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Thomas D Cushion

Showing results (1-10 of 16) with videos related to

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Frontiers in Cell and Developmental Biology|March 6, 2023
MAPping tubulin mutationsThomas D Cushion, Ines Leca, David A Keays
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 28, 2014
The genetics of lissencephalyAndrew E Fry, Thomas D Cushion, Daniela T Pilz
European Journal of Medical Genetics|July 18, 2018
Tubulin genes and malformations of cortical developmentRomina Romaniello, Filippo Arrigoni, Andrew E Fry, et al.
Brain : a Journal of Neurology|September 14, 2013
Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delayRhys H Thomas, Seo-Kyung Chung, Sian E Wood, et al.
American Journal of Human Genetics|April 8, 2014
De novo mutations in the beta-tubulin gene TUBB2A cause simplified gyral patterning and infantile-onset epilepsyThomas D Cushion, Alex R Paciorkowski, Daniela T Pilz, et al.
Human Molecular Genetics|May 15, 2010
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulinsRavinesh A Kumar, Daniela T Pilz, Timothy D Babatz, et al.
Brain : a Journal of Neurology|January 31, 2013
Overlapping cortical malformations and mutations in TUBB2B and TUBA1AThomas D Cushion, William B Dobyns, Jonathan G L Mullins, et al.
Human Molecular Genetics|July 2, 2015
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genesRenske Oegema, Thomas D Cushion, Ian G Phelps, et al.
Neurobiology of Disease|January 11, 2014
A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypesAnn J Johnston, Jing-Qiong Kang, Wangzhen Shen, et al.
Science Advances|August 28, 2020
The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensorTobias Hochstoeger, Tarek Al Said, Dante Maestre, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Frontiers in Cell and Developmental Biology|March 6, 2023
MAPping tubulin mutationsThomas D Cushion, Ines Leca, David A Keays
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 28, 2014
The genetics of lissencephalyAndrew E Fry, Thomas D Cushion, Daniela T Pilz
European Journal of Medical Genetics|July 18, 2018
Tubulin genes and malformations of cortical developmentRomina Romaniello, Filippo Arrigoni, Andrew E Fry, et al.
Brain : a Journal of Neurology|September 14, 2013
Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delayRhys H Thomas, Seo-Kyung Chung, Sian E Wood, et al.
American Journal of Human Genetics|April 8, 2014
De novo mutations in the beta-tubulin gene TUBB2A cause simplified gyral patterning and infantile-onset epilepsyThomas D Cushion, Alex R Paciorkowski, Daniela T Pilz, et al.
Human Molecular Genetics|May 15, 2010
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulinsRavinesh A Kumar, Daniela T Pilz, Timothy D Babatz, et al.
Brain : a Journal of Neurology|January 31, 2013
Overlapping cortical malformations and mutations in TUBB2B and TUBA1AThomas D Cushion, William B Dobyns, Jonathan G L Mullins, et al.
Human Molecular Genetics|July 2, 2015
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genesRenske Oegema, Thomas D Cushion, Ian G Phelps, et al.
Neurobiology of Disease|January 11, 2014
A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypesAnn J Johnston, Jing-Qiong Kang, Wangzhen Shen, et al.
Science Advances|August 28, 2020
The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensorTobias Hochstoeger, Tarek Al Said, Dante Maestre, et al.
Pageof 2