Connection

STEVEN SCHERER to Connexins

This is a "connection" page, showing publications STEVEN SCHERER has written about Connexins.
Connection Strength

1.683
  1. Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct. J Neurosci Res. 2008 Apr; 86(5):992-1006.
    View in: PubMed
    Score: 0.286
  2. The effects of a dominant connexin32 mutant in myelinating Schwann cells. Mol Cell Neurosci. 2006 Jul; 32(3):283-98.
    View in: PubMed
    Score: 0.253
  3. Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells. J Neurosci. 2005 Aug 03; 25(31):7111-20.
    View in: PubMed
    Score: 0.238
  4. Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice. J Neurosci. 2005 Feb 09; 25(6):1550-9.
    View in: PubMed
    Score: 0.230
  5. Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations. Sci Rep. 2017 01 10; 7:40166.
    View in: PubMed
    Score: 0.131
  6. A new mutation in GJC2 associated with subclinical leukodystrophy. J Neurol. 2014 Oct; 261(10):1929-38.
    View in: PubMed
    Score: 0.111
  7. Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1). Hum Mol Genet. 2013 Nov 01; 22(21):4329-38.
    View in: PubMed
    Score: 0.103
  8. Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain. 2009 Feb; 132(Pt 2):426-38.
    View in: PubMed
    Score: 0.075
  9. Pannexin1 is expressed by neurons and glia but does not form functional gap junctions. Glia. 2007 Jan 01; 55(1):46-56.
    View in: PubMed
    Score: 0.066
  10. Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants. Brain. 2023 10 03; 146(10):4336-4349.
    View in: PubMed
    Score: 0.052
  11. Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system. Exp Neurol. 2023 02; 360:114277.
    View in: PubMed
    Score: 0.049
  12. Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1). Neurology. 2017 Aug 29; 89(9):927-935.
    View in: PubMed
    Score: 0.034
  13. CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. J Neurol Neurosurg Psychiatry. 2015 Aug; 86(8):873-8.
    View in: PubMed
    Score: 0.028
  14. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science. 1993 Dec 24; 262(5142):2039-42.
    View in: PubMed
    Score: 0.027
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.