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 *

115 related articles for article (PubMed ID: 15948199)

  • 21. Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia.
    Ikegawa S; Ohashi H; Nishimura G; Kim KC; Sannohe A; Kimizuka M; Fukushima Y; Nagai T; Nakamura Y
    Hum Genet; 1998 Dec; 103(6):633-8. PubMed ID: 9921895
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Comparison of orthopaedic manifestations of multiple epiphyseal dysplasia caused by MATN3 versus COMP mutations: a case control study.
    Seo SG; Song HR; Kim HW; Yoo WJ; Shim JS; Chung CY; Park MS; Oh CW; Jeong C; Song KS; Kim OH; Park SS; Choi IH; Cho TJ
    BMC Musculoskelet Disord; 2014 Mar; 15():84. PubMed ID: 24629099
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Progress of molecular genetic research on pseudoachon-droplasia and multiple epiphyseal dysplasia].
    Wang JJ; Guo YB
    Yi Chuan; 2008 May; 30(5):537-42. PubMed ID: 18487141
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMD.
    Borochowitz ZU; Scheffer D; Adir V; Dagoneau N; Munnich A; Cormier-Daire V
    J Med Genet; 2004 May; 41(5):366-72. PubMed ID: 15121775
    [No Abstract]   [Full Text] [Related]  

  • 25. Multiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African family.
    Ballo R; Briggs MD; Cohn DH; Knowlton RG; Beighton PH; Ramesar RS
    Am J Med Genet; 1997 Feb; 68(4):396-400. PubMed ID: 9021009
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita.
    Unger S; Korkko J; Krakow D; Lachman RS; Rimoin DL; Cohn DH
    Am J Med Genet; 2001 Nov; 104(2):140-6. PubMed ID: 11746045
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pseudoachondroplasia and multiple epiphyseal dysplasia: mutation review, molecular interactions, and genotype to phenotype correlations.
    Briggs MD; Chapman KL
    Hum Mutat; 2002 May; 19(5):465-78. PubMed ID: 11968079
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix.
    Rimoin DL; Rasmussen IM; Briggs MD; Roughley PJ; Gruber HE; Warman ML; Olsen BR; Hsia YE; Yuen J; Reinker K
    Hum Genet; 1994 Mar; 93(3):236-42. PubMed ID: 7907311
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel and recurrent exon 13 mutations of COMP in pseudoachondroplasia.
    Nakashima E; Mabuchi A; Kubota M; Ishikiriyama S; Ohashi H; Nishimura G; Ikegawa S
    Am J Med Genet A; 2005 Jan; 132A(1):108-9. PubMed ID: 15523619
    [No Abstract]   [Full Text] [Related]  

  • 30. Multilayered patella: similar radiographic findings in pseudoachondroplasia and recessive multiple epiphyseal dysplasia.
    Vatanavicharn N; Lachman RS; Rimoin DL
    Am J Med Genet A; 2008 Jul; 146A(13):1682-6. PubMed ID: 18546327
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Review: clinical variability and genetic heterogeneity in multiple epiphyseal dysplasia.
    Chapman KL; Briggs MD; Mortier GR
    Pediatr Pathol Mol Med; 2003; 22(1):53-75. PubMed ID: 12687890
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of cartilage oligomeric matrix protein (COMP) gene mutations in patients with pseudoachondroplasia and multiple epiphyseal dysplasia.
    Song HR; Lee KS; Li QW; Koo SK; Jung SC
    J Hum Genet; 2003; 48(5):222-225. PubMed ID: 12768438
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Multiple epiphyseal dysplasia and pseudoachondroplasia due to novel mutations in the calmodulin-like repeats of cartilage oligomeric matrix protein.
    Susic S; McGrory J; Ahier J; Cole WG
    Clin Genet; 1997 Apr; 51(4):219-24. PubMed ID: 9184241
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Autosomal dominant precocious osteoarthropathy due to a mutation of the cartilage oligomeric matrix protein (COMP) gene: further expansion of the phenotypic variations of COMP defects.
    Kawaji H; Nishimura G; Watanabe S; Mabuchi A; Ikeda T; Ohashi H; Sasaki A; Sano T; Ikegawa S
    Skeletal Radiol; 2002 Dec; 31(12):730-7. PubMed ID: 12483437
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Decreased chondrocyte proliferation and dysregulated apoptosis in the cartilage growth plate are key features of a murine model of epiphyseal dysplasia caused by a matn3 mutation.
    Leighton MP; Nundlall S; Starborg T; Meadows RS; Suleman F; Knowles L; Wagener R; Thornton DJ; Kadler KE; Boot-Handford RP; Briggs MD
    Hum Mol Genet; 2007 Jul; 16(14):1728-41. PubMed ID: 17517694
    [TBL] [Abstract][Full Text] [Related]  

  • 36. MATN3 Mutation Causing Spondyloepimetaphyseal Dysplasia.
    Shyamasundar LG; Loganathan L; Kumar A; Selina A; Madhuri V
    Indian J Pediatr; 2020 Mar; 87(3):227-228. PubMed ID: 31724101
    [No Abstract]   [Full Text] [Related]  

  • 37. Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene.
    Briggs MD; Hoffman SM; King LM; Olsen AS; Mohrenweiser H; Leroy JG; Mortier GR; Rimoin DL; Lachman RS; Gaines ES
    Nat Genet; 1995 Jul; 10(3):330-6. PubMed ID: 7670472
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasia.
    Deere M; Sanford T; Francomano CA; Daniels K; Hecht JT
    Am J Med Genet; 1999 Aug; 85(5):486-90. PubMed ID: 10405447
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations in the cartilage oligomeric matrix protein (COMP) gene in pseudoachondroplasia and multiple epiphyseal dysplasia.
    Cohn DH; Briggs MD; King LM; Rimoin DL; Wilcox WR; Lachman RS; Knowlton RG
    Ann N Y Acad Sci; 1996 Jun; 785():188-94. PubMed ID: 8702126
    [No Abstract]   [Full Text] [Related]  

  • 40. A novel mutation of the COMP gene in a Thai family with pseudoachondroplasia.
    Shotelersuk V; Punyashthiti R
    Int J Mol Med; 2002 Jan; 9(1):81-4. PubMed ID: 11745002
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.