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UnknownGeneration and rescue of a murine model of platelet dysfunction: the Bernard-Soulier syndrome.
Not available
S-EPMC16010 | biostudies-literature
UnknownA GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome.
Not available
S-EPMC8777725 | biostudies-literature
UnknownQuaternary organization of GPIb-IX complex and insights into Bernard-Soulier syndrome revealed by the structures of GPIbβ and a GPIbβ/GPIX chimera.
Not available
S-EPMC3217411 | biostudies-literature
UnknownLentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C.
Not available
S-EPMC10320622 | biostudies-literature
UnknownA novel mutation in GP1BA gene in a family with autosomal dominant Bernard Soulier syndrome variant: A case report.
Not available
S-EPMC7903392 | biostudies-literature
ProteomicsActinomycin targets NPM1c-primed mitochondria in AML
Acute myeloid leukemia (AML) pathogenesis often involves a mutation in the NPM1 nucleolar chaperone, but the bases for its transforming properties and association with favorable outcome remain incompletely understood. Here we demonstrate that an oncogenic mutant form of NPM1 (NPM1c) hampers formatio...
ORGANISM(S): Homo sapiens (Human) 
2021-12-17 | PXD025507 | Pride
Pml Lfq Actinomycin d Mitochondria Npm1c Qexactive Senescence 
TranscriptomicsGenomic profiling by array-CGH/SNP of paired xenograft and diagnosis T-cell Acute Lymphoblastic Leukemia (T-ALL) samples.
Arrays-CGH and/or SNP-array data from n=25 patients with T-ALL, including diagnosis, xenografted, remission and/or relapse samples (total 62 samples).
ORGANISM(S): Homo sapiens 
2011-03-23 | E-MTAB-593 | biostudies-arrayexpress
UnknownAn interactive murine single-cell atlas of the lung responses to radiation injury.
Not available
S-EPMC10147670 | biostudies-literature
TranscriptomicsN-Me duplication in T-cell acute lymphoblastic leukemia cases
Arrays-CGH data from n=8 T-cell acute lymphoblastic leukemia
ORGANISM(S): Homo sapiens 
2014-09-07 | E-MTAB-2775 | biostudies-arrayexpress
TranscriptomicsBM clonal evolution in Fanconi anemia patients
Arrays-CGH and/or SNP-array data from n=57 Fanconi anemia BM and n=36 paired fibroblasts
ORGANISM(S): Homo sapiens 
2011-07-28 | E-MTAB-529 | biostudies-arrayexpress
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