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Littérature scientifique sur le sujet « Aneuploidiya »

Auteur : Grafiati

Publié le 7 juin 2025

Mis à jour le 2 août 2025

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Articles de revues sur le sujet "Aneuploidiya"

Zhuchenko, Lyudmila Aleksandrovna, Elena Nikolaevna Andreeva, Fatima Katabinovna Lagkuyeva, et al. "The main results and a current state of the program of the combined prenatal screening of 1 trimester in the Russian Federation." Journal of obstetrics and women's diseases 62, no. 3 (2013): 20–25. http://dx.doi.org/10.17816/jowd62320-25.

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Prenatal diagnostics of anatomic and chromosomal defects at future child is represents high-allowing technology in system of obstetric monitoring behind the course of pregnancy and a condition of a fruit. Carrying out reform of system of prenatal screening in territorial subjects of the Russian Federation within transition to the international standard of diagnostics to early terms of the pregnancy which is carried out with support of the Government, demands regular audit. The analysis of the first results innovative for the country of mass combined PS of 1 trimester is carried out with use of

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Rodrigo, Lorena, Mónica Clemente-Císcar, Inmaculada Campos-Galindo, Vanessa Peinado, Carlos Simón, and Carmen Rubio. "Characteristics of the IVF Cycle that Contribute to the Incidence of Mosaicism." Genes 11, no. 10 (2020): 1151. http://dx.doi.org/10.3390/genes11101151.

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Highly sensitive next-generation sequencing (NGS) platforms applied to preimplantation genetic testing for aneuploidy (PGT-A) allow the classification of mosaicism in trophectoderm biopsies. However, the incidence of mosaicism reported by these tests can be affected by a wide number of analytical, biological, and clinical factors. With the use of a proprietary algorithm for automated diagnosis of aneuploidy and mosaicism, we retrospectively analyzed a large series of 115,368 trophectoderm biopsies from 27,436 PGT-A cycles to determine whether certain biological factors and in vitro fertilizati

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WILKINS-HAUG, LOUISE, and REBECCA REIMERS. "Unique Challenges of NIPT for Sex Chromosome Aneuploidy." Clinical Obstetrics & Gynecology 66, no. 3 (2023): 568–78. http://dx.doi.org/10.1097/grf.0000000000000804.

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Noninvasive prenatal testing (NIPT) for the sex chromosome aneuploidies (45,X, 47,XXY, 47,XXX, and 47,XYY) differs significantly from that for the autosomal aneuploidies (trisomy 13, 18, and 21). As a group, sex chromosome aneuploidies occur more commonly (1/400) than any one isolated autosomal aneuploidy, the phenotypic variation is greater, the role of mosaicism more challenging, and the positive predictive value of a high-risk NIPT result is substantially lower. These considerations should be identified during pretest counseling, the inclusion of sex chromosome testing offered separately, a

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Sheppard, Olivia, Frances K. Wiseman, Aarti Ruparelia, Victor L. J. Tybulewicz, and Elizabeth M. C. Fisher. "Mouse Models of Aneuploidy." Scientific World Journal 2012 (2012): 1–6. http://dx.doi.org/10.1100/2012/214078.

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Abnormalities of chromosome copy number are called aneuploidies and make up a large health load on the human population. Many aneuploidies are lethal because the resulting abnormal gene dosage is highly deleterious. Nevertheless, some whole chromosome aneuploidies can lead to live births. Alterations in the copy number of sections of chromosomes, which are also known as segmental aneuploidies, are also associated with deleterious effects. Here we examine how aneuploidy of whole chromosomes and segmental aneuploidy of chromosomal regions are modeled in the mouse. These models provide a whole an

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Zhang, Shuai, Ruixue Wang, Ludan Zhang, James A. Birchler, and Lin Sun. "Inverse and Proportional Trans Modulation of Gene Expression in Human Aneuploidies." Genes 15, no. 5 (2024): 637. http://dx.doi.org/10.3390/genes15050637.

