(Q46158738)

English

Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models

scientific article published on 16 January 2009

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Bernhard Aigner

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

11

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Martin Hrabě de Angelis

10

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Martin Hrabé de Angelis

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Ulrike Mayer

8

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author name string

Birgit Rathkolb

2

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Matthias Klaften

3

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Reinhard Sedlmeier

4

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Martina Klempt

5

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Sibylle Wagner

6

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Dian Michel

7

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Thomas Klopstock

9

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

publication date

16 January 2009

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Experimental Physiology

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

94

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

4

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

412-421

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

Diabetes models by screen for hyperglycemia in phenotype-driven ENU mouse mutagenesis projects

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

X chromosome-linked muscular dystrophy (mdx) in the mouse

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Mouse functional genomics requires standardization of mouse handling and housing conditions

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Genetic background determines metabolic phenotypes in the mouse

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Introducing the German Mouse Clinic: open access platform for standardized phenotyping.

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Novel phenotypes identified by plasma biochemical screening in the mouse

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2.

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: revisited.

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Genotype-specific environmental impact on the variance of blood values in inbred and F1 hybrid mice

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Hypercholesterolemia in ENU-induced mouse mutants

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Defective integrin switch and matrix composition at alpha 7-deficient myotendinous junctions precede the onset of muscular dystrophy in mice.

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Mutations in dynein link motor neuron degeneration to defects in retrograde transport

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Generation of ENU-Induced Mouse Mutants with Hypocholesterolemia: Novel Tools for Dissecting Plasma Lipoprotein Homeostasis

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Dominant-Negative Effects of a Novel Mutated Ins2 Allele Causes Early-Onset Diabetes and Severe -Cell Loss in Munich Ins2C95S Mutant Mice

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

The clinical-chemical screen in the Munich ENU Mouse Mutagenesis Project: screening for clinically relevant phenotypes

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2008.045864

21 January 2018

Identifiers

10.1113/EXPPHYSIOL.2008.045864

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19151073

ResearchGate publication ID

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