Works matching Nondisjunction (Genetics)

Results: 37

Dental Care for an adolescent with chromosome pentasomy: rare case report with a two year follow-up.

Published in:

2015

By:

ALVES, Nayara Silva;
ASSAF, Andréa Videira;
MARTINS, Ângela Maria;
Rodrigues CAJAZEIRA, Marlus Roberto;
ANTUNES, Leonardo Santos;
SILVEIRA, Flávia Maia

Publication type:

Case Study

Genetic Variation in Rates of Nondisjunction: Association of Two Naturally Occurring....

Published in:

Genetics, 1999, v. 152, n. 4, p. 1605, doi. 10.1093/genetics/152.4.1605

By:

Zwick, Michael E.;
Salstrom, Jennifer L.

Publication type:

Article

Transmission and Drive Involving Parasitic B Chromosomes.

Published in:

Genes, 2018, v. 9, n. 8, p. 388, doi. 10.3390/genes9080388

By:

Jones, R.N.

Publication type:

Article

Screening for Fetal Aneuploidies in 1st Trimester.

Published in:

Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2016, v. 10, n. 2, p. 147, doi. 10.5005/jp-journals-10009-1458

By:

Athanasiadis, Apostolos P.;
Zavlanos, A. I.

Publication type:

Article

A case of penta X syndrome caused by nondisjunction in maternal meiosis 1 and 2.

Published in:

Clinical Case Reports, 2017, v. 5, n. 7, p. 1136, doi. 10.1002/ccr3.1004

By:

Markholt, Sara;
Graakjaer, Jesper;
Thim, Signe Bødker;
Høst, Bente;
Skytte, Anne‐Bine

Publication type:

Article

Footprintless disruption of prosurvival genes in aneuploid cancer cells using CRISPR/Cas9 technology.

Published in:

Biochemistry & Cell Biology, 2016, v. 94, n. 3, p. 289, doi. 10.1139/bcb-2015-0150

By:

Krachulec, Justyna M.;
Sedlmeier, Georg;
Thiele, Wilko;
Sleeman, Jonathan P.

Publication type:

Article

GENETIC CONSIDERATIONS IN NONDISJUNCTION.

Published in:

Annals of the New York Academy of Sciences, 1969, v. 171, n. 2, p. 391, doi. 10.1111/j.1749-6632.1970.tb39348.x

By:

Young, William J.

Publication type:

Article

Analysis of B chromosome nondisjunction induced by the r-X1 deficiency in maize.

Published in:

Chromosome Research, 2018, v. 26, n. 3, p. 153, doi. 10.1007/s10577-017-9567-7

By:

Tseng, Shih-Hsuan;
Peng, Shu-Fen;
Cheng, Ya-Ming

Publication type:

Article

First trimester maternal serum biochemical markers of aneuploidy in pregnancies with abnormally invasive placentation.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2015, v. 122, n. 10, p. 1370, doi. 10.1111/1471-0528.13298

By:

Thompson, O;
Otigbah, C;
Nnochiri, A;
Sumithran, E;
Spencer, K

Publication type:

Article

Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases.

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 2, p. 265, doi. 10.1007/s10815-017-1069-1

By:

Pylyp, Larysa Y.;
Spynenko, Lyudmyla O.;
Verhoglyad, Nataliya V.;
Mishenko, Anna O.;
Mykytenko, Dmytro O.;
Zukin, Valery D.

Publication type:

Article

Correlation between oocyte morphology and the embryo aneuploidy rate in IVF cycles.

Published in:

Gynecological Endocrinology, 2015, v. 31, p. 61, doi. 10.3109/09513590.2015.1086511

By:

Dolgushina, Nataliya V.;
Syrkasheva, Anastasiia G.;
Makarova, Nataliya P.;
Kovalskaya, Eugenia V.;
Kalinina, Elena A.;
Sukhikh, Gennady T.

Publication type:

Article

Prolonged duration of persistent cell-free fetal DNA from vanishing twin.

Published in:

2018

By:

Niles, K. M.;
Murji, A.;
Chitayat, D.;
Niles, Kirsten M;
Murji, Ally;
Chitayat, David

Publication type:

Case Study

Dynamic Sequence Evolution of a Sex-Associated B Chromosome in Lake Malawi Cichlid Fish.

Published in:

Journal of Heredity, 2017, v. 108, n. 1, p. 53, doi. 10.1093/jhered/esw059

By:

Clark, Frances E.;
Conte, Matthew A.;
Ferreira-Bravo, Irani A.;
Poletto, Andreia B.;
Martins, Cesar;
Kocher, Thomas D.

