The renal phenotype of allopurinol-treated HPRT-deficient mouse.

about

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

Item

http://www.wikidata.org/entity/Q36304281

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@ast

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@en

type

Item

label

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@ast

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@en

prefLabel

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@ast

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@en

P1476

The renal phenotype of allopurinol-treated HPRT-deficient mouse.

@en

P2093

Alessandro Corbelli

http://www.w3.org/2001/XMLSchema#string

Cristina Zennaro

http://www.w3.org/2001/XMLSchema#string

Federica Tonon

http://www.w3.org/2001/XMLSchema#string

Gianluca Paredi

http://www.w3.org/2001/XMLSchema#string

Luca Ronda

http://www.w3.org/2001/XMLSchema#string

Maria Pia Rastaldi

http://www.w3.org/2001/XMLSchema#string

Marialaura Marchetti

http://www.w3.org/2001/XMLSchema#string

Michele Carraro

http://www.w3.org/2001/XMLSchema#string

Milan Clai

http://www.w3.org/2001/XMLSchema#string

Paola Zarattini

http://www.w3.org/2001/XMLSchema#string

P2860

Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome

Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II

Xanthine stone in the urinary bladder of a male child

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

Fabry nephropathy: a review - how can we optimize the management of Fabry nephropathy?

Four generations of transition-state analogues for human purine nucleoside phosphorylase.

HPRT deficiency coordinately dysregulates canonical Wnt and presenilin-1 signaling: a neuro-developmental regulatory role for a housekeeping gene?

Treating gout with pegloticase, a PEGylated urate oxidase, provides insight into the importance of uric acid as an antioxidant in vivo.

Structure and function of xanthine oxidoreductase: where are we now?

Efficient determination of purine metabolites in brain tissue and serum by high-performance liquid chromatography with electrochemical and UV detection.

P304

e0173512

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0173512

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-03-10T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28282408

http://www.w3.org/2001/XMLSchema#string

P932

5345830

http://www.w3.org/2001/XMLSchema#string