Protoplasma
Laboratory of Nuclear Proteins, Faculty of Biotechnology, University of Wrocław, Joliot- Curie 14a, 50-383, Wrocław, Poland.
Published: January 2020
The original publication of this paper contains a mistake.
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http://dx.doi.org/10.1007/s00709-019-01474-z | DOI Listing |
Front Pharmacol
August 2024
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Belgrade, Belgrade, Serbia.
[This corrects the article DOI: 10.3389/fphar.2024.
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May 2024
Center of Excellence in Genomic Medicine Research, Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Congenital heart disease (CHD) encompasses a diverse range of structural and functional anomalies that affect the heart and the major blood vessels. Epidemiological studies have documented a global increase in CHD prevalence, which can be attributed to advancements in diagnostic technologies. Extensive research has identified a plethora of CHD-related genes, providing insights into the biochemical pathways and molecular mechanisms underlying this pathological state.
View Article and Find Full Text PDFBrain
July 2024
Department of Neuroscience, Physiology and Pharmacology, University College London, London, WC1E 6BT, UK.
GABABRs are key membrane proteins that continually adapt the excitability of the nervous system. These G-protein coupled receptors are activated by the brain's premier inhibitory neurotransmitter GABA. They are obligate heterodimers composed of GABA-binding GABABR1 and G-protein-coupling GABABR2 subunits.
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May 2024
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati OH 45229, USA.
The gastrointestinal (GI) tract is complex and consists of multiple organs with unique functions. Rare gene variants can cause congenital malformations of the human GI tract, although the molecular basis of these has been poorly studied. We identified a patient with compound-heterozygous variants in RFX6 presenting with duodenal malrotation and atresia, implicating RFX6 in development of the proximal intestine.
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