Valeria Spina

researcher

Valeria Spina is …
instance of (P31):
humanQ5

P734family nameSpinaQ37298921
SpinaQ37298921
SpinaQ37298921
P735given nameValeriaQ7385728
ValeriaQ7385728
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q58000942A variant of the LRP4 gene affects the risk of chronic lymphocytic leukaemia transformation to Richter syndrome
Q52615711Alteration of BIRC3 and multiple other NF-κB pathway genes in splenic marginal zone lymphoma.
Q43043063Analysis of NOTCH1 mutations in monoclonal B-cell lymphocytosis
Q45924363Analysis of SF3B1 mutations in monoclonal B-cell lymphocytosis.
Q51025698Association between molecular lesions and specific B-cell receptor subsets in chronic lymphocytic leukemia.
Q46585922Biological and clinical risk factors of chronic lymphocytic leukaemia transformation to Richter syndrome
Q33595764Clinical impact of small TP53 mutated subclones in chronic lymphocytic leukemia
Q37216310Clinical impact of small subclones harboring NOTCH1, SF3B1 or BIRC3 mutations in chronic lymphocytic leukemia
Q42504372Diffuse large B-cell lymphoma genotyping on the liquid biopsy
Q52621343Disruption of BIRC3 associates with fludarabine chemorefractoriness in TP53 wild-type chronic lymphocytic leukemia.
Q46719544Epigenetic inactivation of suppressors of cytokine signalling in Philadelphia-negative chronic myeloproliferative disorders
Q37697850Genetic lesions associated with chronic lymphocytic leukemia chemo-refractoriness
Q51548976Genome-wide DNA profiling better defines the prognosis of chronic lymphocytic leukaemia.
Q54538115High density genome-wide DNA profiling reveals a remarkably stable profile in hairy cell leukaemia.
Q28394721Integrated mutational and cytogenetic analysis identifies new prognostic subgroups in chronic lymphocytic leukemia
Q46755084MGA, a suppressor of MYC, is recurrently inactivated in high risk chronic lymphocytic leukemia
Q58001001Molecular and clinical features of chronic lymphocytic leukaemia with stereotyped B cell receptors: results from an Italian multicentre study
Q52614373Molecular history of Richter syndrome: origin from a cell already present at the time of chronic lymphocytic leukemia diagnosis.
Q27851685Mutations of NOTCH1 are an independent predictor of survival in chronic lymphocytic leukemia
Q58001002Stereotyped B-Cell Receptor Is an Independent Risk Factor of Chronic Lymphocytic Leukemia Transformation to Richter Syndrome
Q36193517The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone development
Q51609722The genetics of Richter syndrome reveals disease heterogeneity and predicts survival after transformation.
Q37243257The genetics of nodal marginal zone lymphoma
Q46490525The prognosis of clinical monoclonal B cell lymphocytosis differs from prognosis of Rai 0 chronic lymphocytic leukaemia and is recapitulated by biological risk factors
Q52591762The prognostic value of TP53 mutations in chronic lymphocytic leukemia is independent of Del17p13: implications for overall survival and chemorefractoriness.