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

199 related items for PubMed ID: 23642587

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.
    Kelly RG, Jerome-Majewska LA, Papaioannou VE.
    Hum Mol Genet; 2004 Nov 15; 13(22):2829-40. PubMed ID: 15385444
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.
    Fagman H, Liao J, Westerlund J, Andersson L, Morrow BE, Nilsson M.
    Hum Mol Genet; 2007 Feb 01; 16(3):276-85. PubMed ID: 17164259
    [Abstract] [Full Text] [Related]

  • 6. Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.
    Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C, Unolt M, Pelliccione E, Anaclerio S, Caprio C, Cioffi S, Bilio M, Baban A, Drago F, Digilio MC, Marino B, Baldini A.
    PLoS One; 2019 Feb 01; 14(4):e0211170. PubMed ID: 30933971
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 10. TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.
    Gao S, Moreno M, Eliason S, Cao H, Li X, Yu W, Bidlack FB, Margolis HC, Baldini A, Amendt BA.
    Hum Mol Genet; 2015 Apr 15; 24(8):2330-48. PubMed ID: 25556186
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome.
    Hasten E, Morrow BE.
    PLoS Genet; 2019 Aug 15; 15(8):e1008301. PubMed ID: 31412026
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 18. Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development.
    Garg V, Yamagishi C, Hu T, Kathiriya IS, Yamagishi H, Srivastava D.
    Dev Biol; 2001 Jul 01; 235(1):62-73. PubMed ID: 11412027
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.
    Hiramoto T, Kang G, Suzuki G, Satoh Y, Kucherlapati R, Watanabe Y, Hiroi N.
    Hum Mol Genet; 2011 Dec 15; 20(24):4775-85. PubMed ID: 21908517
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.