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Items: 1 to 20 of 66

1.
Abnormal myelination in the spinal cord of PTPα-knockout mice
Quan-Hong Ma, Tao Xiang, Zara Zhuyun Yang, Xu Zhang, Jude Taylor, Zhi-Cheng Xiao
Cell Adh Migr. 2013 Jul 1; 7(4): 370–376. Published online 2013 Jul 17. doi: 10.4161/cam.25652
PMCID:
PMC3739814
AbstractArticlePDF–1.9M
2.
Cognitive correlates of abnormal myelination in psychosis
Lucy D. Vanes, Elias Mouchlianitis, Erica Barry, Krisna Patel, Katie Wong, Sukhwinder S. Shergill
Sci Rep. 2019; 9: 5162. Published online 2019 Mar 26. doi: 10.1038/s41598-019-41679-z
PMCID:
PMC6435797
AbstractArticlePDF–1.7M
3.
Understanding the Role of Oxidative Stress, Neuroinflammation and Abnormal Myelination in Excessive Aggression Associated with Depression: Recent Input from Mechanistic Studies
Anna Gorlova, Evgeniy Svirin, Dmitrii Pavlov, Raymond Cespuglio, Andrey Proshin, Careen A. Schroeter, Klaus-Peter Lesch, Tatyana Strekalova
Int J Mol Sci. 2023 Jan; 24(2): 915. Published online 2023 Jan 4. doi: 10.3390/ijms24020915
PMCID:
PMC9861430
AbstractArticlePDF–914K
4.
AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate
Marni J. Falk, Dong Li, Xiaowu Gai, Elizabeth McCormick, Emily Place, Francesco M. Lasorsa, Frederick G. Otieno, Cuiping Hou, Cecilia E. Kim, Nada Abdel-Magid, Lyam Vazquez, Frank D. Mentch, Rosetta Chiavacci, Jinlong Liang, Xuanzhu Liu, Hui Jiang, Giulia Giannuzzi, Eric D. Marsh, Guo Yiran, Lifeng Tian, Ferdinando Palmieri, Hakon Hakonarson
JIMD Rep. 2014; 14: 77–85. Published online 2014 Feb 11. doi: 10.1007/8904_2013_287
Correction in:
JIMD Rep. 2014; 14: 119.
PMCID:
PMC4213337
AbstractArticlePDF–579K
5.
Region-Specific Myelin Pathology in Mice Lacking the Golli Products of the Myelin Basic Protein Gene
Erin C. Jacobs, Thomas M. Pribyl, Kathy Kampf, Celia Campagnoni, Christopher S. Colwell, Samuel D. Reyes, Melanie Martin, Vance Handley, Timothy D. Hiltner, Carol Readhead, Russell E. Jacobs, Albee Messing, Robin S. Fisher, Anthony T. Campagnoni
J Neurosci. 2005 Jul 27; 25(30): 7004–7013. doi: 10.1523/JNEUROSCI.0288-05.2005
Correction in:
J Neurosci. 2005 Dec 14; 25(50): np.
PMCID:
PMC6724835
AbstractArticlePDF–896K
6.
Gap junctions in inherited human disorders of the central nervous system
Charles K. Abrams, Steven S. Scherer
Biochim Biophys Acta. Author manuscript; available in PMC 2013 Sep 12.
Published in final edited form as: Biochim Biophys Acta. 2012 Aug; 1818(8): 2030–2047. Published online 2011 Aug 16. doi: 10.1016/j.bbamem.2011.08.015
PMCID:
PMC3771870
AbstractArticlePDF–1.5M
7.
