193 related articles for article (PubMed ID: 11448020)
21. Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia.
Zeng L; Wei J; Han D; Liu H; Liu Y; Zhao N; Sun S; Wang Y; Feng H
Mutagenesis; 2017 Jul; 32(4):437-443. PubMed ID: 28505335
[TBL] [Abstract][Full Text] [Related]
22. Delayed tooth eruption and suppressed osteoclast number in the eruption pathway of heterozygous Runx2/Cbfa1 knockout mice.
Yoda S; Suda N; Kitahara Y; Komori T; Ohyama K
Arch Oral Biol; 2004 Jun; 49(6):435-42. PubMed ID: 15099800
[TBL] [Abstract][Full Text] [Related]
23. [Clinical and image features, and identification of pathogenic gene mutation of two cleidocranial dysplasia families].
Wang GX; Ma LX; Xu WF; Song FL; Sun RP
Zhonghua Er Ke Za Zhi; 2010 Nov; 48(11):834-8. PubMed ID: 21215027
[TBL] [Abstract][Full Text] [Related]
24. Cleidocranial dysplasia: clinical and molecular genetics.
Mundlos S
J Med Genet; 1999 Mar; 36(3):177-82. PubMed ID: 10204840
[TBL] [Abstract][Full Text] [Related]
25. A RUNX2/PEBP2alphaA/CBFA1 mutation in cleidocranial dysplasia revealing the link between the gene and Smad.
Ito Y; Zhang YW
J Bone Miner Metab; 2001; 19(3):188-94. PubMed ID: 11368305
[TBL] [Abstract][Full Text] [Related]
26. A novel missense mutation of the CBFA1 gene in a family with cleidocranial dysplasia (CCD) and variable expressivity.
Golan I; Preising M; Wagener H; Baumert U; Niederdellmann H; Lorenz B; Müssig D
J Craniofac Genet Dev Biol; 2000; 20(3):113-20. PubMed ID: 11321595
[TBL] [Abstract][Full Text] [Related]
27. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients.
Bufalino A; Paranaíba LM; Gouvêa AF; Gueiros LA; Martelli-Júnior H; Junior JJ; Lopes MA; Graner E; De Almeida OP; Vargas PA; Coletta RD
Oral Dis; 2012 Mar; 18(2):184-90. PubMed ID: 22023169
[TBL] [Abstract][Full Text] [Related]
28. A novel small deletion mutation in RUNX2 gene in one Chinese family with cleidocranial dysplasia.
Chen T; Hou J; Hu LL; Gao J; Wu BL
Int J Clin Exp Pathol; 2014; 7(5):2490-5. PubMed ID: 24966961
[TBL] [Abstract][Full Text] [Related]
29. CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.
Zhou G; Chen Y; Zhou L; Thirunavukkarasu K; Hecht J; Chitayat D; Gelb BD; Pirinen S; Berry SA; Greenberg CR; Karsenty G; Lee B
Hum Mol Genet; 1999 Nov; 8(12):2311-6. PubMed ID: 10545612
[TBL] [Abstract][Full Text] [Related]
30. Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
Suda N; Hattori M; Kosaki K; Banshodani A; Kozai K; Tanimoto K; Moriyama K
Orthod Craniofac Res; 2010 Nov; 13(4):197-202. PubMed ID: 21040462
[TBL] [Abstract][Full Text] [Related]
31. A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment.
Çamtosun E; Akıncı A; Demiral E; Tekedereli İ; Sığırcı A
J Clin Res Pediatr Endocrinol; 2019 Sep; 11(3):301-305. PubMed ID: 30468148
[TBL] [Abstract][Full Text] [Related]
32. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
Jaruga A; Hordyjewska E; Kandzierski G; Tylzanowski P
Clin Genet; 2016 Nov; 90(5):393-402. PubMed ID: 27272193
[TBL] [Abstract][Full Text] [Related]
33. New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia.
Machuca-Tzili L; Monroy-Jaramillo N; González-del Angel A; Kofman-Alfaro S
Clin Genet; 2002 May; 61(5):349-53. PubMed ID: 12081718
[TBL] [Abstract][Full Text] [Related]
34. Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia.
Gong L; Odilov B; Han F; Liu F; Sun Y; Zhang N; Zuo X; Yang J; Wang S; Hou X; Ren J
Genes Genomics; 2022 Jun; 44(6):683-690. PubMed ID: 35235174
[TBL] [Abstract][Full Text] [Related]
35. A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia.
Xu W; Chen Q; Liu C; Chen J; Xiong F; Wu B
BMC Med Genet; 2017 Feb; 18(1):13. PubMed ID: 28173761
[TBL] [Abstract][Full Text] [Related]
36. Novel mutation of RUNX2 gene in a patient with cleidocranial dysplasia.
Guo YW; Chiu CY; Liu CL; Jap TS; Lin LY
Int J Clin Exp Pathol; 2015; 8(1):1057-62. PubMed ID: 25755819
[TBL] [Abstract][Full Text] [Related]
37. [Identification of three novel frameshift mutations in the RUNX2 gene in three sporadic Chinese cases with cleidocranial dysplasia].
Qi Z; Yang W; Meng Y; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):415-9. PubMed ID: 25119901
[TBL] [Abstract][Full Text] [Related]
38. A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia.
Fang CY; Xue JJ; Tan L; Jiang CH; Gao QP; Liang DS; Wu LQ
Genet Mol Res; 2011 Dec; 10(4):3539-44. PubMed ID: 22194205
[TBL] [Abstract][Full Text] [Related]
39. RUNX2 mutations in cleidocranial dysplasia patients.
Ryoo HM; Kang HY; Lee SK; Lee KE; Kim JW
Oral Dis; 2010 Jan; 16(1):55-60. PubMed ID: 19744171
[TBL] [Abstract][Full Text] [Related]
40. Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip.
Yamachika E; Tsujigiwa H; Ishiwari Y; Mizukawa N; Nagai N; Sugahara T
J Oral Pathol Med; 2001 Jul; 30(6):381-3. PubMed ID: 11459326
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]