Literature DB >> 22496548

Alexander disease.

Albee Messing1, Michael Brenner, Mel B Feany, Maiken Nedergaard, James E Goldman.   

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Year:  2012        PMID: 22496548      PMCID: PMC3336214          DOI: 10.1523/JNEUROSCI.5384-11.2012

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


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  53 in total

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Authors:  Maiken Nedergaard; Bruce Ransom; Steven A Goldman
Journal:  Trends Neurosci       Date:  2003-10       Impact factor: 13.837

2.  Alexander disease: diagnosis with MR imaging.

Authors:  M S van der Knaap; S Naidu; S N Breiter; S Blaser; H Stroink; S Springer; J C Begeer; R van Coster; P G Barth; N H Thomas; J Valk; J M Powers
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5.  Activity-dependent extracellular K+ accumulation in rat optic nerve: the role of glial and axonal Na+ pumps.

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Authors:  R Blattner; A Von Moers; P A J Leegwater; F A Hanefeld; M S Van Der Knaap; W Köhler
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7.  Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.

Authors:  Erika Stumpf; Hélène Masson; Antoine Duquette; France Berthelet; Julia McNabb; Anne Lortie; Jacques Lesage; Jacques Montplaisir; Bernard Brais; Patrick Cossette
Journal:  Arch Neurol       Date:  2003-09

Review 8.  GFAP mutations in Alexander disease.

Authors:  Rong Li; Albee Messing; James E Goldman; Michael Brenner
Journal:  Int J Dev Neurosci       Date:  2002 Jun-Aug       Impact factor: 2.457

9.  Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.

Authors:  Michito Namekawa; Yoshihisa Takiyama; Yoko Aoki; Norio Takayashiki; Kumi Sakoe; Haruo Shimazaki; Tomohiro Taguchi; Yasufumi Tanaka; Masatoyo Nishizawa; Ken Saito; Yoichi Matsubara; Imaharu Nakano
Journal:  Ann Neurol       Date:  2002-12       Impact factor: 10.422

10.  Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease.

Authors:  M Brenner; A B Johnson; O Boespflug-Tanguy; D Rodriguez; J E Goldman; A Messing
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

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  91 in total

Review 1.  Translational potential of astrocytes in brain disorders.

Authors:  Alexei Verkhratsky; Luca Steardo; Vladimir Parpura; Vedrana Montana
Journal:  Prog Neurobiol       Date:  2015-09-16       Impact factor: 11.685

2.  Alexander Disease: A Novel Mutation in GFAP Leading to Epilepsia Partialis Continua.

Authors:  Daniel J Bonthius; Bahri Karacay
Journal:  J Child Neurol       Date:  2015-12-29       Impact factor: 1.987

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5.  Identification of a novel nonsense mutation in the rod domain of GFAP that is associated with Alexander disease.

Authors:  Tai-Seung Nam; Jin Hee Kim; Chi-Hsuan Chang; Woong Yoon; Yoon Seok Jung; Sa-Yoon Kang; Boo Ahn Shin; Ming-Der Perng; Seok-Yong Choi; Myeong-Kyu Kim
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Review 6.  The role of glia in stress: polyamines and brain disorders.

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Review 7.  Astrogliosis.

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8.  GFAP Mutations in Astrocytes Impair Oligodendrocyte Progenitor Proliferation and Myelination in an hiPSC Model of Alexander Disease.

Authors:  Li Li; E Tian; Xianwei Chen; Jianfei Chao; Jeremy Klein; Qiuhao Qu; Guihua Sun; Guoqiang Sun; Yanzhou Huang; Charles D Warden; Peng Ye; Lizhao Feng; Xinqiang Li; Qi Cui; Abdullah Sultan; Panagiotis Douvaras; Valentina Fossati; Neville E Sanjana; Arthur D Riggs; Yanhong Shi
Journal:  Cell Stem Cell       Date:  2018-08-02       Impact factor: 24.633

9.  Astrocytic TDP-43 pathology in Alexander disease.

Authors:  Adam K Walker; Christine M LaPash Daniels; James E Goldman; John Q Trojanowski; Virginia M-Y Lee; Albee Messing
Journal:  J Neurosci       Date:  2014-05-07       Impact factor: 6.167

10.  Phenotypic conversions of "protoplasmic" to "reactive" astrocytes in Alexander disease.

Authors:  Alexander A Sosunov; Eileen Guilfoyle; Xiaoping Wu; Guy M McKhann; James E Goldman
Journal:  J Neurosci       Date:  2013-04-24       Impact factor: 6.167

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