Works matching DE "X chromosome"

Results: 3912

Schizophrenia and sex chromosome anomalies.

Published in:

1994

By:

DeLisi, Lynn E.;
Friedrich, Ursula;
Wahlstrom, Jan;
Boccio-Smith, Angela;
Forsman, Anders;
Eklund, Kurt;
Crow, Timothy J.

Publication type:

Journal Article

Genetic transmission of major affective disorders: Quantitative models and linkage analyses.

Published in:

1990

By:

Faraone, Stephen V.;
Kremen, William S.;
Tsuang, Ming T.

Publication type:

Journal Article

Prospects for the Genetic Analysis of Schizophrenia.

Published in:

1989

By:

Pato, Carlos N.;
Lander, Eric S.;
Schulz, S. Charles

Publication type:

Journal Article

Evidence for a Sex Chromosome Locus for Schizophrenia.

Published in:

1989

By:

DeLisi, Lynn E.;
Crow, Timothy J.

Publication type:

Journal Article

Familial correlational analyses, sex differences, and the X-linked gene hypothesis.

Published in:

1983

By:

Thomas, Hoben

Publication type:

Journal Article

Topological organization of multichromosomal regions by the long intergenic noncoding RNA Firre.

Published in:

Nature Structural & Molecular Biology, 2014, v. 21, n. 2, p. 198, doi. 10.1038/nsmb.2764

By:

Hacisuleyman, Ezgi;
Goff, Loyal A;
Trapnell, Cole;
Williams, Adam;
Henao-Mejia, Jorge;
Sun, Lei;
McClanahan, Patrick;
Hendrickson, David G;
Sauvageau, Martin;
Kelley, David R;
Morse, Michael;
Engreitz, Jesse;
Lander, Eric S;
Guttman, Mitch;
Lodish, Harvey F;
Flavell, Richard;
Raj, Arjun;
Rinn, John L

Publication type:

Article

Transcriptional control of a whole chromosome: emerging models for dosage compensation.

Published in:

Nature Structural & Molecular Biology, 2014, v. 21, n. 2, p. 118, doi. 10.1038/nsmb.2763

By:

Ferrari, Francesco;
Alekseyenko, Artyom A;
Park, Peter J;
Kuroda, Mitzi I

Publication type:

Article

Human inactive X chromosome is compacted through a PRC2-independent SMCHD1-HBiX1 pathway.

Published in:

Nature Structural & Molecular Biology, 2013, v. 20, n. 5, p. 566, doi. 10.1038/nsmb.2532

By:

Nozawa, Ryu-Suke;
Nagao, Koji;
Igami, Ken-Taro;
Shibata, Sachiko;
Shirai, Natsuko;
Nozaki, Naohito;
Sado, Takashi;
Kimura, Hiroshi;
Obuse, Chikashi

Publication type:

Article

A lncRNA for the active X.

Published in:

Nature Structural & Molecular Biology, 2013, v. 20, n. 3, p. 308, doi. 10.1038/nsmb.2538

By:

Chen, Inês

Publication type:

Article

Chromatin proteins captured by ChIP-mass spectrometry are linked to dosage compensation in Drosophila.

Published in:

Nature Structural & Molecular Biology, 2013, v. 20, n. 2, p. 202, doi. 10.1038/nsmb.2477

By:

Wang, Charlotte I;
Alekseyenko, Artyom A;
LeRoy, Gary;
Elia, Andrew EH;
Gorchakov, Andrey A;
Britton, Laura-Mae P;
Elledge, Stephen J;
Kharchenko, Peter V;
Garcia, Benjamin A;
Kuroda, Mitzi I

Publication type:

Article

Claims and counterclaims of X-chromosome compensation.

Published in:

Nature Structural & Molecular Biology, 2012, v. 19, n. 1, p. 3, doi. 10.1038/nsmb.2218

By:

Birchler, James A

Publication type:

Article

Structural basis for MOF and MSL3 recruitment into the dosage compensation complex by MSL1.

