(Q35658778)

English

Fine-mapping and comprehensive transcript analysis reveals nonsynonymous variants within a novel 1.17 Mb blood pressure QTL region on rat chromosome 10.

scientific article published on 10 January 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

9 August 2017

Fine-mapping and comprehensive transcript analysis reveals nonsynonymous variants within a novel 1.17 Mb blood pressure QTL region on rat chromosome 10. (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

author name string

Yasser Saad

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Michael R Garrett

2

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Ezhilarasi Manickavasagam

3

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Shane Yerga-Woolwine

4

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Phyllis Farms

5

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Tracy Radecki

6

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Europe PubMed Central

PubMed publication ID

9 August 2017

Bina Joe

7

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

publication date

10 January 2007

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Europe PubMed Central

PubMed publication ID

9 August 2017

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Europe PubMed Central

PubMed publication ID

9 August 2017

89

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Europe PubMed Central

PubMed publication ID

9 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

343-353

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Functional genomics in rat models of hypertension: using differential expression and congenic strains to identify and evaluate candidate genes

1 reference

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Combining mapping and arraying: An approach to candidate gene identification.

1 reference

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Renal medullary genes in salt-sensitive hypertension: a chromosomal substitution and cDNA microarray study

1 reference

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27 July 2018

Rat genetics: attaching physiology and pharmacology to the genome

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The major murine systemic lupus erythematosus susceptibility locus, Sle1, is a cluster of functionally related genes

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Functional alterations of the Nppa promoter are linked to cardiac ventricular hypertrophy in WKY/WKHA rat crosses

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Short tandem repeat polymorphic markers for the rat genome from marker-selected libraries

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Linkage map and congenic strains to localize blood pressure QTL on rat chromosome 10.

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Heart mass and blood pressure have separate genetic determinants in the New Zealand genetically hypertensive (GH) rat

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Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.

1 reference

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Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.

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Locus for the inducible, but not a constitutive, nitric oxide synthase cosegregates with blood pressure in the Dahl salt-sensitive rat.

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Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats

1 reference

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27 July 2018

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

1 reference

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The corticotropin-releasing factor receptor type 2a contains an N-terminal pseudo signal peptide.

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25 September 2018

Fine mapping of Lvm1: a quantitative trait locus controlling heart size independently of blood pressure

1 reference

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Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus

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Genomic map of cardiovascular phenotypes of hypertension in female Dahl S rats

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25 September 2018

Time-Course Genetic Analysis of Albuminuria in Dahl Salt-Sensitive Rats on Low-Salt Diet

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25 September 2018

Use of a panel of congenic strains to evaluate differentially expressed genes as candidate genes for blood pressure quantitative trait loci

1 reference

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25 September 2018

High-resolution mapping of the blood pressure QTL on chromosome 7 using Dahl rat congenic strains

1 reference

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25 September 2018

Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats.

1 reference

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25 September 2018

Angiotensin I converting enzyme gene cosegregates with blood pressure and heart weight in F2 progeny derived from spontaneously hypertensive and normotensive Wistar-Kyoto rats

1 reference

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Defining the blood pressure QTL on chromosome 7 in Dahl rats by a 177-kb congenic segment containing Cyp11b1

1 reference

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7 January 2021

Cosegregation of blood pressure with angiotensin converting enzyme and atrial natriuretic peptide receptor genes using Dahl salt-sensitive rats

1 reference

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7 January 2021

Genome scan and congenic strains for blood pressure QTL using Dahl salt-sensitive rats

1 reference

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Complete genome searches for quantitative trait loci controlling blood pressure and related traits in four segregating populations derived from Dahl hypertensive rats

1 reference

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Genetic mapping of blood pressure quantitative trait loci in Milan hypertensive rats

1 reference

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Two linked blood pressure quantitative trait loci on chromosome 10 defined by dahl rat congenic strains

1 reference

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Utilization of marker-assisted congenics to map two blood pressure quantitative trait loci in Dahl rats

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Epistasis, not numbers, regulates functions of clustered Dahl rat quantitative trait loci applicable to human hypertension

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Novel quantitative trait loci for blood pressure and related traits on rat chromosomes 1, 10, and 18

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The region of rat chromosome 10 (the ngfr gene locus) is associated with blood pressure increase in response to emotional stress

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Aging and salt-loading modulate blood pressure QTLs in rats

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Interaction between blood pressure quantitative trait loci in rats in which trait variation at chromosome 1 is conditional upon a specific allele at chromosome 10

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Independent genetic susceptibility to cardiac hypertrophy in inherited hypertension

1 reference

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Genetic determination of cardiac mass in normotensive rats: results from an F344xWKY cross

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1 reference

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1 reference

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10.1016/J.YGENO.2006.12.005

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Europe PubMed Central

PubMed publication ID

9 August 2017

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9 August 2017

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9 August 2017

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