Results 71 to 80 of about 250,409 (302)

EU Law as Private International Law? Re-Conceptualising the Country-Of-Origin Principle as Vested Rights Theory [PDF]

open access: yes, 2006
One of the most pertinent issues in contemporary European conflict of laws is the tension between Community law and traditional choice of law rules.
Michaels, Ralf
core   +1 more source

Does local financial development matter? [PDF]

open access: yes, 2003
We study the effects of differences in local financial development within an integrated financial market. We construct a new indicator of financial development by estimating a regional effect on the probability that, ceteris paribus, a household is shut ...
Guiso, Luigi   +2 more
core   +3 more sources

Context‐Aware Semiautonomous Control for Upper‐Limb Prostheses

open access: yesAdvanced Intelligent Systems, EarlyView.
A semiautonomous prosthetic control strategy integrates electromyographic‐based intention with computer vision‐driven grasp adaptation and wrist orientation. Comparative experiments with functional tasks evaluate performance, usability, and cognitive workload.
Gianmarco Cirelli   +7 more
wiley   +1 more source

Considerations regarding the general rule provided by the article 4 of the Rome II regulation

open access: yesAnnals of Spiru Haret University Economic Series, 2010
This article addresses certain issues related to the enforcement of the Rome II Regulation. The mentioned Regulation was adopted in order to unify, within the European Union, the rules regarding choice of law concerning non-contractual obligations.
Adrian PRICOPI, Claudiu BUTCULESCU
doaj  

HGF modulates actin cytoskeleton remodeling and contraction in testicular myoid cells [PDF]

open access: yes, 2015
The presence of the HGF/Met system in the testicular myoid cells was first discovered by our group. However, the physiological role of this pathway remains poorly understood. We previously reported that HGF increases uPA secretion and TGF-β activation in
Angela, Catizone   +6 more
core   +1 more source

Genotypes and Phenotypes of Patients With TSPEAR‐Related Disorder: Evidence of a Predominant Dental Phenotype

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani   +17 more
wiley   +1 more source

Genetic predisposition to porto‐sinusoidal vascular disorder: A functional genomic‐based, multigenerational family study

open access: yesHepatology, EarlyView., 2022
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan   +19 more
wiley   +1 more source

ІНСТИТУТ НЕДОГОВІРНИХ ЗОБОВ’ЯЗАНЬ У ЄВРОПЕЙСЬКІЙ ПРАВОВІЙ СИСТЕМІ ВІД ЧАСІВ РИМСЬКОГО ПРАВА ДО РЕГЛАМЕНТУ РИМ ІІ [PDF]

open access: yes, 2015
Прийняття Регламенту (ЄС) №864/2007 Європейського парламенту і Ради від 11 липня 2007 року про право, що застосовується до недоговірних зобов’язань стало важливим етапом законодавчої та доктринальної еволюції інституту недоговірних зобов’язань.
Трощенко, І. О.
core   +1 more source

Divergent lncRNAs take the lead on pluripotent cell differentiation [PDF]

open access: yes, 2016
[No abstract ...
Ballarino, Monica, Rosa, Alessandro
core   +1 more source

Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous ALS2 Exons 24–25 Deletion: Expanding the Genotypic Spectrum

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We describe a novel homozygous intragenic deletion in the ALS2 gene in an 8‐year‐old boy with Infantile‐onset Ascending Hereditary Spastic Paraplegia (IAHSP) and oculomotor apraxia, thereby contributing to the expanding genetic landscape of ALS2‐related disorders.
Vito Luigi Colona   +15 more
wiley   +1 more source

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