絞り込み

16633

広告

「"Raimbault A "[Author]」の検索結果

17件中 1件~17件表示    検索結果をPubMedで見る PubMedで見る

The Fraction of CD117/c-KIT-Expressing Erythroid Precursors Predicts ESA Response in Low-Risk Myelodysplastic Syndromes.

A chiral unified chromatography-mass spectrometry method to analyze free amino acids.

Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.

A recurrent clonally distinct burkitt lymphoma case highlights genetic key events contributing to oncogenesis.

Downregulation of TREM-like transcript (TLT)-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.

First inter-laboratory study of a Supercritical Fluid Chromatography method for the determination of pharmaceutical impurities.

CD13 expression in B cell malignancies is a hallmark of plasmacytic differentiation.

A landscape of germline mutations in a cohort of inherited bone marrow failure patients.

UHPLC method for multiproduct pharmaceutical analysis by Quality-by-Design.

Plasma cell leukemia revealing a G6PD deficiency.

Comprehensive Proteomic Analysis of Human Erythropoiesis.

APG101 efficiently rescues erythropoiesis in lower risk myelodysplastic syndromes with severe impairment of hematopoiesis.

Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletion.

Molecular and biochemical characterization of mannitol-1-phosphate dehydrogenase from the model brown alga Ectocarpus sp.

Radionecrosis of malignant glioma and cerebral metastasis: a diagnostic challenge in MRI.

Flow cytometry thresholds of myeloperoxidase detection to discriminate between acute lymphoblastic or myeloblastic leukaemia.

Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression.

Sort by
※並べ替えは表示に時間がかかります