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Gotowe bibliografie tematyczne / Cytogenetic Variation

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Gotowa bibliografia na temat „Cytogenetic Variation”

Autor: Grafiati

Data publikacji: 5 czerwca 2025

Data aktualizacji: 1 sierpnia 2025

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Artykuły w czasopismach na temat "Cytogenetic Variation"

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Atli, Emine, Hakan Gurkan, Engin Atli, et al. "THE IMPORTANCE OF TARGETED NEXT-GENERATION SEQUENCING USAGE IN CYTOGENETICALLY NORMAL MYELOID MALIGNANCIES." Mediterranean Journal of Hematology and Infectious Diseases 13, no. 1 (2020): e2021013. http://dx.doi.org/10.4084/mjhid.2021.013.

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Advanced diagnostic methods give an advantage for the identification of the abnormalities in myeloid malignancies. Various researchers have shown the potential importance of genetic tests both before the onset of the disease and during the remission. Large testing panels prevents false negative results in myeloid malignancies. But the important question is how the results of conventional cytogenetic and molecular cytogenetic techniques can be merged together with NGS technologies. In this paper, we drew an algorithm for evaluation of the myeloid malignancies. In order to evaluate genetic abnor

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ABDULAZIZ, ABDUJABAR, and KIFLE DAGNE Dr. "A REVIEW ON CYTOGENETICAL STATUS OF PLANT-PARASITIC ROOTKNOT NEMATODE (Meloidogyne spp)." International Journal of Recent Research in Life Sciences 9, no. 2 (2022): 35–45. https://doi.org/10.5281/zenodo.6524808.

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<strong>Abstracts: </strong>Root‐knot nematodes (RKN), (<em>Meloidogyne</em> spp.) are obligate endoparasites of more than 3000 species of plants, which results in $80 billion worth of economic loss every year, worldwide. Considerable variation in ability to break crop resistance and to reproduce on different crop species is observed both between and within <em>Meloidogyne</em>. The main feature of plant-parasitic root-knot nematode is its potential host range encompassing more than 3,000 plant species. The adaptation of root-knot nematodes to its various environments of plant hosts

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Campbell, Lynda J., Stephen J. Farish, and Joanne S. White. "Seasonal Variation in New Adult Acute Myeloid Leukemia." Blood 104, no. 11 (2004): 3017. http://dx.doi.org/10.1182/blood.v104.11.3017.3017.

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Abstract Investigations into seasonal trends for the onset of leukemia have produced conflicting results. The majority of studies demonstrating seasonal variation have done so for childhood ALL and have suggested a role for an infectious agent. Few investigations have studied adult AML and none have looked at the potential differences between various AML subtypes. An infectious etiology for adult AML will more likely be reflected by cases that are truly de novo and that have not arisen by transformation from a pre-leukemic phase or from prior exposure to a carcinogenic agent. The Victorian Can

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Li, Ruzhong, David M. Stelly, and Norma L. Trolinder. "Cytogenetic abnormalities in cotton (Gossypium hirsutum L.) cell cultures." Genome 32, no. 6 (1989): 1128–34. http://dx.doi.org/10.1139/g89-566.

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High frequencies of somaclonal phenotypic and cytogenetic variation have been observed previously among regenerants from cotton (Gossypium hirsutum L., 2n = 4x = 52). In this study we endeavored to determine if cytogenetic abnormalities would be detectable in cotton cell cultures and if so, whether or not the observed abnormalities would parallel those expected on the basis of previous cytogenetic analyses of cotton somaclones. Paired samples from suspension cultures established from 21-month-old 'Coker 312' and 8-month-old 'Coker 315' calli were pretreated or not pretreated with colchicine to

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Linacero, R., and A. M. Vazquez. "Cytogenetic variation in rye regenerated plants and their progeny." Genome 35, no. 3 (1992): 428–30. http://dx.doi.org/10.1139/g92-063.

