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The Journal of Biological Chemistry
|
February 5, 2002
Genetic analysis of the mammalian K+ channel beta subunit Kvbeta 2 (Kcnab2)
Ken McCormack, Jolien X Connor, Lei Zhou, et al.
ASN Neuro
|
February 21, 2012
Neurological diseases as primary gliopathies: a reassessment of neurocentrism
Alexei Verkhratsky, Michael V Sofroniew, Albee Messing, et al.
Annals of Clinical and Translational Neurology
|
September 30, 2025
Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease
Tracy L Hagemann, Michelle M Sonsalla, Cora Luzinski, et al.
Journal of Neuropathology and Experimental Neurology
|
May 8, 2010
Alexander disease mutant glial fibrillary acidic protein compromises glutamate transport in astrocytes
Rujin Tian, Xiaoping Wu, Tracy L Hagemann, et al.
Antioxidants & Redox Signaling
|
August 18, 2010
Inhibition of Na+/H+ exchanger isoform 1 is neuroprotective in neonatal hypoxic ischemic brain injury
Pelin Cengiz, Neil Kleman, Kutluay Uluc, et al.
Human Molecular Genetics
|
February 16, 2008
Autophagy induced by Alexander disease-mutant GFAP accumulation is regulated by p38/MAPK and mTOR signaling pathways
Guomei Tang, Zhenyu Yue, Zsolt Talloczy, et al.
Cancer Cell
|
August 16, 2005
Early inactivation of p53 tumor suppressor gene cooperating with NF1 loss induces malignant astrocytoma
Yuan Zhu, Frantz Guignard, Dawen Zhao, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 9, 2014
Astrocytic TDP-43 pathology in Alexander disease
Adam K Walker, Christine M LaPash Daniels, James E Goldman, et al.
Human Molecular Genetics
|
March 3, 2011
P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice
Pietro Fratta, Paola Saveri, Desiree Zambroni, et al.
Archives of Neurology
|
October 12, 2011
Archetypal and new families with Alexander disease and novel mutations in GFAP
Albee Messing, Rong Li, Sakkubai Naidu, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 103) with videos related to
Sort By:
Page
of 11
The Journal of Biological Chemistry
|
February 5, 2002
Genetic analysis of the mammalian K+ channel beta subunit Kvbeta 2 (Kcnab2)
Ken McCormack, Jolien X Connor, Lei Zhou, et al.
ASN Neuro
|
February 21, 2012
Neurological diseases as primary gliopathies: a reassessment of neurocentrism
Alexei Verkhratsky, Michael V Sofroniew, Albee Messing, et al.
Annals of Clinical and Translational Neurology
|
September 30, 2025
Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease
Tracy L Hagemann, Michelle M Sonsalla, Cora Luzinski, et al.
Journal of Neuropathology and Experimental Neurology
|
May 8, 2010
Alexander disease mutant glial fibrillary acidic protein compromises glutamate transport in astrocytes
Rujin Tian, Xiaoping Wu, Tracy L Hagemann, et al.
Antioxidants & Redox Signaling
|
August 18, 2010
Inhibition of Na+/H+ exchanger isoform 1 is neuroprotective in neonatal hypoxic ischemic brain injury
Pelin Cengiz, Neil Kleman, Kutluay Uluc, et al.
Human Molecular Genetics
|
February 16, 2008
Autophagy induced by Alexander disease-mutant GFAP accumulation is regulated by p38/MAPK and mTOR signaling pathways
Guomei Tang, Zhenyu Yue, Zsolt Talloczy, et al.
Cancer Cell
|
August 16, 2005
Early inactivation of p53 tumor suppressor gene cooperating with NF1 loss induces malignant astrocytoma
Yuan Zhu, Frantz Guignard, Dawen Zhao, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 9, 2014
Astrocytic TDP-43 pathology in Alexander disease
Adam K Walker, Christine M LaPash Daniels, James E Goldman, et al.
Human Molecular Genetics
|
March 3, 2011
P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice
Pietro Fratta, Paola Saveri, Desiree Zambroni, et al.
Archives of Neurology
|
October 12, 2011
Archetypal and new families with Alexander disease and novel mutations in GFAP
Albee Messing, Rong Li, Sakkubai Naidu, et al.
Page
of 11