Works matching MSX genes

Results: 89

Differential regulation of msx genes in the development of the gonopodium, an intromittent organ, and of the “sword,” a sexually selected trait of swordtail fishes (Xiphophorus ).

Published in:

Evolution & Development, 2003, v. 5, n. 5, p. 466, doi. 10.1046/j.1525-142X.2003.03053.x

By:

Zauner, Hans;
Begemann, Gerrit;
Marí-Beffa, Manuel;
Meyer, Axel

Publication type:

Article

Msx genes are expressed in the carapacial ridge of turtle shell: a study of the European pond turtle, Emys orbicularis.

Published in:

Development Genes & Evolution, 2003, v. 213, n. 9, p. 464, doi. 10.1007/s00427-003-0347-3

By:

Vincent, Christine;
Bontoux, Martine;
Le Douarin, Nicole M.;
Pieau, Claude;
Monsoro-Burq, Anne-Hèl&e´ne

Publication type:

Article

Uterine inactivation of muscle segment homeobox (Msx) genes alters epithelial cell junction proteins during embryo implantation.

Published in:

FASEB Journal, 2016, v. 30, n. 4, p. 1425, doi. 10.1096/fj.15-282798

By:

Xiaofei Sun;
Park, Craig B.;
Wenbo Deng;
Potter, S. Steven;
Dey, Sudhansu K.

Publication type:

Article

Msx Homeobox Genes Critically Regulate Embryo Implantation by Controlling Paracrine Signaling between Uterine Stroma and Epithelium.

Published in:

PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002500

By:

Nallasamy, Shanmugasundaram;
Quanxi Li;
Bagchi, Milan K.;
Bagchi, Indrani C.

Publication type:

Article

BMPs Regulate msx Gene Expression in the Dorsal Neuroectoderm of Drosophila and Vertebrates by Distinct Mechanisms.

Published in:

PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004625

By:

Esteves, Francisco F.;
Springhorn, Alexander;
Kague, Erika;
Taylor, Erika;
Pyrowolakis, George;
Fisher, Shannon;
Bier, Ethan

Publication type:

Article

Msx genes delineate a novel molecular map of the developing cerebellar neuroepithelium.

Published in:

Frontiers in Molecular Neuroscience, 2024, p. 01, doi. 10.3389/fnmol.2024.1356544

By:

Gupta, Ishita;
Yeung, Joanna;
Rahimi-Balaei, Maryam;
Sih-Rong Wu;
Goldowitz, Dan

Publication type:

Article

Dlx homeobox gene family expression in osteoclasts.

Published in:

Journal of Cellular Physiology, 2010, v. 223, n. 3, p. 779, doi. 10.1002/jcp.22095

By:

LÉZOT, F.;
THOMAS, B. L.;
BLIN-WAKKACH, C.;
CASTANEDA, B.;
BOLANOS, A.;
HOTTON, D.;
SHARPE, P. T.;
HEYMANN, D.;
CARLES, G. F.;
GRIGORIADIS, A. E.;
BERDAL, A.

Publication type:

Article

Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers.

Published in:

BMC Evolutionary Biology, 2009, v. 9, p. 1, doi. 10.1186/1471-2148-9-18

By:

Finnerty, John R.;
Mazza, Maureen E.;
Jezewski, Peter A.

Publication type:

Article

Msx Homeobox Genes Act Downstream of BMP2 to Regulate Endometrial Decidualization in Mice and in Humans.

Published in:

Endocrinology, 2019, v. 160, n. 7, p. 1631, doi. 10.1210/en.2019-00131

By:

Nallasamy, Shanmugasundaram;
Okur, Hatice S Kaya;
Bhurke, Arpita;
Davila, Juanmahel;
Li, Quanxi;
Young, Steven L;
Taylor, Robert N;
Bagchi, Milan K;
Bagchi, Indrani C

Publication type:

Article

Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia.

Published in:

European Journal of Oral Sciences, 2003, v. 111, n. 3, p. 272, doi. 10.1034/j.1600-0722.2003.00036.x

By:

Mostowska, Adrianna;
Kobielak, Agnieszka;
Biedziak, Barbara;
Trzeciak, Wieslaw H.

