Literature DB >> 15237237

Genetics of rare diseases of the kidney: learning from mouse models.

C Zoja1, M Morigi, A Benigni, G Remuzzi.   

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Year:  2004        PMID： 15237237     DOI： 10.1159/000078222

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN： 1424-8581            Impact factor:   1.636


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  2 in total

1.  Loss of the BMP antagonist USAG-1 ameliorates disease in a mouse model of the progressive hereditary kidney disease Alport syndrome.

Authors:  Mari Tanaka; Misako Asada; Atsuko Y Higashi; Jin Nakamura; Akiko Oguchi; Mayumi Tomita; Sachiko Yamada; Nariaki Asada; Masayuki Takase; Tomohiko Okuda; Hiroshi Kawachi; Aris N Economides; Elizabeth Robertson; Satoru Takahashi; Takeshi Sakurai; Roel Goldschmeding; Eri Muso; Atsushi Fukatsu; Toru Kita; Motoko Yanagita
Journal:  J Clin Invest       Date:  2010-02-08       Impact factor: 14.808

Review 2.  Animal models for metabolic, neuromuscular and ophthalmological rare diseases.

Authors:  Guillaume Vaquer; Frida Rivière; Maria Mavris; Fabrizia Bignami; Jordi Llinares-Garcia; Kerstin Westermark; Bruno Sepodes
Journal:  Nat Rev Drug Discov       Date:  2013-03-15       Impact factor: 84.694
  2 in total

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