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Artykuły w czasopismach na temat "Molecular markers"
Sorscher, Steve. "Molecular Markers of Molecular Markers". Journal of Clinical Oncology 37, nr 25 (1.09.2019): 2291. http://dx.doi.org/10.1200/jco.19.00746.
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 źródłaChesnokov, Yu V. "GENETIC MARKERS: COMPARATIVE CLASSIFICATION OF MOLECULAR MARKERS". Vegetable crops of Russia, nr 3 (25.07.2018): 11–15. http://dx.doi.org/10.18619/2072-9146-2018-3-11-15.
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 źródłaCalifano, J. "Molecular markers". Radiotherapy and Oncology 82 (luty 2007): S4. http://dx.doi.org/10.1016/s0167-8140(07)80015-6.
Pełny tekst źródłaDolanská, L., i V. Čurn. "Identification of white clover (Trifolium repens L.) cultivars using molecular markers". Plant, Soil and Environment 50, No. 3 (6.12.2011): 95–100. http://dx.doi.org/10.17221/4013-pse.
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 źródłaSzczechura, Wojciech, Mirosława Staniaszek i Hanna Habdas. "Tomato Molecular Markers". Vegetable Crops Research Bulletin 74, nr 1 (1.01.2011): 5–23. http://dx.doi.org/10.2478/v10032-011-0001-y.
Pełny tekst źródłaChinnappareddy, L. R. D., K. Khandagale, A. Chennareddy i V. G. Ramappa. "Molecular markers in the improvement of Allium crops". Czech Journal of Genetics and Plant Breeding 49, No. 4 (26.11.2013): 131–39. http://dx.doi.org/10.17221/111/2013-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 źródłaRozprawy doktorskie na temat "Molecular markers"
Cai, Na. "Molecular markers of stress". Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:95826e79-6ef0-4148-8478-5778994f97fc.
Pełny tekst źródłaPinto, Diana Maria de Figueiredo. "Molecular markers for diabetic nephropathy". Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15953.
Pełny tekst źródłaType 2 diabetes is one of the most common metabolic disorders in the world. Globally, the prevalence of this disorder is predicted to increase, along with the risk of developing diabetic related complications. One of those complications is diabetic nephropathy, defined by a progressive increase in proteinuria and a gradual decline in renal function. Approximately 25% to 30% of type 2 diabetic individuals develop this complication. However, its underlying genetic mechanisms remain unclear. Thus, the aim of this study is to contribute to the discovery of the genetic mechanisms involved in the development and progression of diabetic nephropathy, through the identification of relevant genetic variants in Portuguese type 2 diabetic individuals. The exomes of 36 Portuguese type 2 diabetic individuals were sequenced on the Ion ProtonTM Sequencer. From those individuals, 19 did not present diabetic nephropathy, being included in the control group, while the 17 individuals that presented the diabetic complication formed the case group. A statistical analysis was then performed to identify candidate common genetic variants, as well as genes accumulating rare variants that could be associated with diabetic nephropathy. From the search for common variants in the study population, the statistically significant (p-value ≤ 0.05) variants rs1051303 and rs1131620 in the LTBP4 gene, rs660339 in UCP2, rs2589156 in RPTOR, rs2304483 in the SLC12A3 gene and rs10169718 present in ARPC2, were considered as the most biologically relevant to the pathogenesis of diabetic nephropathy. The variants rs1051303 and rs1131620, as well as the variants rs660339 and rs2589156 were associated with protective effects in the development of the complication, while rs2304483 and rs10169718 were considered risk variants, being present in individuals with diagnosed diabetic nephropathy. In the rare variants approach, the genes with statistical significance (p-value ≤ 0.05) found, the STAB1 gene, accumulating 9 rare variants, and the CUX1 gene, accumulating 2 rare variants, were identified as the most relevant. Both genes were considered protective, with the accumulated rare variants mainly present in the group without the renal complication. The present study provides an initial analysis of the genetic evidence associated with the development and progression of diabetic nephropathy, and the results obtained may contribute to a deeper understanding of the genetic mechanisms associated with this diabetic complication.
