Results 301 to 310 of about 204,221 (349)
Clinical features of dentatorubral-pallidoluysian atrophy: A survey of Chinese patients. [PDF]
J Int Med ResZheng N, Li M, Wang YX, Yao GE.
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Development and validation of an interpretable machine learning model for predicting chronic atrophic gastritis in elderly patients. [PDF]
Front Med (Lausanne)Fan W +7 more
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Combined oral and peripheral blood detection of <i>Porphyromonas</i> gingivalis associates with coronary heart disease and gut microbiota alterations in a coronary angiography cohort. [PDF]
J Oral MicrobiolWu Y +8 more
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Coastlines, Cags and Communications
Media International Australia, 2008This paper layers communication theory over a cultural context by examining how Community Action Groups (CAGs) have responded to development along Australian coastlines. It analyses how communication and media strategies and techniques have been adopted by the third sector to challenge commercial and government organisations which have proposed coastal
Johnston, Jane, Gration, Steve
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Pathology of CAG repeat diseases
Neuropathology, 2000Neuronal intranuclear inclusions have become the neuropathological signature of the CAG repeat diseases, although their cytotoxicity is a matter of controversy. It has been demonstrated that the inclusions in dentatorubral–pallidoluysian atrophy (DRPLA) and Machado–Joseph disease (MJD) were immunopositive for several transcription factors such as TATA ...
M, Yamada, S, Tsuji, H, Takahashi
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Neurology, 1997
Molecular genetics has had a major impact on neurology. The genes for many neurodevelopmental and neurodegenerative disorders have been identified, and molecular diagnosis has replaced invasive and cumbersome diagnostic procedures. The hereditary ataxias may have benefited most from molecular studies.
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Molecular genetics has had a major impact on neurology. The genes for many neurodevelopmental and neurodegenerative disorders have been identified, and molecular diagnosis has replaced invasive and cumbersome diagnostic procedures. The hereditary ataxias may have benefited most from molecular studies.
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Cas9-mediated replacement of expanded CAG repeats in a pig model of Huntington’s disease
Nature Biomedical Engineering, 2023Sen Yan +17 more
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Neurology, 1999
Many neurodegenerative diseases are caused by expansions in DNA sequences called trinucleotide repeats.1-3 Huntington’s disease (HD), dentatorubropallidoluysian atrophy, and most of the autosomal dominant cerebellar ataxias (ADCAs) are caused by expansions in CAG repeat sequences that code for a string of glutamine residues at the amino acid level ...
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Many neurodegenerative diseases are caused by expansions in DNA sequences called trinucleotide repeats.1-3 Huntington’s disease (HD), dentatorubropallidoluysian atrophy, and most of the autosomal dominant cerebellar ataxias (ADCAs) are caused by expansions in CAG repeat sequences that code for a string of glutamine residues at the amino acid level ...
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