about
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyPreaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRSSeeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function.Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathyCDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly.A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family.Genetic heterogeneity in Pakistani microcephaly families revisited.Prevention of beta-thalassemia in a large Pakistani family through cascade testing.Mutations in multiple components of the nuclear pore complex cause nephrotic syndromeNesprin-1 impact on tumorigenic cell phenotypesUnilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome profiling
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Muhammad Sajid Hussain
@ast
Muhammad Sajid Hussain
@en
Muhammad Sajid Hussain
@es
Muhammad Sajid Hussain
@nl
Muhammad Sajid Hussain
@sl
type
label
Muhammad Sajid Hussain
@ast
Muhammad Sajid Hussain
@en
Muhammad Sajid Hussain
@es
Muhammad Sajid Hussain
@nl
Muhammad Sajid Hussain
@sl
prefLabel
Muhammad Sajid Hussain
@ast
Muhammad Sajid Hussain
@en
Muhammad Sajid Hussain
@es
Muhammad Sajid Hussain
@nl
Muhammad Sajid Hussain
@sl
P106
P31
P496
0000-0002-1353-8809