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1.
Bone Joint J ; 100-B(12): 1559-1564, 2018 12.
Article in English | MEDLINE | ID: mdl-30499313

ABSTRACT

AIMS: Cementless femoral stems must be correctly sized and well-seated to obtain satisfactory biological fixation. The change in sound that occurs during impaction of the femoral broach is said to indicate good fit, but this has not been widely studied. We set out to find whether the presence or absence of these sound changes could predict correct sizing. PATIENTS AND METHODS: We recorded the sound generated during femoral broaching for 105 cementless total hip arthroplasties using the Corail stem. Four cases were excluded, leaving 101 recordings for analysis. There were 36 male patients and 65 female patients, with a mean age of 69.9 years (sd 12.3) and median body mass index (BMI) of 29 kg/m 2 (interquartile range (IQR) 26 to 32). The recordings were analyzed to identify the frequencies of the sounds produced during impaction of the femoral broach. RESULTS: The emergence of a low-frequency band of sound in the 1 kHz range, during the final femoral broaching, was a strong predictor of a well-sized implant stem. The frequency was related to femoral length, supporting our hypothesis that the sound arose from the bone itself. CONCLUSION: The low-frequency sound generated during femoral broaching can be monitored spectrographically, its frequency can be predicted from femoral length, and it is a good predictor of appropriate stem sizing.


Subject(s)
Arthroplasty, Replacement, Hip , Hip Joint/physiopathology , Hip Prosthesis , Monitoring, Intraoperative/methods , Osteoarthritis, Hip/surgery , Sound Localization , Sound Spectrography/methods , Aged , Bone Cements , Female , Humans , Male , Prosthesis Design
2.
Curr Oncol ; 23(3): e196-220, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27330357

ABSTRACT

BACKGROUND: The incidence of hepatocellular carcinoma (hcc) and the complexity of its diagnosis and treatment are increasing. We estimated trends in net health care utilization, costs of care attributable to hcc in Ontario, and rate ratios of resource use at various stages of care. METHODS: This population-based retrospective cohort study identified hcc patients and non-cancer control subjects, and health care resource utilization between 2002 and 2009. Generalized estimating equations were then used to estimate net health care utilization (hcc patients vs. the matched control subjects) and net costs of care attributable to hcc. Generalized linear models were used to analyze rate ratios of resource use. RESULTS: We identified 2832 hcc patients and 2808 matched control subjects. In comparison with the control subjects, hcc patients generally used a greater number of health care services. Overall, the mean net cost of care per 30 patient-days (2013 Canadian dollars) attributable to outpatient visits and hospitalizations was highest in the pre-diagnosis (1 year before diagnosis), initial (1st year after diagnosis), and end-of-life (last 6 months before death, short-term survivors) phases. Mean net homecare costs were highest in the end-of-life phase (long-term survivors). In the end-of-life phase (short-term survivors), mean net costs attributable to outpatient visits and total services significantly increased to $14,220 from $1,547 and to $33,121 from $14,450 (2008-2009 and 2002-2003 respectively). CONCLUSIONS: In hcc, our study found increasing resource use and net costs of care, particularly in the end-of-life phase among short-term survivors. Our findings offer a basis for resource allocation decisions in the area of cancer prevention and control.

4.
J Evol Biol ; 25(3): 431-7, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22221661

ABSTRACT

Spite occurs when an individual harms itself in the act of harming others. Spiteful behaviour may be more pervasive in nature than commonly thought. One of the clearest examples of spite is the costly production and release of bacteriocins, antimicrobial toxins noted for their ability to kill conspecifics. A key question is to what extent these toxins provide a fitness advantage to kin of the producer cell, especially in natural communities. Additionally, when bacteria are involved in parasitic relationships, spiteful interactions are predicted to lower bacterial densities within a host, causing a reduction in parasite-induced virulence. Using five sympatric, field-collected genotypes of the insect pathogen Xenorhabdus bovienii, we experimentally demonstrate that bacteriocin production benefits kin within the host, and that it slows the mortality rate of the host. These results confirm that spite among naturally coexisting bacterial clones can be a successful kin-selected strategy that has emergent effects on virulence.