A diabetes tipo 2 é um dos distúrbios metabólicos mais comuns no mundo. Globalmente, está previsto um aumento da sua prevalência, assim como um aumento do risco de desenvolver complicações associadas. Uma dessas complicações é a nefropatia diabética, definida pelo aumento progressivo de proteinúria e um declínio gradual da função renal. Aproximadamente 25% a 30% dos indivíduos com diabetes tipo 2 desenvolvem esta complicação. No entanto, os mecanismos genéticos associados permanecem por esclarecer. Posto isto, o objetivo deste estudo é contribuir para a identificação dos mecanismos envolvidos no desenvolvimento e progressão desta complicação, através da identificação de variantes genéticas relevantes, em indivíduos com diabetes tipo 2 na população portuguesa. Para isso, os exomas de 36 portugueses com diabetes tipo 2 foram sequenciados na plataforma Ion ProtonTM. Desses individuos, 19 não apresentavam nefropatia diabética, tendo sido incluídos no grupo de controlo, e os restantes 17 individuos, com a complicação diagnosticada, formaram o grupo dos casos. Uma análise estatística foi depois realizada para identificar, com base nas diferenças genéticas entre os dois grupos, variantes comuns, assim como genes que acumulam variantes raras candidatas, que podem explicar o risco acrescido ou diminuído para desenvolver a complicação. Na pesquisa das variantes comuns, as variantes rs1051303 e o rs1131620 no gene LTBP4, a variante rs660339 no UCP2, a variante rs2589156 no gene RPTOR, a variante rs2304483 no SLC12A3 e, por fim, a variante rs10169718 presente no gene ARPC2, foram, de todas aquelas consideradas estatisticamente significativas (p-value ≤ 0,05), as mais relevantes para a patogénese da nefropatia diabética. O rs1051303 e o rs1131620, assim como o rs660339 e o rs2589156, têm um efeito protetor, enquanto o rs2304483 e o rs10169718 foram considerados de risco, estando associados a indivíduos que sofrem da complicação referida. Pela abordagem utilizada para identificar as variantes raras, o gene STAB1, que acumula 9 variantes, e o gene CUX1, que acumula 2, foram, de todos os genes com significado estatístico (p-value ≤ 0,05), aqueles que se evidenciaram como sendo biologicamente relevantes. Ambos os genes foram considerados protetores, já que as suas variantes raras acumuladas estavam presentes maioritariamente nos indivíduos que não apresentam esta complicação renal. Este estudo providencia uma análise inicial das evidências genéticas associadas ao desenvolvimento e progressão da nefropatia diabética, podendo os seus reultados contribuir para uma melhor compreensão dos mecanismos genéticos que estão por detrás do seu surgimento.
Weigelt, Britta. "Molecular markers of breast cancer metastasis". [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2005. http://dare.uva.nl/document/88848.
Pełny tekst źródłaSwagell, Christopher Dean. "Molecular markers of obesity and diabetes". Thesis, Queensland University of Technology, 2007. https://eprints.qut.edu.au/35762/1/Christopher_Swagell_Thesis.pdf.
Pełny tekst źródłaBitalo, 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.
Valdman, Alexander. "Molecular genetic markers of prostate cancer development /". Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-618-9/.
Pełny tekst źródłaLarkin, Samantha. "Molecular characterisation of prostate cancer progression markers". Thesis, University of Portsmouth, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.511205.
Pełny tekst źródłaSteele, Katherine A. "Molecular markers in yellow rust of wheat". Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243712.
Pełny tekst źródłaHemmings, Karen Emily. "Cellular and molecular markers of oocyte quality". Thesis, University of Leeds, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.445945.
Pełny tekst źródłaLaird, Alexander. "Molecular prognostic markers in renal cell carcinoma". Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/17873.
Pełny tekst źródłaKsiążki na temat "Molecular markers"
Singh, Bhim Pratap, i Vijai Kumar Gupta, red. Molecular Markers in Mycology. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-34106-4.
Pełny tekst źródłaHenry, Robert J., red. Molecular Markers in Plants. Oxford, UK: Blackwell Publishing Ltd., 2012. http://dx.doi.org/10.1002/9781118473023.
Pełny tekst źródłaHenry, Robert J. Molecular markers in plant improvement. Hoboken, N.J: John Wiley & Sons, 2013.
Znajdź pełny tekst źródłaSrivastava, P. S., Alka Narula i Sheela Srivastava, red. Plant Biotechnology and Molecular Markers. Dordrecht: Kluwer Academic Publishers, 2005. http://dx.doi.org/10.1007/1-4020-3213-7.
