Case study: polycystic livers in a transgenic mouse line

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Case study: polycystic livers in a transgenic mouse line

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article científic

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article scientifique

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artigo científico

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bilimsel makale

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scientific article published on April 2014

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Case study: polycystic livers in a transgenic mouse line

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Case study: polycystic livers in a transgenic mouse line.

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Case study: polycystic livers in a transgenic mouse line

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Case study: polycystic livers in a transgenic mouse line.

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Case study: polycystic livers in a transgenic mouse line

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Case study: polycystic livers in a transgenic mouse line.

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P1476

Case study: polycystic livers in a transgenic mouse line

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P2093

Christopher J Ward

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James E Artwohl

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Jamie Lovaglio

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Jeffrey D Fortman

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Thomas Gh Diekwisch

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Yoshihiro Ito

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P2860

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3

Liver and kidney disease in ciliopathies

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease

Mutations in SEC63 cause autosomal dominant polycystic liver disease

Polycystic disease of the liver

Genetic deletion of Lsamp causes exaggerated behavioral activation in novel environments

Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly

Mutation of murine adenylate kinase 7 underlies a primary ciliary dyskinesia phenotype.

Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion

P304

115-120

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P31

scholarly article

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P478

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P577

2014-04-01T00:00:00Z

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P698

24674586

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3997289

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