All papers authored by Victor Hernandez
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Marian Seda ,
Emma Peskett,
Naila Haq ,
Avishek Prasai,
Georg Otto ,
Jeshmi Jeyabalan Srikaran ,
Victor Hernandez ,
Gaurav D. Diwan,
Robert B. Russell ,
Marius Ueffing ,
Martina Huranova
and 3 other authors
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Andrew W. Stoker,
Dagan Jenkins
Download from www.karger.com
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Julie Kennedy,
Robin van der Lee,
Erik de Vrieze,
Kirsten A. Wunderlich ,
Suzanne Rix,
Gerard W. Dougherty,
Nils J. Lambacher,
Chunmei Li,
Victor L. Jensen,
Michael R. Leroux,
Rim Hjeij,
Nicola Horn,
Yves Texier ,
Yasmin Wissinger
and 33 other authors
CiliaCarta: An Integrated And Validated Compendium Of Ciliary Genes
Download from doi.org
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Angela Brady,
Dagan Jenkins,
Jenny Morton,
Soren W. Hansen,
Chiara Bacchelli,
Philip L. Beales,
Victor Hernandez-Hernandez
COLEC10 is mutated in 3MC patients and regulates early craniofacial development
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Advances in the understanding of the BBSome complex structure and function
Download from dx.doi.org
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Rm Roccasecca,
Fiona McMurray,
Victor Hernandez-Hernandez ,
Sriparna Mukherjee,
Inês Barroso,
Derek Stemple,
Roger Cox,
Pl Beales,
Sonia Christou-Savina
Download from doi.org
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Priyanka Pravincumar,
Anna Diaz-Font,
Helen May-Simera,
Dagan Jenkins,
Martin Knight,
Philip L. Beales
Bardet–Biedl syndrome proteins control the cilia length through regulation of actin polymerization
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Kayalvizhi Madhivanan,
Debarati Mukherjee,
Cb B. Hanna,
Irene Barinaga-Rementeria Ramirez,
Martin Lowe,
Philip L. Beales,
Rc Claudio Aguilar,
R. Claudio Aguilar,
Hernandez V Madhivanan K Mukherjee D Hanna CB Barinaga-Rementeria Ramirez I Lowe M Beales PL Aguilar R.-C. Coon Bg
The Lowe syndrome protein OCRL1 is involved in primary cilia assembly
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H. Shamseldin,
J. Kenny,
A. Waters,
D. Jenkins,
Aa Kaissi,
Gf Leal
and 15 other authors
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Elyes Chabchoub,
Victor Hernandez-Hernandez ,
Hanan Shamseldin,
Joanna Kenny,
Aoife Waters,
Dagan Jenkins,
A. Al Kaissi,
Ali Al Kaissi,
Gf Leal,
Bruno Dallapiccola,
Franco Carnevale,
Maria Bitner-Glindzicz
and 7 other authors
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome
Download from www.ncbi.nlm.nih.gov
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Victor Hernández Hernández; David Bueno,
David Bueno
Dorsal view of a flattened isthmus hybridised with the riboprobe 24 h after plasmids electroporation
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Victor Hernández Hernández; David Bueno,
David Bueno
Embryos co-electroporated with a pool of DIG-labelled siRNAs and the pEGFP-C2 plasmid
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David Bueno
Transversal sections of the neural tube at the isthmus level
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J. Kenny,
D. Jenkins,
A. Al Kaissi,
G. Leal,
C; Diaz-Foint A; Osborn D; Chabchoub E; Hernandez-Hernandez V; Shamselding H; Kenny J; Waters A; Jenkins D; Al Kaissi A; Leal G; Dallapiccola B; Carnavale F; Bitner-Glindzicz M; Lees M; Hennekam R; Stanier F; Burns A; Peeters Hilde; U0035066; Alkrakya F; B Rooryck,
B. Dallapiccola,
F. Carnavale,
M. Bitner-Glindzicz
and 6 other authors
Mutations in lectin complement pathway genes COLEC11 and MASO1 cause 3MC syndrome
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