Published in:

Nature Structural & Molecular Biology, 2011, v. 18, n. 2, p. 142, doi. 10.1038/nsmb.1960

By:

Kadlec, Jan;
Hallacli, Erinc;
Lipp, Michael;
Holz, Herbert;
Sanchez-Weatherby, Juan;
Cusack, Stephen;
Akhtar, Asifa

Publication type:

Article

The A-repeat links ASF/SF2-dependent Xist RNA processing with random choice during X inactivation.

Published in:

Nature Structural & Molecular Biology, 2010, v. 17, n. 8, p. 948, doi. 10.1038/nsmb.1877

By:

Royce-Tolland, Morgan E.;
Andersen, Angela A.;
Koyfman, Hannah R.;
Talbot, Dale J.;
Wutz, Anton;
Tonks, Ian D.;
Kay, Graham F.;
Panning, Barbara

Publication type:

Article

Corecognition of DNA and a methylated histone tail by the MSL3 chromodomain.

Published in:

Nature Structural & Molecular Biology, 2010, v. 17, n. 8, p. 1027, doi. 10.1038/nsmb.1856

By:

Daesung Kim;
Blus, Bartlomiej J.;
Chandra, Vikas;
Pengxiang Huang;
Rastinejad, Fraydoon;
Khorasanizadeh, Sepideh

Publication type:

Article

The histone variant macroH2A is an epigenetic regulator of key developmental genes.

Published in:

Nature Structural & Molecular Biology, 2009, v. 16, n. 10, p. 1074, doi. 10.1038/nsmb.1665

By:

Buschbeck, Marcus;
Uribesalgo, Iris;
Wibowo, Indra;
Rué, Pau;
Martin, David;
Gutierrez, Arantxa;
Morey, Lluís;
Guigó, Roderic;
López-Schier, Hernán;
Di Croce, Luciano

Publication type:

Article

Drosophila MSL complex globally acetylates H4K16 on the male X chromosome for dosage compensation.

Published in:

Nature Structural & Molecular Biology, 2009, v. 16, n. 8, p. 825, doi. 10.1038/nsmb.1644

By:

Gelbart, Marnie E.;
Larschan, Erica;
Shouyong Peng;
Park, Peter J.;
Kuroda, Mitzi I.

Publication type:

Article

Hit and run: X marks the spot!

Published in:

Nature Structural & Molecular Biology, 2009, v. 16, n. 8, p. 801, doi. 10.1038/nsmb0809-801

By:

Weake, Vikki M.;
Workman, Jerry L.

Publication type:

Article

The MSL3 chromodomain directs a key targeting step for dosage compensation of the Drosophila melanogaster X chromosome.

Published in:

Nature Structural & Molecular Biology, 2008, v. 15, n. 12, p. 1318, doi. 10.1038/nsmb.1520

By:

Sural, Tuba H.;
Peng, Shouyong;
Li, Bing;
Workman, Jerry L.;
Park, Peter J.;
Kuroda, Mitzi I.

Publication type:

Article

The retinitis pigmentosa 2 gene product is a GTPase-activating protein for Arf-like 3.

Published in:

Nature Structural & Molecular Biology, 2008, v. 15, n. 4, p. 373, doi. 10.1038/nsmb.1396

By:

Veltel, Stefan;
Gasper, Raphael;
Eisenacher, Elke;
Wittinghofer, Alfred

Publication type:

Article

X chromosome exposé.

Published in:

Nature Structural & Molecular Biology, 2007, v. 14, n. 9, p. 794, doi. 10.1038/nsmb0907-794

By:

Lall, Sabbi

Publication type:

Article

Keeping the right dosage.

Published in:

Nature Structural & Molecular Biology, 2007, v. 14, n. 2, p. 97, doi. 10.1038/nsmb0207-97

By:

Lall, Sabbi

Publication type:

Article

UNRaveling the regulation of dosage compensation.

