Works matching DE "FOXP2 gene"

Results: 43

Genome-Wide Identification and Characterization of Fox Genes in the Honeybee, Apis cerana, and Comparative Analysis with Other Bee Fox Genes.

Published in:

International Journal of Genomics, 2018, p. 1, doi. 10.1155/2018/5702061

By:

Nie, Hongyi;
Geng, Haiyang;
Lin, Yan;
Xu, Shupeng;
Li, Zhiguo;
Zhao, Yazhou;
Su, Songkun

Publication type:

Article

FOXL2 molecular status in adult granulosa cell tumors of the ovary: A study of primary and metastatic cases.

Published in:

2016

By:

ZANNONI, GIAN FRANCO;
IMPROTA, GIUSEPPINA;
PETRILLO, MARCO;
PETTINATO, ANGELA;
SCAMBIA, GIOVANNI;
FRAGGETTA, FILIPPO

Publication type:

Case Study

Multiple microRNAs regulate human FOXP2 gene expression by targeting sequences in its 3' untranslated region.

Published in:

Molecular Brain, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13041-014-0071-0

By:

Lijuan Fu;
Zhimin Shi;
Guanzheng Luo;
Weihong Tu;
XiuJie Wang;
Zhide Fang;
XiaoChing Li

Publication type:

Article

Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila.

Published in:

PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0211652

By:

Castells-Nobau, Anna;
Eidhof, Ilse;
Fenckova, Michaela;
Brenman-Suttner, Dova B.;
Scheffer-de Gooyert, Jolanda M.;
Christine, Sheren;
Schellevis, Rosa L.;
van der Laan, Kiran;
Quentin, Christine;
van Ninhuijs, Lisa;
Hofmann, Falko;
Ejsmont, Radoslaw;
Fisher, Simon E.;
Kramer, Jamie M.;
Sigrist, Stephan J.;
Simon, Anne F.;
Schenck, Annette

Publication type:

Article

A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.

Published in:

Frontiers in Behavioral Neuroscience, 2016, v. 10, p. 1, doi. 10.3389/fnbeh.2016.00197

By:

Chabout, Jonathan;
Sarkar, Abhra;
Patel, Sheel R.;
Radden, Taylor;
Dunson, David B.;
Fisher, Simon E.;
Jarvis, Erich D.

Publication type:

Article

Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population.

Published in:

Journal of Neural Transmission, 2017, v. 124, n. 7, p. 891, doi. 10.1007/s00702-017-1723-x

By:

Rao, Wenwang;
Du, Xiangdong;
Zhang, Yingyang;
Yu, Qiong;
Hui, Li;
Yu, Yaqin;
Kou, Changgui;
Yin, Guangzhong;
Zhu, Xiaomin;
Man, Lijuan;
Soares, Jair;
Zhang, Xiang

Publication type:

Article

A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment.

Published in:

Clinical Case Reports, 2015, v. 3, n. 2, p. 110, doi. 10.1002/ccr3.167

By:

Hao Song;
Yuka Makino;
Emiko Noguchi;
Tadao Arinami

Publication type:

Article

<i>Drosophila</i> FoxP Mutants Are Deficient in Operant Self-Learning.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100648

By:

Mendoza, Ezequiel;
Colomb, Julien;
Rybak, Jürgen;
Pflüger, Hans-Joachim;
Zars, Troy;
Scharff, Constance;
Brembs, Björn

Publication type:

Article

Detection of FOXP3 gene expression in patients with Epstein-Barr Virus.

Published in:

International Journal of Pharmaceutical Research (09752366), 2019, v. 11, n. 1, p. 1621

By:

ALMEHANYAH, RAWAQ HAYDER;
ALKAABI, SIHAM JASIM

Publication type:

Article

Enhanced Procedural Learning of Speech Sound Categories in a Genetic Variant of FOXP2.

Published in:

Journal of Neuroscience, 2015, v. 35, n. 20, p. 7808, doi. 10.1523/JNEUROSCI.4706-14.2015

By:

Chandrasekaran, Bharath;
Han-Gyol Yi;
Blanco, Nathaniel J.;
McGeary, John E.;
Maddox, W. Todd

Publication type:

Article

FoxP2 Overexpression Impedes Song Learning.

