Personal information

Genetics, Hearing Loss, Cancer, Memory,
New Zealand

Biography

My research focus is Human Molecular Genetics. This involves identifying genetic changes that contribute to hereditary disorders common in New Zealand and will provide further insight into the molecular and cellular mechanisms that cause these observable phenotypic changes (ie, characteristic changes).

This research will involve using a variety of bioinformatic, genetic, cell and molecular biology techniques. All research students acquire basic research skills and a knowledge of techniques, as well as training in specialist disciplines.

Activities

Employment (1)

University of Waikato: Hamilton, NZ

Senior Lecturer in Molecular Biology
Employment
Source: Self-asserted source
Linda Peters

Works (15)

Denigrins H–L: Sulfated Derivatives of Denigrins D and E from a New Zealand Dictyodendrilla c.f. dendyi Marine Sponge

Marine Drugs
2024-05-20 | Journal article
Contributors: Lauren Gris; Michèle R. Prinsep; Linda M. Peters; Christopher N. Battershill
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Biomedical Ti–Cu–Mn alloys with antibacterial capability

Journal of Materials Research and Technology
2021-01 | Journal article
Part of ISSN: 2238-7854
Source: Self-asserted source
Linda Peters

Microstructure, mechanical behaviour and antibacterial activity of biomedical Ti-xMn-yCu alloys

Journal of Alloys and Compounds
2020-12 | Journal article
Part of ISSN: 0925-8388
Source: Self-asserted source
Linda Peters

Ternary Ti alloys functionalised with antibacterial activity

Scientific Reports
2020-12 | Journal article
Part of ISSN: 2045-2322
Source: Self-asserted source
Linda Peters

Antibacterial Ti-Mn-Cu alloys for biomedical applications

Regenerative Biomaterials
2020-12-03 | Journal article
Part of ISSN: 2056-3418
Part of ISSN: 2056-3426
Source: Self-asserted source
Linda Peters

Chitosan: A review of sources and preparation methods.

International journal of biological macromolecules
2020-12-03 | Journal article
Source: Self-asserted source
Linda Peters

Design of β-eutectoid bearing Ti alloys with antibacterial functionality

Materials Letters
2020-11 | Journal article
Part of ISSN: 0167-577X
Source: Self-asserted source
Linda Peters

Are our beaches safe? Quantifying the human health impact of anthropogenic beach litter on people in New Zealand.

The Science of the total environment
2018-10-11 | Journal article
Source: Self-asserted source
Linda Peters

Development of a qPCR method to measure mitochondrial and genomic DNA damage with application to chemotherapy-induced DNA damage and cryopreserved cells

Biology
2016 | Journal article
EID:

2-s2.0-84994056173

Contributors: Evans, S.O.; Jameson, M.B.; Cursons, R.T.M.; Peters, L.M.; Bird, S.; Jacobson, G.M.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier

Mutations in Grxcr1 Are The Basis for Inner Ear Dysfunction in the Pirouette Mouse

American Journal of Human Genetics
2010 | Journal article
EID:

2-s2.0-76049130314

Contributors: Odeh, H.; Hunker, K.L.; Belyantseva, I.A.; Azaiez, H.; Avenarius, M.R.; Zheng, L.; Peters, L.M.; Gagnon, L.H.; Hagiwara, N.; Skynner, M.J. et al.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1

Clinical Genetics
2008 | Journal article
EID:

2-s2.0-40749100281

Contributors: Peters, L.M.; Fridell, R.A.; Boger, E.T.; San Agustin, T.B.; Madeo, A.C.; Griffith, A.J.; Friedman, T.B.; Morell, R.J.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier

Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear

Genomics
2007 | Journal article
EID:

2-s2.0-33845985328

Contributors: Peters, L.M.; Belyantseva, I.A.; Lagziel, A.; Battey, J.F.; Friedman, T.B.; Morell, R.J.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

Nature Genetics
2002 | Journal article
EID:

2-s2.0-0036510053

Contributors: Kurima, K.; Peters, L.M.; Yang, Y.; Riazuddin, S.; Ahmed, Z.M.; Naz, S.; Arnaud, D.; Drury, S.; Mo, J.; Makishima, T. et al.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

Human Molecular Genetics
2002 | Journal article
EID:

2-s2.0-0036849301

Contributors: Peters, L.M.; Anderson, D.W.; Griffith, A.J.; Grundfast, K.M.; San Agustin, T.B.; Madeo, A.C.; Friedman, T.B.; Morell, R.J.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

American Journal of Human Genetics
2001 | Journal article
EID:

2-s2.0-0035168168

Contributors: Bork, J.M.; Peters, L.M.; Riazuddin, S.; Ahmed, Z.M.; Li, X.C.; Griffith, A.J.; Wilcox, E.R.; Friedman, T.B.; Morell, R.J.; Griffith, A.J. et al.
Source: Self-asserted source
Linda Peters via Scopus - Elsevier