Results 171 to 180 of about 1,763,257 (296)

P704: ASCIMINIB PROVIDES DURABLE MOLECULAR RESPONSES IN PATIENTS (PTS) WITH CHRONIC MYELOID LEUKEMIA IN CHRONIC PHASE (CML-CP) WITH THE T315I MUTATION: UPDATED EFFICACY AND SAFETY DATA FROM A PHASE I TRIAL

open access: gold, 2022
Timothy P. Hughes   +20 more
openalex   +1 more source

Perspectives in educating molecular pathologists on liquid biopsy: Toward integrative, equitable, and decentralized precision oncology

open access: yesMolecular Oncology, EarlyView.
Liquid biopsy enables minimally invasive, real‐time molecular profiling through analysis of circulating biomarkers in biological fluids. This Perspective highlights the importance of training pathologists through integrative educational programs, such as the European Masters in Molecular Pathology, to ensure effective and equitable implementation of ...
Marius Ilié   +13 more
wiley   +1 more source

Platelet Gs hypofunction and abnormal morphology resulting from a heterozygous RGS2 mutation

open access: green, 2010
Laura Noé   +10 more
openalex   +2 more sources

A PCR plus restriction enzyme-based technique for detecting target-enzyme mutations at position Pro-106 in glyphosate-resistant Lolium perenne

open access: gold, 2021
Hossein Ghanizadeh   +4 more
openalex   +1 more source

Transcriptional network analysis of PTEN‐protein‐deficient prostate tumors reveals robust stromal reprogramming and signs of senescent paracrine communication

open access: yesMolecular Oncology, EarlyView.
Combining PTEN protein assessment and transcriptomic profiling of prostate tumors, we uncovered a network enriched in senescence and extracellular matrix (ECM) programs associated with PTEN loss and conserved in a mouse model. We show that PTEN‐deficient cells trigger paracrine remodeling of the surrounding stroma and this information could help ...
Ivana Rondon‐Lorefice   +16 more
wiley   +1 more source

TP53 mutation heterogeneity reveals distinct prognoses in mantle cell lymphoma. [PDF]

open access: yesAnn Hematol
Liu S   +9 more
europepmc   +1 more source

c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia [PDF]

open access: gold, 2017
Ali Shalash   +11 more
openalex   +1 more source

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