Results 101 to 110 of about 179,623 (305)

Threonine 348 regulates the subcellular localization of PTEN

open access: yesFEBS Open Bio, EarlyView.
Thr348 in the C2 domain is a key contributor to PTEN subcellular localization. The PTEN350 fragment and PTENA4 accumulated in the nucleus, whereas PTENK13R,A4 predominantly localized to the plasma membrane. In contrast, substitution of Thr348 with Asp (T348D) disrupted these characteristic localization patterns, resulting in predominant cytoplasmic ...
Takashi Kato, Suzu Tanaka, Miyu Ohashi
wiley   +1 more source

Word-Formation Capabilities of Russian Colloquial Speech in the Multilingual Space of Modern Russia

open access: yesНаучный диалог, 2018
Hybrid new word formations recorded in the oral conversational speech of residents of the Volgograd region, caused by contacts with foreign people are analyzed in the article. The method of eco-linguistic monitoring is used.
M. V. Milovanova, E. V. Terentyeva
doaj   +1 more source

Salmonella enterica serovar typhi limits the potency of typhoid toxin and ADP‐ribosylating toxin AB to establish a persistent infection

open access: yesFEBS Open Bio, EarlyView.
The two catalytic subunits of typhoid toxin dissociate from the holotoxin in the ER of an intoxicated cell, but only CdtB exits the ER to generate immunosuppressive effects. PltA is retained in the ER and sequestered from its cytosolic target, thus allowing the anti‐inflammatory effects of CdtB to promote intestinal colonization.
Maria C. Zabala‐Rodriguez   +4 more
wiley   +1 more source

Estimation of parameters and truncation point for the Gompertz distribution

open access: yes, 1993
In this article we discuss the problem of estimating the parameters of the left and the right trun-cated Gompertz distribution when truncation points are unknown. Maximum likelihood estimators and estimators involving expected values of appropriate order
Al-Yousef, M.H.
core  

The C‐terminal truncated splicing variant of NK1R negatively modulates substance P‐stimulated NK1R signaling

open access: yesFEBS Open Bio, EarlyView.
The neurokinin 1 receptor exists as full‐length (NK1L) and C‐terminally truncated (NK1S) splice variants. We show that NK1S heterodimerizes with NK1L, impairing Gαq coupling and Ca2+ mobilization while enhancing β‐arrestin1 recruitment. NK1S suppresses substance P‐driven gene expression and cell migration, revealing NK1S as an endogenous biased ...
Lan Phuong Nguyen   +8 more
wiley   +1 more source

On truncated Weyl modules

open access: yesCommunications in Algebra, 2019
Minor revision.
Fourier, Ghislain   +2 more
openaire   +2 more sources

The C‐terminal domain of yeast Arginyltransferase1 is essential for its catalytic activity

open access: yesFEBS Open Bio, EarlyView.
Arginyltransferase 1 (Ate1), a eukaryotic enzyme, catalyses arginylation, transferring arginine from tRNA‐Arg to the amino terminus of the target protein. Overexpression of Ate1 in yeast is lethal and is dependent on arginylation. This study elucidates how mutations in the cofactor‐binding and active site of Ate1 and truncation of its structural ...
Vikas Kumar Yadav   +4 more
wiley   +1 more source

A Behavioral Approach to Passivity and Bounded Realness Preserving Balanced Truncation with Error Bounds

open access: yes
In this paper we revisit the problems of passivity and bounded realness preserving model reduction by balanced truncation. In the behavioral framework, these problems can be considered as special cases of balanced truncation of strictly half line ...
Trentelman, Harry L., Rapisarda, Paolo
core   +1 more source

Truncation and wildcards

open access: yes, 2020
A short video tutorial on using truncation and wildcards in your database search.
Vicki Farmilo
core   +3 more sources

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

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