(Q44918251)

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Phenotypic and genetic analyses of subcongenic BB.SHR rat lines shorten the region on chromosome 4 bearing gene(s) for underlying facets of metabolic syndrome

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Phenotypic and genetic analyses of subcongenic BB.SHR rat lines shorten the region on chromosome 4 bearing gene(s) for underlying facets of metabolic syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

metabolic syndrome

1 reference

based on heuristic

inferred from title

Ingrid Klöting

3

object named as

Ingrid Klöting

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

1

object named as

Nora Klöting

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

author name string

Barbara Wilke

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

publication date

11 August 2004

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Europe PubMed Central

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7 December 2017

Physiological Genomics

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Europe PubMed Central

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7 December 2017

18

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Europe PubMed Central

PubMed publication ID

7 December 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

325-330

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 gene

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Genetics of experimental hypertension.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Diabetes mellitus and exocrine pancreatic dysfunction in perk-/- mice reveals a role for translational control in secretory cell survival

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Mapping of genetic loci predisposing to hypertriglyceridaemia in the hereditary hypertriglyceridaemic rat: analysis of genetic association with related traits of the insulin resistance syndrome

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Diabetes and hypertension in rodent models

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Congenic BB.SHR (D4Mit6-Npy-Spr) rats: a new aid to dissect the genetics of obesity

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Quantitative trait loci for body weight, blood pressure, blood glucose, and serum lipids: linkage analysis with wild rats (Rattus norvegicus).

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Sex-specific and sex-independent quantitative trait loci for facets of the metabolic syndrome in WOKW rats

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Congenic BB.SHR rat provides evidence for effects of a chromosome 4 segment (D4Mit6-Npy approximately 1 cm) on total serum and lipoprotein lipid concentration and composition after feeding a high-fat, high-cholesterol diet

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Genetics of Cd36 and the hypertension metabolic syndrome

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Wolcott-Rallison syndrome: diabetes mellitus and spondyloepiphyseal dysplasia.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Long-term course of neonatal diabetes.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

The PERK eukaryotic initiation factor 2 alpha kinase is required for the development of the skeletal system, postnatal growth, and the function and viability of the pancreas

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00047.2004

21 January 2018

Identifiers

10.1152/PHYSIOLGENOMICS.00047.2004

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

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