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Regenerated plants obtained from immature embryo-derived calluses of four cultivars of rye, as well as their progeny, were cytologically analyzed. Chromosome number modified plants were found among the regenerants. The progeny of apparently normal diploid regenerated plants was tested and in some cases chromosomally abnormal plants appeared. Equally, meiotic abnormalities were observed in some of the regenerated plants and their progenies. The cytological variations observed were inheritable and in some cases both types of abnormalities could be related. The nature of the variations is discuss

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Akkari, Yassmine M. N., Linda B. Baughn, Adrian M. Dubuc, et al. "Guiding the global evolution of cytogenetic testing for hematologic malignancies." Blood 139, no. 15 (2022): 2273–84. http://dx.doi.org/10.1182/blood.2021014309.

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Abstract Cytogenetics has long represented a critical component in the clinical evaluation of hematologic malignancies. Chromosome banding studies provide a simultaneous snapshot of genome-wide copy number and structural variation, which have been shown to drive tumorigenesis, define diseases, and guide treatment. Technological innovations in sequencing have ushered in our present-day clinical genomics era. With recent publications highlighting novel sequencing technologies as alternatives to conventional cytogenetic approaches, we, an international consortium of laboratory geneticists, pathol

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Spies, J. J., and G. E. Gibbs Russell. "Variation in important pasture grasses. II. Cytogenetic and reproductive variation." Journal of the Grassland Society of Southern Africa 5, no. 1 (1988): 22–25. http://dx.doi.org/10.1080/02566702.1988.9648104.

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Frana, Vitor André, Weferson Júnio da Graça, Éder André Gubiani, Jocicléia Thums Konerat, and Vladimir Pavan Margarido. "Evidence of the color pattern variation in populations of Gymnotus pantanal (Gymnotiformes) from three streams in the upper Paraná River basin, Brazil." Neotropical Ichthyology 9, no. 2 (2011): 343–50. http://dx.doi.org/10.1590/s1679-62252011005000013.

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Color pattern is an important character in the systematics and alpha-taxonomy of electric fishes of the genus Gymnotus. This paper presents evidence of color variation in populations of G. pantanal found in the streams Jacutinga and Pinheirinho, in the upper Paraná River basin, southern Brazil. Color variations were corroborated for morphological and cytogenetic data. Our results show the importance of integrating morphologic and cytogenetic data in the taxonomy of the Gymnotus species.

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GARCIA, L., M. PONSÀ, J. EGOZCUE, and M. GARCIA. "Cytogenetic variation in Ctenomys perrensi (Rodentia, Octodontidae)." Biological Journal of the Linnean Society 71, no. 4 (2000): 615–24. http://dx.doi.org/10.1111/j.1095-8312.2000.tb01281.x.

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Fouroutan, Parisa, Masoud Sheidai, and Fahimeh Koohdar. "The role of chromosomal rearrangements, polyploidy, and genome size variation in the diversity and ecological distribution of Asparagus L. species: a landscape cytogenetics meta-analysis approach." Caryologia 77, no. 2 (2024): 3–18. https://doi.org/10.36253/caryologia-2672.

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The Asparagus genus includes a group of plants with economic and medicinal importance. Although numerous cytogenetic and genetic studies have been conducted on Asparagus species, there are no reports on landscape genetics, landscape cytogenetics, or Asparagus cultivation in response to climate change. Therefore, we designed this study to answer the above-mentioned objectives. We performed a meta-analysis involving landscape genetic studies based on available cytogenetic data and reported DNA C-values for several Asparagus species from different countries. Additionally, species distribution mod

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Rozprawy doktorskie na temat "Cytogenetic Variation"

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Cavell, Jane Sarah. "Cytogenetic and RFLP analyses of somaclonal variation in Nicotiana tabacum." Thesis, University of Bath, 1989. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328517.

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Nascimento, Juliana 1982. "Análise da diversidade cariotípica e de homeologias cromossômicas dentre anuros da Amazônia do gênero Physalaemus (Anura, Leptodactylidade)." [s.n.], 2014. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317679.

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Orientador: Luciana Bolsoni Lourenço<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia<br>Made available in DSpace on 2018-08-26T03:48:33Z (GMT). No. of bitstreams: 1 Nascimento_Juliana_D.pdf: 2106853 bytes, checksum: f64fce074a208a02085fbde516c48f9c (MD5) Previous issue date: 2014<br>Resumo: Recentes análises filogenéticas e citogenéticas têm revelado grande diversidade dentre leiuperídeos do grupo Physalaemus cuvieri. O parafiletismo de P. cuvieri em relação a Physalaemus ephippifer foi inferido com base na análise de sequências de DNA, e linhagens reconhecidas

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Ke, Chien-Ying, and 柯見螢. "Using cytogenetic, RAPD markers, somatic embryogenesis to evaluate variation of Spathiphyllum cultivars." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/40408825954892658075.

