Connection

RALF KRAHE to Gene Expression

This is a "connection" page, showing publications RALF KRAHE has written about Gene Expression.
Connection Strength

0.131
  1. Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. Neuromuscul Disord. 2014 Mar; 24(3):227-40.
    View in: PubMed
    Score: 0.065
  2. Expression and fine mapping of murine vasoactive intestinal peptide receptor 1. J Mol Neurosci. 2001 Dec; 17(3):311-24.
    View in: PubMed
    Score: 0.028
  3. Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders. Muscle Nerve. 2010 Dec; 42(6):856-63.
    View in: PubMed
    Score: 0.013
  4. Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands. Neuromuscul Disord. 2003 Sep; 13(7-8):589-96.
    View in: PubMed
    Score: 0.008
  5. Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 2000 Jul 15; 96(2):405-9.
    View in: PubMed
    Score: 0.006
  6. The gamma-tubulin gene family in humans. Genomics. 2000 Jul 15; 67(2):164-70.
    View in: PubMed
    Score: 0.006
  7. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat. Hum Mol Genet. 1995 Oct; 4(10):1919-25.
    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.