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Journal Abstract Search

226 related items for PubMed ID: 23718693

  • 41.
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  • 43. Evidence of the involvement of the polymorphisms near MSX1 gene in non-syndromic cleft lip with or without cleft palate.
    Gurramkonda VB, Syed AH, Murthy J, Lakkakula BV.
    Int J Pediatr Otorhinolaryngol; 2015 Jul; 79(7):1081-4. PubMed ID: 25953455
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  • 44. MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
    Zhu Y, Zhang Y, Dong J, Ruan W, Yang S, Huang P, Duan X.
    Oral Dis; 2023 Nov; 29(8):3168-3172. PubMed ID: 36478500
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  • 45. MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies.
    Park J, Park BY, Kim HS, Lee JE, Suh I, Nam CM, Kang DR, Kim S, Yun JE, Go EN, Jee SH, Beaty TH.
    Yonsei Med J; 2007 Feb 28; 48(1):101-8. PubMed ID: 17326252
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  • 46. Gene-gene interaction for nonsyndromic cleft lip with or without cleft palate in Chilean case-parent trios.
    Suazo J, Santos JL, Colombo A, Pardo R.
    Arch Oral Biol; 2018 Jul 28; 91():91-95. PubMed ID: 29694940
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  • 47. MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.
    Jagomägi T, Nikopensius T, Krjutskov K, Tammekivi V, Viltrop T, Saag M, Metspalu A.
    Eur J Oral Sci; 2010 Jun 28; 118(3):213-20. PubMed ID: 20572854
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  • 48.
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  • 49. What could be the role of genetic tests and machine learning of AXIN2 variant dominance in non-syndromic hypodontia? A case-control study in orthodontically treated patients.
    Alhazmi N, Alaqla A, Almuzzaini B, Aldrees M, Alnaqa G, Almasoud F, Aldibasi O, Alshamlan H.
    Prog Orthod; 2024 Aug 26; 25(1):31. PubMed ID: 39183201
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  • 51. 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.
    Tatematsu T, Kimura M, Nakashima M, Machida J, Yamaguchi S, Shibata A, Goto H, Nakayama A, Higashi Y, Miyachi H, Shimozato K, Matsumoto N, Tokita Y.
    PLoS One; 2015 Aug 26; 10(6):e0128227. PubMed ID: 26030286
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  • 52.
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  • 53. MSX1 gene polymorphisms and non-syndromic cleft lip with or without palate (NSCL/P): A meta-analysis.
    Tasanarong P, Pabalan N, Tharabenjasin P, Jarjanazi H.
    Oral Dis; 2019 Sep 26; 25(6):1492-1501. PubMed ID: 31132300
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  • 54. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.
    Šerý O, Bonczek O, Hloušková A, Černochová P, Vaněk J, Míšek I, Krejčí P, Izakovičová Hollá L.
    Eur J Oral Sci; 2015 Apr 26; 123(2):65-71. PubMed ID: 25683653
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  • 55. Investigation of Parental Transmission of RUNX2 Single Nucleotide Polymorphism and Its Association With Nonsyndromic Cleft Lip With or Without Palate.
    Jung SH, Lee AY, Park JW, Baek SH, Kim YH.
    Cleft Palate Craniofac J; 2014 Mar 26; 51(2):234-9. PubMed ID: 23909516
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  • 58. Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development.
    Nakatomi M, Ludwig KU, Knapp M, Kist R, Lisgo S, Ohshima H, Mangold E, Peters H.
    Development; 2020 Jun 24; 147(21):. PubMed ID: 32467233
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  • 59. Association of MSX1 and TGF-β1 genetic polymorphisms with hypodontia: meta-analysis.
    Zhang W, Qu HC, Zhang Y.
    Genet Mol Res; 2014 Nov 28; 13(4):10007-16. PubMed ID: 25501212
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  • 60. [Association study on microsatellite polymorphisms of MSX1 gene and nonsyndromic cleft lip and palate].
    Wu PA, Li YL, Fan GZ, Wang K.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun 28; 24(3):325-7. PubMed ID: 17557248
    [Abstract] [Full Text] [Related]

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