Croatian Accession to the European Union: Institutional Challenges [PDF]
This paper analyses the quality of governance and public administration as key determinants for successful functioning within the European Union (EU).
Katarina Ott, Marijana Badjun
core +24 more sources
Croatian Accession to the European Union: Economic and Legal Challenges [PDF]
The ability of a country to meet the criteria for financial convergence on the EU depends on four key factors: the behaviour and structure of the banks and non-banking financial service providers, the degree of development of the money and capital ...
Katarina Ott, Velimir Sonje
core +27 more sources
Croatian Accession to the European Union: Facing the Challenges of Negotiations [PDF]
This paper investigates how one particular aspect of the freedom of movement of capital – the right of EU residents to acquire real estate in EU member states – might shape Croatia’s EU accession negotiations and affect its real estate market, the ...
Dubravko Mihaljek, Katarina Ott
core +18 more sources
The roles of endoglin gene in cerebrovascular diseases. [PDF]
, 2017 Endoglin (ENG, also known as CD105) is a transforming growth factor β (TGFβ) associated receptor and is required for both vasculogenesis and angiogenesis.
Ma, Li, Su, Hua, Zhang, Rui, Zhu, Wan
core +2 more sources
The effectiveness of the creativity trigger module in achieving higher levels of creative thinking among prospective teachers [PDF]
, 2021 The unoptimised level of creative thinking is seen as an issue among Semester 8 prospective teachers in Malaysian Teacher-Education Institutes (IPG).
Chew, Eng Sun
core
Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension
BMC Genetics, 2016 BackgroundPulmonary arterial hypertension (PAH) is a rare vascular disorder characterized by a capillary wedge pressure ≤ 15 mmHg and a mean pulmonary arterial pressure ≥ 25 mmHg at rest.
Guillermo Pousada +4 more
semanticscholar +1 more source
ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia
Molecular Genetics & Genomic Medicine, 2017 Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disorder caused by mutations in ENG, ACVRL1, or SMAD4. Around 90% of HHT patients present with a heterozygous pathogenic genetic variation. Almost all cases of HHT have a family
P. Torring +3 more
semanticscholar +1 more source
An oral SARS-CoV-2 Mpro inhibitor clinical candidate for the treatment of COVID-19
Science, 2021 Description Path to another drug against COVID-19 The rapid development of vaccines has been crucial in battling the ongoing COVID-19 pandemic. However, access challenges remain, breakthrough infections occur, and emerging variants present increased risk.
D. Owen +42 more
semanticscholar +1 more source
BURIALS OF THE FALLEN IN ANCIENT GREECE
Zbornik radova Filozofskog fakulteta u Splitu, 2021 The paper evaluates works of ancient authors who mention and provide details of the burial of fallen soldiers in ancient Greece, and then it compares them with preserved archaeological finds.
Lucia Nováková
doaj
The influence of fibre orientation on the post-cracking tensile behaviour of steel fibre reinforced self-compacting concrete [PDF]
Fracture and Structural Integrity, 2015 Adding fibres to concrete provides several advantages, especially in terms of controlling the crack opening width and propagation after the cracking onset.
A. Abrishambaf +2 more
doaj +1 more source