Projects per year
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
- 1 Finished
Structural and Functional Studies of the Novel DBD Domain of MKP5
8/1/08 → 5/31/14
Project: Research project
Dimerization
DNA
Phosphotransferases
Consensus Sequence
Neoplasms
Research Output 1996 2019
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 journal › Article
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 journal › Comment/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 journal › Article
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 journal › Article
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 journal › Article
Phosphorylation
Tyrosine
Cell Proliferation
Epithelial-Mesenchymal Transition
Serine