Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1995 1
1997 3
1998 1
2003 1
2004 1
2005 1
2020 0
Text availability
Article attribute
Article type
Publication date

Search Results

9 results
Results by year
Filters applied: . Clear all
Page 1
Carboxyfullerenes as neuroprotective agents.
Dugan LL, Turetsky DM, Du C, Lobner D, Wheeler M, Almli CR, Shen CK, Luh TY, Choi DW, Lin TS. Dugan LL, et al. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9434-9. doi: 10.1073/pnas.94.17.9434. Proc Natl Acad Sci U S A. 1997. PMID: 9256500 Free PMC article.
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
Clement AM, Nguyen MD, Roberts EA, Garcia ML, Boillée S, Rule M, McMahon AP, Doucette W, Siwek D, Ferrante RJ, Brown RH Jr, Julien JP, Goldstein LS, Cleveland DW. Clement AM, et al. Science. 2003 Oct 3;302(5642):113-7. doi: 10.1126/science.1086071. Science. 2003. PMID: 14526083 Free article.
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 Jr, Ferrante RJ. Ryu H, et al. J Neurochem. 2005 Jun;93(5):1087-98. doi: 10.1111/j.1471-4159.2005.03077.x. J Neurochem. 2005. PMID: 15934930 Free article.
Molecular signature of late-stage human ALS revealed by expression profiling of postmortem spinal cord gray matter.
Dangond F, Hwang D, Camelo S, Pasinelli P, Frosch MP, Stephanopoulos G, Stephanopoulos G, Brown RH Jr, Gullans SR. Dangond F, et al. Physiol Genomics. 2004 Jan 15;16(2):229-39. doi: 10.1152/physiolgenomics.00087.2001. Physiol Genomics. 2004. PMID: 14645737
A low expressor line of transgenic mice carrying a mutant human Cu,Zn superoxide dismutase (SOD1) gene develops pathological changes that most closely resemble those in human amyotrophic lateral sclerosis.
Dal Canto MC, Gurney ME. Dal Canto MC, et al. Acta Neuropathol. 1997 Jun;93(6):537-50. doi: 10.1007/s004010050650. Acta Neuropathol. 1997. PMID: 9194892
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes.
Bejaoui K, Liu J, McKenna-Yasek D, Le Paslier D, Bossie K, Gilligan DM, Brown RH. Bejaoui K, et al. Neurogenetics. 1998 Mar;1(3):189-96. doi: 10.1007/s100480050028. Neurogenetics. 1998. PMID: 10737122