Search Results - "Curtain, R. P."

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine by LEA, R. A, NYHOLT, D. R, RILEY, J. H, SMITHIES, Y. J, KINRADE, S, GRIFFITHS, L. R, CURTAIN, R. P, OVCARIC, M, SCIASCIA, R, BELLIS, C, MACMILLAN, J, QUINLAN, S, GIBSON, R. A, MCCARTHY, L. C

“…Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on…”
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Familial typical migraine : significant linkage and localization of a gene to Xq24-28 by NYHOLT, D. R, CURTAIN, R. P, GRIFFITHS, L. R

“…In a previous study we found evidence for an X-linked genetic component for familial typical migraine in two large Australian white pedigrees, designated MF7…”
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Migraine association and linkage studies of an endothelial nitric oxide synthase (NOS3) gene polymorphism by GRIFFITHS, L. R, NYHOLT, D. R, CURTAIN, R. P, GOADSBY, P. J, BRIMAGE, P. J

“…Migraine shows strong familial aggregation. However, the number of genes involved in the disorder is unknown and not identified. Nitric oxide is involved in…”
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Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension by RUTHERFORD, Sue, JOHNSON, Matthew P, CURTAIN, Robert P, GRIFFITHS, Lyn R

“…Essential hypertension is a common multifactorial trait that results in a significantly increased risk for heart attack and stroke. The condition has a genetic…”
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Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees by Curtain, R. P., Lea, R. A., Tajouri, L., Haupt, L. M., Ovcaric, M., MacMillan, J., Griffiths, L. R.

“…Objectives: The aims of the study were: (i) to extend our linkage analysis of chromosome 1q microsatellite markers in predominately migraine with aura…”
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Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene by Nyholt, D R, Curtain, R P, Gaffney, P T, Brimage, P, Goadsby, P J, Griffiths, L R

“…5-Hydroxytryptamine (5HT), commonly known as serotonin, which predominantly serves as an inhibitory neurotransmitter in the brain, has long been implicated in…”
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Association of a low density lipoprotein receptor microsatellite variant with obesity by RUTHERFORD, S, NYHOLT, D. R, CURTAIN, R. P, QUINLAN, S. R, GAFFNEY, P. T, MORRIS, B. J, GRIFFITHS, L. R

“…To determine whether a microsatellite polymorphism located towards the 3' end of the low density lipoprotein receptor gene (LDLR) is associated with obesity. A…”
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Influence of Family History on Frequency of Glucagon Receptor Gly40Ser Mutation in Hypertensive Subjects by Morris, Brian J, Jeyasingam, Cheryl L, Zhang, Weiyi, Curtain, Robert P, Griffiths, Lyn R

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Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility by Lea, Rod A., Curtain, Robert P., Hutchins, Colin, Brimage, Peter J., Griffiths, Lyn R.

“…Typical migraine is a complex neurological disorder comprised of two main subtypes: migraine with (MA) and without aura (MO). The disease etiology is still…”
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No evidence for involvement of the human inducible nitric oxide synthase (iNOS) gene in susceptibility to typical migraine by Lea, Rod A., Curtain, Robert P., Shepherd, A. Graeme, Brimage, Peter J., Griffiths, Lyn R.

“…Migraine is a debilitating disorder affecting approximately 12% of Caucasian populations. The disease has a large genetic component, although at present the…”
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Familial typical migraine: significant linkage and localization of a gene to Xq24-28 by Nyholt, DR, Curtain, R P, Griffiths, L R

“…In a previous study we found evidence for an X-linked genetic component for familial typical migraine in two large Australian white pedigrees, designated MF7…”
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Cross-sectional study of a microsatellite marker in the low density lipoprotein receptor gene in obese normotensives by Griffiths, L R, Nyholt, D R, Curtain, R P, Gaffney, P T, Morris, B J

“…1. The low density lipoprotein receptor is an important regulator of serum cholesterol which may have implications for the development of both hypertension and…”
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Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma by Curtain, Robert P., Smith, Robert L., Ovcaric, Mick, Griffiths, Lyn R.

“…Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel,…”
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A typical migraine susceptibility region localizes to chromosome 1q31 by LEA, Rod A, SHEPHERD, A. Graeme, CURTAIN, Robert P, NYHOLT, Dale R, QUINLAN, Sharon, BRIMAGE, Peter J, GRIFFITHS, Lyn R

“…Migraine (with and without aura) is a prevalent neurovascular disease that shows strong familial aggregation, although the number of genes involved and the…”
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An investigation of the 5-HT2C receptor gene as a migraine candidate gene by Johnson, Matthew P., Lea, Rod A., Curtain, Robert P., MacMillan, John C., Griffiths, Lyn R.

“…Migraine is a common complex disorder, currently classified into two main subtypes, migraine with aura (MA) and migraine without aura (MO). The strong…”
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Investigation of an inducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population by Tajouri, Lotti, Martin, Virginie, Ovcaric, Micky, Curtain, Rob P, Lea, Rod A, Csurhes, Peter, Pender, Michael P, Griffiths, Lyn R

“…Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide…”
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