Hemocyte

We describe here the isolation and initial characterization of hemomucin, a novel cell surface molecule from a Drosophila hemocyte cell line. Hemomucin was isolated using H.p. lectin, a snail lectin that enhances induction of T-lymphocytes and induces the antibacterial response in mbn-2 cells. The induction is lectin-dependent because it could be inhibited by addition of the H.p. lectin-specific sugar. Although hemomucin is the only hemocyte protein that could be detected in Western blots and affinity purification using H.p. lectin, minor undetected glycoproteins or glycolipids might have led to the observed effects. Nevertheless, hemomucin is the major target for H.p. lectin on the cell surface and a likely candidate for mediating the lectin-dependent induction. The isolation and characterization of the corresponding cDNA predicts a protein that contains typical mucin domains 10 12, 43 ; . Hemomucin shows no sequence similarity to CD43, the major surface mucin on human T-lymphocytes, which is recognized by H.p. lectin 44 ; . The cellular location of hemomucin in mbn-2 cells and the presence of an amino-terminal hydrophobic domain in the mature protein suggest that it is attached to the membrane of these cells by this domain, which serves as a transmembrane anchor. Two proteins of different molecular mass 100 and 220 kDa ; were recognized by the lectin, similar to other surface mucins that exist in different glycoforms 45 ; . Because the two proteins contained identical tryptic peptides, we conclude that they are encoded by the same gene and that the size difference is due to post-translational modifications. One such difference between the two proteins was shown to be a phosphorylation of the.
Hemocyte products
Radiotherapy For The Treatment Of Cancer CA Cancer J Clin 1966; 16; 186-190 DOI: 10.3322 canjclin.16.5.186. Developmental Factors and Prognosis Younger people tend to recover more rapidly from brain injury than older people. Injury in preschool years is associated with a recovery curve that plateaus at 6 months whilst in older children the figure is more like 12 months.3 A more extensive 2-year recovery phase is quoted for adults with brain injury. This difference may reflect either faster neuronal recovery in the child or less recovery potential due to attenuated developmental processes in the child. The so-called Kennard Principle proposes that it is better to have a brain injury earlier than later in life. This is not necessarily the case, and disagreement on this issue is probably due to confusion in the meaning of `outcome' or ignorance about the nature of brain plasticity.4 Although children and adolescents are more likely than adults to survive following brain injury, such an event will alter the entire subsequent developmental trajectory for a child. The relative contribution of plasticity and vulnerability in the developing nervous system has been discussed at length in the literature in an attempt to explain outcome. On one hand, the earlier the damage, the greater the potential for recovery due to plasticity.5 On the other hand, early disruption can cause vulnerability to severe and global maldevelopment.6 Developmental neuropsychology provides a synthesis of these views. It is likely that cognitive development involves a process of interaction between genetic determination and experience that effects a gradual modularisation of cognitive functions.7 In the young child, lack of early module development gives greater plasticity; hence modules can be relocated in early but not late lesions. Conversely this leads to vulnerability as there are no modules present in early lesions, so the system has to learn the whole function of the module from scratch with potentially impaired experience. Adults. 5. Goldman L, Weinstein MC, Goldman PA, William LW Cost-effectiveness of HMG-Co-A reductase inhibition for primary and secondary prevention of coronary heart disease. JAMA 1991.

Hemocyte drug interactions
Table 1 Average fresh mass, body fat, hemocyte density, and encapsulation rate of winner and loser C. virgo males after contest Winner Mean Fresh mass mg ; Hemocyte density cells ll ; Body fat mg ; Encapsulation rate 112.4 2464.0 3.0 SD 12.1 1356.0 1.5 Loser Mean 110.4 3888.0 2.1 SD 9.0 3327.0 1.2 Paired t test n 27 21 0.88 df 26 20 .39.

