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TranscriptomicsTranscription profiling by array of parotid tissue from Primary Sjögren’s Syndrome and controls
Primary Sjögren’s syndrome (pSS) is a chronic autoimmune disease with complex etiopathogenesis. Here we use Affymetrix U133 plus 2.0 microarray gene expression data from human parotid tissue. Parotid gland tissues were harvested from 17 pSS and 14 14 non-pSS sicca patients and 18 controls. The data ...
ORGANISM(S): Homo sapiens 
2012-09-06 | E-GEOD-40611 | biostudies-arrayexpress
UnknownMicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.
Not available
S-EPMC9329941 | biostudies-literature
TranscriptomicsTranscription profiling of human prostate cancer primary cell line vs metastasis cell line reveals Protein 4.1B suppresses prostate cancer progression and metastasis
Protein 4.1B is a 4.1/ezrin/radixin/moesin (FERM) domain-containing protein whose expression is frequently lost in a variety of human tumors, including meningiomas, non-small-cell lung cancers and breast carcinomas. However, its potential tumor suppressive function under in vivo conditions remains t...
ORGANISM(S): Homo sapiens 
2008-06-15 | E-GEOD-7930 | biostudies-arrayexpress
UnknownA novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer.
Not available
S-EPMC10071693 | biostudies-literature
TranscriptomicsGastric cancer subtyping (Singapore Patient Cohort, batch B)
Genome-wide mRNA expression profiles of 56 primary gastric tumors from the Singapore patient cohort, batch B. Like many cancers, gastric adenocarcinomas (gastric cancers) show considerable heterogeneity between patients. Thus, there is intense interest in using gene expression profiles to discover s...
ORGANISM(S): Homo sapiens 
2014-09-05 | E-GEOD-34942 | biostudies-arrayexpress
UnknownDietary manganese, type 2 diabetes, and cardiovascular disease: A UK Biobank cohort study and meta-analysis of over 270,000 individuals.
Not available
S-EPMC12756635 | biostudies-literature
UnknownExpanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes.
Not available
S-EPMC8863643 | biostudies-literature
Genomics4dbf9af0-d667-494b-b3d9-c80c112d0527 - samples
high depth WGS sequencing of 8 sites of a RET fusion tumour
EGAD00001006878 | EGA
Genomicsdc7d6e29-28d7-43ec-895c-d530c18112cf - samples
Deep WGS sequencing (160x) of 2 different sites of disease of a patient with a RET fusion positive cancer. Amplicon sequencing of 19 other sites of the same patients for the RET fusion.
EGAD00001005776 | EGA
GenomicsMulti-regional tumour biopsies of a RET fusion patient
Identifying modes of resistance to a new experimental drug for a patient resistant to other therapies
EGAS00001004023 | EGA
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