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UnknownRevision of the family Chalcididae (Hymenoptera, Chalcidoidea) from Vietnam, with the description of 13 new species.
Not available
S-EPMC4829922 | biostudies-literature
UnknownN-cadherin in neuroblastoma disease: expression and clinical significance.
Not available
S-EPMC3280274 | biostudies-literature
UnknownThe Magnetic Genome of Two-Dimensional van der Waals Materials.
Not available
S-EPMC9134533 | biostudies-literature
UnknownN-cadherin stabilises neural identity by dampening anti-neural signals.
Not available
S-EPMC6857587 | biostudies-literature
UnknownA structurally dynamic N-terminal region drives function of the staphylococcal peroxidase inhibitor (SPIN).
Not available
S-EPMC5818189 | biostudies-literature
UnknownGlutamate excitotoxicity in neurons triggers mitochondrial and endoplasmic reticulum accumulation of Parkin, and, in the presence of N-acetyl cysteine, mitophagy.
Not available
S-EPMC4322770 | biostudies-literature
GenomicssWGS on paired cfDNA and tissue DNA from pediatric cancer patients
We performed shallow whole genome sequencing (WGS) on circulating free (cf)DNA extracted from plasma or cerebrospinal fluid (CSF), and shallow WGS on the tissue DNA extracted from the biopsy in order to evaluate the correlation between the two biomaterials. After library construction and sequencing ...
ORGANISM(S): Homo sapiens 
2021-11-17 | E-MTAB-10548 | biostudies-arrayexpress
TranscriptomicsMinimally invasive classification of pediatric solid tumors using reduced representation bisulfite sequencing of cell-free DNA: a proof-of-principle study
This submission contains the data from https://www.biorxiv.org/content/10.1101/795047v2.full This dataset contains processed data of cell-free reduced representation bisulfite sequencing from 60 pediatric cancer samples, in order to classify them according to histopathological diagnosis. Files are ...
ORGANISM(S): Homo sapiens 
2020-02-27 | E-MTAB-8770 | biostudies-arrayexpress
UnknownA highly conserved region essential for NMD in the Upf2 N-terminal domain.
Not available
S-EPMC4871600 | biostudies-literature
TranscriptomicsDevelopment of gene expression signatures with lncRNAs for 15 T-ALL patients
Genetic studies in T-cell acute lymphoblastic leukemia have uncovered a remarkable complexity of oncogenic and loss-of-function mutations. Amongst this plethora of genetic changes, NOTCH1 activating mutations stand out as the most frequently occurring genetic defect, identified in more than 50% of T...
ORGANISM(S): Homo sapiens 
2014-10-27 | E-GEOD-61863 | biostudies-arrayexpress
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