Jonathan M. Harris

ORCID: 0000-0003-4209-2380
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About
Contact & Profiles
Research Areas
  • Biochemical and Structural Characterization
  • Estrogen and related hormone effects
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Prostate Cancer Treatment and Research
  • Hormonal and reproductive studies
  • Peptidase Inhibition and Analysis
  • Schizophrenia research and treatment
  • Phytochemical compounds biological activities
  • Chemical Synthesis and Analysis
  • Glutathione Transferases and Polymorphisms
  • Mass Spectrometry Techniques and Applications
  • Functional Brain Connectivity Studies
  • Genomics, phytochemicals, and oxidative stress
  • Reproductive tract infections research
  • Transgenic Plants and Applications
  • HER2/EGFR in Cancer Research
  • Breast Cancer Treatment Studies
  • Protease and Inhibitor Mechanisms
  • Advanced Neuroimaging Techniques and Applications
  • Mental Health and Psychiatry
  • Biochemical and Molecular Research
  • Mitochondrial Function and Pathology
  • Menopause: Health Impacts and Treatments
  • Retinoids in leukemia and cellular processes
  • Antimicrobial Peptides and Activities

Queensland University of Technology
2015-2025

University of Wisconsin–Milwaukee
2024

King's College London
2015-2023

Abu Dhabi National Oil (United Arab Emirates)
2021

Maimonides Medical Center
2017

Cancer Research UK
1992-2016

University of Edinburgh
2004-2009

Royal Edinburgh Hospital
2003-2008

NHS Lothian
2007

Memorial Sloan Kettering Cancer Center
2006

Aldo Scarpa David K. Chang Kátia Nones Vincenzo Corbo Ann‐Marie Patch and 95 more Peter J. Bailey Rita T. Lawlor Amber L. Johns David K. Miller Andrea Mafficini Borislav C. Rusev Maria Scardoni Davide Antonello Stefano Barbi Katarzyna Sikora Sara Cingarlini Caterina Vicentini Skye McKay Michael C. Quinn Timothy J. C. Bruxner Angelika N. Christ Ivon Harliwong Senel Idrisoglu Suzanne McLean Craig Nourse Ehsan Nourbakhsh Peter J. Wilson Matthew J. Anderson J. Lynn Fink Felicity Newell Nick M. Waddell Oliver Holmes Stephen H. Kazakoff Conrad Leonard Scott Wood Qinying Xu Shivashankar H. Nagaraj Eliana Amato Irene Dalai Samantha Bersani Ivana Cataldo Angelo Paolo Dei Tos Paola Capelli Maria Vittoria Davì Luca Landoni Anna Malpaga Marco Miotto Vicki Whitehall Barbara Leggett Janelle L. Harris Jonathan M. Harris Marc D. Jones Jeremy L. Humphris Lorraine A. Chantrill Venessa Chin Adnan Nagrial Marina Pajic Christopher J. Scarlett Andreia V. Pinho Ilse Rooman Christopher W. Toon Jianmin Wu Mark Pinese Mark J. Cowley Andrew P. Barbour Amanda Mawson Emily S. Humphrey Emily K. Colvin Angela Chou Jessica A. Lovell Nigel B. Jamieson Fraser R. Duthie Marie‐Claude Gingras William E. Fisher Rebecca A. Dagg Loretta M. S. Lau Michael Lee Hilda A. Pickett Roger R. Reddel Jaswinder S. Samra James G. Kench Neil D. Merrett Krishna Epari Nam Q. Nguyen Nikolajs Zeps Massimo Falconi Michele Simbolo Giovanni Butturini George Van Buren Stefano Partelli Matteo Fassan Kum Kum Khanna Anthony J. Gill David A. Wheeler Richard A. Gibbs Elizabeth A. Musgrove Claudio Bassi Giampaolo Tortora Paolo Pederzoli John V. Pearson

10.1038/nature21063 article EN Nature 2017-02-14

Abstract There is emerging evidence that the balance between estrogen receptor-α (ERα) and androgen receptor (AR) signaling a critical determinant of growth in normal malignant breast. In this study, we assessed AR status cohort 215 invasive ductal breast carcinomas. ERα were coexpressed majority (80-90%) tumor cells. Kaplan-Meier product limit analysis multivariate Cox regression showed an independent prognostic factor ERα-positive disease, with low level (less than median 75% positive...

10.1158/0008-5472.can-09-0452 article EN Cancer Research 2009-07-29

Cytosolic glutathione S-transferases (GSTs) are a supergene family of dimeric enzymes capable detoxifying number carcinogenic electrophiles. Of the numerous components tobacco smoke, polycyclic aromatic hydrocarbons appear to be principal compounds that yield substrates for these enzymes, GSTM1-1 being effective with those PAH derivatives so far studied; however, gene locus GSTM1 is polymorphic, containing two well-characterized expressing genes and null allele. Use cDNA or appropriate...

