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    Ian Welsh, PhD

    TitlePostdoctoral Scholar
    SchoolUCSF School of Dentistry
    DepartmentOrofacial Sciences
    Address401 Parnassus Ave, LangPorter
    San Francisco CA 94143
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      Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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      1. Welsh IC, Kwak H, Chen FL, Werner M, Shopland LS, Danko CG, Lis JT, Zhang M, Martin JF, Kurpios NA. Chromatin Architecture of the Pitx2 Locus Requires CTCF- and Pitx2-Dependent Asymmetry that Mirrors Embryonic Gut Laterality. Cell Rep. 2015 Oct 13; 13(2):337-49. PMID: 26411685; PMCID: PMC4617833.
      2. Mahadevan A, Welsh IC, Sivakumar A, Gludish DW, Shilvock AR, Noden DM, Huss D, Lansford R, Kurpios NA. The left-right Pitx2 pathway drives organ-specific arterial and lymphatic development in the intestine. Dev Cell. 2014 Dec 22; 31(6):690-706. PMID: 25482882; PMCID: PMC4326534 [Available on 12/22/15].
      3. Welsh IC, Thomsen M, Gludish DW, Alfonso-Parra C, Bai Y, Martin JF, Kurpios NA. Integration of left-right Pitx2 transcription and Wnt signaling drives asymmetric gut morphogenesis via Daam2. Dev Cell. 2013 Sep 30; 26(6):629-44. PMID: 24091014; PMCID: PMC3965270.
      4. Lyndaker AM, Modzelewski AJ, Welsh IC. Reproductive and developmental genomics retreat at Cornell University, 2012. Mol Reprod Dev. 2012 Sep; 79(9):588-91. PMID: 22933246; PMCID: PMC4104196.
      5. Welsh IC, O'Brien TP. Signaling integration in the rugae growth zone directs sequential SHH signaling center formation during the rostral outgrowth of the palate. Dev Biol. 2009 Dec 1; 336(1):53-67. PMID: 19782673; PMCID: PMC2789450.
      6. Munroe RJ, Prabhu V, Acland GM, Johnson KR, Harris BS, O'Brien TP, Welsh IC, Noden DM, Schimenti JC. Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. BMC Dev Biol. 2009; 9:27. PMID: 19379485; PMCID: PMC2676275.
      7. Welsh IC, Hagge-Greenberg A, O'Brien TP. A dosage-dependent role for Spry2 in growth and patterning during palate development. Mech Dev. 2007 Sep-Oct; 124(9-10):746-61. PMID: 17693063; PMCID: PMC2043129.
      8. Han L, Dias Figueiredo M, Berghorn KA, Iwata TN, Clark-Campbell PA, Welsh IC, Wang W, O'brien TP, Lin DM, Roberson MS. Analysis of the gene regulatory program induced by the homeobox transcription factor distal-less 3 in mouse placenta. Endocrinology. 2007 Mar; 148(3):1246-54. PMID: 17110422.
        View in: PubMed
      9. Burgess RW, Peterson KA, Johnson MJ, Roix JJ, Welsh IC, O'Brien TP. Evidence for a conserved function in synapse formation reveals Phr1 as a candidate gene for respiratory failure in newborn mice. Mol Cell Biol. 2004 Feb; 24(3):1096-105. PMID: 14729956; PMCID: PMC321423.
      10. Frank AC, Meyers KA, Welsh IC, O'Brien TP. Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice. Proc Natl Acad Sci U S A. 2003 Nov 25; 100(24):14103-8. PMID: 14615591; PMCID: PMC283553.
      11. Krebs LT, Iwai N, Nonaka S, Welsh IC, Lan Y, Jiang R, Saijoh Y, O'Brien TP, Hamada H, Gridley T. Notch signaling regulates left-right asymmetry determination by inducing Nodal expression. Genes Dev. 2003 May 15; 17(10):1207-12. PMID: 12730124; PMCID: PMC196059.
      12. Welsh IC, O'Brien TP. Loss of late primitive streak mesoderm and interruption of left-right morphogenesis in the Ednrb(s-1Acrg) mutant mouse. Dev Biol. 2000 Sep 1; 225(1):151-68. PMID: 10964471.
        View in: PubMed
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