforms. In this thesis SARP2 was the isoform used. The complex was found to be enriched in sperm, and this discovery lead to further studies on the possible role of this complex in sperm functions. The relevance of using SARP2 as a putative molecular marker to distinguish normal and abnormal spermatozoa was studied. Since nowadays there is a urgent need to change the way in which men infertility is being diagnosed, especially by the use of the traditional semen parameters evaluated in a spermogram, the biomarker discovery could be a way. In this thesis it was discovered a subcellular localization within human spermatozoa different from the one described before. The expression pattern of SARP2 is very variable; there are fourteen other patterns besides the normal one. Although, it was not possible to confirm with certain that we had a putative molecular marker. The present study gave enough data to proceed in the future, with the elaboration of an optimized experimental plan using more volunteers, to get a representative sample of the Portuguese population. Finally, it is necessary to complement this study with parallel tests (DNA fragmentation, ROS, etc) to ascertain if having a spermatozoon classified as normal, according to our study, is always synonymous of having a normal spermatozoon.
Liu, Kejun. "Software and Methods for Analyzing Molecular Genetic Marker Data". NCSU, 2003. http://www.lib.ncsu.edu/theses/available/etd-07182003-122001/.
Pełny tekst źródłaBerry, Simon. "Molecular marker analysis of cultivated sunflower (Helianthus annus L.)". Thesis, University of Reading, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301959.
Pełny tekst źródłaChani, Eduard. "Molecular marker analysis of a segregating monoploid potato family". Diss., Virginia Tech, 1998. http://hdl.handle.net/10919/29792.
Pełny tekst źródłaPh. D.
Mills, Claire A. "Molecular and non-molecular approaches to creating marker-free transgenic wheat (Triticum aestivum L.) /". [S.l.] : [s.n.], 2000. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=13687.
Pełny tekst źródłaJung, Renata. "Identification of Molecular Markers for Marker-Assisted Selection of Malting Quality and Associated Traits in Barley". Diss., North Dakota State University, 2015. http://hdl.handle.net/10365/25241.
Pełny tekst źródłaAmerican Malting Barley Association
Książki na temat "Molecular marker"
Swapna, M. Molecular marker applications for sugar content in sugarcane. New York: Springer, 2012.
Znajdź pełny tekst źródłaH, Lörz, i Wenzel Gerhard, red. Molecular marker systems in plant breeding and crop improvement. Berlin: Springer, 2008.
Znajdź pełny tekst źródłaLörz, Horst, i Gerhard Wenzel, red. Molecular Marker Systems in Plant Breeding and Crop Improvement. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b137756.
Pełny tekst źródłaSwapna, M., i Sangeeta Srivastava. Molecular Marker Applications for Improving Sugar Content in Sugarcane. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-2257-0.
Pełny tekst źródłaH, Lörz, i Wenzel Gerhard, red. Molecular marker systems in plant breeding and crop improvement. Berlin: Springer, 2005.
Znajdź pełny tekst źródłaH, Augenlicht Leonard, red. Cell and molecular biology of colon cancer. Boca Raton, Fla: CRC Press, 1989.
Znajdź pełny tekst źródłaTian, Jichun, Zhiying DENG, Kunpu Zhang, Haixia Yu i Xiaoling Jiang. Genetic Analyses of Wheat and Molecular Marker-Assisted Breeding, Volume 1. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-7390-4.
Pełny tekst źródłaTian, Jichun, Jiansheng Chen, Guangfeng Chen, Peng Wu, Han Zhang i Yong Zhao. Genetic Analyses of Wheat and Molecular Marker-Assisted Breeding, Volume 2. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-7447-5.
Pełny tekst źródłaSvensson, Ann-Cathrin. Molecular analyses of human endogenous retrovirus ERV9: Marker for HLA-DR haplotype evolution. Uppsala: Sveriges Lantbruksuniversitet, 1996.
Znajdź pełny tekst źródłaM, Gratzl, i Langley Keith, red. Markers for neural and endocrine cells: Molecular and cell biology, diagnostic applications. Weinheim (Federal Republic of Germany): VCH, 1990.
Znajdź pełny tekst źródłaCzęści książek na temat "Molecular marker"
Lai, Kaitao, Michał Tadeusz Lorenc i David Edwards. "Molecular Marker Databases". W Methods in Molecular Biology, 49–62. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1966-6_4.
Pełny tekst źródłaBrar, Darshan S. "Molecular Marker Assisted Breeding". W Molecular Techniques in Crop Improvement, 55–83. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-017-2356-5_3.
