Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 5 of 5 for “"DiGeorge syndrome"”.
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Characterization of Stress Responsive MicroRNAs and Their Roles in T Cell Development
… in almost all individuals with 22q11.2 deletion/DiGeorge syndrome that can present with immune, cardiac, parathyroid, and psychological problems. The molecular targets of miR-185 in thymocytes are unknown. Transgenic expression of miR-185 attenuated thymopoiesis at the TCRβ-selection checkpoint …
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Analysis and characterisation of the mouse Hic2 gene
… homolog HIC2, Hic2 could be involved in some syndromes. Patients with a 22q11 deletion have disrupted brain development which may involve abnormal neural crest cell migration, (Van Amelsvoort et al., 2001). It is now recognized that the 22q11.2 deletion syndrome encompasses the phenotypes …
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Generation and Characterization of Human Blood-Brain Barrier Models for Investigating Neuropsychiatric Disorders and Tumor Metastasis
… by BMECs is compromised in 22q11.2 deletion syndrome (also called DiGeorge syndrome), which is one of the validated genetic risk factors for schizophrenia, a 2D iBBB (induced BBB) on a Transwell filter was generated from human microvascular endothelial cells (HBMECs) derived from the induced …
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The Role of Sonic Hedgehog in Outflow Tract Development
<p>The two major contributing populations to the outflow tract of the heart are the secondary heart field and the cardiac neural crest. These two populations are responsible for providing the myocardium that supports the outflow tract valves, the smooth muscle that surrounds these valves and the …
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Caracterización clínica de pacientes pediátricos con síndrome de deleción 22q11 atendidos en Hospital de Bogotá, durante el periodo de 2010 a 2020
El síndrome de deleción 22q11 (22q11DS) es el segundo síndrome genético más común y la segunda causa de cardiopatía congénita en la infancia (1). El 90-95% de los casos se deben a microdeleciones de novo, con un riesgo de recurrencia de ∼1%. El 22q11DS afecta múltiples sistemas que incluyen el …