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碩士<br>國立屏東科技大學<br>熱帶農業研究所<br>88<br>The purposes of this study are to evaluate genetic variation in Spathiphyllum germplasms based on morphological traits, RAPD markers, somatic embryogenesis and karyotype analysis. We examined morphological traits, such as leaf length, plant height and leaf numbers of 12 Spathiphyllum cultivars. The results showed that morphological traits were significantly different among cultivars. Both S. 'Max' and S. 'Sensation' were shown to be triploid with 2n = 45. Other cultivars, including S. 'Pallas', S. 'Luna', S. 'Ceres', S. 'Stephanie', S. 'Illusion', S. 'Vanessa

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Książki na temat "Cytogenetic Variation"

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Taški-Ajduković, Ksenija. Regeneracija somatskih hibrida u rodu Helianthus. Zadužbina Andrejević, 2006.

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Gerhart, John. Cells, embryos, and evolution: Toward a cellular and developmental understanding of phenotypic variation and evolutionary adaptability. Blackwell Science, 1997.

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Części książek na temat "Cytogenetic Variation"

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Fourré, J. L., P. Berger, and P. André. "Somatic Embryogenesis and Somaclonal Variation in Norway Spruce: Cytogenetic and Molecular Approaches." In Somatic Cell Genetics and Molecular Genetics of Trees. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-3983-0_6.

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Feldman, Moshe, and Avraham A. Levy. "Introduction." In Wheat Evolution and Domestication. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-30175-9_1.

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AbstractThe chapter presents topics that will be further detailed within the book such as origin of wheat, identification of its wild progenitors, processes leading to its domestication, and evolution under cultivation. These topics have been the object of extensive botanical, genetic, cytogenetic, molecular, and evolutionary studies, most of which are reviewed in the book. Given that only a small number of wild genotypes were selected for domestication, the genetic basis of domesticated wheat is relatively narrow, representing only a fraction of the large genetic variation that exist in its w

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Lawce, Helen J., and Luke Boyd. "Human chromosomes: identification and variations." In The AGT Cytogenetics Laboratory Manual. John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119061199.ch7.

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Mpumelelo Casper, Rikhotso, Kachienga Leonard, Magwalivha Mpho, and Nethathe Bono. "Recent Molecular Techniques in Cytogenetics." In Recent Advances in Cytogenetics Unraveling Casualties of Genetic Variations [Working Title]. IntechOpen, 2025. https://doi.org/10.5772/intechopen.1005877.

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Cytogenetics involves all aspects of chromosome biology. Through the application of molecular cytogenetic techniques in biology and medicine, we gain insights into the structural and functional organization of chromosomes, chromosomal abnormalities, and genomic variations in developmental, medical, and cancer genetics. This chapter explores recent advancements in molecular cytogenetics and their implications for managing hereditary diseases. It explores cutting-edge molecular methodologies such as spectral karyotyping, fluorescence in situ hybridization, and next-generation sequencing alongsid

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Tymowska, Janina. "Polyploidy and Cytogenetic Variation in Frogs of the Genus Xenopus." In Amphibian Cytogenetics and Evolution. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-12-297880-7.50016-0.

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Kumar Dey, Subrata. "Technological Advances in Cancer Cytogenetics." In Recent Advances in Cytogenetics [Working Title]. IntechOpen, 2024. https://doi.org/10.5772/intechopen.1008240.