Subject(s)
Adaptation, Biological/physiology , Bacteriocins/metabolism , Moths/parasitology , Nematoda/microbiology , Xenorhabdus/metabolism , Xenorhabdus/pathogenicity , Analysis of Variance , Animals , Genotype , Host-Pathogen Interactions , Indiana , Selection, Genetic , Virulence , Xenorhabdus/genetics , Xenorhabdus/physiology
5.
Am J Physiol Lung Cell Mol Physiol ; 281(4): L913-21, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11557595

ABSTRACT

The long-term disposition of circulating neutrophils and the site of disappearance from circulation remain unclear. We investigated neutrophil localization in mice using (111)In-labeled murine peripheral blood neutrophils, mature bone marrow neutrophils, and peritoneal exudate neutrophils to track in vivo localization of these different cell populations. Infused peripheral neutrophils were found to localize equally between liver and marrow sites by 4 h (31.2 +/- 1.9 vs. 31.9 +/- 1.8%), whereas exudate neutrophils predominantly localized to liver (42.0 +/- 1.1%) and marrow-derived neutrophils to the marrow (65.9 +/- 6.6%) where they were found to localize predominantly in the hematopoietic cords. Stimulation of marrow neutrophils before infusion caused a shift in localization from marrow to liver, and subsequent induction of an inflammatory site after infusion and marrow sequestration led to remobilization of infused marrow neutrophils but not of peripheral neutrophils. These results indicate that the marrow participates in removing neutrophils from circulation, with evidence supporting both storage and perhaps disposal functions. Furthermore, models for circulating neutrophil homeostasis should consider that the site of retention is governed by the maturation and activation states of the cell.


Subject(s)
Chemotaxis, Leukocyte/immunology , Neutrophils/cytology , Neutrophils/immunology , Actins/metabolism , Animals , Bone Marrow Cells/cytology , Bone Marrow Cells/immunology , Cell Differentiation/immunology , Chemotaxis, Leukocyte/drug effects , Exudates and Transudates/cytology , Exudates and Transudates/immunology , Indium Radioisotopes , Kinetics , Lipopolysaccharides/pharmacology , Liver/cytology , Liver/immunology , Mice , Mice, Inbred C57BL , Neutrophils/metabolism , Superoxides/metabolism
6.
J Digit Imaging ; 14(2 Suppl 1): 195-6, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11442094

ABSTRACT

As medical technology advances at a rapid pace, clinicians become further and further removed from the design of their own technological tools. This is particularly evident with information management. For radiologists, clinical histories, patient reports, and other pertinent information require sophisticated tools for data handling. However, as databases grow more powerful and sophisticated, systems require the expertise of programmers and information technology personnel. The radiologist, the clinician end-user, must maintain involvement in the development of system tools to insure effective information management. Conceptual database modeling is a design method that serves to bridge the gap between the technological aspects of information management and its clinical applications. Conceptual database modeling involves developing information systems in simple language so that anyone can have input into the overall design. This presentation describes conceptual database modeling, using object role modeling, as a means by which end-users (clinicians) may participate in database development.


Subject(s)
Radiology Information Systems , Database Management Systems , Humans , Mammography
7.
Radiographics ; 21(3): 781-7, 2001.
Article in English | MEDLINE | ID: mdl-11353124

ABSTRACT

In response to rising health care costs and changing expectations concerning the quality of health care, information management is becoming increasingly important in the practice of medicine; more specifically, it is beginning to effect significant changes in radiology practice and patient care. Radiologic applications of information management include reporting diagnostic information generated from film interpretation as well as tracking utilization patterns of different imaging modalities and the variability of clinical outcomes, documenting the type of information sought by and provided to clinicians, and evaluating departmental quality standards and performance goals. Conceptual database modeling enables radiologists to understand and participate in the development of information systems, thereby improving the likelihood of successful results. In object-role modeling, groups of relevant objects and roles are identified and used to create elementary facts that form the "building blocks" for information models. The resultant models can easily be communicated, reviewed, and revised, allowing decreased development time and optimizing inclusion of relevant features in the target relational database. Increasing the amount of clinical and management input in the development process may help information systems better meet user needs, become accepted and more often used, and ultimately succeed.


