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Journal Abstract Search


176 related items for PubMed ID: 19623272

  • 41. Hox genes and regional patterning of the vertebrate body plan.
    Mallo M, Wellik DM, Deschamps J.
    Dev Biol; 2010 Aug 01; 344(1):7-15. PubMed ID: 20435029
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  • 42. Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of hoxd-11.
    Davis AP, Capecchi MR.
    Development; 1994 Aug 01; 120(8):2187-98. PubMed ID: 7925020
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  • 43. Pbx1/Pbx2 govern axial skeletal development by controlling Polycomb and Hox in mesoderm and Pax1/Pax9 in sclerotome.
    Capellini TD, Zewdu R, Di Giacomo G, Asciutti S, Kugler JE, Di Gregorio A, Selleri L.
    Dev Biol; 2008 Sep 15; 321(2):500-14. PubMed ID: 18691704
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  • 44. Identification of cis-HOX-HOXC10 axis as a therapeutic target for colorectal tumor-initiating cells without APC mutations.
    Chen Z, Wu J, Liu B, Zhang G, Wang Z, Zhang L, Wang K, Fan Z, Zhu P.
    Cell Rep; 2021 Jul 27; 36(4):109431. PubMed ID: 34320348
    [Abstract] [Full Text] [Related]

  • 45. Hox C cluster genes are dispensable for overall body plan of mouse embryonic development.
    Suemori H, Noguchi S.
    Dev Biol; 2000 Apr 15; 220(2):333-42. PubMed ID: 10753520
    [Abstract] [Full Text] [Related]

  • 46. Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex.
    O'Brien TP, Metallinos DL, Chen H, Shin MK, Tilghman SM.
    Genetics; 1996 May 15; 143(1):447-61. PubMed ID: 8722795
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  • 47. Dlk1-Dio3 locus-derived lncRNAs perpetuate postmitotic motor neuron cell fate and subtype identity.
    Yen YP, Hsieh WF, Tsai YY, Lu YL, Liau ES, Hsu HC, Chen YC, Liu TC, Chang M, Li J, Lin SP, Hung JH, Chen JA.
    Elife; 2018 Oct 12; 7():. PubMed ID: 30311912
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  • 48. Role of HOXC10 in Cancer.
    Fang J, Wang J, Yu L, Xu W.
    Front Oncol; 2021 Oct 12; 11():684021. PubMed ID: 34113572
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  • 49. Retinoic acid regulates a subset of Cdx1 function in vivo.
    Houle M, Sylvestre JR, Lohnes D.
    Development; 2003 Dec 12; 130(26):6555-67. PubMed ID: 14660544
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  • 50. Coordinated actions of the forkhead protein Foxp1 and Hox proteins in the columnar organization of spinal motor neurons.
    Rousso DL, Gaber ZB, Wellik D, Morrisey EE, Novitch BG.
    Neuron; 2008 Jul 31; 59(2):226-40. PubMed ID: 18667151
    [Abstract] [Full Text] [Related]

  • 51. Early mitotic degradation of the homeoprotein HOXC10 is potentially linked to cell cycle progression.
    Gabellini D, Colaluca IN, Vodermaier HC, Biamonti G, Giacca M, Falaschi A, Riva S, Peverali FA.
    EMBO J; 2003 Jul 15; 22(14):3715-24. PubMed ID: 12853486
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  • 52. Abnormalities of vertebral formation and Hox expression in congenital kyphoscoliotic rats.
    Seki T, Shimokawa N, Iizuka H, Takagishi K, Koibuchi N.
    Mol Cell Biochem; 2008 May 15; 312(1-2):193-9. PubMed ID: 18327665
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  • 53. The mouse Ulnaless mutation deregulates posterior HoxD gene expression and alters appendicular patterning.
    Peichel CL, Prabhakaran B, Vogt TF.
    Development; 1997 Sep 15; 124(18):3481-92. PubMed ID: 9342041
    [Abstract] [Full Text] [Related]

  • 54. Interleukin 1β-mediated HOXC10 Overexpression Promotes Hepatocellular Carcinoma Metastasis by Upregulating PDPK1 and VASP.
    Dang Y, Chen J, Feng W, Qiao C, Han W, Nie Y, Wu K, Fan D, Xia L.
    Theranostics; 2020 Sep 15; 10(8):3833-3848. PubMed ID: 32206125
    [Abstract] [Full Text] [Related]

  • 55. Transcription factors Nkx3.1 and Nkx3.2 (Bapx1) play an overlapping role in sclerotomal development of the mouse.
    Herbrand H, Pabst O, Hill R, Arnold HH.
    Mech Dev; 2002 Sep 15; 117(1-2):217-24. PubMed ID: 12204261
    [Abstract] [Full Text] [Related]

  • 56. New insights into the role of Jmjd3 and Utx in axial skeletal formation in mice.
    Naruse C, Shibata S, Tamura M, Kawaguchi T, Abe K, Sugihara K, Kato T, Nishiuchi T, Wakana S, Ikawa M, Asano M.
    FASEB J; 2017 Jun 15; 31(6):2252-2266. PubMed ID: 28188179
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  • 57. Developmental Patterning as a Quantitative Trait: Genetic Modulation of the Hoxb6 Mutant Skeletal Phenotype.
    Kappen C.
    PLoS One; 2016 Jun 15; 11(1):e0146019. PubMed ID: 26800342
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  • 58. Postnatal Msx1 expression pattern in craniofacial, axial, and appendicular skeleton of transgenic mice from the first week until the second year.
    Orestes-Cardoso SM, Nefussi JR, Hotton D, Mesbah M, Orestes-Cardoso MD, Robert B, Berdal A.
    Dev Dyn; 2001 May 15; 221(1):1-13. PubMed ID: 11357189
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  • 59. Hindlimb patterning and mandible development require the Ptx1 gene.
    Lanctôt C, Moreau A, Chamberland M, Tremblay ML, Drouin J.
    Development; 1999 May 15; 126(9):1805-10. PubMed ID: 10101115
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  • 60. Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in mice.
    Fisher CL, Lee I, Bloyer S, Bozza S, Chevalier J, Dahl A, Bodner C, Helgason CD, Hess JL, Humphries RK, Brock HW.
    Dev Biol; 2010 Jan 01; 337(1):9-15. PubMed ID: 19833123
    [Abstract] [Full Text] [Related]


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