Publication type:

Article

BMP-Mediated Functional Cooperation between Dlx5;Dlx6 and Msx1;Msx2 during Mammalian Limb Development.

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0051700

By:

Vieux-Rochas, Maxence;
Bouhali, Kamal;
Mantero, Stefano;
Garaffo, Giulia;
Provero, Paolo;
Astigiano, Simonetta;
Barbieri, Ottavia;
Caratozzolo, Mariano F.;
Tullo, Apollonia;
Guerrini, Luisa;
Lallemand, Yvan;
Robert, Benoît;
Levi, Giovanni;
Merlo, Giorgio R.

Publication type:

Article

Early Events During Avian Skin Appendage Regeneration: Dependence on Epithelial-Mesenchymal Interaction and order of Molecular Reappearance.

Published in:

Journal of Investigative Dermatology, 1996, v. 107, n. 4, p. 639, doi. 10.1111/1523-1747.ep12584254

By:

Cheng-Ming Chuong;
Widelitz, Randall B.;
Ting-Berreth, Sheree;
Jiang, Ting-Xin

Publication type:

Article

Isolation, characterization, and expression of Le-msx, a maternally expressed member of the msx gene family from the glossiphoniid leech, Helobdella.

Published in:

Developmental Dynamics, 1996, v. 207, n. 4, p. 404, doi. 10.1002/(SICI)1097-0177(199612)207:4<404::AID-AJA5>3.0.CO;2-L

By:

Master, Viraj A.;
Kourakis, Matthew J.;
Martindale, Mark Q.

Publication type:

Article

Expression of an Msx homeobox gene in ascidians: Insights into the archetypal chordate expression pattern.

Published in:

Developmental Dynamics, 1996, v. 205, n. 3, p. 308, doi. 10.1002/(SICI)1097-0177(199603)205:3<308::AID-AJA10>3.0.CO;2-0

By:

Ma, Liang;
Swalla, Billie J.;
Zhou, Jing;
Dobias, Sonia L.;
Bell, Jeffrey R.;
Chen, Juan;
Maxson, Robert E.;
Jeffery, William R.

Publication type:

Article

Regulation of Msx2 gene expression by steroid hormones in human nonmalignant and malignant breast cancer explants cultured in vitro.

Published in:

2005

By:

Malewski, T.;
Milewicz, T.;
Krzysiek, J.;
Gregoraszczuk, Ewa L.;
Augustowska, K.;
Gregoraszczuk, E L

Publication type:

journal article

Examination of the MSX1 gene in patients with Parkinson’s disease.

Published in:

Acta Neurologica Scandinavica, 2009, v. 120, n. 6, p. 442, doi. 10.1111/j.1600-0404.2009.01271.x

By:

Deng, H.;
Zhu, S. H.;
Le, W. D.;
Yang, H. R.;
Lv, H. W.;
Xu, H. B.;
Xie, W. J.;
Jankovic, J.

Publication type:

Article

Msx2 promotes cardiovascular calcification by activating paracrine Wnt signals.

Published in:

Journal of Clinical Investigation, 2005, v. 115, n. 5, p. 1210, doi. 10.1172/JCI200524140

By:

Jian-su Shao;
Su-Li Cheng;
Pingsterhaus, Joyce M.;
Chariton-Kachigian, Nichole;
Loewy, Arleen P.;
Towler, Dwight A.

Publication type:

Article

IDENTIFICATION OF MSX1 GENE MUTATION IN KELANTANESE PATIENTS WITH VARIOUS TYPES OF NON-SYNDROMIC CLEFT LIP AND PALATE.

Published in:

Malaysian Journal of Medical Sciences, 2006, v. 13, p. 100

By:

A. R., Nurhanini;
W. S., Wan Azman;
B. P., Hoh;
B. A., Zilfalil

Publication type:

Article

MSX3 Switches Microglia Polarization and Protects from Inflammation-Induced Demyelination.

Published in:

Journal of Neuroscience, 2015, p. 6350, doi. 10.1523/JNEUROSCI.2468-14.2015

By:

Zhongwang Yu;
Dingya Sun;
Jifeng Feng;
Weixing Tan;
Xue Fang;
Ming Zhao;
Xiaolin Zhao;
Yingyan Pu;
Aijun Huang;
Zhenghua Xiang;
Li Cao;
Cheng He

Publication type:

Article

Association Between MSX1 Variants and Oral Clefts in Han Chinese in Western China.

