ROCK2 is a major regulator of axonal degeneration, neuronal death and axonal regeneration in the CNS

Por Koch, J C, Tönges, L, Barski, E, Michel, U, Bähr, M, Lingor, P
Publicado em 2014

Pain and quality of life in leprosy patients in an endemic area of Northeast Brazil: a cross-sectional study

Por Santos, Victor S., Santana, Jamilly C. V., Castro, Fabrícia D. N., Oliveira, Laudice S., Santana, Julianne C. V., Feitosa, Vera L. C., Gurgel, Ricardo Q., Cuevas, Luis E.
Publicado no Infect Dis Poverty (2016)

Bioinformatics Data Mining Approach Suggests Coexpression of AGTPBP1 with an ALS-linked Gene C9orf72

Por Kitano, Shouta, Kino, Yoshihiro, Yamamoto, Yoji, Takitani, Mika, Miyoshi, Junko, Ishida, Tsuyoshi, Saito, Yuko, Arima, Kunimasa, Satoh, Jun-ichi
Publicado no J Cent Nerv Syst Dis (2015)

Association of brain-derived neurotrophic factor and nerve growth factor gene polymorphisms with susceptibility to migraine

Por Coskun, Salih, Varol, Sefer, Ozdemir, Hasan H, Agacayak, Elif, Aydın, Birsen, Kapan, Oktay, Camkurt, Mehmet Akif, Tunc, Saban, Cevik, Mehmet Ugur
Publicado no Neuropsychiatr Dis Treat (2016)

Characterization of skin function associated with obesity and specific correlation to local/systemic parameters in American women

Por Mori, Shinobu, Shiraishi, Akiko, Epplen, Karen, Butcher, Desiree, Murase, Daiki, Yasuda, Yuka, Murase, Takatoshi
Publicado no Lipids Health Dis (2017)

Myasthenia gravis

Por Juel, Vern C, Massey, Janice M
Publicado em 2007

JNK2 and JNK3 are major regulators of axonal injury-induced retinal ganglion cell death

Por Fernandes, Kimberly A., Harder, Jeffrey M., Fornarola, Laura B, Freeman, Robert S, Clark, Abbot F., Pang, Iok-Hou, John, Simon W.M., Libby, Richard T.
Publicado em 2012

Molecular Network Analysis Suggests a Logical Hypothesis for the Pathological Role of C9orf72 in Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

Por Satoh, Jun-ichi, Yamamoto, Yoji, Kitano, Shouta, Takitani, Mika, Asahina, Naohiro, Kino, Yoshihiro
Publicado em 2014

S113R mutation in SLC33A1 leads to neurodegeneration and augmented BMP signaling in a mouse model

Por Liu, Pingting, Jiang, Baichun, Ma, Jian, Lin, Pengfei, Zhang, Yinshuai, Shao, Changshun, Sun, Wenjie, Gong, Yaoqin
Publicado no Dis Model Mech (2017)

Mechanisms of multiple neurotransmitters in the effects of Lycopene on brain injury induced by Hyperlipidemia

Por Yang, Weichun, Shen, Ziyi, Wen, Sixian, Wang, Wei, Hu, Minyu
Publicado no Lipids Health Dis (2018)

Dynamin-related protein 1 is required for normal mitochondrial bioenergetic and synaptic function in CA1 hippocampal neurons

Por Shields, L Y, Kim, H, Zhu, L, Haddad, D, Berthet, A, Pathak, D, Lam, M, Ponnusamy, R, Diaz-Ramirez, L G, Gill, T M, Sesaki, H, Mucke, L, Nakamura, K
Publicado no Cell Death Dis (2015)

Dock3 protects myelin in the cuprizone model for demyelination

Por Namekata, K, Kimura, A, Harada, C, Yoshida, H, Matsumoto, Y, Harada, T
Publicado no Cell Death Dis (2014)

Late infantile metachromatic leukodystrophy: Clinical manifestations of five Taiwanese patients and Genetic features in Asia

Por Liaw, Hsiang-Ru, Lee, Hsiu-Fen, Chi, Ching-Shiang, Tsai, Chi-Ren
Publicado no Orphanet J Rare Dis (2015)

Selective cognitive and psychiatric manifestations in Wolfram Syndrome

Por Bischoff, Allison N., Reiersen, Angela M., Buttlaire, Anna, Al-lozi, Amal, Doty, Tasha, Marshall, Bess A., Hershey, Tamara
Publicado no Orphanet J Rare Dis (2015)

Visual evoked potentials of Niemann-Pick type C1 mice reveal an impairment of the visual pathway that is rescued by 2-hydroxypropyl-ß-cyclodextrin

Por Palladino, Giampiero, Loizzo, Stefano, Fortuna, Andrea, Canterini, Sonia, Palombi, Fioretta, Erickson, Robert P., Mangia, Franco, Fiorenza, Maria Teresa
Publicado no Orphanet J Rare Dis (2015)

Longitudinal hearing loss in Wolfram syndrome

Por Karzon, Roanne, Narayanan, Anagha, Chen, Ling, Lieu, Judith E. C., Hershey, Tamara
Publicado no Orphanet J Rare Dis (2018)

Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy

Por Leruez, Stéphanie, Verny, Christophe, Bonneau, Dominique, Procaccio, Vincent, Lenaers, Guy, Amati-Bonneau, Patrizia, Reynier, Pascal, Scherer, Clarisse, Prundean, Adriana, Orssaud, Christophe, Zanlonghi, Xavier, Rougier, Marie-Bénédicte, Tilikete, Caroline, Miléa, Dan
Publicado no Orphanet J Rare Dis (2018)

The p38α mitogen-activated protein kinase is a key regulator of myelination and remyelination in the CNS

Por Chung, S-H, Biswas, S, Selvaraj, V, Liu, X-B, Sohn, J, Jiang, P, Chen, C, Chmilewsky, F, Marzban, H, Horiuchi, M, Pleasure, D E, Deng, W
Publicado no Cell Death Dis (2015)

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

Por McMillan, Hugh J., Telegrafi, Aida, Singleton, Amanda, Cho, Megan T., Lelli, Daniel, Lynn, Francis C., Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E., Koolen, David A., Haaxma, Charlotte A., Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J., Henderson, Lindsay B., McLaughlin, Heather, Molday, Laurie L., Molday, Robert S., Yoon, Grace
Publicado no Orphanet J Rare Dis (2018)