Subject(s)
Databases, Factual , Information Management/methods , Models, Theoretical , Radiology , Humans
9.
J Immunol ; 164(4): 2151-9, 2000 Feb 15.
Article in English | MEDLINE | ID: mdl-10657669

ABSTRACT

Early inflammatory events include cytokine release, activation, and rapid accumulation of neutrophils, with subsequent recruitment of mononuclear cells. The p38 mitogen-activated protein kinase (MAPK) intracellular signaling pathway plays a central role in regulating a wide range of inflammatory responses in many different cells. A murine model of mild LPS-induced lung inflammation was developed to investigate the role of the p38 MAPK pathway in the initiation of pulmonary inflammation. A novel p38 MAPK inhibitor, M39, was used to determine the functional consequences of p38 MAPK activation. In vitro exposure to M39 inhibited p38 MAPK activity in LPS-stimulated murine and human neutrophils and macrophages, blocked TNF-alpha and macrophage inflammatory protein-2 (MIP-2) release, and eliminated migration of murine neutrophils toward the chemokines MIP-2 and KC. In contrast, alveolar macrophages required a 1000-fold greater concentration of M39 to block release of TNF-alpha and MIP-2. Systemic inhibition of p38 MAPK resulted in significant decreases in the release of TNF-alpha and neutrophil accumulation in the airspaces following intratracheal administration of LPS. Recovery of MIP-2 and KC from the airspaces was not affected by inhibition of p38 MAPK, and accumulation of mononuclear cells was not significantly reduced. When KC was instilled as a proinflammatory stimulus, neutrophil accumulation was significantly decreased by p38 MAPK inhibition independent of TNF-alpha or LPS. Together, these results demonstrate a much greater dependence on the p38 MAPK cascade in the neutrophil when compared with other leukocytes, and suggest a means of selectively studying and potentially modulating early inflammation in the lung.


Subject(s)
Calcium-Calmodulin-Dependent Protein Kinases/physiology , Lung/enzymology , Lung/pathology , Mitogen-Activated Protein Kinases , Aminopyridines/pharmacology , Animals , Bronchoalveolar Lavage Fluid/immunology , Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors , Chemotaxis, Leukocyte/immunology , Cytokines/metabolism , Enzyme Activation/drug effects , Enzyme Activation/immunology , Enzyme Inhibitors/pharmacology , Female , Humans , Imidazoles/pharmacology , Inflammation/enzymology , Inflammation/immunology , Inflammation/pathology , Intubation, Intratracheal , Leukocyte Count , Lipopolysaccharides/administration & dosage , Lipopolysaccharides/immunology , Macrophages, Alveolar/immunology , Mice , Mice, Inbred C57BL , N-Formylmethionine Leucyl-Phenylalanine/pharmacology , Neutrophils/enzymology , Neutrophils/immunology , Neutrophils/pathology , p38 Mitogen-Activated Protein Kinases
11.
Dev Psychol ; 35(5): 1189-97, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10493645

ABSTRACT

The role of infant and toddler temperament in the prediction of empathy in 2-year-old children was examined. Assessments of temperament included reactivity and affect observed at 4 months of age, as well as inhibition at Age 2. Empathy was measured in 2-year-old children's responses to simulations of distress performed by their mothers and by an unfamiliar person. Children showed relatively more concern for the mother's distress, but they were also responsive to unfamiliar victims. Infants who were unreactive and showed little affect also showed less empathy toward the unfamiliar adult almost 2 years later. Inhibition toward an unfamiliar adult (but not toward the mother) at 2 years of age was negatively related to empathy. Inhibited temperament may thus have a major impact on young children's empathy in unfamiliar contexts. Findings also highlight the need to consider early underarousal as another dimension of temperament that may dampen expressions of empathic concern.


