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Ines Leca

Showing results (1-10 of 9) 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
Scientific Reports|January 21, 2023
Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in miceInes Leca, Alexander William Phillips, Lyubov Ushakova, et al.
Molecular and Cellular Neurosciences|March 29, 2017
Tubulins and brain development - The origins of functional specificationMartin 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 mouseInes 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 stabilityMartin 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 humansThomas 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 humansThomas 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 disorderFabian 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 MalformationsRatna Tripathy, Ines Leca, Tessa van Dijk, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Frontiers in Cell and Developmental Biology|March 6, 2023
MAPping tubulin mutationsThomas 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 miceInes Leca, Alexander William Phillips, Lyubov Ushakova, et al.
Molecular and Cellular Neurosciences|March 29, 2017
Tubulins and brain development - The origins of functional specificationMartin 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 mouseInes 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 stabilityMartin 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 humansThomas 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 humansThomas 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 disorderFabian 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 MalformationsRatna Tripathy, Ines Leca, Tessa van Dijk, et al.
Pageof 1