Works matching X chromosome

Results: 5000

The making of a Barr body: the mosaic of factors that eXIST on the mammalian inactive X chromosome.

Published in:

Biochemistry & Cell Biology, 2016, v. 94, n. 1, p. 56, doi. 10.1139/bcb-2015-0016

By:

Dixon-McDougall, Thomas;
Brown, Carolyn

Publication type:

Article

Getting to the center of X-chromosome inactivation: the role of transgenes.

Published in:

Biochemistry & Cell Biology, 2009, v. 87, n. 5, p. 759, doi. 10.1139/O09-040

By:

Minks, Jakub;
Brown, Carolyn J.

Publication type:

Article

X chromosome inactivation: heterogeneity of heterochromatin.

Published in:

Biochemistry & Cell Biology, 2008, v. 86, n. 5, p. 370, doi. 10.1139/O08-100

By:

Sidhu, Sharan K.;
Minks, Jakub;
Chang, Samuel C.;
Cotton, Allison M.;
Brown, Carolyn J.

Publication type:

Article

Characterization of chromatin at structurally abnormal inactive X chromosomes reveals potential evidence of a rare hybrid active and inactive isodicentric X chromosome.

Published in:

Chromosome Research, 2020, v. 28, n. 2, p. 155, doi. 10.1007/s10577-019-09621-1

By:

Chadwick, Brian P.

Publication type:

Article

Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements.

Published in:

Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01121-6

By:

Kawashima, Sayaka;
Hattori, Atsushi;
Suzuki, Erina;
Matsubara, Keiko;
Toki, Machiko;
Kosaki, Rika;
Hasegawa, Yukihiro;
Nakabayashi, Kazuhiko;
Fukami, Maki;
Kagami, Masayo

Publication type:

Article

X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study.

Published in:

Respiratory Research, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12931-023-02337-1

By:

Hayden, Lystra P.;
Hobbs, Brian D.;
Busch, Robert;
Cho, Michael H.;
Liu, Ming;
Lopes-Ramos, Camila M.;
Lomas, David A.;
Bakke, Per;
Gulsvik, Amund;
Silverman, Edwin K.;
Crapo, James D.;
Beaty, Terri H.;
Laird, Nan M.;
Lange, Christoph;
DeMeo, Dawn L.

Publication type:

Article

A region of euchromatin coincides with an extensive tandem repeat on the mouse ( Mus musculus) inactive X chromosome.

Published in:

Chromosome Research, 2014, v. 22, n. 3, p. 335, doi. 10.1007/s10577-014-9424-x

By:

Darrow, Emily;
Seberg, Andrew;
Das, Sunny;
Figueroa, Debbie;
Sun, Zhuo;
Moseley, Shawn;
Chadwick, Brian

Publication type:

Article

Twenty Years Later: A Comprehensive Review of the X Chromosome Use in Forensic Genetics.

Published in:

Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.00926

By:

Gomes, Iva;
Pinto, Nádia;
Antão-Sousa, Sofia;
Gomes, Verónica;
Gusmão, Leonor;
Amorim, António

Publication type:

Article

Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion.

Published in:

Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00101

By:

Santos-Rebouças, Cíntia B.;
Boy, Raquel;
Vianna, Evelyn Q.;
Gonçalves, Andressa P.;
Piergiorge, Rafael M.;
Abdala, Bianca B.;
dos Santos, Jussara M.;
Calassara, Veluma;
Machado, Filipe B.;
Medina-Acosta, Enrique;
Pimentel, Márcia M. G.

Publication type:

Article

Molecular cytogenetic characterization of a de novo derivative chromosome X with an unbalanced t(X;9) translocation in a fetus and literature review.

Published in:

Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00603-3

By:

Wu, Qiong;
Kong, Hui;
Shen, Yanyan;
Chen, Jing

Publication type:

Article

The Inactive X Chromosome: A Genetic Driver of Female‐Biased Rheumatic Autoimmune Disorders?