Subject(s)
Child Behavior/psychology , Empathy , Temperament/physiology , Adult , Child, Preschool , Female , Humans , Inhibition, Psychological , Male , Psychology, Child
12.
Clin Immunol ; 92(3): 300-10, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10479535

ABSTRACT

Wound healing is a complex process that involves inflammation, apoptosis, growth, and tissue remodeling. The autoimmune-prone inbred mouse strain MRL/+ manifests accelerated and extensive healing to ear punch wounds, suggesting a link between immune defects and wound healing. Prior studies with lupus-prone mice have shown that hematopoietic cells of lupus-prone strains can transfer disease to otherwise non-autoimmune-prone recipients. In this study we performed reciprocal bone marrow transfers between MRL and the control strain B10.BR and found that radioresistant MRL/+ host cells, rather than hematopoietic cells, are required for the healing response. We have also made the novel observations that, compared to normal controls, MRL/+ hematopoietic cells overproduce TGF-beta1 and manifest impaired inflammatory responses to lipopolysaccharide challenge. These features suggest that the aberrant wound healing phenotype of MRL mice is independent of their propensity to develop autoimmunity.


Subject(s)
Mice, Inbred MRL lpr/metabolism , Transforming Growth Factor beta/metabolism , Wound Healing/physiology , Aging/genetics , Aging/physiology , Animals , Bone Marrow Transplantation , Bronchoalveolar Lavage Fluid/cytology , Genotype , Hematopoietic Stem Cells/metabolism , Inflammation Mediators/metabolism , Lipopolysaccharides/pharmacology , Mice , Neutrophils/cytology , Pneumonia/physiopathology , Transplantation Chimera , Wound Healing/genetics
14.
J Clin Invest ; 103(6): 851-8, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10079106

ABSTRACT

Activation of leukocytes by proinflammatory stimuli selectively initiates intracellular signal transduction via sequential phosphorylation of kinases. Lipopolysaccharide (LPS) stimulation of human neutrophils is known to result in activation of p38 mitogen-activated protein kinase (MAPk); however, the upstream activator(s) of p38 MAPk is unknown, and consequences of p38 MAPk activation remain largely undefined. We investigated the MAPk kinase (MKK) that activates p38 MAPk in response to LPS, the p38 MAPk isoforms that are activated as part of this pathway, and the functional responses affected by p38 MAPk activation. Although MKK3, MKK4, and MKK6 all activated p38 MAPk in experimental models, only MKK3 was found to activate recombinant p38 MAPk in LPS-treated neutrophils. Of p38 MAPk isoforms studied, only p38alpha and p38delta were detected in neutrophils. LPS stimulation selectively activated p38alpha. Specific inhibitors of p38alpha MAPk blocked LPS-induced adhesion, nuclear factor-kappa B (NF-kappaB) activation, and synthesis of tumor necrosis factor-alpha (TNF-alpha). Inhibition of p38alpha MAPk resulted in a transient decrease in TNF-alpha mRNA accumulation but persistent loss of TNF-alpha synthesis. These findings support a pathway by which LPS stimulation of neutrophils results in activation of MKK3, which in turn activates p38alpha MAPk, ultimately regulating adhesion, NF-kappaB activation, enhanced gene expression of TNF-alpha, and regulation of TNF-alpha synthesis.


Subject(s)
Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Lipopolysaccharides/pharmacology , Mitogen-Activated Protein Kinase Kinases , Mitogen-Activated Protein Kinases , Neutrophils/drug effects , Cell Adhesion , Down-Regulation , Enzyme Activation/drug effects , Humans , Isoenzymes/metabolism , Lipopolysaccharide Receptors/metabolism , MAP Kinase Kinase 3 , Models, Biological , NF-kappa B/metabolism , Protein Serine-Threonine Kinases/metabolism , Protein-Tyrosine Kinases/metabolism , Signal Transduction , Tumor Necrosis Factor-alpha/biosynthesis , p38 Mitogen-Activated Protein Kinases
15.
J Mol Med (Berl) ; 77(1): 211-4, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9930965

ABSTRACT

Continuous delivery of therapeutic peptide to the systemic circulation would be the optimal treatment for a variety of diseases. The Baxter TheraCyte system is a membrane encapsulation system developed for implantation of tissues, cells such as endocrine cells or cell lines genetically engineered for therapeutic peptide delivery in vivo. To demonstrate the utility of this system, cell lines were developed which expressed human growth hormone (hGH) at levels exceeding 1 microgram per million cells per day. These were loaded into devices which were then implanted into juvenile nude rats. Significant levels of hGH of up to 2.5 ng/ml were detected in plasma throughout the six month duration of the study. In contrast, animals implanted with free cells showed peak plasma levels of 0.5 to 1.2 ng four days after implantation with no detectable hGH beyond 10 days. Histological examination of explanted devices showed they were vascularized and contained cells that were viable and morphologically healthy. After removal of the implants, no hGH could be detected which confirmed that the source of hGH was from cells contained within the device. The long term expression of human growth hormone as a model peptide has implications for the peptide therapies for a variety of human diseases using membrane encapsulated cells.


