Results 71 to 80 of about 618,994 (277)

Neuid: A Novel Neuron‐Enriched LncRNA that Connects Epigenetic Gene Silencing to Alzheimer's Disease

open access: yesAdvanced Science, EarlyView.
ABSTRACT The increasing evidence that non‐coding RNAs can become deregulated during pathogenesis is dramatically expanding the space for drug discovery beyond the protein‐coding genome. Long noncoding RNAs (lncRNAs) are emerging as key regulators of cellular function, yet most remain uncharacterized.
Ranjit Pradhan   +17 more
wiley   +1 more source

Analyse des retombées économiques directes de la Balade des Divins à Sion [PDF]

open access: yes, 2014
L’office du tourisme de Sion organise depuis 2009, la balade des Divins, une activité qui a pour but d’animer et de faire connaitre la ville. Aujourd’hui, après trois ans, le comité d’organisation aimerait connaitre les retombées économiques directes ...
Scaglione, Miriam, Zosso, Violaine
core  

An $xp$ model on $AdS_2$ spacetime

open access: yes, 2013
In this paper we formulate the $xp$ model on the AdS$_2$ spacetime. We find that the spectrum of the Hamiltonian has positive and negative eigenvalues, whose absolute values are given by a harmonic oscillator spectrum, which in turn coincides with that ...
Molina-Vilaplana, Javier   +1 more
core   +1 more source

Xanthelasma palpebrarum with arcus cornea: A clinical and biochemical study

open access: yesIndian Journal of Dermatology, 2016
Background: Xanthelasma palpebrarum (XP) is characterized by sharply demarcated yellowish flat plaques on upper and lower eyelids. It is commonly seen in women with a peak incidence at 30–50 years.
Pragya Ashok Nair   +4 more
doaj   +1 more source

On the Origins of Toughness in Corymbia calophylla (Marri Tree) Nuts

open access: yesAdvanced Science, EarlyView.
We uncover the natural toughening mechanisms of the marri nut, including fiber pullout, crack deflection, and a viscoelastic matrix, which enable exceptional energy absorption and ductility comparable to Teflon, with an elastic modulus similar to acrylic.
Wegood M. Awad   +7 more
wiley   +1 more source

PSION Organiser II XP [PDF]

open access: yesJurPC, 1989
In den Computershops findet der interessierte Anwender ein kleines, graues Kastchen (14x8x3 .cm, 286 g inklusive Batterie) mit einem schmalen LC-Display, das, versteckt unter einem Schutzschuber der sich nach unt&n schieben last, 36 Tasten besijtzt. Fur 499,D M , in der Grundversion, erhalt der Anwender eine Datenbank, eine Uhr, einen Terminkalender ...
openaire   +1 more source

Atrophic Skeletal Muscle‐Derived Extracellular Vesicles Transfer miR‐125a‐5p to Inhibit Bone Formation in Osteoporosis during Aging

open access: yesAdvanced Science, EarlyView.
A muscle‐bone endocrine pathway in aging is revealed in which extracellular vesicles released from atrophic skeletal muscle (Aged‐SKM‐EVs) inhibit bone formation. These EVs deliver miR‐125a‐5p to osteoblasts, thereby suppressing the SIRT7‐Sp7 signaling axis and osteogenic differentiation.
Xiaoyan Shao   +22 more
wiley   +1 more source

L’utilité d’une crèche / UAPE dans la commune d’Orsières: projet de création d’une structure d’accueil extrascolaire de type crèche et UAPE [PDF]

open access: yes, 2016
Actuellement, de plus en plus de parents se voient dans l’obligation de travailler, mais de plus en plus de parents ont le désir d’exercer un emploi tous les deux. A cette volonté voire obligation d’activité professionnelle s’entremêle une problématique
Abelenda, Lucie, Délez Marie-Luce
core  

Genetic insight into putative causes of xanthelasma palpebrarum: a Mendelian randomization study

open access: yesFrontiers in Immunology
Xanthelasma palpebrarum (XP) is the most common form of cutaneous xanthoma, with a prevalence of 1.1%~4.4% in the population. However, the cause of XP remains largely unknown.
Wenting Hu   +3 more
doaj   +1 more source

Identification of a novel DDB2 mutation in a Chinese Han family with Xeroderma pigmentosum group E:a case report and literature review

open access: yesBMC Medical Genetics, 2020
Background Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis. There are eight complementation groups of XP (XP-A to G and a variant form).
Rui Yang   +4 more
doaj   +1 more source

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