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation
Dongxue Mao, Chloe M. Reuter, Maura R.Z. Ruzhnikov, Anita E. Beck, Emily G. Farrow, Lisa T. Emrick, Jill A. Rosenfeld, Katherine M. Mackenzie, Laurie Robak, Matthew T. Wheeler, Lindsay C. Burrage, Mahim Jain, Pengfei Liu, Daniel Calame, Sébastien Küry, Martin Sillesen, Klaus Schmitz-Abe, Davide Tonduti, Luigina Spaccini, Maria Iascone, Casie A. Genetti, Mary K. Koenig, Madeline Graf, Alyssa Tran, Mercedes Alejandro, Undiagnosed Diseases Network, Brendan H. Lee, Isabelle Thiffault, Pankaj B. Agrawal, Jonathan A. Bernstein, Hugo J. Bellen, Hsiao-Tuan Chao
Am J Hum Genet. 2020 Apr 2; 106(4): 570–583. Published online 2020 Mar 19. doi: 10.1016/j.ajhg.2020.02.016
PMCID:
PMC7118694
AbstractArticlePDF–2.0M
8.
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia
Veronika Boczonadi, Juliane S. Müller, Angela Pyle, Jennifer Munkley, Talya Dor, Jade Quartararo, Ileana Ferrero, Veronika Karcagi, Michele Giunta, Tuomo Polvikoski, Daniel Birchall, Agota Princzinger, Yuval Cinnamon, Susanne Lützkendorf, Henriett Piko, Mojgan Reza, Laura Florez, Mauro Santibanez-Koref, Helen Griffin, Markus Schuelke, Orly Elpeleg, Luba Kalaydjieva, Hanns Lochmüller, David J. Elliott, Patrick F. Chinnery, Shimon Edvardson, Rita Horvath
Nat Commun. 2014 Jul 3; 5: 4287. Published online 2014 Jul 3. doi: 10.1038/ncomms5287
PMCID:
PMC4102769
AbstractArticlePDF–5.3M
9.
POLR3A variants with striatal involvement and extrapyramidal movement disorder
Inga Harting, Murtadha Al-Saady, Ingeborg Krägeloh-Mann, Annette Bley, Maja Hempel, Tatjana Bierhals, Stephanie Karch, Ute Moog, Geneviève Bernard, Richard Huntsman, Rosalina M. L. van Spaendonk, Maaike Vreeburg, Agustí Rodríguez-Palmero, Aurora Pujol, Marjo S. van der Knaap, Petra J. W. Pouwels, Nicole I. Wolf
Neurogenetics. 2020; 21(2): 121–133. Published online 2020 Jan 15. doi: 10.1007/s10048-019-00602-4
PMCID:
PMC7064625
AbstractArticlePDF–3.3M
10.
Myelin Gene Expression after Experimental Contusive Spinal Cord Injury
Jean R. Wrathall, Wen Li, Lynn D. Hudson
J Neurosci. 1998 Nov 1; 18(21): 8780–8793. doi: 10.1523/JNEUROSCI.18-21-08780.1998
PMCID:
PMC6793561
AbstractArticlePDF–2.1M
11.
Aberrant Growth and Differentiation of Oligodendrocyte Progenitors in Neurofibromatosis Type 1 Mutants
Michael R. Bennett, Tilat A. Rizvi, Saikumar Karyala, Randall D. McKinnon, Nancy Ratner
J Neurosci. 2003 Aug 6; 23(18): 7207–7217. doi: 10.1523/JNEUROSCI.23-18-07207.2003
PMCID:
PMC6740670
AbstractArticlePDF–491K
12.
Molecular and phenotypic analysis of Attractin mutant mice.
T M Gunn, T Inui, K Kitada, S Ito, K Wakamatsu, L He, D M Bouley, T Serikawa, G S Barsh
Genetics. 2001 Aug; 158(4): 1683–1695. doi: 10.1093/genetics/158.4.1683
PMCID:
PMC1461748
SummaryPDF–429K
13.
Myosin Va Controls Oligodendrocyte Morphogenesis and Myelination
Jacob A. Sloane, Timothy K. Vartanian
J Neurosci. 2007 Oct 17; 27(42): 11366–11375. doi: 10.1523/JNEUROSCI.2326-07.2007
PMCID:
PMC6673025
AbstractArticlePDF–21M
14.
