(Q28512820)

25 January 2017

title

Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype (English)

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Intraflagellar transport 88

25 January 2017

main subject

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GOA release 2020-03-11

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C. Sommardahl

1

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25 January 2017

M. Cottrell

2

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25 January 2017

J. E. Wilkinson

3

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25 January 2017

R. P. Woychik

4

1 reference

25 January 2017

D. K. Johnson

5

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25 January 2017

publication date

21 December 2001

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25 January 2017

published in

Physiological Genomics

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25 January 2017

volume

7

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25 January 2017

issue

2

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25 January 2017

page(s)

127–134

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Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic

25 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Genetic dissection of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Overview of QTL mapping software and introduction to map manager QT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Efficient localization of mutations by interval haplotype analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

Genetic identification of two major modifier loci of polycystic kidney disease progression in pcy mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00089.2001

10.1152/PHYSIOLGENOMICS.00089.2001

21 January 2018

Identifiers

DOI

0 references

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