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UnknownA novel model for treatment of hypertrophic pachymeningitis.
Not available
S-EPMC6414490 | biostudies-literature
UnknownImmunohistochemistry for identification of CCND1, NSD2, and MAF gene rearrangements in plasma cell myeloma.
Not available
S-EPMC6676137 | biostudies-literature
UnknownComprehensive analysis of serum cytokines in patients with multiple myeloma before and after lenalidomide and dexamethasone.
Not available
S-EPMC11259000 | biostudies-literature
UnknownLower expression of activating transcription factors 3 and 4 correlates with shorter progression-free survival in multiple myeloma patients receiving bortezomib plus dexamethasone therapy.
Not available
S-EPMC4735074 | biostudies-literature
UnknownCase report: Genomic analysis of a therapy-related chronic myelomonocytic leukemia with KMT2A rearrangement that progressed to acute myeloid leukemia with acute promyelocytic leukemia-like features.
Not available
S-EPMC9981998 | biostudies-literature
TranscriptomicsTranscription profiling of Arabidopsis CAF-1 depletion/gamma-irradiation
CAF-1 is involved in nucleosome assembly following DNA replication and nucleotide excision repair. In Arabidopsis thaliana, the 3 CAF-1 subunits p150, p60 and p48 are encoded by FAS1, FAS2 and, most likely, MSI1, respectively.fas mutants exhibited increased levels of DNA double-strand breaks, a G2 p...
ORGANISM(S): Arabidopsis thaliana 
2008-06-13 | E-GEOD-5043 | biostudies-arrayexpress
UnknownCyclin-dependent kinase 9 as a potential specific molecular target in NK-cell leukemia/lymphoma.
Not available
S-EPMC6269314 | biostudies-literature
UnknownClinical significance of tryptophan catabolism in Hodgkin lymphoma.
Not available
S-EPMC5765298 | biostudies-literature
UnknownTargeting Overexpressed IDO in Stromal Cells as a Potential Therapeutic Strategy in Multiple Myeloma.
Not available
S-EPMC12861097 | biostudies-literature
ProteomicsProteome analysis of brain vessels (the anterior cerebral artery and the middle cerebral artery) from 24-month-old Htra1 KO and wild type mice
CARASIL (cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy) is a hereditary cerebral small-vessel disease caused by loss of function mutations of HTRA1, which is a serine protease with a variety of targets, including extracellular matrix proteins. We isolate...
ORGANISM(S): Mus Musculus (mouse) 
2021-11-02 | PXD022298 | JPOST Repository
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