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Volumn 1472, Issue , 2012, Pages 124-137

Distribution and frequency of intranuclear inclusions in female CGG KI mice modeling the fragile X premutation

Author keywords

CGG KI mouse; Fragile X premutation; Intranuclear inclusions; Trinucleotide repeat disorder

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN CORTEX; CELL NUCLEUS INCLUSION BODY; CLINICAL FEATURE; COGNITION; CONTROLLED STUDY; FEMALE; FRAGILE X ASSOCIATED TREMOR ATAXIA SYNDROME; FRAGILE X SYNDROME; HISTOLOGY; IMMUNOCYTOCHEMISTRY; LIFESPAN; MACROGLIA; MOUSE; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; SUBCORTEX; TRINUCLEOTIDE REPEAT;

EID: 84865686138     PISSN: 00068993     EISSN: 18726240     Source Type: Journal    
DOI: 10.1016/j.brainres.2012.06.052     Document Type: Article
Times cited : (12)

References (56)
  • 2
    • 34548424947 scopus 로고    scopus 로고
    • Fragile X premutation in a woman with cognitive impairment, tremor, and history of premature ovarian failure
    • J.T. Al-Hinti, N. Nagan, and S.I. Harik Fragile X premutation in a woman with cognitive impairment, tremor, and history of premature ovarian failure Alzheimer Dis. Assoc. Disord. 21 2007 262 264
    • (2007) Alzheimer Dis. Assoc. Disord. , vol.21 , pp. 262-264
    • Al-Hinti, J.T.1    Nagan, N.2    Harik, S.I.3
  • 3
    • 67949106844 scopus 로고    scopus 로고
    • Seattle (WA): Allen Institute for Brain Science ©. Available from
    • Allen Mouse Brain Atlas [Internet], 2009. Seattle (WA): Allen Institute for Brain Science ©. Available from: 〈http://mouse.brain-map. org〉.
    • (2009) Allen Mouse Brain Atlas [Internet]
  • 4
    • 74249092236 scopus 로고    scopus 로고
    • Mouse models of fragile X-associated tremor ataxia
    • R.F. Berman, and R. Willemsen Mouse models of fragile X-associated tremor ataxia J. Invest. Med. 57 8 2009 837 841
    • (2009) J. Invest. Med. , vol.57 , Issue.8 , pp. 837-841
    • Berman, R.F.1    Willemsen, R.2
  • 5
    • 11144233958 scopus 로고    scopus 로고
    • Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation
    • E. Berry-Kravis, K. Potanos, D. Weinberg, L. Zhou, and C.G. Goetz Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation Ann. Neurol. 57 2005 144 147
    • (2005) Ann. Neurol. , vol.57 , pp. 144-147
    • Berry-Kravis, E.1    Potanos, K.2    Weinberg, D.3    Zhou, L.4    Goetz, C.G.5
  • 6
    • 56749165180 scopus 로고    scopus 로고
    • CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome
    • J.R. Brouwer, K. Huizer, L.A. Severijnen, R.K. Hukema, R.F. Berman, B.A. Oostra, and R. Willemsen CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome J. Neurochem. 107 6 2008 1671 1682
    • (2008) J. Neurochem. , vol.107 , Issue.6 , pp. 1671-1682
    • Brouwer, J.R.1    Huizer, K.2    Severijnen, L.A.3    Hukema, R.K.4    Berman, R.F.5    Oostra, B.A.6    Willemsen, R.7
  • 10
    • 78049436586 scopus 로고    scopus 로고
    • Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome
    • W. Chonchaiya, F. Tassone, P. Ashwood, D. Hessl, A. Schneider, L. Campos, D.V. Nguyen, and R.J. Hagerman Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome Hum. Genet. 128 2010 539 548
    • (2010) Hum. Genet. , vol.128 , pp. 539-548
    • Chonchaiya, W.1    Tassone, F.2    Ashwood, P.3    Hessl, D.4    Schneider, A.5    Campos, L.6    Nguyen, D.V.7    Hagerman, R.J.8