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Genomic imbalance in aneuploidy is often detrimental to organisms. To gain insight into the molecular basis of aneuploidies in humans, we analyzed transcriptome data from several autosomal and sex chromosome aneuploidies. The results showed that in human aneuploid cells, genes located on unvaried chromosomes are inversely or proportionally trans-modulated, while a subset of genes on the varied chromosomes are compensated. Less genome-wide modulation is found for sex chromosome aneuploidy compared with autosomal aneuploidy due to X inactivation and the retention of dosage sensitive regulators o

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Zou, Ying, and Jaclyn Murry. "Live-Born Double Aneuploidy at the Johns Hopkins Cytogenomics Laboratory: Case Report and Review of the Literature." OBM Genetics 06, no. 04 (2022): 1–16. http://dx.doi.org/10.21926/obm.genet.2204168.

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Double aneuploidy is the co-occurrence of aneuploidy of two different chromosomes within the same individual. Genomic imbalance associated with two aneuploidies in humans is associated with early lethality, and observation in live-born humans is rare. In isolation, trisomy of chromosomes 13, 18, 21, X, and Y may be better tolerated, whereas monosomy of X is the only such type of aberration that may be compatible with life. It is hypothesized that two successive malsegregation events must occur in early development to be observed constitutionally. Mechanisms like trisomy rescue or selection aga

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He, Meng, Eun Jung Kim, Yangmeng Wang, Alejandro Chibly, and Kristel Dorighi. "Abstract 4305: Targeting the exonuclease domain of POLE to induce synthetic lethality in highly aneuploidic tumor cells." Cancer Research 85, no. 8_Supplement_1 (2025): 4305. https://doi.org/10.1158/1538-7445.am2025-4305.

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Abstract Aneuploidy is a hallmark of cancer evolution, it is associated with fast disease progression and drug resistance across many tumor types. The underlying molecular aberration that causes aneuploidy remains largely unknown. Currently, there are no established therapeutics for tumors with high levels of aneuploidy. We propose that inhibition of the exonuclease domain of the DNA polymerase, POLE, could induce synthetic lethality in tumor cells with high levels of aneuploidy. We observed that loss of function mutations in the exonuclease domain of POLE are mutually exclusive with high leve

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Rubio, Carmen, Lorena Rodrigo, and Carlos Simón. "PREIMPLANTATION GENETIC TESTING: Chromosome abnormalities in human embryos." Reproduction 160, no. 5 (2020): A33—A44. http://dx.doi.org/10.1530/rep-20-0022.

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Aneuploidy is a frequent event in human embryos, and its incidence is higher in oocytes and embryos from women of advanced maternal age. Aneuploidy may also be a contributing factor in infertile populations, such as couples with recurrent miscarriages, repetitive implantation failure, or male infertility. For these reasons, preimplantation genetic testing for aneuploidy (PGT-A) has been proposed to prevent miscarriages and increase live birth rates in infertile couples undergoing in vitro fertilisation. Next-generation sequencing is currently being applied for the detection of aneuploidies in

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Krepischi, Ana Cristina Victorino. "Revisitando a origem cromossômica do câncer: aneuploidias promovem ou suprimem o processo tumorigênico?" Semina: Ciências Biológicas e da Saúde 38, no. 1supl (2018): 34. http://dx.doi.org/10.5433/1679-0367.2017v38n1suplp34.

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Alterações citogenéticas que modificam o número de cópias cromossômicas (aneuploidias) são marca do câncer. Entretanto, o papel das aneuploidias no início e na progressão tumoral ainda não é totalmente elucidado. Parte da dificuldade no estudo de seu efeito provém do conjunto complexo e diverso de anormalidades cromossômicas dos diferentes tipos de tumores. Evidências recentes mostram que aneuloidias poderiam agir para antagonizar a tumorigênese em certos contextos genômicos. Ao contrário de mutações de ponto, que afetam poucos genes, ganho ou perda de um cromossomo altera a transcrição de cen

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Akutsu, Silvia Natsuko, Kazumasa Fujita, Keita Tomioka, Tatsuo Miyamoto, and Shinya Matsuura. "Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders." Cells 9, no. 1 (2020): 239. http://dx.doi.org/10.3390/cells9010239.

