Results 61 to 70 of about 1,844,634 (338)

The multidrug and toxin extrusion (MATE) transporter DTX51 antagonizes non‐cell‐autonomous HLS1–AMP1 signaling in a region‐specific manner

open access: yesFEBS Letters, EarlyView.
The Arabidopsis mutants hls1 hlh1 and amp1 lamp1 exhibit pleiotropic developmental phenotypes. Although the functions of the causative genes remain unclear, they act in the same genetic pathway and are thought to generate non‐cell‐autonomous signals.
Takashi Nobusawa, Makoto Kusaba
wiley   +1 more source

Phase diagram of Hertzian spheres [PDF]

open access: yesThe Journal of Chemical Physics, 2009
We report the phase diagram of interpenetrating Hertzian spheres. The Hertz potential is purely repulsive, bounded at zero separation, and decreases monotonically as a power law with exponent 5/2, vanishing at the overlapping threshold. This simple functional describes the elastic interaction of weakly deformable bodies and, therefore, it is a reliable
Pàmies, J.C., Cacciuto, A., Frenkel, D.
openaire   +6 more sources

Three-dimensional phase diagram of disordered HgTe/CdTe Quantum spin-Hall wells

open access: yes, 2011
We compute the phase diagram of the HgTe/CdTe quantum wells in the 3 dimensional (3D) parameter space of Dirac mass, Fermi level and disorder strength. The phase diagram reveals the Quantum spin-Hall, the metallic and the normal insulating phases.
Prodan, Emil
core   +1 more source

Micro- vs. macro-phase separation in binary blends of poly(styrene)-poly(isoprene) and poly(isoprene)-poly(ethylene oxide) diblock copolymers [PDF]

open access: yes, 2001
In this paper we present an experimentally determined phase diagram of binary blends of the diblock copolymers poly(styrene)-poly(isoprene) and poly(isoprene)-poly(ethylene oxide). At high temperatures, the blends form an isotropic mixture. Upon lowering
A. J Ryan   +12 more
core   +1 more source

Ergothioneine supplementation improves pup phenotype and survival in a murine model of spinal muscular atrophy

open access: yesFEBS Letters, EarlyView.
Spinal muscular atrophy (SMA) is a genetic disease affecting motor neurons. Individuals with SMA experience mitochondrial dysfunction and oxidative stress. The aim of the study was to investigate the effect of an antioxidant and neuroprotective substance, ergothioneine (ERGO), on an SMNΔ7 mouse model of SMA.
Francesca Cadile   +8 more
wiley   +1 more source

Facets of the QCD Phase-Diagram

open access: yesEPJ Web of Conferences, 2011
In this contribution we will discuss two aspects of the matter created in ultra-relativistic heavy ion collisions. First we will attempt to define a universal measure for the fluidity of a substance, which will allow a correct comparison between the ...
Bzdak A., Koch V., Liao J.
doaj   +1 more source

Preparation and characterization of vemurafenib microemulsion

open access: yesIraqi Journal of Pharmaceutical Sciences, 2023
Human melanoma is the most common and malignant type of skin cancer. Vemurafenib has been used for the treatment of malignant or metastatic melanoma. Oral vemurafenib has serious adverse drug reactions including QTc sigment prolongation of heart ECG ...
Mohammed Jassim Neamah   +1 more
doaj   +1 more source

Shock dynamics of phase diagrams [PDF]

open access: yesAnnals of Physics, 2014
A thermodynamic phase transition denotes a drastic change of state of a physical system due to a continuous change of thermodynamic variables, as for instance pressure and temperature. The classical van der Waals equation of state is the simplest model that predicts the occurrence of a critical point associated with the gas-liquid phase transition ...
openaire   +3 more sources

Phase Diagram of Coupled Ladders

open access: yes, 1998
The 2-leg t-J ladder forms a spin liquid at half-filling which evolves to a Luther-Emery liquid upon doping. Our aim is to obtain a complete phase diagram for isotropic coupling (i.e.
B. Frischmuth   +28 more
core   +1 more source

C9orf72 ALS‐causing mutations lead to mislocalization and aggregation of nucleoporin Nup107 into stress granules

open access: yesFEBS Letters, EarlyView.
Mutations in the C9orf72 gene represent the most common genetic cause of amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease. Using patient‐derived neurons and C. elegans models, we find that the nucleoporin Nup107 is dysregulated in C9orf72‐associated ALS. Conversely, reducing Nup107 levels mitigates disease‐related changes.
Saygın Bilican   +7 more
wiley   +1 more source

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