From owner-contents@net.bio.net Wed Oct 27 19:03:00 1999
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Subject: Diseases of Aquatic Organisms, vol. 38, no. 01, 11 October 1999
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CC Inter-Research Science Publisher
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CC Diseases of Aquatic Organisms Volume 38, Number 1, table of contents
CC -------------------------------------------------------------------
CC Abstracts from Inter-Research journals, along with a searchable
CC index, are available on the Internet (http://www.int-res.com).
CC Contents are also sent to a mailing list (contents@int-res.com).

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CC Copyright Inter-Research, Oldendorf/Luhe, 1999
CC -------------------------------------------------------------------
CC -------------------------------------------------------------------
CC Diseases of Aquatic Organisms (ISSN 0177-5103)
CC Volume 38, Number 1 (1999)
CC October 11
CC -------------------------------------------------------------------


CC RESEARCH ARTICLES
AU Sukhumsirichart-W.  Wongteerasupaya-C.  Boonsaeng-V.  Panyim-S.
   Sriurairatana-S.  Withyachumnarnkul-B.  Flegel-T-W.
TI Characterization and PCR detection of hepatopancreatic parvovirus (HPV)
   from Penaeus monodon in Thailand.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:1-10.

AU Harris-L-J.  Owens-L.
TI Production of exotoxins by two luminous Vibrio harveyi strains known to
   be primary pathogens of Penaeus monodon larvae.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:11-22.

AU Senson-P-R.  Stevenson-R-M-W.
TI Production of the 57 kDa major surface antigen by a non-agglutinating
   strain of the fish pathogen Renibacterium salmoninarum.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:23-31.

AU Dykova-I.  Figueras-A.  Novoa-B.
TI Epizoic amoebae from the gills of turbot Scophthalmus maximus.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:33-38.

AU Lom-J.  Dykova-I.  Tonguthai-K.
TI Kabataia gen. n., a new genus proposed for Microsporidium spp.
   infecting trunk muscles of fishes.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:39-46.

AU Sangmaneedet-S.  Smith-S-A.
TI Efficacy of various chemotherapeutic agents on the growth of
   Spironucleus vortens, an intestinal parasite of the freshwater
   angelfish.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:47-52.

CC REVIEW
AU Van-Bressem-M-F.  Van-Waerebeek-K.  Raga-J-A.
TI A review of virus infections of cetaceans and the potential impact of
   morbilliviruses, poxviruses and papillomaviruses on host population
   dynamics.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:53-65.

CC NOTES
AU Otta-S-K.  Shubha-G.  Joseph-B,Chakraborty-A.  Karunasagar-I.
   Karunasagar-I.
TI Polymerase chain reaction (PCR) detection of white spot syndrome virus
   (WSSV) in cultured and wild crustaceans in India.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:67-70.

AU Nagelkerken-I.  Smith-G-W.  Snelders-E.  Karel-M.  James-S.
TI Sea urchin Meoma ventricosa die-off in Curacao (Netherlands Antilles)
   associated with a pathogenic bacterium.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:71-74.

AU McKibben-C-L.  Pascho-R-J.
TI Shedding of Renibacterium salmoninarum by infected chinook salmon
   Oncorhynchus tschawytscha.
SO Dis-Aquat-Org.  1999 Oct 11.  38(1).  P DAO 38:75-79.


From owner-contents@net.bio.net Wed Oct 27 19:06:00 1999
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From: BIOSCI Administrator <biosci-help@net.bio.net>
Newsgroups: bionet.journals.contents
Subject: Aquatic Microbial Ecology, vol. 19, no. 03, 27 October 1999
Date: 27 Oct 1999 13:06:54 -0700
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CC Aquatic Microbial Ecology Volume 19, Number 3, table of contents
CC -------------------------------------------------------------------
CC Abstracts from Inter-Research journals, along with a searchable
CC index, are available on the Internet (http://www.int-res.com).
CC Contents are also sent to a mailing list (contents@int-res.com).