Subject(s)
Fibroblasts/metabolism , Fibroblasts/transplantation , Genetic Therapy/methods , Human Growth Hormone/biosynthesis , Human Growth Hormone/genetics , Animals , Cell Line , Cell Transplantation , Genetic Engineering , Human Growth Hormone/blood , Humans , Membranes, Artificial , Rats
17.
Injury ; 29(10): 751-6, 1998 Dec.
Article in English | MEDLINE | ID: mdl-10341898

ABSTRACT

Fourteen consecutive cases with type 4 fracture of the medial epicondyle were evaluated following open reduction and internal fixation of the displaced medial epicondyle. The mean age was 9.7 years (range 6-16) and the mean follow-up was 17.2 months (range 12-24). Operative treatment yielded excellent results with no loss of functional range of motion, residual deformity or instability. There were three cases with pre-operative symptoms of ulnar nerve injury which made a good recovery following neurolysis of the ulnar nerve. Type 4 fractures are commonly associated with intra-articular entrapment of the ulnar nerve and result from serious damage to the soft tissues on the medial side of the elbow. Assessing instability is therefore of key importance, as is the intra-operative gravity stress-valgus test in assessing instability.


Subject(s)
Elbow Injuries , Fracture Fixation, Internal/methods , Humeral Fractures/surgery , Adolescent , Child , Elbow Joint/diagnostic imaging , Female , Follow-Up Studies , Humans , Humeral Fractures/diagnostic imaging , Male , Radiography , Ulnar Nerve Compression Syndromes/etiology , Ulnar Nerve Compression Syndromes/surgery
18.
Int J Dermatol ; 36(9): 673-6, 1997 Sep.
Article in English | MEDLINE | ID: mdl-9352408

ABSTRACT

BACKGROUND: Pyogenic granulomas (lobular capillary hemangiomas) and condyloma acuminata share similar locations and risk factors. Human papillomavirus (HPV) types 6 and 11 are commonly associated with condyloma acuminata, but their association with pyogenic granulomas has not been evaluated. The purpose of this study was to determine whether pyogenic granulomas contain evidence of infection with condyloma-producing HPVs. METHODS: Polymerase chain reaction assays for the E6 and E7 gene sequences of HPV types 6 and 11 and another assay for the E7 region of HPV types 16, 31, 33, 35, 42, and 58 were used to evaluate deoxyribonucleic acid (DNA) extracted from archival pyogenic granuloma biopsies taken from cutaneous and oral epithelium. RESULTS: Neither cutaneous nor oral pyogenic granulomas contain amplifiable E6 or E7 sequences from any of these viruses. CONCLUSIONS: Pyogenic granulomas are not caused by HPV 6, 11, 16, 31, 33, 35, 42, or 58. This study does not exclude the possibility that other viruses may be responsible for these tumors.


Subject(s)
DNA, Viral/analysis , Granuloma, Pyogenic/virology , Mouth Diseases/virology , Papillomaviridae/isolation & purification , Papillomavirus Infections/complications , Skin Diseases/virology , Tumor Virus Infections/complications , Base Sequence , Biopsy, Needle , Culture Techniques , Granuloma, Pyogenic/pathology , Humans , Molecular Sequence Data , Mouth Diseases/pathology , Polymerase Chain Reaction , Reference Values , Sensitivity and Specificity , Skin Diseases/pathology
19.
Article in English | MEDLINE | ID: mdl-9195622

