137 related articles for article (PubMed ID: 36478500)
41. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia.
Goldenberg M; Das P; Messersmith M; Stockton DW; Patel PI; D'Souza RN
J Dent Res; 2000 Jul; 79(7):1469-75. PubMed ID: 11005730
[TBL] [Abstract][Full Text] [Related]
42. A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis.
AlFawaz S; Plagnol V; Wong FS; Kelsell DP
Arch Oral Biol; 2015 Jul; 60(7):982-8. PubMed ID: 25874811
[TBL] [Abstract][Full Text] [Related]
43. Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis.
Nakatomi M; Wang XP; Key D; Lund JJ; Turbe-Doan A; Kist R; Aw A; Chen Y; Maas RL; Peters H
Dev Biol; 2010 Apr; 340(2):438-49. PubMed ID: 20123092
[TBL] [Abstract][Full Text] [Related]
44. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.
Mostowska A; Biedziak B; Jagodzinski PP
Arch Oral Biol; 2012 Jun; 57(6):790-5. PubMed ID: 22297032
[TBL] [Abstract][Full Text] [Related]
45. Novel MSX1 variants identified in families with nonsyndromic oligodontia.
Zheng J; Yu M; Liu H; Cai T; Feng H; Liu Y; Han D
Int J Oral Sci; 2021 Jan; 13(1):2. PubMed ID: 33419968
[TBL] [Abstract][Full Text] [Related]
46. Morphological variations of median maxillary labial frenum: A clinical study.
Dasgupta P; Kamath G; Hs S; Babshet M; Doddamani L
J Stomatol Oral Maxillofac Surg; 2017 Dec; 118(6):337-341. PubMed ID: 28697985
[TBL] [Abstract][Full Text] [Related]
47. A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
Vastardis H; Karimbux N; Guthua SW; Seidman JG; Seidman CE
Nat Genet; 1996 Aug; 13(4):417-21. PubMed ID: 8696335
[TBL] [Abstract][Full Text] [Related]
48. Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?
Bock NC; Lenz S; Ruiz-Heiland G; Ruf S
J Orofac Orthop; 2017 Mar; 78(2):112-120. PubMed ID: 28204848
[TBL] [Abstract][Full Text] [Related]
49. MSX1 gene polymorphisms in Mexican patients with non-syndromic cleft lip/palate.
Ibarra-Arce A; Albavera-Giles T; Zavaleta-Villa B; Ortiz de Zárate-Alarcón G; Flores-Peña L; Sierra-Romero MD; Romero-Valdovinos M; Olivo-Díaz A
Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():119-124. PubMed ID: 27729116
[TBL] [Abstract][Full Text] [Related]
50. Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation.
Koskinen S; Keski-Filppula R; Alapulli H; Nieminen P; Anttonen V
Clin Oral Investig; 2019 Nov; 23(11):4107-4111. PubMed ID: 30809714
[TBL] [Abstract][Full Text] [Related]
51. Msx1 mutations: how do they cause tooth agenesis?
Wang Y; Kong H; Mues G; D'Souza R
J Dent Res; 2011 Mar; 90(3):311-6. PubMed ID: 21297014
[TBL] [Abstract][Full Text] [Related]
52. Establishment of a congenital tooth agenesis related gene MSX1 knockout human embryonic stem cell lines by CRISPR-Cas9 technology.
Xue Y; Zhu M; Qin D; Li Y; Cen X; Sun X; Lian W; Liao B
Stem Cell Res; 2017 Oct; 24():151-154. PubMed ID: 29034883
[TBL] [Abstract][Full Text] [Related]
53. Mutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth.
Pawlowska E; Janik-Papis K; Wisniewska-Jarosinska M; Szczepanska J; Blasiak J
Tohoku J Exp Med; 2009 Apr; 217(4):307-12. PubMed ID: 19346736
[TBL] [Abstract][Full Text] [Related]
54. Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis.
Vieira AR
J Dent Res; 2003 Mar; 82(3):162-5. PubMed ID: 12598542
[TBL] [Abstract][Full Text] [Related]
55. [Transmission disequilibrium test for nonsyndromic cleft lip and palate and segment homeobox gene-1 gene].
Wu PA; Li YL; Wu HJ; Wang K; Fan GZ
Zhonghua Kou Qiang Yi Xue Za Zhi; 2007 Sep; 42(9):561-3. PubMed ID: 18070437
[TBL] [Abstract][Full Text] [Related]
56. Genes affecting tooth morphogenesis.
Kapadia H; Mues G; D'Souza R
Orthod Craniofac Res; 2007 Aug; 10(3):105-13. PubMed ID: 17651126
[TBL] [Abstract][Full Text] [Related]
57. [Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate].
Vieira AR; Castillo Taucher S; Aravena T; Astete C; Sanz P; Tastets ME; Monasterio L; Murray JC
Rev Med Chil; 2004 Jul; 132(7):816-22. PubMed ID: 15379328
[TBL] [Abstract][Full Text] [Related]
58. Genes affecting tooth morphogenesis.
Kapadia H; Mues G; D'Souza R
Orthod Craniofac Res; 2007 Nov; 10(4):237-44. PubMed ID: 17973693
[TBL] [Abstract][Full Text] [Related]
59. Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate.
Lace B; Vasiljeva I; Dundure I; Barkane B; Akota I; Krumina A
Stomatologija; 2006; 8(1):21-4. PubMed ID: 16687911
[TBL] [Abstract][Full Text] [Related]
60. [Research advances in tooth agenesis].
Feng HL; Zhang XX; Wu H
Beijing Da Xue Xue Bao Yi Xue Ban; 2007 Feb; 39(1):13-7. PubMed ID: 17304318
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]