Search Results - "Aaraj, Yassmin Al"
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Distinct plasma gradients of microRNA-204 in the pulmonary circulation of patients suffering from WHO Groups I and II pulmonary hypertension
Published in Pulmonary circulation (01-04-2019)“…Pulmonary hypertension (PH), a heterogeneous vascular disease, consists of subtypes with overlapping clinical phenotypes. MicroRNAs, small non-coding RNAs that…”
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Frataxin deficiency promotes endothelial senescence in pulmonary hypertension
Published in The Journal of clinical investigation (01-06-2021)“…The dynamic regulation of endothelial pathophenotypes in pulmonary hypertension (PH) remains undefined. Cellular senescence is linked to PH with intracardiac…”
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Profiling of repetitive RNA sequences in the blood plasma of patients with cancer
Published in Nature biomedical engineering (01-12-2023)“…Liquid biopsies provide a means for the profiling of cell-free RNAs secreted by cells throughout the body. Although well-annotated coding and non-coding…”
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Single Nucleotide Polymorphism rs9277336 Controls the Nuclear Alpha Actinin 4-Human Leukocyte Antigen-DPA1 Axis and Pulmonary Endothelial Pathophenotypes in Pulmonary Arterial Hypertension
Published in Journal of the American Heart Association (04-04-2023)“…Background Pulmonary arterial hypertension (PAH) is a complex, fatal disease where disease severity has been associated with the single nucleotide polymorphism…”
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Computational repurposing of therapeutic small molecules from cancer to pulmonary hypertension
Published in Science advances (22-10-2021)“…Cancer therapies are being considered for treating rare noncancerous diseases like pulmonary hypertension (PH), but effective computational screening is…”
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Long-term Outcomes for Teen Mothers Who Participated in a Mentoring Program to Prevent Repeat Teen Pregnancy
Published in Journal of the National Medical Association (01-06-2019)“…Each year in the United States (US), one million adolescents are pregnant, of which approximately 20% are repeat pregnancies. Adolescent motherhood is…”
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Abstract 15579: Stem Cell Modeling of a Candidate Genetic Variant in a Family With Complex Inherited Cardiomyopathy
Published in Circulation (New York, N.Y.) (07-11-2023)“…Abstract only Introduction: Inherited cardiomyopathies, such as arrhythmogenic right (or left) ventricular cardiomyopathy (ARVC; ALVC) and dilated…”
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Abstract 10137: Functional Brain Imaging Reveals Decreased Cerebellar Volume and Altered Brain Connectivity in Pulmonary Arterial Hypertension
Published in Circulation (New York, N.Y.) (16-11-2021)“…IntroductionPsychiatric and cognitive deficiencies are increasingly appreciated in pulmonary arterial hypertension (PAH). Brain abnormalities potentially…”
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Abstract 17196: Genetic and Acquired DHCR7 Deficiency Upregulates 7β-hydroxycholesterol to Drive Endothelial Apoptosis and Pulmonary Hypertension
Published in Circulation (New York, N.Y.) (07-11-2023)“…Abstract only Introduction: Pulmonary hypertension (PH) is a fatal disease without a cure, in which endothelial dysfunction drives pathologic remodeling of the…”
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Abstract 9770: Endothelial Loss of Amphiregulin Drives Inflammation and Endothelial Apoptosis in Pulmonary Hypertension
Published in Circulation (New York, N.Y.) (16-11-2021)“…Pulmonary hypertension (PH) is a vascular disease characterized by elevated pulmonary arterial pressure (PAP), leading to right ventricular failure and death…”
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Abstract 10096: Genetic Control of Lysosomal Dysfunction Reprograms Sterol Metabolism in Pulmonary Arterial Hypertension
Published in Circulation (New York, N.Y.) (08-11-2022)“…Background Vascular inflammation critically regulates endothelial pathophenotypes, yet causative mechanisms remain incompletely defined, particularly in…”
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Dietary intake and glutamine-serine metabolism control pathologic vascular stiffness
Published in Cell metabolism (04-06-2024)“…Perivascular collagen deposition by activated fibroblasts promotes vascular stiffening and drives cardiovascular diseases such as pulmonary hypertension (PH)…”
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Abstract 15826: SCUBE1 Controls BMPR2-relevant Pulmonary Endothelial Function: Implications for Diagnostic Marker Development in Pulmonary Arterial Hypertension
Published in Circulation (New York, N.Y.) (17-11-2020)“…IntroductionPulmonary arterial hypertension (PAH) is a morbid vascular disease where mutations of bone morphogenetic protein receptor 2 (BMPR2) control…”
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Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension
Published in Science translational medicine (10-01-2024)“…Hypoxic reprogramming of vasculature relies on genetic, epigenetic, and metabolic circuitry, but the control points are unknown. In pulmonary arterial…”
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Reversal of inflammatory reprogramming by vasodilator agents in pulmonary hypertension
Published in ERJ open research (08-08-2024)“…Background Pulmonary arterial hypertension (PAH) is a deadly disease without effective non-invasive diagnostic and prognostic testing. It remains unclear…”
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Loss of Amphiregulin drives inflammation and endothelial apoptosis in pulmonary hypertension
Published in Life science alliance (01-11-2022)“…Pulmonary hypertension (PH) is a vascular disease characterized by elevated pulmonary arterial pressure, leading to right ventricular failure and death…”
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SCUBE1 Controls BMPR2-Relevant Pulmonary Endothelial Function: Implications for Diagnostic Marker Development in Pulmonary Arterial Hypertension
Published in JACC. Basic to translational science (01-11-2020)“…Utilizing publicly available ribonucleic acid sequencing data, we identified as a BMPR2-related gene differentially expressed between induced pluripotent stem…”
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Computational repurposing of therapeutic small molecules from cancer to pulmonary hypertension
Published in Science advances (22-10-2021)“…Cancer therapies are being considered for treating rare noncancerous diseases like pulmonary hypertension (PH), but effective computational screening is…”
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SCUBE1 Controls BMPR2-Relevant Pulmonary Endothelial Function
Published in JACC. Basic to translational science (01-11-2020)“…[Display omitted] •Guided by public sequencing data of iPSC-derived BMPR2-mutant ECs derived from patients with PAH and related family members, SCUBE1 was…”
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