Suchergebnisse - "Sheikh, Taimoor I"

PubPharm (4)

1

Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations

enthalten in: Translational psychiatry | 2022

von Mok, R. | Zhang, W. | Sheikh, T. | +16

2

Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability

enthalten in: Translational psychiatry | 2021

von Sheikh, T. | Vasli, N. | Pastore, S. | +19

3

From Function to Phenotype : Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2

enthalten in: Scientific reports | 2016

von Sheikh, T. | Ausió, J. | Faghfoury, H. | +6

4

Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment

enthalten in: Human molecular genetics | 2015

von Ahmed, I. | Buchert, R. | Zhou, M. | +20

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