9 results match your criteria: "Hubrecht Institute-KNAW and UMC Utrecht[Affiliation]"

Article Synopsis
  • Gain-of-function mutations in SHP2 are commonly found in sporadic juvenile myelomonocytic leukemia (JMML) and myeloproliferative neoplasms (MPN) associated with Noonan syndrome (NS).
  • Researchers studied the gene expression of hematopoietic stem and progenitor cells (HSPCs) with SHP2 mutations from JMML patients and a new zebrafish model, finding an inflammatory gene pattern.
  • Treatment with an anti-inflammatory agent improved the JMML-like MPN in zebrafish embryos, suggesting inflammation in HSPCs might be a potential therapeutic target for JMML.
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Background: The epicardium is the outer mesothelial layer of the heart. It encloses the myocardium and plays key roles in heart development and regeneration. It derives from the proepicardium (PE), cell clusters that appear in the dorsal pericardium (DP) close to the atrioventricular canal and the venous pole of the heart, and are released into the pericardial cavity.

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We report here a de novo missense variant in HIST1H4J resulting in a complex syndrome combining growth delay, microcephaly and intellectual disability. Trio whole exome sequencing (WES) revealed that the proband was heterozygous for a de novo c.274 A > G p.

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Mutations in genes encoding K channel subunits have been reported for pancreatic disorders and Cantú syndrome. Here, we report a syndrome in six patients from two families with a consistent phenotype of mild intellectual disability, similar facies, myopathy, and cerebral white matter hyperintensities, with cardiac systolic dysfunction present in the two oldest patients. Patients are homozygous for a splice-site mutation in ABCC9 (c.

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Actin dynamics and the Bmp pathway drive apical extrusion of proepicardial cells.

Development

July 2019

Development of the Epicardium and its Role During Regeneration Laboratory, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Melchor Fernández Almagro 3, 28029 Madrid, Spain

Article Synopsis
  • The epicardium is the outer layer of the heart that is crucial for its development and healing.
  • Researchers used zebrafish and advanced imaging techniques to understand how a group of cells called the proepicardium forms from surrounding heart tissue.
  • They discovered that specific signaling pathways and cellular movements help these proepicardium cells to leave their original position, allowing them to develop into the epicardium.
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Organoids are self-organizing 3D structures grown from stem cells that recapitulate essential aspects of organ structure and function. Here, we describe a method to establish long-term-expanding human airway organoids from broncho-alveolar resections or lavage material. The pseudostratified airway organoids consist of basal cells, functional multi-ciliated cells, mucus-producing secretory cells, and CC10-secreting club cells.

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Article Synopsis
  • The zebrafish is an ideal model for studying organ development and function due to its clear visibility and quick growth in embryos.
  • Researchers have been using genetically modified zebrafish to explore potential new drugs, although previous methods of modeling human diseases had limitations in replicating specific mutations.
  • The study successfully introduces point mutations associated with cardiovascular disorders into zebrafish, resulting in observable disease symptoms, which highlights the potential of zebrafish for accurately modeling human genetic diseases and developing new treatments.
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Retriever fetches integrins from endosomes.

Nat Cell Biol

September 2017

Hubrecht Institute/KNAW and UMC Utrecht, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands; and the Department of Cell Biology, UMC Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.

Recycling from endosomes to the plasma membrane is an important step in cell homeostasis. The retromer/SNX27/WASH complex recycles numerous receptors, but key ones are still unaccounted for. Now a related conserved heterotrimer, called retriever, has been identified that, together with SNX17, the CCC complex and WASH, mediates the recycling of αβ integrins.

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Pkd1 regulates lymphatic vascular morphogenesis during development.

Cell Rep

May 2014

Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia. Electronic address:

Lymphatic vessels arise during development through sprouting of precursor cells from veins, which is regulated by known signaling and transcriptional mechanisms. The ongoing elaboration of vessels to form a network is less well understood. This involves cell polarization, coordinated migration, adhesion, mixing, regression, and shape rearrangements.

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