Connection

STEVEN SCHERER to Animals

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

0.522
  1. Peripheral Nervous System (PNS) Myelin Diseases. Cold Spring Harb Perspect Biol. 2024 05 02; 16(5).
    View in: PubMed
    Score: 0.049
  2. A recessive Trim2 mutation causes an axonal neuropathy in mice. Neurobiol Dis. 2020 07; 140:104845.
    View in: PubMed
    Score: 0.036
  3. 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: 0.032
  4. 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: 0.019
  5. A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy. Ann Neurol. 2009 Dec; 66(6):759-70.
    View in: PubMed
    Score: 0.018
  6. 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: 0.016
  7. 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: 0.015
  8. The effects of a dominant connexin32 mutant in myelinating Schwann cells. Mol Cell Neurosci. 2006 Jul; 32(3):283-98.
    View in: PubMed
    Score: 0.014
  9. The finished DNA sequence of human chromosome 12. Nature. 2006 03 16; 440(7082):346-51.
    View in: PubMed
    Score: 0.014
  10. 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: 0.013
  11. 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: 0.013
  12. SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain. 2024 Sep 03; 147(9):3131-3143.
    View in: PubMed
    Score: 0.012
  13. Disease mechanisms in inherited neuropathies. Nat Rev Neurosci. 2003 Sep; 4(9):714-26.
    View in: PubMed
    Score: 0.012
  14. 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: 0.012
  15. Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World. PLoS Negl Trop Dis. 2023 04; 17(4):e0010862.
    View in: PubMed
    Score: 0.011
  16. 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: 0.011
  17. 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: 0.011
  18. 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: 0.010
  19. A High-throughput Approach to Identify Effective Systemic Agents for the Treatment of Anaplastic Thyroid Carcinoma. J Clin Endocrinol Metab. 2021 09 27; 106(10):2962-2978.
    View in: PubMed
    Score: 0.010
  20. Molecular organization of the nodal region is not altered in spontaneously diabetic BB-Wistar rats. J Neurosci Res. 2001 Jul 15; 65(2):139-49.
    View in: PubMed
    Score: 0.010
  21. Ezrin, radixin, and moesin are components of Schwann cell microvilli. J Neurosci Res. 2001 Jul 15; 65(2):150-64.
    View in: PubMed
    Score: 0.010
  22. Internodal specializations of myelinated axons in the central nervous system. Cell Tissue Res. 2001 Jul; 305(1):53-66.
    View in: PubMed
    Score: 0.010
  23. 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: 0.009
  24. Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A. Ann Neurol. 2019 03; 85(3):316-330.
    View in: PubMed
    Score: 0.008
  25. 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: 0.008
  26. 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: 0.008
  27. 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: 0.008
  28. 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: 0.007
  29. Multifaceted biological insights from a draft genome sequence of the tobacco hornworm moth, Manduca sexta. Insect Biochem Mol Biol. 2016 09; 76:118-147.
    View in: PubMed
    Score: 0.007
  30. Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy. Proc Natl Acad Sci U S A. 2016 Apr 26; 113(17):E2421-9.
    View in: PubMed
    Score: 0.007
  31. Pseudomonas helleri sp. nov. and Pseudomonas weihenstephanensis sp. nov., isolated from raw cow's milk. Int J Syst Evol Microbiol. 2016 Mar; 66(3):1163-1173.
    View in: PubMed
    Score: 0.007
  32. The genomes of two key bumblebee species with primitive eusocial organization. Genome Biol. 2015 Apr 24; 16:76.
    View in: PubMed
    Score: 0.006
  33. A massive expansion of effector genes underlies gall-formation in the wheat pest Mayetiola destructor. Curr Biol. 2015 Mar 02; 25(5):613-20.
    View in: PubMed
    Score: 0.006
  34. The first myriapod genome sequence reveals conservative arthropod gene content and genome organisation in the centipede Strigamia maritima. PLoS Biol. 2014 Nov; 12(11):e1002005.
    View in: PubMed
    Score: 0.006
  35. Comparative validation of the D. melanogaster modENCODE transcriptome annotation. Genome Res. 2014 Jul; 24(7):1209-23.
    View in: PubMed
    Score: 0.006
  36. 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: 0.006
  37. A genetic map of Xenopus tropicalis. Dev Biol. 2011 Jun 01; 354(1):1-8.
    View in: PubMed
    Score: 0.005
  38. The genome of the model beetle and pest Tribolium castaneum. Nature. 2008 Apr 24; 452(7190):949-55.
    View in: PubMed
    Score: 0.004
  39. The genetic structure of mouse ornithine transcarbamylase. Nucleic Acids Res. 1988 Feb 25; 16(4):1593-601.
    View in: PubMed
    Score: 0.004
  40. Recurrent duplication-driven transposition of DNA during hominoid evolution. Proc Natl Acad Sci U S A. 2006 Nov 21; 103(47):17626-31.
    View in: PubMed
    Score: 0.004
  41. 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: 0.004
  42. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 2006 Apr 27; 440(7088):1194-8.
    View in: PubMed
    Score: 0.003
  43. The DNA sequence of the human X chromosome. Nature. 2005 Mar 17; 434(7031):325-37.
    View in: PubMed
    Score: 0.003
  44. Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution. Genome Res. 2005 Jan; 15(1):1-18.
    View in: PubMed
    Score: 0.003
  45. 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: 0.003
  46. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 2004 04 01; 428(6982):493-521.
    View in: PubMed
    Score: 0.003
  47. Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence. Genome Biol. 2002; 3(12):RESEARCH0079.
    View in: PubMed
    Score: 0.003
  48. Notch1 control of oligodendrocyte differentiation in the spinal cord. J Cell Biol. 2002 Aug 19; 158(4):709-18.
    View in: PubMed
    Score: 0.003
  49. Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. J Neurosci Res. 2002 Feb 15; 67(4):443-9.
    View in: PubMed
    Score: 0.003
  50. 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
  51. Axon-Schwann cell interactions regulate the expression of fibroblast growth factor-5 (FGF-5). J Neurosci Res. 2001 Oct 01; 66(1):16-22.
    View in: PubMed
    Score: 0.003
  52. 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
  53. A global profile of germline gene expression in C. elegans. Mol Cell. 2000 Sep; 6(3):605-16.
    View in: PubMed
    Score: 0.002
  54. 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: 0.002
  55. p200, a collagen secreted by Schwann cells, is expressed in developing nerves and in adult nerves following axotomy. J Neurosci Res. 1999 May 01; 56(3):284-94.
    View in: PubMed
    Score: 0.002
  56. Accumulation of F-spondin in injured peripheral nerve promotes the outgrowth of sensory axons. J Neurosci. 1998 Nov 01; 18(21):8875-85.
    View in: PubMed
    Score: 0.002
  57. Expression and regulation of kainate and AMPA receptors in uncommitted and committed neural progenitors. Neurochem Res. 1995 May; 20(5):549-60.
    View in: PubMed
    Score: 0.002
  58. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science. 1993 Dec 24; 262(5142):2039-42.
    View in: PubMed
    Score: 0.001
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.