Connection

STEVEN SCHERER to Mice

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

0.398
  1. A recessive Trim2 mutation causes an axonal neuropathy in mice. Neurobiol Dis. 2020 07; 140:104845.
    View in: PubMed
    Score: 0.048
  2. Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E. Exp Neurol. 2018 10; 308:13-25.
    View in: PubMed
    Score: 0.043
  3. A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes. Neuron Glia Biol. 2010 Nov; 6(4):213-23.
    View in: PubMed
    Score: 0.026
  4. A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy. Ann Neurol. 2009 Dec; 66(6):759-70.
    View in: PubMed
    Score: 0.024
  5. 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: 0.021
  6. 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: 0.019
  7. The effects of a dominant connexin32 mutant in myelinating Schwann cells. Mol Cell Neurosci. 2006 Jul; 32(3):283-98.
    View in: PubMed
    Score: 0.019
  8. 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: 0.018
  9. 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: 0.017
  10. Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history. Brain. 2023 09 01; 146(9):3826-3835.
    View in: PubMed
    Score: 0.015
  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: 0.015
  12. Disruption of Endosomal Sorting in Schwann Cells Leads to Defective Myelination and Endosomal Abnormalities Observed in Charcot-Marie-Tooth Disease. J Neurosci. 2022 06 22; 42(25):5085-5101.
    View in: PubMed
    Score: 0.014
  13. Novel Anaplastic Thyroid Cancer PDXs and Cell Lines: Expanding Preclinical Models of Genetic Diversity. J Clin Endocrinol Metab. 2021 10 21; 106(11):e4652-e4665.
    View in: PubMed
    Score: 0.014
  14. Internodal specializations of myelinated axons in the central nervous system. Cell Tissue Res. 2001 Jul; 305(1):53-66.
    View in: PubMed
    Score: 0.013
  15. TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model. Elife. 2020 05 28; 9.
    View in: PubMed
    Score: 0.012
  16. Schwann cell-derived periostin promotes autoimmune peripheral polyneuropathy via macrophage recruitment. J Clin Invest. 2018 10 01; 128(10):4727-4741.
    View in: PubMed
    Score: 0.011
  17. PMP22 antisense oligonucleotides reverse Charcot-Marie-Tooth disease type 1A features in rodent models. J Clin Invest. 2018 01 02; 128(1):359-368.
    View in: PubMed
    Score: 0.010
  18. Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP). J Neuropathol Exp Neurol. 1997 Jul; 56(7):811-21.
    View in: PubMed
    Score: 0.010
  19. Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies. Am J Hum Genet. 2016 09 01; 99(3):607-623.
    View in: PubMed
    Score: 0.009
  20. Modality-based organization of ascending somatosensory axons in the direct dorsal column pathway. J Neurosci. 2013 Nov 06; 33(45):17691-709.
    View in: PubMed
    Score: 0.008
  21. The genetic structure of mouse ornithine transcarbamylase. Nucleic Acids Res. 1988 Feb 25; 16(4):1593-601.
    View in: PubMed
    Score: 0.005
  22. Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circ Res. 2006 Sep 15; 99(6):646-55.
    View in: PubMed
    Score: 0.005
  23. Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom. Neurobiol Dis. 2004 Nov; 17(2):290-9.
    View in: PubMed
    Score: 0.004
  24. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 2004 04 01; 428(6982):493-521.
    View in: PubMed
    Score: 0.004
  25. Notch1 control of oligodendrocyte differentiation in the spinal cord. J Cell Biol. 2002 Aug 19; 158(4):709-18.
    View in: PubMed
    Score: 0.004
  26. Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells. Mol Cell Neurosci. 2001 Dec; 18(6):606-18.
    View in: PubMed
    Score: 0.003
  27. Alpha4 integrin is expressed during peripheral nerve regeneration and enhances neurite outgrowth. J Neurosci. 2001 Sep 01; 21(17):6732-44.
    View in: PubMed
    Score: 0.003
  28. Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system. J Neurobiol. 2000 Jul; 44(1):7-19.
    View in: PubMed
    Score: 0.003
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.