Published in:

Journal of Neuroscience, 2015, v. 35, n. 7, p. i

By:

Heston, Jonathan B.;
White, Stephanie A.

Publication type:

Article

Correction.

Published in:: 2014
Publication type:: Correction Notice

FOXC2 Expression is Associated with Tumor Proliferation and Invasion Potential in Oral Tongue Squamous Cell Carcinoma.

Published in:

Pathology & Oncology Research, 2015, v. 21, n. 3, p. 783, doi. 10.1007/s12253-014-9891-6

By:

Imayama, Naomi;
Yamada, Shin-ichi;
Yanamoto, Souichi;
Naruse, Tomofumi;
Matsushita, Yuki;
Takahashi, Hidenori;
Seki, Sachiko;
Fujita, Shuichi;
Ikeda, Tohru;
Umeda, Masahiro

Publication type:

Article

Bee venom enhances the differentiation of human regulatory T cells.

Published in:

Allergy, 2015, v. 70, n. 10, p. 1340, doi. 10.1111/all.12691

By:

Caramalho, I.;
Melo, A.;
Pedro, E.;
Barbosa, M. M. P.;
Victorino, R. M. M.;
Pereira Santos, M. C.;
Sousa, A. E.

Publication type:

Article

Association study of FOXP3 gene and the risk of 0020 pre-eclampsia.

Published in:

Clinical & Experimental Hypertension, 2018, v. 40, n. 7, p. 613, doi. 10.1080/10641963.2017.1411500

By:

Gholami, Milad;
Mirfakhraie, Reza;
Pirjani, Reihaneh;
Taheripanah, Robabeh;
Bayat, Sahar;
Daryabari, Seyyedeh Anita;
Noori, Matina;
Ghaderian, Sayyed Mohamad Hossein

Publication type:

Article

Analysis of FOXL2 detects three novel mutations and an atypical phenotype of blepharophimosis-ptosis-epicanthus inversus syndrome.

Published in:

Clinical & Experimental Ophthalmology, 2016, v. 44, n. 9, p. 757, doi. 10.1111/ceo.12783

By:

Krepelova, Anna;
Simandlova, Martina;
Vlckova, Marketa;
Kuthan, Pavel;
Vincent, Andrea L;
Liskova, Petra

Publication type:

Article

Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78531-8

By:

Urbanus, Bastiaan H. A.;
Peter, Saša;
Fisher, Simon E.;
De Zeeuw, Chris I.

Publication type:

Article

Foxc2 and BMP2 Induce Osteogenic/Odontogenic Differentiation and Mineralization of Human Stem Cells from Apical Papilla.

Published in:

Stem Cells International, 2018, p. 1, doi. 10.1155/2018/2363917

By:

Zhang, Wen;
Zhang, Xiaolei;
Li, Junyuan;
Zheng, Jianmao;
Hu, Xiaoli;
Xu, Meng;
Mao, Xueli;
Ling, Junqi

Publication type:

Article

The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 3, p. 338, doi. 10.1038/ejhg.2013.147

By:

Nazaryan, Lusine;
Stefanou, Eunice G;
Hansen, Claus;
Kosyakova, Nadezda;
Bak, Mads;
Sharkey, Freddie H;
Mantziou, Theodora;
Papanastasiou, Anastasios D;
Velissariou, Voula;
Liehr, Thomas;
Syrrou, Maria;
Tommerup, Niels

Publication type:

Article

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.

Published in:

Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0148-1

By:

Moralli, Daniela;
Nudel, Ron;
Chan, May T. M.;
Green, Catherine M.;
Volpi, Emanuela V.;
Benítez-Burraco, Antonio;
Newbury, Dianne F.;
García-Bellido, Paloma

Publication type:

Article

FOXP2 and language alterations in psychiatric pathology.

Published in:

Salud Mental, 2019, v. 42, n. 6, p. 297, doi. 10.17711/SM.0185-3325.2019.039

By:

Castro Martínez, Xochitl Helga;
Moltó Ruiz, María Dolores;
Morales Marin, Mirna Edith;
Flores Lázaro, Julio César;
González Fernández, Javier;
Gutiérrez Najera, Nora Andrea;
Alvarez Amado, Daniel Eduardo;
Nicolini Sánchez, José Humberto

Publication type:

Article

RARE VARIANTS IN LAMA5 GENE ASSOCIATED WITH FLT4 AND FOXC2 MUTATIONS IN PRIMARY LYMPHEDEMA MAY CONTRIBUTE TO SEVERITY.

