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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

177 related items for PubMed ID: 15525660

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  • 2. Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.
    Rozeman LB, Sangiorgi L, Briaire-de Bruijn IH, Mainil-Varlet P, Bertoni F, Cleton-Jansen AM, Hogendoorn PC, Bovée JV.
    Hum Mutat; 2004 Dec; 24(6):466-73. PubMed ID: 15523647
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  • 3. [Cytokines in bone diseases. Genetic defects of PTH/PTHrP receptor in chondrodysplasia].
    Ogata N.
    Clin Calcium; 2010 Oct; 20(10):1481-8. PubMed ID: 20890029
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  • 9. PTHR1 mutations associated with Ollier disease result in receptor loss of function.
    Couvineau A, Wouters V, Bertrand G, Rouyer C, Gérard B, Boon LM, Grandchamp B, Vikkula M, Silve C.
    Hum Mol Genet; 2008 Sep 15; 17(18):2766-75. PubMed ID: 18559376
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  • 10. [Parathyroid hormone (PTH)/PTH-related peptide (PTHrP) receptor gene recombinant mice].
    Amizuka N, Li M.
    Nihon Rinsho; 2005 Oct 15; 63 Suppl 10():300-5. PubMed ID: 16279651
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  • 12. Climbing exercise enhances osteoblast differentiation and inhibits adipogenic differentiation with high expression of PTH/PTHrP receptor in bone marrow cells.
    Menuki K, Mori T, Sakai A, Sakuma M, Okimoto N, Shimizu Y, Kunugita N, Nakamura T.
    Bone; 2008 Sep 15; 43(3):613-20. PubMed ID: 18567552
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  • 13. Loss of function of parathyroid hormone receptor 1 induces Notch-dependent aortic defects during zebrafish vascular development.
    Gray C, Bratt D, Lees J, daCosta M, Plant K, Watson OJ, Solaymani-Kohal S, Tazzyman S, Serbanovic-Canic J, Crossman DC, Keavney BD, Haase A, McMahon K, Gering M, Roehl H, Evans PC, Chico TJ.
    Arterioscler Thromb Vasc Biol; 2013 Jun 15; 33(6):1257-63. PubMed ID: 23559631
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  • 15. Absence of functional type 1 parathyroid hormone (PTH)/PTH-related protein receptors in humans is associated with abnormal breast development and tooth impaction.
    Wysolmerski JJ, Cormier S, Philbrick WM, Dann P, Zhang JP, Roume J, Delezoide AL, Silve C.
    J Clin Endocrinol Metab; 2001 Apr 15; 86(4):1788-94. PubMed ID: 11297619
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  • 17. Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.
    Bowen ME, Boyden ED, Holm IA, Campos-Xavier B, Bonafé L, Superti-Furga A, Ikegawa S, Cormier-Daire V, Bovée JV, Pansuriya TC, de Sousa SB, Savarirayan R, Andreucci E, Vikkula M, Garavelli L, Pottinger C, Ogino T, Sakai A, Regazzoni BM, Wuyts W, Sangiorgi L, Pedrini E, Zhu M, Kozakewich HP, Kasser JR, Seidman JG, Kurek KC, Warman ML.
    PLoS Genet; 2011 Apr 15; 7(4):e1002050. PubMed ID: 21533187
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  • 18. A new acro-osteolysis syndrome caused by duplications including PTHLH.
    Gray MJ, van Kogelenberg M, Beddow R, Morgan T, Wordsworth P, Shears DJ, Robertson SP, Hurst JA.
    J Hum Genet; 2014 Sep 15; 59(9):484-7. PubMed ID: 25007883
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  • 19. Association of parathyroid hormone-like hormone (PTHLH) and its receptor (PTHR1) with the number of functional and inverted teats in pigs.
    Tetzlaff S, Chomdej S, Jonas E, Ponsuksili S, Murani E, Phatsara C, Schellander K, Wimmers K.
    J Anim Breed Genet; 2009 Jun 15; 126(3):237-41. PubMed ID: 19646152
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