Works matching Nondisjunction and aneuploidy

Results: 42

Cell biology: Nondisjunction, aneuploidy and tetraploidy.

Published in:

Nature, 2006, v. 442, n. 7104, p. E9, doi. 10.1038/nature05139

By:

Weaver, Beth A. A.;
Silk, Alain D.;
Cleveland, Don W.

Publication type:

Article

Screening for parental mitotic nondisjunction as a cause of fetal aneuploidy.

Published in:

Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 26, doi. 10.4103/MXE.MXE_1_18

By:

Hussen, Dalia F.;
Hammad, Saida A.;
Refaat, Khaled M.;
Ashaat, Engy A.;
Gaber, Khaled R.;
Aglan, Mona S.;
Otaify, Ghada A.;
Abdel Ghany, Asia E.;
Temtamy, Samia A.

Publication type:

Article

Cell biology: Nondisjunction, aneuploidy and tetraploidy (Reply).

Published in:

Nature, 2006, v. 442, n. 7104, p. E10, doi. 10.1038/nature05140

By:

Shi, Qinghua;
King, Randall W.

Publication type:

Article

Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction.

Published in:

Clinical Genetics, 1984, v. 26, n. 1, p. 43, doi. 10.1111/j.1399-0004.1984.tb00786.x

By:

Hecht, Frederick;
Hecht, Barbara K.;
Berger, Carol S.

Publication type:

Article

Aneuploidy in human oocytes: nondisjunction or predivision?

Published in:

Cytogenetics & Cell Genetics, 2001, v. 94, n. 3/4, p. 241, doi. 10.1159/000048823

By:

Rosenbusch, B.;
Giaeser, B.;
Schneider, M.

Publication type:

Article

Does the Assessment of Nondisjunction Provide a More Sensitive Assay for the Detection of Aneugens?

Published in:

Toxicological Sciences, 2017, v. 157, n. 1, p. 20, doi. 10.1093/toxsci/kfx014

By:

Elloway, Joanne M.;
Davies, Alexandra K.;
Hayes, Julie E.;
Doherty, Ann T.

Publication type:

Article

Fitness consequences of sex chromosome aneuploidy in Drosophila melanogaster.

Published in:

PLoS Genetics, 2025, v. 21, n. 6, p. 1, doi. 10.1371/journal.pgen.1011703

By:

Makovec, Elizabeth R.;
Kestell, Caitlin C.;
Janke, Kayla K.;
Carter, Ethan J.;
Ragsdale, Aaron P.;
Sharp, Nathaniel P.

Publication type:

Article

Double Aneuploidy: 48,XXY,+18 in a Bedouin Boy.

Published in:

Medical Principles & Practice, 1999, v. 8, n. 3, p. 241, doi. 10.1159/000026099

By:

AI-Awadi, S.A.;
AI-Naggar, R.L.;
Tayel, S.M.;
Uma, R.

Publication type:

Article

Recurrent triploidy of maternal origin.

Published in:

2003

By:

Brancati, Francesco;
Mingarelli, Rita;
Dallapiccola, Bruno

Publication type:

Report

Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 206, doi. 10.1159/000086891

By:

Pellestor, F.;
Anahory, T.;
Hamamah, S.

Publication type:

Article

Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 3/4, p. 237, doi. 10.1159/000086894

By:

Delhanty, J. D. A.

Publication type:

Article

Reconsideration of the safety and effectiveness of human oocyte cryopreservation.

Published in:

Reproductive Biology & Endocrinology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12958-023-01071-z

By:

Kwan, Helen C. K.

Publication type:

Article

Indication for thresholds of chromosome non-disjunction versus chromosome lagging induced by spindle inhibitors in vitro in human lymphocytes.

Published in:

Mutagenesis, 1997, v. 12, n. 3, p. 133, doi. 10.1093/mutage/12.3.133

By:

Elhajouji, Azeddine;
Tibaldi, Fabian;
Kirsch-Volders, Micheline

Publication type:

Article

Premature separation of sister chromatids in human male meiosis.

Published in:

Human Reproduction, 2008, v. 23, n. 4, p. 982, doi. 10.1093/humrep/dem427

By:

Laia Uroz;
Osvaldo Rajmil;
Cristina Templado

Publication type:

Article

Chromosomal FISH analysis of unfertilized human oocytes and polar bodies.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 9, p. 488, doi. 10.1007/s100380200071

By:

Honda, N.;
Miharu, N.;
Hara, T.;
Samura, O.;
Honda, H.;
Ohama, K.

Publication type:

Article

Study of the effects of 0.15 terahertz radiation on genome integrity of adult fibroblasts.