Pełny tekst źródłaYoon, Jae Bok, Soon-Wook Kwon, Tae-Ho Ham, Sunggil Kim, Michael Thomson, Sherry Lou Hechanova, Kshirod K. Jena i Younghoon Park. "Marker-Assisted Breeding". W Current Technologies in Plant Molecular Breeding, 95–144. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-9996-6_4.
Pełny tekst źródłaHayward, Alice C., Reece Tollenaere, Jessica Dalton-Morgan i Jacqueline Batley. "Molecular Marker Applications in Plants". W Methods in Molecular Biology, 13–27. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1966-6_2.
Pełny tekst źródłaEbinuma, Hiroyasu, i Kazuya Nanto. "Marker-Free Targeted Transformation". W Molecular Techniques in Crop Improvement, 527–43. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2967-6_22.
Pełny tekst źródłaSexton, Timothy R., i Frances M. Shapter. "Amplicon Sequencing for Marker Discovery". W Molecular Markers in Plants, 35–56. Oxford, UK: Blackwell Publishing Ltd., 2012. http://dx.doi.org/10.1002/9781118473023.ch3.
Pełny tekst źródłaGillies, Susan. "Transcriptome Sequencing for Marker Discovery". W Molecular Markers in Plants, 57–66. Oxford, UK: Blackwell Publishing Ltd., 2012. http://dx.doi.org/10.1002/9781118473023.ch4.
Pełny tekst źródłaSimeone, Ester, Antonio M. Grimaldi i Paolo A. Ascierto. "Marker Utility for Combination Therapy". W Methods in Molecular Biology, 97–115. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-727-3_7.
Pełny tekst źródłaRajendrakumar, P. "Molecular Marker Development Using Bioinformatic Tools". W Sorghum Molecular Breeding, 179–95. New Delhi: Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2422-8_8.
Pełny tekst źródłaScharnagl, Hubert, Winfried März, Markus Böhm, Thomas A. Luger, Federico Fracassi, Alessia Diana, Thomas Frieling i in. "Additional Marker Chromosome 15". W Encyclopedia of Molecular Mechanisms of Disease, 32. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8982.
Pełny tekst źródłaStreszczenia konferencji na temat "Molecular marker"
Wang, Xiaojia, Zhihui Wang, Siyu Zhang, Jundou Liu i Xun Wang. "Screening citrus SSR molecular marker primers". W 2018 7th International Conference on Energy and Environmental Protection (ICEEP 2018). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/iceep-18.2018.311.
Pełny tekst źródłaKnopf, A., A. Pickhard, K. Fritsche i K. El Shabrawi. "TIMP1 as molecular marker in distant metastatic outgrowth". W Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1710970.
Pełny tekst źródłaQi, Shuhong, Lisen Lu i Zhihong Zhang. "ALDH3A2 as a potential molecular marker for nasopharyngeal carcinoma". W Biophotonics and Immune Responses XIV, redaktor Wei R. Chen. SPIE, 2019. http://dx.doi.org/10.1117/12.2506121.
Pełny tekst źródłaListanto, Edy, Ahmad Warsun, Ahmad Dadang, Eny Ida Riyanti, Saptowo Jumali Pardal, Sustiprijatno i Mastur. "Agroforensic, a new emerging study using molecular marker technique". W THE SECOND INTERNATIONAL CONFERENCE ON GENETIC RESOURCES AND BIOTECHNOLOGY: Harnessing Technology for Conservation and Sustainable Use of Genetic Resources for Food and Agriculture. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0075164.
Pełny tekst źródłaWang, Shiying, F. William Mauldin, Sunil Unnikrishnan, Alexander L. Klibanov i John A. Hossack. "Ultrasound quantification of molecular marker concentration in large blood vessels". W 2014 IEEE International Ultrasonics Symposium (IUS). IEEE, 2014. http://dx.doi.org/10.1109/ultsym.2014.0204.
Pełny tekst źródłaIuchi, Toshihiko, Sana Yokoi, Miki Ohira, Hajime Kageyama, Makiko Itami, Yuzo Hasegawa, Koichiro Kawasaki, Tsukasa Sakaida i Akira Nakagawara. "Abstract 4592: Sox8 as a molecular marker of oligodendroglial tumors". W Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-4592.