ABSTRACT

A workshop to discuss primary oral melanomas was convened at the annual Western Society of Teachers of Oral Pathology meeting in Bannf, Alberta, Canada. Fifty oral melanomas, identified from the files of the participants, were reviewed in order to better understand the clinical features, histologic spectrum, and natural history of these perplexing lesions. Results confirmed that oral melanomas occur in adults almost three times more frequently in men than women and have a decided predilection for the palate and gingiva. Some lesions exhibit a clinically detectable and prolonged in situ growth phase, whereas others seem to lack this property and exhibit only or predominantly invasive characteristics. Recurrences, metastases, and death from tumor were characteristic of the follow-up of a limited number of patients. Until definitive prospective data are collected that elucidate natural history, oral mucosal melanomas should be tracked separately from cutaneous lesions. All oral pigmented lesions that are not clinically diagnostic should be biopsied. Lesions with equivocal histopathologic features might be referred to as "atypical melanocytic proliferation" and should be excised. Recognition of lesions in an early in situ phase and aggressive treatment should have a favorable effect on prognosis. To enhance future or prospective study of these rare neoplasms, guidelines for reporting oral melanomas are suggested.


Subject(s)
Melanoma/pathology , Mouth Neoplasms/pathology , Adult , Aged , Aged, 80 and over , Alberta , Female , Humans , Male , Melanoma/classification , Melanoma/therapy , Middle Aged , Mouth Neoplasms/classification , Mouth Neoplasms/therapy , Prognosis , Sex Ratio , Terminology as Topic
20.
J Clin Invest ; 99(5): 975-86, 1997 Mar 01.
Article in English | MEDLINE | ID: mdl-9062356

ABSTRACT

Stimulation of human neutrophils with chemoattractants FMLP or platelet activating factor (PAF) results in different but overlapping functional responses. We questioned whether these differences might reflect patterns of intracellular signal transduction. Stimulation with either PAF or FMLP resulted in equivalent phosphorylation and activation of the mitogen-activated protein kinase (MAPk) homologue 38-kD murine MAP kinase homologous to HOG-1 (p38) MAPk. Neither FMLP nor PAF activated c-jun NH2-terminal MAPk (JNKs). Under identical conditions, FMLP but not PAF, resulted in significant p42/44 (ERK) MAPk activation. Both FMLP and PAF activated MAP kinase kinase-3 (MKK3), a known activator of p38 MAPk. Both MAP ERK kinase kinase-1 (MEKK1) and Raf are activated strongly by FMLP, but minimally by PAF. Pertussis toxin blocked FMLP-induced activation of the p42/44 (ERK) MAPk cascade, but not that of p38 MAPk. A specific p38 MAPk inhibitor (SK&F 86002) blocked superoxide anion production in response to FMLP and reduced adhesion and chemotaxis in response to PAF or FMLP. These results demonstrate distinct patterns of intracellular signaling for two chemoattractants and suggest that selective activation of intracellular signaling cascades may underlie different patterns of functional responses.


Subject(s)
MAP Kinase Kinase Kinase 1 , Mitogen-Activated Protein Kinases , N-Formylmethionine Leucyl-Phenylalanine/pharmacology , Neutrophils/metabolism , Platelet Activating Factor/pharmacology , Saccharomyces cerevisiae Proteins , Signal Transduction , Calcium-Calmodulin-Dependent Protein Kinases/immunology , Calcium-Calmodulin-Dependent Protein Kinases/isolation & purification , Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Cell Adhesion/drug effects , Chemotaxis/drug effects , Chromatography, Ion Exchange , Electrophoresis, Polyacrylamide Gel , Humans , Imidazoles/pharmacology , Mitogen-Activated Protein Kinase Kinases , Pertussis Toxin , Phosphorylation , Precipitin Tests , Protein Kinases/immunology , Protein Kinases/metabolism , Protein Serine-Threonine Kinases/immunology , Protein Serine-Threonine Kinases/isolation & purification , Protein Serine-Threonine Kinases/metabolism , Protein-Tyrosine Kinases/immunology , Protein-Tyrosine Kinases/isolation & purification , Protein-Tyrosine Kinases/metabolism , Proto-Oncogene Proteins/immunology , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-jun/metabolism , Proto-Oncogene Proteins c-raf , Recombinant Proteins/pharmacology , Superoxides/metabolism , Thiazoles/pharmacology , Time Factors , Virulence Factors, Bordetella/pharmacology
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