Published in:

DNA & Cell Biology, 2011, v. 30, n. 12, p. 1057, doi. 10.1089/dna.2010.1208

By:

Huang, Yong-qing;
Ma, Jian;
Ma, Min;
Deng, Ying;
Li, Ya-di;
Ren, Hong-wang;
Zhao, Gui-zhi;
Guo, Sheng-sheng;
Wang, Yang-yang;
Zhang, Gen-xun;
Shi, Bing

Publication type:

Article

Effects of DLX2 overexpression on the osteogenic differentiation of MC3T3-E1 cells.

Published in:

Experimental & Therapeutic Medicine, 2015, v. 9, n. 6, p. 2173, doi. 10.3892/etm.2015.2378

By:

HAO SUN;
ZHIXU LIU;
BIAO LI;
JIEWEN DAI;
XUDONG WANG

Publication type:

Article

A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.

Published in:

2006

By:

Ghassibé, Michella;
Bernier, Vincent;
Boon, Laurence M.;
Vikkula, Miikka;
Ghassibé, Michella

Publication type:

journal article

Dlx3 Transcriptional Regulation of Osteoblast Differentiation: Temporal Recruitment of Msx2, Dlx3, and Dlx5 Homeodomain Proteins to Chromatin of the Osteocalcin Gene.

Published in:

Molecular & Cellular Biology, 2004, v. 24, n. 20, p. 9248, doi. 10.1128/MCB.24.20.9248-9261.2004

By:

Hassan, Mohammad Q.;
Javed, Amjad;
Morasso, Maria I.;
Karlin, Jeremy;
Montecino, Martin;
Van Wijnen, Andre J.;
Stein, Gary S.;
Stein, Janet L.;
Lian, Jane B.

Publication type:

Article

The Role of Msx Genes in Mammalian Developmenta.

Published in:

Annals of the New York Academy of Sciences, 1996, v. 785, n. 1, p. 171, doi. 10.1111/j.1749-6632.1996.tb56256.x

By:

Maas, Richard;
Chen, Yi Ping;
Bei, Marianna;
Woo, Ian;
Satokata, Ichiro

Publication type:

Article

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.

Published in:

Mutagenesis, 2014, v. 29, n. 5, p. 319, doi. 10.1093/mutage/geu019

By:

Wong, Sing-Wai;
Liu, Hao-Chen;
Han, Dong;
Chang, Huai-Guang;
Zhao, Hong-Shan;
Wang, Yi-Xiang;
Feng, Hai-Lan

Publication type:

Article

MSX1 Mutation in Witkop Syndrome; A Case Report.

Published in:

Iranian Journal of Medical Sciences, 2013, v. 38, p. 191

By:

Ghaderi, Faezeh;
Hekmat, Somaye;
Ghaderi, Reza;
Fardaei, Majid

Publication type:

Article

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 2, p. 151, doi. 10.1038/sj.ejhg.5201526

By:

Mavrogiannis, Lampros A;
Taylor, Indira B;
Davies, Sally J;
Ramos, Feliciano J;
Olivares, José L;
Wilkie, Andrew O M

Publication type:

Article

Rattling the core of a well-established paradigm: is retinoic acid really necessary for meiosis entry?

Published in:

McGill Science Undergraduate Research Journal, 2012, v. 7, n. 1, p. 17, doi. 10.26443/msurj.v7i1.98

By:

Brian Chang

Publication type:

Article

Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 755, doi. 10.1038/jhg.2011.95

By:

Salahshourifar, Iman;
Halim, Ahmad Sukari;
Wan Sulaiman, Wan Azman;
Zilfalil, Bin Alwi

Publication type:

Article

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 5, p. 419, doi. 10.1007/s10038-008-0265-3

By:

Furuichi, Tatsuya;
Maeda, Koichi;
Chung-Tei Chou;
Yu-Fen Liu;
Ting-Chun Liu;
Miyamoto, Yoshinari;
Takahashi, Atsushi;
Mori, Kanji;
Ikari, Katsunori;
Kamatani, Naoyuki;
Kurosawa, Hisashi;
Inoue, Hisashi;
Tsai, Shih-Feng;
Ikegawa, Shiro

Publication type:

Article

A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 10, p. 872, doi. 10.1007/s10038-006-0037-x

By:

Chishti, Muhammad S.;
Muhammad, Dost;
Haider, Mahmud;
Ahmad, Wasim

Publication type:

Article

Accelerated closure of skin wounds in mice deficient in the homeobox gene Msx2.

