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Biomedicines
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December 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, et al.
Nucleic Acids Research
|
March 20, 2018
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome
Giovanni Iacono, Aline Dubos, Hamid Méziane, et al.
Scientific Reports
|
January 3, 2024
The Rogdi knockout mouse is a model for Kohlschütter-Tönz syndrome
Alexandra Jimenez-Armijo, Supawich Morkmued, José Tomás Ahumada, et al.
Plos Genetics
|
September 29, 2021
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome
Véronique Brault, Thu Lan Nguyen, Javier Flores-Gutiérrez, et al.
Genome Biology
|
November 16, 2023
Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein
Perrine F Kretz, Christel Wagner, Anna Mikhaleva, et al.
Human Molecular Genetics
|
April 17, 2018
A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterations
Aline Dubos, Hamid Meziane, Giovanni Iacono, et al.
Plos One
|
December 24, 2010
Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse F2 intercross
Jonathan M J Derry, Hua Zhong, Cliona Molony, et al.
Current Protocols
|
June 17, 2026
Standardized Pipeline for Metabolism and Cognition in GO-DS21 Mouse Model: Investigating Down Syndrome Comorbidities
Mohammed Selloum, Patricia da Silva-Buttkus, Fabrice Riet, et al.
Human Molecular Genetics
|
September 18, 2015
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration
Aline Dubos, Anna Castells-Nobau, Hamid Meziane, et al.
Plos Genetics
|
July 14, 2017
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition
Thomas Arbogast, Giovanni Iacono, Claire Chevalier, et al.
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Search research articles
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Showing results (11-20 of 37) with videos related to
Sort By:
Page
of 4
Biomedicines
|
December 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, et al.
Nucleic Acids Research
|
March 20, 2018
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome
Giovanni Iacono, Aline Dubos, Hamid Méziane, et al.
Scientific Reports
|
January 3, 2024
The Rogdi knockout mouse is a model for Kohlschütter-Tönz syndrome
Alexandra Jimenez-Armijo, Supawich Morkmued, José Tomás Ahumada, et al.
Plos Genetics
|
September 29, 2021
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome
Véronique Brault, Thu Lan Nguyen, Javier Flores-Gutiérrez, et al.
Genome Biology
|
November 16, 2023
Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein
Perrine F Kretz, Christel Wagner, Anna Mikhaleva, et al.
Human Molecular Genetics
|
April 17, 2018
A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterations
Aline Dubos, Hamid Meziane, Giovanni Iacono, et al.
Plos One
|
December 24, 2010
Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse F2 intercross
Jonathan M J Derry, Hua Zhong, Cliona Molony, et al.
Current Protocols
|
June 17, 2026
Standardized Pipeline for Metabolism and Cognition in GO-DS21 Mouse Model: Investigating Down Syndrome Comorbidities
Mohammed Selloum, Patricia da Silva-Buttkus, Fabrice Riet, et al.
Human Molecular Genetics
|
September 18, 2015
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration
Aline Dubos, Anna Castells-Nobau, Hamid Meziane, et al.
Plos Genetics
|
July 14, 2017
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition
Thomas Arbogast, Giovanni Iacono, Claire Chevalier, et al.
Page
of 4