Radiolabeled anti-CD20 antibodies produce responses in 60% to 95% of patients with relapsed non-Hodgkin lymphoma NHL however, absorbed radiation ratios between tumors and normal organs are relatively low, and many patients have relapses. In this study we compared the abilities of anti-CD45 BC8 ; and anti-CD20 1F5 ; antibodies to target human Ramos lymphoma xenografts in athymic mice. When direct radioiodination was performed with conventional methods, BC8 delivered 2- to 4-fold more radioiodine to tumors than 1F5, with tumor-tonormal organ ratios as high as 20: 1 using radiolabeled BC8 compared with a maximal ratio of 9.8: 1 using radioiodinated 1F5. To opti and heparin. We have previously shown that embryonic hemocytes rapidly chemotax toward an epithelial wound Stramer et al., 2005 ; in a process resembling the vertebrate inflammatory response. To determine whether Pvf signals play a chemotactic role during this inflammatory response, we made laser ablations to pvr mutants expressing p35. 1 h after wounding, these embryos show a robust wild-type response from the mutant hemocytes, demonstrating that wound chemotaxis is independent of PVR expression Fig. 6, A and B; Rorth, P., personal communication ; . To further study the wound chemotactic response, we developed a wounding assay using beads that allow the treatment of the wound region with inhibitory drugs. Such beads are routinely used in embryonic studies for the local application of chemical inhibitors in vivo Kawakami et al., 2003 ; . Implanting a bead into a D. melanogaster embryo creates an epithelial wound approximately the same diameter as the bead Fig. 6 C ; . the case with laser-induced wounds, application of untreated beads to a stage 16 embryo leads to rapid accumulation of hemocytes at the wound site until, by 30 min, they surround the bead Fig. 6 D ; . Like unstimulated midline hemocytes, these cells exhibit large dynamic membrane ruffles and filopodia as they surround and seemingly try to collectively phagocytose the invasive bead Fig. 6 E and Video 2, available at : jcb cgi content full jcb.200508161 DC1 ; . These actin-rich protrusive structures are one of the most distinctive features of moving cells and are generally considered to be critical for single-cell migration. To directly test the requirement of cytoskeletal protrusions during hemocyte chemotaxis, we presoaked beads in one of two actin polymerization blocking drugs, Cytochalasin D or Latrunculin B, before bead implantation and examined hemocyte recruitment in embryos 1 h after bead insertion. We found that treatment with either drug blocks this chemotactic response so that drug-treated beads show little or no hemocytes in direct contact with the bead and those hemocytes close to the bead exhibit small or no actin protrusions and are much less motile when compared with their wild-type counterparts Figs. 6, F and G; and Video 2 ; . In both cases, effects of drug treatment can be seen up to 50 away from the bead, as hemocytes that lie further away from the bead exhibit normal dynamic lamellipodia Fig. 6 F ; . assume that this reflects a drop off in drug concentration as a result of drug diffusion away from the bead.

