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Mental retardation in Down syndrome: From gene dosage imbalance to molecular and cellular mechanisms

Neuroscience research, 2007-12, Vol.59 (4), p.349-369

2007

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Mental retardation and associated neurological dysfunctions in Down syndrome: A consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways

European journal of paediatric neurology, 2008-05, Vol.12 (3), p.168-182

2008

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Molecular and Cellular Mechanisms Elucidating Neurocognitive Basis of Functional Impairments Associated with Intellectual Disability in Down Syndrome

American journal on intellectual and developmental disabilities, 2010-03, Vol.115 (2), p.83-112

2010

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Insights into the genetic makeup of French Polynesian peripheral populations of the small giant clam Tridacna maxima

Aquatic conservation, 2023-12, Vol.33 (12), p.1514-1534

2023

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Expression of the Mnb (dyrk) Protein in Adult and Embryonic Mouse Tissues

Biochemical and biophysical research communications, 1998-12, Vol.253 (2), p.514-518

1998

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A quantitative assessment of gene expression (QAGE) reveals differential overexpression of DOPEY2, a candidate gene for mental retardation, in Down syndrome brain regions

International journal of developmental neuroscience, 2009-06, Vol.27 (4), p.393-398

2009

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New cerebellar phenotypes in YAC transgenic mouse in vivo library of human Down syndrome critical region-1

Biochemical and biophysical research communications, 2007-12, Vol.364 (3), p.488-494

2007

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Differential transcription of Barhl1 homeobox gene in restricted functional domains of the central nervous system suggests a role in brain patterning

International journal of developmental neuroscience, 2006-02, Vol.24 (1), p.35-44

2006

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Spatial and temporal localization during embryonic and fetal human development of the transcription factor SIM2 in brain regions altered in Down syndrome

International journal of developmental neuroscience, 2005-08, Vol.23 (5), p.475-484

2005

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C21orf5, a new member of Dopey family involved in morphogenesis, could participate in neurological alterations and mental retardation in Down syndrome

DNA research, 2005, Vol.12 (3), p.203-210

2005

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BARHL1 homeogene, the human ortholog of the mouse Barhl1 involved in cerebellum development, shows regional and cellular specificities in restricted domains of developing human central nervous system

Biochemical and biophysical research communications, 2006-01, Vol.339 (1), p.296-304

2006

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The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice

Biochemical and biophysical research communications, 2003-06, Vol.305 (4), p.915-924

2003

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Erratum to “The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice” [Biochem. Biophys. Res. Commun. 305 (2003) 915–924]

Biochemical and biophysical research communications, 2003-12, Vol.312 (3), p.865-865

2003

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Erratum to “The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice” [Biochem. Biophys. Res. Commun. 305 (2003) 915–924]

Biochemical and biophysical research communications, 2003-08, Vol.307 (3), p.758-758

2003

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Down Syndrome-Critical Region Contains a Gene Homologous to Drosophila sim Expressed During Rat and Human Central Nervous System Development

Proceedings of the National Academy of Sciences - PNAS, 1995-09, Vol.92 (20), p.9191-9195

1995

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Characterization of the dCaMKII-GAL4 driver line whose expression is controlled by the Drosophila Ca 2+ /calmodulin-dependent protein kinase II promoter

Cell and tissue research, 2002-11, Vol.310 (2), p.237-252

2002

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The CASK/Lin-2 Drosophila Homologue, Camguk, Could Play a Role in Epithelial Patterning and in Neuronal Targeting

Biochemical and biophysical research communications, 2001-06, Vol.284 (4), p.1004-1010

2001

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Characterization of the dCaMKII-GAL4 driver line whose expression is controlled by the Drosophila Ca2+/calmodulin-dependent protein kinase II promoter

Cell and tissue research, 2002-11, Vol.310 (2), p.237-252

2002

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An integrated YAC-overlap and ‘cosmid-pocket’ map of the human chromosome 21

Human molecular genetics, 1994-05, Vol.3 (5), p.759-770

1994

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Dynamic expression pattern of Ca(2+)/calmodulin-dependent protein kinase II gene in the central nervous system of Drosophila throughout development

