Shyma Hamdan

33 Cleveland Street, W1W 7FF
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 8 publications

Correction: Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo.

Correction: Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo.

Journal: Acta neuropathologica

Published: March 30, 2026

Modification of early behavioural, physiological and neuropathological endpoints by syntaxin-6 knockout in a humanised P301S transgenic model of tauopathy.

Modification of early behavioural, physiological and neuropathological endpoints by syntaxin-6 knockout in a humanised P301S transgenic model of tauopathy.

Journal: Acta neuropathologica

Published: January 22, 2026

Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo.

Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo.

Journal: Acta neuropathologica

Published: August 02, 2025

Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo.

Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo.

Journal: Acta neuropathologica

Published: August 02, 2025

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.

Journal: PLoS biology

Published: October 17, 2019

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

Journal: PLoS pathogens

Published: March 06, 2015

A naturally occurring variant of the human prion protein completely prevents prion disease.

A naturally occurring variant of the human prion protein completely prevents prion disease.

Journal: Nature

Published: January 28, 2015

Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.

Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.

Journal: PLoS pathogens

Published: August 05, 2013

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Last Updated: 09/26/2026