Background: Gen1 mutation can cause various phenotypes of congenital anomaly of the kidney and urinary tract (CAKUT). An intrauterine low-protein isocaloric diet can also cause CAKUT phenotypes in offspring. However, single factors such as gene mutation or abnormal environmental factor during pregnancy can only explain part of the pathogenesis of CAKUT. Objectives: A low-protein isocaloric diet was fed to Gen1-mutant mice throughout pregnancy to establish a Gen1-mutant mouse model exposed to a low-protein isocaloric intrauterine environment. The mice were divided into 4 groups: normal (22%) protein diet (ND) + wild-type mice (CON group), ND + Gen1PB/+ mice (Gen1PB/+ group), low (6%)-protein isocaloric diet (LD) + wild-type mice (LD group), ...
In the SWV strain of mice, old females have a severe increase in water intake and urine output. This...
Congenital urinary tract obstructions are the leading cause of chronic kidney disease and end-stage ...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of inherited rena...
BackgroundLow birth weight (LBW) neonates have impaired kidney development that leaves them suscepti...
Smith. Bradykinin B2 null mice are prone to renal dyspla-sia: gene-environment interactions in kidne...
Kidney diseases lead to the failure of urinary excretion of metabolism products. In the Munich ethyl...
BACKGROUND: Increased levels of blood plasma urea were used as phenotypic parameter for establishing...
Human epidemiological data associating birth weight with adult disease suggest that organogenesis is...
A maternal low protein (LP) diet in rodents often results in low nephron endowment and renal pathoph...
Chronic kidney disease (CKD) is a growing medical problem and a significant risk factor for the deve...
Background/Aim: Phenotype-driven screening of a great pool of randomly mutant mice and subsequent se...
Abstract Background Increased levels of blood plasma urea were used as phenotypic parameter for esta...
Heterozygous 1Neu mice transmit a single base pair insertion mutation within the paired domain (exon...
In the almost 30 years that have passed since the postulation of the “Developmental Origins of Healt...
Early embryonic development is known to be susceptible to maternal undernutrition, leading to a dise...
In the SWV strain of mice, old females have a severe increase in water intake and urine output. This...
Congenital urinary tract obstructions are the leading cause of chronic kidney disease and end-stage ...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of inherited rena...
BackgroundLow birth weight (LBW) neonates have impaired kidney development that leaves them suscepti...
Smith. Bradykinin B2 null mice are prone to renal dyspla-sia: gene-environment interactions in kidne...
Kidney diseases lead to the failure of urinary excretion of metabolism products. In the Munich ethyl...
BACKGROUND: Increased levels of blood plasma urea were used as phenotypic parameter for establishing...
Human epidemiological data associating birth weight with adult disease suggest that organogenesis is...
A maternal low protein (LP) diet in rodents often results in low nephron endowment and renal pathoph...
Chronic kidney disease (CKD) is a growing medical problem and a significant risk factor for the deve...
Background/Aim: Phenotype-driven screening of a great pool of randomly mutant mice and subsequent se...
Abstract Background Increased levels of blood plasma urea were used as phenotypic parameter for esta...
Heterozygous 1Neu mice transmit a single base pair insertion mutation within the paired domain (exon...
In the almost 30 years that have passed since the postulation of the “Developmental Origins of Healt...
Early embryonic development is known to be susceptible to maternal undernutrition, leading to a dise...
In the SWV strain of mice, old females have a severe increase in water intake and urine output. This...
Congenital urinary tract obstructions are the leading cause of chronic kidney disease and end-stage ...
Background: Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of inherited rena...