Results 21 to 30 of about 6,328 (292)

Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study

open access: yesHepatology, EarlyView., 2022
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel   +93 more
wiley   +1 more source

lissa

open access: yes, 2022
In der Seeschlacht von Lissa traf 1866 vor der kroatischen Insel Vis die k.u.k.-Marine auf die Flotte Italiens, der Sieg machte Admiral Tegethoff zum österreichischen Helden, war aber letztlich historisch bedeutungslos.
Straub, Wolfgang   +2 more
openaire   +1 more source

Poljske ljudske pesmi v priredbi Ludwiga van Beethovna

open access: yesMuzikološki Zbornik, 1973
Poljske ljudske pesmi v priredbi Ludwiga van ...
Zofia Lissa
doaj   +1 more source

A Visit to Lissa and Pelagosa [PDF]

open access: yesJournal of the Royal Geographical Society of London, 1879
n ...
openaire   +2 more sources

JuanmaCopia/lissa: Third Release

open access: yes, 2022
Added some descriptions to help to better understand the artifact.
Pablo Ponzio, Juan Manuel Copia
core   +1 more source

Development of a benthic macroinvertebrate-based multimetric index to quantify riverbed substrate condition in Swedish streams

open access: yesJournal of Freshwater Ecology
Human activities have degraded riverbed substrate structure via reduced heterogeneity of substrate particle sizes and increased fine sediment loadings. Despite increasing recognition of the importance of substrate quality in river ecosystems, our ability
Peter E. Carlson
doaj   +1 more source

Proteasomal degradation of intracellularly expressed Amblyomin‐X limits suicide gene therapy potential in melanoma cells

open access: yesFEBS Open Bio, EarlyView.
This study explores the feasibility of expressing the antitumoral protein Amblyomin‐X through a suicide gene therapy approach and investigates its intracellular fate after gene delivery. Although the gene is efficiently expressed, melanoma cells rapidly degrade the Amblyomin‐X protein via proteasome activity.
Victor Dal Posolo Cinel   +4 more
wiley   +1 more source

JuanmaCopia/lissa: First Release

open access: yes, 2022
First version of the ASE ...
Juan Manuel Copia
core   +1 more source

Unraveling 4‐Phenylbutyrate's Therapeutic Role in SLC6A1 Disorders: Pharmacochaperoning Over HDAC Inhibition

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw   +5 more
wiley   +1 more source

Discordance Between Patient and Physician Global Assessments in Early Systemic Sclerosis

open access: yesArthritis Care &Research, EarlyView.
Objective This study aims to identify factors associated with patient global assessment (PtGA) and physician global assessment (PhGA) and discordance between them in systemic sclerosis (SSc). Methods Data from adults with early SSc (<5 years) from the Collaborative National Quality and Efficacy Registry were included.
Ellen Romich   +35 more
wiley   +1 more source

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