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., Barinaga-Rementeria Ramirez, I., 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