Published in:

Nature Structural & Molecular Biology, 2006, v. 13, n. 3, p. 189, doi. 10.1038/nsmb0306-189

By:

Shyu, Ann-Bin

Publication type:

Article

Does the X-Chromosome Carry the Gene Responsible for Bipolar Disorder?

Published in:

Klinik Psikofarmakoloji Bulteni, 2013, v. 23, n. 3, p. 267, doi. 10.5455/bcp.20130318061411

By:

Edgunlu, Tuba Gokdogan;
Duvarci, Ibrahim;
Cetin, Esin Sakalli

Publication type:

Article

Ethics in pre-ART genetics: a missed X-linked Menkes disease case.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 4, p. 811, doi. 10.1007/s10815-023-02778-z

By:

Gerdes, A.-M. A.;
Møller, L. Birk;
Horn, N.

Publication type:

Article

Genomic testing for copy number and single nucleotide variants in spermatogenic failure.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 9, p. 2103, doi. 10.1007/s10815-022-02538-5

By:

Hardy, J.;
Pollock, N.;
Gingrich, T.;
Sweet, P.;
Ramesh, A.;
Kuong, J.;
Basar, A.;
Jiang, H.;
Hwang, K.;
Vukina, J.;
Jaffe, T.;
Olszewska, M.;
Kurpisz, M.;
Yatsenko, A. N.

Publication type:

Article

Not just carriers: experiences of X-linked female heterozygotes.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 10, p. 2757, doi. 10.1007/s10815-021-02270-6

By:

Choi, Jennifer;
Kane, Taylor;
Propst, Lauren;
Spencer, Sara;
Kostialik, Jamie;
Arjunan, Aishwarya

Publication type:

Article

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 6, p. 1421, doi. 10.1007/s10815-020-01779-6

By:

Wu, Huan;
Gao, Yang;
Ma, Cong;
Shen, Qunshan;
Wang, Jiajia;
Lv, Mingrong;
Liu, Chunyu;
Cheng, Huiru;
Zhu, Fuxi;
Tian, Shixiong;
Elshewy, Nagwa;
Ni, Xiaoqing;
Tan, Qing;
Xu, Xiaofeng;
Zhou, Ping;
Wei, Zhaolian;
Zhang, Feng;
He, Xiaojin;
Cao, Yunxia

Publication type:

Article

Unbalanced X;9 translocation in an infertile male with de novo duplication Xp22.31p22.33.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 4, p. 769, doi. 10.1007/s10815-019-01405-0

By:

Roumelioti, Fani-Marlen;
Louizou, Eirini;
Karras, Spyridon;
Neroutsou, Rozalia;
Velissariou, Voula;
Gagos, Sarantis

Publication type:

Article

Male infertility: establishing sperm aneuploidy thresholds in the laboratory.

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 3, p. 371, doi. 10.1007/s10815-018-1385-0

By:

García-Mengual, Elena;
Triviño, Juan Carlos;
Sáez-Cuevas, Alba;
Bataller, Juan;
Ruíz-Jorro, Miguel;
Vendrell, Xavier

Publication type:

Article

Possible influence of menstrual cycle on lymphocyte X chromosome mosaicism.

Published in:

Journal of Assisted Reproduction & Genetics, 2015, v. 32, n. 1, p. 111, doi. 10.1007/s10815-014-0377-y

By:

Gersak, K.;
Perme-Pohar, M.;
Veble, A.;
Gersak, B.

Publication type:

Article

An infertile 45,X male with a SRY-bearing chromosome 13: a clinical case report and literature review.

