Results 71 to 80 of about 978,459 (257)

Tight Bounds for Online Edge Coloring

open access: yes, 2019
Vizing's celebrated theorem asserts that any graph of maximum degree Delta admits an edge coloring using at most Delta + 1 colors. In contrast, Bar-Noy, Motwani and Naor showed over a quarter century ago that the trivial greedy algorithm, which uses 2 ...
Peng, Binghui   +5 more
core   +1 more source

Invisible but not inaccessible—Revealing transient oligomers formed by intrinsically disordered proteins with solution NMR and complementary methods

open access: yesFEBS Letters, EarlyView.
Transient oligomers formed by intrinsically disordered proteins may be ‘invisible’ to direct detection yet remain accessible to solution NMR through equilibrium‐exchange measurements and pressure‐jump experiments. Complementary methods report on mass, stoichiometry, selected distance distributions, morphology, and internal packing.
Martin D. Gelenter, Ad Bax
wiley   +1 more source

List Star Edge-Coloring of Subcubic Graphs [PDF]

open access: yes, 2018
A star edge-coloring of a graph G is a proper edge coloring such that every 2-colored connected subgraph of G is a path of length at most 3. For a graph G, let the list star chromatic index of G, ch′st(G), be the minimum k such that for any k-uniform ...
Kostochka Alexandr   +8 more
core   +2 more sources

Twin edge colorings of certain square graphs and product graphs

open access: yesElectronic Journal of Graph Theory and Applications, 2016
A twin edge $k\!$-coloring of a graph $G$ is a proper edge $k$-coloring of $G$ with the elements of $\mathbb{Z}_k$ so that the induced vertex $k$-coloring, in which the color of a vertex $v$ in $G$ is the sum in $\mathbb{Z}_k$ of the colors of the edges ...
R Rajarajachozhan, R. Sampathkumar
doaj   +1 more source

Soft motions encoded by the fold and mediated by conserved hinge sites drive V‐ATPase allosteric machinery and autoinhibition

open access: yesFEBS Letters, EarlyView.
Vacuolar H+‐ATPase (V‐ATPase) is a multisubunit rotary proton pump that acidifies intracellular compartments. Using elastic network models, we identified conserved hinge residues that govern its large‐scale functional motions. We show that intrinsically encoded ‘soft modes’ drive critical functional transitions, including rotary catalysis and ...
Diksha Parwana   +3 more
wiley   +1 more source

Unlocking the potential of cell‐permeable nanobodies for intracellular applications

open access: yesFEBS Letters, EarlyView.
This review outlines current strategies for delivery of nanobodies into cells and highlights recent examples of functional applications. By addressing and manipulating intracellular targets, these molecules hold great potential for treating cancer, respiratory diseases and neurological disorders, making this a vibrant area of research in the biomedical
Mariona Gené‐Verdés   +2 more
wiley   +1 more source

Vertex Coloring Edge-Weighting of Coronation by Path Graphs [PDF]

open access: yes, 2019
In this paper, we study vertex coloring edge of corona graph. A k-edge weigting of graph G is mapping w : (EG) ! f1; 2; ; kg. An edge-weighting w induces a vertex coloring Fw : V (G) ! N de ned by fw(v) = P v2e w(e).
KRISTIANA, Arika Indah   +5 more
core  

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

Strong edge coloring sparse graphs

open access: yes, 2015
International audienceA strong edge coloring of a graph is a proper edge coloring such that no edge has two incident edges of the same color. Erdős and Nešetřil conjectured in 1989 that $5 /4∆2$ colors are always enough for a strong edge coloring, where $
Hocquard, Hervé   +2 more
core   +1 more source

Developmental programmes drive cellular plasticity, disease progression and therapy resistance in lung adenocarcinoma

open access: yesMolecular Oncology, EarlyView.
This study shows that lung adenocarcinomas exploit developmental branching morphogenesis to acquire a therapy resistant basal‐like tumour cell state. This process was found to be regulated by combined TP53 loss‐of‐function and type‐I interferon signalling, identifying a novel axis for biomarker and therapeutic target discovery.
Kamila J Bienkowska   +13 more
wiley   +1 more source

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