Fingerprint Fingerprint is based on mining the text of the persons scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 10 Similar Profiles
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Neurons Medicine & Life Sciences
Mutation Medicine & Life Sciences
Transgenic Mice Medicine & Life Sciences
Mutant Proteins Medicine & Life Sciences
TDP-43 Proteinopathies Medicine & Life Sciences
Poisons Medicine & Life Sciences
Proteolysis Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Grants 2013 2022

Research Output 1997 2018

  • 1312 Citations
  • 18 h-Index
  • 28 Article
  • 3 Review article
  • 1 Comment/debate
  • 1 Short survey

Overexpression of a conserved HSP40 chaperone reduces toxicity of several neurodegenerative disease proteins

Park, S. K., Arslan, F., Kanneganti, V., Barmada, S. J., Purushothaman, P., Verma, S. C. & Liebman, S. W. Jan 30 2018 (Accepted/In press) In : Prion. p. 1-7 7 p.

Research output: Contribution to journalArticle

Neurodegenerative diseases
Neurodegenerative Diseases
Proteasome Endopeptidase Complex

TDP43 and RNA instability in amyotrophic lateral sclerosis

Weskamp, K. & Barmada, S. J. Jan 1 2018 (Accepted/In press) In : Brain Research.

Research output: Contribution to journalArticle

RNA Stability
Amyotrophic Lateral Sclerosis
Nuclear RNA

The ubiquitin conjugating enzyme Ube2W regulates solubility of the Huntington's disease protein, huntingtin

Wang, B., Zeng, L., Merillat, S. A., Fischer, S., Ochaba, J., Thompson, L. M., Barmada, S. J., Scaglione, K. M. & Paulson, H. L. Jan 1 2018 In : Neurobiology of Disease. 109, p. 127-136 10 p.

Research output: Contribution to journalArticle

Ubiquitin-Conjugating Enzymes
Huntington Disease

Inhibition of PIP4Kγ ameliorates the pathological effects of mutant huntingtin protein

Al-Ramahi, I., Giridharan, S. S. P., Chen, Y. C., Patnaik, S., Safren, N., Hasegawa, J., de Haro, M., Gee, A. K. W., Titus, S. A., Jeong, H., Clarke, J., Krainc, D., Zheng, W., Irvine, R. F., Barmada, S., Ferrer, M., Southall, N., Weisman, L. S., Botas, J. & Marugan, J. J. Dec 26 2017 In : eLife. 6, e29123

Research output: Contribution to journalArticle

Huntington Disease
Mutant Proteins

Overexpression of the essential Sis1 chaperone reduces TDP-43 effects on toxicity and proteolysis

Park, S. K., Hong, J. Y., Arslan, F., Kanneganti, V., Patel, B., Tietsort, A., Tank, E. M. H., Li, X., Barmada, S. J. & Liebman, S. W. May 1 2017 In : PLoS Genetics. 13, 5, e1006805

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Cell Shape