Published in:

European Journal of Immunology, 2025, v. 55, n. 5, p. 1, doi. 10.1002/eji.202451331

By:

Ferrayé, Léa;
Nieucel, Mélissa;
Savignac, Magali;
Chaumeil, Julie;
Guéry, Jean‐Charles

Publication type:

Article

X chromosome inactivation in mammalian embryonic development.

Published in:

CES Medicina Veterinaria & Zootecnica, 2013, v. 8, n. 2, p. 108

By:

Acosta Lobo, Mariano Eliécer;
Vásquez Araque, Neil Aldrin;
Londoño Franco, Luis Fernando

Publication type:

Article

Statistical methods for testing X chromosome variant associations: application to sex-specific characteristics of bipolar disorder.

Published in:

Biology of Sex Differences, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13293-019-0272-4

By:

Jons, William A.;
Colby, Colin L.;
McElroy, Susan L.;
Frye, Mark A.;
Biernacka, Joanna M.;
Winham, Stacey J.

Publication type:

Article

Forensic Applications of Markers Present on the X Chromosome.

Published in:

Genes, 2022, v. 13, n. 9, p. 1597, doi. 10.3390/genes13091597

By:

Garcia, Fernanda M.;
Bessa, Bárbara G. O.;
dos Santos, Eldamária V. W.;
Pereira, Julia D. P.;
Alves, Lyvia N. R.;
Vianna, Lucas A.;
Casotti, Matheus C.;
Trabach, Raquel S. R.;
Stange, Victor S.;
Meira, Débora D.;
Louro, Iuri D.

Publication type:

Article

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis.

Published in:

PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0158550

By:

Kanaan, Sami B.;
Onat, Onur E.;
Balandraud, Nathalie;
Martin, Gabriel V.;
Nelson, J. Lee;
Azzouz, Doua F.;
Auger, Isabelle;
Arnoux, Fanny;
Martin, Marielle;
Roudier, Jean;
Ozcelik, Tayfun;
Lambert, Nathalie C.

Publication type:

Article

Case Report: De novo DDX3X mutation caused intellectual disability in a female with skewed X-chromosome inactivation on the mutant allele.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.999442

By:

Yixi Sun;
Yangwen Qian;
Hai-Xi Sun;
Min Chen;
Yuqin Luo;
Xiaojing Xu;
Kai Yan;
Liya Wang;
Junjie Hu;
Minyue Dong

Publication type:

Article

DNA replication timing: Coordinating genome stability with genome regulation on the X chromosome and beyond.

Published in:

BioEssays, 2014, v. 36, n. 10, p. 997, doi. 10.1002/bies.201400077

By:

Koren, Amnon

Publication type:

Article

Characterization of X-Chromosome Gene Expression in Bovine Blastocysts Derived by In vitro Fertilization and Somatic Cell Nuclear Transfer.

Published in:

Frontiers in Genetics, 2017, p. 1, doi. 10.3389/fgene.2017.00042

By:

Byungkuk Min;
Jung Sun Park;
Kyuheum Jeon;
Yong-Kook Kang

Publication type:

Article

Sex differences in number of X chromosomes and X-chromosome inactivation in females promote greater variability in hearing among males.

Published in:

Biology of Sex Differences, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13293-022-00457-9

By:

Summers, Van

Publication type:

Article

Cross-species examination of X-chromosome inactivation highlights domains of escape from silencing.

Published in:

Epigenetics & Chromatin, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13072-021-00386-8

By:

Balaton, Bradley P.;
Fornes, Oriol;
Wasserman, Wyeth W.;
Brown, Carolyn J.

Publication type:

Article

Live Cell Imaging of the Nascent Inactive X Chromosome during the Early Differentiation Process of Naive ES Cells towards Epiblast Stem Cells.

Published in:

PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0116109

By:

Guyochin, Aurélia;
Maenner, Sylvain;
Chu, Erin Tsi-Jia;
Hentati, Asma;
Attia, Mikael;
Avner, Philip;
Clerc, Philippe

Publication type:

Article

Low-level X chromosome mosaicism in women with sporadic premature ovarian failure.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2011, v. 22, n. 4, p. 399, doi. 10.1016/j.rbmo.2011.01.002

By:

Gersak, K.;
Veble, A.

