Projects per year
Fingerprint Dive into the research topics where Amjad Farooq is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
Ligands
Medicine & Life Sciences
Proteins
Medicine & Life Sciences
Mutation
Medicine & Life Sciences
Transcription Factors
Medicine & Life Sciences
DNA
Medicine & Life Sciences
Early Growth Response Protein 1
Medicine & Life Sciences
Calorimetry
Medicine & Life Sciences
Thermodynamics
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
Interplay between HGAL and Grb2 proteins regulates B-cell receptor signaling
Jiang, X., Lu, X., Zhang, Y., Lacaria, L., Schuchardt, B. J., Mikles, D. C., Magistri, M., García-Ramírez, I., Sanchez-Garcia, I., Farooq, A., Verdun, R. E., Abdulreda, M. H., Moy, V. T. & Lossos, I. S., Aug 13 2019, In : Blood Advances. 3, 15, p. 2286-2297 12 p.Research output: Contribution to journal › Article
Open Access
GRB2 Adaptor Protein
B-Lymphocytes
Germinal Center
Binding Sites
Phosphopeptides
Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss
Diaz-Horta, O., Bademci, G., Tokgoz-Yilmaz, S., Guo, S., Zafeer, F., Sineni, C. J., Duman, D., Farooq, A. & Tekin, M., Jan 1 2019, (Accepted/In press) In : Clinical Genetics.Research output: Contribution to journal › Article
Stereocilia
Hearing Loss
Mutation
Actins
Auditory Perception
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., Mnatsakanova, D., Mathews, K., Yang, H., Schon, E., Zuchner, S. & 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
12
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