  • 12
    • 84856771413 scopus 로고    scopus 로고
    • Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching task
    • A.A. Diep, M.R. Hunsaker, R. Kwock, K. Kim, R. Willemsen, and R.F. Berman Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching task Neurobiol. Learn. Mem. 97 2 2012 229 234
    • (2012) Neurobiol. Learn. Mem. , vol.97 , Issue.2 , pp. 229-234
    • Diep, A.A.1    Hunsaker, M.R.2    Kwock, R.3    Kim, K.4    Willemsen, R.5    Berman, R.F.6
  • 13
    • 34247637636 scopus 로고    scopus 로고
    • Regional FMRP deficits and large repeat expansions into the full mutation range in a new fragile X premutation mouse model
    • A. Entezam, R. Biacsi, B. Orrison, T. Saha, G.E. Hoffman, E. Grabczyk, R.L. Nussbaum, and K. Usdin Regional FMRP deficits and large repeat expansions into the full mutation range in a new fragile X premutation mouse model Gene 395 1-2 2007 125 134
    • (2007) Gene , vol.395 , Issue.12 , pp. 125-134
    • Entezam, A.1    Biacsi, R.2    Orrison, B.3    Saha, T.4    Hoffman, G.E.5    Grabczyk, E.6    Nussbaum, R.L.7    Usdin, K.8
  • 14
    • 84858017006 scopus 로고    scopus 로고
    • Intercellular (mis)communication in neurodegenerative disease
    • G.A. Garden, and A.R. La Spada Intercellular (mis)communication in neurodegenerative disease Neuron 73 5 2012 886 901
    • (2012) Neuron , vol.73 , Issue.5 , pp. 886-901
    • Garden, G.A.1    La Spada, A.R.2
  • 16
    • 82955198526 scopus 로고    scopus 로고
    • Adult female fragile X premutation carriers exhibit age- and CGG repeat length-related impairments on an attentionally based enumeration task
    • N.J. Goodrich-Hunsaker, L.M. Wong, Y. McLennan, F. Tassone, D. Harvey, S.M. Rivera, and T.J. Simon Adult female fragile X premutation carriers exhibit age- and CGG repeat length-related impairments on an attentionally based enumeration task Front. Hum. Neurosci. 5 2011 63
    • (2011) Front. Hum. Neurosci. , vol.5 , pp. 63
    • Goodrich-Hunsaker, N.J.1    Wong, L.M.2    McLennan, Y.3    Tassone, F.4    Harvey, D.5    Rivera, S.M.6    Simon, T.J.7
  • 18
    • 0036019165 scopus 로고    scopus 로고
    • Mechanisms of cell death in neurodegenerative diseases: Fashion, fiction, and facts
    • M.B. Graeber, and L.B. Moran Mechanisms of cell death in neurodegenerative diseases: fashion, fiction, and facts Brain Pathol. 12 3 2002 385 390
    • (2002) Brain Pathol. , vol.12 , Issue.3 , pp. 385-390
    • Graeber, M.B.1    Moran, L.B.2
  • 22
    • 57049092347 scopus 로고    scopus 로고
    • Testing for fragile X gene mutations throughout the life span
    • R.J. Hagerman, and P.J. Hagerman Testing for fragile X gene mutations throughout the life span J. Am. Med. Assoc. 300 2008 2419 2421
    • (2008) J. Am. Med. Assoc. , vol.300 , pp. 2419-2421
    • Hagerman, R.J.1    Hagerman, P.J.2
  • 25
    • 77953917097 scopus 로고    scopus 로고
    • Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation
    • M.R. Hunsaker, N.J. Goodrich-Hunsaker, R. Willemsen, and R.F. Berman Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation Behav. Brain Res. 213 2 2010 263 268
    • (2010) Behav. Brain Res. , vol.213 , Issue.2 , pp. 263-268
    • Hunsaker, M.R.1    Goodrich-Hunsaker, N.J.2    Willemsen, R.3    Berman, R.F.4
  • 27
    • 79957468734 scopus 로고    scopus 로고
