Connection

JOHN BELMONT to Animals

This is a "connection" page, showing publications JOHN BELMONT has written about Animals.
Connection Strength

0.543
  1. Genetic architecture of laterality defects revealed by whole exome sequencing. Eur J Hum Genet. 2019 04; 27(4):563-573.
    View in: PubMed
    Score: 0.036
  2. Genetic basis of congenital cardiovascular malformations. Eur J Med Genet. 2014 Aug; 57(8):402-13.
    View in: PubMed
    Score: 0.026
  3. Strategic approaches to unraveling genetic causes of cardiovascular diseases. Circ Res. 2011 May 13; 108(10):1252-69.
    View in: PubMed
    Score: 0.021
  4. Identification of a novel role of ZIC3 in regulating cardiac development. Hum Mol Genet. 2007 Jul 15; 16(14):1649-60.
    View in: PubMed
    Score: 0.016
  5. Craniofacial, skeletal, and cardiac defects associated with altered embryonic murine Zic3 expression following targeted insertion of a PGK-NEO cassette. Front Biosci. 2007 Jan 01; 12:1680-90.
    View in: PubMed
    Score: 0.016
  6. Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway. Dev Dyn. 2006 Jun; 235(6):1631-7.
    View in: PubMed
    Score: 0.015
  7. Zic3 is critical for early embryonic patterning during gastrulation. Dev Dyn. 2006 Mar; 235(3):776-85.
    View in: PubMed
    Score: 0.015
  8. Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation. Am J Hum Genet. 2006 Feb; 78(2):303-14.
    View in: PubMed
    Score: 0.015
  9. Molecular genetics of heterotaxy syndromes. Curr Opin Cardiol. 2004 May; 19(3):216-20.
    View in: PubMed
    Score: 0.013
  10. Genome-wide linkage disequilibrium and haplotype maps. Am J Pharmacogenomics. 2004; 4(4):253-62.
    View in: PubMed
    Score: 0.013
  11. Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects. Am J Hum Genet. 2004 Jan; 74(1):93-105.
    View in: PubMed
    Score: 0.013
  12. The dual specificity JKAP specifically activates the c-Jun N-terminal kinase pathway. J Biol Chem. 2002 Sep 27; 277(39):36592-601.
    View in: PubMed
    Score: 0.012
  13. Cell cycle-dependent expression and nucleolar localization of hCAP-H. Mol Biol Cell. 2001 Nov; 12(11):3527-37.
    View in: PubMed
    Score: 0.011
  14. Long-distance DD-PCR and cDNA microarrays. Curr Opin Microbiol. 2000 Jun; 3(3):316-21.
    View in: PubMed
    Score: 0.010
  15. Molecular determinants of left and right outflow tract obstruction. Am J Med Genet. 2000; 97(4):297-303.
    View in: PubMed
    Score: 0.010
  16. The molecular basis of vascular disorders. Am J Hum Genet. 1999 Mar; 64(3):678-84.
    View in: PubMed
    Score: 0.009
  17. Gene trap screening using negative selection: identification of two tandem, differentially expressed loci with potential hematopoietic function. Dev Genet. 1999; 25(1):49-63.
    View in: PubMed
    Score: 0.009
  18. Genomic stability and the mechanisms of chromatid separation in mammalian cells. Mol Genet Metab. 1998 Oct; 65(2):105-12.
    View in: PubMed
    Score: 0.009
  19. Recent progress in the molecular genetics of congenital heart defects. Clin Genet. 1998 Jul; 54(1):11-9.
    View in: PubMed
    Score: 0.009
  20. Identification and cloning of differentially expressed genes by long-distance differential display. Anal Biochem. 1998 Jun 01; 259(2):235-44.
    View in: PubMed
    Score: 0.009
  21. Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains. Genome Res. 1997 Apr; 7(4):315-29.
    View in: PubMed
    Score: 0.008
  22. Differential mRNA display using anchored oligo-dT and long sequence-specific primers as arbitrary primers. Trends Genet. 1996 Dec; 12(12):502-4.
    View in: PubMed
    Score: 0.008
  23. Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans. Am J Hum Genet. 2016 Oct 06; 99(4):886-893.
    View in: PubMed
    Score: 0.008
  24. Multi-omic profiles of hepatic metabolism in TPN-fed preterm pigs administered new generation lipid emulsions. J Lipid Res. 2016 09; 57(9):1696-711.
    View in: PubMed
    Score: 0.008
  25. Genetic control of X inactivation and processes leading to X-inactivation skewing. Am J Hum Genet. 1996 Jun; 58(6):1101-8.
    View in: PubMed
    Score: 0.008
  26. Insights into lymphocyte development from X-linked immune deficiencies. Trends Genet. 1995 Mar; 11(3):112-6.
    View in: PubMed
    Score: 0.007
  27. The receptor tyrosine kinase-related gene (ryk) demonstrates lineage and stage-specific expression in hematopoietic cells. J Immunol. 1995 Feb 01; 154(3):1157-66.