Publication type:

Article

Efficiency of non-invasive prenatal screening in pregnant women at advanced maternal age.

Published in:

2021

By:

Zhu, Hui;
Jin, Xiaoxiao;
Xu, Yuqing;
Zhang, Weihua;
Liu, Xiaodan;
Jin, Jinglei;
Qian, Yeqing;
Dong, Minyue

Publication type:

journal article

Association between telomere length and chromosome 21 nondisjunction in the oocyte.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1263, doi. 10.1007/s00439-015-1603-0

By:

Albizua, I.;
Rambo-Martin, B.;
Allen, E.;
He, W.;
Amin, A.;
Sherman, S.

Publication type:

Article

MOLECULAR CHARACTERIZATION OF LOCALLY ADOPTED SUGARCANE (Saccharum officinarum L.) VARIETIES USING MICROSATELLITE MARKERS.

Published in:

JAPS: Journal of Animal & Plant Sciences, 2017, v. 27, n. 1, p. 164

By:

Ahmed, M. S.;
Gardezi, S. D. A.

Publication type:

Article

An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099560

By:

Oliver, Tiffany Renee;
Middlebrooks, Candace D.;
Tinker, Stuart W.;
Allen, Emily Graves;
Bean, Lora J. H.;
Begum, Ferdouse;
Feingold, Eleanor;
Chowdhury, Reshmi;
Cheung, Vivian;
Sherman, Stephanie L.

Publication type:

Article

Evolutionary justifications for human reproductive limitations.

Published in:

Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 12, p. 2133, doi. 10.1007/s10815-018-1285-3

By:

Lubinsky, Mark

Publication type:

Article

Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis.

Published in:

Human Reproduction Update, 2004, v. 10, n. 5, p. 401, doi. 10.1093/humupd/dmh036

By:

Anver Kuliev

Publication type:

Article

Is there a role for fetal ductus venosus and hepatic artery Doppler in screening for fetal aneuploidy in the first trimester?

Published in:

2015

By:

Togrul, Cihan;
Ozaksit, Gulnur M.;
Seckin, Kerem D.;
Baser, Eralp;
Karsli, Mehmet F.;
Gungor, Tayfun

Publication type:

journal article

Chromosome-Specific and Global Effects of Aneuploidy in Saccharomyces cerevisiae.

Published in:

Genetics, 2016, v. 202, n. 4, p. 1395, doi. 10.1534/genetics.115.185660

By:

Dodgson, Stacie E.;
Kim, Sharon;
Costanzo, Michael;
Baryshnikova, Anastasia;
Morse, Darcy L.;
Kaiser, Chris A.;
Boone, Charles;
Amon, Angelika

Publication type:

Article

Too Much of a Good Thing: The Unique and Repeated Paths Toward Copper Adaptation.

Published in:

Genetics, 2015, v. 199, n. 2, p. 555, doi. 10.1534/genetics.114.171124

By:

Gerstein, Aleeza C.;
Ono, Jasmine;
Lo, Dara S.;
Campbell, Marcus L.;
Kuzmin, Anastasia;
Otto, Sarah P.

Publication type:

Article

Are paternal or grandmaternal age associated with higher probability of trisomy 21 in offspring? A population‐based, matched case‐control study, 1995‐2015.

Published in:

Paediatric & Perinatal Epidemiology, 2021, v. 35, n. 3, p. 281, doi. 10.1111/ppe.12737

By:

Schliep, Karen C.;
Feldkamp, Marcia L.;
Hanson, Heidi A.;
Hollingshaus, Michael;
Fraser, Alison;
Smith, Ken R.;
Panushka, Katherine A.;
Varner, Michael W.

Publication type:

Article

Linear dose response of acrocentric chromosome associations to gamma irradiation in human lymphocytes.

Published in:

Strahlentherapie und Onkologie, 2023, v. 199, n. 2, p. 182, doi. 10.1007/s00066-022-01978-3

By:

Samarth, Ravindra M;
Gandhi, Puneet;
Chaudhury, Nabo Kumar

Publication type:

Article

Epidemiology of Down Syndrome: New Insight Into the Multidimensional Interactions Among Genetic and Environmental Risk Factors in the Oocyte.

Published in:

American Journal of Epidemiology, 2011, v. 174, n. 9, p. 1009, doi. 10.1093/aje/kwr240

By:

Ghosh, Sujoy;
Hong, Chang-Sook;
Feingold, Eleanor;
Ghosh, Papiya;
Ghosh, Priyanka;
Bhaumik, Pranami;
Dey, Subrata Kumar

Publication type:

Article

Correlacion genotipo-fenotipo y analisis molecular en pacientes con sindrome Down.