CC Inter-Research, Nordbuente 23, D-21385 Oldendorf/Luhe, Germany
CC Tel: (+49)(0) 4132 7127
CC Fax: (+49)(0) 4132 8883
CC E-mail: ir@int-res.com

CC Copyright Inter-Research, Oldendorf/Luhe, 1999
CC -------------------------------------------------------------------
CC -------------------------------------------------------------------
CC Aquatic Microbial Ecology (ISSN 0948-3055)
CC Volume 19, Number 3 (1999)
CC October 27
CC -------------------------------------------------------------------


CC RESEARCH ARTICLES
AU Guixa-Boixereu-N.  Vaque-D.  Gasol-J-M.  Pedros-Alio-C-P.
TI Distribution of viruses and their potential effect on bacterioplankton
   in an oligotrophic marine system.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 205-213.

AU Ducklow-H.  Carlson-C.  Smith-W.
TI Bacterial growth in experimental plankton assemblages and seawater
   cultures from the Phaeocystis antarctica bloom in the Ross Sea,
   Antarctica.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 215-227.

AU Carlson-C-A.  Bates-N-R.  Ducklow-H-W.  Hansell-D-A.
TI Estimation of bacterial respiration and growth efficiency in the Ross
   Sea, Antarctica.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 229-244.

AU Reitner-B.  Herzig-A.  Herndl-G-J.
TI Dynamics in bacterioplankton production in a shallow, temperate lake
   (Lake Neusiedl, Austria): evidence for dependence on macrophyte
   production rather than on phytoplankton.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 245-254.

AU Lebaron-P.  Servais-P.  Troussellier-M.  Courties-C.  Vives-Rego-J.
   Muyzer-G.  Bernard-L.  Guindulain-T.  Schaefer-H.  Stackebrandt-E.
TI Changes in bacterial community structure in seawater mesocosms
   differing in their nutrient status.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 255-267.

AU Wulff-A.  Nilsson-C.  Sundbaeck-K.  Waengberg-S-A.  Odmark-S.
TI UV radiation effects on microbenthos-a four month field experiment.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 269-278.

AU Newbold-R-W.  Jensen-P-R.  Fenical-W.  Pawlik-J-R.
TI Antimicrobial activity of Caribbean sponge extracts.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 279-284.

AU Chung-W-K.  King-G-M.
TI Biogeochemical transformations and potential polyaromatic hydrocarbon
   degradation in macrofaunal burrow sediments.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 285-295.

AU Battin-T-J.  Butturini-A.  Sabater-F.
TI Immobilization and metabolism of dissolved organic carbon by natural
   sediment biofilms in a Mediterranean and temperate stream.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 297-305.

CC NOTE
AU Cantin-G.  Levasseur-M.  Schultes-S.  Michaud-S.
TI Dimethylsulfide (DMS) production by size-fractionated particles in the
   Labrador Sea.
SO Aquat-Microb-Ecol.  1999 Oct 27.  19(3).  P 307-312.

From owner-contents@net.bio.net Wed Oct 27 19:11:00 1999
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From: BIOSCI Administrator <biosci-help@net.bio.net>
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Subject: Biotecnologia Aplicada, vol. 16, no. 04, 1999
Date: 27 Oct 1999 13:11:10 -0700
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CC BIOTECNOLOGIA APLICADA
CC Vol. 16 No. 4 (October-December, 1999)
CC ISSN 0864-4551 (printed)
CC ISSN 1027-2852 (electronic)
CC Copyright 1999, Elfos Scientiae.

CC Founded in 1983 and published as Interferon y
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CC Correspondence and subscriptions
CC Ave. 31 entre 158 y 190,
CC Cubanacan, Playa
CC Ciudad de La Habana,
CC Apdo. 6072, Habana 6, Cuba.
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CC Full papers are available online through BIOLINE System
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CC tion or single document purchase are possible. Contact
CC the following for further information:
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CC E-mail address: bio@biostrat.demon.co.uk

