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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

175 related items for PubMed ID: 15721141

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  • 23. Comparative analysis of the genomic organization of Pax9 and its conserved physical association with Nkx2-9 in the human, mouse, and pufferfish genomes.
    Santagati F, Gerber JK, Blusch JH, Kokubu C, Peters H, Adamski J, Werner T, Balling R, Imai K.
    Mamm Genome; 2001 Mar; 12(3):232-7. PubMed ID: 11252173
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  • 24. Molecular morphogenetic fields in the development of human dentition.
    Line SR.
    J Theor Biol; 2001 Jul 07; 211(1):67-75. PubMed ID: 11407892
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  • 26. Pax1/Pax9-Related genes in an agnathan vertebrate, Lampetra japonica: expression pattern of LjPax9 implies sequential evolutionary events toward the gnathostome body plan.
    Ogasawara M, Shigetani Y, Hirano S, Satoh N, Kuratani S.
    Dev Biol; 2000 Jul 15; 223(2):399-410. PubMed ID: 10882524
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  • 27. Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.
    Mostowska A, Kobielak A, Trzeciak WH.
    Eur J Oral Sci; 2003 Oct 15; 111(5):365-70. PubMed ID: 12974677
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  • 29. Malleal processus brevis is dispensable for normal hearing in mice.
    Zhang Z, Zhang X, Avniel WA, Song Y, Jones SM, Jones TA, Fermin C, Chen Y.
    Dev Dyn; 2003 May 15; 227(1):69-77. PubMed ID: 12701100
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  • 34. Familial human hypodontia--is it all in the genes?
    Cobourne MT.
    Br Dent J; 2007 Aug 25; 203(4):203-8. PubMed ID: 17721480
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  • 35. 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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  • 39. Novel PAX9 mutations cause non-syndromic tooth agenesis.
    Mitsui SN, Yasue A, Masuda K, Watanabe K, Horiuchi S, Imoto I, Tanaka E.
    J Dent Res; 2014 Mar 13; 93(3):245-9. PubMed ID: 24436340
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