<p>a) The CAST-derived segment of Chr 4 corresponding to <i>Mpkd1-2</i> interval is delimited by the marker, D4Mit80 (shaded area). The breakpoint between the proximal CAST/E-derived and distal B6-derived segment of Chr 4 occurred between markers D4Mit80 (37.7 cM) and D4Mit175 (45.7 cM). b) The predicted cystic disease-modulating effects of the CAST-derived <i>Mpkd1-2</i> loci was tested by comparing the renal cystic phenotypes in <i>Cys1</i><sup><i>cpk/cpk</i></sup> mutants that were heterozygotes for the CAST-derived (CAST/Ei; n = 9) <i>Mpkd1-2</i> interval to <i>Cys1</i><sup><i>cpk/cpk</i></sup> mutants from the same cross that were homozygous B6 for the <i>Mpkd1-2</i> interval (n = 14). The genetic background of both groups was B6. Diam...
Autosomal dominant polycystic kidney disease (ADPKD) occurs by germline mutation in PKD1 or PKD2. Ev...
The cpk mouse is the most extensively characterized model of autosomal recessive polycystic kidney d...
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Numerous m...
<p>a) The CAST-derived segment of Chr 4 corresponding to <i>Mpkd1-3</i> interval is delimited by the...
<p>We adapted a deletion mapping approach to fine map the dominant cystic disease-modulating effects...
<div><p>We have previously mapped the interval on Chromosome 4 for a major polycystic kidney disease...
Numerous mouse models of polycystic kidney disease (PKD) have been described in which the mutant phe...
We have previously mapped the interval on Chromosome 4 for a major polycystic kidney disease modifie...
Polycystic kidney disease (PKD) is a genetically heterogeneous disorder. In addition to the many PKD...
<p>all reported areas are in mm<sup>2</sup>; SEM = standard error of the mean; <i>p-value</i> = sign...
The genetic analysis of rodent disease models provides a powerful tool to investigate how modifier l...
Location of mutations within the PKD2 gene influences clinical outcome.BackgroundSince the cloning o...
New mouse model for polycystic kidney disease with both recessive and dominant gene effects. In the ...
Cystic kidney disease is characterized by the progressive development of multiple fluid-filled cysts...
Cystic kidney disease is characterized by the progressive development of multiple fluid-filled cysts...
Autosomal dominant polycystic kidney disease (ADPKD) occurs by germline mutation in PKD1 or PKD2. Ev...
The cpk mouse is the most extensively characterized model of autosomal recessive polycystic kidney d...
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Numerous m...
<p>a) The CAST-derived segment of Chr 4 corresponding to <i>Mpkd1-3</i> interval is delimited by the...
<p>We adapted a deletion mapping approach to fine map the dominant cystic disease-modulating effects...
<div><p>We have previously mapped the interval on Chromosome 4 for a major polycystic kidney disease...
Numerous mouse models of polycystic kidney disease (PKD) have been described in which the mutant phe...
We have previously mapped the interval on Chromosome 4 for a major polycystic kidney disease modifie...
Polycystic kidney disease (PKD) is a genetically heterogeneous disorder. In addition to the many PKD...
<p>all reported areas are in mm<sup>2</sup>; SEM = standard error of the mean; <i>p-value</i> = sign...
The genetic analysis of rodent disease models provides a powerful tool to investigate how modifier l...
Location of mutations within the PKD2 gene influences clinical outcome.BackgroundSince the cloning o...
New mouse model for polycystic kidney disease with both recessive and dominant gene effects. In the ...
Cystic kidney disease is characterized by the progressive development of multiple fluid-filled cysts...
Cystic kidney disease is characterized by the progressive development of multiple fluid-filled cysts...
Autosomal dominant polycystic kidney disease (ADPKD) occurs by germline mutation in PKD1 or PKD2. Ev...
The cpk mouse is the most extensively characterized model of autosomal recessive polycystic kidney d...
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. Numerous m...