AU Rosa A Serra, Maureen McDonnell, April Bragg
IN Department of Molecular and Cellular Physiology.
   University of Cincinnati School of Medicine.
   Cincinnati, OH 45267, USA. E-mail: serrar@email.uc.edu
   Department of Cell Biology,
   Vanderbilt University Medical Center.
   Nashville, TN, USA 37232.
TI Transforming Growth Factor-beta in Development
   and Disease
DE BMP
DE differentiation
DE mechanism of action
DE signaling
DE Smad
DE TGF
SO Biotecnologia Aplicada 1999;16:205-218
AB The transforming growth factor-beta (TGF-beta)
   superfamily consists of multifunctional
   peptides that control many aspects of cell
   growth and differentiation. Because of the
   multifunctional nature of the TGF-betas, an
   understanding of the mechanism of TGF-beta
   action should provide significant information
   regarding the pathogenesis of many diseases.
   This review will focus on the role and
   mechanisms of TGF-beta signaling in the mammary
   gland, skin, lung, and skeleton and will
   discuss how alterations in TGF-beta signaling
   may result in disease.
CC Review article
CC Language: English

AU Nieves Santos, Jorge Aguiar, Julio Fernandez,
   Maria Vazquez, George Auburger, Suzana Gispert,
   Yssel Mendoza, Julia Garcia, Luis Velazquez
IN Department of Neurology. Lenin Hospital. Holguin, Cuba.
   Department of Pharmaceutics.
   Center for Genetic Engineering and Biotechnology.
   PO Box 6162, Havana 10600, Cuba.
   Phone (53-7) 21 8008; 336008; E-mail: jaguiar@cigb.edu.cu
   Department of Neurology. University Hospital.
   Düsseldorf, Germany.
TI Molecular diagnosis of a sample of the Cuban population
   with spinocerebellar ataxia type 2
DE CAG repeat expansions
DE disease
DE spinocerebellar ataxia 2
SO Biotecnologia Aplicada 1999;16:219-221
AB CAG repeat unstable expansions causing spinocerebellar
   ataxia 2 (SCA2) disease were localized into a CpG island
   on the exon 1 of the SCA2 gene, previously linked to the
   chromosomic region 12q23-24.1 of human chromosome 12. At
   molecular level, 392 patients with dominant ataxia from
   Holguin, Cuba, were analyzed, showing an inverse
   correlation between CAG repeat length and the age of
   disease onset. The smallest CAG repeat expansion causing
   neurodegeneration among the SCA2 patients was also found.
   For SCA2 patients with (CAG)n stretches of 32 to 40
   repeats, there is a high variability with respect to the
   age of disease manifestation. These findings suggest that
   for each patient other specific genetic and/or
   environmental factors are very significant for the
   begining and evolution of the disease for small sizes of
   CAG repeat expansions.
CC Research Article
CC Language: Spanish

AU Angel Valdivia, Danay Chacon, Clara Savon, Odalys Valdes,
   Grehete Gonzalez, Reynel Cancio, Julio C Sanchez,
   German Roges, Blanca Garcia-Barreno, Jose A Melero,
   Angel Goyenechea
IN Deparment of Virology. Institute of Tropical Medicine
   "Pedro Kouri". PO Box 601, Marianao 13, Havana, Cuba.
   Fax: (53-7) 24 6051, 22 0633;
   E-mail: a.valdivia@ipk.sld.cu
   Center for Genetic Engineering and Biotechnology.
   PO Box 6162. Havana 6, Cuba.
   National Center of Fundamental Biology, Majadahonda 28220
   Madrid, Spain.
TI Confirmation of Unusual Epidemiological Behavior of the
   Human Respiratory Syncytial Virus During Two Consecutive
   Epidemics (Seasons 94/95 and 95/96) in Havana City, Cuba
DE HRSV
DE molecular epidemiology
DE respiratory syncytial virus
SO Biotecnologia Aplicada 1999;16:222-225
AB Twenty-seven strains of the human respiratory syncytial
   virus, isolated from three consecutive outbreaks, were
   sequenced at the National Center of Fundamental Biology
   (Madrid, Spain). The nucleotide sequence showed two
   unique characteristics related to what had been
   previously reported in the literature: (i) all of them
   were identical, and (ii) all showed a great homology with
   the Spanish Long reference strain (with only five
   changes). Upon this unusual finding and with the main
   objective of excluding a probable contamination with
   another Long strain from Sweden, selected regions of both
   reference strains and other laboratory strains were
   sequenced. The Spanish Long strain was only used as a
   confirmatory control of the results obtained in
   laboratories from Spain. The results obtained by the
   authors discarded any possible contamination when the
   percentages of homology between the sequenced regions of
   the two foreign strains and the Cuban isolates were
   analyzed and compared. The results also corroborated that
   the Swedish Long strain was even more separated from the
   Cuban isolates than the Spanish strain. This report
   presents a theory to explain the unusual epidemiological
   behavior of this virus in Cuba.
CC Research article
CC Language: English

