Disease modeling in genetic kidney diseases: mice.

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Disease modeling in genetic kidney diseases: mice.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Disease modeling in genetic kidney diseases: mice.

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Disease modeling in genetic kidney diseases: mice.

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Disease modeling in genetic kidney diseases: mice.

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Disease modeling in genetic kidney diseases: mice.

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Disease modeling in genetic kidney diseases: mice.

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Disease modeling in genetic kidney diseases: mice.

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P1476

Disease modeling in genetic kidney diseases: mice

@en

P2093

Andreas F Hofmeister

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Ivica Grgic

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Stefanie Weber

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P2860

Gitelman syndrome

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

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

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

Alpha-actinin binding kinetics modulate cellular dynamics and force generation

Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

P2888

s00441-017-2639-3

P304

159-170

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P31

scholarly article

P356

10.1007/S00441-017-2639-3

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P433

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P478

369

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P50

Martin Kömhoff

P577

2017-06-10T00:00:00Z

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P698

28601904

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