Abbink, Truus E.M.
Emma Kinderziekenhuis · Amsterdam Neuroscience · Amsterdam University Medical Centers · Vrije Universiteit Amsterdam
6 papers on CoChatORCID 0000-0001-6932-0449
Most cited papers
- Verified
A novel long distance base-pairing interaction in human immunodeficiency virus type 1 RNA occludes the Gag start codon
Abbink, T. E. M., & Berkhout, B. (2003) · Journal of Biological Chemistry
RNA and protein synthesis mechanismsHIV Research and Treatment
Cited by 203
- Verified
The HIV-1 leader RNA conformational switch regulates RNA dimerization but does not regulate mRNA translation
Abbink, T. E. M., Ooms, M., Haasnoot, P. C. J., & Berkhout, B. (2005) · Biochemistry
RNA and protein synthesis mechanismsHIV Research and Treatment
Cited by 122
- Verified
Cathepsin A–related arteriopathy with strokes and leukoencephalopathy (CARASAL)
Bugiani, M., Kevelam, S. H., Bakels, H. S., Waisfisz, Q., Ceuterick-de Groote, C., Niessen, H. W. M., Abbink, T. E. M., Lesnik Oberstein, S. A. M. J., & van der Knaap, M. S. (2016) · Neurology
Cerebrovascular and genetic disordersMetabolism and Genetic Disorders
Cited by 111
- Verified
Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy
van Berge, L., Hamilton, E. M., Linnankivi, T., Uziel, G., Steenweg, M. E., Isohanni, P., Wolf, N. I., Krageloh-Mann, I., Brautaset, N. J., Andrews, P. I., et al. (2014) · Brain
Metabolism and Genetic DisordersMitochondrial Function and Pathology
Cited by 109
- Verified
Evidence that the endosomal sorting complex required for transport-II (ESCRT-II) is required for efficient human immunodeficiency virus-1 (HIV-1) production
Meng, B., Ip, N. C. Y., Prestwood, L. J., Abbink, T. E. M., & Lever, A. M. L. (2015) · Retrovirology
HIV Research and TreatmentCellular transport and secretion
Cited by 65
- Verified
Genome sequencing in persistently unsolved white matter disorders
Helman, G., Lajoie, B. R., Crawford, J., Takanohashi, A., Walkiewicz, M., Dolzhenko, E., Gross, A. M., Gainullin, V. G., Bent, S. J., Jenkinson, E. M., et al. (2020) · Annals of Clinical and Translational Neurology
Genomics and Rare DiseasesHereditary Neurological Disorders
Cited by 39
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free