Moderate interactions abc plus senior , abc to z , acarbose , acetohexamide , acid relief , adeks , adgyn estro , aerodiol , aerolate iii , aerolate jr , aerolate sr , alka-mints , alkets , alkums , allbee-c 800 with iron , aloh-gel , alora , alternagel , alu-cap , alu-tab , aluminum carbonate , aluminum hydroxide , amaryl , ami-natal plus one improved , amilac , aminatal plus , aminatal plus new formula , aminatal plus one , aminate , aminate with 90 mg iron , aminophylline , aminophylline extended release , amitone , amobarbital , amphojel , amytal sodium , anabolin la , andro la 200 , andro-cyp 100 , andro-cyp 200 , androderm , androgel , androgel 25 g actuation , androgel 5 g packet , androgel 5 g packet , android , android-10 , android-25 , androlone-d , andryl 200 , anemagen , anemagen fa , anemagen ob , anhydrous calcium iodide , anisindione , antioxid caplets , antioxidant formula , antioxidant ultra formula , apatate forte , apetimar with iron , apidra , apidra opticlik cartridge , aquadeks , aquadeks pediatric , aquaphyllin , aquest , asmalix , avail calcium intensive , b-plex plus minerals , bacmin , basaljel , becomax rx , bedol , bee-zee , beelith , berocca plus , berplex plus , betamed , biotin forte with zinc , bright beginnings , bronkodyl , bugs bunny complete , bugs bunny with iron chewable , busodium , butabarbital , butalbital , butisol sodium , cal oys , cal-gest , cal-nate , calafol rx , calcarb , calcet plus , calci mix , calci-chew , calcifol , calcifolic-d , calcionate , calciquid , calcitab , calcium acetate , calcium carbonate , calcium citrate , calcium concentrate , calcium glubionate , calcium gluconate , calcium lactate , calcium liquid softgel , calcium oyster , calcium oyster shell , calcium phosphate, tribasic , calphron , caltrate , caltrate 600 plus , caltrate plus , caltro , carbamazepine , carbamazepine extended release , carbatrol , carbonyl iron , cardoxin , carenatal dha , caromega , cenestin , cenogen ultra , centavite , central , central-vite , centrum , centrum jr , centrum jr with extra c , centrum jr with extra calcium , centrum kids complete dora the explorer , centrum kids complete spongebob squarepants , centrum kids complete variety , centrum performance , centrum silver , centrum singles , century , century-vite , cerovite advanced formula , cerovite junior , cerovite liquid , cerovite senior , certa-vite , certa-vite senior plus lutein , certagen , certagen senior , certagen senior with lutein , certavite , cezin-s , cf vite , chem-sol , chlorotrianisene , chlorpropamide , choledyl , choledyl sa , cholestyramine , cholestyramine light , chooz , chromagen , chromagen obsolete ; 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4. Discussion The present study tested the impact of food supply on the biochemical composition and hemocyte parameters of oysters over an annual cycle under experimentally-controlled conditions. A histological study was simultaneously performed by Enriquez-Diaz 2004 ; , so discussion of the biochemical and hemocyte changes during reproductive process is possible. Combined, these data will contribute to a better understanding of the interactions between energetic, hemocyte parameters and reproductive processes. 4.1. Changes related to the reproductive processes Irrespective of dietary rations, changes in all energetic and hemocyte parameters can be separated into two successive phases related to reproductive processes: a gametogenesis phase and a growth phase including glycogen storage and somatic growth. Measures of energy status, such as the carbohydrate content and adenylate energy charge AEC ; , revealed that there was a significant consumption of energy reserves from May to August and then a restoration of this compartment from October to February. Changes in these two parameters were significantly inversely correlated with seawater temperature in the rearing tanks. It is well known that increase and utilization of carbohydrate storage is a result of the balance between food supply and energy demands of two successive biological processes, reproduction and growth, both of which are temperature dependent. So, the depletion of carbohydrate content and AEC from May to August is considered to be a consequence of utilization of reserves for the gametogenic processes taking place during this period Moal et al., 1991 a and b ; . This result is in agreement with studies of Mori et al. 1965 ; , Perdue and Erickson 1984 ; , Ruiz et al. 1992 ; and more recently Li et al. 2000 ; and Berthelin et al. 2000 ; . Thereafter, there is a restoration of the energy reserves of oysters in the fall September-November ; . Histological analyses of Enriquez-Diaz 2004 ; Figure 8 ; confirmed that those changes were related to the balance between the reproductive process, energy storage, and growth.

Side effects of Hemocyte

Of the fully colonized light organ by 12 h Doino and McFall-Ngai, 1995 ; . Like this signal for morphogenesis, the reinforcing signal for hemocyte infiltration may be delivered within the ducts or the crypts, a process that would require some system of signal transduction to the epithelial fields on the surface. However, the surge in hemocyte infiltration at 12 h also roughly coincident with the time of the first venting of 95% of the crypt contents at dawn Lee and Ruby, 1994; Boettcher et al., 1996 ; . Thus, it is also possible that this second signal for infiltration may be triggered by the ventate as it is expelled through the ducts and onto the surface, where PGN fragments can interact directly with receptors on the epithelium and stimulate these cells to release more chemotactic factor into the appendage sinuses. The onset of hemocyte infiltration into the light organ precedes all signs of symbiont-induced morphogenesis, including apoptosis, and the cell sloughing that represents the onset of epithelial regression. Similarly, studies of microbial and parasitic infections in molluscs often report hemocyte infiltration prior to other signs of tissue remodeling Mackin, 1951; Farley, 1968; Lauckner, 1983; Villalba et al., 1997; Lee et al., 2001 ; . In these studies, the hemocytes appear to take an active role in the destruction of the basement membrane, cell sloughing, histolysis, or atrophy associated with pathogenic tissue remodeling. Likewise, several studies have documented the infiltration of hemocytes prior to, or concurrent with, signs of developmental morphogenesis in insects Nardi and Miklasz, 1989; Rheuben, 1992; Kiger et al., 2001; Nardi et al., 2001 ; . In these cases, the hemocytes participate in the destruction of the extracellular matrix in target tissues during metamorphosis-associated remodeling. Blood cell infiltration can also be a late-stage event during both vertebrate and invertebrate larval metamorphosis Weber, 1964; Whitten, 1964; Scharrer, 1966; Crossley, 1968; Kinoshita et al., 1985 ; . In these instances the blood cells participate as phagocytes that take up and dispose of the apoptotic cells and debris that are the remnants of previously degraded larval tissues. In the morphogenic squid light organ, previous work has described the symbiont-induced apoptosis of cells of the epithelial fields; however, we have found no evidence that these cells are removed by phagocytosis Foster and McFall-Ngai, 1998 ; . Although hemocyte infiltration is not necessary for the induction of the early signs of light organ morphogenesis, it is possible that the basal population of hemocytes in the nascent epithelial fields can participate in these early morphogenic events. Additionally, a timely infiltration of hemocytes correlates with a more advanced stage of regression in wild-type V. fischeri-colonized organs Fig. 4 thus hemocytes apparently facilitate the regression process. To determine whether these phagocytic cells are indeed required for organ morphogenesis, they might be eliminated using phagocyte-specific toxins such as phenylalanine and herceptin.

