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The multisubunit complex transcription factor IIH (TFIIH) has dual functions in transcriptional initiation and nucleotide… Expand Non-recurrent microdeletion (≤2 Mb in size) in 7p22.1 is a rarely described cytogenetic aberration, only recently reported in… Expand F‐box proteins play pivotal roles in multiple cellular processes; however, little is known about their functions in glioma… Expand Dominantly inherited mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common causes of familial Parkinson's disease… Expand There are no published reports of patients harboring microdeletions involving the 7p22.1 region. Although 7p22.1 microdeletions… Expand Fbxl7, a subunit of the SCF (Skp-Cul1-F-box protein) complex induces mitotic arrest in cells; however, molecular factors that… Expand Amyloid precursor protein (APP) is best known for its involvement in the pathogenesis of Alzheimer’s disease. We have previously… Expand Introduction. More than 60 cases of 7p22 duplications and deletions have been reported with over 16 of them occurring without… Expand