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Journal Abstract Search

127 related items for PubMed ID: 9611267

  • 1. Isolation of a Drosophila T-box gene closely related to human TBX1.
    Porsch M, Hofmeyer K, Bausenwein BS, Grimm S, Weber BH, Miassod R, Pflugfelder GO.
    Gene; 1998 Jun 08; 212(2):237-48. PubMed ID: 9611267
    [Abstract] [Full Text] [Related]

  • 2. Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
    Chieffo C, Garvey N, Gong W, Roe B, Zhang G, Silver L, Emanuel BS, Budarf ML.
    Genomics; 1997 Aug 01; 43(3):267-77. PubMed ID: 9268629
    [Abstract] [Full Text] [Related]

  • 3. Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19.
    Yi CH, Terrett JA, Li QY, Ellington K, Packham EA, Armstrong-Buisseret L, McClure P, Slingsby T, Brook JD.
    Genomics; 1999 Jan 01; 55(1):10-20. PubMed ID: 9888994
    [Abstract] [Full Text] [Related]

  • 4. T-box genes and cardiac development.
    Ryan K, Chin AJ.
    Birth Defects Res C Embryo Today; 2003 Feb 01; 69(1):25-37. PubMed ID: 12768655
    [Abstract] [Full Text] [Related]

  • 5. Cloning and mapping of a human gene (TBX2) sharing a highly conserved protein motif with the Drosophila omb gene.
    Campbell C, Goodrich K, Casey G, Beatty B.
    Genomics; 1995 Jul 20; 28(2):255-60. PubMed ID: 8530034
    [Abstract] [Full Text] [Related]

  • 6. Evolution of mouse T-box genes by tandem duplication and cluster dispersion.
    Agulnik SI, Garvey N, Hancock S, Ruvinsky I, Chapman DL, Agulnik I, Bollag R, Papaioannou V, Silver LM.
    Genetics; 1996 Sep 20; 144(1):249-54. PubMed ID: 8878690
    [Abstract] [Full Text] [Related]

  • 7. Structure of the DNA-bound T-box domain of human TBX3, a transcription factor responsible for ulnar-mammary syndrome.
    Coll M, Seidman JG, Müller CW.
    Structure; 2002 Mar 20; 10(3):343-56. PubMed ID: 12005433
    [Abstract] [Full Text] [Related]

  • 8. T-box genes in human disorders.
    Packham EA, Brook JD.
    Hum Mol Genet; 2003 Apr 01; 12 Spec No 1():R37-44. PubMed ID: 12668595
    [Abstract] [Full Text] [Related]

  • 9. Cloning, mapping, and expression analysis of TBX15, a new member of the T-Box gene family.
    Agulnik SI, Papaioannou VE, Silver LM.
    Genomics; 1998 Jul 01; 51(1):68-75. PubMed ID: 9693034
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
    Berti L, Mittler G, Przemeck GK, Stelzer G, Günzler B, Amati F, Conti E, Dallapiccola B, Hrabé de Angelis M, Novelli G, Meisterernst M.
    Genomics; 2001 Jun 15; 74(3):320-32. PubMed ID: 11414760
    [Abstract] [Full Text] [Related]

  • 12. Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.
    Chapman DL, Garvey N, Hancock S, Alexiou M, Agulnik SI, Gibson-Brown JJ, Cebra-Thomas J, Bollag RJ, Silver LM, Papaioannou VE.
    Dev Dyn; 1996 Aug 15; 206(4):379-90. PubMed ID: 8853987
    [Abstract] [Full Text] [Related]

  • 13. TBX10, a member of the Tbx1-subfamily of conserved developmental genes, is located at human chromosome 11q13 and proximal mouse chromosome 19.
    Law DJ, Garvey N, Agulnik SI, Perlroth V, Hahn OM, Rhinehart RE, Gebuhr TC, Silver LM.
    Mamm Genome; 1998 May 15; 9(5):397-9. PubMed ID: 9545502
    [No Abstract] [Full Text] [Related]

  • 14. The lethal(1)optomotor-blind gene of Drosophila melanogaster is a major organizer of optic lobe development: isolation and characterization of the gene.
    Pflugfelder GO, Roth H, Poeck B, Kerscher S, Schwarz H, Jonschker B, Heisenberg M.
    Proc Natl Acad Sci U S A; 1992 Feb 15; 89(4):1199-203. PubMed ID: 1741374
    [Abstract] [Full Text] [Related]

  • 15. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
    Li QY, Newbury-Ecob RA, Terrett JA, Wilson DI, Curtis AR, Yi CH, Gebuhr T, Bullen PJ, Robson SC, Strachan T, Bonnet D, Lyonnet S, Young ID, Raeburn JA, Buckler AJ, Law DJ, Brook JD.
    Nat Genet; 1997 Jan 15; 15(1):21-9. PubMed ID: 8988164
    [Abstract] [Full Text] [Related]

  • 16. Facilitated isolation of rare recombinants by ligase chain reaction: selection for intragenic crossover events in the Drosophila optomotor-blind gene.
    Balles J, Pflugfelder GO.
    Mol Gen Genet; 1994 Dec 15; 245(6):734-40. PubMed ID: 7830721
    [Abstract] [Full Text] [Related]

  • 17. Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation.
    Stoller JZ, Epstein JA.
    Hum Mol Genet; 2005 Apr 01; 14(7):885-92. PubMed ID: 15703190
    [Abstract] [Full Text] [Related]

  • 18. A human gene similar to Drosophila melanogaster peanut maps to the DiGeorge syndrome region of 22q11.
    McKie JM, Sutherland HF, Harvey E, Kim UJ, Scambler PJ.
    Hum Genet; 1997 Nov 01; 101(1):6-12. PubMed ID: 9385360
    [Abstract] [Full Text] [Related]

  • 19. An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus.
    Bollag RJ, Siegfried Z, Cebra-Thomas JA, Garvey N, Davison EM, Silver LM.
    Nat Genet; 1994 Jul 01; 7(3):383-9. PubMed ID: 7920656
    [Abstract] [Full Text] [Related]

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