Published in:

Wound Repair & Regeneration, 2009, v. 17, n. 5, p. 639, doi. 10.1111/j.1524-475X.2009.00535.x

By:

Yeh, Jennifer;
Green, Lydia M.;
Jiang, Ting‐Xin;
Plikus, Maksim;
Huang, Eunice;
Chang, Richard N.;
Hughes, Michael W.;
Chuong, Cheng‐Ming;
Tuan, Tai‐Lan

Publication type:

Article

Fibroblast growth factor-induced gene expression and cartilage pattern formation in chick limb bud recombinants.

Published in:

Development, Growth & Differentiation, 2001, v. 43, n. 2, p. 165, doi. 10.1046/j.1440-169X.2001.00561.x

By:

Akiba, Eiji;
Yonei-Tamura, Sayuri;
Yajima, Hiroshi;
Omi, Minoru;
Tanaka, Mikiko;
Sato-Maeda, Mika;
Tamura, Koji;
Ide, Hiroyuki

Publication type:

Article

PATHOLOGY CLINIC. Cherubism.

Published in:

ENT: Ear, Nose & Throat Journal, 2015, v. 94, n. 1, p. 22

By:

Thompson, Lester D. R.

Publication type:

Article

MSX2 is an oncogenic downstream target of activated WNT signaling in ovarian endometrioid adenocarcinoma.

Published in:

Oncogene, 2011, v. 30, n. 40, p. 4152, doi. 10.1038/onc.2011.123

By:

Zhai, Y;
Iura, A;
Yeasmin, S;
Wiese, A B;
Wu, R;
Feng, Y;
Fearon, E R;
Cho, K R

Publication type:

Article

A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.

Published in:

European Journal of Oral Sciences, 2015, v. 123, n. 2, p. 65, doi. 10.1111/eos.12170

By:

Šerý, Omar;
Bonczek, Ondřej;
Hloušková, Alena;
Černochová, Pavlína;
Vaněk, Jiří;
Míšek, Ivan;
Krejčí, Přemysl;
Izakovičová Hollá, Lydie

Publication type:

Article

MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.

Published in:

European Journal of Oral Sciences, 2010, v. 118, n. 3, p. 213, doi. 10.1111/j.1600-0722.2010.00729.x

By:

Jagomägi, Triin;
Nikopensius, Tiit;
Krjutškov, Kaarel;
Tammekivi, Veronika;
Viltrop, Triin;
Saag, Mare;
Metspalu, Andres

Publication type:

Article

Increased vitamin D-driven signalling and expression of the vitamin D receptor, MSX2, and RANKL in tooth resorption in cats.

Published in:

European Journal of Oral Sciences, 2010, v. 118, n. 1, p. 39, doi. 10.1111/j.1600-0722.2009.00707.x

By:

Booij‐Vrieling, Henriëtte E.;
Ferbus, Didier;
Tryfonidou, Marianna A.;
Riemers, Frank M.;
Penning, Louis C.;
Berdal, Ariane;
Everts, Vincent;
Hazewinkel, Herman A. W.

Publication type:

Article

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 11, p. 892, doi. 10.1038/sj.ejhg.5201062

By:

Garcia-Miñaur, Sixto;
Mavrogiannis, Lampros A.;
Rannan-Eliya, Sahan V.;
Hendry, Michael A.;
Liston, William A.;
Porteous, Mary E.M.;
Wilkie, Andrew O.M.

Publication type:

Article

Expression of Bone Morphogenetic Proteins and Msx Genes during Root Formation.