Side effects of Hemocyte

When Ruditapes philippinarum was challenged with the bacterium, the number o circulating hemocytes inf creased significantly p 0.01 ; between 0 and 3 d Fig. 1A. B ; . In the long-term experiment, the hemocyte density remained constant after the third day at high values 4000 vs 2800 cells at Day 0 ; . From 1 d to wk, all the values obtained after challenge with the bacterium were significantly greater p 0.01 ; than those observed for clams who received a seawater inoculum. At 1 d, these control clams showed a slight decrease in hemocyte density which was not observed later. This initial decrease in circulating hemocytes at.

Hemocyte drug

Implementation date remains the same. For other providers who bill Medicare carriers, fiscal intermediaries, including Regional Home Health Intermediaries, and or Part A B Medicare Administrative Contractors A B MAC ; , the implementation date is now April 7, 2008. The CR transmittal date, number, and Web address for accessing CR5452 were also changed. All other information remains the same and hms. Gels are not completely immersed. Keratin contamination from skin in the samples. It is a laboratory device intended for the analysis of elements having atomic numbers higher than 16 in solid, liquid and powdered samples. The principle of operation is based on the low resolution of X-ray fluorescence and its block diagram is and humalog.
Staining kit specific for V. cholerae O1 New Horizons Diagnostics Corporation, Columbia, Md. detection of MSHA activity was performed by using chicken erythrocytes as described previously 25 ; . Escherichia coli MG1655 CGSC6300 ; 15 ; carrying type 1 fimbriae and the unfimbriated derivative AAEC072 fim 2 ; were also used. The presence of type 1 fimbriae in MG1655 was confirmed by both bacterial ability to cause D-mannose-sensitive agglutination of yeast cells Saccharomyces cerevisiae ; 14 ; and electron microscopy analysis of negatively stained bacterial preparations 12 ; . All cultures were grown in Luria-Bertani LB ; broth or agar 27 ; under static conditions at 37C. To radiolabel bacteria, strains were grown overnight in LB broth containing 10 Ci of [methyl-3H]thymidine 25 Ci mmol ; ml 1. Cells were then harvested by centrifugation 3, 000 g for 15 min at 4C ; , washed three times with phosphate-buffered saline PBS; 0.1 M KH2PO4, 0.1 M Na2HPO4, 0.15 M NaCl, pH 7.2 to 7.4 ; , and resuspended in PBS at an A650 of 1 2 109 to 4 109 CFU ml 1 ; . The number of counts per minute cpm ; per milliliter and the number of CFU per milliliter were evaluated to calculate the efficiency of cell labeling number of CFU per cpm ; that varied in different bacterial preparations from 150 to 300. Artificial seawater ASW ; prepared following the methods of La Roche et al. 22 ; , 35 wt vol ; salinity, pH 7.9, and filtered onto 0.22- m-pore-size Millipore filters Bedford, Mass. ; was used throughout the experiments. Mussels M. galloprovincialis Lam ; were obtained from the depuration plant Casa del Pescatore Cattolica, Italy ; during the spring of 2002. Average monthly temperature and salinity at the collection site were 15C and 35, respectively. Mussels were transferred to the laboratory, gently scrubbed to remove epibiota, moistened with 100% ethanol to sterilize the surface, and kept in an aquarium at 16C in static tanks containing ASW 1 liter animal ; for 1 to 3 days before use; seawater was changed daily. Hemolymph extraction, preparation of hemolymph serum i.e., hemolymph free of cells ; , determination of hemocyte concentration, and preparation of hemocyte monolayers on coverslips were as previously described 4, 5 ; . Bacterial adherence to and association with hemocytes were evaluated as previously described 4 ; . Briefly, aliquots 1.5 ml ; of either ASW or hemolymph serum containing radiolabeled bacteria at the final concentration of about 107 CFU ml 1 were added to monolayers on coverslips contained in plastic culture dishes hemocytes bacteria ratio, about 1: 10 the dishes were then incubated with gentle shaking at either 18C to evaluate all associated bacteria, i.e., attached plus internalized ; or 4C to evaluate attached bacteria only ; . Bacterial binding to hemocytes was also evaluated at 18C