Page last updated: 2024-10-16

formic acid and Dementias, Transmissible

formic acid has been researched along with Dementias, Transmissible in 4 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.

Research Excerpts

ExcerptRelevanceReference
"Human prion diseases are associated with a range of clinical presentations, and they are classified by both clinicopathological syndrome and etiology, with subclassification according to molecular criteria."1.46Methods for Molecular Diagnosis of Human Prion Disease. ( Adamson, G; Beck, JA; Brandner, S; Brock, L; Collinge, J; Joiner, S; Linehan, JM; Mead, S; Powell, C; Wadsworth, JDF, 2017)
"However, disease-associated gliosis and deposition of misfolded prion protein PrP(Sc) were identical in infected Tg2576-mice and non-transgenic littermate controls."1.35Prion infection of mice transgenic for human APPSwe: increased accumulation of cortical formic acid extractable Abeta(1-42) and rapid scrapie disease development. ( Apelt, J; Baier, M; Bamme, T; Burwinkel, M; Gültner, S; Riemer, C; Schliebs, R; Schwarz, A, 2008)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wadsworth, JDF1
Adamson, G1
Joiner, S1
Brock, L1
Powell, C1
Linehan, JM1
Beck, JA1
Brandner, S1
Mead, S1
Collinge, J1
Baier, M1
Apelt, J1
Riemer, C1
Gültner, S1
Schwarz, A1
Bamme, T1
Burwinkel, M1
Schliebs, R1
Zaborowski, A1
Kordek, R1
Botts, GT1
Liberski, PP1
Rubenstein, R1
Kascsak, RJ1
Papini, M1
Kascsak, R1
Carp, RI1
LaFauci, G1
Meloen, R1
Langeveld, J1

Other Studies

4 other studies available for formic acid and Dementias, Transmissible

ArticleYear
Methods for Molecular Diagnosis of Human Prion Disease.
    Methods in molecular biology (Clifton, N.J.), 2017, Volume: 1658

    Topics: Anti-Infective Agents, Local; Base Sequence; Brain; Brain Chemistry; Electrophoresis, Polyacrylamide

2017
Prion infection of mice transgenic for human APPSwe: increased accumulation of cortical formic acid extractable Abeta(1-42) and rapid scrapie disease development.
    International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 2008, Volume: 26, Issue:7

    Topics: Alzheimer Disease; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Animals; Cerebral Cortex;

2008
Immunohistochemical investigations of the prion protein accumulation in human spongiform encephalopathies. Special report II.
    Polish journal of pathology : official journal of the Polish Society of Pathologists, 2003, Volume: 54, Issue:1

    Topics: Antibodies, Monoclonal; Brain; Creutzfeldt-Jakob Syndrome; Formates; Gerstmann-Straussler-Scheinker

2003
Immune surveillance and antigen conformation determines humoral immune response to the prion protein immunogen.
    Journal of neurovirology, 1999, Volume: 5, Issue:4

    Topics: Amino Acid Sequence; Animals; Antibodies; Blotting, Western; Epitopes; Formates; Humans; Molecular S

1999