Published in:

Revista Ciencias de la Salud, 2012, v. 10, n. 3, p. 295

By:

Contreras Bravo, Nora Constanza;
Silva Aldana, Claudia Tamar;
Mateus Arbelaez, Heidi Eliana

Publication type:

Article

Unusual Longevity of Edwards Syndrome: A Case Report.

Published in:

Genes, 2020, v. 11, n. 12, p. 1466, doi. 10.3390/genes11121466

By:

Alshami, Abbas;
Douedi, Steven;
Guida, Melissa;
Ajam, Firas;
Desai, Dhaval;
Zales, Vincent;
Calderon, Dawn M

Publication type:

Article

Turner syndrome and genetic polymorphism: a systematic review.

Published in:

Revista Paulista de Pediatria, 2015, v. 33, n. 3, p. 363, doi. 10.1016/j.rpped.2014.11.014

By:

de Marqui, Alessandra Bernadete Trovó

Publication type:

Article

Parental balanced chromosomal rearrangement leading to major genomic imbalance and an autosomal trisomy resulting in consecutive pregnancy loss: a case report.

Published in:

Journal of Genetics, 2021, v. 100, n. 2, p. 1, doi. 10.1007/s12041-021-01304-3

By:

Shrivastava, Anushka;
Thakur, Seema;
Nath, Tara;
Debnath, Abhipsa V. F.;
Bakshi, Sonal R.

Publication type:

Article

Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone.

Published in:

Human Molecular Genetics, 2001, v. 10, n. 9, p. 963, doi. 10.1093/hmg/10.9.963

By:

Bean, Christopher J.

Publication type:

Article

Genotoxic evaluation of two oral antidiabetic agents in the Drosophila wing spot test.

Published in:

Toxicology & Industrial Health, 2014, v. 30, n. 4, p. 376, doi. 10.1177/0748233712456091

By:

Gürbüzel, Mehmet;
Çapoğlu, İlyas;
Kızılet, Halit;
Halıcı, Zekai;
Özçiçek, Fatih;
Demirtaş, Levent

Publication type:

Article

MTHFR C677T and A1298C polymorphisms are risk factors for Down’s syndrome in Indian mothers.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 278, doi. 10.1007/s10038-005-0356-3

By:

Rai, Amit Kumar;
Singh, Satya;
Mehta, Stuti;
Kumar, Ashok;
Pandey, L. K.;
Raman, Rajiva

Publication type:

Article

A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.

Published in:

PLoS Genetics, 2019, v. 15, n. 12, p. 1, doi. 10.1371/journal.pgen.1008414

By:

Chernus, Jonathan M.;
Allen, Emily G.;
Zeng, Zhen;
Hoffman, Eva R.;
Hassold, Terry J.;
Feingold, Eleanor;
Sherman, Stephanie L.

Publication type:

Article

Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening.

Published in:

Cell Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41421-022-00457-4

By:

Xu, Chenming;
Li, Jianli;
Chen, Songchang;
Cai, Xiaoqiang;
Jing, Ruilin;
Qin, Xiaomei;
Pan, Dong;
Zhao, Xin;
Ma, Dongyang;
Xu, Xiufeng;
Liu, Xiaojun;
Wang, Can;
Yang, Bingxin;
Zhang, Lanlan;
Li, Shuyuan;
Chen, Yiyao;
Pan, Nina;
Tang, Ping;
Song, Jieping;
Liu, Nian

Publication type:

Article

Differences in crossover frequency and distribution among three sibling species of Drosophila.

Published in:

Genetics, 1996, v. 142, n. 2, p. 507, doi. 10.1093/genetics/142.2.507

By:

True, John R.;
Mercer, John M.

Publication type:

Article

Long-tract mitotic gene conversion in yeast: Evidence for triparental contribution during...

Published in:

Genetics, 1994, v. 137, n. 2, p. 439, doi. 10.1093/genetics/137.2.439

By:

Bethke, Bruce D.;
Golin, John

Publication type:

Article

Down syndrome: genetic recombination and the origin of the extra chromosome 21.

Published in:

Clinical Genetics, 2000, v. 57, n. 2, p. 95, doi. 10.1034/j.1399-0004.2000.570201.x

By:

Hassold, Terry;
Sherman, Stephanie

Publication type:

Article