The C3H/HeJ inbred mouse is a model of vesico-ureteric reflux with a susceptibility locus on chromosome 12 (Q84083024)

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31 January 2020

title

The C3H/HeJ inbred mouse is a model of vesico-ureteric reflux with a susceptibility locus on chromosome 12 (English)

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31 January 2020

author name string

Inga J Murawski

1

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31 January 2020

Rita W Maina

2

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31 January 2020

Lisa M Guay-Woodford

4

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31 January 2020

Mary Fujiwara

6

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31 January 2020

Kenneth Morgan

7

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31 January 2020

Indra R Gupta

8

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31 January 2020

language of work or name

English

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publication date

21 April 2010

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31 January 2020

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31 January 2020

volume

78

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31 January 2020

issue

3

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31 January 2020

page(s)

269-278

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Hereditary and familial vesicoureteral reflux

31 January 2020

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Prevalence of hypertension in children with primary vesicoureteral reflux

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End-stage reflux nephropathy

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Position and configuration of the ureteral orifice and its relationship to renal scarring in adults

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The Ureteral Orifice: Its Configuration and Competency

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Does treatment of vesicoureteric reflux in childhood prevent end-stage renal disease attributable to reflux nephropathy?

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Vesicoureteral reflux

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Sibling vesicoureteral reflux in multiple gestation births

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Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.

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Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds

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A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5

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7 January 2021

A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity

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7 January 2021

A genome-wide scan for genes involved in primary vesicoureteric reflux.

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Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux

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Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/- mouse

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7 January 2021

Overexpression of RET leads to vesicoureteric reflux in mice

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7 January 2021

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

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7 January 2021

Autosomal dominant optic nerve colobomas, vesicoureteral reflux, and renal anomalies.

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RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec.

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7 January 2021

What is the normal prevalence of vesicoureteral reflux?

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Comprehensive ultrasound versus voiding cysturethrography in the diagnosis of vesicoureteral reflux

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Congenitally small kidneys with reflux as a common cause of nephropathy in boys

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Morphogenesis during mouse embryonic kidney explant culture

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7 January 2021

Relation of age, sex, and infection to reflux: Data indicating high spontaneous cure rate in pediatric patients

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7 January 2021

Theory of Maturation of the Intravesical Ureter

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7 January 2021

Natural history of vesicoureteral reflux in siblings

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7 January 2021

Characterization of blood pressure and morphological traits in cardiovascular-related organs in 13 different inbred mouse strains

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7 January 2021

Blood pressure in 15 inbred mouse strains and its lack of relation with obesity and insulin resistance in the progeny of an NZO/HILtJ x C3H/HeJ intercross

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Low pressure reflux: relation of vesicoureteral reflux to intravesical pressure

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Kidney Weight in Mice: Strain Differences and Genetic Determination

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7 January 2021

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