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Longer titles found: Multisystem proteinopathy (view)

searching for proteinopathy 10 found (26 total)

alternate case: Proteinopathy

Riluzole (1,137 words) [view diff] exact match in snippet view article find links to article

release from presynaptic terminals. Since CK1δ plays a key role in TDP-43 proteinopathy, a pathological hallmark of ALS, this could help to better decipher
Amyotrophic lateral sclerosis (17,684 words) [view diff] exact match in snippet view article find links to article
up to 50% of FTD patients. In December 2021 a paper found the TDP-43 proteinopathy is in turn caused by defective cyclophilin A which regulates TARDBP
Hippocampal sclerosis (1,744 words) [view diff] exact match in snippet view article find links to article
(Jan 2015). "Hippocampal sclerosis in Lewy body disease is a TDP-43 proteinopathy similar to FTLD-TDP Type A". Acta Neuropathol. 129 (1): 53–64. doi:10
Genetics of amyotrophic lateral sclerosis (3,945 words) [view diff] exact match in snippet view article find links to article
in the prion-like domains of hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS". Nature. 495 (7442): 467–73. doi:10.1038/nature11922. PMC 3756911
Lou Gehrig (9,323 words) [view diff] exact match in snippet view article find links to article
March 25, 2019. Retrieved August 1, 2016. McKee, A.C., et al.: TDP-43 Proteinopathy and Motor Neuron Disease in Chronic Traumatic Encephalopathy. Journal
Alzheimer's disease (17,602 words) [view diff] exact match in snippet view article find links to article
microglial lysosomal system in Alzheimer's disease: Guardian against proteinopathy". Ageing Research Reviews. 71: 101444. doi:10.1016/j.arr.2021.101444
Lary Walker (1,837 words) [view diff] exact match in snippet view article find links to article
and Harry LeVine introduced the term 'proteopathy' (also known as 'proteinopathy') to describe diseases characterized by the misfolding and aggregation
N6-Methyladenosine (5,212 words) [view diff] exact match in snippet view article find links to article
"Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS". Nature. 495 (7442): 467–73. Bibcode:2013Natur.495..467K. doi:10
Stress granule (12,254 words) [view diff] exact match in snippet view article find links to article
(2012). "Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitination"
Andrew E. Budson (1,931 words) [view diff] exact match in snippet view article find links to article
J., Cantu, R. C., Kowall, N. W., ... & Budson, A. E. (2010). TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy. Journal