Pełny tekst źródłaEganhouse, Robert P., red. Molecular Markers in Environmental Geochemistry. Washington, DC: American Chemical Society, 1997. http://dx.doi.org/10.1021/bk-1997-0671.
Pełny tekst źródła1948-, Eganhouse Robert P., American Chemical Society. Division of Environmental Chemistry., American Chemical Society. Division of Geochemistry. i American Chemical Society Meeting, red. Molecular markers in environmental geochemistry. Washington, DC: American Chemical Society, 1997.
Znajdź pełny tekst źródłaWunder, Jay S. Molecular markers for musculoskeletal sarcomas. Ottawa: National Library of Canada, 1990.
Znajdź pełny tekst źródłaS, Srivastava P., Narula Alka, Srivastava Sheela i Bhojwani S. S, red. Plant biotechnology and molecular markers. Boston: Kluwer Academic Publishers, 2004.
Znajdź pełny tekst źródłaCentre, World Agroforestry. Molecular markers for tropical trees. Nairobi, Kenya: World Agroforestry Centre, 2009.
Znajdź pełny tekst źródłaS, Hulka Barbara, Wilcosky Timothy C i Griffith Jack D, red. Biological markers in epidemiology. New York: Oxford University Press, 1990.
Znajdź pełny tekst źródłaCzęści książek na temat "Molecular markers"
Agrawal, Pavan Kumar, i Rahul Shrivastava. "Molecular Markers". W Advances in Biotechnology, 25–39. New Delhi: Springer India, 2013. http://dx.doi.org/10.1007/978-81-322-1554-7_3.
Pełny tekst źródłaMondal, Tapan Kumar. "Molecular Markers". W Breeding and Biotechnology of Tea and its Wild Species, 93–123. New Delhi: Springer India, 2014. http://dx.doi.org/10.1007/978-81-322-1704-6_6.
Pełny tekst źródłaMondal, Tapan Kumar. "Molecular Markers". W Tea: Genome and Genetics, 139–94. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-8868-6_6.
Pełny tekst źródłaSpangenberg, Germán, Zeng-Yu Wang i Ingo Potrykus. "Molecular Markers". W Monographs on Theoretical and Applied Genetics, 147–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72051-2_9.
Pełny tekst źródłaBetsy, C. Judith, i C. Siva. "Molecular Markers". W Fisheries Biotechnology and Bioinformatics, 141–51. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-6991-3_15.
Pełny tekst źródłaLivneh, O., i E. Vardi. "Molecular Genetic Markers". W Hybrid Cultivar Development, 201–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-07822-8_8.
Pełny tekst źródłaBahler, David. "Prognostic Markers". W Molecular Pathology Library, 65–72. Boston, MA: Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-5698-9_3.
Pełny tekst źródłaSienko, Anna, Timothy Craig Allen i Philip T. Cagle. "Prognostic Markers". W Molecular Pathology Library, 193–99. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-72430-0_18.
Pełny tekst źródłaJahoor, Ahmed. "RFLP Markers". W Molecular Tools for Screening Biodiversity, 229–36. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-009-0019-6_45.
Pełny tekst źródłaEoli, M., A. Di Stefano i G. Finocchiaro. "Molecular Markers of Gliomas". W Therapeutic Ribonucleic Acids in Brain Tumors, 157–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-00475-9_8.
Pełny tekst źródłaStreszczenia konferencji na temat "Molecular markers"
Gubenko, Marina, Lali Kogonia i Turna Ashkhatsava. "NEW MOLECULAR MARKERS OF GLIOBLASTOMA". W XVIII INTERNATIONAL INTERDISCIPLINARY CONGRESS NEUROSCIENCE FOR MEDICINE AND PSYCHOLOGY. LCC MAKS Press, 2022. http://dx.doi.org/10.29003/m2730.sudak.ns2022-18/110-111.
Pełny tekst źródłaSchmitz, Georg, Michal Mleczko i Monica Siepmann. "Retrieving multidimensional ultrasonic image information of molecular markers". W 2008 IEEE International Conference on Multimedia and Expo (ICME). IEEE, 2008. http://dx.doi.org/10.1109/icme.2008.4607488.
Pełny tekst źródłaIngram, Whitney. "Biomedical wellness monitoring system based upon molecular markers". W SPIE Defense, Security, and Sensing, redaktorzy Harold Szu i Liyi Dai. SPIE, 2012. http://dx.doi.org/10.1117/12.918838.
