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Select item 36829651.

Oral and Craniofacial Manifestations and Two Novel Missense Mutations of the NTRK1 Gene Identified in the Patient with Congenital Insensitivity to Pain with Anhidrosis

Li Gao, Hao Guo, Nan Ye, Yudi Bai, Xin Liu, Ping Yu, Yang Xue, Shufang Ma, Kewen Wei, Yan Jin, Lingying Wen, Kun Xuan

PLoS One. 2013; 8(6): e66863. Published online 2013 Jun 14. doi: 10.1371/journal.pone.0066863

PMCID:: PMC3682965

Abstract Article PDF–8.9M

Select item 33589212.

Neonatal chimerization with human glial progenitor cells can both remyelinate and rescue the otherwise lethally hypomyelinated shiverer mouse

Martha Windrem, Steve Schanz, Min Guo, Guo-Feng Tian, Vaughn Washco, Nancy Stanwood, Matthew Rasband, Neeta S. Roy, Maiken Nedergaard, Leif A. Havton, Su Wang, Steven A. Goldman

Cell Stem Cell. Author manuscript; available in PMC 2012 May 23.

Published in final edited form as: Cell Stem Cell. 2008 Jun 5; 2(6): 553–565. doi: 10.1016/j.stem.2008.03.020

PMCID:: PMC3358921

Abstract Article PDF–5.4M

Select item 34013603.

Identification of Drug Modulators Targeting Gene-Dosage Disease CMT1A

Sung-Wook Jang, Camila Lopez-Anido, Ryan MacArthur, John Svaren, James Inglese

ACS Chem Biol. Author manuscript; available in PMC 2013 Jul 20.

Published in final edited form as: ACS Chem Biol. 2012 Jul 20; 7(7): 1205–1213. Published online 2012 May 2. doi: 10.1021/cb300048d

PMCID:: PMC3401360

Abstract Article PDF–3.3M

Select item 34480864.

Experimental Alcohol-Related Peripheral Neuropathy: Role of Insulin/IGF Resistance

Van Anh Nguyen, Tran Le, Ming Tong, Michelle Mellion, James Gilchrist, Suzanne M. de la Monte

Nutrients. 2012 Aug; 4(8): 1042–1057. Published online 2012 Aug 17. doi: 10.3390/nu4081042

PMCID:: PMC3448086

Abstract Article PDF–830K

Select item 34848705.

Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development

Jimann Shin, Arun Padmanabhan, Eric D. de Groh, Jeong-Soo Lee, Sam Haidar, Suzanne Dahlberg, Feng Guo, Shuning He, Marc A. Wolman, Michael Granato, Nathan D. Lawson, Scot A. Wolfe, Seok-Hyung Kim, Lilianna Solnica-Krezel, John P. Kanki, Keith L. Ligon, Jonathan A. Epstein, A. Thomas Look

Dis Model Mech. 2012 Nov; 5(6): 881–894. Published online 2012 Jul 5. doi: 10.1242/dmm.009779

PMCID:: PMC3484870

Abstract Article

Select item 35115986.

Gene-Dosage-Dependent Association of DYRK1A with the Cytoskeleton in the Brain and Lymphocytes of Down Syndrome Patients

Karol Dowjat, Tatyana Adayev, Wojciech KaczmarskiPhD, Jerzy Wegiel, Yu-Wen Hwang

J Neuropathol Exp Neurol. Author manuscript; available in PMC 2013 Dec 1.

Published in final edited form as: J Neuropathol Exp Neurol. 2012 Dec; 71(12): 1100–1112. doi: 10.1097/NEN.0b013e31827733c8

PMCID:: PMC3511598

Abstract Article PDF–1.8M

Select item 35438707.

Large Kindred Evaluation of Mitofusin 2 Novel Mutation, Extremes of Neurologic Presentations, and Preserved Nerve Mitochondria

Dr. Christopher J. Klein, Ms. Grace W. Kimmel, Dr. Sean J. Pittock, Ms. JaNean E. Engelstad, Dr. Julie M. Cunningham, Dr. Yanhong Wu, Dr. Peter J. Dyck

Arch Neurol. Author manuscript; available in PMC 2013 Jan 13.

Published in final edited form as: Arch Neurol. 2011 Oct; 68(10): 1295–1302. doi: 10.1001/archneurol.2011.225

PMCID:: PMC3543870

Abstract Article PDF–2.8M

Select item 35482538.

A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease

Paschalis Nicolaou, Carlo Cianchetti, Anna Minaidou, Giovanni Marrosu, Eleni Zamba-Papanicolaou, Lefkos Middleton, Kyproula Christodoulou

Eur J Hum Genet. 2013 Feb; 21(2): 190–194. Published online 2012 Jul 11. doi: 10.1038/ejhg.2012.146

PMCID:: PMC3548253

Abstract Article PDF–949K

Select item 35781599.

Striatal development involves a switch in gene expression networks, followed by a myelination event: implications for neuropsychiatric disease

Gabriela Novak, Theresa Fan, Brian F. O’Dowd, Susan R. George

Synapse. Author manuscript; available in PMC 2014 Apr 1.

Published in final edited form as: Synapse. 2013 Apr; 67(4): 179–188. Published online 2012 Dec 27. doi: 10.1002/syn.21628

PMCID:: PMC3578159

Abstract Article PDF–457K

Select item 358192310.

