… of DICER1 alterations in pineoblastoma given the finding of biallelic inactivating alterations
in the gene in a subset of cases (de Kock et al., 2014; de Kock et al., 2019; Lee et al., 2019). …

DICER1 syndrome is a rare tumor predisposition syndrome with manifestations that predominantly
affect children and young adults. The syndrome is typically caused by heterozygous …

Objective: To identify reliable predictors of outcome in comatose patients after cardiac arrest
using a single routine EEG and standardized interpretation according to the terminology …

… " (De Kock 23) was decisively broken. But for all this, there were some misgivings. Breyten
Breytenbach clearly felt disturbed by the dangers of a new "alternative" consensus for culture …

… Leanne de Kock … d Expression and detection rates of differentially expressed genes
commonly induced in warm-dissociated samples (differentially expressed in at least four cell types). …

Individuals harboring germ-line DICER1 mutations are predisposed to a rare cancer
syndrome, the DICER1 Syndrome or pleuropulmonary blastoma-familial tumor and dysplasia …

Nanocellulose has over the past decades attracted considerable interest due to its favourable
properties compared to the commonly used polymeric materials in the fabrication of …

Germ-line RB-1 mutations predispose to pineoblastoma (PinB), but other predisposing genetic
factors are not well established. We recently identified a germ-line DICER1 mutation in a …

Ovarian Sertoli-Leydig cell tumors (SLCTs) are uncommon sex cord-stromal tumors associated
with both germ-line and somatic DICER1 mutations, the frequency of which has varied …

Context: Carriers of germline DICER1 mutations are predisposed to a rare cancer syndrome,
the DICER1 syndrome. Thyroid abnormalities are a common finding in DICER1 syndrome …