M. Percy

发表

Molecular Shuttle Chelation: The Use of Ascorbate, Desferrioxamine and Feralex-G in Combination to Remove Nuclear Bound Aluminum

J. Cui, W. Lukiw, T. Kruck, 2004, Cellular and Molecular Neurobiology.

Celiac Disease: Its Many Faces and Relevance to Developmental Disabilities

M. Percy, E. Propst, 2008 .

Metal-Sulfate Induced Generation of ROS in Human Brain Cells: Detection Using an Isomeric Mixture of 5- and 6-Carboxy-2′,7′-Dichlorofluorescein Diacetate (Carboxy-DCFDA) as a Cell Permeant Tracer

Aileen I. Pogue, Walter J. Lukiw, Yuhai Zhao, 2012, International journal of molecular sciences.

Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: II. Further cytogenetic analysis of the marker and characterization of the high-level repeat sequences using fluorescence in situ hybridization.

M. Somerville, E. Jabs, D. Miller, 1993, American journal of medical genetics.

Peripheral Markers of Alzheimer’s

M. Percy, H. Potter, D. Andrews, 2000 .

Nanomolar aluminum induces pro-inflammatory and pro-apoptotic gene expression in human brain cells in primary culture.

W. Lukiw, T. Kruck, M. Percy, 2005, Journal of inorganic biochemistry.

Synergistic effects of iron and aluminum on stress-related gene expression in primary human neural cells.

J. Cui, W. Lukiw, T. Kruck, 2005, Journal of Alzheimer's disease : JAD.

Hemochromatosis and the enigma of misplaced iron: Implications for infectious disease and survival

M. Percy, E. Weinberg, S. Moalem, 2004, Biometals.

Relation between apolipoprotein E genotype, hepatitis b virus status, and thyroid status in a sample of older persons with down syndrome

A. Warren, T. Mazzulli, A. Dalton, 2003, American journal of medical genetics. Part A.

Age-associated chromosome 21 loss in Down syndrome: possible relevance to mosaicism and Alzheimer disease.

M. Somerville, A. Dalton, M. Percy, 1993, American journal of medical genetics.

Serum creatine kinase and pyruvate kinase in duchenne muscular dystrophy carrier detection

M. W. Thompson, M. Percy, C. Verellen-Dumoulin, 1979, Muscle & nerve.

Involvement of ApoE E4 and H63D in sporadic Alzheimer's disease in a folate-supplemented Ontario population.

M. Freedman, M. Somerville, Katherine Zanibbi, 2008, Journal of Alzheimer's disease : JAD.

A microRNA cluster (let-7c, miRNA-99a, miRNA-125b, miRNA-155 and miRNA-802) encoded at chr21q21.1-chr21q21.3 and the phenotypic diversity of Down's syndrome (DS; trisomy 21).

W. Lukiw, M. Percy, Yuhai Zhao, 2017, Journal of nature and science.

CBC – The Nature of Things with David Suzuki : Autism Enigma Abstract

A. F. Schormans, M. Percy, I. Brown, 2013 .

Human papillomavirus infection of morphologically normal cervical epithelium adjacent to squamous dysplasia and invasive carcinoma.

T. Colgan, M. Percy, D. Andrews, 1989, Human pathology.

G protein-coupled receptors disrupted in human genetic disease.

M. Thompson, D. Cole, M. Percy, 2008, Methods in molecular biology.

Chromosome 1p36 in migraine with aura: association study of the 5HT1D locus

G. Ebers, M. Thompson, M. Percy, 2012, Neuroreport.

Localization of a new ferritin heavy chain sequence present in human brain mRNA to chromosome 11.

M. Percy, J. Joshi, M. Dhar, 1995, Genome.

Selective accumulation of aluminum in cerebral arteries in Alzheimer's disease (AD).

W. Lukiw, James M. Hill, T. Kruck, 2013, Journal of inorganic biochemistry.

Neurofilament Light and Polyadenylated mRNA Levels Are Decreased in Amyotrophic Lateral Sclerosis Motor Neurons

M. Somerville, C. Bergeron, M. Percy, 1994, Journal of neuropathology and experimental neurology.

Epidemic pathogenic selection: an explanation for hereditary hemochromatosis?