Published in:

Journal of Dental Research, 2003, v. 82, n. 3, p. 172, doi. 10.1177/154405910308200305

By:

Yamashiro, T.;
Tummers, M.;
Thesleff, I.

Publication type:

Article

Role of MSX1 in Osteogenic Differentiation of Human Dental Pulp Stem Cells.

Published in:

Stem Cells International, 2016, p. 1, doi. 10.1155/2016/8035759

By:

Goto, Noriko;
Fujimoto, Katsumi;
Fujii, Sakiko;
Ida-Yonemochi, Hiroko;
Ohshima, Hayato;
Kawamoto, Takeshi;
Noshiro, Mitsuhide;
Shukunami, Chisa;
Kozai, Katsuyuki;
Kato, Yukio

Publication type:

Article

The Msx1 Homeoprotein Recruits G9a Methyltransferase to Repressed Target Genes in Myoblast Cells.

Published in:

PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037647

By:

Wang, Jingqiang;
Abate-Shen, Cory

Publication type:

Article

Extracting Fluorescent Reporter Time Courses of Cell Lineages from High-Throughput Microscopy at Low Temporal Resolution.

Published in:

PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0027886

By:

Downey, Mike J.;
Jeziorska, Danuta M.;
Ott, Sascha;
Katherine Tamai, T.;
Koentges, Georgy;
Vance, Keith W.;
Bretschneider, Till

Publication type:

Article

Nucleotide sequence changes in the MSX1 and IRF6 genes in Lithuanian patients with nonsyndromic orofacial clefting.

Published in:

Acta Medica Lituanica, 2006, v. 13, n. 4, p. 219

By:

Morkunienė, Aušra;
Steponavičiūtė, Danguolė;
Kasnauskienė, Jūratė;
Kučinskas, Vaidutis

Publication type:

Article

MSX2 in ameloblast cell fate and activity.

Published in:

Frontiers in Physiology, 2015, v. 5, p. 1, doi. 10.3389/fphys.2014.00510

By:

Babajko, Sylvie;
de La Dure-Molla, Muriel;
Jedeon, Katia;
Berdal, Ariane

Publication type:

Article

The Regenerative Plasticity of Isolated Urodele Myofibers and Its Dependence on Msx1.

Published in:

PLoS Biology, 2004, v. 2, n. 8, p. 0, doi. 10.1371/journal.pbio.0020218

By:

Kumar, Anoop;
Velloso, Cristiana P.;
Imokawa, Yutaka;
Brockes, Jeremy P.

Publication type:

Article

Effort-related motivational effects of the pro-inflammatory cytokine interleukin-6: pharmacological and neurochemical characterization.

Published in:

Psychopharmacology, 2016, v. 233, n. 19/20, p. 3575, doi. 10.1007/s00213-016-4392-9

By:

Yohn, Samantha;
Arif, Yumna;
Haley, Allison;
Tripodi, Guiseppe;
Baqi, Younis;
Müller, Christa;
Miguel, Noemi;
Correa, Mercè;
Salamone, John

Publication type:

Article

Neuronal development genes are key elements mediating the reinforcing effects of methamphetamine, amphetamine, and methylphenidate.

Published in:

Psychopharmacology, 2013, v. 230, n. 3, p. 399, doi. 10.1007/s00213-013-3168-8

By:

dela Peña, Ike;
Jeon, Se Jin;
Lee, Eunyoung;
Ryu, Jong Hoon;
Shin, Chan Young;
Noh, Minsoo;
Cheong, Jae Hoon

Publication type:

Article

Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-13

By:

Jamsheer, Aleksander;
Sowińska, Anna;
Simon, Dorota;
Jamsheer-Bratkowska, Ma łgorzata;
Trzeciak, Tomasz;
Latos-Bieleńska, Anna

Publication type:

Article

Cross-Talk Between Msx/Dlx Homeobox Genes and Vitamin D During Tooth Mineralization.

Published in:

Connective Tissue Research, 2002, v. 43, n. 2/3, p. 509

By:

Lézot, F.;
Descroix, V.;
Mesbah, M.;
Hotton, D.;
Blin, C.;
Papagerakis, P.;
Mauro, N.;
Kato, S.;
MacDougall, M.;
Sharpe, P.;
Berdal, A.

Publication type:

Article