Published in:

Environmental & Molecular Mutagenesis, 2018, v. 59, n. 6, p. 476, doi. 10.1002/em.22192

By:

Franchini, Valeria;
De Sanctis, Stefania;
Marinaccio, Jessica;
De Amicis, Andrea;
Coluzzi, Elisa;
Di Cristofaro, Sara;
Lista, Florigio;
Regalbuto, Elisa;
Doria, Andrea;
Giovenale, Emilio;
Gallerano, Gian Piero;
Bei, Roberto;
Benvenuto, Monica;
Masuelli, Laura;
Udroiu, Ion;
Sgura, Antonella

Publication type:

Article

Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes.

Published in:

Human Genetics, 2003, v. 112, n. 2, p. 195, doi. 10.1007/s00439-002-0852-x

By:

Pellestor, Franck;
Andréo, Brigitte;
Arnal, Françoise;
Humeau, Claude;
Demaille, Jacques

Publication type:

Article

On the rate of aneuploidy reversion in a wild yeast model.

Published in:

Genetics, 2025, v. 229, n. 2, p. 1, doi. 10.1093/genetics/iyae196

By:

Hose, James;
Zheng, Qi;
Sharp, Nathaniel P;
Gasch, Audrey P

Publication type:

Article

Adaptation by Loss of Heterozygosity in Saccharomyces cerevisiae Clones Under Divergent Selection.

Published in:

Genetics, 2019, v. 213, n. 2, p. 665, doi. 10.1534/genetics.119.302411

By:

James, Timothy Y.;
Michelotti, Lucas A.;
Glasco, Alexander D.;
Clemons, Rebecca A.;
Powers, Robert A.;
James, Ellen S.;
Simmons, D. Rabern;
Fengyan Bai;
Shuhua Ge

Publication type:

Article

Centromere-Proximal Meiotic Crossovers in Drosophila melanogaster Are Suppressed by Both HighlyRepetitive Heterochromatin and Proximity tothe Centromere.

Published in:

Genetics, 2019, v. 213, n. 1, p. 113, doi. 10.1534/genetics.119.302509

By:

Hartmann, Michaelyn;
Umbanhowar, James;
Sekelsky, Jeff

Publication type:

Article

Loss of Drosophila Mei-41/ATR Alters Meiotic Crossover Patterning.

Published in:

Genetics, 2018, v. 208, n. 2, p. 579, doi. 10.1534/genetics.117.300634

By:

Brady, Morgan M.;
McMahan, Susan;
Sekelsky, Jeff

Publication type:

Article

Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype.

Published in:

Molecular Human Reproduction, 2000, v. 6, n. 2, doi. 10.1093/molehr/6.2.107

By:

Rives, N.;
Joly, G.;
Machy, A.;
Siméon, N.;
Leclerc, P.;
Macé, B.

Publication type:

Article

Folate Deficiency Triggers the Abnormal Segregation of a Region With Large Cluster of CG-Rich Trinucleotide Repeats on Human Chromosome 2.

Published in:

Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.695124

By:

Garribba, Lorenza;
Vogel, Ivan;
Lerdrup, Mads;
Gonçalves Dinis, Marisa M.;
Ren, Liqun;
Liu, Ying

Publication type:

Article

Selfish centromeres and the wastefulness of human reproduction.

Published in:

PLoS Biology, 2022, v. 20, n. 7, p. 1, doi. 10.1371/journal.pbio.3001671

By:

Hurst, Laurence D.

Publication type:

Article

Nondisjunction and transmission ratio distortion ofChromosome 2 in a (2.8) Robertsonian translocation mouse strain.

Published in:

Mammalian Genome, 2006, v. 17, n. 3, p. 239, doi. 10.1007/s00335-005-0126-8

By:

Schulz, Reiner;
Underkoffler, Lara A.;
Collins, Joelle N.;
Oakey, Rebecca J.

Publication type:

Article

The origin of aneuploidy in humans: where we've been, where we're going.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 20, p. S8, doi. 10.1016/S1472-6483(10)62283-3

By:

Hassold, T.

Publication type:

Article

Cleavage versus blastocyst-stage embryo transfer.

Published in:

2008

By:

Jansen, R. P. S.

Publication type:

Abstract

Fertility assessment in hybrids between monobrachially homologous Rb races of the house mouse from the island of Madeira: implications for modes of chromosomal evolution.

Published in:

Heredity, 2011, v. 106, n. 2, p. 348, doi. 10.1038/hdy.2010.74

By:

Nunes, A. C.;
Catalan, J.;
Lopez, J.;
Ramalhinho, M. da Graça;
Mathias, M. da Luz;
Britton-Davidian, J.

Publication type:

Article

Population monitoring of trisomy 21: problems and approaches.

