These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 34088323)

  • 1. A novel mutation of COL2A1 in a large Chinese family with avascular necrosis of the femoral head.
    Zhang Z; Zhu K; Dai H; Wang Q; Zhang C; Zhang Z
    BMC Med Genomics; 2021 Jun; 14(1):147. PubMed ID: 34088323
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral head.
    Li N; Yu J; Cao X; Wu QY; Li WW; Li TF; Zhang C; Cui YX; Li XJ; Yin ZM; Xia XY
    PLoS One; 2014; 9(6):e100505. PubMed ID: 24949742
    [TBL] [Abstract][Full Text] [Related]  

  • 3. COL2A1 mutation (c.3508G>A) leads to avascular necrosis of the femoral head in a Chinese family: A case report.
    Liu F; Xiong Z; Liu Q; Hu J; Li W; Zhang N
    Mol Med Rep; 2018 Jul; 18(1):254-260. PubMed ID: 29750297
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Type II collagen gene variants and inherited osteonecrosis of the femoral head.
    Liu YF; Chen WM; Lin YF; Yang RC; Lin MW; Li LH; Chang YH; Jou YS; Lin PY; Su JS; Huang SF; Hsiao KJ; Fann CS; Hwang HW; Chen YT; Tsai SF
    N Engl J Med; 2005 Jun; 352(22):2294-301. PubMed ID: 15930420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Age at onset-dependent presentations of premature hip osteoarthritis, avascular necrosis of the femoral head, or Legg-Calvé-Perthes disease in a single family, consequent upon a p.Gly1170Ser mutation of COL2A1.
    Su P; Li R; Liu S; Zhou Y; Wang X; Patil N; Mow CS; Mason JC; Huang D; Wang Y
    Arthritis Rheum; 2008 Jun; 58(6):1701-6. PubMed ID: 18512791
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening of the COL2A1 mutation in idiopathic osteonecrosis of the femoral head.
    Sakamoto Y; Yamamoto T; Miyake N; Matsumoto N; Iida A; Nakashima Y; ; Iwamoto Y; Ikegawa S
    J Orthop Res; 2017 Apr; 35(4):768-774. PubMed ID: 27183340
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family.
    Zhou T; Yang X; Chen Z; Zhou Y; Cao X; Zhao C; Zhao J
    J Clin Lab Anal; 2021 Apr; 35(4):e23728. PubMed ID: 33590889
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation in the COL2A1 gene in a Chinese family with Spondyloepiphyseal dysplasia congenita.
    Li S; Zhou H; Qin H; Guo H; Bai Y
    Joint Bone Spine; 2014 Jan; 81(1):86-9. PubMed ID: 23932928
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Avascular necrosis of the femoral head due to a novel C propeptide mutation in COL2A1.
    Kannu P; O'Rielly DD; Hyland JC; Kokko LA
    Am J Med Genet A; 2011 Jul; 155A(7):1759-62. PubMed ID: 21671384
    [No Abstract]   [Full Text] [Related]  

  • 10. Association of gene variants of transcription factors PPARγ, RUNX2, Osterix genes and COL2A1, IGFBP3 genes with the development of osteonecrosis of the femoral head in Chinese population.
    Song Y; Du Z; Ren M; Yang Q; Wang Q; Chen G; Zhao H; Li Z; Wang J; Zhang G
    Bone; 2017 Aug; 101():104-112. PubMed ID: 28476574
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association Between the Angiotensin-Converting Enzyme Gene Insertion/Deletion Polymorphism and Avascular Necrosis of the Femoral Head.
    Zhang Y; Zhao Z; Wang C; Wang Z; Ren Y; Wang Y; Liu J
    Genet Test Mol Biomarkers; 2019 Nov; 23(11):778-782. PubMed ID: 31633405
    [No Abstract]   [Full Text] [Related]  

  • 12. Identification of a novel COL2A1 mutation (c.1744G>A) in a Japanese family: a case report.
    Kishiya M; Nakamura Y; Ohishi H; Furukawa K; Ishibashi Y
    J Med Case Rep; 2014 Aug; 8():276. PubMed ID: 25124518
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of sterol regulatory element binding protein 2 and insulin-like growth factor binding protein 3 genetic polymorphisms with avascular necrosis of the femoral head in the Chinese population.
    Song Y; Du ZW; Li QJ; Zhang GZ; Wang LL; Wu N; Wang JC; Gao ZL
    Chin Med J (Engl); 2012 Nov; 125(22):4037-43. PubMed ID: 23158139
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A genetic pedigree analysis to identify gene mutations involved in femoral head necrosis.
    Wang L; Pan H; Zhu ZA
    Mol Med Rep; 2014 Oct; 10(4):1835-8. PubMed ID: 25050885
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome.
    Wang X; Jia X; Xiao X; Li S; Li J; Li Y; Wei Y; Liang X; Guo X
    Mol Vis; 2016; 22():697-704. PubMed ID: 27390512
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation in COL2A1 leading to spondyloepiphyseal dysplasia congenita in a three-generation family.
    Xu L; Qiu X; Zhu Z; Yi L; Qiu Y
    Eur Spine J; 2014 May; 23 Suppl 2():271-7. PubMed ID: 24736929
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Morphology and immunohistochemistry of traumatic and non-traumatic necrosis of the femoral head].
    Zhang Y; Li Q; Zhang Y; Wang Z
    Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2010 Jan; 24(1):17-22. PubMed ID: 20135964
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report.
    Chen J; Ma X; Zhou Y; Li G; Guo Q
    BMC Pediatr; 2017 Jul; 17(1):175. PubMed ID: 28738883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New insights into the pathogenesis of glucocorticoid-induced avascular necrosis: microarray analysis of gene expression in a rat model.
    Kerachian MA; Cournoyer D; Harvey EJ; Chow TY; Bégin LR; Nahal A; Séguin C
    Arthritis Res Ther; 2010; 12(3):R124. PubMed ID: 20579363
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Identification of a novel mutation of COL2A1 gene in a Chinese family affected with spondyloepiphyseal dysplasia congenita].
    Li H; Ji A; Ma L; Wang B; Li Y; Cui Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):240-4. PubMed ID: 25863096
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.