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TranscriptomicsA novel unusual chromosome 11 abnormality: a homozygous somatic deletion of the entire WT1 gene within a heterozygous 11p13 deletion and UPD limited to 11p15 in a Wilms tumor and establishment of an immortalized cell line
We describe a stromal predominant Wilms tumor with a complex, tumor specific chromosome 11 aberration: a homozygous deletion of the entire WT1 gene within a heterozygous 11p13 deletion and an additional region of uniparental disomy (UPD) limited to 11p15.5-p15.2 including the IGF2 gene. The tumor ca...
ORGANISM(S): Homo sapiens 
2016-06-01 | E-GEOD-71265 | biostudies-arrayexpress
UnknownAutoreactive T cells specific for insulin B:11-23 recognize a low-affinity peptide register in human subjects with autoimmune diabetes.
Not available
S-EPMC4205657 | biostudies-literature
UnknownHeterotaxy in Caenorhabditis: widespread natural variation in left-right arrangement of the major organs.
Not available
S-EPMC5104504 | biostudies-literature
UnknownBrentuximab vedotin in the front-line treatment of patients with CD30+ peripheral T-cell lymphomas: results of a phase I study.
Not available
S-EPMC4171358 | biostudies-literature
UnknownThe cleaved cytoplasmic tail of polycystin-1 regulates Src-dependent STAT3 activation.
Not available
S-EPMC4116067 | biostudies-literature
UnknownCrystal deposition triggers tubule dilation that accelerates cystogenesis in polycystic kidney disease.
Not available
S-EPMC6763267 | biostudies-literature
TranscriptomicsNo-match ORESTES explored as tumor markers
Sequencing technologies together with new bioinformatics tools have led to the complete sequencing of various genomes. However, information regarding the human transcriptome and its annotation is yet to be completed. The Human Cancer Genome Project, using ORESTES (open reading frame EST sequences) m...
ORGANISM(S): Homo sapiens 
2009-04-13 | E-GEOD-12737 | biostudies-arrayexpress
TranscriptomicsMicroarray Analysis in Vestibular Schwannomas
Vestibular Schwannomas are benign neoplasms that arise from the vestibular nerve. The hallmark of these tumors is the biallelic inactivation of NF2. Transcriptomic alterations, such as the Nrg1/ErbB2 pathway, have been described in Schwannomas. Here, we have performed a whole transcriptomic analysis...
ORGANISM(S): Homo sapiens 
2013-03-01 | E-GEOD-39645 | biostudies-arrayexpress
UnknownMethionine Adenosyltransferase α1 Is Targeted to the Mitochondrial Matrix and Interacts with Cytochrome P450 2E1 to Lower Its Expression.
Not available
S-EPMC6842664 | biostudies-literature
UnknownIdentical and Nonidentical Twins: Risk and Factors Involved in Development of Islet Autoimmunity and Type 1 Diabetes.
Not available
S-EPMC6341285 | biostudies-literature
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