Published in:

Lymphology, 2016, v. 49, n. 4, p. 192

By:

Liu, N.-f.;
Yu, Z.-y.;
Sun, D.;
Lou, Y.

Publication type:

Article

Disturbances of Modulating Molecules (FOXP3, CTLA-4/CD28/B7, and CD40/CD40L) mRNA Expressions in the Orbital Tissue from Patients with Severe Graves’ Ophthalmopathy.

Published in:

Mediators of Inflammation, 2015, v. 2015, p. 1, doi. 10.1155/2015/340934

By:

Pawlowski, Przemyslaw;
Wawrusiewicz-Kurylonek, Natalia;
Eckstein, Anja;
Reszec, Joanna;
Luczynski, Wlodzimierz;
Johnson, Kristian;
Kretowski, Adam;
Bakunowicz-Lazarczyk, Alina;
Gorska, Maria;
Szamatowicz, Jacek;
Chyczewski, Lech;
Mysliwiec, Janusz

Publication type:

Article

Contactin-associated protein-like 2 expression in SH-SY5Y cells is upregulated by a FOXP2 mutant with a shortened poly-glutamine tract.

Published in:

Molecular Medicine Reports, 2015, v. 12, n. 6, p. 8162, doi. 10.3892/mmr.2015.4483

By:

YUNJING ZHAO;
XIAOLIANG LIU;
HONGWEI SUN;
YUEPING WANG;
WENZHU YANG;
HONGWEI MA

Publication type:

Article

Association of two FOXP3 polymorphisms with breast cancer susceptibility in Chinese Han women.

Published in:

Cancer Management & Research, 2018, v. 10, p. 867, doi. 10.2147/CMAR.S158433

By:

Tian, Tian;
Wang, Meng;
Zheng, Yi;
Yang, Tielin;
Zhu, Wenge;
Li, Hongtao;
Lin, Shuai;
Liu, Kang;
Xu, Peng;
Deng, Yujiao;
Zhou, Linghui;
Dai, Zhijun

Publication type:

Article

Mapping of Human FOXP2 Enhancers Reveals Complex Regulation.

Published in:

Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00047

By:

Becker, Martin;
Devanna, Paolo;
Fisher, Simon E.;
Vernes, Sonja C.

Publication type:

Article

Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System.

Published in:

Frontiers in Molecular Neuroscience, 2017, v. 10, p. 1, doi. 10.3389/fnmol.2017.00112

By:

Mendoza, Ezequiel;
Scharff, Constance

Publication type:

Article

Talking Convergence: Growing Evidence Links FOXP2 and Retinoic Acid in Shaping Speech-Related Motor Circuitry.

Published in:

Frontiers in Neuroscience, 2017, v. 11, p. 1, doi. 10.3389/fnins.2017.00019

By:

Negwer, Moritz;
Schubert, Dirk;
Scharff, Constance

Publication type:

Article

p47phox-Dependent Reactive Oxygen Species Stimulate Nuclear Translocation of the FoxO1 Transcription Factor During Metabolic Inhibition in Cardiomyoblasts.

Published in:

Cell Biochemistry & Biophysics, 2018, v. 76, n. 3, p. 401, doi. 10.1007/s12013-018-0847-4

By:

ter Horst, Ellis N.;
Hahn, Nynke E.;
Geerts, Dirk;
Musters, René J. P.;
Paulus, Walter J.;
van Rossum, Albert C.;
Meischl, Christof;
Piek, Jan J.;
Niessen, Hans W. M.;
Krijnen, Paul A. J.

Publication type:

Article

Dissecting FOXP2 Oligomerization and DNA Binding.

Published in:

Angewandte Chemie, 2019, v. 131, n. 23, p. 7744, doi. 10.1002/ange.201901734

By:

Häußermann, Katharina;
Young, Gavin;
Kukura, Philipp;
Dietz, Hendrik

Publication type:

Article

FOXN1 in Organ Development and Human Diseases.