    View in: PubMed
    Score: 0.007
  28. Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice. PLoS One. 2014; 9(4):e94390.
    View in: PubMed
    Score: 0.007
  29. The phosphatase JKAP/DUSP22 inhibits T-cell receptor signalling and autoimmunity by inactivating Lck. Nat Commun. 2014 Apr 09; 5:3618.
    View in: PubMed
    Score: 0.007
  30. Thymic nurse cells are sites of thymocyte apoptosis. J Immunol. 1994 Mar 15; 152(6):2645-51.
    View in: PubMed
    Score: 0.006
  31. The biology of the human ligand for CD40. J Clin Immunol. 1993 Nov; 13(6):373-80.
    View in: PubMed
    Score: 0.006
  32. Enrichment and functional characterization of Sca-1+WGA+, Lin-WGA+, Lin-Sca-1+, and Lin-Sca-1+WGA+ bone marrow cells from mice with an Ly-6a haplotype. Blood. 1993 Nov 01; 82(9):2673-83.
    View in: PubMed
    Score: 0.006
  33. MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development. Hum Mol Genet. 2013 Nov 01; 22(21):4339-48.
    View in: PubMed
    Score: 0.006
  34. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet. 1992 Dec; 51(6):1229-39.
    View in: PubMed
    Score: 0.006
  35. Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left-right patterning and heart development. Hum Mol Genet. 2013 Mar 01; 22(5):879-89.
    View in: PubMed
    Score: 0.006
  36. NPHP4 variants are associated with pleiotropic heart malformations. Circ Res. 2012 Jun 08; 110(12):1564-74.
    View in: PubMed
    Score: 0.006
  37. Leukemia inhibitory factor improves survival of retroviral vector-infected hematopoietic stem cells in vitro, allowing efficient long-term expression of vector-encoded human adenosine deaminase in vivo. J Exp Med. 1991 Oct 01; 174(4):837-45.
    View in: PubMed
    Score: 0.005
  38. Stimulation of retroviral vector infection of murine hematopoietic progenitors. Int J Cell Cloning. 1991 Sep; 9(5):491-502.
    View in: PubMed
    Score: 0.005
  39. RNA secondary structure analysis of the packaging signal for Moloney murine leukemia virus. Virology. 1991 Aug; 183(2):611-9.
    View in: PubMed
    Score: 0.005
  40. V gamma 3 T cell receptor rearrangement and expression in the adult thymus. J Immunol. 1991 Feb 15; 146(4):1348-52.
    View in: PubMed
    Score: 0.005
  41. Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning. Proc Natl Acad Sci U S A. 2011 Feb 15; 108(7):2915-20.
    View in: PubMed
    Score: 0.005
  42. Evaluation of lymphoid-specific enhancer addition or substitution in a basic retrovirus vector. Hum Gene Ther. 1991; 2(4):307-15.
    View in: PubMed
    Score: 0.005
  43. Effects of leukemia inhibitory factor (LIF) on gene transfer efficiency into murine hematolymphoid progenitors. Adv Exp Med Biol. 1991; 292:131-8.
    View in: PubMed
    Score: 0.005
  44. CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet. 2011 Jan; 43(1):72-8.
    View in: PubMed
    Score: 0.005
  45. Murine leukemia inhibitory factor enhances retroviral-vector infection efficiency of hematopoietic progenitors. Blood. 1990 Sep 15; 76(6):1098-103.
    View in: PubMed
    Score: 0.005
  46. Human adenosine deaminase expression in mice. Blood. 1990 May 15; 75(10):2085-92.
    View in: PubMed
    Score: 0.005
  47. Stable RNA secondary structure in a retroviral vector insert terminates reverse transcriptase elongation in vitro but not in cultured cells. Hum Gene Ther. 1990; 1(3):269-76.
    View in: PubMed
    Score: 0.005
  48. BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects. Eur J Hum Genet. 2009 Oct; 17(10):1325-35.
    View in: PubMed
    Score: 0.005
  49. Expression vectors for human adenosine deaminase gene therapy. Genome. 1989; 31(2):832-9.
    View in: PubMed
    Score: 0.005
  50. Expression of human adenosine deaminase in murine hematopoietic cells. Mol Cell Biol. 1988 Dec; 8(12):5116-25.
    View in: PubMed
    Score: 0.005
  51. 20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits. J Med Genet. 2009 Mar; 46(3):168-75.
    View in: PubMed
    Score: 0.004
  52. Lipocalin 2 is required for BCR-ABL-induced tumorigenesis. Oncogene. 2008 Oct 16; 27(47):6110-9.
    View in: PubMed
    Score: 0.004
  53. NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling. Hum Mol Genet. 2008 Sep 15; 17(18):2886-93.
    View in: PubMed
    Score: 0.004
  54. Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly. Am J Hum Genet. 2008 Jul; 83(1):18-29.
