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UnknownPredicting Oncogenic Missense Mutations.
Not available
S-EPMC8901086 | biostudies-literature
ProteomicsPresentation of DNAJB1-PRKACA fusion neoantigens by different HLA class I alleles
Fibrolamellar carcinoma (FLC) is a liver tumor with a high mortality burden and few treatment options. A promising therapeutic vulnerability in this disease is its highly conserved driver mutation: a gene fusion between DNAJB1 and PRKACA, which is expressed in virtually all FLC tumors and could be a...
ORGANISM(S): Homo sapiens (Human) 
2024-05-24 | PXD042316 | Pride
Fusion neoantigens Hla class i Cd8 t cell Dnajb1-prkaca Fibrolamellar carcinoma 
UnknownHybrid magnonics in hybrid perovskite antiferromagnets.
Not available
S-EPMC10067936 | biostudies-literature
UnknownCOMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstruction.
Not available
S-EPMC12808943 | biostudies-literature
UnknownEarly-Onset Pancreas Cancer: Clinical Descriptors, Genomics, and Outcomes.
Not available
S-EPMC8418394 | biostudies-literature
UnknownEvaluating Immune Checkpoint Blockade in Metastatic Castration-Resistant Prostate Cancers with Deleterious CDK12 Alterations in the Phase 2 IMPACT Trial.
Not available
S-EPMC11293970 | biostudies-literature
UnknownInactivation of CDK12 Delineates a Distinct Immunogenic Class of Advanced Prostate Cancer.
Not available
S-EPMC6084431 | biostudies-literature
UnknownRNA-Puzzles Round III: 3D RNA structure prediction of five riboswitches and one ribozyme.
Not available
S-EPMC5393176 | biostudies-literature
TranscriptomicsA missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family B)
Affymetrix 6.0 SNP data for haplotype comparison of patients from two different families sharing the same homozygous mutation in TFRC, to determine if the families were related to each other Peripheral blood was used for patients who had no history of hematopoietic stem cell transplant (HSCT). Fibro...
ORGANISM(S): Homo sapiens 
2015-11-25 | E-GEOD-75349 | biostudies-arrayexpress
TranscriptomicsA missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency (Family A)
Affymetrix 6.0 SNP data for genome-wide linkage scans of a consanguineous Kuwaiti family with a combined immunodeficiency Peripheral blood or saliva were used for patients who had no history of hematopoietic stem cell transplant (HSCT). Fibroblasts cell lines were used as a source of DNA for individ...
ORGANISM(S): Homo sapiens 
2015-11-25 | E-GEOD-75314 | biostudies-arrayexpress
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