BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 17373680)

  • 1. Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation.
    Bocciardi R; Giorda R; Buttgereit J; Gimelli S; Divizia MT; Beri S; Garofalo S; Tavella S; Lerone M; Zuffardi O; Bader M; Ravazzolo R; Gimelli G
    Hum Mutat; 2007 Jul; 28(7):724-31. PubMed ID: 17373680
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype.
    Moncla A; Missirian C; Cacciagli P; Balzamo E; Legeai-Mallet L; Jouve JL; Chabrol B; Le Merrer M; Plessis G; Villard L; Philip N
    Hum Mutat; 2007 Dec; 28(12):1183-8. PubMed ID: 17676597
    [TBL] [Abstract][Full Text] [Related]  

  • 3. C-type natriuretic peptide and overgrowth.
    Bocciardi R; Ravazzolo R
    Endocr Dev; 2009; 14():61-6. PubMed ID: 19293575
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypomorphic mutation in mouse Nppc gene causes retarded bone growth due to impaired endochondral ossification.
    Tsuji T; Kondo E; Yasoda A; Inamoto M; Kiyosu C; Nakao K; Kunieda T
    Biochem Biophys Res Commun; 2008 Nov; 376(1):186-90. PubMed ID: 18775416
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dwarfism and early death in mice lacking C-type natriuretic peptide.
    Chusho H; Tamura N; Ogawa Y; Yasoda A; Suda M; Miyazawa T; Nakamura K; Nakao K; Kurihara T; Komatsu Y; Itoh H; Tanaka K; Saito Y; Katsuki M; Nakao K
    Proc Natl Acad Sci U S A; 2001 Mar; 98(7):4016-21. PubMed ID: 11259675
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype-Phenotype Correlation of 2q37 Deletions Including NPPC Gene Associated with Skeletal Malformations.
    Tassano E; Buttgereit J; Bader M; Lerone M; Divizia MT; Bocciardi R; Napoli F; Pala G; Sloan-Béna F; Gimelli S; Gimelli G
    PLoS One; 2013; 8(6):e66048. PubMed ID: 23805197
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chronically elevated plasma C-type natriuretic peptide level stimulates skeletal growth in transgenic mice.
    Kake T; Kitamura H; Adachi Y; Yoshioka T; Watanabe T; Matsushita H; Fujii T; Kondo E; Tachibe T; Kawase Y; Jishage K; Yasoda A; Mukoyama M; Nakao K
    Am J Physiol Endocrinol Metab; 2009 Dec; 297(6):E1339-48. PubMed ID: 19808910
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cyclic GMP-dependent protein kinase II plays a critical role in C-type natriuretic peptide-mediated endochondral ossification.
    Miyazawa T; Ogawa Y; Chusho H; Yasoda A; Tamura N; Komatsu Y; Pfeifer A; Hofmann F; Nakao K
    Endocrinology; 2002 Sep; 143(9):3604-10. PubMed ID: 12193576
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Skeletal overgrowth syndrome caused by overexpression of C-type natriuretic peptide in a girl with balanced chromosomal translocation, t(1;2)(q41;q37.1).
    Ko JM; Bae JS; Choi JS; Miura K; Lee HR; Kim OH; Kim NK; Oh SK; Ozono K; Lee CK; Choi IH; Park WY; Cho TJ
    Am J Med Genet A; 2015 May; 167A(5):1033-8. PubMed ID: 25728306
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Circulating C-type natriuretic peptide (CNP) rescues chondrodysplastic CNP knockout mice from their impaired skeletal growth and early death.
    Fujii T; Komatsu Y; Yasoda A; Kondo E; Yoshioka T; Nambu T; Kanamoto N; Miura M; Tamura N; Arai H; Mukoyama M; Nakao K
    Endocrinology; 2010 Sep; 151(9):4381-8. PubMed ID: 20610569
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Significance of C-type natriuretic peptide (CNP) in endochondral ossification: analysis of CNP knockout mice.
    Komatsu Y; Chusho H; Tamura N; Yasoda A; Miyazawa T; Suda M; Miura M; Ogawa Y; Nakao K
    J Bone Miner Metab; 2002; 20(6):331-6. PubMed ID: 12434160
    [No Abstract]   [Full Text] [Related]  

  • 12. The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies.
    Panza E; Gimelli G; Passalacqua M; Cohen A; Gimelli S; Giglio S; Ghezzi C; Sparatore B; Heye B; Zuffardi O; Rugarli E; Meitinger T; Romeo G; Ravazzolo R; Seri M
    Int J Mol Med; 2007 Mar; 19(3):429-35. PubMed ID: 17273791
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Skeletal analysis of the long bone abnormality (lbab/lbab) mouse, a novel chondrodysplastic C-type natriuretic peptide mutant.
    Kondo E; Yasoda A; Tsuji T; Fujii T; Miura M; Kanamoto N; Tamura N; Arai H; Kunieda T; Nakao K
    Calcif Tissue Int; 2012 Apr; 90(4):307-18. PubMed ID: 22271248
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation.
    Bernheim A; Toujani S; Guillaud-Bataille M; Richon C; Waxin H; Dessen P; Berger R
    Cytogenet Genome Res; 2007; 119(3-4):185-90. PubMed ID: 18253027
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cloning and chromosomal assignment of the mouse C-type natriuretic peptide (CNP) gene (Nppc): comparison with the human CNP gene (NPPC).
    Ogawa Y; Itoh H; Yoshitake Y; Inoue M; Yoshimasa T; Serikawa T; Nakao K
    Genomics; 1994 Nov; 24(2):383-7. PubMed ID: 7698765
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.
    Boyadjiev SA; South ST; Radford CL; Patel A; Zhang G; Hur DJ; Thomas GH; Gearhart JP; Stetten G
    Genomics; 2005 May; 85(5):622-9. PubMed ID: 15820314
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
    Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
    Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retarded skeletal development in transgenic mice with a type II collagen mutation.
    Savontaus M; Metsranta M; Vuorio E
    Am J Pathol; 1996 Dec; 149(6):2169-82. PubMed ID: 8952549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.