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Connection

Ivan Moskowitz to Mice

This is a "connection" page, showing publications Ivan Moskowitz has written about Mice.
Connection Strength

1.446
  1. A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus. Hum Mol Genet. 2011 Oct 01; 20(19):3725-37.
    View in: PubMed
    Score: 0.150
  2. A Genomic Link From Heart Failure to Atrial Fibrillation Risk: FOG2 Modulates a TBX5/GATA4-Dependent Atrial Gene Regulatory Network. Circulation. 2024 Apr 09; 149(15):1205-1230.
    View in: PubMed
    Score: 0.090
  3. Hedgehog signaling activates a mammalian heterochronic gene regulatory network controlling differentiation timing across lineages. Dev Cell. 2022 09 26; 57(18):2181-2203.e9.
    View in: PubMed
    Score: 0.082
  4. Hedgehog-FGF signaling axis patterns anterior mesoderm during gastrulation. Proc Natl Acad Sci U S A. 2020 07 07; 117(27):15712-15723.
    View in: PubMed
    Score: 0.070
  5. Enhancer transcription identifies cis-regulatory elements for photoreceptor cell types. Development. 2020 02 05; 147(3).
    View in: PubMed
    Score: 0.068
  6. Atrial fibrillation risk loci interact to modulate Ca2+-dependent atrial rhythm homeostasis. J Clin Invest. 2019 11 01; 129(11):4937-4950.
    View in: PubMed
    Score: 0.067
  7. Evolutionarily conserved Tbx5-Wnt2/2b pathway orchestrates cardiopulmonary development. Proc Natl Acad Sci U S A. 2018 11 06; 115(45):E10615-E10624.
    View in: PubMed
    Score: 0.063
  8. Transcription-factor-dependent enhancer transcription defines a gene regulatory network for cardiac rhythm. Elife. 2017 12 27; 6.
    View in: PubMed
    Score: 0.059
  9. Pitx2 modulates a Tbx5-dependent gene regulatory network to maintain atrial rhythm. Sci Transl Med. 2016 08 31; 8(354):354ra115.
    View in: PubMed
    Score: 0.054
  10. Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms. Hum Mol Genet. 2016 07 15; 25(14):3011-3028.
    View in: PubMed
    Score: 0.053
  11. Foxf genes integrate tbx5 and hedgehog pathways in the second heart field for cardiac septation. PLoS Genet. 2014 Oct; 10(10):e1004604.
    View in: PubMed
    Score: 0.048
  12. A common genetic variant within SCN10A modulates cardiac SCN5A expression. J Clin Invest. 2014 Apr; 124(4):1844-52.
    View in: PubMed
    Score: 0.046
  13. TBX5 drives Scn5a expression to regulate cardiac conduction system function. J Clin Invest. 2012 Jul; 122(7):2509-18.
    View in: PubMed
    Score: 0.040
  14. Inducible recombination in the cardiac conduction system of minK: CreERT² BAC transgenic mice. Genesis. 2011 Nov; 49(11):878-84.
    View in: PubMed
    Score: 0.038
  15. Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development. [corrected] Proc Natl Acad Sci U S A. 2011 Mar 08; 108(10):4006-11.
    View in: PubMed
    Score: 0.037
  16. sonic hedgehog is required in pulmonary endoderm for atrial septation. Development. 2009 May; 136(10):1761-70.
    View in: PubMed
    Score: 0.032
  17. A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development. Cell. 2007 Jun 29; 129(7):1365-76.
    View in: PubMed
    Score: 0.029
  18. The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system. Development. 2004 Aug; 131(16):4107-16.
    View in: PubMed
    Score: 0.023
  19. An Anterior Second Heart Field Enhancer Regulates the Gene Regulatory Network of the Cardiac Outflow Tract. Circulation. 2023 11 21; 148(21):1705-1722.
    View in: PubMed
    Score: 0.022
  20. Frem1 activity is regulated by Sonic hedgehog signaling in the cranial neural crest mesenchyme during midfacial morphogenesis. Dev Dyn. 2023 04; 252(4):483-494.
    View in: PubMed
    Score: 0.021
  21. Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Circulation. 2023 03 07; 147(10):824-840.
    View in: PubMed
    Score: 0.021
  22. Detecting critical transition signals from single-cell transcriptomes to infer lineage-determining transcription factors. Nucleic Acids Res. 2022 09 09; 50(16):e91.
    View in: PubMed
    Score: 0.020
  23. Identification of direct transcriptional targets of NFATC2 that promote ß cell proliferation. J Clin Invest. 2021 11 01; 131(21).
    View in: PubMed
    Score: 0.019
  24. Tbx5 drives Aldh1a2 expression to regulate a RA-Hedgehog-Wnt gene regulatory network coordinating cardiopulmonary development. Elife. 2021 10 13; 10.
    View in: PubMed
    Score: 0.019
