• 2571 Citations
19962019
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Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

Ligands Medicine & Life Sciences
Proteins Medicine & Life Sciences
Transcription Factors Medicine & Life Sciences
DNA Medicine & Life Sciences
Mutation Medicine & Life Sciences
Early Growth Response Protein 1 Medicine & Life Sciences
Nitrogen Isotopes Medicine & Life Sciences
Carbon Isotopes Medicine & Life Sciences

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

Projects 2008 2014

Dimerization
DNA
Phosphotransferases
Consensus Sequence
Neoplasms

Research Output 1996 2019

  • 2571 Citations
  • 89 Article
  • 1 Comment/debate

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

Li, C., Bademci, G., Subasioglu, A., Diaz-Horta, O., Zhu, Y., Liu, J., Mitchell, T. G., Abad, C., Seyhan, S., Duman, D., Cengiz, F. B., Tokgoz-Yilmaz, S., Blanton, S. H., Farooq, A., Walz, K., Zhai, R. G. & Tekin, M., Jan 22 2019, In : Proceedings of the National Academy of Sciences of the United States of America. 116, 4, p. 1347-1352 6 p.

Research output: Contribution to journalArticle

GRB2 Adaptor Protein
Sensorineural Hearing Loss
Phosphotransferases
Proteins
Auditory Hair Cells

Erratum: SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency (Brain (2018) 141 (662-672) DOI: 10.1093/brain/awx369)

Rebelo, A., Dimah, S., Pereira, C., Farooq, A., Huff, T., Abreu, L., Moraes, C. T., Mnatsakanova, D., Mathews, K., Yang, H., Schon, E., Zuchner, S. L. & Shy, M., Apr 1 2018, In : Brain. 141, 4, e32.

Research output: Contribution to journalComment/debate

Charcot-Marie-Tooth Disease
Names
Copper
Mutation
Brain
6 Citations (Scopus)

SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency

Rebelo, A. P., Saade, D., Pereira, C. V., Farooq, A., Huff, T. C., Abreu, L., Moraes, C. T., Mnatsakanova, D., Mathews, K., Yang, H., Schon, E. A., Zuchner, S. L. & Shy, M. E., Mar 1 2018, In : Brain. 141, 3, p. 662-672 11 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Copper
Mutation
Oxidoreductases
Polyneuropathies
3 Citations (Scopus)

Characterization of ATPase activity of P2RX2 cation channel

Mittal, R., Grati, M., Sedlacek, M., Yuan, F., Chang, Q., Yan, D., Lin, X., Kachar, B., Farooq, A., Chapagain, P., Zhang, Y. & Liu, X. Z., 2016, In : Frontiers in Physiology. 7, MAY, 186.

Research output: Contribution to journalArticle

Adenosine Triphosphatases
Cations
Adenosine Triphosphate
Ion Channel Gating
Hydrolysis
7 Citations (Scopus)

Phosphorylation of Tyr188 in the WW domain of YAP1 plays an essential role in YAP1-induced cellular transformation

Li, Y. W., Guo, J., Shen, H., Li, J., Yang, N., Frangou, C., Wilson, K. E., Zhang, Y., Mussell, A. L., Sudol, M., Farooq, A., Qu, J. & Zhang, J., Sep 16 2016, In : Cell Cycle. 15, 18, p. 2497-2505 9 p.

Research output: Contribution to journalArticle

Phosphorylation
Tyrosine
Cell Proliferation
Epithelial-Mesenchymal Transition
Serine