214 related articles for article (PubMed ID: 22762947)
1. Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations.
Sako W; Ito H; Yoshida M; Koizumi H; Kamada M; Fujita K; Hashizume Y; Izumi Y; Kaji R
Clin Neuropathol; 2012; 31(6):418-23. PubMed ID: 22762947
[TBL] [Abstract][Full Text] [Related]
2. [Inflammatory mechanisms in amyotrophic lateral sclerosis].
Fujita K; Izumi Y; Kaji R
Brain Nerve; 2012 Mar; 64(3):273-8. PubMed ID: 22402721
[TBL] [Abstract][Full Text] [Related]
3. Optineurin suppression causes neuronal cell death via NF-κB pathway.
Akizuki M; Yamashita H; Uemura K; Maruyama H; Kawakami H; Ito H; Takahashi R
J Neurochem; 2013 Sep; 126(6):699-704. PubMed ID: 23721573
[TBL] [Abstract][Full Text] [Related]
4. Activation of signal transducer and activator of transcription-3 in the spinal cord of sporadic amyotrophic lateral sclerosis patients.
Shibata N; Kakita A; Takahashi H; Ihara Y; Nobukuni K; Fujimura H; Sakoda S; Sasaki S; Iwata M; Morikawa S; Hirano A; Kobayashi M
Neurodegener Dis; 2009; 6(3):118-26. PubMed ID: 19372705
[TBL] [Abstract][Full Text] [Related]
5. Sodium phenylbutyrate prolongs survival and regulates expression of anti-apoptotic genes in transgenic amyotrophic lateral sclerosis mice.
Ryu H; Smith K; Camelo SI; Carreras I; Lee J; Iglesias AH; Dangond F; Cormier KA; Cudkowicz ME; Brown RH; Ferrante RJ
J Neurochem; 2005 Jun; 93(5):1087-98. PubMed ID: 15934930
[TBL] [Abstract][Full Text] [Related]
6. Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients.
van Blitterswijk M; van Vught PW; van Es MA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 May; 33(5):1016.e1-7. PubMed ID: 21802176
[TBL] [Abstract][Full Text] [Related]
7. Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis.
Nakazawa S; Oikawa D; Ishii R; Ayaki T; Takahashi H; Takeda H; Ishitani R; Kamei K; Takeyoshi I; Kawakami H; Iwai K; Hatada I; Sawasaki T; Ito H; Nureki O; Tokunaga F
Nat Commun; 2016 Aug; 7():12547. PubMed ID: 27552911
[TBL] [Abstract][Full Text] [Related]
8. [Identification of a new causative gene of amyotrophic lateral sclerosis; optineurin].
Maruyama H
Rinsho Shinkeigaku; 2012; 52(1):1-5. PubMed ID: 22260971
[TBL] [Abstract][Full Text] [Related]
9. Mutations of optineurin in amyotrophic lateral sclerosis.
Maruyama H; Morino H; Ito H; Izumi Y; Kato H; Watanabe Y; Kinoshita Y; Kamada M; Nodera H; Suzuki H; Komure O; Matsuura S; Kobatake K; Morimoto N; Abe K; Suzuki N; Aoki M; Kawata A; Hirai T; Kato T; Ogasawara K; Hirano A; Takumi T; Kusaka H; Hagiwara K; Kaji R; Kawakami H
Nature; 2010 May; 465(7295):223-6. PubMed ID: 20428114
[TBL] [Abstract][Full Text] [Related]
10. A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany.
Weishaupt JH; Waibel S; Birve A; Volk AE; Mayer B; Meyer T; Ludolph AC; Andersen PM
Neurobiol Aging; 2013 May; 34(5):1516.e9-15. PubMed ID: 23062601
[TBL] [Abstract][Full Text] [Related]
11. NF-κB deficit in spinal motoneurons in patients with sporadic amyotrophic lateral sclerosis--a pilot study.
Sulejczak D; Chrapusta SJ; Dziewulska D; Rafałowska J
Folia Neuropathol; 2015; 53(4):367-76. PubMed ID: 26785371
[TBL] [Abstract][Full Text] [Related]
12. Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.
Iida A; Hosono N; Sano M; Kamei T; Oshima S; Tokuda T; Nakajima M; Kubo M; Nakamura Y; Ikegawa S
Neurobiol Aging; 2012 Aug; 33(8):1843.e19-24. PubMed ID: 22402017
[TBL] [Abstract][Full Text] [Related]
13. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
Kato S; Funakoshi H; Nakamura T; Kato M; Nakano I; Hirano A; Ohama E
Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786
[TBL] [Abstract][Full Text] [Related]
14. Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model.
Nakamura M; Ito H; Wate R; Nakano S; Hirano A; Kusaka H
Acta Neuropathol; 2008 Mar; 115(3):327-34. PubMed ID: 18210139
[TBL] [Abstract][Full Text] [Related]
15. Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation.
Ito H; Nakamura M; Komure O; Ayaki T; Wate R; Maruyama H; Nakamura Y; Fujita K; Kaneko S; Okamoto Y; Ihara M; Konishi T; Ogasawara K; Hirano A; Kusaka H; Kaji R; Takahashi R; Kawakami H
Acta Neuropathol; 2011 Aug; 122(2):223-9. PubMed ID: 21644038
[TBL] [Abstract][Full Text] [Related]
16. Optineurin and amyotrophic lateral sclerosis.
Maruyama H; Kawakami H
Geriatr Gerontol Int; 2013 Jul; 13(3):528-32. PubMed ID: 23279185
[TBL] [Abstract][Full Text] [Related]
17. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation.
Kamada M; Izumi Y; Ayaki T; Nakamura M; Kagawa S; Kudo E; Sako W; Maruyama H; Nishida Y; Kawakami H; Ito H; Kaji R
Neuropathology; 2014 Feb; 34(1):64-70. PubMed ID: 23889540
[TBL] [Abstract][Full Text] [Related]
18. Persistent cleavage and nuclear translocation of apoptosis-inducing factor in motor neurons in the spinal cord of sporadic amyotrophic lateral sclerosis patients.
Shibata N; Kakita A; Takahashi H; Ihara Y; Nobukuni K; Fujimura H; Sakoda S; Sasaki S; Yamamoto T; Kobayashi M
Acta Neuropathol; 2009 Dec; 118(6):755-62. PubMed ID: 19669652
[TBL] [Abstract][Full Text] [Related]
19. Novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS.
Tümer Z; Bertelsen B; Gredal O; Magyari M; Nielsen KC; Lucamp ; Grønskov K; Brøndum-Nielsen K
Neurobiol Aging; 2012 Jan; 33(1):208.e1-5. PubMed ID: 21852022
[TBL] [Abstract][Full Text] [Related]
20. Survival motor neuron (SMN) protein in the spinal anterior horn cells of patients with sporadic amyotrophic lateral sclerosis.
Piao Y; Hashimoto T; Takahama S; Kakita A; Komori T; Morita T; Takahashi H; Mizutani T; Oyanagi K
Brain Res; 2011 Feb; 1372():152-9. PubMed ID: 21122798
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
