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Academic Journal

Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation.

Authors : Ribchester, Richard R.¹ (AUTHOR); Thomson, Derek¹ (AUTHOR); Wood, Nigel I.² (AUTHOR)

Source: European Journal of Neuroscience. Dec2004, Vol. 20 Issue 11, p3092-3114. 23p.

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Academic Journal

Werner helicase polymorphism is not associated with Alzheimer's disease.

Authors : Payãao, Spencer Luiz Marques^1,2; De Labio, Roger Willian¹; Gatti, Luciano Lobo^1,2

Source: Journal of Alzheimer's Disease. 2004, Vol. 6 Issue 6, p591-594. 4p. 1 Chart.

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Academic Journal

PRNPpolymorphisms in Chinese ovine, caprine and bovine breeds.

Authors : Zhang, L.¹; Li, N.¹ ; Fan, B.¹

Source: Animal Genetics. Dec2004, Vol. 35 Issue 6, p457-461. 5p.

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Academic Journal

New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications.

Authors : Moutou, Céline¹; Gardes, Nathalie¹; Viville, Stéphane^1,2

Source: European Journal of Human Genetics. Dec2004, Vol. 12 Issue 12, p1007-1014. 8p.

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Academic Journal

Early onset Huntington disease: a neuronal degeneration syndrome.

Authors : Seneca, Sara¹ ; Fagnart, Dominique²; Keymolen, Kathelijn¹

Source: European Journal of Pediatrics. Dec2004, Vol. 163 Issue 12, p717-721. 5p. 1 Black and White Photograph.

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Academic Journal

Rodent Abeta(1-42) exhibits oxidative stress properties similar to those of human Abeta(1-42): Implications for proposed mechanisms of toxicity.

Authors : Boyd-Kimball, Debra¹; Sultana, Rukhsana¹; Mohmmad-Abdul, Hafiz¹

Source: Journal of Alzheimer's Disease. 2004, Vol. 6 Issue 5, p515-525. 11p. 3 Black and White Photographs, 1 Diagram, 5 Graphs.

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Academic Journal

Molecular targets for neuroprotection.

Authors : Przedborski, Serge¹

Source: Amyotrophic Lateral Sclerosis & Other Motor Neuron Disorders. Sep2004 Supplement 1, Vol. 5, p14-18. 5p.

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Academic Journal

Polymorphism in candidate genes: implications for the risk and treatment of idiopathic Parkinson's disease.

Authors : Gilgun-Sherki, Y.^1,2; Djaldetti, R.^1,2 ; Melamed, E.^1,2

Source: Pharmacogenomics Journal. 2004, Vol. 4 Issue 5, p291-306. 16p. 1 Diagram, 3 Charts.

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Academic Journal

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families.

Authors : Mariotti, C.¹ ; Gellera, C.¹; Rimoldi, M.¹

Source: Neurological Sciences. Jul2004, Vol. 25 Issue 3, p130-137. 8p.

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Academic Journal

Specific caspase interactions and amplification are involved in selective neuronal vulnerability in Huntington's disease.

Authors : Hermel, E.^1,2; Gafni, J.¹; Propp, S.S.¹

Source: Cell Death & Differentiation. Apr2004, Vol. 11 Issue 4, p424-438. 15p.

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فلترة النتائج

Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation.

Werner helicase polymorphism is not associated with Alzheimer's disease.

PRNPpolymorphisms in Chinese ovine, caprine and bovine breeds.

New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications.

Early onset Huntington disease: a neuronal degeneration syndrome.

Rodent Abeta(1-42) exhibits oxidative stress properties similar to those of human Abeta(1-42): Implications for proposed mechanisms of toxicity.

Molecular targets for neuroprotection.

Polymorphism in candidate genes: implications for the risk and treatment of idiopathic Parkinson's disease.

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families.

Specific caspase interactions and amplification are involved in selective neuronal vulnerability in Huntington's disease.

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