Published in:

Journal of Assisted Reproduction & Genetics, 2015, v. 32, n. 1, p. 107, doi. 10.1007/s10815-014-0376-z

By:

Peng, Di;
Zhang, Yong-Sheng;
Zhang, Xin-Yue;
Hu, Cong;
Liu, Mei-Han;
Liu, Rui-Zhi

Publication type:

Article

Nuclear DNA fragmentation negatively affects zona binding competence of Y bearing mouse spermatozoa.

Published in:

Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 12, p. 1611, doi. 10.1007/s10815-013-0123-x

By:

Kumar, Dayanidhi;
Upadhya, Dinesh;
Uppangala, Shubhashree;
Salian, Sujit Raj;
Kalthur, Guruprasad;
Adiga, Satish Kumar

Publication type:

Article

Ubiquitin-specific protease ( USP26) gene alterations associated with male infertility and recurrent pregnancy loss (RPL) in Iranian infertile patients.

Published in:

Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 7, p. 923, doi. 10.1007/s10815-013-0027-9

By:

Asadpor, U.;
Totonchi, M.;
Sabbaghian, M.;
Hoseinifar, H.;
Akhound, M.;
Zari Moradi, Sh.;
Haratian, K.;
Sadighi Gilani, M.;
Gourabi, H.;
Mohseni Meybodi, A.

Publication type:

Article

The role of genetic and autoimmune factors in premature ovarian failure.

Published in:

Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 5, p. 617, doi. 10.1007/s10815-013-9974-4

By:

Shamilova, Nigyar;
Marchenko, Larisa;
Dolgushina, Nataliya;
Zaletaev, Dmitry;
Sukhikh, Gennady

Publication type:

Article

Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports.

Published in:

2013

By:

Gao, Xuefeng;
Chen, Guian;
Huang, Jing;
Bai, Quan;
Zhao, Nan;
Shao, Minjie;
Jiao, Liping;
Wei, Yanling;
Chang, Liang;
Li, Dan;
Yang, Liping

Publication type:

Report

Genetic and epigenetic X-chromosome variations in a parthenogenetic human embryonic stem cell line.

Published in:

Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 4, p. 303, doi. 10.1007/s10815-010-9517-1

By:

Liu, Weiqiang;
Yin, Yifei;
Jiang, Yonghua;
Kou, Chaohui;
Luo, Yumei;
Huang, Shengchang;
Zheng, Yuhong;
Li, Shaoying;
Li, Qing;
Guo, Liyuan;
Gao, Shaorong;
Sun, Xiaofang

Publication type:

Article

A normal birth following preimplantation genetic diagnosis by FISH determination in the carriers of der(15)t(Y;15) (Yq12;15p11) translocations: two case reports.

Published in:

Journal of Assisted Reproduction & Genetics, 2007, v. 24, n. 10, p. 483, doi. 10.1007/s10815-007-9163-4

By:

Yongjian Chen;
Guian Chen;
Ying Lian;
Xuefeng Gao;
Jin Huang;
Jie Qiao

Publication type:

Article

Predictive value of preimplantation genetic diagnosis for aneuploidy screening in repeated IVF-ET cycles among women with recurrent implantation failure.

Published in:

Journal of Assisted Reproduction & Genetics, 2008, v. 25, n. 2/3, p. 103, doi. 10.1007/s10815-008-9200-y

By:

Pagidas, K.;
Ying, Y.;
Keefe, D.

Publication type:

Article

Accuracy of fetal gender detection using a conventional nested PCR assay of maternal plasma in daily practice.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2008, v. 48, n. 5, p. 501, doi. 10.1111/j.1479-828X.2008.00906.x

By:

Tungwiwat, Warunee;
Fucharoen, Supan;
Fucharoen, Goonnapa;
Ratanasiri, Thawalwong;
Sanchaisuriya, Kanokwan

Publication type:

Article

Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2006, v. 46, n. 5, p. 384, doi. 10.1111/j.1479-828X.2006.00622.x

By:

Bagislar, Sevgi;
Ustuner, Isik;
Cengiz, Bora;
Soylemez, Feride;
Akyerli, Cemaliye Boylu;
Ceylaner, Serdar;
Ceylaner, Gulay;
Acar, Aynur;
Ozcelik, Tayfun

Publication type:

Article

Characteristics of a Novel Activator of RNA Polymerase II Transcription.

