Results 221 to 230 of about 1,669,600 (380)

Regional variation in firm formation: Panel and cross-sectional data evidence from Finland [PDF]

open access: yes
This paper investigates regional variation in firm formation in Finland between 1989 and 1993. Firstly, the paper describes the firm formation process in 19 regions and 88 subregions, and finds that there has been a clear variation in firm formation ...
Aki Kangasharju
core  

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

Incidence and Mortality of Mycosis Fungoides and Sezary Syndrome: A Nationwide Registry Study in Finland. [PDF]

open access: yesActa Derm Venereol
Partanen A   +9 more
europepmc   +1 more source

Forty-year trends in cardiovascular risk factors in Finland.

open access: yesEuropean Journal of Public Health, 2015
K. Borodulin   +9 more
semanticscholar   +1 more source

Molecular Profiling of Genes Associated With Methylphenidate Pathway Therapy and Discovery of New Variants in Amazonian Amerindian Populations

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT In Attention Deficit Hyperactivity Disorder (ADHD), methylphenidate is one of the most widely used drugs, in which patient response significantly impacts prognosis. This study aimed to characterize the molecular profile of 10 genes associated with methylphenidate therapy.
Aline Pasquini Santos   +14 more
wiley   +1 more source

Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non‐Finnish Patients

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cytosolic phosphoenoylpyruvate carboxykinase (PEPCK‐C) is an essential, rate‐limiting enzyme in the gluconeogenesis pathway. PEPCK‐C deficiency presents with hypoglycaemia, hyperlactataemia and hepatopathy, and was first reported in association with bi‐allelic PCK1 variants in 2014.
Isaac Bernhardt   +9 more
wiley   +1 more source

Sensitized Disequilibration of Water‐Soluble Azopolymers

open access: yesAngewandte Chemie, EarlyView.
Disequilibration by sensitization under confinement (DESC) is a promising strategy for efficient visible‐light‐induced azobenzene E→Z isomerization. In this article, we explored key factors for adapting DESC to azopolymers, eventually achieving efficiencies up to 85% compared to direct excitation and laying the foundation for more complex systems ...
Henning Jörn Meteling   +4 more
wiley   +2 more sources

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