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Select item 108780741.

Intrahepatic homeobox protein MSX-1 is a novel host restriction factor of hepatitis B virus

Zhongliang Shen, Shenyan Zhang, Zixiang Gao, Xueping Yu, Jinyu Wang, Shaokun Pan, Ning Kang, Nannan Liu, Huijun Xu, Mu Liu, Yang Yang, Qiang Deng, Jing Liu, Youhua Xie, Jiming Zhang

J Virol. 2024 Feb; 98(2): e01345-23. Published online 2024 Jan 16. doi: 10.1128/jvi.01345-23

PMCID:: PMC10878074

Currently embargoed: Free in PMC on Jul 16, 2024; PubMed

Select item 107676052.

Characterization of novel MSX1 variants causally associated with non‐syndromic oligodontia in Chinese families

Ya Zhao, Jiabao Ren, Lingqiang Meng, Yan Hou, Chunyan Liu, Guozhong Zhang, Wenjing Shen

Mol Genet Genomic Med. 2024 Jan; 12(1): e2334. Published online 2023 Dec 8. doi: 10.1002/mgg3.2334

PMCID:: PMC10767605

Abstract Article PDF–5.0M

Select item 101921523.

MSX1-expression during the different phases in healthy human endometrium

Simon Eppich, Christina Kuhn, Elisa Schmoeckel, Doris Mayr, Sven Mahner, Udo Jeschke, Julia Gallwas, Helene Hildegard Heidegger

Arch Gynecol Obstet. 2023; 308(1): 273–279. Published online 2023 Apr 27. doi: 10.1007/s00404-023-07033-5

PMCID:: PMC10192152

Abstract Article PDF–1.2M

Select item 87834544.

Family and case–control genetic study of MSX1 polymorphisms in peg-shaped teeth Jordanian population

Rami Alkhatib, Razan Hawamdeh, Laith Al-Eitan, Nour Abdo, Fadi Obeidat, Mohamed Al-Bataineh, Hatem Aman

BMC Oral Health. 2022; 22: 16. Published online 2022 Jan 22. doi: 10.1186/s12903-022-02051-2

PMCID:: PMC8783454

Abstract Article PDF–1.0M

Select item 80735575.

Association of Polymorphic and Haplotype Variants of the MSX1 Gene and the Impacted Teeth Phenomenon

Grzegorz Trybek, Aleksandra Jaroń, Anna Grzywacz

Genes (Basel) 2021 Apr; 12(4): 577. Published online 2021 Apr 16. doi: 10.3390/genes12040577

PMCID:: PMC8073557

Abstract Article PDF–715K

Select item 77945566.

Novel MSX1 variants identified in families with nonsyndromic oligodontia

Jinglei Zheng, Miao Yu, Haochen Liu, Tao Cai, Hailan Feng, Yang Liu, Dong Han

Int J Oral Sci. 2021; 13: 2. Published online 2021 Jan 8. doi: 10.1038/s41368-020-00106-0

PMCID:: PMC7794556

Abstract Article PDF–3.3M

Select item 73502657.

MSX1—A Potential Marker for Uterus-Preserving Therapy of Endometrial Carcinomas

Simon Eppich, Christina Kuhn, Elisa Schmoeckel, Doris Mayr, Sven Mahner, Udo Jeschke, Julia Gallwas, Helene Hildegard Heidegger

Int J Mol Sci. 2020 Jun; 21(12): 4529. Published online 2020 Jun 25. doi: 10.3390/ijms21124529

PMCID:: PMC7350265

Abstract Article PDF–8.0M

Select item 69488258.

Two novel mutations in MSX1 causing oligodontia

Le Yang, Jia Liang, Haitang Yue, Zhuan Bian

PLoS One. 2020; 15(1): e0227287. Published online 2020 Jan 8. doi: 10.1371/journal.pone.0227287

PMCID:: PMC6948825

Abstract Article PDF–1.2M

Select item 61285269.

Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia

Ondřej Bonczek, Peter Bielik, Přemysl Krejčí, Tomáš Zeman, Lýdie Izakovičová-Hollá, Jana Šoukalová, Jiří Vaněk, Tereza Gerguri, Vladimir J. Balcar, Omar Šerý

PLoS One. 2018; 13(9): e0202989. Published online 2018 Sep 7. doi: 10.1371/journal.pone.0202989

PMCID:: PMC6128526

Abstract Article PDF–21M

Select item 599915710.

Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma

A. M. J. van Nistelrooij, R. van Marion, W. F. J. van Ijcken, A. de Klein, A. Wagner, K. Biermann, M. C. W. Spaander, J. J. B. van Lanschot, W. N. M. Dinjens, B. P. L. Wijnhoven

Fam Cancer. 2018; 17(3): 435–440. Published online 2017 Nov 13. doi: 10.1007/s10689-017-0054-2

PMCID:: PMC5999157

Abstract Article PDF–1.1M

Select item 590279511.

MSX1-Induced Neural Crest-Like Reprogramming Promotes Melanoma Progression

Markus V. Heppt, Joshua X. Wang, Denitsa M. Hristova, Zhi Wei, Ling Li, Brianna Evans, Marilda Beqiri, Samir Zaman, Jie Zhang, Martin Irmler, Carola Berking, Robert Besch, Johannes Beckers, Frank J. Rauscher, 3rd, Rick A. Sturm, David E. Fisher, Meenhard Herlyn, Mizuho Fukunaga-Kalabis

J Invest Dermatol. Author manuscript; available in PMC 2018 Apr 17.