Published in:

Doklady Biochemistry & Biophysics, 2005, v. 402, n. 1-6, p. 204, doi. 10.1007/s10628-005-0071-1

By:

Shidlovskii, Yu. V.;
Krasnov, A. N.;
Nikolenko, Yu. V.;
Georgieva, S. G.;
Nabirochkina, E. N.

Publication type:

Article

Ex vivo disease modelling of Rett syndrome: the transcriptomic and metabolomic implications of direct neuronal conversion.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09915-6

By:

Karaosmanoglu, Beren;
Imren, Gozde;
Ozisin, M. Samil;
Reçber, Tuba;
Simsek Kiper, Pelin Ozlem;
Haliloglu, Goknur;
Alikaşifoğlu, Mehmet;
Nemutlu, Emirhan;
Taskiran, Ekim Z.;
Utine, Gulen Eda

Publication type:

Article

Morphological plasticity in the rice root nematode, Hirschmanniella oryzae (van Breda de Haan, 1902) Luc & Goodey, 1964 from Korea, with inferences from its ribosomal and mitochondrial DNA.

Published in:

European Journal of Plant Pathology, 2022, v. 164, n. 3, p. 337, doi. 10.1007/s10658-022-02563-1

By:

Mwamula, Abraham Okki;
Lim, Tae Heon;
Kim, Yiseul;
Lee, Ho-wook;
Kim, Young Ho;
Lee, Dong Woon

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

Sex chromosome differentiation via changes in the Y chromosome repeat landscape in African annual killifishes Nothobranchius furzeri and N. kadleci.

Published in:

Chromosome Research, 2022, v. 30, n. 4, p. 309, doi. 10.1007/s10577-022-09707-3

By:

Štundlová, Jana;
Hospodářská, Monika;
Lukšíková, Karolína;
Voleníková, Anna;
Pavlica, Tomáš;
Altmanová, Marie;
Richter, Annekatrin;
Reichard, Martin;
Dalíková, Martina;
Pelikánová, Šárka;
Marta, Anatolie;
Simanovsky, Sergey A.;
Hiřman, Matyáš;
Jankásek, Marek;
Dvořák, Tomáš;
Bohlen, Joerg;
Ráb, Petr;
Englert, Christoph;
Nguyen, Petr;
Sember, Alexandr

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

Meiotic pairing and double-strand break formation along the heteromorphic threespine stickleback sex chromosomes.

Published in:

Chromosome Research, 2022, v. 30, n. 4, p. 429, doi. 10.1007/s10577-022-09699-0

By:

Nath, Shivangi;
Welch, Lucille A.;
Flanagan, Mary K.;
White, Michael A.

Publication type:

Article

Non-random chromosome segregation and chromosome eliminations in the fly Bradysia (Sciara).

Published in:

Chromosome Research, 2022, v. 30, n. 2/3, p. 273, doi. 10.1007/s10577-022-09701-9

By:

Gerbi, Susan A.

Publication type:

Article

The fate of a suppressed X-linked meiotic driver: experimental evolution in Drosophila simulans.

Published in:

Chromosome Research, 2022, v. 30, n. 2/3, p. 141, doi. 10.1007/s10577-022-09698-1

By:

Bastide, Héloïse;
Ogereau, David;
Montchamp-Moreau, Catherine;
Gérard, Pierre R.

Publication type:

Article

The maize abnormal chromosome 10 meiotic drive haplotype: a review.

Published in:

Chromosome Research, 2022, v. 30, n. 2/3, p. 205, doi. 10.1007/s10577-022-09693-6

By:

Dawe, R. Kelly

Publication type:

Article