Publication type:

Article

Female predisposition to TLR7-driven autoimmunity: gene dosage and the escape from X chromosome inactivation.

Published in:

Seminars in Immunopathology, 2019, v. 41, n. 2, p. 153, doi. 10.1007/s00281-018-0712-y

By:

Souyris, Mélanie;
Mejía, José E.;
Chaumeil, Julie;
Guéry, Jean-Charles

Publication type:

Article

Study of methylation of histone H3 lysine 9 and H3 lysine 27 during X chromosome inactivation in three types of cells.

Published in:

Chromosome Research, 2012, v. 20, n. 6, p. 769, doi. 10.1007/s10577-012-9311-2

By:

Li, Yan;
Tan, Tan;
Zong, Le;
He, Dacheng;
Tao, Wei;
Liang, Qianjin

Publication type:

Article

Escape from X chromosome inactivation and female bias of autoimmune diseases.

Published in:

Molecular Medicine, 2020, v. 26, n. 1, p. 1, doi. 10.1186/s10020-020-00256-1

By:

Mousavi, Mohammad Javad;
Mahmoudi, Mahdi;
Ghotloo, Somayeh

Publication type:

Article

X-chromosome association study reveals genetic susceptibility loci of hypospadias in southern Chinese population.

Published in:

World Journal of Urology, 2025, v. 43, n. 1, p. 1, doi. 10.1007/s00345-025-05667-5

By:

Liu, Yanqing;
Li, Binyao;
Deng, Fuming;
Zhao, Xinying;
Liu, Zhihai;
Zhao, Jinglu;
Fu, Wen;
Zhang, Yan;
Zuo, Xiaoyu

Publication type:

Article

Relationship between Glucose-6-Phosphate Dehydrogenase Deficiency, X-Chromosome Inactivation and Inflammatory Markers.

Published in:

Antioxidants, 2023, v. 12, n. 2, p. 334, doi. 10.3390/antiox12020334

By:

Errigo, Alessandra;
Bitti, Angela;
Galistu, Franca;
Salis, Roberta;
Pes, Giovanni Mario;
Dore, Maria Pina

Publication type:

Article

Perturbed maintenance of transcriptional repression on the inactive X-chromosome in the mouse brain after Xist deletion.

Published in:

Epigenetics & Chromatin, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13072-018-0219-8

By:

Adrianse, Robin L.;
Smith, Kaleb;
Gatbonton-Schwager, Tonibelle;
Sripathy, Smitha P.;
Lao, Uyen;
Foss, Eric J.;
Boers, Ruben G.;
Boers, Joachim B.;
Gribnau, Joost;
Bedalov, Antonio

Publication type:

Article

Loss of SETDB1 decompacts the inactive X chromosome in part through reactivation of an enhancer in the IL1RAPL1 gene.

Published in:

Epigenetics & Chromatin, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13072-018-0218-9

By:

Sun, Zhuo;
Chadwick, Brian P.

Publication type:

Article

The Mbd1-Atf7ip-Setdb1 pathway contributes to the maintenance of X chromosome inactivation.

Published in:

Epigenetics & Chromatin, 2014, v. 7, n. 1, p. 1, doi. 10.1186/1756-8935-7-12

By:

Minkovsky, Alissa;
Sahakyan, Anna;
Rankin-Gee, Elyse;
Bonora, Giancarlo;
Patel, Sanjeet;
Plath, Kathrin

Publication type:

Article

Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders.