CFTR-deficient pigs display peripheral nervous system defects at birth

Leah R. Reznikov, Qian Dong, Jeng-Haur Chen, Thomas O. Moninger, Jung Min Park, Yuzhou Zhang, Jianyang Du, Michael S. Hildebrand, Richard J. H. Smith, Christoph O. Randak, David A. Stoltz, Michael J. Welsh

Proc Natl Acad Sci U S A. 2013 Feb 19; 110(8): 3083–3088. Published online 2013 Feb 4. doi: 10.1073/pnas.1222729110

PMCID:: PMC3581923

Abstract Article PDF–1.0M

Select item 364095811.

Peripheral nerve injury is accompanied by chronic transcriptome-wide changes in the mouse prefrontal cortex

Sebastian Alvarado, Maral Tajerian, Magali Millecamps, Mathew Suderman, Laura S Stone, Moshe Szyf

Mol Pain. 2013; 9: 21. Published online 2013 Apr 18. doi: 10.1186/1744-8069-9-21

PMCID:: PMC3640958

Abstract Article PDF–994K

Select item 364609712.

Peptide Mimetic of the S100A4 Protein Modulates Peripheral Nerve Regeneration and Attenuates the Progression of Neuropathy in Myelin Protein P₀ Null Mice

Mihai Moldovan, Volodymyr Pinchenko, Oksana Dmytriyeva, Stanislava Pankratova, Kåre Fugleholm, Jorg Klingelhofer, Elisabeth Bock, Vladimir Berezin, Christian Krarup, Darya Kiryushko

Mol Med. 2013; 19(1): 43–53. Published online 2013 Mar 8. doi: 10.2119/molmed.2012.00248

PMCID:: PMC3646097

Abstract Article PDF–7.6M

Select item 365717513.

Hand weakness in Charcot-Marie-Tooth disease 1X

P.J. Arthur-Farraj, S.M. Murphy, M. Laura, M.P. Lunn, H. Manji, J. Blake, G. Ramdharry, Z. Fox, M.M. Reilly

Neuromuscul Disord. 2012 Jul; 22(7): 622–626. doi: 10.1016/j.nmd.2012.02.008

PMCID:: PMC3657175

Abstract Article

Select item 367835214.

Role of Semaphorin III in the Developing Rodent Trigeminal System

Emel Ulupinar, Akash Datwani, Oded Behar, Hajime Fujisawa, Reha Erzurumlu

Mol Cell Neurosci. Author manuscript; available in PMC 2013 Jun 11.

Published in final edited form as: Mol Cell Neurosci. 1999 Apr; 13(4): 281–292. doi: 10.1006/mcne.1999.0747

PMCID:: PMC3678352

Abstract Article PDF–3.1M

Select item 329315215.

Dual-mode Modulation of Smad Signaling by Smad-interacting Protein Sip1 is Required for Myelination in the CNS

Qinjie Weng, Ying Chen, Haibo Wang, Xiaomei Xu, Bo Yang, Qiaojun He, Weinian Shou, Yan Chen, Yujiro Higashi, Veronique van den Berghe, Eve Seuntjens, Steven G. Kernie, Polina Bukshpun, Elliott H. Sherr, Danny Huylebroeck, Q. Richard Lu

Neuron. Author manuscript; available in PMC 2013 Feb 23.

Published in final edited form as: Neuron. 2012 Feb 23; 73(4): 713–728. doi: 10.1016/j.neuron.2011.12.021

Correction in:: volume 76 on page 462

PMCID:: PMC3293152

Abstract Article PDF–3.3M

Select item 370748616.

NIBP, a Novel NIK and IKKβ-binding Protein That Enhances NF-κB Activation

Wen-Hui Hu, Julie S. Pendergast, Xian-Ming Mo, Roberta Brambilla, Valerie Bracchi-Ricard, Fang Li, Winston M. Walters, Bas Blits, Li He, Sandra M. Schaal, John R. Bethea

J Biol Chem. Author manuscript; available in PMC 2013 Jul 10.

Published in final edited form as: J Biol Chem. 2005 Aug 12; 280(32): 29233–29241. Published online 2005 Jun 10. doi: 10.1074/jbc.M501670200

PMCID:: PMC3707486

Abstract Article PDF–712K

Select item 371836117.

Genetic Deletion of Cadm4 Results in Myelin Abnormalities Resembling Charcot-Marie-Tooth Neuropathy

Neev Golan, Elena Kartvelishvily, Ivo Spiegel, Daniela Salomon, Helena Sabanay, Katya Rechav, Anya Vainshtein, Shahar Frechter, Galia Maik-Rachline, Yael Eshed-Eisenbach, Takashi Momoi, Elior Peles

J Neurosci. 2013 Jul 3; 33(27): 10950–10961. doi: 10.1523/JNEUROSCI.0571-13.2013

PMCID:: PMC3718361

Abstract Article PDF–5.9M

Select item 372815118.

Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

Hyeon Jin Kim, Young Bin Hong, Jin-Mo Park, Yu-Ri Choi, Ye Jin Kim, Bo Ram Yoon, Heasoo Koo, Jeong Hyun Yoo, Sang Beom Kim, Minhwa Park, Ki Wha Chung, Byung-Ok Choi

Orphanet J Rare Dis. 2013; 8: 104. Published online 2013 Jul 12. doi: 10.1186/1750-1172-8-104