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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

214 related items for PubMed ID: 7649395

  • 41.
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  • 42. Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins.
    Joosten PH, Hol FA, van Beersum SE, Peters H, Hamel BC, Afink GB, van Zoelen EJ, Mariman EC.
    Proc Natl Acad Sci U S A; 1998 Nov 24; 95(24):14459-63. PubMed ID: 9826722
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  • 44. The floor plate is sufficient for development of the sclerotome and spine without the notochord.
    Ando T, Semba K, Suda H, Sei A, Mizuta H, Araki M, Abe K, Imai K, Nakagata N, Araki K, Yamamura K.
    Mech Dev; 2011 Nov 24; 128(1-2):129-40. PubMed ID: 21111815
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  • 45. Association between palatal morphogenesis and Pax9 expression pattern in CL/Fr embryos with clefting during palatal development.
    Hamachi T, Sasaki Y, Hidaka K, Nakata M.
    Arch Oral Biol; 2003 Aug 24; 48(8):581-7. PubMed ID: 12828987
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  • 46. Histochemistry of the developing notochord, perichordal sheath and vertebrae in Danforth's short-tail (sd) and normal C57BL/6 mice.
    Paavola LG, Wilson DB, Center EM.
    J Embryol Exp Morphol; 1980 Feb 24; 55():227-45. PubMed ID: 7373196
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  • 50. Pax1(EGFP): new wildtype and mutant EGFP mouse lines for molecular and fate mapping studies.
    Sivakamasundari V, Kraus P, Jie S, Lufkin T.
    Genesis; 2013 Jun 24; 51(6):420-9. PubMed ID: 23377878
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  • 51.
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  • 52. Meox homeodomain proteins are required for Bapx1 expression in the sclerotome and activate its transcription by direct binding to its promoter.
    Rodrigo I, Bovolenta P, Mankoo BS, Imai K.
    Mol Cell Biol; 2004 Apr 24; 24(7):2757-66. PubMed ID: 15024065
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  • 53. Pax genes and organogenesis: Pax9 meets tooth development.
    Peters H, Neubüser A, Balling R.
    Eur J Oral Sci; 1998 Jan 24; 106 Suppl 1():38-43. PubMed ID: 9541201
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  • 54. The scoliosis (sco) mouse: a new allele of Pax1.
    Adham IM, Gille M, Gamel AJ, Reis A, Dressel R, Steding G, Brand-Saberi B, Engel W.
    Cytogenet Genome Res; 2005 Jan 24; 111(1):16-26. PubMed ID: 16093716
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  • 55. Undulated short-tail deletion mutation in the mouse ablates Pax1 and leads to ectopic activation of neighboring Nkx2-2 in domains that normally express Pax1.
    Kokubu C, Wilm B, Kokubu T, Wahl M, Rodrigo I, Sakai N, Santagati F, Hayashizaki Y, Suzuki M, Yamamura K, Abe K, Imai K.
    Genetics; 2003 Sep 24; 165(1):299-307. PubMed ID: 14504237
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  • 56.
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  • 57. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.
    Peters H, Neubüser A, Kratochwil K, Balling R.
    Genes Dev; 1998 Sep 01; 12(17):2735-47. PubMed ID: 9732271
    [Abstract] [Full Text] [Related]

  • 58. Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans.
    Mensah JK, Ogawa T, Kapadia H, Cavender AC, D'Souza RN.
    J Biol Chem; 2004 Feb 13; 279(7):5924-33. PubMed ID: 14607846
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  • 59. A developmental transcriptomic analysis of Pax1 and Pax9 in embryonic intervertebral disc development.
    Sivakamasundari V, Kraus P, Sun W, Hu X, Lim SL, Prabhakar S, Lufkin T.
    Biol Open; 2017 Feb 15; 6(2):187-199. PubMed ID: 28011632
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  • 60.
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