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J Gault

Showing results (21-30 of 35) with videos related to

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Restorative Neurology and Neuroscience|April 3, 2003
Nicotinic receptors, smoking and schizophreniaS Leonard, J Gault, C Adams, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 11, 2014
Cholesteatoma has a high prevalence in Turner syndrome, highlighting the need for earlier diagnosis and the potential benefits of otoscopy training for paediatriciansD B N Lim, E J Gault, H Kubba, et al.
Nature Structural & Molecular Biology|May 10, 2011
Nemo kinase phosphorylates β-catenin to promote ommatidial rotation and connects core PCP factors to E-cadherin-β-cateninIvana Mirkovic, William J Gault, Maryam Rahnama, et al.
European Journal of Pharmacology|April 20, 2000
Smoking and schizophrenia: abnormal nicotinic receptor expressionS Leonard, C Breese, C Adams, et al.
American Journal of Human Genetics|January 1, 1993
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragmentJ Zonana, J Gault, K J Davies, et al.
Circulation|January 1, 1978
Cryoablation of drug-resistant ventricular tachycardia in a patient with a variant of sclerodermaJ J Gallagher, R W Anderson, J Kasell, et al.
Human Molecular Genetics|October 1, 1993
Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA)N S Thomas, J Chelly, J Zonana, et al.
Molecular and Cellular Biology|September 16, 2003
Puralpha is essential for postnatal brain development and developmentally coupled cellular proliferation as revealed by genetic inactivation in the mouseKamel Khalili, Luis Del Valle, Vandhana Muralidharan, et al.
Human Molecular Genetics|October 14, 2008
Phosphatase-defective LEOPARD syndrome mutations in PTPN11 gene have gain-of-function effects during Drosophila developmentKimihiko Oishi, Hui Zhang, William J Gault, et al.
American Journal of Medical Genetics|May 17, 2000
Inhibitory neurophysiological deficit as a phenotype for genetic investigation of schizophreniaR Freedman, C E Adams, L E Adler, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Restorative Neurology and Neuroscience|April 3, 2003
Nicotinic receptors, smoking and schizophreniaS Leonard, J Gault, C Adams, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 11, 2014
Cholesteatoma has a high prevalence in Turner syndrome, highlighting the need for earlier diagnosis and the potential benefits of otoscopy training for paediatriciansD B N Lim, E J Gault, H Kubba, et al.
Nature Structural & Molecular Biology|May 10, 2011
Nemo kinase phosphorylates β-catenin to promote ommatidial rotation and connects core PCP factors to E-cadherin-β-cateninIvana Mirkovic, William J Gault, Maryam Rahnama, et al.
European Journal of Pharmacology|April 20, 2000
Smoking and schizophrenia: abnormal nicotinic receptor expressionS Leonard, C Breese, C Adams, et al.
American Journal of Human Genetics|January 1, 1993
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragmentJ Zonana, J Gault, K J Davies, et al.
Circulation|January 1, 1978
Cryoablation of drug-resistant ventricular tachycardia in a patient with a variant of sclerodermaJ J Gallagher, R W Anderson, J Kasell, et al.
Human Molecular Genetics|October 1, 1993
Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA)N S Thomas, J Chelly, J Zonana, et al.
Molecular and Cellular Biology|September 16, 2003
Puralpha is essential for postnatal brain development and developmentally coupled cellular proliferation as revealed by genetic inactivation in the mouseKamel Khalili, Luis Del Valle, Vandhana Muralidharan, et al.
Human Molecular Genetics|October 14, 2008
Phosphatase-defective LEOPARD syndrome mutations in PTPN11 gene have gain-of-function effects during Drosophila developmentKimihiko Oishi, Hui Zhang, William J Gault, et al.
American Journal of Medical Genetics|May 17, 2000
Inhibitory neurophysiological deficit as a phenotype for genetic investigation of schizophreniaR Freedman, C E Adams, L E Adler, et al.
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