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Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele

Cox, Gregory A, Mahaffey, Connie L, Frankel, Wayne N·1998·Neuron
DOI 10.1016/s0896-6273(00)80652-2
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  • Mutation of SMBP2 causes mouse neuromuscular degeneration, a disease similar to human spinal muscular atrophy and linked to miRNA-containing complex.

    “Mutation of this protein causes mouse neuromuscular degeneration (Cox et al. 1998), a disease similar to human spinal muscular atrophy and linked to miRNA-containing complex (see above).”

    From A microRNA array reveals extensive regulation of microRNAs during brain development (2003) · cites this paper as Cox et al. 1998

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Research works printed but not linked: 14

  1. [1]1. Appelbaum, J.S ∙ Roos, R.P ∙ Salazar Grueso, E.F ... Intrafamilial heterogeneity in hereditary motor neuron disease Neurology. 1992; 42:1488-1492 Crossref PubMed Google Scholar
  2. [2]2. Biswas, S.B ∙ Chen, P.H ∙ Biswas, E.E Purification and characterization of DNA polymerase alpha-associated replication protein A–dependent yeast DNA helicase A Biochemistry. 1997; 36:13270-13276 Crossref Scopus (17) PubMed Google Scholar
  3. [3]3. Biswas, E.E ∙ Fricke, W.M ∙ Chen, P.H ... Yeast DNA helicase Acloning, expression, purification, and enzymatic characterization Biochemistry. 1997; 36:13277-13284 Crossref Scopus (16) PubMed Google Scholar
  4. [4]4. Chance, P.F ∙ Rabin, B.A ∙ Ryan, S.G ... Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34 Am. J. Hum. Genet. 1998; 62:633-640 Full Text Full Text (PDF) Scopus (180) PubMed Google Scholar
  5. [5]5. Cook, S.A ∙ Johnson, K.R ∙ Bronson, R.T ... Neuromuscular degeneration (nmd)a mutation on mouse chromosome 19 that causes motor neuron degeneration Mamm. Genome. 1995; 6:187-191 Crossref Scopus (43) PubMed Google Scholar
  6. [6]6. Cox, G.A ∙ Phelps, S.F ∙ Chapman, V.M ... New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin Nat. Genet. 1993; 4:87-93 Crossref Scopus (172) PubMed Google Scholar
  7. [7]7. de Boer, J ∙ de Wit, J ∙ van Steeg, H ... A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy Mol. Cell. 1998; 1:981-990 Full Text Full Text (PDF) Scopus (180) PubMed Google Scholar
  8. [8]8. de Boer, J ∙ Donker, I ∙ de Wit, J ... Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality Cancer Res. 1998; 58:89-94 PubMed Google Scholar
  9. [9]9. Deng, H.X ∙ Hentati, A ∙ Tainer, J.A ... Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase Science. 1993; 261:1047-1051 Crossref Scopus (1416) PubMed Google Scholar
  10. [10]10. Fanning, E ∙ Knippers, R Structure and function of simian virus 40 large tumor antigen Annu. Rev. Biochem. 1992; 61:55-85 Crossref Scopus (499) PubMed Google Scholar
  11. [11]11. Fischer, U ∙ Liu, Q ∙ Dreyfuss, G The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis Cell. 1997; 90:1023-1029 Full Text Full Text (PDF) Scopus (570) PubMed Google Scholar
  12. [12]12. Frankel, W.N ∙ Sweet, H.O ∙ Davisson, M.T The stumbler mutation maps to proximal mouse Chromosome 2 Mamm. Genome. 1994; 5:659-662 Crossref Scopus (5) PubMed Google Scholar
  13. [13]13. Frankel, W.N ∙ Valenzuela, A ∙ Lutz, C.M ... New seizure frequency QTL and the complex genetics of epilepsy in EL mice Mamm. Genome. 1995; 6:830-838 Crossref Scopus (77) PubMed Google Scholar
  14. [14]14. Fukita, Y ∙ Mizuta, T.R ∙ Shirozu, M ... The human S mu bp-2, a DNA-binding protein specific to the single-stranded guanine-rich sequence related to the immunoglobulin mu chain switch region J. Biol. Chem. 1993; 268:17463-17470

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Authors
Cox, G. A., Mahaffey, C. L., & Frankel, W. N.
Venue
Neuron
Publisher
Elsevier BV
Published
1998-12
Volume
21
Issue
6
Pages
1327-1337
ISSN
0896-6273
DOI
10.1016/s0896-6273(00)80652-2
Cited by
107
References
0
Language
en
Licence

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