loss of function allele for murine Staufen1 leads to impairment of dendritic Staufen1-RNP delivery and dendritic spine morphogenesis
Vessey, John P, Macchi, Paolo, Stein, Joel M, Mikl, Martin, Hawker, Kelvin N, Vogelsang, Petra, Wieczorek, Krzysztof, Vendra, Georgia, Riefler, Julia, Tübing, Fabian, Aparicio, Samuel A.J, Abel, Ted, Kiebler, Michael A
Published in Proceedings of the National Academy of Sciences - PNAS (21.10.2008)
Published in Proceedings of the National Academy of Sciences - PNAS (21.10.2008)
Get full text
Journal Article
Disproportionate language impairment in children using cochlear implants
Hawker, Kelvin, Ramirez-Inscoe, Jayne, Bishop, Dorothy V M, Twomey, Tracey, O'Donoghue, Gerard M, Moore, David R
Published in Ear and hearing (01.06.2008)
Published in Ear and hearing (01.06.2008)
Get more information
Journal Article
Organization of the Fugu rubripes Hox clusters: evidence for continuing evolution of vertebrate Hox complexes
Aparicio, Samuel, Hawker, Kelvin, Cottage, Amanda, Mikawa, Yoshikazu, Zuo, Lin, Venkatesh, Byrappa, Chen, Elson, Krumlauf, Robb, Brenner, Sydney
Published in Nature genetics (01.05.1997)
Published in Nature genetics (01.05.1997)
Get full text
Journal Article
Imprinted Expression of Neuronatin from Modified BAC Transgenes Reveals Regulation by Distinct and Distant Enhancers
John, Rosalind M., Aparicio, Samuel A.J.R., Ainscough, Justin F-X., Arney, Katharine L., Khosla, Sanjeev, Hawker, Kelvin, Hilton, Kathy J., Barton, Sheila C., Surani, M.Azim
Published in Developmental biology (15.08.2001)
Published in Developmental biology (15.08.2001)
Get full text
Journal Article
The PufferfishSLP-1Gene, a New Member of theSCL/TAL-1Family of Transcription Factors
Göttgens, Berthold, Gilbert, James G.R, Barton, Linda M, Aparicio, Samuel, Hawker, Kelvin, Mistry, Shailesh, Vaudin, Mark, King, Andrew, Bentley, David, Elgar, Greg, Green, Anthony R
Published in Genomics (San Diego, Calif.) (01.02.1998)
Published in Genomics (San Diego, Calif.) (01.02.1998)
Get full text
Journal Article
A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice
Calvert, Jennifer A., Dedos, Skarlatos G., Hawker, Kelvin, Fleming, Michelle, Lewis, Morag A., Steel, Karen P.
Published in Mammalian genome (01.06.2011)
Published in Mammalian genome (01.06.2011)
Get full text
Journal Article
Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4 Dos nuevos ratones mutantes con defectos vestibulares hallados en el altamente mutable locus del cromosoma 4
Hawker, Kelvin, Fuchs, Helmut, Angelis, Martin Hrabéde, Steel, Karen P.
Published in International journal of food sciences and nutrition (01.03.2005)
Published in International journal of food sciences and nutrition (01.03.2005)
Get full text
Journal Article
The pufferfish SLP-1 gene, a new member of the SCL/TAL-1 family of transcription factors
GÖTTGENS, B, GILBERT, J. G. R, GREEN, A. R, BARTON, L. M, APARICIO, S, HAWKER, K, MISTRY, S, VAUDIN, M, KING, A, BENTLEY, D, ELGAR, G
Published in Genomics (San Diego, Calif.) (15.02.1998)
Published in Genomics (San Diego, Calif.) (15.02.1998)
Get full text
Journal Article
Evolution of plasminogen-related growth factors (HGF/SF and HGF1/MSP)
Gherardi, E, Gonzalez Manzano, R, Cottage, A, Hawker, K, Aparicio, S
Published in Ciba Foundation symposium (1997)
Get more information
Published in Ciba Foundation symposium (1997)
Journal Article