Pełny tekst źródłaMaral, A. R. S., C. M. R. Caridade, P. Albuquerque, M. V. Mendes i F. Tavares. "Automatic detection of molecular markers in digital images". W 2009 Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2009. http://dx.doi.org/10.1109/iembs.2009.5333807.
Pełny tekst źródłaКузьмина, Л. П., А. Г. Хотулева, М. М. Коляскина, Л. М. Безрукавникова i Н. А. Анварул. "Molecular genetic markers for assessing individual sensitivity to lead". W III International Scientific Forum "Health And Safety At The Workplace". Polikraft, 2019. http://dx.doi.org/10.31089/978-985-7153-76-3-2019-1-3-175-179.
Pełny tekst źródłaDesai, B., J. Mattson, H. Paintal, M. Nathan, M. Beaumont, M. Malinao, F. Shen i in. "Differential Cellular and Molecular Markers in Idiopathic Pulmonary Fibrosis." 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.a3488.
Pełny tekst źródłaSupari, Nurhaziqah, Yilmaz Kaya, Maral Biroudian i Muhammad Arshad Javed. "Molecular characterization of Malaysian rice cultivars using SSR markers". W PROCEEDINGS OF THE 2ND INTERNATIONAL CONFERENCE ON BIOSCIENCES AND MEDICAL ENGINEERING (ICBME2019): Towards innovative research and cross-disciplinary collaborations. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5125520.
Pełny tekst źródłaCherkasova, O., S. Kuznetsov, M. Konnikova, A. Rybak, D. Utkin i N. Nikolaev. "DETECTION OF GLIOMA MOLECULAR MARKERS BY TERAHERTZ NANOANTENNA SENSOR". W Terahertz and Microwave Radiation: Generation, Detection and Applications (ТЕRА-2023). Moscow: Our Style, 2023. http://dx.doi.org/10.59043/9785604953914_79.
Pełny tekst źródłaMohapatra, Monalisa, i Ashok K. Mishra. "Fluorescent molecular probes based on excited state prototropism". W Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications III. SPIE, 2011. http://dx.doi.org/10.1117/12.881132.
Pełny tekst źródłaAshley, H. W., i J. Fareed. "MOLECULAR MARKERS OF HEMOSTATIC ACTIVATION: COMPARISON OF PLASMA AND URINARY LEVELS". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643826.
Pełny tekst źródłaRaporty organizacyjne na temat "Molecular markers"
Olopade, Olufunmilayo I. Molecular Markers in Hereditary Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, październik 2001. http://dx.doi.org/10.21236/ada403325.
Pełny tekst źródłaThompson, Henry J. Modulation of Molecular Markers by CLA. Fort Belvoir, VA: Defense Technical Information Center, październik 1998. http://dx.doi.org/10.21236/ada366915.
Pełny tekst źródłaThompson, Henry J. Modulation of Molecular Markers by CLA. Fort Belvoir, VA: Defense Technical Information Center, październik 1996. http://dx.doi.org/10.21236/ada320113.
Pełny tekst źródłaOlopade, Olufunmilayo I. Molecular Markers in Hereditary Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, październik 2002. http://dx.doi.org/10.21236/ada412814.
Pełny tekst źródłaOlopade, Olufunmilayo I. Molecular Markers in Hereditary Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, październik 2003. http://dx.doi.org/10.21236/ada420426.
Pełny tekst źródłaRosen, Jeffrey M. Molecular Markers for Breast Cancer Susceptibility. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1997. http://dx.doi.org/10.21236/ada340575.
Pełny tekst źródłaThompson, Henry J. Modulation of Molecular Markers by CLA. Fort Belvoir, VA: Defense Technical Information Center, październik 1997. http://dx.doi.org/10.21236/ada346554.
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 źródłaShugart, L. R. Biological (molecular and cellular) markers of toxicity. Office of Scientific and Technical Information (OSTI), październik 1990. http://dx.doi.org/10.2172/6441197.
Pełny tekst źródłaRitter, Mark A. Molecular Markers and Prostate Cancer Radiation Response. Fort Belvoir, VA: Defense Technical Information Center, styczeń 2003. http://dx.doi.org/10.21236/ada415011.
Pełny tekst źródła