E-LIB Suche - Ergebnisse für: Sheikh, Taimoor I.

1

Wide spectrum of neuronal and network phenotypes in human s..:

Mok, Rebecca S. F. ; Zhang, Wenbo ; Sheikh, Taimoor I....
Translational Psychiatry. 12 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

2

Heterozygous De Novo Truncating Mutation of Nucleolin in an..:

Sheikh, Taimoor I. ; Harripaul, Ricardo ; Vasli, Nasim...
Genes. 13 (2021) 1 - p. 51 , 2021

Link: https://doi.org/10.3390/..

3

Biallelic mutations in the death domain of PIDD1 impair cas..:

Sheikh, Taimoor I. ; Vasli, Nasim ; Pastore, Stephen...
Translational Psychiatry. 11 (2021) 1 - p. , 2021

Link: https://doi.org/10.1038/..

4

MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bou..:

Martínez de Paz, Alexia ; Khajavi, Leila ; Martin, Hélène...
Epigenetics & Chromatin. 12 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

5

Biallelic missense variants in ZBTB11 can cause intellectua..:

Fattahi, Zohreh ; Sheikh, Taimoor I ; Musante, Luciana...
Human Molecular Genetics. 27 (2018) 18 - p. 3177-3188 , 2018

Link: https://doi.org/10.1093/..

6

MeCP2_E1 N-terminal modifications affect its degradation ra..:

Sheikh, Taimoor I ; de Paz, Alexia Martínez ; Akhtar, Shamim..
Human Molecular Genetics. 26 (2017) 21 - p. 4132-4141 , 2017

Link: https://doi.org/10.1093/..

7

From Function to Phenotype: Impaired DNA Binding and Cluste..:

Sheikh, Taimoor I. ; Ausió, Juan ; Faghfoury, Hannah...
Scientific Reports. 6 (2016) 1 - p. , 2016

Link: https://doi.org/10.1038/..

8

Mutations in DCPS and EDC3 in autosomal recessive intellect..:

Ahmed, Iltaf ; Buchert, Rebecca ; Zhou, Mi...
Human Molecular Genetics. 24 (2015) 11 - p. 3172-3180 , 2015

Link: https://doi.org/10.1093/..

9

Identification of a homozygous splice site mutation in the ..:

Ahmed, Iltaf ; Mittal, Kirti ; Sheikh, Taimoor I....
Human Genetics. 133 (2014) 11 - p. 1419-1429 , 2014

Link: https://doi.org/10.1007/..

10

A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a c..:

Sheikh, Taimoor I ; Mittal, Kirti ; Willis, Mary J.
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013

Link: https://doi.org/10.1186/..

11

Expression of EBV Encoded viral RNA 1, 2 and anti-inflammat..:

Sheikh, Taimoor I ; Qadri, Ishtiaq
Diagnostic Pathology. 6 (2011) 1 - p. , 2011

Link: https://doi.org/10.1186/..

12

Wide spectrum of neuronal and network phenotypes in human s..:

Mok, Rebecca SF ; Zhang, Wenbo ; Sheikh, Taimoor I...
qt8xq9276p. , 2022

Link: https://escholarship.org..

13

Wide spectrum of neuronal and network phenotypes in human s..:

Mok, Rebecca S. F ; Zhang, Wenbo ; Sheikh, Taimoor I...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576700/. , 2022

Link: http://www.ncbi.nlm.nih...

14

Heterozygous De Novo Truncating Mutation of Nucleolin in an..:

Sheikh, Taimoor I ; Harripaul, Ricardo ; Vasli, Nasim...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774667/. , 2021

Link: http://www.ncbi.nlm.nih...

15

Heterozygous De Novo Truncating Mutation of Nucleolin in an..:

Sheikh, Taimoor I ; Harripaul, Ricardo ; Vasli, Nasim...
Genes 13 (1): 51 (2022). , 2021

Link: http://hdl.handle.net/18..