AU Santiago Dueñas-Carrera, Juan Morales,
   Nelson Acosta-Rivero, Lazaro J Lorenzo, Ciro Garcia,
   Thelvia Ramos, Ivis Guerra, Maxlenin Peña
IN Centro de Ingenieria Genetica y Biotecnologia.
   AP 6162, CP 10600, Habana, Cuba. Fax: (53-7) 214764;
   E-mail: juan.morales@cigb.edu.cu
TI Variable Level Expression of Hepatitis C Virus Core
   Protein in a Prokaryotic System. Analysis of the Humoral
   Response against It in Rabbits
DE E. coli
DE expression
DE HCV
DE hepatitis C virus
DE immunogenicity
DE nucleocapsid core protein
DE purification
SO Biotecnologia Aplicada 1999;16:226-231
AB Experimental evidence suggests that the hepatitis C virus
   (HCV) core protein has several biological properties and
   is implicated as a viral factor in HCV-mediated
   pathogenesis. In this study, CoE1.339, Co.176 and Co.120
   variants of the HCV capsid protein were produced at
   variable levels in Escherichia coli from pNCoE1, pN12 and
   pSLCo120 plasmids, respectively. The chimera CoE1.339
   spans the first 339 amino acids of the viral polyprotein,
   fused to the 45 amino acids stabilizer peptide from P64K
   protein of Neisseria meningitidis. Co.176 is a non-fused
   variant encompassing amino acids 1-176 of the capsid
   protein sequence. Both CoE1.339 and Co.176 were expressed
   under the transcriptional control of the tryptophan
   promoter and the protein was only detected by Western
   blot. However, Co.120, a variant truncated at the C
   terminus which contains amino acids 1-120 of the HCV core
   protein fused to a leader tag of six histidines, was
   successfully produced under the control of the T7
   promoter in BL21 (DE3) cells. Like Co.176 and CoE1.339,
   Co.120 was efficiently recognized by human anti-HCV
   positive serum. Purified Co.120 antigen showed to be
   immunogenic in rabbits. Synthetic peptides covering amino
   acids 1-40 of the core protein showed the greatest
   reactivity to the rabbit anti-Co.120 serum.
CC Research Article
CC Language: English

AU Diana Garcia del Barco, Alina Rodriguez, Elsa Rodriguez,
   Caridad Tamayo, Julio R Fernandez, Maria M Vasquez,
   Maria P Rodriguez, Ricardo Lleonart
IN Division de Genetica de Celulas de Mamiferos.
   Centro de Ingenieria Genetica y Biotecnologia.
   AP 6162, CP 10600, La Habana, Cuba. Telf: (53-7) 21 8164;
   Fax: (53-7) 33 6008; E-mail: diana.garcia@cigb.edu.cu
TI Erythropoietin gene co-amplification in
   methotrexate-resistant Chinese hamster ovary dhfr- cells.
DE CHO
DE EPO
DE erythropoietin
DE gene amplification
SO Biotecnologia Aplicada 1999;16:232-235
AB Gene amplification plays an important role in cellular
   regulatory mechanisms. To study the amplification and
   expression of the human erythropoietin (EPO) gene,
   Chinese hamster ovary (CHO) dhfr- cells co-transfected
   with chimeric genes for the expression of EPO and
   dihydrofolate reductase (DHFR) and selected in the
   presence of increasing concentrations of methotrexate,
   were used. The results evidenced a three-fold gene
   amplification, accompanied by an increase in EPO
   expression of up to 33 pg/cell/day. The amplicon, which
   contains host genomic sequences, shows rearrangements
   originated during the integration-amplification process
CC Research Article
CC Language: Spanish

