Search Results - (Author, Cooperation:F. Nicole)
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1J. L. Magnard ; A. Roccia ; J. C. Caissard ; P. Vergne ; P. Sun ; R. Hecquet ; A. Dubois ; L. Hibrand-Saint Oyant ; F. Jullien ; F. Nicole ; O. Raymond ; S. Huguet ; R. Baltenweck ; S. Meyer ; P. Claudel ; J. Jeauffre ; M. Rohmer ; F. Foucher ; P. Hugueney ; M. Bendahmane ; S. Baudino
American Association for the Advancement of Science (AAAS)
Published 2015Staff ViewPublication Date: 2015-07-04Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Molecular Sequence Data ; Monoterpenes/*metabolism ; *Odors ; Plastids/*enzymology ; Pyrophosphatases/*biosynthesis/genetics ; Rosa/*enzymology/genetics ; Terpenes/*metabolism ; Transcriptome ; Volatile Organic Compounds/*metabolismPublished by: -
2Beckel, Nicole F. ; O'Toole, Therese E. ; Rozanski, Elizabeth A. ; Labato, Mary A.
Oxford, UK : Blackwell Science Ltd
Published 2005Staff ViewISSN: 1476-4431Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineNotes: Objective: To describe the use of peritoneal dialysis (PD) in the management of 5 dogs with acute renal failure (ARF) caused by leptospirosis.Case Series Summary: All dogs were treated for leptospirosis with intravenous (IV) fluids and ampicillin prior to PD. Median age of dogs was 5 years (range 2–6 years). All dogs had positive titers for Leptospira bratislava. Median duration of PD was 4 days (range 3–16 days). PD resulted in a decrease in azotemia in all dogs. Median serum blood urea nitrogen at the start of PD was 192 mg/dL (range 140–235 mg/dL) and at the end of PD was 63 mg/dL (range 48–139 mg/dL). Median serum creatinine at the start of PD and the end was 12.8 mg/dL (range 7.7–16.9 mg/dL) and 3.4 mg/dL (range 1.4–11.1 mg/dL), respectively. Complications identified during PD included hypokalemia (n=3, 60%), hypoalbuminemia (n=2, 40%), hypomagnesemia (n=1, 20%), pelvic limb edema (n=2, 40%), central nervous system signs (n=2, 40%), dialysate retention (n=1, 20%), and leakage from the catheter site (n=1, 20%). Peritonitis was not identified in any of the dogs. Four dogs (80%) survived to discharge from the hospital. PD was effective for management of uremia in dogs with ARF caused by leptospirosis.Type of Medium: Electronic ResourceURL: -
3Delovitch, Terry L. ; Semple, John W. ; Naquet, Philippe ; Bernard, Nicole F. ; Elllis, Janet ; Champagne, PAT ; Phillips, M. Laurie
Oxford, UK : Blackwell Publishing Ltd
Published 1988Staff ViewISSN: 1600-065XSource: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineType of Medium: Electronic ResourceURL: -
4PRODJOSUDJADI, Wiguno ; DET, Nicole F ; VERHAGEN, Nicole AM ; GERRITSMA, Jort SJ ; BRUIJN, Jan A ; DAHA, Mohamed R ; ES, Leendert A
Oxford, UK : Blackwell Publishing Ltd
Published 1995Staff ViewISSN: 1440-1797Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineNotes: Summary: Mediators released by glomerular macrophages may stimulate glomerular visceral epithelial cells (GVEC) to produce cytokines, growth factors or extracellular matrix components. This study describes that human GVEC produce monocyte chemoattractant protein-1 (MCP-1), a monocyte-specific chemotactic factor, and the effects of interleukin-lα (IL-1α) and tumour necrosis factor-α (TNF-a) on the production of MCP-1 by GVEC.We observed that the intensity of MCP-1 staining in GVEC is stronger in membranous nephropathy and glomerulosclerosis than in normal kidneys. Various cell lines of GVEC produced significant amounts of MCP-1, as assessed by inhibition radio-immunoassay. the presence of IL-1α and TNF-α during culture of GVEC enhanced the production of MCP-1 in a dose- and time-dependent manner. Glomerular visceral epithelial cells in culture express mRNA for MCP-1 and the expression is upregulated 2.0- and 1.4-fold in the presence of optimal concentration of IL-1α and TNF-α, respectively. De novo synthesis of MCP-1 is supported by the observation that MCP-1 production is fully inhibited by cydoheximide. Monocyte chemoattractant protein-1 isolated from GVEC supernatants exhibits a molecular size of 12 and 10 kDa as determined by gel filtration chromatography. Both sizes of MCP-1 is chemotactically active for monocytes.This study shows increased MCP-1 production by cultured human GVEC after stimulation with the inflammatory cytokines IL-1α and TNF-α. the expression of MCP-1 in GVEC was found to be upregulated in membranous nephropathy and glomerulosclerosis. These findings suggest that MCP-1 may be involved in glomerular injury in these diseases. the possible role of MCP-1 in the pathogenesis of human glomerulonephritis is discussed.Type of Medium: Electronic ResourceURL: -
5Kirman, Jacob H. ; Kirman, Nicole F.
Provincetown, Mass., etc. : Periodicals Archive Online (PAO)
Published 1985Staff ViewISSN: 0022-1309Topics: PsychologyURL: -
6Wolfish, Norman M. ; Delbrouck, Nicole F. ; Shanon, Amir ; Matzinger, Mary Ann ; Stenstrom, Robert ; McLaine, Peter N.
Springer
Published 1994Staff ViewISSN: 1432-198XSource: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: -
7Amit A. Vernekar, Gilles Berger, Anna E. Czapar, Frank A. Veliz, David I. Wang, Nicole F. Steinmetz and Stephen J. Lippard
American Chemical Society (ACS)
Published 2018Staff ViewPublication Date: 2018-03-20Publisher: American Chemical Society (ACS)Print ISSN: 0002-7863Electronic ISSN: 1520-5126Topics: Chemistry and PharmacologyPublished by: -
8Staff View
Publication Date: 2018-05-15Publisher: American Heart Association (AHA)Electronic ISSN: 1524-4539Topics: MedicineKeywords: Cardiopulmonary Arrest, Statements and GuidelinesPublished by: -
9Dispersal and population state of an endangered island lizard following a conservation translocationNicole F. Angeli, Ian F. Lundgren, Clayton G. Pollock, Zandy M. Hillis-Starr, Lee A. Fitzgerald
Wiley-Blackwell
Published 2018Staff ViewPublication Date: 2018-01-20Publisher: Wiley-BlackwellPrint ISSN: 1051-0761Electronic ISSN: 1939-5582Topics: BiologyPublished by: