Connection

JOHN BELMONT to Molecular Sequence Data

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

0.921
  1. Atypical presentation of moyamoya disease in an infant with a de novo RNF213 variant. Am J Med Genet A. 2015 Nov; 167A(11):2742-7.
    View in: PubMed
    Score: 0.086
  2. 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: 0.044
  3. 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: 0.038
  4. 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: 0.035
  5. Cell cycle-dependent expression and nucleolar localization of hCAP-H. Mol Biol Cell. 2001 Nov; 12(11):3527-37.
    View in: PubMed
    Score: 0.033
  6. 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: 0.027
  7. 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: 0.024
  8. 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: 0.024
  9. Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy. Am J Hum Genet. 2016 Mar 03; 98(3):562-570.
    View in: PubMed
    Score: 0.022
  10. Inhibition of HIV-1 by a double transdominant fusion gene. Gene Ther. 1995 May; 2(3):181-6.
    View in: PubMed
    Score: 0.021
  11. Insights into lymphocyte development from X-linked immune deficiencies. Trends Genet. 1995 Mar; 11(3):112-6.
    View in: PubMed
    Score: 0.021
  12. 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: 0.021
  13. Thymic nurse cells are sites of thymocyte apoptosis. J Immunol. 1994 Mar 15; 152(6):2645-51.
    View in: PubMed
    Score: 0.020
  14. A sensitive reporter cell line for HIV-1 tat activity, HIV-1 inhibitors, and T cell activation effects. AIDS Res Hum Retroviruses. 1994 Mar; 10(3):295-301.
    View in: PubMed
    Score: 0.020
  15. Application of carrier testing to genetic counseling for X-linked agammaglobulinemia. Am J Hum Genet. 1994 Jan; 54(1):25-35.
    View in: PubMed
    Score: 0.019
  16. The biology of the human ligand for CD40. J Clin Immunol. 1993 Nov; 13(6):373-80.
    View in: PubMed
    Score: 0.019
  17. 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: 0.019
  18. Trinucleotide repeat polymorphism at DXS101. Hum Mol Genet. 1993 Sep; 2(9):1508.
    View in: PubMed
    Score: 0.019
  19. TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet. 2013 Aug 08; 93(2):197-210.
    View in: PubMed
    Score: 0.019
  20. Dinucleotide repeat polymorphism in the human CD40 ligand gene. Hum Mol Genet. 1993 Jun; 2(6):828.
    View in: PubMed
    Score: 0.019
  21. 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: 0.018
  22. Dinucleotide repeat polymorphism at the DXS178 locus. Hum Mol Genet. 1992 Jun; 1(3):216.
    View in: PubMed
    Score: 0.017
  23. NPHP4 variants are associated with pleiotropic heart malformations. Circ Res. 2012 Jun 08; 110(12):1564-74.
    View in: PubMed
    Score: 0.017
  24. Stromal support enhances cell-free retroviral vector transduction of human bone marrow long-term culture-initiating cells. Blood. 1992 Mar 15; 79(6):1393-9.
    View in: PubMed
    Score: 0.017
  25. SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing. Genome Biol. 2011 Sep 21; 12(9):R91.
    View in: PubMed
    Score: 0.016
  26. Stimulation of retroviral vector infection of murine hematopoietic progenitors. Int J Cell Cloning. 1991 Sep; 9(5):491-502.
    View in: PubMed
    Score: 0.016
  27. RNA secondary structure analysis of the packaging signal for Moloney murine leukemia virus. Virology. 1991 Aug; 183(2):611-9.
    View in: PubMed
    Score: 0.016
  28. Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications. Hum Mol Genet. 2011 May 15; 20(10):1975-88.
    View in: PubMed
    Score: 0.016
  29. 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: 0.016
  30. 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: 0.016
  31. Murine leukemia inhibitory factor enhances retroviral-vector infection efficiency of hematopoietic progenitors. Blood. 1990 Sep 15; 76(6):1098-103.
    View in: PubMed
    Score: 0.015
  32. Human adenosine deaminase expression in mice. Blood. 1990 May 15; 75(10):2085-92.
    View in: PubMed
    Score: 0.015
  33. 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: 0.015
  34. Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly. Mol Genet Metab. 2009 Sep-Oct; 98(1-2):225-34.
    View in: PubMed
    Score: 0.014
  35. Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations. Hum Mol Genet. 2009 Mar 01; 18(5):861-71.
    View in: PubMed
    Score: 0.014
  36. 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: 0.013
  37. 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: 0.013
  38. 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: 0.012
  39. Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. PLoS Genet. 2005 Sep; 1(3):e41.
    View in: PubMed
    Score: 0.011
  40. Disturbance of muscle fiber differentiation in congenital hypomyelinating neuropathy caused by a novel myelin protein zero mutation. Ann Neurol. 2003 Sep; 54(3):398-402.
    View in: PubMed
    Score: 0.009
  41. Supravalvular aortic stenosis: genetic and molecular dissection of a complex mutation in the elastin gene. Hum Genet. 2001 Nov; 109(5):512-20.
    View in: PubMed
    Score: 0.008
  42. 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: 0.007
  43. 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: 0.006
  44. DNA deletion confined to the iduronate-2-sulfatase promoter abolishes IDS gene expression. Hum Mutat. 1998; 11(2):121-6.
    View in: PubMed
    Score: 0.006
  45. A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome. J Clin Invest. 1996 Jan 01; 97(1):196-201.
    View in: PubMed
    Score: 0.006
  46. Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci. Mamm Genome. 1995 May; 6(5):334-8.
    View in: PubMed
    Score: 0.005
  47. 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: 0.005
  48. The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia. Immunogenetics. 1994; 40(5):319-24.
    View in: PubMed
    Score: 0.005
  49. 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: 0.005
  50. Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22. Genomics. 1993 Feb; 15(2):342-9.
    View in: PubMed
    Score: 0.005
  51. Use of cell-free retroviral vector preparations for transduction of cells from the marrow of chronic phase and blast crisis chronic myelogenous leukemia patients and from normal individuals. Hum Gene Ther. 1992 Apr; 3(2):137-45.
    View in: PubMed
    Score: 0.004
  52. Characterization of two missense mutations in human galactose-1-phosphate uridyltransferase: different molecular mechanisms for galactosemia. Genomics. 1992 Mar; 12(3):596-600.
    View in: PubMed
    Score: 0.004
  53. 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: 0.004
  54. Gene transfer of adenosine deaminase into primitive human hematopoietic progenitor cells. Hum Gene Ther. 1991; 2(3):203-13.
    View in: PubMed
    Score: 0.004
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.