after 30 min of treatment of hemocyte monolayers with cytochalasin D CD ; at final concentration of 5 g Triplicate preparations were made for each sample. After 120 min of incubation the coverslips were rinsed three times with 3 ml of cold ASW to remove nonadherent bacteria and were transferred to PICO-FLUOR15 scintillation fluid Packard Instruments Company Inc., Meriden, Conn. ; . The number of cpm per coverslip was evaluated by using a Beckman L5 1801 scintillation counter. For each sample the number of bacteria per monolayer was calculated by multiplying the cpm values by the efficiency of cell. Time to Postoperative Angiogram Greater than . Years ; 5 4 3 Number of Angiograms 25 47 72 Angiograms in the Specific Yearly Interval 22 25 22 and humira. The only monthly journal devoted solely to thje specialty. The aim of the Journal is the prompt pubhcation of ongmal articles which advance knowledge m all branches of anaesthesiology, particularly those winch describe progress in ongmal research and the results of recent chnipal investigations Annual Subscription; post free. To be obtained from any bookseller or subscription agency or direct from the Publishers. JOHN SHERRATT & SON, Park R o a England and hemocyte. Appl Environ Microbiol 1996 Jul; 62 7 ; : 2540-6 Production of a polyhydroxyalkanoate biopolymer in insect cells with a Published erratum appears in Appl Environ modified eucaryotic fatty acid synthase. Microbiol 1998 Jan; 64 1 ; : 383 and hyaluronan. Mol ; for the hemocyte counting with a hemocytometer, 0.1 ml for the LR assay and 0.2 ml for the phagocytosis assay. The operation was repeated for the 4 mussels contained in each bag and hemolymph was then pooled for a total of 5 pools of 4 individuals each per aquarium and each sampling day. Lysosome retention LR ; : LR was evaluated by using neutral red dye following the technique described by Lowe & Pipe 1994 ; . Aliquots of 100 l pooled hemolymph were added to 200 l 2% neutral red dye in TBS, in a sterile centrifuge tube, and incubated at room temperature for 5 h. The cells were then washed with TBS, fixed 2% glutaraldehyde in TBS, and centrifuged at 800 g for 10 min. The fixative solution was then removed with a Pasteur pipette, 1 ml of TBS was added and the preparation was stored cold in the dark. Prior to the readings, TBS was removed and 1 ml extraction solution consisting of 1% v v ; acetic acid plus 50% v v ; ethanol in distilled water was added for 30 min Grundy et al. 1996 ; . Neutral red retained by the hemocytes was displaced by the addition of the extraction solution and measured at 540 nm on a PerkinElmer spectrophotometer, calibrated with the extraction solution. Data reported are optical densities and were standardized to 106 cells. Membrane injury MI ; : Quantification of MI to hemocytes was carried out with a nigrosine dye test. The dark blue dye enhances the contrast of the outer cell membrane and enables detection of abnormal cell shape. Pooled hemolymph 100 l ; was placed in a clean well, overlaid with an equal volume of 0.2% nigrosine in TBS and incubated at room temperature for 1 to 5 min. The percentage of damaged cells was calculated from 150 cells examined under a phase contrast microscope at 40 magnification. Phagocytic activity PA ; and hemocyte count HC ; : The fluorescent dye, fluorescein-isothiocyanate FITC ; suspended in TBS solution, was added to the yeast zymosan type 1 in excess, and incubated for 2 h at room temperature with periodic mixing. The labeled yeast were then washed repeatedly with TBS until the supernatant contained no yellow fluorescence. Subsamples of 1 ml were then frozen at 20C until used. Densities of the labeled yeast were ascertained in all samples with a fluorescence microscope and ranged from 4 to 5 107 ml1. Hemocyte numbers in 0.4 ml hemolymph, pooled from mussels at 0.1 ml each and adjusted to 1 ml, were determined using an Improved Neubauer hematocytometer. Fluorescent yeast were then added to the hemocyte solution in a 100: 1 density ratio and left to incubate at room temperature in the dark for 5 h, after which they were evaluated for PA. To prevent dehydration of samples, 0.5 ml of a 4% Bovine Serum Albumin BSA ; solution diluted in RPMI 1640 Sigma ; was.

