Results 91 to 100 of about 28,866 (196)

Magnesium Deficiency Accelerates Gut Aging and Increases Susceptibility to Colitis

open access: yesAging Cell, Volume 25, Issue 3, March 2026.
Aging is associated with a gut‐specific decline in magnesium (Mg), which accelerates intestinal aging and aggravates colitis in aged mice. Mechanistically, Mg deficiency reshapes the phosphoproteome and N‐glycoproteome, destabilizing adhesion complexes.
Rou Zhang   +16 more
wiley   +1 more source

Tongue schwannomas associated with neurofibromatosis type 2

open access: yesOral and Maxillofacial Surgery Cases, 2018
Schwannomas are typically solitary benign neural tumors; however, multiple lesions associated with the rare genetic disorder neurofibromatosis type 2 (NF2) have been reported in some cases.
Harusachi Kanazawa   +6 more
doaj   +1 more source

Meflin/ISLR is a meningeal cell‐specific marker involved in the development of meninges and meningioma progression

open access: yesBrain Pathology, Volume 36, Issue 2, March 2026.
Mesenchymal stromal cell‐and fibroblast‐expressing Linx paralogue (Meflin) is expressed in embryonic meninges and contributes to meningeal homeostasis. In meningiomas, elevated Meflin correlates with higher grade and recurrence. Single‐cell RNA sequencing revealed a Meflin‐high tumor cell subset marked by reduced proliferation, WNT6 expression, and ...
Yukihiro Shiraki   +13 more
wiley   +1 more source

Multiplicity fluctuation and correlation of mesons and baryons in ultra-relativistic heavy-ion collisions at LHC

open access: yes, 2017
We study the multiplicity fluctuation and correlation of identified mesons and baryons formed at the hadronization by the quark combination mechanism in the context of ultra-relativistic heavy-ion collisions. Based on the statistical method of free quark
Li, Hai-hong, Shao, Feng-lan, Song, Jun
core   +1 more source

Identification of BCL2L11 as a Candidate Gene for Hereditary Predisposition to Non‐Medullary Thyroid Cancer Using Familial Whole‐Exome‐Sequencing

open access: yesClinical Genetics, Volume 109, Issue 3, Page 458-469, March 2026.
Whole‐exome sequencing of five families with non‐medullary thyroid cancer revealed three candidate genes. Functional analyses confirmed BCL2L11 as a strong candidate gene for hereditary predisposition to non‐medullary thyroid cancer. ABSTRACT Familial non‐medullary thyroid cancer, defined as two or more affected first‐degree relatives, accounts for 3 ...
Duygu Abbasoglu   +9 more
wiley   +1 more source

TANC1::HTRA1 fusion in schwannomas

open access: yes
Brain Pathology, EarlyView.
Ilay Caliskan   +3 more
wiley   +1 more source

The Impact of Next‐Generation Sequencing on Interobserver Agreement and Diagnostic Accuracy of Deep Penetrating Melanocytic Neoplasms

open access: yesJournal of Cutaneous Pathology, Volume 53, Issue 3, Page 293-301, March 2026.
ABSTRACT Background Next‐generation sequencing (NGS) is becoming more commonly used for diagnosis in dermatopathology. It's critical to appraise its efficacy and limitations. Distinguishing benign deep penetrating nevi (DPN) from deep penetrating like‐melanoma (DPN‐M) is a challenging diagnostic scenario even for experienced dermatopathologists ...
Julia Edwin Jeyakumar   +37 more
wiley   +1 more source

The Morphology of N=6 Chern-Simons Theory

open access: yes, 2009
We tabulate various properties of the language of N=6 Chern-Simons Theory, in the sense of Polyakov. Specifically we enumerate and compute character formulas for all syllables of up to four letters, i.e.
A. Hanany   +38 more
core   +1 more source

Merlin, the NF2 Gene Product

open access: yesPathology & Oncology Research, 2013
Merlin, the protein product of NF2 gene, is one of the most versatile tumor suppressors capable of integrating different mechanisms that regulate cell proliferation, motility, survival and signaling pathways underlying and governing those mechanisms. Merlin is considered a member of the band 4.1 families of cytoskeleton-associated proteins also called ...
openaire   +2 more sources

Additional file 3 of Distinct genomic subclasses of high-grade/progressive meningiomas: NF2-associated, NF2-exclusive, and NF2-agnostic

open access: yes, 2020
Additional file 3: Figure S2: a stacked bar graph demonstrates the most frequently detected mutations in meningiomas, based on their WHO grading. In 13 cases, WHO grading was not available. Those cases included: four meningiomas with NF2 mutations and alterations in PTEN (n= 1), ARID1A (n= 1), BAP1 (n= 1) and PTEN (n= 1).
Williams, Erik A.   +13 more
openaire   +1 more source

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