BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 27060301)

  • 1. [Analysis of type IV osteogenesis imperfecta caused by two mutations occurred simultaneously in COL1A1 gene in a Chinese child].
    Ju M; Zhang T; Bai X; Ren X; Li K; Li G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):140-4. PubMed ID: 27060301
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Screening and analysis of a new mutation of COL1A1 gene in a family with osteogenesis imperfecta].
    Bai X; Li K; Ren X; He X; Wang Y; Guan S; Jing Y; Li G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):344-7. PubMed ID: 24928016
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic screening of a pedigree with osteogenesis imperfecta type Ⅰ and identification of a novel mutation in COL1A2 pathogenic gene.
    Li R; Guo YP; Pan JX; Guo YB
    Yi Chuan; 2015 Jan; 37(1):41-47. PubMed ID: 25608812
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family.
    Xia XY; Cui YX; Huang YF; Pan LJ; Yang B; Wang HY; Li XJ; Shi YC; Lu HY; Zhou YC
    Clin Chim Acta; 2008 Dec; 398(1-2):148-51. PubMed ID: 18755172
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Analysis of COL1A1 gene mutation in an ethnic Han Chinese family from Henan affected with osteogenesis imperfecta].
    Huang Y; Guo L; Wang D; Yang M; Yang B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):653-6. PubMed ID: 27577215
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta.
    Zhang ZL; Zhang H; Ke YH; Yue H; Xiao WJ; Yu JB; Gu JM; Hu WW; Wang C; He JW; Fu WZ
    J Bone Miner Metab; 2012 Jan; 30(1):69-77. PubMed ID: 21667357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation spectrum of COL1A1/COL1A2 screening by high-resolution melting analysis of Chinese patients with osteogenesis imperfecta.
    Ju M; Bai X; Zhang T; Lin Y; Yang L; Zhou H; Chang X; Guan S; Ren X; Li K; Wang Y; Li G
    J Bone Miner Metab; 2020 Mar; 38(2):188-197. PubMed ID: 31414283
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mutation analysis and prenatal diagnosis of COL1A1 gene in a Chinese family with type I osteogenesis imperfecta].
    Zhang H; Wu D; Hou Q; Liu Z; Qin L; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):730-2. PubMed ID: 25449076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in COL1A1 of type I collagen genes in Chinese patients with osteogenesis imperfecta.
    Wang Z; Yang Z; Ke Z; Yang S; Shi H; Wang L
    J Investig Med; 2009 Jun; 57(5):662-7. PubMed ID: 19491628
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Gene mutation analysis of a Chinese family with osteogenesis imperfecta].
    Wang Z; Xu DL; Hu JY; Liao YH; Yang Z; Liang Q; Wang LT
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):192-4. PubMed ID: 16604495
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I].
    Ke LF; Zheng LW; Xie HH; Yan AZ; Zhu ZY; Lan FH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):50-3. PubMed ID: 19199251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Spectrum of COL1A1/2 mutations and gene diagnosis in Chinese patients with osteogenesis imperfecta].
    Zhao X; Xiao J; Wang H; Ren X; Gao J; Wu Y; Lu C; Zhang X
    Zhonghua Yi Xue Za Zhi; 2015 Nov; 95(43):3484-9. PubMed ID: 26813269
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A new mutation in COL1A1 gene in a family with osteogenesis imperfecta].
    Wang Z; Xu DL; Chen Z; Hu JY; Yang Z; Wang LT
    Zhonghua Yi Xue Za Zhi; 2006 Jan; 86(3):170-3. PubMed ID: 16638323
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation characteristics in type I collagen genes in Chinese patients with osteogenesis imperfecta.
    Yang Z; Ke ZF; Zeng C; Wang Z; Shi HJ; Wang LT
    Genet Mol Res; 2011 Feb; 10(1):177-85. PubMed ID: 21341209
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patients.
    Lu Y; Ren X; Wang Y; Li T; Li F; Wang S; Xu C; Wu G; Li H; Li G; Zhao F; Wang Z; Mo X; Han J
    Clin Endocrinol (Oxf); 2014 Apr; 80(4):524-31. PubMed ID: 24147872
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.
    Zhang H; Yue H; Wang C; Hu W; Gu J; He J; Fu W; Hu Y; Li M; Zhang Z
    Mol Med Rep; 2016 Nov; 14(5):4918-4926. PubMed ID: 27748872
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Identification of a novel splicing mutation in COL1A1 gene in a Chinese family affected with typeⅠosteogenesis imperfecta].
    Song Y; Jin X; Kong J; Zhao D; Guo Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):472-5. PubMed ID: 25119913
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compound phenotype of osteogenesis imperfecta and Ehlers-Danlos syndrome caused by combined mutations in
    Lin Z; Zeng J; Wang X
    Biosci Rep; 2019 Jul; 39(7):. PubMed ID: 31239369
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta.
    Xi L; Zhang H; Zhang ZL
    J Bone Miner Metab; 2021 May; 39(3):416-422. PubMed ID: 33070251
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Analysis of gross deletions of COL1A1/2 genes in Chinese families affected with osteogenesis imperfecta].
    Wang H; Zhao X; Ren X; Xiao J; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):431-4. PubMed ID: 27454992
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.