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Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

Nature, 2006-09, Vol.443 (7107), p.50-55

2006

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Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn

Mammalian genome, 2011-12, Vol.22 (11-12), p.685-691

2011

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Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (27), p.9415-9420

2008

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Loss of Correlations among Proteins in Brains of the Ts65Dn Mouse Model of Down Syndrome

Journal of proteome research, 2012-02, Vol.11 (2), p.1251-1263

2012

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Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

American journal of human genetics, 2001-11, Vol.69 (5), p.981-988

2001

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Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (44), p.18108-18113

2011

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Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

Nature genetics, 1997-05, Vol.16 (1), p.19-27

1997

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Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome

Behavioural brain research, 2002-08, Vol.134 (1), p.185-200

2002

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A spontaneous mutation in contactin 1 in the mouse

PloS one, 2011-12, Vol.6 (12), p.e29538-e29538

2011

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Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse

Genomics (San Diego, Calif.), 2006-05, Vol.87 (5), p.673-677

2006

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Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome

BioTechniques, 2003-12, Vol.35 (6), p.1170-1180

2003

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Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice

Nature genetics, 1999-04, Vol.21 (4), p.405-409

1999

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A-to-I pre-mRNA editing of the serotonin 2C receptor: Comparisons among inbred mouse strains

Gene, 2006-11, Vol.382, p.39-46

2006

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Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice

Nature genetics, 2006-02, Vol.38 (2), p.245-250

2006

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Age Exacerbates Abnormal Protein Expression in a Mouse Model of Down Syndrome

Neurobiology of aging, 2017-09, Vol.57, p.120-132

2017

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A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers

Kidney international, 2014-06, Vol.85 (6), p.1461-1468

2014

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Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease

Human molecular genetics, 2013-09, Vol.22 (17), p.3397-3414

2013

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A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis

Journal of bone and mineral research, 2003-09, Vol.18 (9), p.1612-1621

2003

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The effects of piracetam on cognitive performance in a mouse model of Down's syndrome

Physiology & behavior, 2002-11, Vol.77 (2), p.403-409

2002

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Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

Gene, 2003-10, Vol.318, p.137-147

2003

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Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1)

Behavioural brain research, 2010-01, Vol.206 (1), p.52

2010

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Love at First Site

BioTechniques, 2003-10, Vol.35 (4), p.651-651

Davisson, Muriel T

2003

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New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice

Mammalian genome, 2004-03, Vol.15 (3), p.151-161

2004

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Chromosomal inversion discovered in C3H/HeJ mice

Genomics (San Diego, Calif.), 2006-02, Vol.87 (2), p.311-313

2006

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Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis

American journal of physiology. Renal physiology, 2015-06, Vol.308 (12), p.F1335-F1342

2015

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Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn

Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome

Loss of Correlations among Proteins in Brains of the Ts65Dn Mouse Model of Down Syndrome

Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse

Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome

A spontaneous mutation in contactin 1 in the mouse

Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse

Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice

A-to-I pre-mRNA editing of the serotonin 2C receptor: Comparisons among inbred mouse strains

Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice

Age Exacerbates Abnormal Protein Expression in a Mouse Model of Down Syndrome

A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers

Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease

A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis

The effects of piracetam on cognitive performance in a mouse model of Down's syndrome

Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1)

Love at First Site

New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice

Chromosomal inversion discovered in C3H/HeJ mice

Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis

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