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The field of cytogenetics has witnessed significant changes due to constant evolution of new methodologies for the detection of chromosomal alterations in number and structure. The discovery of Philadelphia chromosome in Chronic Myelogenous Leukemia (CML) ushered in new era in cancer cytogenetics. Classical cytogenetics is based on G-banded chromosome analysis and karyotyping, which can detect alterations in structure and number of chromosomes in a diploid set. Subsequent development of molecular cytogenetic techniques such as Fluorescence In situ Hybridization (FISH) where fluorescent dye-lab

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Hameed Zargar, Mahrukh, Tahir Mohiuddin Malla, Faisel Ahmed, Zafar A. Shah, Jaffar Abass Wani, and Asra Kirmani. "Cytogenetics and Microdeletion Syndromes." In Recent Advances in Cytogenetics [Working Title]. IntechOpen, 2024. https://doi.org/10.5772/intechopen.1006054.

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The emergence of molecular cytogenetic technologies has transformed the process of identifying new microdeletion syndromes. Traditional methods of identifying these syndromes relied on the chance discovery of patients exhibiting specific clinical features and visible chromosomal rearrangements through techniques like G-banding. However, with the introduction of comparative genomic hybridization using microarrays, it has become possible to detect previously unknown and recurring imbalances in individuals presenting with conditions such as mental retardation and nonspecific features. In contrast

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Norppa Hannu. "Relationship between Biomarkers of Effect (CAs, MNi, SCEs) and Risk of Cancer." In NATO Science for Peace and Security Series - E: Human and Societal Dynamics. IOS Press, 2010. https://doi.org/10.3233/978-1-60750-645-4-51.

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Chromosomal aberrations (CAs), micronuclei (MNi), and sister chromatid exchanges (SCEs) in peripheral lymphocytes have widely been used as biomarkers of genotoxic exposure and effects in humans. International collaborative studies have shown that a high level of CAs in lymphocytes is associated with an increased risk of overall cancer. The CA-cancer association is seen in subjects with known carcinogenic exposure but also in individuals with no known history of exposure to carcinogens. This suggests that a high CA level is an indicator of increased cancer risk regardless of the reason for the

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Singh Bakala, Harmeet, Kamalpreet Singh Mandahal, Ankita, Loveleen Kaur Sarao, and Puja Srivastava. "Breeding Wheat for Biotic Stress Resistance: Achievements, Challenges and Prospects." In Current Trends in Wheat Research [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97359.

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Wheat (T. aestivum) is one of the key food grain crops and is a prominent source of calories and proteins globally. In addition to mushrooming population and rising abiotic stresses in this ongoing climate change era, biotic stresses pose a great threat to wheat production over the globe. Fungal diseases such as rusts, mildew, along with pests like aphid, hinder the potential yield performance of the elite wheat cultivars to a huge extent. The complex nature of plant-parasite interactions is shown to be the decisive factor for the ultimate resistance expression in wheat. However, the advanceme

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Cebulska-Wasilewska Antonina, Miszczyk Justyna, Balegenowa Nazym, et al. "Studies of the Susceptibility to Radiation of Prostate Cancer or BPH Patients and Healthy Donors." In NATO Science for Peace and Security Series - E: Human and Societal Dynamics. IOS Press, 2010. https://doi.org/10.3233/978-1-60750-645-4-211.

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Genetic constitution, health condition and lifestyle of an individual, e.g. diet and a level of physical activity, can affect his response to various exogenous factors, including accidental exposure to radiation or therapeutic treatment. As a consequence, in a population at emergency, posing a threat to public of any hazardous exposure (physical, biological or chemical), subjects at various stage of disease development may constitute a quite large subgroup, potentially in a higher health risk as more vulnerable to the exposure. The aim of our studies was to compare, on molecular and cellular l

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Streszczenia konferencji na temat "Cytogenetic Variation"

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Wolff, BM, YG Oliveira, VT Almeida, et al. "CYTOGENOMIC DELINEATION OF A RARE 15Q TRIPLICATION CASE." In Resumos do 54º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2022. http://dx.doi.org/10.5327/1516-3180.140s1.5930.

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Objective: The proximal long arm of human chromosome 15 is frequently involved in molecular rearrangements including duplications, deletions, triplications, translocations, and inversions, as well as in the formation of supernumerary marker chromosomes. It happens due to the presence of low copy repeats (LCR), which mediate non-allelic homologous recombination (NAHR), resulting in these genomic rearrangements. In this study, we made a molecular characterization of the patient and his family. Method: We report a 14-year-old boy, the product of healthy and nonconsaguineous couple who has an intr

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