Published in:

Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00703-w

By:

Tolmacheva, Ekaterina N.;
Kashevarova, Anna A.;
Fonova, Elizaveta A.;
Salyukova, Olga A.;
Seitova, Gulnara N.;
Nazarenko, Lyudmila P.;
Agafonova, Anna A.;
Minaycheva, Larisa I.;
Ravzhaeva, Ekaterina G.;
Petrova, Valeria V.;
Lopatkina, Maria E.;
Belyaeva, Elena O.;
Vovk, Svetlana L.;
Fedotov, Dmitry A.;
Vasilyeva, Oksana Y.;
Skryabin, Nikolay A.;
Lebedev, Igor N.

Publication type:

Article

Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome.

Published in:

Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00593-2

By:

Luo, Hunjin;
Ni, Liu;
Yang, Yi-Qiong;
Zhang, Xiao-Min;
Huang, Hongping;
Tan, Sainan;
Ling, Chen;
Liang, Li;
Wang, Ling;
Dan, Tang;
Zhou, Shu-Xiang;
Yang, Chunliu

Publication type:

Article

Regions of XY homology in the pig X chromosome and the boundary of the pseudoautosomal region.

Published in:

BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-3

By:

Skinner, Benjamin M;
Lachani, Kim;
Sargent, Carole A;
Affara, Nabeel A

Publication type:

Article

Cdk8 and Hira mutations trigger X chromosome elimination in naive female hybrid mouse embryonic stem cells.

Published in:

Chromosome Research, 2024, v. 32, n. 4, p. 1, doi. 10.1007/s10577-024-09756-w

By:

Halter, Kevin;
Chen, Jingyi;
Priklopil, Tadeas;
Monfort, Asun;
Wutz, Anton

Publication type:

Article

Constitutive heterochromatin propagation contributes to the X chromosome inactivation.

Published in:

Chromosome Research, 2022, v. 30, n. 4, p. 289, doi. 10.1007/s10577-022-09706-4

By:

Shevchenko, Alexander I.;
Rifel, Nikita A.;
Zakian, Suren M.;
Zakharova, Irina S.

Publication type:

Article

A quantum mechanical approach to random X chromosome inactivation.

Published in:

AIMS Biophysics, 2021, v. 8, n. 4, p. 322, doi. 10.3934/biophy.2021026

By:

Lobato, Rodrigo

Publication type:

Article

Mechanisms of Choice in X-Chromosome Inactivation.

Published in:

Cells (2073-4409), 2022, v. 11, n. 3, p. 535, doi. 10.3390/cells11030535

By:

Furlan, Giulia;
Galupa, Rafael

Publication type:

Article

An investigation of a hemophilia A female with heterozygous intron 22 inversion and skewed X chromosome inactivation.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2024.1500167

By:

Tan, Xiaoyan;
Yang, Yi;
Wu, Xia;
Zhu, Jing;
Wang, Teng;
Jiang, Huihui;
Chen, Shu;
Lou, Shifeng

Publication type:

Article

Genes on the X chromosome affect development of collagen-induced arthritis in mice.

Published in:

1993

By:

Jansson, L.;
Holmdahl, R.

Publication type:

Abstract

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

Published in:

Journal of Human Genetics, 2007, v. 52, n. 5, p. 397, doi. 10.1007/s10038-007-0127-4

By:

Hayashi, Shin;
Honda, Shozo;
Minaguchi, Maki;
Makita, Yoshio;
Okamoto, Nobuhiko;
Kosaki, Rika;
Okuyama, Torayuki;
Imoto, Issei;
Mizutani, Shuki;
Inazawa, Johji

Publication type:

Article

A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 11, p. 1030, doi. 10.1007/s10038-006-0049-6

By:

Cau, Milena;
Addis, Maria;
Congiu, Rita;
Meloni, Cristiana;
Cao, Antonio;
Santaniello, Simona;
Loi, Mario;
Emma, Francesco;
Zuffardi, Orsetta;
Ciccone, Roberto;
Sole, Gabriella;
Melis, Maria

Publication type:

Article

Did the creeping vole sex chromosomes evolve through a cascade of adaptive responses to a selfish x chromosome?

Published in:

BioEssays, 2023, v. 45, n. 12, p. 1, doi. 10.1002/bies.202100164

By:

Roy, Scott William

Publication type:

Article

X-chromosome inactivation in female patients with Fabry disease.

