A third HSAN5 mutation disrupts the nerve growth factor furin cleavage site

por Shaikh, Samiha S, Nahorski, Michael S, Woods, C Geoffrey
Publicado 2018

Before progressing from “exomes” to “genomes”… don’t forget splicing variants

por Shaikh, Samiha S., Nahorski, Michael S., Rai, Harjeet, Woods, C. Geoffrey
Publicado 2018

A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV)

por Shaikh, Samiha S., Chen, Ya‐Chun, Halsall, Sally‐Anne, Nahorski, Michael S., Omoto, Kiyoyuki, Young, Gareth T., Phelan, Anne, Woods, Christopher Geoffrey
Publicado 2016

Clathrin heavy chain 22 contributes to the control of neuropeptide degradation and secretion during neuronal development

por Nahorski, Michael S., Borner, Georg H. H., Shaikh, Samiha S., Davies, Alexandra K., Al-Gazali, Lihadh, Antrobus, Robin, Woods, C. Geoffrey
Publicado 2018

Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons

por Tanudjojo, Benedict, Shaikh, Samiha S., Fenyi, Alexis, Bousset, Luc, Agarwal, Devika, Marsh, Jade, Zois, Christos, Heman-Ackah, Sabrina, Fischer, Roman, Sims, David, Melki, Ronald, Tofaris, George K.
Publicado 2021

A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development

por Nahorski, Michael S., Al-Gazali, Lihadh, Hertecant, Jozef, Owen, David J., Borner, Georg H. H., Chen, Ya-Chun, Benn, Caroline L., Carvalho, Ofélia P., Shaikh, Samiha S., Phelan, Anne, Robinson, Margaret S., Royle, Stephen J., Woods, C. Geoffrey
Publicado 2015