Results 281 to 290 of about 1,460,723 (393)

Landscape of BRAF transcript variants in human cancer

open access: yesMolecular Oncology, EarlyView.
We investigate the annotation of BRAF variants, focusing on protein‐coding BRAF‐220 (formerly BRAF‐reference) and BRAF‐204 (BRAF‐X1). The IsoWorm pipeline allows us to quantify these variants in human cancer, starting from RNA‐sequencing data. BRAF‐204 is more abundant than BRAF‐220 and impacts patient survival.
Maurizio S. Podda   +5 more
wiley   +1 more source

Overview of Next‐Generation Sequencing Technologies

open access: yesCurrent Protocols in Molecular Biology, 2018
B. Slatko, A. F. Gardner, F. Ausubel
semanticscholar   +1 more source

Comparative of metagenomic and targeted next-generation sequencing in lower respiratory tract fungal infections. [PDF]

open access: yesFront Cell Infect Microbiol
Chen Z   +9 more
europepmc   +1 more source

TRPM8 levels determine tumor vulnerability to channel agonists

open access: yesMolecular Oncology, EarlyView.
TRPM8 is a Ca2+ permissive channel. Regardless of the amount of its transcript, high levels of TRPM8 protein mark different tumors, including prostate, breast, colorectal, and lung carcinomas. Targeting TRPM8 with channel agonists stimulates inward calcium currents followed by emptying of cytosolic Ca2+ stores in cancer cells.
Alessandro Alaimo   +18 more
wiley   +1 more source

Next-generation sequencing in cancer diagnosis and treatment: clinical applications and future directions. [PDF]

open access: yesDiscov Oncol
Ghoreyshi N   +6 more
europepmc   +1 more source

The anticancer effect of the HDAC inhibitor belinostat is enhanced by inhibitors of Bcl‐xL or Mcl‐1 in ovarian cancer

open access: yesMolecular Oncology, EarlyView.
The pan‐HDAC inhibitor belinostat increases the expression of the pro‐apoptotic proteins Bim, Puma, and Noxa and induces apoptosis in ovarian cancer cell lines and patient‐derived tumor organoids when used at high concentrations. Moreover, inhibiting the anti‐apoptotic proteins Bcl‐xL or Mcl‐1 sensitizes these preclinical models to the cytotoxic effect
Cécilia Thomine   +10 more
wiley   +1 more source

Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3

open access: green, 2010
Kimia Kahrizi   +11 more
openalex   +2 more sources

A Retrospective Analysis of Ambiguous Spitz Tumors Using Next-Generation Sequencing. [PDF]

open access: yesCancers (Basel)
Teufer M   +8 more
europepmc   +1 more source

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