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Connection

Frederic Depreux to Animals

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

0.148
  1. Antisense oligonucleotides delivered to the amniotic cavity in utero modulate gene expression in the postnatal mouse. Nucleic Acids Res. 2016 Nov 16; 44(20):9519-9529.
    View in: PubMed
    Score: 0.032
  2. Molecular cloning and characterization of porcine calcineurin-alpha subunit expression in skeletal muscle. J Anim Sci. 2010 Feb; 88(2):562-71.
    View in: PubMed
    Score: 0.020
  3. Eya4-deficient mice are a model for heritable otitis media. J Clin Invest. 2008 Feb; 118(2):651-8.
    View in: PubMed
    Score: 0.017
  4. Paylean alters myosin heavy chain isoform content in pig muscle. J Anim Sci. 2002 Jul; 80(7):1888-94.
    View in: PubMed
    Score: 0.012
  5. Antisense oligonucleotide therapy rescues disruptions in organization of exploratory movements associated with Usher syndrome type 1C in mice. Behav Brain Res. 2018 02 15; 338:76-87.
    View in: PubMed
    Score: 0.009
  6. Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment. J Assoc Res Otolaryngol. 2018 02; 19(1):1-16.
    View in: PubMed
    Score: 0.009
  7. Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide. Hum Mol Genet. 2017 09 15; 26(18):3482-3494.
    View in: PubMed
    Score: 0.008
  8. Lunatic fringe-mediated Notch signaling regulates adult hippocampal neural stem cell maintenance. Elife. 2017 07 12; 6.
    View in: PubMed
    Score: 0.008
  9. Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates. Elife. 2016 12 14; 5.
    View in: PubMed
    Score: 0.008
  10. Gene expression, chromosome position and lamin A/C mutations. Nucleus. 2011 May-Jun; 2(3):162-7.
    View in: PubMed
    Score: 0.005
  11. Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods. Proc Natl Acad Sci U S A. 2009 Dec 22; 106(51):21813-8.
    View in: PubMed
    Score: 0.005
  12. Nesprin-1 mutations in human and murine cardiomyopathy. J Mol Cell Cardiol. 2010 Apr; 48(4):600-8.
    View in: PubMed
    Score: 0.005
  13. An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line. Proc Natl Acad Sci U S A. 2007 Nov 20; 104(47):18537-42.
    View in: PubMed
    Score: 0.004
  14. Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss. Nat Genet. 2005 Apr; 37(4):418-22.
    View in: PubMed
    Score: 0.004
  15. Myostatin expression in porcine tissues: tissue specificity and developmental and postnatal regulation. Am J Physiol. 1998 10; 275(4):R1265-73.
    View in: PubMed
    Score: 0.002
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.