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Chromosomal segregation errors in germ cells and early embryonic development underlie aneuploidies, which are numerical chromosomal abnormalities causing fetal absorption, developmental anomalies, and carcinogenesis. It has been considered that human aneuploidy disorders cannot be resolved by radical treatment. However, recent studies have demonstrated that aneuploidies can be rescued to a normal diploid state using genetic engineering in cultured cells. Here, we summarize a series of studies mainly applying genome editing to eliminate an extra copy of human chromosome 21, the cause of the mos

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Thèses sur le sujet "Aneuploidiya"

Cortez, Beatriz de Araujo. "Diferentes abordagens para o entendimento da aneuploidia: interferindo na mitose com o uso de crisotila e vincristina." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-15122014-143541/.

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A aneuploidia é uma característica dos tumores sólidos. Ela pode ser resultado de diferentes erros durante a mitose, como a amplificação centrossômica, mitoses multipolares, e anormalidades durante a citocinese. Hoje se sabe que a aneuploidia pode estar relacionada à supressão ou progressão tumoral dependendo do grau da aneuploidia e do contexto genético das células, e assim esforços vem sendo feitos a fim de elucidar quais erros durante a mitose estão relacionados à formação de células aneuploides viáveis e inviáveis. Estudos prévios do nosso grupo mostraram que tratamentos de células em cult

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Cortez, Beatriz de Araujo. "Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-05042010-134617/.

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Asbesto é um nome geral dado a seis tipos de fibras minerais encontradas naturalmente na crosta terrestre. Estas fibras vêm sendo exploradas industrialmente desde 1970, porém diversos trabalhadores expostos às fibras apresentaram patologias no trato respiratório, como fibroses e carcinomas. Alguns tipos de fibra foram banidos do mercado, porém o tipo de asbesto crisotila ainda pode ser comercializado na maioria dos países. Estudos in vivo e in vitro tentam elucidar as alterações causadas pela exposição à asbesto nos tecidos e nas células que possam estar relacionadas ao aparecimento de doenças

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Santos-Silva, Alan Roger 1981. "Analise das caracteristicas clinico-patologicas e da ploidia do DNA em pacientes jovens com carcinoma espinocelular de lingua : um estudo colaborativo internacional." [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/287850.

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Orientador: Marcio Ajudarte Lopes Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba Made available in DSpace on 2018-08-15T17:55:17Z (GMT). No. of bitstreams: 1 Santos-Silva_AlanRoger_D.pdf: 1071923 bytes, checksum: 996d56a5e4895653ebcd0b9e1636e7e2 (MD5) Previous issue date: 2010 Resumo: Predominantemente, o carcinoma espinocelular (CEC) de boca afeta pacientes idosos e com frequência se desenvolve em associação com o consumo de fumo e álcool. Todavia, evidências científicas têm sugerido o aumento da incidência desta malignidade em paciente

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Nakagawa, Elly Kayoko. "Estudo do significado biológico da multinucleação induzida por vincristina em células em cultura." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19092007-173841/.

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O estudo de agentes que interferem no funcionamento das proteínas relacionadas com o ciclo celular é importante para a compreensão dos processos de transformação e de morte celular. Alterações de ploidia, embora presentes na maioria dos tumores humanos, não têm ainda seu papel conhecido no processo de oncogênese. A alteração do número cromossômico é conseqüência primária de erros que envolvem o fuso mitótico e o cinetócoro. Dessa maneira, drogas que agem sobre os microtúbulos são consideradas aneugênicas potenciais. O presente trabalho enfocou o estudo do mecanismo pelo qual drogas que atuam s

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Romão, Daniela 1993. "Systemic effects of chromosomal instability induced tumorigenesis : A role of JAK/STAT and cytokine secretion in coupling inflammation to maturation defects in Drosophila." Doctoral thesis, TDX (Tesis Doctorals en Xarxa), 2021. http://hdl.handle.net/10803/672640.