FTY720 Improves Behavior, Increases Brain Derived Neurotrophic Factor and Reduces α-Synuclein Pathology in Parkinsonian GM2+/− Mice
Guadalupe Vidal-Martinez, Katherine Najera, Julie D. Miranda, Carolina Gil-Tommee, Barbara Yang, Javier Vargas-Medrano, Valeria Diaz-Pacheco, Ruth G. Perez
Neuroscience. Author manuscript; available in PMC 2020 Jul 15.
Published in final edited form as: Neuroscience. 2019 Jul 15; 411: 1–10. Published online 2019 May 23. doi: 10.1016/j.neuroscience.2019.05.029
PMCID:
PMC6612448
AbstractArticlePDF–1.1M
15.
Identification of a novel de novo p.Phe932Ile KCNT1 mutation in a patient with leukoencephalopathy and severe epilepsy
Adeline Vanderver, Cas Simons, Johanna L. Schmidt, Philip L. Pearl, Miriam Bloom, Bennett Lavenstein, David Miller, Sean M. Grimmond, Ryan J. Taft
Pediatr Neurol. Author manuscript; available in PMC 2015 Jan 22.
Published in final edited form as: Pediatr Neurol. 2014 Jan; 50(1): 112–114. Published online 2013 Oct 10. doi: 10.1016/j.pediatrneurol.2013.06.024
PMCID:
PMC4303471
AbstractArticlePDF–492K
16.
Characterization of a Novel Variant in Siblings with Asparagine Synthetase Deficiency
Stephanie J. Sacharow, Elizabeth E. Dudenhausen, Carrie L. Lomelino, Lance Rodan, Christelle Moufawad El Achkar, Heather E. Olson, Casie A Genetti, Pankaj B. Agrawal, Robert McKenna, Michael S. Kilberg
Mol Genet Metab. Author manuscript; available in PMC 2019 Mar 1.
Published in final edited form as: Mol Genet Metab. 2018 Mar; 123(3): 317–325. Published online 2017 Dec 20. doi: 10.1016/j.ymgme.2017.12.433
PMCID:
PMC5832599
AbstractArticlePDF–944K
17.
GlcNAc6ST-1 regulates sulfation of N-glycans and myelination in the peripheral nervous system
Takeshi Yoshimura, Akiko Hayashi, Mai Handa-Narumi, Hirokazu Yagi, Nobuhiko Ohno, Takako Koike, Yoshihide Yamaguchi, Kenji Uchimura, Kenji Kadomatsu, Jan Sedzik, Kunio Kitamura, Koichi Kato, Bruce D. Trapp, Hiroko Baba, Kazuhiro Ikenaka
Sci Rep. 2017; 7: 42257. Published online 2017 Feb 10. doi: 10.1038/srep42257
PMCID:
PMC5301494
AbstractArticlePDF–2.0M
18.
Diffusion-Weighted and Conventional MR Imaging Findings of Neuroaxonal Dystrophy
R. Nuri Sener
AJNR Am J Neuroradiol. 2004 Aug; 25(7): 1269–1273.
PMCID:
PMC7976545
AbstractArticlePDF–296K
19.
Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria
Julien L Marcadier, Amanda M Smith, Daniela Pohl, Jeremy Schwartzentruber, Osama Y Al-Dirbashi, Jacek Majewski, Sacha Ferdinandusse, Ronald JA Wanders, Dennis E Bulman, Kym M Boycott, Pranesh Chakraborty, Michael T Geraghty
Orphanet J Rare Dis. 2013; 8: 98. Published online 2013 Jul 9. doi: 10.1186/1750-1172-8-98
PMCID:
PMC3710243
AbstractArticlePDF–692K
20.
Oligodendrocyte Regeneration after Neonatal Hypoxia Requires FoxO1-Mediated p27Kip1 Expression
Beata Jablonska, Joseph Scafidi, Adan Aguirre, Flora Vaccarino, Vien Nguyen, Erzsebet Borok, Tamas L. Horvath, David H. Rowitch, Vittorio Gallo
J Neurosci. 2012 Oct 17; 32(42): 14775–14793. doi: 10.1523/JNEUROSCI.2060-12.2012
PMCID:
PMC3517297
AbstractArticlePDF–12M

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