Dr Victor Hernandez
Senior Lecturer in Biomedical Sciences
Heinz Wolff 226
- Email: victor.hernandez@brunel.ac.uk
- Tel: +44 (0)1895 267635
Freke, GM., Martins, T., Davies, RJ., Beyer, T., Seda, M., Peskett, E., et al. (2023) 'De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of Bbs1'. Cells, 12 (22). pp. 1 - 21. ISSN: 2073-4409 Open Access Link
Gupta, S., Dovey, OM., Domingues, AF., Cyran, OW., Cash, CM., Giotopoulos, G., et al. (2022) 'Transcriptional variability accelerates pre-leukemia by cell diversification and perturbation of protein synthesis'. Science advances, 8 (31). pp. 1 - 15. ISSN: 2375-2548 Open Access Link
Gupta, S., Dovey, OM., Domingues, AF., Cyran, OW., Cash, CM., Giotopoulos, G., et al. (2021) 'Transcriptional variability accelerates pre-leukemia by cell diversification and 2 perturbation of protein synthesis'. biorXiv.Open Access Link
van Dam, MA., Kennedy, J., van der Lee, R., de Vrieze, E., Wunderlich, KA., Rix, S., et al. (2019) 'CiliaCarta: An integrated and validated compendium of ciliary genes'. PLOS ONE, 14 (5). pp. e0216705 - e0216705. ISSN: 1932-6203 Open Access Link
Kretschmer, V., Patnaik, SR., Kretschmer, F., Chawda, MM., Hernandez-Hernandez, V. and May-Simera, HL. (2019) 'Progressive Characterization of Visual Phenotype in Bardet-Biedl Syndrome Mutant Mice'. Investigative Ophthalmology & Visual Science, 60 (4). pp. 1132 - 1143. ISSN: 1552-5783 Open Access Link
Seda, M., Geerlings, M., Lim, P., Jeyabalan-Srikaran, J., Cichon, A-C., Scambler, PJ., et al. (2018) 'An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis'. Molecular Syndromology, 10 (1-2). pp. 98 - 114. ISSN: 1661-8769 Open Access Link
Munye, MM., Diaz-Font, A., Ocaka, L., Henriksen, ML., Lees, M., Brady, A., et al. (2017) 'COLEC10 is mutated in 3MC patients and regulates early craniofacial development'. PLoS Genetics, 13 (3). pp. 1 - 15. ISSN: 1553-7390 Open Access Link
Hernandez-Hernandez, V. and Jenkins, D. (2015) 'Advances in the understanding of the BBSome complex structure and function'. Research and Reports in Biology, 2015 (6). pp. 191 - 201. ISSN: 1179-7274 Open Access Link
Osborn, DPS., Roccasecca, RM., McMurray, F., Hernandez-Hernandez, V., Mukherjee, S., Barroso, I., et al. (2014) 'Loss of FTO Antagonises Wnt Signaling and Leads to Developmental Defects Associated with Ciliopathies'. PLoS ONE, 9 (2). pp. e87662 - e87662. ISSN: 1932-6203 Open Access Link
Hernandez-Hernandez, V., Pravincumar, P., Diaz-Font, A., May-Simera, H., Jenkins, D., Knight, M. and et al. (2013) 'Bardet–Biedl syndrome proteins control the cilia length through regulation of actin polymerization'. Human Molecular Genetics, 22 (19). pp. 3858 - 3868. ISSN: 0964-6906 Open Access Link
Hernandez, V., Pravincumar, P., Diaz-Font, A., May-Simera, H., Jenkins, D., Knight, M. and et al. (2012) 'Bardet-Biedl syndrome proteins control cilia length through regulation of actin polymerisation'. Cilia, 1 (S1). pp. P88 - P88. ISSN: 2046-2530
Hernandez, V., Coon, BG., Madhivanan, K., Mukherjee, D., Hanna, CB., Barinaga-Rementeria Ramirez, I., et al. (2012) 'The Lowe syndrome protein OCRL1 is involved in primary cilia assembly'. Cilia, 1 (S1). pp. P87 - P87. ISSN: 2046-2530
Coon, BG., Hernandez, V., Madhivanan, K., Mukherjee, D., Hanna, CB., Ramirez, IBR., et al. (2012) 'The lowe syndrome protein OCRL1 is involved in primary cilia assembly'. Human Molecular Genetics, 21 (8). pp. 1835 - 1847. ISSN: 0964-6906
Rooryck, C., Diaz-Font, A., Osborn, DPS., Chabchoub, E., Hernandez-Hernandez, V., Shamseldin, H., et al. (2011) 'Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome'. Nature Genetics, 43 (3). pp. 197 - 203. ISSN: 1061-4036 Open Access Link
Bueno, D., Fernàndez-Rodríguez, J., Cardona, A., Hernàndez-Hernàndez, V. and Romero, R. (2002) 'A Novel Invertebrate Trophic Factor Related to Invertebrate Neurotrophins Is Involved in Planarian Body Regional Survival and Asexual Reproduction'. Developmental Biology, 252 (2). pp. 188 - 201. ISSN: 0012-1606