Results 61 to 70 of about 28,866 (196)

NF2/Merlin suppresses proliferation and induces apoptosis in colorectal cancer cells

open access: yesFrontiers in Bioscience-Landmark, 2020
Merlin ((Moesin-ezrin-radixin-like protein, also known as schwannomin) is a tumor suppressor protein which is encoded by the neurofibromatosis type 2 gene, NF2.
Xingli Wu   +6 more
doaj   +1 more source

Merlin deficiency alters the redox management program in breast cancer

open access: yesMolecular Oncology, 2021
The expression of Merlin tumor suppressor protein encoded by Neurofibromin 2 (NF2) gene is remarkably decreased in metastatic breast cancer tissues.
Mateus Mota   +6 more
doaj   +1 more source

Gene replacement therapy in a schwannoma mouse model of neurofibromatosis type 2

open access: yesMolecular Therapy: Methods & Clinical Development, 2022
Loss of function of the neurofibromatosis type 2 (NF2) tumor suppressor gene leads to the formation of schwannomas, meningiomas, and ependymomas, comprising ∼50% of all sporadic cases of primary nervous system tumors.
Shilpa Prabhakar   +15 more
doaj   +1 more source

First-principles calculations of the electronic structure of open-shell condensed matter systems

open access: yes, 2012
We develop a Green's function approach to quasiparticle excitations of open-shell systems within the GW approximation. It is shown that accurate calculations of the characteristic multiplet structure require a precise knowledge of the self energy and, in
Deslippe, Jack   +3 more
core   +1 more source

Inhibition of cyclin-dependent kinase 7 down-regulates yes-associated protein expression in mesothelioma cells. [PDF]

open access: yes, 2020
Cyclin-dependent kinase 7 (CDK7) is a protein kinase that plays a major role in transcription initiation. Yes-associated protein (YAP) is a main effector of the Hippo/YAP signalling pathway.
Bin, Hu   +12 more
core  

Pediatric spinal ependymomas: Long‐term surgical outcomes in a cohort of 61 cases

open access: yesPediatric Investigation, EarlyView.
Spinal ependymomas are rare in children, with limited long‐term outcome data. In this retrospective study of 61 pediatric patients undergoing surgical resection, gross total resection was achieved in 62.3% and was associated with favorable functional improvement. Recurrence was observed in 31.1% of cases.
Liang Zhang   +3 more
wiley   +1 more source

Brigatinib causes tumor shrinkage in both NF2-deficient meningioma and schwannoma through inhibition of multiple tyrosine kinases but not ALK.

open access: yesPLoS ONE, 2021
Neurofibromatosis Type 2 (NF2) is an autosomal dominant genetic syndrome caused by mutations in the NF2 tumor suppressor gene resulting in multiple schwannomas and meningiomas.
Long-Sheng Chang   +40 more
doaj   +1 more source

Renal cell carcinoma with atypical omental metastasis: A case report and literature review

open access: yesUroPrecision, EarlyView.
Abstract Background Renal cell carcinoma (RCC) is the most common type of kidney cancer in adults, with common metastatic sites including the lungs, bones, liver, and brain. Omental metastasis is exceedingly rare and usually occurs postoperatively. Fumarate hydratase‐deficient (FH‐deficient) RCC, a recently classified and highly aggressive subtype of ...
Andrew Jing   +4 more
wiley   +1 more source

Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition

open access: yesClinical Case Reports, 2023
We report the case of a teenager with neurofibromatosis type 2 (NF2) presenting a locked‐in syndrome due to a brainstem ischemic syndrome. The presence of sudden or rapidly worsening onset of neurological deficits in NF2 patients should evoke this ...
Aglaë Blauen   +3 more
doaj   +1 more source

Merlin Phosphorylation by p21-activated Kinase 2 and Effects of Phosphorylation on Merlin Localization [PDF]

open access: yes, 2002
The Nf2 tumor suppressor gene product merlin is related to the membrane-cytoskeleton linker proteins of the band 4.1 superfamily, including ezrin, radixin, and moesin (ERMs). Merlin is regulated by phosphorylation in a Rac/cdc42-dependent fashion.
Eckman, Matthew S.   +3 more
core   +1 more source

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