Results 91 to 100 of about 32,140 (211)

Cutwidth and degeneracy of graphs

open access: yes, 2010
v2: slightly shortened, some typos corrected.We prove an inequality involving the degeneracy, the cutwidth and the sparsity of graphs. It implies a quadratic lower bound on the cutwidth in terms of the degeneracy for all graphs and an improvement of it ...
Kloeckner, Benoit
core  

Figure 6-Association complexity degeneracy

open access: yes, 2011
Association between complexity and degeneracy for evolved genetic networks with and without feedback ...
Elena, Santiago F.   +5 more
core   +1 more source

Global Rather Than Vertical‐Selective Saccadic Abnormalities in Progressive Supranuclear Palsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To test whether vertical saccades are preferentially affected in Progressive Supranuclear Palsy (PSP). Methods PSP patients (n = 24) were compared to age‐matched controls (n = 94) and two degenerative groups (Alzheimer's disease, n = 20; Lewy body disease, n = 50).
Duy Duan Nguyen   +6 more
wiley   +1 more source

Symmetry-adapted HAM/3 method and its application to some symmetric molecules

open access: yesJournal of the Brazilian Chemical Society, 2004
The semiempirical HAM/3 method developed by Lindholm and coworkers about two decades ago has been known to have a deficiency that splits energies for the degenerate energy states.
Narita Susumu   +3 more
doaj  

Validation of a Cellular Imaging‐Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Hereditary Spastic Paraplegia (HSP) comprises a group of rare genetic diseases characterized by length‐dependent axonal degeneration of the corticospinal tracts and dorsal columns, whose main clinical feature is spastic gait. Pathogenic variants in the SPG4 gene cause Spastic Paraplegia Type 4 (SPG4‐HSP), the most common form of HSP.
Gaia Fattorini   +12 more
wiley   +1 more source

Morphogenetic degeneracies in the actomyosin cortex

open access: yeseLife, 2018
One of the great challenges in biology is to understand the mechanisms by which morphogenetic processes arise from molecular activities. We investigated this problem in the context of actomyosin-based cortical flow in C.
Sundar Ram Naganathan   +7 more
doaj   +1 more source

Diabetes‐Associated Cognitive Impairment: Pathophysiology and Emerging Therapies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Diabetes‐associated cognitive impairment (DACI) is a common yet underrecognized condition, manifesting along a spectrum from mild cognitive impairment to dementia. DACI encompasses patients who develop vascular dementia (VaD) or Alzheimer's disease (AD) with diabetes as a risk factor; however, in certain patients, particularly those lacking ...
Osman Corbali   +4 more
wiley   +1 more source

Octant Degeneracy and Plots of Parameter Degeneracy in Neutrino Oscillations Revisited [PDF]

open access: yes
The three kinds of parameter degeneracy in neutrino oscillation, the intrinsic, sign and octant degeneracy, form an eight-fold degeneracy. The nature of this eight-fold degeneracy can be visualized on the ($\sin^22\theta_{13}$, $1/\sin^2\theta_{23 ...
Yasuda, Osamu, Sugama, Sho
core  

Re‐Purposing Sapropterin (Kuvan) for ACTA2‐Related Multisystemic Smooth Muscle Dysfunction Syndrome: A Translational Mechanistic and First‐In‐Human Therapeutic Report

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Multisystemic smooth muscle dysfunction syndrome (MSMDS) is an ultra‐rare, ACTA2‐related disorder characterized by severe cerebrovascular disease, aortic aneurysms, and smooth muscle dysfunction. Using molecular dynamics simulations and in silico drug screening, we identified that sapropterin dihydrochloride (Kuvan) is a candidate capable of ...
Moran Hausman‐Kedem   +9 more
wiley   +1 more source

Relativistic Degeneracy [PDF]

open access: yesMonthly Notices of the Royal Astronomical Society, 1935
Moller, Chr., Chandrasekhar, S.
openaire   +2 more sources

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