Literature DB >> 20544945

Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice.

Glen B Banks1, Ariana C Combs, Jeffrey S Chamberlain.   

Abstract

Currently available polymerase chain reaction (PCR) genotyping methods for point mutations in the mouse dystrophin gene can lead to false positives and result in wasted time and money due to breeding or treating the wrong mice. Here we describe a simple and accurate method for sequencing the point mutations in mdx, mdx(4cv), and mdx(5cv) mice. This method clearly distinguishes between wildtype, heterozygous, and mutant transcripts, and thereby time and money can be saved by avoiding false positives.

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Year:  2010        PMID: 20544945      PMCID: PMC3155817          DOI: 10.1002/mus.21700

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  7 in total

1.  The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy.

Authors:  I Danko; V Chapman; J A Wolff
Journal:  Pediatr Res       Date:  1992-07       Impact factor: 3.756

Review 2.  Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue.

Authors:  T Haenggi; J-M Fritschy
Journal:  Cell Mol Life Sci       Date:  2006-07       Impact factor: 9.261

3.  Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

Authors:  V M Chapman; D R Miller; D Armstrong; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

4.  X chromosome-linked muscular dystrophy (mdx) in the mouse.

Authors:  G Bulfield; W G Siller; P A Wight; K J Moore
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

5.  The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.

Authors:  P Sicinski; Y Geng; A S Ryder-Cook; E A Barnard; M G Darlison; P J Barnard
Journal:  Science       Date:  1989-06-30       Impact factor: 47.728

6.  Differential expression of dystrophin isoforms in strains of mdx mice with different mutations.

Authors:  W B Im; S F Phelps; E H Copen; E G Adams; J L Slightom; J S Chamberlain
Journal:  Hum Mol Genet       Date:  1996-08       Impact factor: 6.150

7.  A novel and simple method for genotyping the mdx mouse using high-resolution melt polymerase chain reaction.

Authors:  Andrea L Trebbin; Andrew J Hoey
Journal:  Muscle Nerve       Date:  2009-05       Impact factor: 3.217

  7 in total
  10 in total

1.  A new method of genotyping MDX4CV mice by PCR-RFLP analysis.

Authors:  Elisia D Tichy; Foteini Mourkioti
Journal:  Muscle Nerve       Date:  2017-03-21       Impact factor: 3.217

2.  Extraocular muscle satellite cells are high performance myo-engines retaining efficient regenerative capacity in dystrophin deficiency.

Authors:  Pascal Stuelsatz; Andrew Shearer; Yunfei Li; Lindsey A Muir; Nicholas Ieronimakis; Qingwu W Shen; Irina Kirillova; Zipora Yablonka-Reuveni
Journal:  Dev Biol       Date:  2014-09-16       Impact factor: 3.582

3.  Genotyping mdx, mdx3cv, and mdx4cv mice by primer competition polymerase chain reaction.

Authors:  Jin-Hong Shin; Chady H Hakim; Keqing Zhang; Dongsheng Duan
Journal:  Muscle Nerve       Date:  2010-12-09       Impact factor: 3.217

4.  A new immuno-, dystrophin-deficient model, the NSG-mdx(4Cv) mouse, provides evidence for functional improvement following allogeneic satellite cell transplantation.

Authors:  Robert W Arpke; Radbod Darabi; Tara L Mader; Yu Zhang; Akira Toyama; Cara-Lin Lonetree; Nardina Nash; Dawn A Lowe; Rita C R Perlingeiro; Michael Kyba
Journal:  Stem Cells       Date:  2013-08       Impact factor: 6.277

5.  Muscle structure influences utrophin expression in mdx mice.

Authors:  Glen B Banks; Ariana C Combs; Guy L Odom; Robert J Bloch; Jeffrey S Chamberlain
Journal:  PLoS Genet       Date:  2014-06-12       Impact factor: 5.917

6.  Recombinase-mediated reprogramming and dystrophin gene addition in mdx mouse induced pluripotent stem cells.

Authors:  Chunli Zhao; Alfonso P Farruggio; Christopher R R Bjornson; Christopher L Chavez; Jonathan M Geisinger; Tawny L Neal; Marisa Karow; Michele P Calos
Journal:  PLoS One       Date:  2014-04-29       Impact factor: 3.240

7.  Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice.

Authors:  Rachel M Faber; John K Hall; Jeffrey S Chamberlain; Glen B Banks
Journal:  Skelet Muscle       Date:  2014-05-23       Impact factor: 4.912

8.  Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function.

Authors:  Arielle Hall; Tatiana Fontelonga; Alec Wright; Katlynn Bugda Gwilt; Jeffrey Widrick; Alessandra Pasut; Francesco Villa; Cynthia K Miranti; Devin Gibbs; Evan Jiang; Hui Meng; Michael W Lawlor; Emanuela Gussoni
Journal:  Skelet Muscle       Date:  2020-11-27       Impact factor: 4.912

9.  Mass Spectrometric Profiling of Extraocular Muscle and Proteomic Adaptations in the mdx-4cv Model of Duchenne Muscular Dystrophy.

Authors:  Stephen Gargan; Paul Dowling; Margit Zweyer; Jens Reimann; Michael Henry; Paula Meleady; Dieter Swandulla; Kay Ohlendieck
Journal:  Life (Basel)       Date:  2021-06-22

10.  Microutrophin expression in dystrophic mice displays myofiber type differences in therapeutic effects.

Authors:  Glen B Banks; Jeffrey S Chamberlain; Guy L Odom
Journal:  PLoS Genet       Date:  2020-11-11       Impact factor: 5.917

  10 in total

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