10.1289/ehp.929887 article EN public-domain Environmental Health Perspectives 1992-11-01

Recent evidence demonstrates that the androgen receptor (AR) continues to influence prostate cancer growth despite medical therapies reduce circulating ligands castrate levels and/or block ligand binding. Whereas mutation, amplification, overexpression of AR, or cross-talk between AR and other factor pathways may explain failure ablation in some cases, there is little supporting a causal role cancer. In this study, we functionally directly address whereby contributes spontaneous progression...

10.1073/pnas.0408925102 article EN Proceedings of the National Academy of Sciences 2005-01-18

NOR-1/NR4A3 is an “orphan member” of the nuclear hormone receptor superfamily. NOR-1 and its close relatives Nurr1 Nur77 are members NR4A subgroup receptors. Members induced through multiple signal transduction pathways. They have been implicated in cell proliferation, differentiation, T-cell apoptosis, chondrosarcomas, neurological disorders, inflammation, atherogenesis. However, mechanism transcriptional activation, coactivator recruitment, agonist-mediated activation remain obscure....

10.1074/jbc.m300088200 article EN cc-by Journal of Biological Chemistry 2003-06-29

Summary Studies of face processing have begun to elucidate the brain regions involved in social cognition, which include frontal and temporal known be reduced volume schizophrenia. In this case-control study participants with schizophrenia (n=20) showed marked deficits their ability interpret cues from faces, those experiencing positive symptoms were impaired recognising even basic facial emotions.

10.1192/bjp.185.2.169 article EN The British Journal of Psychiatry 2004-07-30

Genome-wide association studies (GWAS) have identified more than 30 prostate cancer (PrCa) susceptibility loci. One of these (rs2735839) is located close to a plausible candidate gene, KLK3, which encodes prostate-specific antigen (PSA). PSA widely used as biomarker for PrCa detection and disease monitoring. To refine the between variants in this region, we genotyping data from two-stage GWAS using samples UK Australia, Cancer Genetic Markers Susceptibility (CGEMS) study. Genotypes were...

10.1007/s00439-011-0981-1 article EN cc-by-nc Human Genetics 2011-04-04

Microplastics contamination has been widely reported in filter feeders yet the < 1 μm size fraction largely ignored. In attempt to characterize this sub and better understand distribution of microplastics feeders, field deployed oysters were characterised using a combination fractionation combined with pyrolysis-gas chromatography-mass spectrometry (Py-GC/MS) as well Fourier Transform-Infrared Spectroscopy (μFT-IR). Sequential filtration followed by Py-GC/MS identified 1–22 contain highest...

10.1016/j.hazl.2021.100021 article EN cc-by-nc-nd Journal of Hazardous Materials Letters 2021-03-21

The androgen receptor (AR), a member of the steroid superfamily nuclear transcription factors, mediates signaling in diverse target tissues. Here we report AR gene mutations identified human prostate cancer and autochthonous transgenic adenocarcinoma mouse model that colocate to residues 668QPIF671 at boundary hinge ligand-binding domain, resulting receptors exhibit 2- 4-fold increased activity compared with wild-type response dihydrotestosterone, estradiol, progesterone, adrenal androgens,...

10.1210/mend.15.1.0581 article EN Molecular Endocrinology 2001-01-01

We have used the autochthonoustransgenic adenocarcinoma of mouseprostate (TRAMP) model to investigate relationship between somatic mutation in androgen receptor (AR) and emergence androgen-independent prostate cancer. Here we report identification, isolation, characterization distinct classes AR variants from spontaneous tumors TRAMP model. Using cDNA cloning, single stranded conformation polymorphism sequencing strategies, 15 unique mutations were identified obtained eight mice 24 29 weeks...

10.1074/jbc.m008207200 article EN cc-by Journal of Biological Chemistry 2001-04-01

A rat liver mitochondrial-matrix fraction was prepared and shown to have 1-chloro-2,4-dinitrobenzene(CDNB)-metabolizing glutathione transferase (GST) activity. Further fractionation by sequential gel filtration, isoelectric focusing or chromatofocusing hydroxyapatite chromatography yielded three GSTs of pI 9.3, 8.9 7.5, none which bound a GSH-agarose affinity matrix. Most the activity associated with pI-9.3 form, selected for further study. Its tested following potential substrates in...

10.1042/bj2780137 article EN Biochemical Journal 1991-08-15

Abstract Although the androgen receptor (AR) is accepted as major determinant of prostate cancer cell survival throughout disease progression, it currently unclear how sustains genomic signaling under conditions systemic ablation. Here, we show that evolutionarily conserved Hsp70/Hsp90 cochaperone, small glutamine–rich tetratricopeptide repeat containing protein α (αSGT), interacts with hinge region human AR in yeast and mammalian cells. Overexpression RNA interference revealed αSGT acts to...

10.1158/0008-5472.can-07-1646 article EN Cancer Research 2007-10-15
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