Connection

WILLIAM CRAIGEN to Molecular Sequence Data

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

0.451
  1. Genetic demonstration that the plasma membrane maxianion channel and voltage-dependent anion channels are unrelated proteins. J Biol Chem. 2006 Jan 27; 281(4):1897-904.
    View in: PubMed
    Score: 0.042
  2. Mitochondrial voltage-dependent anion channel gene family in Drosophila melanogaster: complex patterns of evolution, genomic organization, and developmental expression. Mol Genet Metab. 2005 Aug; 85(4):308-17.
    View in: PubMed
    Score: 0.041
  3. The tissue-specific, alternatively spliced single ATG exon of the type 3 voltage-dependent anion channel gene does not create a truncated protein isoform in vivo. Mol Genet Metab. 2000 May; 70(1):69-74.
    View in: PubMed
    Score: 0.029
  4. Revised fine mapping of the human voltage-dependent anion channel loci by radiation hybrid analysis. Mamm Genome. 1999 Oct; 10(10):1041-2.
    View in: PubMed
    Score: 0.027
  5. Retrotransposition of glycerol kinase-related genes from the X chromosome to autosomes: functional and evolutionary aspects. Genomics. 1999 Aug 01; 59(3):282-90.
    View in: PubMed
    Score: 0.027
  6. A novel isoform of the mitochondrial outer membrane protein VDAC3 via alternative splicing of a 3-base exon. Functional characteristics and subcellular localization. J Biol Chem. 1998 Nov 13; 273(46):30482-6.
    View in: PubMed
    Score: 0.026
  7. The murine voltage-dependent anion channel gene family. Conserved structure and function. J Biol Chem. 1997 Jul 25; 272(30):18966-73.
    View in: PubMed
    Score: 0.024
  8. Isolation, mapping, and functional expression of the mouse X chromosome glycerol kinase gene. Genomics. 1996 Sep 15; 36(3):530-4.
    View in: PubMed
    Score: 0.022
  9. A novel mouse mitochondrial voltage-dependent anion channel gene localizes to chromosome 8. Genomics. 1996 Aug 15; 36(1):192-6.
    View in: PubMed
    Score: 0.022
  10. Isolation, characterization, and mapping of two mouse mitochondrial voltage-dependent anion channel isoforms. Genomics. 1996 Apr 15; 33(2):283-8.
    View in: PubMed
    Score: 0.022
  11. Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):579-83.
    View in: PubMed
    Score: 0.019
  12. Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications. Eur J Hum Genet. 2015 Jul; 23(7):915-21.
    View in: PubMed
    Score: 0.019
  13. Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. Am J Hum Genet. 2013 Sep 05; 93(3):471-81.
    View in: PubMed
    Score: 0.018
  14. Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder. Neurogenetics. 2009 Oct; 10(4):363-9.
    View in: PubMed
    Score: 0.013
  15. 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: 0.013
  16. The function, structure and regulation of E. coli peptide chain release factors. Biochimie. 1987 Oct; 69(10):1031-41.
    View in: PubMed
    Score: 0.012
  17. 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: 0.011
  18. The physiological properties of a novel family of VDAC-like proteins from Drosophila melanogaster. Biophys J. 2004 Jan; 86(1 Pt 1):152-62.
    View in: PubMed
    Score: 0.009
  19. Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia. Proc Natl Acad Sci U S A. 2002 Aug 06; 99(16):10282-6.
    View in: PubMed
    Score: 0.008
  20. Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet. 2000 Jul 01; 9(11):1587-95.
    View in: PubMed
    Score: 0.007
  21. Cloning and characterization of a putative human d-2-hydroxyacid dehydrogenase in chromosome 9q. Biochem Biophys Res Commun. 2000 Feb 16; 268(2):298-301.
    View in: PubMed
    Score: 0.007
  22. Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII. Hum Genet. 2000 Jan; 106(1):19-28.
    View in: PubMed
    Score: 0.007
  23. Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles. Hum Mutat. 1998; 11(4):286-94.
    View in: PubMed
    Score: 0.006
  24. Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiency. Hum Mol Genet. 1996 Dec; 5(12):1925-30.
    View in: PubMed
    Score: 0.006
  25. Ahch, the mouse homologue of DAX1: cloning, characterization and synteny with GyK, the glycerol kinase locus. Gene. 1996 Oct 31; 178(1-2):31-4.
    View in: PubMed
    Score: 0.006
  26. Cloning and expression of a mammalian peptide chain release factor with sequence similarity to tryptophanyl-tRNA synthetases. Proc Natl Acad Sci U S A. 1990 May; 87(9):3508-12.
    View in: PubMed
    Score: 0.004
  27. Rapid and precise mapping of the Escherichia coli release factor genes by two physical approaches. J Bacteriol. 1988 Oct; 170(10):4537-41.
    View in: PubMed
    Score: 0.003
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