Published in final edited form as: J Invest Dermatol. 2018 Jan; 138(1): 141–149. Published online 2017 Sep 18. doi: 10.1016/j.jid.2017.05.038

PMCID:: PMC5902795

Abstract Article PDF–879K

Select item 511792812.

MSX1 mutations and associated disease phenotypes: genotype-phenotype relations

Jia Liang, Johannes Von den Hoff, Joanna Lange, Yijin Ren, Zhuan Bian, Carine E L Carels

Eur J Hum Genet. 2016 Dec; 24(12): 1663–1670. Published online 2016 Jul 6. doi: 10.1038/ejhg.2016.78

PMCID:: PMC5117928

Abstract Article PDF–1.3M

Select item 499165713.

Reduced homeobox protein MSX1 in human endometrial tissue is linked to infertility

Alan D. Bolnick, Jay M. Bolnick, Brian A. Kilburn, Tamika Stewart, Jonathan Oakes, Javier Rodriguez-Kovacs, Hamid-Reza Kohan-Ghadr, Jing Dai, Michael P. Diamond, Yasushi Hirota, Sascha Drewlo, Sudhansu K. Dey, D. Randall Armant

Hum Reprod. 2016 Sep; 31(9): 2042–2050. Published online 2016 Aug 19. doi: 10.1093/humrep/dew143

PMCID:: PMC4991657

Abstract Article PDF–8.4M

Select item 484955814.

Epigenetic regulation of the homeobox gene MSX1 associates with platinum resistant disease in high grade serous epithelial ovarian cancer

Nair A. Bonito, Jane Borley, Charlotte S. Wilhelm-Benartzi, Sadaf Ghaem-Maghami, Robert Brown

Clin Cancer Res. Author manuscript; available in PMC 2016 Dec 15.

Published in final edited form as: Clin Cancer Res. 2016 Jun 15; 22(12): 3097–3104. Published online 2016 Jan 13. doi: 10.1158/1078-0432.CCR-15-1669

PMCID:: PMC4849558

Abstract Article PDF–1.3M

Select item 464050315.

Characterization of Transcriptional Repressor Gene MSX1 Variations for Possible Associations with Congenital Heart Diseases

Fei-Feng Li, Ying Han, Shuai Shi, Xia Li, Xi-Dong Zhu, Jing Zhou, Qing-Liang Shao, Xue-Qi Li, Shu-Lin Liu

PLoS One. 2015; 10(11): e0142666. Published online 2015 Nov 10. doi: 10.1371/journal.pone.0142666

PMCID:: PMC4640503

Abstract Article PDF–862K

Select item 445115016.

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

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

PLoS One. 2015; 10(6): e0128227. Published online 2015 Jun 1. doi: 10.1371/journal.pone.0128227

PMCID:: PMC4451150

Abstract Article PDF–2.6M

Select item 412515217.

Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis

Seishi Yamaguchi, Junichiro Machida, Munefumi Kamamoto, Masashi Kimura, Akio Shibata, Tadashi Tatematsu, Hitoshi Miyachi, Yujiro Higashi, Peter Jezewski, Atsuo Nakayama, Kazuo Shimozato, Yoshihito Tokita

PLoS One. 2014; 9(8): e102944. Published online 2014 Aug 7. doi: 10.1371/journal.pone.0102944

PMCID:: PMC4125152

Abstract Article PDF–3.0M

Select item 385934018.

MSX1 gene and nonsyndromic oral clefts in a Southern Brazilian population

L.T. Souza, T.W. Kowalski, M.V.M. Collares, T.M. Félix

Braz J Med Biol Res. 2013 Jul; 46(7): 555–558. Published online 2013 Aug 10. doi: 10.1590/1414-431X20133054

PMCID:: PMC3859340

Abstract Article PDF–80K

Select item 361730319.

Association between MSX1 SNPs and Nonsyndromic Cleft Lip with or without Cleft Palate in the Korean Population

Na Young Kim, Young Ho Kim, Ji Wan Park, Seung-Hak Baek

J Korean Med Sci. 2013 Apr; 28(4): 522–526. Published online 2013 Mar 27. doi: 10.3346/jkms.2013.28.4.522

PMCID:: PMC3617303

Abstract Article PDF–419K

Select item 320699120.

Genetic Studies in the Nigerian Population Implicate a MSX1 Mutation in Complex Oral Facial Clefting Disorders

A Butali, P.A Mossey, W.L Adeyemo, P.A Jezewski, C.K Onwuamah, M.O Ogunlewe, V.I. Ugboko, O Adejuyigbe, A.I. Adigun, L.O Abdur-Rahman, I.I. Onah, R.A Audu, E.O. Idigbe, M.A. Mansilla, E.A Dragan, A.L Petrin, S.A Bullard, A.O. Uduezue, O. Akpata, A.O Osaguona, H.O Olasoji, T.O Ligali, B.M Kejeh, K.R Iseh, P.B Olaitan, A.R Adebola, E Efunkoya, O.A Adesina, O.M Oluwatosin, J.C Murray, The NigeriaCRAN collaboration

Cleft Palate Craniofac J. Author manuscript; available in PMC 2011 Nov 3.

Published in final edited form as: Cleft Palate Craniofac J. 2011 Nov; 48(6): 646–653. Published online 2011 Jul 8. doi: 10.1597/10-133

PMCID:: PMC3206991

Abstract Article PDF–389K

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