T. Kruck, M. Percy, S. Moalem, 2002, Medical hypotheses.

Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis

P. Fraser, W. Tatton, P. George-Hyslop, 1994, Neuron.

Serum creatine kinase in the detection of duchenne muscular dystrophy carriers: Effects of season and multiple testing

M. W. Thompson, M. Percy, D. Andrews, 1982, Muscle & nerve.

Immunoglobulin G subclasses in older persons with Down syndrome

H. Wiśniewski, P. Mehta, A. Dalton, 1993, Journal of the Neurological Sciences.

Creatine kinase–“no phospho‐, please!”

M. W. Thompson, M. Percy, Margaret W. Thompson, 1981, Muscle & nerve.

Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.

C. Gunter, C. Schwartz, W. Brown, 1999, American journal of medical genetics.

G protein-coupled receptor mutations and human genetic disease.

M. Thompson, D. Bichet, G. Hendy, 2014, Methods in molecular biology.

Early insight into the potential contribution of aluminum to neurodegeneration - A tribute to the research work of Robert D. Terry, Igor Klatzo, Henryk M. Wisniewski and Donald R.C. Mclachlan.

M. Percy, J. Hill, W. Lukiw, 2019, Journal of inorganic biochemistry.

Creatine kinase isozyme transition in chicks with hereditary muscular dystrophy

M. W. Thompson, P. Stewart, M. Percy, 1981, Muscle and Nerve.

Metal sulfate-mediated induction of pathogenic genes and repression by phenyl butyl nitrone and Feralex-G

W. Lukiw, T. Kruck, M. Percy, 2008, Neuroreport.

Accumulation of S100 beta mRNA and protein in cerebellum during infancy in Down syndrome and control subjects.

D. O’Hanlon, L. Becker, M. Percy, 1996, Brain research. Molecular brain research.

Autoimmune thyroiditis associated with mild "subclinical" hypothyroidism in adults with Down syndrome: a comparison of patients with and without manifestations of Alzheimer disease.

M. Somerville, A. Dalton, M. Percy, 1990, American journal of medical genetics.

Accumulation of S100β mRNA and protein in cerebellum during infancy in Down syndrome and control subjects

D. O’Hanlon, L. Becker, M. Percy, 1996 .

A comprehensive guide to intellectual and developmental disabilities

M. Percy, I. Brown, 2007 .

RETRACTED ARTICLE: Aluminum in Neurological and Neurodegenerative Disease

W. J. Walsh, C. Bergeron, W. Lukiw, 2019, Molecular Neurobiology.

Hyperphosphatasia with neurologic deficit: a pyridoxine-responsive seizure disorder?

M. Thompson, D. Cole, M. Percy, 2006, Pediatric neurology.

Towards the prevention of potential aluminum toxic effects and an effective treatment for Alzheimer's disease.

W. Lukiw, T. Kruck, M. Percy, 2011, Journal of inorganic biochemistry.

Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: I. Application of a new model for estimation of the risk of disease associated with the marker.

M. Percy, D. Andrews, D. Crapper McLachlan, 1991, American journal of medical genetics.

Aluminum in neurological disease – a 36 year multicenter study

W. J. Walsh, C. Bergeron, W. Lukiw, 2018, Journal of Alzheimer's disease & Parkinsonism.

Copper/zinc superoxide dismutase mRNA levels are increased in sporadic amyotrophic lateral sclerosis motorneurons

M. Somerville, C. Bergeron, M. Percy, 1994, Brain Research.

Mutations in the open reading frame of the β-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease

E. Rogaev, P. S. St George-Hyslop, H. Medeiros, 2001, Neurogenetics.

Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.

J. Rommens, Y. Agid, R. Sherrington, 1996, Human molecular genetics.

Is heart disease a risk factor for low dementia test battery scores in older persons with Down syndrome? Exploratory, pilot study, and commentary

W. Lukiw, M. Percy, 2017, International journal of developmental disabilities.

Epilepsy and Developmental Disability Part I : Developmental Disorders in Which Epilepsy May be Comorbid

M. Thompson, M. Percy, Vasan Persad, 2004 .

Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination.

M. W. Thompson, M. Percy, D. Andrews, 1982, American journal of medical genetics.

Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination.

M. W. Thompson, M. Percy, D. Andrews, 1981, American journal of medical genetics.

Risk factors for development of dementia in a unique six-year cohort study. I. An exploratory, pilot study of involvement of the E4 allele of apolipoprotein E, mutations of the hemochromatosis-HFE gene, type 2 diabetes, and stroke.

M. Somerville, Angeles A. Garcia, M. Percy, 2013, Journal of Alzheimer's disease : JAD.

Aluminum and its potential contribution to Alzheimer's disease (AD)

Walter J. Lukiw, Yuhai Zhao, W. Lukiw, 2014, Front. Aging Neurosci..

