Connection

DAVID NELSON to Amino Acid Sequence

This is a "connection" page, showing publications DAVID NELSON has written about Amino Acid Sequence.
Connection Strength

0.508
  1. HlyU is a positive regulator of hemolysin expression in Vibrio anguillarum. J Bacteriol. 2011 Sep; 193(18):4779-89.
    View in: PubMed
    Score: 0.068
  2. FMR2 function: insight from a mouse knockout model. Cytogenet Genome Res. 2003; 100(1-4):129-39.
    View in: PubMed
    Score: 0.038
  3. The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism. Genomics. 2002 Aug; 80(2):185-94.
    View in: PubMed
    Score: 0.037
  4. Alternative splicing in the murine and human FXR1 genes. Genomics. 1999 Jul 15; 59(2):193-202.
    View in: PubMed
    Score: 0.030
  5. Cytochrome P450 Monooxygenase CYP139 Family Involved in the Synthesis of Secondary Metabolites in 824 Mycobacterial Species. Int J Mol Sci. 2019 May 31; 20(11).
    View in: PubMed
    Score: 0.029
  6. Blooming of Unusual Cytochrome P450s by Tandem Duplication in the Pathogenic Fungus Conidiobolus coronatus. Int J Mol Sci. 2018 06 09; 19(6).
    View in: PubMed
    Score: 0.027
  7. Comparative analyses and structural insights of the novel cytochrome P450 fusion protein family CYP5619 in Oomycetes. Sci Rep. 2018 04 26; 8(1):6597.
    View in: PubMed
    Score: 0.027
  8. CYP79 P450 monooxygenases in gymnosperms: CYP79A118 is associated with the formation of taxiphyllin in Taxus baccata. Plant Mol Biol. 2017 Sep; 95(1-2):169-180.
    View in: PubMed
    Score: 0.026
  9. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. Nat Genet. 1996 May; 13(1):109-13.
    View in: PubMed
    Score: 0.024
  10. A muscle-specific DNase I-like gene in human Xq28. Hum Mol Genet. 1995 Sep; 4(9):1557-64.
    View in: PubMed
    Score: 0.023
  11. Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome. Nat Genet. 1995 Aug; 10(4):483-5.
    View in: PubMed
    Score: 0.023
  12. Diversity and evolution of cytochrome P450 monooxygenases in Oomycetes. Sci Rep. 2015 Jul 01; 5:11572.
    View in: PubMed
    Score: 0.022
  13. Alternative splicing in the fragile X gene FMR1. Hum Mol Genet. 1993 Aug; 2(8):1348.
    View in: PubMed
    Score: 0.020
  14. Alternative splicing in the fragile X gene FMR1. Hum Mol Genet. 1993 Apr; 2(4):399-404.
    View in: PubMed
    Score: 0.019
  15. Site-specific phosphorylation of the middle molecular weight human neurofilament protein in transfected non-neuronal cells. J Neurosci. 1990 Jul; 10(7):2428-37.
    View in: PubMed
    Score: 0.016
  16. The human mid-size neurofilament subunit: a repeated protein sequence and the relationship of its gene to the intermediate filament gene family. EMBO J. 1987 Jun; 6(6):1617-26.
    View in: PubMed
    Score: 0.013
  17. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain. Neuron. 2002 Jun 13; 34(6):961-72.
    View in: PubMed
    Score: 0.009
  18. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 1991 May 31; 65(5):905-14.
    View in: PubMed
    Score: 0.008
  19. Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma). Am J Hum Genet. 2001 Mar; 68(3):765-71.
    View in: PubMed
    Score: 0.008
  20. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins. Hum Mol Genet. 2000 Jun 12; 9(10):1487-93.
    View in: PubMed
    Score: 0.008
  21. A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence. Proc Natl Acad Sci U S A. 1998 Sep 29; 95(20):11751-6.
    View in: PubMed
    Score: 0.007
  22. X-linked situs abnormalities result from mutations in ZIC3. Nat Genet. 1997 Nov; 17(3):305-8.
    View in: PubMed
    Score: 0.007
  23. Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Hum Mol Genet. 1997 Jul; 6(7):991-1002.
    View in: PubMed
    Score: 0.006
  24. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat. Nat Genet. 1993 Jul; 4(3):244-51.
    View in: PubMed
    Score: 0.005
  25. Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiae. Nucleic Acids Res. 1992 Sep 11; 20(17):4649-55.
    View in: PubMed
    Score: 0.005
  26. The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase. Nature. 1992 Jul 16; 358(6383):239-42.
    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.