    View in: PubMed
    Score: 0.004
  55. Liposome-incorporated Grb2 antisense oligodeoxynucleotide increases the survival of mice bearing bcr-abl-positive leukemia xenografts. Int J Oncol. 2007 Nov; 31(5):1243-50.
    View in: PubMed
    Score: 0.004
  56. Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans. Am J Hum Genet. 2007 Nov; 81(5):987-94.
    View in: PubMed
    Score: 0.004
  57. Sesn1 is a novel gene for left-right asymmetry and mediating nodal signaling. Hum Mol Genet. 2006 Nov 15; 15(22):3369-77.
    View in: PubMed
    Score: 0.004
  58. Expression of human adenosine deaminase in murine haematopoietic progenitor cells following retroviral transfer. Nature. 1986 Jul 24-30; 322(6077):385-7.
    View in: PubMed
    Score: 0.004
  59. Towards gene therapy for adenosine deaminase deficiency. Ann Clin Res. 1986; 18(5-6):322-6.
    View in: PubMed
    Score: 0.004
  60. Bcr-Abl-mediated suppression of normal hematopoiesis in leukemia. Oncogene. 2005 May 05; 24(20):3246-56.
    View in: PubMed
    Score: 0.004
  61. Correlation between CXCR4 and homing or engraftment of acute myelogenous leukemia. Cancer Res. 2004 Sep 15; 64(18):6832 author reply 6832-3.
    View in: PubMed
    Score: 0.003
  62. Engraftment of acute myeloid leukemia in NOD/SCID mice is independent of CXCR4 and predicts poor patient survival. Stem Cells. 2004; 22(2):188-201.
    View in: PubMed
    Score: 0.003
  63. A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice. Development. 2002 May; 129(9):2293-302.
    View in: PubMed
    Score: 0.003
  64. Divalent cations and cytochalasin B-sensitive processes in activation, synthesis, and release of mixed leukocyte reaction suppressor factor. Cell Immunol. 1981 Jul 01; 61(2):353-64.
    View in: PubMed
    Score: 0.003
  65. BCR gene expression blocks Bcr-Abl induced pathogenicity in a mouse model. Oncogene. 2001 Apr 05; 20(15):1873-81.
    View in: PubMed
    Score: 0.003
  66. Physiology of mixed leukocyte reaction suppressor factor. I. Role of cytoskeleton and protein synthesis in production and secretion. J Immunol. 1979 Mar; 122(3):1022-8.
    View in: PubMed
    Score: 0.002
  67. Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development. Am J Hum Genet. 1999 Mar; 64(3):712-21.
    View in: PubMed
    Score: 0.002
  68. Comparative sequence analysis of a gene-rich cluster at human chromosome 12p13 and its syntenic region in mouse chromosome 6. Genome Res. 1998 Jan; 8(1):29-40.
    View in: PubMed
    Score: 0.002
  69. In vivo marking of spontaneous or vaccine-induced fibrosarcomas in the domestic house cat, using an adenoviral vector containing a bifunctional fusion protein, GAL-TEK. Hum Gene Ther. 1995 Sep; 6(9):1215-23.
    View in: PubMed
    Score: 0.002
  70. Disruption of the adenosine deaminase gene causes hepatocellular impairment and perinatal lethality in mice. Proc Natl Acad Sci U S A. 1995 Apr 25; 92(9):3673-7.
    View in: PubMed
    Score: 0.002
  71. Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12. Genomics. 1995 Jan 01; 25(1):334-5.
    View in: PubMed
    Score: 0.002
  72. Delivery of a secretable adenosine deaminase through microcapsules--a novel approach to somatic gene therapy. Hum Gene Ther. 1994 Dec; 5(12):1445-55.
    View in: PubMed
    Score: 0.002
  73. A new family of murine retroviral vectors with extended multiple cloning sites for gene insertion. Hum Gene Ther. 1994 Mar; 5(3):307-12.
    View in: PubMed
    Score: 0.002
  74. Expression of human CD18 in murine granulocytes and improved efficiency for infection of deficient human lymphoblasts. Hum Gene Ther. 1993 Feb; 4(1):25-34.
    View in: PubMed
    Score: 0.002
  75. Characterization of recombinant helper retroviruses from Moloney-based vectors in ecotropic and amphotropic packaging cell lines. Virology. 1991 Feb; 180(2):849-52.
    View in: PubMed
    Score: 0.001
  76. Gene therapy: a new approach for the treatment of genetic disorders. Clin Pharmacol Ther. 1990 Jan; 47(1):1-11.
    View in: PubMed
    Score: 0.001
  77. Human gene expression in murine hemopoietic cells in vivo. Adv Exp Med Biol. 1988; 241:123-7.
    View in: PubMed
    Score: 0.001
  78. Gene replacement therapy for inborn errors of purine metabolism. Cold Spring Harb Symp Quant Biol. 1986; 51 Pt 2:1065-71.
    View in: PubMed
    Score: 0.001
Connection Strength

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