Pełny tekst źródłaYanmei, Wang, Wang Jiahui, Liu Zhen i Li Shirong. "Analysis of fine individual no-cones platanus acerifoliaby ISSR molecular marker". W 2011 International Conference on Human Health and Biomedical Engineering (HHBE). IEEE, 2011. http://dx.doi.org/10.1109/hhbe.2011.6028377.
Pełny tekst źródłaYu, Xiao-Ling, Ming-Wang Shi, Xiao-Jian Zhang, Zhi-Feng Xiang i Gang-Cai Wei. "Mathematical Relation between Types, Effect of Genes and Molecular Marker Genotype". W 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2009). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163031.
Pełny tekst źródłaLI, Xue-Bin, Xiaoling Yu, Zhifeng Xiang, Kun Zhao i Xiaojian Zhang. "Locating QTLs Based on Estimating Gene Effect by Molecular Marker Regression Model". W 2009 2nd International Conference on Biomedical Engineering and Informatics. IEEE, 2009. http://dx.doi.org/10.1109/bmei.2009.5305516.
Pełny tekst źródłaMahayu, Weda Makarti, i Taryono. "Coconut (Cocos nucifera L.) diversity in Indonesia based on SSR molecular marker". W 1ST INTERNATIONAL CONFERENCE ON BIOINFORMATICS, BIOTECHNOLOGY, AND BIOMEDICAL ENGINEERING (BIOMIC 2018). Author(s), 2019. http://dx.doi.org/10.1063/1.5098418.
Pełny tekst źródłaRaporty organizacyjne na temat "Molecular marker"
Mote, B. E., N. Deeb, O. Southwood i Max F. Rothschild. Using Molecular Marker Technology for Improvement in Sow Reproductive Longevity. Ames (Iowa): Iowa State University, styczeń 2005. http://dx.doi.org/10.31274/ans_air-180814-1069.
Pełny tekst źródłaRocheford, Torbert, Yaakov Tadmor, Robert Lambert i Nurit Katzir. Molecular Marker Mapping of Genes Enhancing Tocol and Carotenoid Composition of Maize Grain. United States Department of Agriculture, grudzień 1995. http://dx.doi.org/10.32747/1995.7571352.bard.
Pełny tekst źródłaLamont, Susan J., E. Dan Heller i Avigdor Cahaner. Prediction of Immunocompetence and Resistance to Disease by Using Molecular Markers of the Major Histocompatibility Complex. United States Department of Agriculture, wrzesień 1994. http://dx.doi.org/10.32747/1994.7568780.bard.
Pełny tekst źródłaJuvik, John A., Avri Bar Zur i Torbert R. Rocheford. Breeding for Quality in Vegetable Maize Using Linked Molecular Markers. United States Department of Agriculture, styczeń 1993. http://dx.doi.org/10.32747/1993.7568764.bard.
Pełny tekst źródłaGunter, L. E. Towards the Development of a Molecular Map in Switchgrass: I. Microsatellite Marker Development. Office of Scientific and Technical Information (OSTI), sierpień 2001. http://dx.doi.org/10.2172/788504.
Pełny tekst źródłaReisch, Bruce, Pinhas Spiegel-Roy, Norman Weeden, Gozal Ben-Hayyim i Jacques Beckmann. Genetic Analysis in vitis Using Molecular Markers. United States Department of Agriculture, kwiecień 1995. http://dx.doi.org/10.32747/1995.7613014.bard.
Pełny tekst źródłaSadka, Avi, Mikeal L. Roose i Yair Erner. Molecular Genetic Analysis of Citric Acid Accumulation in Citrus Fruit. United States Department of Agriculture, marzec 2001. http://dx.doi.org/10.32747/2001.7573071.bard.
Pełny tekst źródłaVeilleux, Richard E., Jossi Hillel, A. Raymond Miller i David Levy. Molecular Analysis by SSR of Genes Associated with Alkaloid Synthesis in a Segregating Monoploid Potato Family. United States Department of Agriculture, maj 1994. http://dx.doi.org/10.32747/1994.7570550.bard.
Pełny tekst źródłaBlum, Abraham, i Henry T. Nguyen. Molecular Tagging of Drought Resistance in Wheat: Osmotic Adjustment and Plant Productivity. United States Department of Agriculture, listopad 2002. http://dx.doi.org/10.32747/2002.7580672.bard.
Pełny tekst źródłaParan, Ilan, i Molly Jahn. Analysis of Quantitative Traits in Pepper Using Molecular Markers. United States Department of Agriculture, styczeń 2000. http://dx.doi.org/10.32747/2000.7570562.bard.
Pełny tekst źródła