Published in:

Molecular Cytogenetics (17558166), 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13039-023-00637-1

By:

Sperling, Karl;
Scherb, Hagen;
Neitzel, Heidemarie

Publication type:

Article

Previous aneuploidic offspring in a young woman does not increase the risk for somatic random aneuploidy in subsequent pregnancies.

Published in:

Acta Obstetricia et Gynecologica Scandinavica, 2006, v. 85, n. 8, p. 1003, doi. 10.1080/00016340600622577

By:

Biron-Shental, Tal;
Amiel, Aliza;
Fejgin, Moshe

Publication type:

Article

Chromosomal Damage Rate, Aging, and Diet<sup>a</sup>.

Published in:

Annals of the New York Academy of Sciences, 1998, v. 854, n. 1, p. 23, doi. 10.1111/j.1749-6632.1998.tb09889.x

By:

FENECH, MICHAEL

Publication type:

Article

The effects of age and abnormal sperm count on the nondisjunction of spermatozoa.

Published in:

Journal of Assisted Reproduction & Genetics, 2000, v. 17, n. 1, p. 51, doi. 10.1023/A:1009454114973

By:

Asada, H.;
Sueoka, K.

Publication type:

Article

Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes...

Published in:

Genetics, 1995, v. 141, n. 2, p. 667, doi. 10.1093/genetics/141.2.667

By:

Oakey, Rebecca J.;
Matteson, Paul G.

Publication type:

Article

Nuclear envelope structural defect underlies the main cause of aneuploidy in ovarian carcinogenesis.

Published in:

BMC Cell Biology, 2016, v. 17, p. 1, doi. 10.1186/s12860-016-0114-8

By:

Capo-chichi, Callinice D.;
Yeasky, Toni M.;
Smith, Elizabeth R.;
Xiang-Xi Xu

Publication type:

Article

Preimplantation lethality of monosomy for mouse chromosome 19.

Published in:

Nature, 1979, v. 280, n. 5718, p. 144, doi. 10.1038/280144a0

By:

EPSTEIN, CHARLES J.;
TRAVIS, BRUCE

Publication type:

Article

A case of double aneuploidy of Down and Klinefelter syndrome in an Indian infant: a detailed case report.

Published in:

Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00602-6

By:

Patel, Sunny Kumar Jignesh Kumar;
Sheikh, Shagufa;
Banerjee, Birendranath

Publication type:

Article

Human Embryonic Stem Cells as Models for Aneuploid Chromosomal Syndromes.

Published in:

Stem Cells, 2010, v. 28, n. 9, p. 1530, doi. 10.1002/stem.483

By:

Biancotti, Juan-Carlos;
Narwani, Kavita;
Buehler, Nicole;
Mandefro, Berhan;
Golan-Lev, Tamar;
Yanuka, Ofra;
Clark, Amander;
Hill, David;
Benvenisty, Nissim;
Lavon, Neta

Publication type:

Article

Pentasomy 49,XXXXY Associated with a Chiari Type 1 Malformation and Cervical Syrinx.

Published in:

Pediatric Neurosurgery, 2007, v. 43, n. 1, p. 47, doi. 10.1159/000097526

By:

Raven, Ramin;
Bingham, Peter M.;
Graupman, Patrick

Publication type:

Article

The Histone Deacetylase Inhibitor Trichostatin A Has Genotoxic Effects in Human Lymphoblasts In Vitro.

Published in:

Toxicological Sciences, 2006, v. 93, n. 2, p. 341, doi. 10.1093/toxsci/kfl068

By:

Olaharski, Andrew J.;
Zhiying Ji;
Ji-Young Woo;
Lim, Sophia;
Hubbard, Alan E.;
Luoping Zhang;
Smith, Martyn T.

Publication type:

Article

Cytogenetic mechanisms of aneuploidy in somatic cells of chemonuclear industry professionals with incorporated plutonium-239.

Published in:

Russian Journal of Genetics, 2010, v. 46, n. 11, p. 1381, doi. 10.1134/S1022795410110141

By:

Vasilyev, S.;
Timoshevsky, V.;
Lebedev, I.

Publication type:

Article

The incidence of aneuploidy in human oocytes assessed by conventional cytogenetic analysis.

Published in:

Hereditas, 2004, v. 141, n. 2, p. 97, doi. 10.1111/j.1601-5223.2004.01803.x

By:

Rosenbusch, Bernd

Publication type:

Article

The decatenation checkpoint.

Published in:

British Journal of Cancer, 2007, v. 96, n. 2, p. 201, doi. 10.1038/sj.bjc.6603537

By:

Damelin, M.;
Bestor, T. H.

Publication type:

Article