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Frontiers in Cell and Developmental Biology
|
March 6, 2023
MAPping tubulin mutations
Thomas D Cushion, Ines Leca, David A Keays
Scientific Reports
|
January 21, 2023
Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice
Ines Leca, Alexander William Phillips, Lyubov Ushakova, et al.
Molecular and Cellular Neurosciences
|
March 29, 2017
Tubulins and brain development - The origins of functional specification
Martin W Breuss, Ines Leca, Thomas Gstrein, et al.
Plos Genetics
|
November 2, 2020
A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse
Ines Leca, Alexander William Phillips, Iris Hofer, et al.
Human Molecular Genetics
|
December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Nature Neuroscience
|
June 8, 2018
Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans
Thomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
Nature Neuroscience
|
January 10, 2018
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans
Thomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
The Journal of Experimental Medicine
|
August 10, 2022
Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder
Fabian M P Kaiser, Sarah Gruenbacher, Maria Roa Oyaga, et al.
Neuron
|
November 20, 2018
Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations
Ratna Tripathy, Ines Leca, Tessa van Dijk, et al.
Page
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Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Frontiers in Cell and Developmental Biology
|
March 6, 2023
MAPping tubulin mutations
Thomas D Cushion, Ines Leca, David A Keays
Scientific Reports
|
January 21, 2023
Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice
Ines Leca, Alexander William Phillips, Lyubov Ushakova, et al.
Molecular and Cellular Neurosciences
|
March 29, 2017
Tubulins and brain development - The origins of functional specification
Martin W Breuss, Ines Leca, Thomas Gstrein, et al.
Plos Genetics
|
November 2, 2020
A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse
Ines Leca, Alexander William Phillips, Iris Hofer, et al.
Human Molecular Genetics
|
December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
Martin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.
Nature Neuroscience
|
June 8, 2018
Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans
Thomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
Nature Neuroscience
|
January 10, 2018
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans
Thomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
The Journal of Experimental Medicine
|
August 10, 2022
Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder
Fabian M P Kaiser, Sarah Gruenbacher, Maria Roa Oyaga, et al.
Neuron
|
November 20, 2018
Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations
Ratna Tripathy, Ines Leca, Tessa van Dijk, et al.
Page
of 1