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List of works by Muriel Davisson

A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice

scientific article published in March 2002

A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis

scientific article

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

scientific article

A mouse model for Meckel syndrome type 3.

scientific article published on 11 February 2009

A spontaneous mutation in contactin 1 in the mouse

scientific article

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

scientific article published on 27 June 2006

Age exacerbates abnormal protein expression in a mouse model of Down syndrome

scientific article published on 10 May 2017

Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene

scientific journal article

Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis

scientific article (publication date: June 2002)

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

scientific article

Behavioral, cognitive and biochemical responses to different environmental conditions in male Ts65Dn mice, a model of Down syndrome

scientific article published in September 2005

Building protein interaction maps for Down's syndrome

scientific article published in August 2004

Centralized mouse repositories

scientific article published on 04 September 2012

Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.

scientific article

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

scientific article published in August 2002

Discovery Genetics - The History and Future of Spontaneous Mutation Research

scientific article

Discovery genetics: serendipity in basic research

scientific article

Editing of the serotonin 2C receptor pre-mRNA: Effects of the Morris Water Maze

scientific article published on 12 January 2007

Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

scientific journal article

FIMRe: Federation of International Mouse Resources: global networking of resource centers

scientific article published in May 2006

Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10

scientific article

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

scientific article published on 24 October 2011

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

scientific article published on April 2015

Know thy mouse

scientific article published on 26 September 2006

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

scientific article published on January 25, 2012

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

scientific article published on April 24, 2013

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

scientific article

Mouse model of subretinal neovascularization with choroidal anastomosis

scientific article published in August 2003

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

scientific article published on October 30, 2003

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

scientific journal article

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

scientific article

Operant conditioning in the Ts65Dn mouse: learning

scientific article published in January 2004

Otitis media in a mouse model for Down syndrome

scientific article

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

scientific article published in December 2003

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).

scientific article

Strategies for managing an ever increasing mutant mouse repository

scientific article

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

scientific journal article

The Mouse Congenital Polycystic Kidney (cpk) Locus Maps within 1.3 cM of the Chromosome 12 Marker D12Nyu2

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

scientific article published in November 2002

The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentials

scientific article

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

scientific article

Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic mice

scientific journal article

VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse

scientific article

ZFP191 is required by oligodendrocytes for CNS myelination

scientific journal article

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