Search Results - "GAROFALO, Mary"
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Resignation and Resilience: Bridging Effective Teaching to the Impacts of Complex and Layered School Culture
Published in Research in educational administration & leadership (28-03-2023)“…This article examines the relationship between teacher efficacy, leadership, and how they intersect with complex and layered school system dynamics. Using the…”
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Germline IKAROS dimerization haploinsufficiency causes hematologic cytopenias and malignancies
Published in Blood (21-01-2021)“…IKAROS is a transcription factor forming homo- and heterodimers and regulating lymphocyte development and function. Germline mutations affecting the IKAROS…”
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Lavinia Dock (1858-1956): picketing, parading, and protesting
Published in American journal of public health (1971) (01-02-2015)“…After graduation, she worked as a visiting nurse for a variety of charitable organizations, supervised a ward in a temporary hospital for those suffering from…”
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Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling
Published in Nature communications (22-06-2023)“…We describe the first cases of germline biallelic null mutations in ARPC5, part of the Arp2/3 actin nucleator complex, in two unrelated patients presenting…”
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Florence Nightingale and the Crimean War
Published in American journal of public health (1971) (01-09-2010)“…Nightingale's accomplishments during the disastrous years the British army experienced in the Crimea were largely the result of her concern with sanitation and…”
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TNF overproduction impairs epithelial staphylococcal response in hyper IgE syndrome
Published in The Journal of clinical investigation (01-08-2018)“…Autosomal dominant hyper IgE syndrome (AD-HIES), or Job's syndrome, is a primary immune deficiency caused by dominant-negative mutations in STAT3. Recurrent…”
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Gain of Function Mutations of PIK3CD as a Cause of Primary Sclerosing Cholangitis
Published in Journal of clinical immunology (01-01-2015)“…Gain of function (GOF) mutation in the p110δ catalytic subunit of the phosphatidylinositol-3-OH kinase ( PIK3CD ) is the cause of a primary immunodeficiency…”
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Florence Nightingale (1820-1910): feminism and hospital reform. 2010
Published in American journal of public health (1971) (01-09-2010)Get full text
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Florence Nightingale (1820–1910): Feminism and Hospital Reform
Published in American journal of public health (1971) (01-09-2010)“…FLORENCE NIGHTINGALE WAS born of wealthy parents who expected her to do all the things young ladies of her class did: to spend much of her time in the drawing…”
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Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism
Published in Journal of allergy and clinical immunology (01-06-2013)“…Background Autosomal dominant hyper-IgE syndrome (AD-HIES) is caused by mutations in signal transducer and activator of transcription 3 (STAT3) . We describe 2…”
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Red Emma (1869-1940): idealistic revolutionary
Published in American journal of public health (1971) (01-06-2011)“…A labor organizer and anarchist leader, she crisscrossed the county lecturing on anarchism, economics, drama, birth control, free love, and women's…”
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The Use of Radiolabelled 18-F-2-Deoxy-2-Fluro-Glucose (18-FDG) in Combined Positron Emission Tomography-Computed Tomography (PET-CT) to Evaluate Infection: Lessons Learned from a Case Series of 23 Patients with Chronic Granulomatous Disease (CGD)
Published in Journal of allergy and clinical immunology (01-02-2015)“…[...]CGD lymphadenopathy observed by CT, but unrelated to infection, lack intense 18-FDG uptake…”
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Suicidality and divalproex sodium: analysis of controlled studies in multiple indications
Published in Annals of general psychiatry (18-01-2011)“…Recent analyses of antiepileptic drugs have indicated an increase in the risk of suicidality. The objective of this report was to provide clinical information…”
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AMD3100 is a potent antagonist at CXCR4R334X, a hyperfunctional mutant chemokine receptor and cause of WHIM syndrome
Published in Journal of cellular and molecular medicine (01-10-2011)“…WHIM is an acronym for a rare immunodeficiency syndrome (OMIM #193670) caused by autosomal dominant mutations truncating the C‐terminus of the chemokine…”
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CRISPR-Cas9 gene repair of hematopoietic stem cells from patients with X-linked chronic granulomatous disease
Published in Science translational medicine (11-01-2017)“…Gene repair of CD34 hematopoietic stem and progenitor cells (HSPCs) may avoid problems associated with gene therapy, such as vector-related mutagenesis and…”
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Faculty Development: Mission and Methods for Practical Integration
Published in Journal of Catholic higher education (2021)“…Current research suggests that faculty development should address a cross-section of personal and professional needs of the faculty, as well as support the…”
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Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype
Published in Blood (28-09-2017)“…NF-κB signaling through its NFKB1-dependent canonical and NFKB2-dependent noncanonical pathways plays distinctive roles in a diverse range of immune processes…”
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T and B cell abnormalities, pneumocystis pneumonia, and chronic lymphocytic leukemia associated with an AIOLOS defect in patients
Published in The Journal of experimental medicine (06-12-2021)“…AIOLOS/IKZF3 is a member of the IKAROS family of transcription factors. IKAROS/IKZF1 mutations have been previously associated with different forms of primary…”
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Glycosylation, Hypogammaglobulinemia, and Resistance to Viral Infections
Published in The New England journal of medicine (24-04-2014)“…In two siblings, a congenital disorder of glycosylation (CDG-IIb) was shown to lead to severe hypogammaglobulinemia but paradoxically impaired viral…”
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Pulmonary Nontuberculous Mycobacterial Disease: Prospective Study of a Distinct Preexisting Syndrome
Published in American journal of respiratory and critical care medicine (15-11-2008)“…Pulmonary nontuberculous mycobacterial (PNTM) disease is increasing, but predisposing features have been elusive. To prospectively determine the morphotype,…”
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