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UnknownPRG-1 transcriptional regulation independent from Nex1/Math2-mediated activation.
Not available
S-EPMC11114846 | biostudies-literature
UnknownWhat's the hype about CDK5RAP2?
Not available
S-EPMC11115181 | biostudies-literature
UnknownNovel Alternative Splice Variants of Mouse Cdk5rap2.
Not available
S-EPMC4556188 | biostudies-literature
UnknownClinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation.
Not available
S-EPMC3639195 | biostudies-literature
UnknownTogaram1 is expressed in the neural tube and its absence causes neural tube closure defects.
Not available
S-EPMC11541697 | biostudies-literature
UnknownPTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients.
Not available
S-EPMC10657312 | biostudies-literature
UnknownHomozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.
Not available
S-EPMC5428974 | biostudies-literature
UnknownCombined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2).
Not available
S-EPMC4230835 | biostudies-literature
UnknownMutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness.
Not available
S-EPMC4284127 | biostudies-literature
UnknownPrecise Somatotopic Thalamocortical Axon Guidance Depends on LPA-Mediated PRG-2/Radixin Signaling.
Not available
S-EPMC5065528 | biostudies-literature
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