An affecting history of the captivity & sufferings of Mrs. Mary Velnet, an Italian lady, who was seven years a slave in Tripoli. Boston, W. Crary. [1804?] Wright bibliography number 7A. Reel: Sup 1 An affecting narrative of the captivity and sufferings of Thomas Nicholson [a native of New Jersey]. Who has been six years a prisoner among the Algerines, and from whom he fortunately made his escape a few months previous to Commodore Decatur's late expedition against the Barbary powers. Boston, Printed for G. Walker. [1816?] Wright bibliography number 7C. Reel: Sup 1 Afloat and ashore: or, A sailor's life. Boston, F. Gleason. 1848 Wright bibliography number 7G. Reel: Sup 1 Arthur, Timothy Shay. Alice Melville; or, The indiscretion. Philadelphia, H.F. Anners. [c1850] Wright bibliography number 53A. Reel: Sup 1 Arthur, Timothy Shay. Lucy Sandford. Philadelphia, T.B. Peterson. [n.d.] Wright bibliography number 108A. Reel: Sup 1 Arthur, Timothy Shay. Madeline, or A daughter's love, and other tales. Philadelphia, H.F. Anners. [c1843] Wright bibliography number 108B. Reel: Sup 1 Arthur, Timothy Shay. Our children: how shall we have them?.Also, Keeping it up, and The problem, by James Nack. The prairie fire, a poem, by J. Pierpont and a number of temperance anecdotes. New York, Oliver & Bro. 1849 Wright bibliography number 133A. Reel: Sup 1 Arthur, Timothy Shay. The ruined gamester; or, Two eras in my life. Philadelphia, H.F. Anners. 1844 Wright bibliography number 151A. Reel: Sup 1 Arthur, Timothy Shay. Sketches of life and character. Phladelphia, J.W. Bradley. 1849 Wright bibliography number 161A. Reel: Sup 1 Arthur, Timothy Shay. Tales of married life. Philadelphia, H.F. Anners. 1850 Wright bibliography number 171A. Reel: Sup 1 Bacon, Josephine Dodge Daskam ; . When Binks came. The memoirs of a baby. New York, Grosset & Dunlap. 1904 Wright bibliography number 5 Sup. Reel: Sup 1 Bonesteel, Mary Greene. The young color guard; or, Tommy Collins at Santiago. New York, Benziger Brothers. c1902 Wright bibliography number 8 Sup. Reel: Sup 1 Brainerd, Eleanor Hoyt. Concerning Belinda. New York, Doubleday, Page. 1905 Wright bibliography number 9 Sup. Reel: Sup 1 Brewster, Frances Stanton. When mother was a little girl. Philadelphia, G.W. Jacobs. c1901 Wright bibliography number 10 Sup. Reel: Sup 1 Connolly, James Brendan. Jeb Hutton. The story of a Georgia boy. New York, C. Scribner's Sons. 1902 Wright bibliography number 11 Sup. Reel: Sup 1 Arthur, Timothy Shay. The widow Morrison; a leaf from the book of human life. Baltimore, Knight & Colburn. 1841 Wright bibliography number 184A. Reel: Sup 2 Ashland, Aria. Dark Sybil: or, The fortunes of the Catherwoods. Boston, F. Gleason. 1848 Wright bibliography number 192A. Reel: Sup 2 Asmodeus [pseud.]. The Jenny Lind mania in Boston; or, a sequel to Barnum's Parnassus. Boston. 1850 Wright bibliography number 193A. Reel: Sup 2 Ayer, I.W. The Hungarian refugee; or, The bold Magyar. Boston, Star Spangled Banner Office. [c1850] Wright bibliography number 214A. Reel: Sup 2 and hydralazine.

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