Results 91 to 100 of about 256,860 (287)

On the Density of Identifying Codes in the Square Lattice [PDF]

open access: yes, 2002
Let G=(V, E) be an undirected graph and C a subset of vertices. If the sets Br(v)∩C, v∈V, are all nonempty and different, where Br(v) denotes the set of all points within distance r from v, we call C an r-identifying code.
Lobstein, Antoine, Honkala, Iiro
core   +1 more source

Phosphoinositides and inositol phosphates as molecular glues

open access: yesFEBS Letters, EarlyView.
Inositol phosphates (IPs) and phosphoinositides (PIPs) regulate diverse eukaryotic processes. Beyond recruiting signaling proteins or acting as structural cofactors, recent studies suggest they mediate protein–protein interactions as natural molecular glues.
Aleshia Seaton‐Terry   +9 more
wiley   +1 more source

Accuracy of national mortality codes in identifying adjudicated cardiovascular deaths [PDF]

open access: yes, 2011
Objective: This study investigated the sensitivity and specificity of the national mortality codes in identifying cardiovascular disease (CVD) deaths and documents methods of verification.Methods: A 12-year retrospective case ascertainment of all ICD ...
D Magliano (13338792)   +17 more
core   +3 more sources

Identifying Codes and the Set Cover Problem [PDF]

open access: yes, 2006
We consider the problem of finding a minimum identifying code in a graph, i.e., a designated set of vertices whose neighborhoods uniquely overlap at any vertex on the graph.
Moshe Laifenfeld   +2 more
core  

Three phosphatase families form a community: The phosphohydrolases that act upon inositol pyrophosphates

open access: yesFEBS Letters, EarlyView.
Inositol pyrophosphates are energy‐rich signaling molecules that perform critical functions in cells. Three different families of phosphatases hydrolyze the β phosphate of the inositol pyrophosphate molecules: two have narrow specificities and one is promiscuous.
Ronda J. Rolfes
wiley   +1 more source

Design and analysis strategies for robust microbiome ageing research

open access: yesFEBS Letters, EarlyView.
The gut microbiome changes with age and associates with age‐related morbidity and mortality, establishing it as a potential biomarker and intervention target for ageing. Realising this potential requires methodological rigour, yet distinguishing biological signals from methodological artefacts remains challenging across cohorts. This review provides an
Mark Olenik   +5 more
wiley   +1 more source

On identifying codes that are robust against edge changes [PDF]

open access: yes, 2007
Assume that G=(V, E) is an undirected graph, and C⊆V. For every v∈V, denote Ir(G; v)={u∈C: d(u,v)≤r}, where d(u,v) denotes the number of edges on any shortest path from u to v in G.
Laihonen, Tero, Honkala, Iiro
core   +1 more source

The role of miR‐335‐5p in the redifferentiation of BRAF p.V600E thyroid cancers

open access: yesMolecular Oncology, EarlyView.
The BRAF p.V600E mutation promotes thyroid cancer dedifferentiation and radioiodine resistance. Using a network approach, we identified miR‐335‐5p as a key regulator of BRAF‐mutated thyroid tumors. Restoring miR‐335‐5p increased thyroid‐specific gene expression and iodine uptake in cells and organoids.
Valeria Pecce   +11 more
wiley   +1 more source

TRAIL‐PEG‐Apt‐PLGA nanosystem as an aptamer‐targeted drug delivery system potential for triple‐negative breast cancer therapy using in vivo mouse model

open access: yesMolecular Oncology, EarlyView.
Aptamers are used both therapeutically and as targeting agents in cancer treatment. We developed an aptamer‐targeted PLGA–TRAIL nanosystem that exhibited superior therapeutic efficacy in NOD/SCID breast cancer models. This nanosystem represents a novel biotechnological drug candidate for suppressing resistance development in breast cancer.
Gulen Melike Demirbolat   +8 more
wiley   +1 more source

Efficient Genome-wide Association in Biobanks Using Topic Modeling Identifies Multiple Novel Disease Loci

open access: yesMolecular Medicine, 2017
Biobanks and national registries represent a powerful tool for genomic discovery, but rely on diagnostic codes that can be unreliable and fail to capture relationships between related diagnoses.
Thomas H. McCoy   +4 more
doaj   +1 more source

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