Suchergebnisse - "Tariq, Muhammad"

PubPharm (10)

1

Whole exome sequencing identifies a novel variant causing cockayne syndrome type I in a consanguineous Pakistani family

enthalten in: The International journal of neuroscience | 2024

von Zulfiqar, S. | Moawia, A. | Waseem, S. | +5

2

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss

enthalten in: Human genetics | 2021

von Ullah, F. | Rauf, W. | Khan, K. | +12

3

A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family

enthalten in: Genes | 2021

von Waseem, S. | Moawia, A. | Budde, B. | +13

4

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family

enthalten in: Genes | 2021

von Ramzan, S. | Tennstedt, S. | Tariq, M. | +12

5

CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly

enthalten in: Molecular genetics and genomics : MGG | 2017

von Sukumaran, S. | Stumpf, M. | Salamon, S. | +13

6

Genetic and functional analyses of ZIC3 variants in congenital heart disease

enthalten in: Human mutation | 2014

von Cowan, J. | Tariq, M. | Ware, S.

7

Drosophila GAGA factor polyglutamine domains exhibit prion-like behavior

enthalten in: BMC genomics | 2013

von Tariq, M. | Wegrzyn, R. | Anwar, S. | +2

8

Distinct roles of Hand2 in initiating polarity and posterior Shh expression during the onset of mouse limb bud development

enthalten in: PLoS genetics | 2010

von Galli, A. | Robay, D. | Osterwalder, M. | +6

9

Epigenetic regulation of transcription in intermediate heterochromatin

enthalten in: EMBO reports | 2006

von Habu, Y. | Mathieu, O. | Tariq, M. | +4

10

Depletion of MOM1 in non-dividing cells of Arabidopsis plants releases transcriptional gene silencing

enthalten in: EMBO reports | 2002

von Tariq, M. | Habu, Y. | Paszkowski, J.

1
[1]