Frans A. Kuypers

ORCID: 0000-0003-0731-1007
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About
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Research Areas
  • Hemoglobinopathies and Related Disorders
  • Erythrocyte Function and Pathophysiology
  • Neonatal Health and Biochemistry
  • Iron Metabolism and Disorders
  • Blood groups and transfusion
  • Hemoglobin structure and function
  • Blood properties and coagulation
  • Peroxisome Proliferator-Activated Receptors
  • Metabolism and Genetic Disorders
  • Lipid Membrane Structure and Behavior
  • Lipid metabolism and biosynthesis
  • Metabolomics and Mass Spectrometry Studies
  • Hematopoietic Stem Cell Transplantation
  • Phagocytosis and Immune Regulation
  • Heme Oxygenase-1 and Carbon Monoxide
  • Bone and Joint Diseases
  • Malaria Research and Control
  • Nitric Oxide and Endothelin Effects
  • Microfluidic and Bio-sensing Technologies
  • Erythropoietin and Anemia Treatment
  • Antioxidant Activity and Oxidative Stress
  • Sphingolipid Metabolism and Signaling
  • Pulmonary Hypertension Research and Treatments
  • Neonatal Respiratory Health Research
  • Folate and B Vitamins Research

Universidad Católica de Santa Fe
2024

University of California, San Francisco
1999-2024

UCSF Benioff Children's Hospital
2020-2022

Oakland University
1991-2016

California State University, East Bay
2005

University of Pittsburgh
2003

Purdue University West Lafayette
2002

Lawrence Berkeley National Laboratory
1994-2001

Albert Einstein College of Medicine
2001

National Institutes of Health
2001

Pulmonary hypertension is a life-threatening complication of sickle cell disease. L-Arginine the nitrogen donor for synthesis nitric oxide, potent vasodilator that deficient during times crisis. This deficiency may play role in pulmonary hypertension. The enzyme arginase hydrolyzes arginine to ornithine and urea, thus, it compete with oxide synthase, leading decreased production. Nitric therapy by inhalation has improved associated acute chest syndrome disease, several studies demonstrate...

10.1164/rccm.200208-967oc article EN American Journal of Respiratory and Critical Care Medicine 2003-03-11

Artemisinin is an important new antimalarial agent containing a bridged endoperoxide. The in vitro activity of artemisinin derivative, arteether, antagonized by two iron chelators, pyridoxal benzoylhydrazone and 1,2-dimethyl-3-hydroxypyrid-4-one. Similarly, the acute toxicity mice another chelator, deferoxamine-hydroxyethylstarch. A combination hemin oxidizes erythrocyte membrane thiols vitro, this oxidation also inhibited chelator. Thus, plays role mechanisms action artemisinin. decreases...

10.1128/aac.37.5.1108 article EN Antimicrobial Agents and Chemotherapy 1993-05-01

Recent studies suggest that a nitric oxide (NO) deficiency and elevated arginase activity may play role in the pathogenesis of asthma. Although much attention has been directed toward measurements exhaled NO asthma, no to date have evaluated levels plasma or arginine, substrate for production, patients with This study, therefore, measured amino acid levels, activity, metabolites blood as well breath. virtually all acids were reduced, asthma exhibited striking reduction arginine compared...

10.1164/rccm.200309-1304oc article EN American Journal of Respiratory and Critical Care Medicine 2004-04-13

Purpose Our objective was to evaluate l-arginine and nitric oxide metabolite (NOx) levels in children with sickle cell disease (SCD) at steady-state during vaso-occlusive crisis (VOC). Because alterations production may have an important role the pathophysiology of SCD, our second aim determine if a relationship exists between these Patients Methods Plasma serum NOx were examined 36 patients SCD 39 episodes VOC 10 steady-state. Daily obtained requiring hospitalization. Results Steady-state...

10.1097/00043426-200011000-00009 article EN ˜The œAmerican journal of pediatric hematology/oncology 2000-11-01

Painful episodes of vaso-occlusion are the leading cause hospitalizations and emergency department visits in sickle cell disease, associated with increased mortality. Low nitric oxide bioavailability contributes to vasculopathy disease. Since arginine is obligate substrate for production, an acute deficiency pain, we hypothesized that may be a beneficial treatment pain related Thirty-eight children disease hospitalized 56 were randomized into this double-blinded placebo-controlled trial....

10.3324/haematol.2013.086637 article EN cc-by-nc Haematologica 2013-05-03

Abstract Nine inbred strains of mice, which are progenitors recombinant sets, were evaluated for aortic lesion formation and plasma liver lipid levels. This survey was done to determine if a semi‐synthetic high‐fat diet could elicit the same extent diet‐induced atherosclerosis as that observed in mice fed natural ingredient highfat discover strain‐specific variants future genetic characterization. Evaluation lesions after 18 wk consumption showed C57BL/6J, C57L/J, SWR/J SM/J susceptible A/J,...

10.1007/bf02536053 article EN Lipids 1993-07-01

By consensus, the acyl-CoA synthetase (ACS) community, with advice of human and mouse genome nomenclature committees, has revised for mammalian long-chain synthetases. ACS is family root name, genes ACSs are termed ACSL1,3-6 Acsl1,3-6, respectively. Splice variants ACSL3, -4, -5, -6 cataloged. Suggestions naming other members nonmammalian synthetases made.

10.1194/jlr.e400002-jlr200 article EN cc-by Journal of Lipid Research 2004-08-02

Abstract The pathogenesis of pulmonary hypertension (PAH), a serious complication in thalassemia, is not well understood. Thromboembolism has been postulated as one the causative factors; however, there are currently limited specific data on its role. To examine whether increased platelet activation and hypercoagulability linked to PAH, 25 β‐thalassemia major intermedia patients were evaluated with Doppler echocardiograms for estimation artery pressure laboratory assays indications...

10.1002/ajh.20640 article EN American Journal of Hematology 2006-06-22

The mammalian RBC lacks de novo lipid synthesis but maintains its membrane composition by rapid turnover of acyl moieties at the sn-2 position phospholipids. Plasma-derived fatty acids are esterified to acyl-CoA synthetases and transferred lysophospholipids acyl-CoA:lysophospholipid acyltransferases. We report characterization three lysophosphatidylcholine (lysoPC) acyltransferases (LPCATs), products AYTL1, -2, -3 genes. These proteins members a LPCAT family, which all genes expressed in an...

10.1073/pnas.0709737104 article EN Proceedings of the National Academy of Sciences 2007-12-22

Summary Sickle cell disease (SCD) is characterized by progressive vascular injury and its pathophysiology strikingly similar to that of atherosclerosis. Statins decrease inflammation improve endothelial function in cardiovascular disease, but their effect SCD not known. In this pilot study, we examined the safety short‐term simvastatin on biomarkers dysfunction SCD. We treated 26 patients with simvastatin, 20 or 40 mg/d, for 21 d. Plasma nitric oxide metabolites (NOx), C‐reactive protein...

10.1111/j.1365-2141.2010.08480.x article EN British Journal of Haematology 2011-04-08
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