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Alterations in developmental transitions are common among animals to compensate for growth disturbances. These variations are usually a consequence of altered steroidal hormone production resulting in puberty delays. Inflammation and high cytokine release seem to be behind these altercations, although in humans no concrete model has been put forward. Here we use a Drosophila epithelial model of Chromosomal Instability-driven malignant transformation to unravel a role of the Upd3 cytokine and JAK/STAT signaling in coupling the development of these tumors with a delay in metamorphosis. We pre

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BISPO, Adriana Valéria Sales. "Investigação de mosaicismo críptico e potenciais fatores de riscos para a não disjunção cromossômica na Síndrome de Turner." Universidade Federal de Pernambuco, 2015. https://repositorio.ufpe.br/handle/123456789/16176.

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Submitted by Fabio Sobreira Campos da Costa (fabio.sobreira@ufpe.br) on 2016-03-30T13:52:07Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) Tese_Adriana_Bispo_final_ficha catalografica.pdf: 4400523 bytes, checksum: b3e9eb79c58483144a4659be5ab2d45c (MD5) Made available in DSpace on 2016-03-30T13:52:07Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) Tese_Adriana_Bispo_final_ficha catalografica.pdf: 4400523 bytes, checksum: b3e9eb79c58483144a4659be5ab2d45c (MD5) Previous issue date: 2

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Sheltzer, Jason (Jason Meyer). "Several consequences of aneuploidy." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101353.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, September 2015. Cataloged from PDF version of thesis. "June 2015." Written on title page: "September 2015." Includes bibliographical references. Whole-chromosome aneuploidy, or a karyotype that is not a multiple of the haploid complement, is the most common cause of miscarriage and developmental delay in humans. Aneuploidy is also a hallmark of cancer: greater than 90% of tumors display chromosomal copy number alterations. Thus, understanding the consequences of aneuploidy has broad relevance for human healt

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Gouvêa, Adriele Ferreira. "Análise clinicopatológica, da expressão imunoistoquímica de KI-67, MCM 2 e geminina e da ploidia do DNA em leucoplasia verrucosa proliferativa." [s.n.], 2011. http://repositorio.unicamp.br/jspui/handle/REPOSIP/287849.

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Orientador: Marcio Ajudarte Lopes Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba Made available in DSpace on 2018-08-17T15:24:01Z (GMT). No. of bitstreams: 1 Gouvea_AdrieleFerreira_D.pdf: 1529519 bytes, checksum: 67d58c675522b5dd769d5fcad163d152 (MD5) Previous issue date: 2011 Resumo: Leucoplasia verrucosa proliferativa (LVP) tem como principais características acometer principalmente mulheres, com idades acima dos 60 anos, sem hábitos nocivos, com lesões multifocais, recorrentes após excisão e com altas taxas de malignização. Alguns est

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Morhan, Alina Raluca. "Aneuploidy in pancreatic intraepithelial neoplasia." Thesis, Swansea University, 2015. https://cronfa.swan.ac.uk/Record/cronfa42775.

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Pancreatic ductal adenocarcinoma has one of the most unfavourable prognoses and survival patterns. Pancreatic intraepithelial ductal neoplasias (PanINs) 1-3 are microscopic precursors which display genetic and epigenetic changes leading to adenocarcinoma. We investigated the chromosomal numeric changes for chromosomes 1, 6, 9 and 18 using fluorescence in situ hybridization in the progressing intraepithelial neoplasias and the corresponding tumours. We also assessed the protein levels for mitotic checkpoint proteins Mad2 and BubRl using immunohistochemistry and applied correlation models to der

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Hermine, T. "Radiation induced aneuploidy in somatic cells." Thesis, Swansea University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637267.

