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Neuroscience and Biobehavioral Reviews
|
March 6, 2014
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action
Francesco Bedogni, Riccardo L Rossi, Francesco Galli, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
January 20, 2018
Lack of Methyl-CpG Binding Protein 2 (MeCP2) Affects Cell Fate Refinement During Embryonic Cortical Development
Clementina Cobolli Gigli, Linda Scaramuzza, Marco De Simone, et al.
Plos One
|
April 21, 2016
MeCP2 Related Studies Benefit from the Use of CD1 as Genetic Background
Clementina Cobolli Gigli, Linda Scaramuzza, Anna Gandaglia, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
May 17, 2015
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms
Francesco Bedogni, Clementina Cobolli Gigli, Davide Pozzi, et al.
The Journal of Biological Chemistry
|
December 21, 2014
Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization
Anna Bergo, Marta Strollo, Marta Gai, et al.
Genes & Development
|
March 17, 2023
Pioneer factor ASCL1 cooperates with the mSWI/SNF complex at distal regulatory elements to regulate human neural differentiation
Oana Păun, Yu Xuan Tan, Harshil Patel, et al.
EMBO Molecular Medicine
|
March 5, 2021
The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes
Linda Scaramuzza, Giuseppina De Rocco, Genni Desiato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2026
Multimodal Genotype-Phenotype Analysis in SMARCB1-Associated Developmental Disorders
Ramy Saad, Clementina Cobolli Gigli, Pleuntje J van der Sluijs, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Neuroscience and Biobehavioral Reviews
|
March 6, 2014
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action
Francesco Bedogni, Riccardo L Rossi, Francesco Galli, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
January 20, 2018
Lack of Methyl-CpG Binding Protein 2 (MeCP2) Affects Cell Fate Refinement During Embryonic Cortical Development
Clementina Cobolli Gigli, Linda Scaramuzza, Marco De Simone, et al.
Plos One
|
April 21, 2016
MeCP2 Related Studies Benefit from the Use of CD1 as Genetic Background
Clementina Cobolli Gigli, Linda Scaramuzza, Anna Gandaglia, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
May 17, 2015
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms
Francesco Bedogni, Clementina Cobolli Gigli, Davide Pozzi, et al.
The Journal of Biological Chemistry
|
December 21, 2014
Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization
Anna Bergo, Marta Strollo, Marta Gai, et al.
Genes & Development
|
March 17, 2023
Pioneer factor ASCL1 cooperates with the mSWI/SNF complex at distal regulatory elements to regulate human neural differentiation
Oana Păun, Yu Xuan Tan, Harshil Patel, et al.
EMBO Molecular Medicine
|
March 5, 2021
The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes
Linda Scaramuzza, Giuseppina De Rocco, Genni Desiato, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2026
Multimodal Genotype-Phenotype Analysis in SMARCB1-Associated Developmental Disorders
Ramy Saad, Clementina Cobolli Gigli, Pleuntje J van der Sluijs, et al.
Page
of 1