Page last updated: 2024-10-16

formic acid and Huntington Disease

formic acid has been researched along with Huntington Disease in 3 studies

formic acid: RN given refers to parent cpd
formic acid : The simplest carboxylic acid, containing a single carbon. Occurs naturally in various sources including the venom of bee and ant stings, and is a useful organic synthetic reagent. Principally used as a preservative and antibacterial agent in livestock feed. Induces severe metabolic acidosis and ocular injury in human subjects.

Huntington Disease: A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)

Research Excerpts

ExcerptRelevanceReference
"Fragmentation of expanded huntingtin in Huntington's disease must result from the operation of multiple proteolytic activities with little specificity and not from that of a specific endopeptidase; subsequent aggregation of the fragments by covalent and non-covalent bonds leads to the formation of the inclusions."1.33Purification of neuronal inclusions of patients with Huntington's disease reveals a broad range of N-terminal fragments of expanded huntingtin and insoluble polymers. ( Djian, P; Hoffner, G; Island, ML, 2005)
" Here we have report that, although expression of Huntingtin derivatives with a pathological poly(Q) expansion are innocuous in yeast, deletion of the flanking proline-rich region alters the shape and number of poly(Q) inclusions and unmasks toxic properties."1.33Critical role of the proline-rich region in Huntingtin for aggregation and cytotoxicity in yeast. ( Bertolotti, A; Dehay, B, 2006)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Iuchi, S1
Hoffner, G2
Verbeke, P1
Djian, P2
Green, H1
Island, ML1
Dehay, B1
Bertolotti, A1

Other Studies

3 other studies available for formic acid and Huntington Disease

ArticleYear
Oligomeric and polymeric aggregates formed by proteins containing expanded polyglutamine.
    Proceedings of the National Academy of Sciences of the United States of America, 2003, Mar-04, Volume: 100, Issue:5

    Topics: Animals; Blotting, Western; Brain; Cell Nucleus; Cerebellum; Cerebral Cortex; COS Cells; Cytosol; Di

2003
Purification of neuronal inclusions of patients with Huntington's disease reveals a broad range of N-terminal fragments of expanded huntingtin and insoluble polymers.
    Journal of neurochemistry, 2005, Volume: 95, Issue:1

    Topics: Adolescent; Adult; Aged; Brain; Cerebral Cortex; Formates; Humans; Huntingtin Protein; Huntington Di

2005
Critical role of the proline-rich region in Huntingtin for aggregation and cytotoxicity in yeast.
    The Journal of biological chemistry, 2006, Nov-24, Volume: 281, Issue:47

    Topics: Centrifugation, Density Gradient; Formates; Gene Deletion; Green Fluorescent Proteins; Heat-Shock Pr

2006