A novel ENU-induced <i>Cpox</i> mutation causes microcytic hypochromic anemia in mice-Reference-Cited by-同舟云学术

A novel ENU-induced <i>Cpox</i> mutation causes microcytic hypochromic anemia in mice

Published:2022 Issue:4 Volume:71 Page:433-441
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

Miyasaka Yuki¹,Okuda Kento¹,Miura Ikuo²,Motegi Hiromi³,Wakana Shigeharu²,Ohno Tamio¹

Affiliation:

1. Division of Experimental Animals, Graduate School of Medicine, Nagoya University, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi 466-8550, Japan

2. Technology and Developmental Team for Mouse Phenotype Analysis, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki 305-0074, Japan

3. Team for Advanced Development and Evaluation of Human Disease Models, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki 305-0074, Japan

Publisher

Japanese Association for Laboratory Animal Science

Subject

General Veterinary,General Biochemistry, Genetics and Molecular Biology,Animal Science and Zoology,General Medicine

Link

https://www.jstage.jst.go.jp/article/expanim/71/4/71_22-0032/_pdf

Reference28 articles.

1. 1. Acevedo-Arozena A, Wells S, Potter P, Kelly M, Cox RD, Brown SD. ENU mutagenesis, a way forward to understand gene function. Annu Rev Genomics Hum Genet. 2008; 9: 49–69.

2. 2. Cordes SP. N-ethyl-N-nitrosourea mutagenesis: boarding the mouse mutant express. Microbiol Mol Biol Rev. 2005; 69: 426–439.

3. 3. Nolan PM, Hugill A, Cox RD. ENU mutagenesis in the mouse: application to human genetic disease. Brief Funct Genomics Proteomics. 2002; 1: 278–289.

4. 4. Rank G, Sutton R, Marshall V, Lundie RJ, Caddy J, Romeo T, et al. Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant. Blood. 2009; 113: 3352–3362.

5. 5. Hughes MR, Anderson N, Maltby S, Wong J, Berberovic Z, Birkenmeier CS, et al. A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis. Exp Hematol. 2011; 39: 305–320, 320.e1–320.e2.

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