Prions - Revision history

Aidan: Text replacement - "Creutzfeld-Jakob disease" to "Creutzfeldt-Jakob disease"

2020-11-06T16:27:06Z

Text replacement - "Creutzfeld-Jakob disease" to "Creutzfeldt-Jakob disease"

← Older revision		Revision as of 16:27, 6 November 2020
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	*Proteinaceous infectious particles that are capable of self-propagating		*Proteinaceous infectious particles that are capable of self-propagating
	*May be acquired by infection (iCJD and vCJD), sporadic mutation (sCJD and sFI), or heritable genetics (fCJD, GSS, and FFI)		*May be acquired by infection (iCJD and vCJD), sporadic mutation (sCJD and sFI), or heritable genetics (fCJD, GSS, and FFI)
	*In human, prion disease generally refers to [[~~Creutzfeld~~-Jakob disease]] and its subtypes, all caused by misfolding of PrP<sup>C</sup>, although there is some evidence that [[amyloidosis]], [[Alzheimer disease]], [[Parkinson disease]], [[frontotemporal dementia]], [[amyotrophic lateral sclerosis]] can be caused by self-propagating proteins		*In human, prion disease generally refers to [[Creutzfeldt-Jakob disease]] and its subtypes, all caused by misfolding of PrP<sup>C</sup>, although there is some evidence that [[amyloidosis]], [[Alzheimer disease]], [[Parkinson disease]], [[frontotemporal dementia]], [[amyotrophic lateral sclerosis]] can be caused by self-propagating proteins

	{\| class="wikitable"		{\| class="wikitable"
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	\|ritualistic cannibalism in Papua New Guinea		\|ritualistic cannibalism in Papua New Guinea
	\|-		\|-
	\|sporadic [[~~Creutzfeld~~-Jakob disease]]		\|sporadic [[Creutzfeldt-Jakob disease]]
	\|sCJD		\|sCJD
	\|human		\|human
	\|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>		\|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>
	\|-		\|-
	\|familial [[~~Creutzfeld~~-Jakob disease]]		\|familial [[Creutzfeldt-Jakob disease]]
	\|fCJD		\|fCJD
	\|human		\|human
Line 31:		Line 31:
	\|mutations in PRNP gene		\|mutations in PRNP gene
	\|-		\|-
	\|iatrogenic [[~~Creutzfeld~~-Jakob disease]]		\|iatrogenic [[Creutzfeldt-Jakob disease]]
	\|iCJD		\|iCJD
	\|human		\|human
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	\|PRNP haplotype 178N-129M		\|PRNP haplotype 178N-129M
	\|-		\|-
	\|variant [[~~Creutzfeld~~-Jakob disease]]		\|variant [[Creutzfeldt-Jakob disease]]
	\|vCJD		\|vCJD
	\|human		\|human

Aidan at 02:22, 5 November 2020

2020-11-05T02:22:25Z

@@ Line 1: / Line 1: @@
 {| class="wikitable"
@@ Line 94: / Line 92: @@
 |lemurs
 |BSE origin
-|}
+|}<br />
 [[Category:Organisms]]

Aidan at 02:15, 5 November 2020

2020-11-05T02:15:25Z

Show changes

Aidan at 01:51, 5 November 2020

2020-11-05T01:51:02Z

← Older revision		Revision as of 01:51, 5 November 2020
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	\|scrapie		\|scrapie
	\|—		\|—
	\|~~ssheep~~ and goats		\|sheep and goats
	\|unknown origin		\|unknown origin
	\|-		\|-

Aidan: Aidan moved page Prion disease to Prions

2020-11-05T01:50:48Z

Aidan moved page Prion disease to Prions

← Older revision	Revision as of 01:50, 5 November 2020
(No difference)

Aidan: Removed redirect to Creutzfeld-Jakob disease

2020-11-05T01:50:31Z

Removed redirect to Creutzfeld-Jakob disease

← Older revision		Revision as of 01:50, 5 November 2020
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			{\| class="wikitable"
⚫	~~#REDIRECT~~ [[Creutzfeld-Jakob disease]]
			!Disease
			!Abbr
			!Host
			!Etiology
			\|-
			! colspan="4" \|Animal Prion Diseases
			\|-
			\|scrapie
			\|—
			\|ssheep and goats
			\|unknown origin
			\|-
			\|[[transmissible mink encephalopathy]]
			\|TME
			\|mink
			\|sheep or cattle origin
			\|-
			\|[[chronic wasting disease]]
			\|CWD
			\|cervids
			\|unknown origin
			\|-
			\|[[bovine spongiform encephalopathy]]
			\|BSE
			\|cattle
			\|unknown origin
			\|-
			\|[[exotic ungulate spongiform encephalopathy]]
			\|EUE
			\|Nyala, Kudu
			\|BSE origin
			\|-
			\|[[feline spongiform encephalopathy]]
			\|FSE
			\|cats
			\|BSE origin
			\|-
			\|[[non-human primate spongiform encephalopathy]]
			\|NHP
			\|lemurs
			\|BSE origin
			\|-
			! colspan="4" \|Human Prion Diseases
			\|-
			\|Kuru
			\|—
			\|human
			\|ritualistic cannibalism
			\|-
		⚫	\|sporadic [[Creutzfeld-Jakob disease]]
			\|sCJD
			\|human
			\|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>
			\|-
			\|familial [[Creutzfeld-Jakob disease]]
			\|fCJD
			\|human
			\|mutations in PRNP gene
			\|-
			\|Gerstmann-Straüssler-Scheinker syndrome
			\|GSS
			\|human
			\|mutations in PRNP gene
			\|-
			\|iatrogenic [[Creutzfeld-Jakob disease]]
			\|iCJD
			\|human
			\|infection from surgical exposure to sCJD
			\|-
			\|fatal familial insomnia
			\|FFI
			\|human
			\|PRNP haplotype 178N-129M
			\|-
			\|variant [[Creutzfeld-Jakob disease]]
			\|vCJD
			\|human
			\|BSE origin
			\|-
			\|sporadic fatal insomnia
			\|sFI
			\|human
			\|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>
			\|-
			\|variably protease-sensitive prionopathy
			\|VPSPr
			\|human
			\|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>
			\|}
			[[Category:Organisms]]

Aidan: Redirected page to Creutzfeld-Jakob disease

2020-08-12T22:13:03Z

Redirected page to Creutzfeld-Jakob disease

New page

#REDIRECT [[Creutzfeld-Jakob disease]]