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3 Publications
2017 |
Published |
Journal Article |
IST-REx-ID: 1016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
M. Breuss, T. Nguyen, A. Srivatsan, I. Leca, G. Tian, T. Fritz, A.H. Hansen, D. Musaev, J. Mcevoy Venneri, J. Kiely, R. Rosti, E. Scott, U. Tan, R. Kolodner, N. Cowan, D. Keays, J. Gleeson, Human Molecular Genetics 26 (2017) 258–269.
View
| DOI
| WoS
M. Breuss, T. Nguyen, A. Srivatsan, I. Leca, G. Tian, T. Fritz, A.H. Hansen, D. Musaev, J. Mcevoy Venneri, J. Kiely, R. Rosti, E. Scott, U. Tan, R. Kolodner, N. Cowan, D. Keays, J. Gleeson, Human Molecular Genetics 26 (2017) 258–269.
2003 |
Published |
Journal Article |
IST-REx-ID: 847
Impact of selection, mutation rate and genetic drift on human genetic variation
S. Sunyaev, F. Kondrashov, P. Bork, V. Ramensky, Human Molecular Genetics 12 (2003) 3325–3330.
View
| DOI
| PubMed | Europe PMC
S. Sunyaev, F. Kondrashov, P. Bork, V. Ramensky, Human Molecular Genetics 12 (2003) 3325–3330.
2001 |
Published |
Journal Article |
IST-REx-ID: 867
Origin of alternative splicing by tandem exon duplication
F. Kondrashov, E. Koonin, Human Molecular Genetics 10 (2001) 2661–2669.
[Published Version]
View
| DOI
| PubMed | Europe PMC
F. Kondrashov, E. Koonin, Human Molecular Genetics 10 (2001) 2661–2669.