Suchergebnisse - "Tariq, Muhammad"

PubPharm (9)

1

Mask exhibits trxG-like behavior and associates with H3K27ac marked chromatin

enthalten in: Developmental biology | 2024

von Shaukat, A. | Bakhtiari, M. | Chaudhry, D. | +8

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

Modifier Genes in Microcephaly : A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ

enthalten in: Genes | 2021

von Makhdoom, E. | Waseem, S. | Iqbal, M. | +22

5

A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency

enthalten in: BMC medical genetics | 2014

von Jameel, M. | Klar, J. | Tariq, M. | +8

6

Drosophila GAGA factor polyglutamine domains exhibit prion-like behavior

enthalten in: BMC genomics | 2013

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

7

Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A

enthalten in: Journal of medical genetics | 2013

von Kalsoom, U. | Klopocki, E. | Wasif, N. | +6

8

The effect of acute dose charge particle radiation on expression of DNA repair genes in mice

enthalten in: Molecular and cellular biochemistry | 2011

von Tariq, M. | Soedipe, A. | Ramesh, G. | +6

ErratumIn: Mol Cell Biochem. 2011 Mar;349(1-2):219 Gridley, Daila S [added]

9

Epigenetic regulation of transcription in intermediate heterochromatin

enthalten in: EMBO reports | 2006

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

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