Is hemochromatosis a risk factor for Alzheimer's disease?

R. Scott, J. Connor, C. Vergani, 2001, Journal of Alzheimer's disease : JAD.

Are hereditary hemochromatosis mutations involved in Alzheimer disease?

A. Warren, A. Dalton, T. Kruck, 2000, American journal of medical genetics.

A Family with Multiple Instances of Definite, Probable and Possible Early-Onset Alzheimer's Disease

M. Percy, R. Becker, H. Karlinsky, 1991, British Journal of Psychiatry.

A human immunoglobulin G with deletions in both heavy and light polypeptide chains.

M. Percy, G. E. Connell, D. M. Parr, 1972, Immunochemistry.

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder

I. Rainero, J. L. Haines, J. A. Hardy, 1990, Nature.

Localization and quantitation of 68 kDa neurofilament and superoxide dismutase-1 mRNA in Alzheimer brains.

M. Somerville, C. Bergeron, D. McLachlan, 1991, Brain research. Molecular brain research.

Deletions in Immunoglobulin Polypeptide Chains as Evidence for Breakage and Repair in DNA

M. Percy, E. Fanning, O. Smithies, 1971, Science.

Red cell superoxide dismutase, glutathione peroxidase and catalase in Down syndrome patients with and without manifestations of Alzheimer disease.

A. Dalton, M. Percy, D. Andrews, 1990, American journal of medical genetics.

Progressive inflammatory pathology in the retina of aluminum-fed 5xFAD transgenic mice.

W. Lukiw, M. Percy, A. Pogue, 2015, Journal of inorganic biochemistry.

Characterization of an NF-kappaB-regulated, miRNA-146a-mediated down-regulation of complement factor H (CFH) in metal-sulfate-stressed human brain cells.

Yuhai Zhao, J. Cui, W. Lukiw, 2009, Journal of inorganic biochemistry.

Up-regulation of NF-kB-sensitive miRNA-125b and miRNA-146a in metal sulfate-stressed human astroglial (HAG) primary cell cultures.

J. Cui, W. Lukiw, T. Kruck, 2011, Journal of inorganic biochemistry.

Advances in Understanding Causes of Autism and Effective Interventions

M. Percy, I. Brown, Indu Joshi, 2003 .

DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.

M. Percy, D. Andrews, P. Brasher, 1986, American journal of medical genetics.

Serum myoglobin in Duchenne muscular dystrophy carrier detection: a comparison with creatine kinase and hemopexin using logistic discrimination.

M. Percy, D. Andrews, L. S. Chang, 1984, American journal of medical genetics.

Generation of Reactive Oxygen Species (ROS) and Pro-Inflammatory Signaling in Human Brain Cells in Primary Culture

W. Lukiw, M. Percy, A. Pogue, 2012, Journal of Alzheimer's disease & Parkinsonism.

Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the β‐amyloid precursor protein gene

J. Haines, P. S. St George-Hyslop, R. Tanzi, 1992, Neurology.

Monozygotic twins concordant for late-onset probable Alzheimer disease with suspected Alzheimer disease in four sibs.

P. S. St George-Hyslop, L. Farrer, P. Ray, 1992, American journal of medical genetics.

Aluminum-Induced Amyloidogenesis and Impairment in the Clearance of Amyloid Peptides from the Central Nervous System in Alzheimer’s Disease

W. Lukiw, M. Percy, A. Pogue, 2014, Front. Neurol..

Molecular Genetic Predictive Testing for Alzheimer's Disease: Deliberations and Preliminary Recommendations

W. Meschino, M. Percy, H. Karlinsky, 1994, Alzheimer disease and associated disorders.

Chromosome 21-Encoded microRNAs (mRNAs): Impact on Down’s Syndrome and Trisomy-21 Linked Disease

W. Lukiw, M. Percy, P. Alexandrov, 2017, Cellular and Molecular Neurobiology.

Localization of the 68,000-Da human neurofilament gene (NF68) using a murine cDNA probe.

M. Somerville, M. Percy, D. McLachlan, 1988, Genome.

Methylation of the 5′ flanking sequences of the ribosomal DNA in human cell lines and in a human‐hamster hybird cell line

M. Rocchi, D. Miller, A. Baldini, 1992, Journal of cellular biochemistry.

Peripheral Markers of Alzheimer's Disease: Directions From the Alzheimer Pathogenic Pathway

M. Percy, H. Potter, D. Andrews, 2000 .