Works matching DE "MSX genes"

Results: 65

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

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

Transcriptional Regulation of Msx1 Natural Antisense Transcript.

Published in:

Cells Tissues Organs, 2011, v. 194, n. 2-4, p. 151, doi. 10.1159/000324466

By:

Babajko, Sylvie;
Méary, Fleur;
Petit, Stéphane;
Fernandes, Isabelle;
Berdal, Ariane

Publication type:

Article

Regulation of Bmp4 Expression in Odontogenic Mesenchyme: From Simple to Complex.

Published in:

Cells Tissues Organs, 2011, v. 194, n. 2-4, p. 156, doi. 10.1159/000324747

By:

Hui Kong;
Ying Wang;
Patel, Manshi;
Mues, Gabriele;
D'Souza, Rena N.

Publication type:

Article

Msx1 Expression Regulation by Its Own Antisense RNA: Consequence on Tooth Development and Bone Regeneration.

Published in:

Cells Tissues Organs, 2008, v. 189, n. 1-4, p. 115, doi. 10.1159/000151748

By:

Babajko, Sylvie;
Petit, Stéphane;
Fernandes, Isabelle;
Méary, Fleur;
LeBihan, Johanne;
Pibouin, Laurence;
Berdal, Ariane

Publication type:

Article

Differential Impact of Msx1 and Msx2 Homeogenes on Mouse Maxillofacial Skeleton.

Published in:

Cells Tissues Organs, 2008, v. 189, n. 1-4, p. 126, doi. 10.1159/000154271

By:

Berdal, Ariane;
Molla, Muriel;
Hotton, Dominique;
Aïoub, Muhanad;
Lézot, Frédéric;
Néfussi, Jean-Raphaël;
Goubin, Gérard

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

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

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

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

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

Case-parent Triads: Estimating Single- and Double-dose Effects of Fetal and Maternal Disease Gene Haplotypes.

Published in:

Annals of Human Genetics, 2006, v. 70, n. 3, p. 382, doi. 10.1111/j.1529-8817.2005.00218.x

By:

Gjessing, H. K.;
Lie, R. T.

Publication type:

Article

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 387, doi. 10.1038/74224

By:

Wilkie, Andrew O.M.;
Tang, Zequn;
Elanko, Navaratnam;
Walsh, Sinead;
Twigg, Stephen R.F.;
Hurst, Jane A.;
Wall, Steven A.;
Chrzanowska, Krystyna H.;
Maxson, Robert E.

Publication type:

Article

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 391, doi. 10.1038/74231

By:

Satokata, Ichiro;
Ma, Liang;
Ohshima, Hayato;
Bei, Marianna;
Woo, Ian;
Nishizawa, Kazumichi;
Maeda, Takeyasu;
Takano, Yoshiro;
Uchiyama, Makoto;
Heaney, Shaun;
Peters, Heiko;
Tang, Zequn;
Maxson, Robert;
Maas, Richard

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

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 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

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

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

Oncogenic deregulation of NKL homeobox gene MSX1 in mantle cell lymphoma.

Published in:

Leukemia & Lymphoma, 2014, v. 55, n. 8, p. 1893, doi. 10.3109/10428194.2013.864762

By:

Nagel, Stefan;
Ehrentraut, Stefan;
Meyer, Corinna;
Kaufmann, Maren;
Drexler, Hans G.;
MacLeod, Roderick A. F.

Publication type:

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

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

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

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

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

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

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

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

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

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

Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2.

Published in:

Journal of Investigative Dermatology, 1999, v. 113, n. 2, p. 0, doi. 10.1046/j.1523-1747.1999.00680.x

By:

Jiang, Ting-Xin;
Liu, Yi-Hsin;
Widelitz, Randall B.;
Kundu, Ramendra K.;
Maxson, Robert E.;
Chuong, C. M.

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

In This Issue...

Published in:

Journal of Investigative Dermatology, 1995, v. 104, n. 5, p. 705, doi. 10.1111/1523-1747.ep12606954

By:

Bickenbach, Jackie 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

Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations.

Published in:

Cell Death & Differentiation, 2014, v. 21, n. 6, p. 990, doi. 10.1038/cdd.2014.21

By:

Miyagawa, S;
Harada, M;
Matsumaru, D;
Tanaka, K;
Inoue, C;
Nakahara, C;
Haraguchi, R;
Matsushita, S;
Suzuki, K;
Nakagata, N;
Ng, R C-L;
Akita, K;
Lui, V C-H;
Yamada, G

Publication type:

Article

Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression.

Published in:

Pulmonary Circulation, 2011, v. 1, n. 3, p. 389, doi. 10.4103/2045-8932.87308

By:

Austin, Eric D.;
Menon, Swapna;
Hemnes, Anna R.;
Robinson, Linda R.;
Talati, Megha;
Fox, Kelly L.;
Cogan, Joy D.;
Hamid, Rizwan;
Hedges, Lora K.;
Robbins, Ivan;
Lane, Kirk;
Newman, John H.;
Loyd, James E.;
West, James

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

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

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

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

Targeted Reduction of Vascular Msx1 and Msx2 Mitigates Arteriosclerotic Calcification and Aortic Stiffness in LDLR-Deficient Mice Fed Diabetogenic Diets.

Published in:

Diabetes, 2014, v. 63, n. 12, p. 4326, doi. 10.2337/db14-0326

By:

Su-Li Cheng;
Behrmann, Abraham;
Jian-Su Shao;
Ramachandran, Bindu;
Krchma, Karen;
Arredondo, Yoanna Bello;
Kovacs, Attila;
Mead, Megan;
Maxson, Robert;
Towler, Dwight A.

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

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

An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family.

Published in:

PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128227

By:

Tatematsu, Tadashi;
Kimura, Masashi;
Nakashima, Mitsuko;
Machida, Junichiro;
Yamaguchi, Seishi;
Shibata, Akio;
Goto, Hiroki;
Nakayama, Atsuo;
Higashi, Yujiro;
Miyachi, Hitoshi;
Shimozato, Kazuo;
Matsumoto, Naomichi;
Tokita, Yoshihito

Publication type:

Article