Published in:

Clinical Genetics, 2016, v. 89, n. 1, p. 44, doi. 10.1111/cge.12613

By:

Echevarria, L.;
Benistan, K.;
Toussaint, A.;
Dubourg, O.;
Hagege, A.A.;
Eladari, D.;
Jabbour, F.;
Beldjord, C.;
De Mazancourt, P.;
Germain, D.P.

Publication type:

Article

Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 6, p. 628, doi. 10.1038/sj.ejhg.5201799

By:

Renault, Nisa K.;
Dyack, Sarah;
Dobson, Melanie J.;
Costa, Teresa;
Lam, Wan L.;
Greer, Wenda L.

Publication type:

Article

X-linked Deficiency in ELF4 in Females with Skewed X Chromosome Inactivation.

Published in:

Journal of Clinical Immunology, 2025, v. 45, n. 1, p. 1, doi. 10.1007/s10875-025-01866-2

By:

Zhao, Rongtao;
Zhang, Zhuo;
Mei, Shiyue;
Sun, Li;
Zhang, Qianlu;
Lv, Qianying;
Zhou, Fang;
Sun, Gan;
Zhou, Lina;
Tang, Xuemei;
An, Yunfei;
Liu, Zhifeng;
Zhao, Xiaodong;
Du, Hongqiang

Publication type:

Article

High frequency of the X-chromosome inactivation in young female patients with high-grade glioma.

Published in:

Diagnostic Pathology, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1746-1596-8-101

By:

Gang Li;
Zhiguo Zhang;
Tianbo Jin;
Hongjuan Liang;
Yanyang Tu;
Li Gong;
Zhongping Chen;
Guodong Gao

Publication type:

Article

Astroblastoma: a distinct tumor entity characterized by alterations of the X chromosome and MN1 rearrangement.

Published in:

Brain Pathology, 2018, v. 28, n. 5, p. 684, doi. 10.1111/bpa.12565

By:

Hirose, Takanori;
Nobusawa, Sumihito;
Sugiyama, Kazuhiko;
Amatya, Vishwa J.;
Fujimoto, Naomi;
Sasaki, Atsushi;
Mikami, Yoshiki;
Kakita, Akiyoshi;
Tanaka, Shinya;
Yokoo, Hideaki

Publication type:

Article

Sex chromosomal dimorphisms narrated by X-chromosome translocation in a spiny frog (Quasipaa boulengeri).

Published in:

Frontiers in Zoology, 2018, v. 15, n. 1, p. N.PAG, doi. 10.1186/s12983-018-0291-8

By:

Yuan, Xiuyun;
Xia, Yun;
Zeng, Xiaomao

Publication type:

Article

BEXCIS: Bayesian methods for estimating the degree of the skewness of X chromosome inactivation.

Published in:

BMC Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12859-022-04721-y

By:

Yu, Wen-Yi;
Zhang, Yu;
Li, Meng-Kai;
Yang, Zi-Ying;
Fung, Wing Kam;
Zhao, Pei-Zhen;
Zhou, Ji-Yuan

Publication type:

Article

Chromosome X-Wide Association Study Identifies Loci for Fasting Insulin and Height and Evidence for Incomplete Dosage Compensation.

Published in:

PLoS Genetics, 2014, v. 10, n. 2, p. 1, doi. 10.1371/journal.pgen.1004127

By:

Tukiainen, Taru;
Pirinen, Matti;
Sarin, Antti-Pekka;
Ladenvall, Claes;
Kettunen, Johannes;
Lehtimäki, Terho;
Lokki, Marja-Liisa;
Perola, Markus;
Sinisalo, Juha;
Vlachopoulou, Efthymia;
Eriksson, Johan G.;
Groop, Leif;
Jula, Antti;
Järvelin, Marjo-Riitta;
Raitakari, Olli T.;
Salomaa, Veikko;
Ripatti, Samuli

Publication type:

Article