Published in:

International Reviews of Immunology, 2014, v. 33, n. 2, p. 83, doi. 10.3109/08830185.2013.870171

By:

Palamaro, Loredana;
Romano, Rosa;
Fusco, Anna;
Giardino, Giuliana;
Gallo, Vera;
Pignata, Claudio

Publication type:

Article

Pathogenic conversion of forkhead box protein 3-positive T cells into T helper 17 cells: Is this also the case for multiple sclerosis?

Published in:

Clinical & Experimental Neuroimmunology, 2014, v. 5, n. 2, p. 112, doi. 10.1111/cen3.12114

By:

Saito, Mineki

Publication type:

Article

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development.

Published in:

PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0152576

By:

Mueller, Kathryn L.;
Murray, Jeffrey C.;
Michaelson, Jacob J.;
Christiansen, Morten H.;
Reilly, Sheena;
Tomblin, J. Bruce

Publication type:

Article

Insights into the Genetic Foundations of Human Communication.

Published in:

Neuropsychology Review, 2015, v. 25, n. 1, p. 3, doi. 10.1007/s11065-014-9277-2

By:

Fisher, Simon;
Graham, Sarah;
Deriziotis, Pelagia

Publication type:

Article

Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release.

Published in:

Brain Structure & Function, 2018, v. 223, n. 9, p. 4211, doi. 10.1007/s00429-018-1746-6

By:

van Rhijn, Jon-Ruben;
Fisher, Simon E.;
Vernes, Sonja C.;
Nadif Kasri, Nael

Publication type:

Article

Functional characterization of two enhancers located downstream FOXP2.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0810-2

By:

Torres-Ruiz, Raúl;
Benítez-Burraco, Antonio;
Martínez-Lage, Marta;
Rodríguez-Perales, Sandra;
García-Bellido, Paloma

Publication type:

Article

FOXP2, retinoic acid, and language: a promising direction.

Published in:

2014

By:

Benítez-Burraco, Antonio;
Boeckx, Cedric

Publication type:

Opinion

FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways.

Published in:

Frontiers in Cellular Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fncel.2014.00305

By:

Devanna1, Paolo;
Middelbeek, Jeroen;
Vernes, Sonja C.

Publication type:

Article

Spatiotemporal expression of foxo4, foxo6a, and foxo6b in the developing brain and retina are transcriptionally regulated by PI3K signaling in zebrafish.

Published in:

Development Genes & Evolution, 2017, v. 227, n. 3, p. 219, doi. 10.1007/s00427-017-0575-6

By:

Lin, Sheng-Jia;
Chiang, Ming-Chang;
Shih, Hung-Yu;
Chiang, Kun-Chun;
Cheng, Yi-Chuan

Publication type:

Article

FoxP2 isoforms delineate spatiotemporal transcriptional networks for vocal learning in the zebra finch.

Published in:

eLife, 2018, p. 1, doi. 10.7554/eLife.30649

By:

Burkett, Zachary Daniel;
Day, Nancy F.;
Kimball, Todd Haswell;
Aamodt, Caitlin M.;
Heston, Jonathan B.;
Hilliard, Austin T.;
Xinshu Xiao;
White, Stephanie A.

Publication type:

Article

The butterfly pattern in a patient with chromosome 7 deletion.

Published in:

2014

By:

Velayuthan, Suji;
Dawson, Amber;
Riel-Romero, Rosario Maria S.;
Gonzalez-Toledo, Eduardo

Publication type:

Letter to the Editor

FoxP2 protein levels regulate cell morphology changes and migration patterns in the vertebrate developing telencephalon.

Published in:

Brain Structure & Function, 2016, v. 221, n. 6, p. 2905, doi. 10.1007/s00429-015-1079-7

By:

Garcia-Calero, Elena;
Botella-Lopez, Arancha;
Bahamonde, Olga;
Perez-Balaguer, Ariadna;
Martinez, Salvador

Publication type:

Article

Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome.

Published in:

BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0217-7

By:

Min Xue;
Jie Zheng;
Qing Zhou;
Fielding Hejtmancik, J.;
Yuan Wang;
Shouling Li

Publication type:

Article