    • Rare intranuclear inclusions in the brains of 3 older adult males with fragile X syndrome: Implications for the spectrum of fragile X-associated disorders
    • M.R. Hunsaker, C.M. Greco, F. Tassone, R.F. Berman, R. Willemsen, R.J. Hagerman, and P.J. Hagerman Rare intranuclear inclusions in the brains of 3 older adult males with fragile X syndrome: implications for the spectrum of fragile X-associated disorders J. Neuropathol. Exp. Neurol. 70 6 2011 462 469
    • (2011) J. Neuropathol. Exp. Neurol. , vol.70 , Issue.6 , pp. 462-469
    • Hunsaker, M.R.1    Greco, C.M.2    Tassone, F.3    Berman, R.F.4    Willemsen, R.5    Hagerman, R.J.6    Hagerman, P.J.7
  • 29
    • 72249123025 scopus 로고    scopus 로고
    • Progressive spatial processing deficits in a mouse model of the fragile X premutation
    • M.R. Hunsaker, H.J. Wenzel, R. Willemsen, and R.F. Berman Progressive spatial processing deficits in a mouse model of the fragile X premutation Behav. Neurosci. 123 6 2009 1315 1324
    • (2009) Behav. Neurosci. , vol.123 , Issue.6 , pp. 1315-1324
    • Hunsaker, M.R.1    Wenzel, H.J.2    Willemsen, R.3    Berman, R.F.4
  • 30
    • 84864583481 scopus 로고    scopus 로고
    • The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): Evidence for a complex inheritance
    • Hunter, J.E., Epstein, M.P., Tinker, S.W., Abramowitz, A., Sherman, S.L. 2011. The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance. Behav. Genet., 42 (3), 415-422.
    • (2011) Behav. Genet. , vol.42 , Issue.3 , pp. 415-422
    • Hunter, J.E.1    Epstein, M.P.2    Tinker, S.W.3    Abramowitz, A.4    Sherman, S.L.5
  • 31
    • 77951758220 scopus 로고    scopus 로고
    • Co-occurring diagnoses among FMR1 premutation allele carriers
    • J.E. Hunter, J.K. Rohr, and S.L. Sherman Co-occurring diagnoses among FMR1 premutation allele carriers Clin. Genet. 77 4 2010 374 381
    • (2010) Clin. Genet. , vol.77 , Issue.4 , pp. 374-381
    • Hunter, J.E.1    Rohr, J.K.2    Sherman, S.L.3
  • 32
    • 84863310075 scopus 로고    scopus 로고
    • Capturing the fragile X premutation phenotypes: A collaborative effort across multiple cohorts
    • Hunter, J.E., Sherman, S., Grigsby, J., Kogan, C., Cornish, K. 2012. Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology, 26 (2), 156-164.
    • (2012) Neuropsychology , vol.26 , Issue.2 , pp. 156-164
    • Hunter, J.E.1    Sherman, S.2    Grigsby, J.3    Kogan, C.4    Cornish, K.5
  • 37
    • 44449102182 scopus 로고    scopus 로고
    • Fragile X associated tremor/ataxia syndrome (FXTAS) with dementia in a female harbouring FMR1 premutation
    • Y. Karmon, and N. Gadoth Fragile X associated tremor/ataxia syndrome (FXTAS) with dementia in a female harbouring FMR1 premutation J. Neurol. Neurosurg. Psychiatry 79 2008 738 739
    • (2008) J. Neurol. Neurosurg. Psychiatry , vol.79 , pp. 738-739
    • Karmon, Y.1    Gadoth, N.2
  • 38
    • 0035394437 scopus 로고    scopus 로고
    • Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers
    • A. Kenneson, F. Zhang, C.H. Hagedorn, and S.T. Warren Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers Hum. Mol. Genet. 10 2001 1449 1454
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 1449-1454
    • Kenneson, A.1    Zhang, F.2    Hagedorn, C.H.3    Warren, S.T.4
  • 39
    • 80054697701 scopus 로고    scopus 로고
    • Fibromyalgia in fragile X mental retardation 1 gene premutation carriers