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This thesis describes the cytogenetic effects of X-irradiation on chromosome segregation. Metaphase analysis of G0 irradiated human lymphocytes showed that X-irradiation resulted mainly in structural aberrations but that non-disjunction (measured as chromosome gains) and polyploidy were also induced. The technology used involved fluorescence in-situ hybridisation with whole chromosome probes for chromosomes 2 & 8. Radiation induced micronuclei were measured in both human fibroblasts and Chinese hamster cell lines using the cytokinesis block micronucleus assay coupled with kinetochore la

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Livres sur le sujet "Aneuploidiya"

Dellarco, Vicki L., Peter E. Voytek, Alexander Hollaender, et al., eds. Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9.

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K, Vig Baldev, and Sandberg Avery A, eds. Aneuploidy. Liss, 1987.

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M, Carpanini F., and European Centre for Ecotoxicology and Toxicology of Chemicals., eds. Aneuploidy. ECETOC, 1997.

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Büchner, Th, Clara D. Bloomfield, W. Hiddemann, D. K. Hossfeld, and J. Schumann, eds. Tumor Aneuploidy. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70458-1.

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Th, Büchner, and Andreeff Michael 1943-, eds. Tumor aneuploidy. Springer-Verlag, 1985.

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Vig, Baldev K., ed. Chromosome Segregation and Aneuploidy. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84938-1.

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L, Dellarco Vicki, Voytek Peter E, Hollaender Alexander 1898-, and Symposium on Aneuploidy: Etiology and Mechanisms (1985 : Carnegie Institution of Washington), eds. Aneuploidy: Etiology and mechanisms. Plenum Press, 1985.

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K, Vig Baldev, and NATO Advanced Research Workshop on Chromosome Segregation and Aneuploidy (1992 : Aghia Pelagia, Greece), eds. Chromosome segregation and aneuploidy. Springer-Verlag, 1993.

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Storchova, Zuzana. Aneuploidy in health and disease. InTech, 2012.

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Klinga, Karin. Aneuploidy in induced autotetraploid forage grasses. [s.n.], 1987.

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Chapitres de livres sur le sujet "Aneuploidiya"

Voytek, Peter E. "Introduction: Assessment of Health Risks." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_1.

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Kline, Jennie, and Zena Stein. "Environmental Causes of Aneuploidy: Why So Elusive?" In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_10.

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Evans, H. J. "Neoplasia and Cytogenetic Abnormalities." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_11.

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Hook, Ernest B. "Roundtable Discussion: Human Aspects of Aneuploidy." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_12.

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Nicklas, R. Bruce. "Mitosis in Eukaryotic Cells: An Overview of Chromosome Distribution." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_13.

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McIntosh, J. Richard. "Spindle Structure and the Mechanisms of Chromosome Movement." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_14.

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Yeh, Elaine, and Kerry Bloom. "Characterization of a Tightly Centromere-Linked Gene Essential for Meiosis in the Yeast Saccharomyces Cerevisiae." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_15.

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Brinkley, B. R., A. Tousson, and M. M. Valdivia. "The Kinetochore of Mammalian Chromosomes: Structure and Function in Normal Mitosis and Aneuploidy." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_16.

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De Brabander, M., F. Aerts, J. De Mey, et al. "Microtubule Dynamics and the Mitotic Cycle: A Model." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_17.

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Hsu, T. C., and K. L. Satya-Prakash. "Aneuploidy Induction by Mitotic Arrestants in Animal Cell Systems: Possible Mechanisms." In Aneuploidy. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2127-9_18.