  25. Chamber-specific transcriptional responses in atrial fibrillation. JCI Insight. 2020 09 17; 5(18).
    View in: PubMed
    Score: 0.018
  26. ZO-1 Regulates Intercalated Disc Composition and Atrioventricular Node Conduction. Circ Res. 2020 07 03; 127(2):e28-e43.
    View in: PubMed
    Score: 0.017
  27. Gata4 regulates hedgehog signaling and Gata6 expression for outflow tract development. PLoS Genet. 2019 05; 15(5):e1007711.
    View in: PubMed
    Score: 0.016
  28. A calcium transport mechanism for atrial fibrillation in Tbx5-mutant mice. Elife. 2019 03 21; 8.
    View in: PubMed
    Score: 0.016
  29. Gata4 potentiates second heart field proliferation and Hedgehog signaling for cardiac septation. Proc Natl Acad Sci U S A. 2017 02 21; 114(8):E1422-E1431.
    View in: PubMed
    Score: 0.014
  30. De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS Genet. 2016 Apr; 12(4):e1005963.
    View in: PubMed
    Score: 0.013
  31. The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model. BMC Dev Biol. 2015 Jul 25; 15:30.
    View in: PubMed
    Score: 0.013
  32. Maternal and zygotic Zfp57 modulate NOTCH signaling in cardiac development. Proc Natl Acad Sci U S A. 2015 Apr 21; 112(16):E2020-9.
    View in: PubMed
    Score: 0.012
  33. MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus. Hum Mol Genet. 2015 Apr 15; 24(8):2375-89.
    View in: PubMed
    Score: 0.012
  34. Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Hum Mol Genet. 2012 Jul 15; 21(14):3255-63.
    View in: PubMed
    Score: 0.010
  35. Enhanced desumoylation in murine hearts by overexpressed SENP2 leads to congenital heart defects and cardiac dysfunction. J Mol Cell Cardiol. 2012 Mar; 52(3):638-49.
    View in: PubMed
    Score: 0.010
  36. Expression of sumoylation deficient Nkx2.5 mutant in Nkx2.5 haploinsufficient mice leads to congenital heart defects. PLoS One. 2011; 6(6):e20803.
    View in: PubMed
    Score: 0.009
  37. Defective sumoylation pathway directs congenital heart disease. Birth Defects Res A Clin Mol Teratol. 2011 Jun; 91(6):468-76.
    View in: PubMed
    Score: 0.009
  38. Complex interactions between genes controlling trafficking in primary cilia. Nat Genet. 2011 Jun; 43(6):547-53.
    View in: PubMed
    Score: 0.009
  39. DNMT3B7, a truncated DNMT3B isoform expressed in human tumors, disrupts embryonic development and accelerates lymphomagenesis. Cancer Res. 2010 Jul 15; 70(14):5840-50.
    View in: PubMed
    Score: 0.009
  40. Genome-wide identification of mouse congenital heart disease loci. Hum Mol Genet. 2010 Aug 15; 19(16):3105-13.
    View in: PubMed
    Score: 0.009
  41. A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines. BMC Genet. 2009 Mar 06; 10:12.
    View in: PubMed
    Score: 0.008
  42. E2F3 plays an essential role in cardiac development and function. Cell Cycle. 2008 Dec; 7(23):3775-80.
    View in: PubMed
    Score: 0.008
  43. The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy. PLoS One. 2008 Jul 09; 3(7):e2642.
    View in: PubMed
    Score: 0.008
  44. Characterization of sinoatrial node in four conduction system marker mice. J Mol Cell Cardiol. 2007 May; 42(5):946-53.
    View in: PubMed
    Score: 0.007
  45. Complex genomic rearrangement in CCS-LacZ transgenic mice. Genesis. 2007 Feb; 45(2):76-82.
    View in: PubMed
    Score: 0.007
  46. Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis. Proc Natl Acad Sci U S A. 2006 Dec 26; 103(52):19836-41.
    View in: PubMed
    Score: 0.007
  47. Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia. Proc Natl Acad Sci U S A. 2005 Dec 13; 102(50):18123-8.
    View in: PubMed
    Score: 0.006
  48. Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice. Genesis. 2003 Nov; 37(3):144-50.
    View in: PubMed
    Score: 0.006
  49. Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome. J Am Coll Cardiol. 2003 Sep 03; 42(5):942-51.
    View in: PubMed
    Score: 0.005
  50. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy. Circulation. 2003 Jun 10; 107(22):2850-6.
    View in: PubMed
    Score: 0.005
  51. Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C gene. Circulation. 2001 Nov 27; 104(22):2734-9.
    View in: PubMed
    Score: 0.005
  52. Comparison of two murine models of familial hypertrophic cardiomyopathy. Circ Res. 2001 Mar 02; 88(4):383-9.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.