cysteine and Alexander Disease

cysteine has been researched along with Alexander Disease in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hasuo, K; Ito, K; Kubota, K; Matsuda, H; Morooka, M; Takeuchi, S1
Goldman, JE; Hagemann, TL; McKhann, GM; Messing, A; Sosunov, AA; Tian, R; Wu, X1
Christen, HJ; Das, AM; Donnerstag, F; Hagedorn, M; Hartmann, H; Herchenbach, J; Ledaal, P; Lücke, T; Meins, M; Stephani, U1

Other Studies

3 other study(ies) available for cysteine and Alexander Disease

ArticleYear
Cerebral blood flow on ECD SPECT in a patient with adult onset Alexander disease.
    Clinical nuclear medicine, 2009, Volume: 34, Issue:12

    Topics: Alexander Disease; Cerebrovascular Circulation; Cerebrovascular Disorders; Cysteine; Female; Humans; Medulla Oblongata; Middle Aged; Organotechnetium Compounds; Radiopharmaceuticals; Tomography, Emission-Computed, Single-Photon

2009
Alexander disease mutant glial fibrillary acidic protein compromises glutamate transport in astrocytes.
    Journal of neuropathology and experimental neurology, 2010, Volume: 69, Issue:4

    Topics: 8-Bromo Cyclic Adenosine Monophosphate; Alexander Disease; Animals; Arginine; Astrocytes; Cells, Cultured; Coculture Techniques; Cysteine; Excitatory Amino Acid Agonists; Excitatory Amino Acid Transporter 2; Flow Cytometry; Gene Expression Regulation; Glial Fibrillary Acidic Protein; Green Fluorescent Proteins; Hippocampus; Kainic Acid; Membrane Potentials; Mutation; Nerve Tissue Proteins; Neurons; Patch-Clamp Techniques; Rats; Transfection

2010
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.
    Neuropediatrics, 2007, Volume: 38, Issue:3

    Topics: Age of Onset; Alanine; Alexander Disease; Cysteine; DNA Mutational Analysis; Exons; Female; Frontal Lobe; Glial Fibrillary Acidic Protein; Humans; Infant; Magnetic Resonance Imaging; Male; Mutation; Protein Structure, Tertiary; Tyrosine; Valine

2007