Connection

JOHN BELMONT to Transcription Factors

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

0.859
  1. Characterization of the interactions of human ZIC3 mutants with GLI3. Hum Mutat. 2008 Jan; 29(1):99-105.
    View in: PubMed
    Score: 0.111
  2. 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: 0.106
  3. 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: 0.103
  4. 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: 0.099
  5. Zic3 is critical for early embryonic patterning during gastrulation. Dev Dyn. 2006 Mar; 235(3):776-85.
    View in: PubMed
    Score: 0.097
  6. 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: 0.084
  7. 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: 0.039
  8. Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2. Am J Med Genet A. 2011 Jul; 155A(7):1574-80.
    View in: PubMed
    Score: 0.035
  9. Molecular genetics of heterotaxy syndromes. Curr Opin Cardiol. 2004 May; 19(3):216-20.
    View in: PubMed
    Score: 0.021
  10. Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy. Circulation. 2003 Nov 25; 108(21):2672-8.
    View in: PubMed
    Score: 0.021
  11. Exclusion of PITX2 mutations as a major cause of CHARGE association. Am J Med Genet. 2002 Jul 22; 111(1):27-30.
    View in: PubMed
    Score: 0.019
  12. 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: 0.019
  13. Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. Am J Med Genet A. 2020 06; 182(6):1387-1399.
    View in: PubMed
    Score: 0.016
  14. Molecular determinants of left and right outflow tract obstruction. Am J Med Genet. 2000; 97(4):297-303.
    View in: PubMed
    Score: 0.016
  15. 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: 0.015
  16. 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: 0.013
  17. Lessons learned from additional research analyses of unsolved clinical exome cases. Genome Med. 2017 03 21; 9(1):26.
    View in: PubMed
    Score: 0.013
  18. 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: 0.012
  19. 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: 0.011
  20. 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: 0.009
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.