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Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice

The Journal of neuroscience, 2005-12, Vol.25 (50), p.11521-11530

2005

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Parent-of-origin allelic contributions to deiodinase-3 expression elicit localized hyperthyroid milieu in the hippocampus

Molecular psychiatry, 2011-08, Vol.16 (8), p.786-787

2011

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Excess folate during adolescence suppresses thyroid function with permanent deficits in motivation and spatial memory

Genes, brain and behavior, 2012-03, Vol.11 (2), p.193-200

2012

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Xist has properties of the X-chromosome inactivation centre

Nature (London), 1997-03, Vol.386 (6622), p.272-275

1997

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The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression

American journal of human genetics, 2001-06, Vol.68 (6), p.1501-1505

2001

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Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11– q13 duplications

Human molecular genetics, 2002-07, Vol.11 (15), p.1707-1718

2002

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Mutation screening and transmission disequilibrium study of ATP10C in autism

American journal of medical genetics, 2002-03, Vol.114 (2), p.137-143

2002

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Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts

American journal of human genetics, 1993-12, Vol.53 (6), p.1206-1216

1993

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Construction of specific cosmids from YACs by homologous recombination in yeast

Nucleic acids research, 1995-10, Vol.23 (19), p.4005-4006

1995

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Novel lacZ-based recombination vectors for mammalian cells

Gene, 1993-12, Vol.137 (2), p.163-169

1993

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Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice

Parent-of-origin allelic contributions to deiodinase-3 expression elicit localized hyperthyroid milieu in the hippocampus

Excess folate during adolescence suppresses thyroid function with permanent deficits in motivation and spatial memory

Xist has properties of the X-chromosome inactivation centre

The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11– q13 duplications

Mutation screening and transmission disequilibrium study of ATP10C in autism

Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts

Construction of specific cosmids from YACs by homologous recombination in yeast

Novel lacZ-based recombination vectors for mammalian cells

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