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Connection

Ursula Storb to Point Mutation

This is a "connection" page, showing publications Ursula Storb has written about Point Mutation.
Connection Strength

0.560
  1. Scarcity of lambda 1 B cells in mice with a single point mutation in C lambda 1 is due to a low BCR signal caused by misfolded lambda 1 light chain. Mol Immunol. 2007 Feb; 44(6):1417-28.
    View in: PubMed
    Score: 0.267
  2. B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. J Exp Med. 1997 Aug 04; 186(3):413-9.
    View in: PubMed
    Score: 0.143
  3. A point mutation in the constant region of Ig lambda1 prevents normal B cell development due to defective BCR signaling. Immunity. 2002 Feb; 16(2):245-55.
    View in: PubMed
    Score: 0.049
  4. Mutation of BCL-6 gene in normal B cells by the process of somatic hypermutation of Ig genes. Science. 1998 Jun 12; 280(5370):1750-2.
    View in: PubMed
    Score: 0.038
  5. The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes. Mol Immunol. 1997 May; 34(7):527-33.
    View in: PubMed
    Score: 0.035
  6. Crossing the SJL lambda locus into kappa-knockout mice reveals a dysfunction of the lambda 1-containing immunoglobulin receptor in B cell differentiation. EMBO J. 1994 Feb 15; 13(4):827-34.
    View in: PubMed
    Score: 0.028
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.