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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

430 related items for PubMed ID: 10742104

  • 1. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.
    Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R.
    Nat Genet; 2000 Apr; 24(4):391-5. PubMed ID: 10742104
    [Abstract] [Full Text] [Related]

  • 2. Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.
    Liu YH, Tang Z, Kundu RK, Wu L, Luo W, Zhu D, Sangiorgi F, Snead ML, Maxson RE.
    Dev Biol; 1999 Jan 15; 205(2):260-74. PubMed ID: 9917362
    [Abstract] [Full Text] [Related]

  • 3. Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation.
    Antonopoulou I, Mavrogiannis LA, Wilkie AO, Morriss-Kay GM.
    J Anat; 2004 Jun 15; 204(6):487-99. PubMed ID: 15198690
    [Abstract] [Full Text] [Related]

  • 4. Msx2 -/- transgenic mice develop compound amelogenesis imperfecta, dentinogenesis imperfecta and periodental osteopetrosis.
    Aïoub M, Lézot F, Molla M, Castaneda B, Robert B, Goubin G, Néfussi JR, Berdal A.
    Bone; 2007 Nov 15; 41(5):851-9. PubMed ID: 17878071
    [Abstract] [Full Text] [Related]

  • 5. Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development.
    Lallemand Y, Nicola MA, Ramos C, Bach A, Cloment CS, Robert B.
    Development; 2005 Jul 15; 132(13):3003-14. PubMed ID: 15930102
    [Abstract] [Full Text] [Related]

  • 6. Fibroblast growth factors lead to increased Msx2 expression and fusion in calvarial sutures.
    Ignelzi MA, Wang W, Young AT.
    J Bone Miner Res; 2003 Apr 15; 18(4):751-9. PubMed ID: 12674336
    [Abstract] [Full Text] [Related]

  • 7. Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.
    Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA, Wall SA, Chrzanowska KH, Maxson RE.
    Nat Genet; 2000 Apr 15; 24(4):387-90. PubMed ID: 10742103
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Msx2 is a repressor of chondrogenic differentiation in migratory cranial neural crest cells.
    Takahashi K, Nuckolls GH, Takahashi I, Nonaka K, Nagata M, Ikura T, Slavkin HC, Shum L.
    Dev Dyn; 2001 Oct 15; 222(2):252-62. PubMed ID: 11668602
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Msx2 controls ameloblast terminal differentiation.
    Bei M, Stowell S, Maas R.
    Dev Dyn; 2004 Dec 15; 231(4):758-65. PubMed ID: 15499554
    [Abstract] [Full Text] [Related]

  • 14. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2.
    Cohen MM.
    J Craniofac Genet Dev Biol; 2000 Dec 15; 20(1):19-25. PubMed ID: 10879654
    [Abstract] [Full Text] [Related]

  • 15. Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.
    Mavrogiannis LA, Antonopoulou I, Baxová A, Kutílek S, Kim CA, Sugayama SM, Salamanca A, Wall SA, Morriss-Kay GM, Wilkie AO.
    Nat Genet; 2001 Jan 15; 27(1):17-8. PubMed ID: 11137991
    [Abstract] [Full Text] [Related]

  • 16. Impaired endochondral bone development and osteopenia in Gli2-deficient mice.
    Miao D, Liu H, Plut P, Niu M, Huo R, Goltzman D, Henderson JE.
    Exp Cell Res; 2004 Mar 10; 294(1):210-22. PubMed ID: 14980515
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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 10; 227(1):69-77. PubMed ID: 12701100
    [Abstract] [Full Text] [Related]

  • 19. Ventral abdominal wall dysmorphogenesis of Msx1/Msx2 double-mutant mice.
    Ogi H, Suzuki K, Ogino Y, Kamimura M, Miyado M, Ying X, Zhang Z, Shinohara M, Chen Y, Yamada G.
    Anat Rec A Discov Mol Cell Evol Biol; 2005 May 10; 284(1):424-30. PubMed ID: 15803476
    [Abstract] [Full Text] [Related]

  • 20. Positionally-dependent chondrogenesis induced by BMP4 is co-regulated by Sox9 and Msx2.
    Semba I, Nonaka K, Takahashi I, Takahashi K, Dashner R, Shum L, Nuckolls GH, Slavkin HC.
    Dev Dyn; 2000 Apr 10; 217(4):401-14. PubMed ID: 10767084
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 22.