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Actes de conférences sur le sujet "Aneuploidiya"

Ramiro, Grazieli Cristina, DANIEL APARECIDO MARASSATTI, RENATO MASSAHARU HASSUNUMA, and PATRÍCIA CARVALHO GARCIA. "ANEUPLOIDIAS HUMANAS: ENSINANDO OS CONCEITOS BÁSICOS EM GENÉTICA A PARTIR DE LIVROS DIGITAIS E UM JOGO EDUCACIONAL." In I Congresso Nacional de Pesquisas e Estudos Genéticos On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/geneticon/6419.

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Introdução: As aneuploidias são doenças genéticas caracterizadas pela alteração no número de cromossomos. Por vezes, a aquisição do conhecimento sobre as estas doenças pode ser dificultada pela quantidade de informações relacionadas a elas. Neste contexto, o uso de resumos e jogos educacionais podem ser considerados um recurso pedagógico motivador no ensino de Genética. Objetivos: O objetivo do trabalho foi o desenvolvimento de dois livros digitais sobre as principais aneuploidias humanas, sendo um livro-texto com resumos sobre as aneuploidias e um livro-jogo. Metodologia: Inicialmente, foi re

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Pinheiro Lucio, Márcio Jamerson, Osvaldo Carlos Silva Leopoldino, Vinicius Ruas Lacerda, and Gabriela de Queiroz Fonseca de Queiroz Fonseca. "PERFIL EPIDEMIOLÓGICO DE ANOMALIAS CROMOSSÔMICAS NO TERRITÓRIO BRASILEIRO." In Congresso Nacional de Genética. CONGRESSE.ME, 2021. http://dx.doi.org/10.54265/ackg1360.

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Introdução: A contagem numérica de cromossomos humanos tem como expressão, em números modais de 46 cromossomos (22 pares de cromossomos somáticos e 1 par de cromossomos sexuais). Podemos definidir anomalias cromossômicas, alterações numéricas destes valores cromossômicos, referindo-se quando o indivíduo possui um número cromossômico anormal, aneuploidias. Estes distúrbios cromossômicos, podem causar significativa deficiência mental, déficit ponderal e estrutural, dismorfismos faciais e malformações.Ademais, as aneuploidias estão entre as anomalias congênitas mais comuns na prática clínica, sen

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Borilli, Nicoly Abido, and Iáskara Vieira De Oliveira. "ANÁLISE CROMOSSÔMICA PRÉ-IMPLANTACIONAL NÃO INVASIVA DE EMBRIÕES." In I Congresso On-line Nacional de Histologia e Embriologia Humana. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/2712.

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Introdução: Em torno de 2016 surgiu a biópsia não invasiva de embriões que consiste, basicamente, na análise do DNA livre no meio de cultivo embrionário para a realização do NICS (do inglês: Non Invasive Chromosome Screening; do português: triagem cromossômica não invasiva), fazendo com que a retirada das células embrionárias não se torne mais necessária. Objetivo: descrever o que é e quais as vantagens da analise não invasiva de embriões e comparar e verificar as taxas de concordância entre as técnicas de biópsia tradicional e NICS por meio de uma revisão de literatura que reuniu e sintetizou

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Hollenbach, Andrew D., Jacob M. Loupe, Patrick J. Miller, et al. "Abstract 2013: The PAX3-FOXO1 oncogene drives aneuploidy and overrides aneuploidy-associated proliferative defects in alveolar rhabdomyosarcoma." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-2013.

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Davoli, Teresa, Wei Xu, Peter Park, and Stephen J. Elledge. "Abstract SY36-03: How aneuploidy drives tumorigenesis." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-sy36-03.

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Davoli, Teresa, Hajima Uno, Andrew Xu, et al. "Abstract SY10-01: How aneuploidy drives cancer." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-sy10-01.

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Lee, Jui-Hao, and Chi-Hung Lin. "Abstract 5091: Aneuploidy is in stomatin overexpressed cells." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-5091.