Biochemical and biophysical research communications, 1999-07, Vol.260 (3), p.707-711

1999

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Genetical analysis ofvisual system disorganizer (vid), a new gene involved in normal development of eye and optic lobe of the brain inDrosophila melanogaster

Genetica, 1997-02, Vol.99 (1), p.31-45

1997

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Dynamic Expression Pattern of Ca2+/Calmodulin-Dependent Protein Kinase II Gene in the Central Nervous System of Drosophila throughout Development

Biochemical and biophysical research communications, 1999-07, Vol.260 (3), p.707-711

1999

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Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome

Genomics (San Diego, Calif.), 1998-02, Vol.48 (1), p.12-23

1998

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Saúde mental e qualidade de vida dos estudantes de faculdades de medicina brasileiras: uma revisão integrativa

Revista Eletrônica Acervo Saúde, 2021-06, Vol.13 (6), p.e6953

2021

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Genetical analysis of visual system disorganizer (vid), a new gene involved in normal development of eye and optic lobe of the brain in Drosophila melanogaster

Genetica, 1997-01, Vol.99 (1), p.31-45

1997

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Mental retardation in Down syndrome: From gene dosage imbalance to molecular and cellular mechanisms

Mental retardation and associated neurological dysfunctions in Down syndrome: A consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways

Molecular and Cellular Mechanisms Elucidating Neurocognitive Basis of Functional Impairments Associated with Intellectual Disability in Down Syndrome

Insights into the genetic makeup of French Polynesian peripheral populations of the small giant clam Tridacna maxima

Expression of the Mnb (dyrk) Protein in Adult and Embryonic Mouse Tissues

A quantitative assessment of gene expression (QAGE) reveals differential overexpression of DOPEY2, a candidate gene for mental retardation, in Down syndrome brain regions

New cerebellar phenotypes in YAC transgenic mouse in vivo library of human Down syndrome critical region-1

Differential transcription of Barhl1 homeobox gene in restricted functional domains of the central nervous system suggests a role in brain patterning

Spatial and temporal localization during embryonic and fetal human development of the transcription factor SIM2 in brain regions altered in Down syndrome

C21orf5, a new member of Dopey family involved in morphogenesis, could participate in neurological alterations and mental retardation in Down syndrome

BARHL1 homeogene, the human ortholog of the mouse Barhl1 involved in cerebellum development, shows regional and cellular specificities in restricted domains of developing human central nervous system

The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice

Erratum to “The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice” [Biochem. Biophys. Res. Commun. 305 (2003) 915–924]

Erratum to “The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice” [Biochem. Biophys. Res. Commun. 305 (2003) 915–924]

Down Syndrome-Critical Region Contains a Gene Homologous to Drosophila sim Expressed During Rat and Human Central Nervous System Development

Characterization of the dCaMKII-GAL4 driver line whose expression is controlled by the Drosophila Ca 2+ /calmodulin-dependent protein kinase II promoter

The CASK/Lin-2 Drosophila Homologue, Camguk, Could Play a Role in Epithelial Patterning and in Neuronal Targeting

Characterization of the dCaMKII-GAL4 driver line whose expression is controlled by the Drosophila Ca2+/calmodulin-dependent protein kinase II promoter

An integrated YAC-overlap and ‘cosmid-pocket’ map of the human chromosome 21

Dynamic expression pattern of Ca(2+)/calmodulin-dependent protein kinase II gene in the central nervous system of Drosophila throughout development

Genetical analysis ofvisual system disorganizer (vid), a new gene involved in normal development of eye and optic lobe of the brain inDrosophila melanogaster

Dynamic Expression Pattern of Ca2+/Calmodulin-Dependent Protein Kinase II Gene in the Central Nervous System of Drosophila throughout Development

Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome

Saúde mental e qualidade de vida dos estudantes de faculdades de medicina brasileiras: uma revisão integrativa

Genetical analysis of visual system disorganizer (vid), a new gene involved in normal development of eye and optic lobe of the brain in Drosophila melanogaster

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