Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease. (Q37164138)

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25 January 2020

title

Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease (English)

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Karen Roos

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Bernardino Ghetti

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Pierluigi Gambetti

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author name string

Xiangzhu Xiao

1

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Leticia Miravalle

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Jue Yuan

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Zhiqian Dong

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Robert Wyza

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Gregory T MacLennan

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Alan M Golichowski

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Geoff Kneale

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Nicholas King

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Qingzhong Kong

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Salvatore Spina

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Ruben Vidal

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Wen-Quan Zou

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language of work or name

English

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publication date

6 April 2009

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The American Journal of Pathology

25 January 2020

published in

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volume

174

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issue

5

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page(s)

1602-1608

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A novel human disease with abnormal prion protein sensitive to protease

25 January 2020

cites work

1 reference

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6 September 2017

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Antibody to DNA detects scrapie but not normal prion protein

6 September 2017

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Acquired prion disease: iatrogenic CJD, variant CJD, kuru

6 September 2017

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Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population

6 September 2017

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Pregnancy status and fetal prion genetics determine PrPSc accumulation in placentomes of scrapie-infected sheep

6 September 2017

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Preferential binding of fd gene 5 protein to tetraplex nucleic acid structures.

6 September 2017

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A new variant of Creutzfeldt-Jakob disease in the UK.

6 September 2017

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

6 September 2017

1 reference

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Prion protein biosynthesis in scrapie-infected and uninfected neuroblastoma cells

6 September 2017

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Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins

6 September 2017

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Iatrogenic Creutzfeldt-Jakob disease: the waning of an era.

6 September 2017

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Scrapie infectivity and proteinase K-resistant prion protein in sheep placenta, brain, spleen, and lymph node: implications for transmission and antemortem diagnosis.

14 September 2017

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Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

27 June 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

27 June 2018

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Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery

27 June 2018

1 reference

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Prion diseases are efficiently transmitted by blood transfusion in sheep.

27 June 2018

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Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains.

3 September 2018

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Sensitive detection of prion protein in human urine

3 September 2018

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Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

3 September 2018

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Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease.

3 September 2018

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Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form

3 September 2018

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Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease

3 September 2018

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Creutzfeldt-Jakob disease in a pregnant woman with an implanted dura mater graft.

3 September 2018

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3 September 2018

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Changing Patterns of Kuru: Epidemiological Changes in the Period of Increasing Contact of the Fore People with Western Civilization

3 September 2018

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3 September 2018

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12 December 2020

Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay

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12 December 2020

Demonstration of the Transmissible Agent in Tissue from a Pregnant Woman with Creutzfeldt–Jakob Disease

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12 December 2020

[Creutzfeldt-Jakob disease and pregnancy]

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Variant Creutzfeldt-Jakob disease in UK children: a national surveillance study

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12 December 2020

10.2353/AJPATH.2009.081045

Identifiers

DOI

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