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Davoli, Teresa. "Abstract IA02: The role of aneuploidy during tumorigenesis." In Abstracts: Fifth AACR-IASLC International Joint Conference: Lung Cancer Translational Science from the Bench to the Clinic; January 8-11, 2018; San Diego, CA. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1557-3265.aacriaslc18-ia02.

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Scofield, H., R. Sharma, V. Harris, et al. "313 Very rare x chromosome aneuploidies in lupus and sjogren’s." In LUPUS 2017 & ACA 2017, (12th International Congress on SLE &, 7th Asian Congress on Autoimmunity). Lupus Foundation of America, 2017. http://dx.doi.org/10.1136/lupus-2017-000215.313.

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Bao, Hua, Ming Han, Yi Shen, Xue Wu, and Yang Shao. "Abstract 2210: Chromosome arm aneuploidy landscape in lung adenocarcinoma." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-2210.

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Rapports d'organisations sur le sujet "Aneuploidiya"

สุขเจริญ, นเรศร, та จิรพรรณ เหงี่ยมวิจาวัฒน์. การตรวจหา Sex chromosome aneuploidy ของอสุจิที่ได้จากท่อนำอสุจิส่วน epididymis ในผู้ป่วยที่ตรวจไม่พบอสุจิในน้ำอสุจิ. จุฬาลงกรณ์มหาวิทยาลัย, 2001. https://doi.org/10.58837/chula.res.2001.22.

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การฉีดอสุจิเข้าในไข่ (intracytoplasmic sperm injection : ICSI) เป็นวิธีการรักษาภาวะที่ไม่พบอสุจิในน้ำอสุจิซึ่งเกิดจากการอุดตันของท่อนำอสุจิโดยใช้อสุจิจากท่อนำอสุจิ (epididymal spermatozoa) ได้อย่างมีประสิทธิภาพ อย่างไรก็ตามยังคงมีความกังวลถึงความเสี่ยงต่อการเกิดความผิดปกติของโครเมโซมชนิด aneuploidy ในทารกที่เกิดจากวิธีดังกล่าวจากบิดา ในปัจจุบันยังมีข้อมูลน้อยมากเกี่ยวกับอุบัติการณ์ของความผิดปกติของโครโมโซมของ epididymal spermatozoa ในผู้ป่วยที่ไม่พบอสุจิในน้ำอสุจิซึ่งเกิดจากการอุดตันของท่อนำอสุจิ ดังนั้นจึงได้ทำการศึกษาถึงอุบัติการณ์ของความผิดปกติของโครโมโซมชนิด aneuploidy และ diploidy ของ epi

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Sharp, David J., and Daniel W. Buster. Chromokinesins: Possible Generators of Cancer-Associated Aneuploidy. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada447643.

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Mueller, Adam. O-GlcNAc Misregulation and Aneuploidy in Breast Cancer. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada506322.

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Mueller, Adam. O-GlcNAc Misregulation and Aneuploidy in Breast Cancer. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada545785.

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Lingle, Wilma. Centrosome Hypertrophy Induced by p53 Mutations Leads to Tumor Aneuploidy. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada392933.

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Pati, Debananda. Linking Sister Chromatid Cohesion to Apoptosis and Aneuploidy in the Development of Breast Cancer. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada418197.

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Wyrobek, W. J., and R. T. Dunlay. Phase II: Automated System for Aneuploidy Detection in Sperm Final Report CRADA No. TC-1554-98. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1399725.

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Wyrobek, A. Phase II: Automated System for Aneuploidy Detection in Sperm Final Report CRADA No. TC-1554-98. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/815176.

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Wyrobek, A. J., and R. T. Dunlay. Automated System for Aneuploidy Detection in Sperm Final Report CRADA No. TC-1364-96: Phase I SBIR. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1406411.

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Wyrobek, A. Automated System for Aneuploidy Detection in Sperm Final Report CRADA No. TC-1364-96: Phase I SBIR. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/790152.

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