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Walter MC

As seen in: PeerJ
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Articles by Walter MC

Predictive value of D4Z4 methylation levels for phenotypic heterogeneity and disease progression in Facioscapulohumeral Muscular Dystrophy with borderline D4Z4 repeat units: a retrospective cohort study

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By Walter MC, Di Leo R, El Hajj N
| PeerJ
Xiaodan Lin conceived and designed the experiments, authored or reviewed drafts of the article, and approved the final draft. Qifang He analyzed the data, prepared figures and/or tables, and approved the final draft. Minghui Zeng performed the experiments, authored or reviewed drafts of the article, and approved the final draft. Yuhua Lin analyzed the data, authored or reviewed drafts of the article, and approved the final draft.
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Comparative analysis of fecal DNA viromes in Large-billed crows and Northern ravens reveals diverse viral profiles

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By Walter MC, da Silva AL, Roy AA, Scott LC
| PeerJ
Comparative analysis of fecal DNA viromes in Large-billed crows and Northern ravens reveals diverse viral profiles 1State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University, Xining, China 2College of Eco-Environmental Engineering, Qinghai University, Xining, China 3Xining Wildlife Park of Qinghai Province, Xining, China 4Federal Research Center of Fundamental and Translational Medicine, Novosibirsk, Russia 5Novosibirsk State University, Novosibirsk, Russia DOI...
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Investigating antimicrobial resistance genes in Kenya, Uganda and Tanzania cattle using metagenomics

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By Byrne BA, Mitchell AL, Walter MC, Omar KM
| PeerJ
Investigating antimicrobial resistance genes in Kenya, Uganda and Tanzania cattle using metagenomics 1Department of Biochemistry and Biotechnology, School of Pure and Applied Sciences, Pwani University, Kilifi, Kenya 2Division of Immunology, Department of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa 3Genetics, Genomics and Bioinformatics Department, National Biotechnology Development Agency, Abuja, Nigeria 4Department of...
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Systemic deletion of DMD exon 51 rescues clinically severe Duchenne muscular dystrophy in a pig model lacking DMD exon 52

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By Stöckl JB, Walter MC
| ncbi.nlm.nih.gov
Save citation to file Format: Add to My Bibliography Your saved search Name of saved search: Search terms: Frequency: Which day? Which day? Report format: Send at most: Send even when there aren't any new results Optional text in email: Create a file for external citation management software
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First metagenomic analysis of the Andean condor (Vultur gryphus) gut microbiome reveals microbial diversity and wide resistome

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By Gilbert JA, Walter MC, Eduardo Martinez-Hernandez J
| PeerJ
Additional Information and Declarations Competing Interests The authors declare that they have no competing interests. Author Contributions J. Eduardo Martinez-Hernandez conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft.
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Transcriptome analysis and exploration of genes involved in the biosynthesis of secoiridoids in Gentiana rhodantha

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By Martin MJ, Walter MC, Kim SH, Jackson JD
| PeerJ
Discussion Secoiridoid is one of the important medicinal components for G. rhodantha (Li et al., 2006; Inao et al., 2004). The analysis of the secoiridoid biosynthesis pathway is very important for quality improvement and breeding for G. rhodantha. First, we sequenced the transcriptome of different organs of G. rhodantha. When comparing with other plants of the same genus, the results showed that sequence splicing quality of G.
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Genomics and cellulolytic, hemicellulolytic, and amylolytic potential of Iocasia fonsfrigidae strain SP3-1 for polysaccharide degradation

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By Walter MC, Lee IM, Randall RJ, Sobroney Heng
| PeerJ
Additional Information and Declarations Competing Interests The authors declare there are no competing interests. Author Contributions Sobroney Heng conceived and designed the experiments, performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the article, and approved the final draft.
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Dominant LGMD2A: alternative diagnosis or hidden digenism?

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By Neurosciences Area, López de Munain, Walter MC, De Paula F
| Oxford University Press (OUP)
We read with great interest the work recently published in Brain (Vissing et al., 2016), in which the findings on limb girdle muscular dystrophy families from the UK, Denmark and Sweden are described. The cases showed a segregation pattern compatible with a dominant transmission. All the affected cases except for one share a heterozygous mutation in the CAPN3 gene previously described in recessive forms of limb girdle muscular dystrophy 2A (LGMD2A) (Richard et al., 1997; Groen et al., 2007).
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