Bilaketaren emaitzak - Kelly Springell
- Erakusten 1 - 8 emaitzak -- 8
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1
The molecular landscape of ASPM mutations in primary microcephaly nork Adeline K. Nicholas, Eric A. Swanson, James J. Cox, Gulshan Karbani, Sabreena Malik, Kelly Springell, Daniel J. Hampshire, M Ahmed, Jacquelyn Bond, Daniela Benedetto, Marco Fichera, Corrado Romano, William B. Dobyns, C. Geoffrey Woods
Argitaratua 2008Artigo -
2
Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome nork C. Geoffrey Woods, Sigmar Stricker, Petra Seemann, Rowena Stern, James J. Cox, E. Sherridan, Emma Roberts, Kelly Springell, Simon Scott, Gulshan Karbani, Saghira Malik Sharif, Carmel Toomes, Jacquelyn Bond, Dheeraj Kumar, Lihadh Al‐Gazali, Stefan Mundlos
Argitaratua 2006Artigo -
3
Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease nork C. Geoffrey Woods, James J. Cox, Kelly Springell, Daniel J. Hampshire, Moin Mohamed, Martin McKibbin, Rowena Stern, F. Lucy Raymond, Richard Sandford, Saghira Malik Sharif, Gulshan Karbani, Mustaq Ahmed, Jacquelyn Bond, David Clayton, Chris F. Inglehearn
Argitaratua 2006Artigo -
4
Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia nork Mohammad Reza Abdollahi, Ewan E. Morrison, Tamara Sirey, Zoltán Molnár, Bruce E. Hayward, Ian Carr, Kelly Springell, C. Geoff Woods, Mushtaq Ahmed, Louise Hattingh, Peter Corry, Daniela T. Pilz, Neil Stoodley, Yanick J. Crow, Graham R. Taylor, David T. Bonthron, Eamonn Sheridan
Argitaratua 2009Artigo -
5
Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size nork Jacquelyn Bond, Sheila Scott, Daniel J. Hampshire, Kelly Springell, Peter Corry, Marc Abramowicz, Ganeshwaran H. Mochida, Raoul C. M. Hennekam, Eamonn R. Maher, Jean‐Pierre Fryns, Abdulrahman Alswaid, Hussain Jafri, Yasmin Abdul Rashid, Ammar F. Mubaidin, Christopher A. Walsh, Emma Roberts, C. Geoffrey Woods
Argitaratua 2003Artigo -
6
An SCN9A channelopathy causes congenital inability to experience pain nork James J. Cox, Frank Reimann, Adeline K. Nicholas, Gemma Thornton, Emma Roberts, Kelly Springell, Gulshan Karbani, Hussain Jafri, Jovaria Mannan, Yasmin Raashid, Lihadh Al‐Gazali, Henan Hamamy, Enza Maria Valente, Shaun Gorman, Richard Williams, Duncan P. McHale, John N. Wood, Fiona M. Gribble, C. Geoffrey Woods
Argitaratua 2006Artigo -
7
The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis nork Mehmet Bakırcıoğlu, Ofélia P. Carvalho, Maryam Khurshid, James J. Cox, Beyhan Tüysüz, Tanyeri Barak, Saliha Yılmaz, Ahmet Okay Çağlayan, Alp Di̇nçer, Adeline K. Nicholas, Oliver Quarrell, Kelly Springell, Gulshan Karbani, Saghira Malik, Caroline Gannon, Eamonn Sheridan, Moira Crosier, Steven Lisgo, Susan Lindsay, Kaya Bilgüvar, Fanni Gergely, Murat Günel, C. Geoffrey Woods
Argitaratua 2011Artigo -
8
Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice nork David Parry, Carmel Toomes, L. Bida, Michael Danciger, Katherine V. Towns, Martin McKibbin, Samuel G. Jacobson, Clare V. Logan, Manir Ali, Jacquelyn Bond, Rebecca K. Chance, Steven Swendeman, Lauren L. Daniele, Kelly Springell, Matthew Adams, Colin A. Johnson, Adam Booth, Hussain Jafri, Yasmin Abdul Rashid, Eyal Banin, Tim M. Strom, Debora B. Farber, Dror Sharon, Carl Blobel, Edward N. Pugh, Eric A. Pierce, Chris F. Inglehearn
Argitaratua 2009Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Biology
Genetics
Gene
Medicine
Anatomy
Mutation
Neuroscience
Phenotype
Cell biology
Pathology
Archaeology
Autosomal recessive inheritance
Biochemistry
Channelopathy
Chemistry
Consanguineous Marriage
Consanguinity
Disease
Disease gene identification
Dystrophy
Epilepsy
Exome sequencing
Exon
Frameshift mutation
G alpha subunit
Genetic heterogeneity
Genotype
Geometry
HEK 293 cells
Heterozygote advantage