    • M.A. Leehey, W. Legg, F. Tassone, and R. Hagerman Fibromyalgia in fragile X mental retardation 1 gene premutation carriers Rheumatology (Oxford) 50 2011 2233 2236
    • (2011) Rheumatology (Oxford) , vol.50 , pp. 2233-2236
    • Leehey, M.A.1    Legg, W.2    Tassone, F.3    Hagerman, R.4
  • 40
    • 0036306870 scopus 로고    scopus 로고
    • Skewed X-chromosome inactivation is a common feature of x-linked mental retardation disorders
    • R.M. Plenge, R.A. Stevenson, H.A. Lubs, C.E. Schwartz, and H.F. Willard Skewed X-chromosome inactivation is a common feature of x-linked mental retardation disorders Am. J. Hum. Genet. 71 2002 168 173
    • (2002) Am. J. Hum. Genet. , vol.71 , pp. 168-173
    • Plenge, R.M.1    Stevenson, R.A.2    Lubs, H.A.3    Schwartz, C.E.4    Willard, H.F.5
  • 41
    • 79961135005 scopus 로고    scopus 로고
    • R Development Core Team R Foundation for Statistical Computing, Vienna, Austria. URL:. ISBN 3-900051-07-0
    • R Development Core Team, 2011. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. URL: 〈http://www.R-project.org/〉. ISBN 3-900051-07-0.
    • (2011) R: A Language and Environment for Statistical Computing
  • 42
    • 74249089729 scopus 로고    scopus 로고
    • Molecular pathogenesis of fragile X-associated tremor/ataxia syndrome
    • C. Raske, and P.J. Hagerman Molecular pathogenesis of fragile X-associated tremor/ataxia syndrome J. Invest. Med. 57 2009 825 829
    • (2009) J. Invest. Med. , vol.57 , pp. 825-829
    • Raske, C.1    Hagerman, P.J.2
  • 45
    • 27744591518 scopus 로고    scopus 로고
    • An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene
    • A. Saluto, A. Brussino, F. Tassone, C. Arduino, C. Cagnoli, P. Pappi, P. Hagerman, N. Migone, and A. Brusco An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene J. Mol. Diagn. 7 5 2005 605 612
    • (2005) J. Mol. Diagn. , vol.7 , Issue.5 , pp. 605-612
    • Saluto, A.1    Brussino, A.2    Tassone, F.3    Arduino, C.4    Cagnoli, C.5    Pappi, P.6    Hagerman, P.7    Migone, N.8    Brusco, A.9
  • 46
    • 0033022410 scopus 로고    scopus 로고
    • Reduction of lipofuscin-like autofluorescence in fluorescently labeled tissue
    • S.A. Schnell, W.A. Staines, and M.W. Wessendorf Reduction of lipofuscin-like autofluorescence in fluorescently labeled tissue J. Histochem. Cytochem. 47 6 1999 719 730
    • (1999) J. Histochem. Cytochem. , vol.47 , Issue.6 , pp. 719-730
    • Schnell, S.A.1    Staines, W.A.2    Wessendorf, M.W.3
  • 50
  • 51
    • 38749141432 scopus 로고    scopus 로고
    • A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations
    • F. Tassone, R. Pan, K. Amiri, A.K. Taylor, and P.J. Hagerman A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations J. Mol. Diagn. 10 2008 43 49
    • (2008) J. Mol. Diagn. , vol.10 , pp. 43-49
    • Tassone, F.1    Pan, R.2    Amiri, K.3    Taylor, A.K.4    Hagerman, P.J.5
  • 53
    • 76449105593 scopus 로고    scopus 로고
    • Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation
    • H.J. Wenzel, M.R. Hunsaker, C.M. Greco, R. Willemsen, and R.F. Berman Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation Brain Res. 1318 2010 155 166
    • (2010) Brain Res. , vol.1318 , pp. 155-166
    • Wenzel, H.J.1    Hunsaker, M.R.2    Greco, C.M.3    Willemsen, R.4    Berman, R.F.5


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