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Profil bibliographique

Scott Jennings

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

65Publications signalées
1183Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Cystic Fibrosis Research AdvancesRenal cell carcinoma treatmentCardiac Valve Diseases and TreatmentsPleural and Pulmonary DiseasesInfective Endocarditis Diagnosis and Management

Les publications récentes

Accès ouvert 2025 article OpenAlex

Myeloperoxidase gene knockout causes local inflammation and dysbiosis in the murine gut

Yawen Hu, Scott Jennings, Meng Luo, Christopher M. Taylor et autres

Myeloperoxidase (MPO), predominantly expressed in neutrophils, catalyzes the production of hypochlorous acid (HOCl) that plays an integral role in the host defense against invading pathogens. However, little is known about its role in maintaining normal gut microbiome and function. Here, we report …

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0 citations Gut Microbes Reports
Accès ouvert 2024 article OpenAlex

Normalization of Cystic Fibrosis Immune System Reverses Intestinal Neutrophilic Inflammation and Significantly Improves the Survival of Cystic Fibrosis Mice

Callie Scull, Yawen Hu, Scott Jennings, Guoshun Wang

BACKGROUND & AIMS: Cystic fibrosis (CF) is an autosomal recessive genetic disorder, affecting multiple organ systems. CF intestinal disease develops early, manifesting as intestinal bacterial overgrowth/dysbiosis, neutrophilic inflammation, and obstruction. As unresolvable infection and inflammation reflect host immune deficiency, we sought to …

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1 citation Cellular and Molecular Gastroenterology and Hepatology
Accès ouvert 2023 article OpenAlex

Loss of CFTR function in macrophages alters the cell transcriptional program and delays lung resolution of inflammation

Dianne Wellems, Yawen Hu, Scott Jennings, Guoshun Wang

Cystic fibrosis (CF) is an autosomal recessive genetic disorder caused by mutations in the CF Transmembrane-conductance Regulator (CFTR) gene. The most severe pathologies of CF occur in the lung, manifesting as chronic bacterial infection, persistent neutrophilic inflammation, and mucopurulent airway obstruction. Despite …

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11 citations Frontiers in Immunology
Accès ouvert 2023 article OpenAlex

Aberrant immune programming in neutrophils in cystic fibrosis

Yawen Hu, Christine M. Bojanowski, Clemente J. Britto, Dianne Wellems et autres

Cystic fibrosis is a life-shortening genetic disorder, caused by mutations in the gene that encodes cystic fibrosis transmembrane-conductance regulator, a cAMP-activated chloride and bicarbonate channel. Persistent neutrophilic inflammation is a major contributor to cystic fibrosis lung disease. However, how cystic fibrosis transmembrane-conductance …

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19 citations Journal of Leukocyte Biology
Accès ouvert 2023 article OpenAlex

Neutrophil defect and lung pathogen selection in cystic fibrosis

Scott Jennings, Yawen Hu, Dianne Wellems, Meng Luo et autres

Cystic fibrosis is a life-threatening genetic disorder caused by mutations in the CFTR chloride channel. Clinically, over 90% of patients with cystic fibrosis succumb to pulmonary complications precipitated by chronic bacterial infections, predominantly by Pseudomonas aeruginosa and Staphylococcus aureus. Despite the well-characterized …

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8 citations Journal of Leukocyte Biology
Accès ouvert 2023 preprint OpenAlex

ABERRANT IMMUNE PROGRAMMING IN NEUTROPHILS IN CYSTIC FIBROSIS

Yawen Hu, Christine M. Bojanowski, Clemente J. Britto, Dianne Wellems et autres

ABSTRACT Cystic fibrosis (CF) is a life-shortening genetic disorder, caused by mutations in the gene that encodes Cystic Fibrosis Transmembrane-conductance Regulator (CFTR), a cAMP-activated chloride and bicarbonate channel. Although multiple organ systems can be affected, CF lung disease claims the most morbidity …

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3 citations medRxiv
Accès ouvert 2022 article OpenAlex

Cftr deletion in mouse epithelial and immune cells differentially influence the intestinal microbiota

Callie Scull, Meng Luo, Scott Jennings, Christopher M. Taylor et autres

Cystic fibrosis (CF) is a life-threatening genetic disorder, caused by mutations in the CF transmembrane-conductance regulator gene (cftr) that encodes CFTR, a cAMP-activated chloride and bicarbonate channel. Clinically, CF lung disease dominates the adult patient population. However, its gastrointestinal illness claims the …

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10 citations Communications Biology
Accès ouvert 2022 review OpenAlex

Comparison of Proportion of Elevated Carcinoembryonic Antigen Levels in Patients With Appendiceal and Colorectal Adenocarcinoma: A Systematic Review and Meta-analysis

Adam Cristaudo, Scott Jennings, David L. Morris

BACKGROUND/AIM: The proportion of patients with liver metastases in patients with appendiceal versus colorectal adenocarcinomas was 3.1 percent and 24 percent, respectively, in our peritonectomy centre. From our internal analyses, carcinoembryonic antigen (CEA) was potentially involved. A hypothesis was proposed regarding the …

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6 citations Anticancer Research
Accès ouvert 2020 article OpenAlex

Myeloid CFTR loss-of-function causes persistent neutrophilic inflammation in cystic fibrosis

Hang Pong Ng, Scott Jennings, Dianne Wellems, Fei Sun et autres

Persistent neutrophilic inflammation is a hallmark of cystic fibrosis (CF). However, the mechanisms underlying this outstanding pathology remain incompletely understood. Here, we report that CFTR in myeloid immune cells plays a pivotal role in control of neutrophilic inflammation. Myeloid CFTR-Knockout (Mye-Cftr-/-) mice …

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12 citations Journal of Leukocyte Biology

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