(Q52531754)

English

Mouse models of genetic disease: new approaches, new paradigms.

scientific article published in August 1998

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scholarly article

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

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Europe PubMed Central

Mouse models of genetic disease: new approaches, new paradigms. (English)

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Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

genetic disease

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author name string

S D Brown

1

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Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

publication date

1 August 1998

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Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

Journal of Inherited Metabolic Disease

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Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

21

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2 May 2018

http://europepmc.org/abstract/MED/9728333

532-539

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Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

5

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Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

https://scigraph.springernature.com/pub.10.1023/a:1005414921109

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Insertional mutagenesis in transgenic mice

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Phenotypic analysis--making the most of your mouse

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https://pubmed.ncbi.nlm.nih.gov/9728333

12 December 2020

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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Positional cloning of the mouse obese gene and its human homologue

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains

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https://pubmed.ncbi.nlm.nih.gov/9728333

12 December 2020

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Comparative genome organization of vertebrates. The First International Workshop on Comparative Genome Organization.

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Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

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Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse

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A Gene Map of the Human Genome

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A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Positional cloning moves from perditional to traditional

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Chemical mutagenesis and fine-structure functional analysis of the mouse genome

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Mutation analysis of the mouse myosin VIIA deafness gene

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Combining mutagenesis and genomics in the mouse--closing the phenotype gap.

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Genes and deafness

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Abnormal splicing of the leptin receptor in diabetic mice

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A type VII myosin encoded by the mouse deafness gene shaker-1

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Mapping the mouse genome: current status and future prospects

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https://pubmed.ncbi.nlm.nih.gov/9728333

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hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis

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https://pubmed.ncbi.nlm.nih.gov/9728333

12 December 2020

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Chromosome engineering in mice

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Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase

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Identification and expression cloning of a leptin receptor, OB-R

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https://pubmed.ncbi.nlm.nih.gov/9728333

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Gene trapping and functional genomics

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https://pubmed.ncbi.nlm.nih.gov/9728333

12 December 2020

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Identifiers

10.1023/A:1005414921109

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

2 May 2018

http://europepmc.org/abstract/MED/9728333

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