(Q34578759)

3 August 2017

1 reference

title

The mousetrap: what we can learn when the mouse model does not mimic the human disease (English)

1 reference

3 August 2017

Sarah H Elsea

1

1 reference

PubMed ID

11917158

3 August 2017

Rebecca E Lucas

series ordinal

2

1 reference

3 August 2017

1 January 2002

1 reference

3 August 2017

1 reference

3 August 2017

43

1 reference

3 August 2017

66-79

1 reference

3 August 2017

2

1 reference

A mouse model of galactose-induced cataracts

3 August 2017

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Pathological features of glycogen storage disease type II highlighted in the knockout mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Decelerated rate of dendrite outgrowth from dopaminergic neurons in primary cultures from brains of hypoxanthine phosphoribosyltransferase-deficient knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Generation and characterization of a delta F508 cystic fibrosis mouse model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Porphyrias: animal models and prospects for cellular and gene therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Modelling cystic fibrosis in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Behavioral and neurochemical evaluation of a transgenic mouse model of Lesch-Nyhan syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Molecular genetics of metachromatic leukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Influence of age and strain on striatal dopamine loss in a genetic mouse model of Lesch-Nyhan disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Brain purines in a genetic mouse model of Lesch-Nyhan disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Clinical and metabolic correction of pompe disease by enzyme therapy in acid maltase-deficient quail

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Demonstration that polyol accumulation is responsible for diabetic cataract by the use of transgenic mice expressing the aldose reductase gene in the lens

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Mouse model of GM2 activator deficiency manifests cerebellar pathology and motor impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

A mouse model for X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Complementation of null CF mice with a human CFTR YAC transgene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Hyperuricemia and mental retardation with athetosis and self-mutilation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Clinical Aspects of Adrenoleukodystrophy and Adrenomyeloneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Galactose metabolism in mice with galactose-1-phosphate uridyltransferase deficiency: sucklings and 7-week-old animals fed a high-galactose diet

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Galactose metabolism by the mouse with galactose-1-phosphate uridyltransferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

alpha-Galactosidase A deficient mice: a model of Fabry disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Modulation of disease severity in mice with targeted disruption of the acid alpha-glucosidase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Production of a severe cystic fibrosis mutation in mice by gene targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Sulfatide storage in visceral organs of arylsulfatase A-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

An animal model for cystic fibrosis made by gene targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Targeted disruption of the methionine synthase gene in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Recombinant human alpha-glucosidase from rabbit milk in Pompe patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Purine nucleotide synthesis in lymphoblasts cultured from normal subjects and a patient with Lesch-Nyhan syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Hyperuricemia and urate nephropathy in urate oxidase-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

A mouse model for the delta F508 allele of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FILAR.43.2.66

21 January 2018

Identifiers

DOI

10.1093/ILAR.43.2.66

1 reference

3 August 2017

1 reference

PubMed ID

11917158