|
1
|
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
|
Nat Genet
|
2001
|
3.15
|
|
2
|
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
|
Nat Genet
|
2001
|
2.95
|
|
3
|
New mouse model for polycystic kidney disease with both recessive and dominant gene effects.
|
Kidney Int
|
1995
|
1.08
|
|
4
|
Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic.
|
Kidney Int
|
1996
|
0.87
|
|
5
|
Encyclopedia of the mouse genome VII. Mouse chromosome 10.
|
Mamm Genome
|
1998
|
0.81
|
|
6
|
Recovery of probes linked to the jcpk locus on mouse chromosome 10 by the use of an improved representational difference analysis technique.
|
Genomics
|
1996
|
0.79
|
|
7
|
Mouse chromosome 10.
|
Mamm Genome
|
1999
|
0.78
|
|
8
|
FRET analysis of actin-myosin interaction in contracting rat aortic smooth muscle.
|
Can J Physiol Pharmacol
|
2009
|
0.78
|
|
9
|
Detection of histidine decarboxylase in rat aorta and cultured rat aortic smooth muscle cells.
|
Inflamm Res
|
2004
|
0.77
|
|
10
|
Scraggly, a new hair loss mutation on mouse chromosome 19.
|
Mamm Genome
|
1999
|
0.77
|
|
11
|
Mouse chromosome 10.
|
Mamm Genome
|
1994
|
0.76
|
|
12
|
Encyclopedia of the mouse genome V. Mouse chromosome 10.
|
Mamm Genome
|
1996
|
0.75
|
|
13
|
Characterization of the region containing the jcpk PKD gene on mouse Chromosome 10.
|
Cytogenet Genome Res
|
2002
|
0.75
|
|
14
|
Mouse chromosome 10.
|
Mamm Genome
|
1997
|
0.75
|