AU Lisset Herrera, Orlene Guerra, Pedro L Ramos,
   Rudy Peral, Ana L Echemendia, Nadia Ramirez,
   Vivian Doreste, Pedro Oramas
IN Laboratory of Biochemistry. Bioplant Center.
   University of Ciego de Avila. Carretera a Moron Km 9,5.
   CP 69450. Ciego de Avila, Cuba.
   Plant Biotechnology Division.
   Center for Genetic Engineering and Biotechnology.
   PO Box 6162, Havana, Cuba. Fax: (53-7) 21 8070;
   E-mail: Pedro.Oramas@cigb.edu.cu
   Instituto de Sanidad Vegetal.
   Playa, Ciudad de La Habana, Cuba.
TI Molecular Techniques for the Detection of Tomato Yellow
   Leaf Curl Geminivirus in Infected Plants and Viruliferous
   Whiteflies
DE Dot blot
DE geminiviruses
DE PCR
DE TYLCV
DE virus diagnosis
SO Biotecnologia Aplicada 1999;16:237-241
AB The tomato yellow leaf curl virus (TYLCV) causes major
   yield losses in tomato production in many tropical and
   subtropical regions. Therefore, there is an increased
   need to apply molecular methods for the detection and
   characterization of the main TYLCV isolates that affect
   Cuban tomato plantations. A DNA fragment containing the
   gene encoding the coat protein of a Cuban TYLCV isolate
   was amplified by polymerase chain reaction (PCR). DNA
   hybridization with specific radiolabeled probes
   corroborated the identity of the amplified product, and
   allowed to analyze the integration into a full-length
   TYLCV genome. The threshold of TYLCV detection by PCR in
   plants and viruliferous whiteflies was within the
   reported range. To detect TYLCV infections, samples
   collected from tomato plantations of several regions in
   Cuba were analyzed by PCR. The amplified coat protein
   gene was also effectively used as a DNA probe in Dot blot
   assays to detect geminivirus in plants
CC Paper on Techniques
CC Language: English

AU Guillermo Pratta, Roxana Zorzoli, Liliana A Picardi
IN Catedra de Genetica. Facultad de Ciencias Agrarias.
   Universidad Nacional de Rosario. CC 14, 2123 Zavalla,
   Argentina. Telf: (54-0341) 497 0080;
   Fax: (54-0341) 497 0085; E-mail: gpratta@fcagr.unr.edu.ar
TI Obtainment and micropropagation of intra- and
   interspecific hybrids of tomato (genus lycopersicon)
DE embryo rescue
DE in vitro plant tissue culture
DE plant breeding
DE plant genetic resources
SO Biotecnologia Aplicada 1999;16:242-245
AB In vitro plant tissue culture is a useful tool for
   overcoming the problems in obtaining hybrids (i.e.,
   embryo abortion,  production of seeds) when wild species
   are incorporated to breeding programs. The ability for
   producing intra- and interspecific hybrids among
   different crosses in the genus Lycopersicon, the adequacy
   of in vitro culture of immature embryos to break the
   unilateral incompatibility, and the micropropagation
   response of the hybrids obtained, were evaluated.
   Different genotypes of the species and varieties of L.
   esculentum, L. esculentum var. cerasiforme, L.
   pimpinellifolium, L. peruvianum, and L. hirsutum, were
   used. Differences in the ability to produce intra- and
   interspecific hybrids were found among the crosses. In
   vitro culture of immature embryos was successful in
   obtainintg interspecific hybrids when the crosses
   presented unilateral incompatibility. In this case, there
   also were differences in the ability to cross among the
   genotypes. The capacity for in vitro regeneration of the
   intra- and interspecific hybrids originated from
   compatible crosses was in general superior to that of the
   parental lines, but a decrease in the regeneration
   capacity was observed in the hybrids originated from
   incompatible crosses, with respect to the parental
   genotypes.
CC Paper on Techniques
CC Language: Spanish

AU Mauro Alfonso, Peter Ifversen, Jesper Zeuthen
IN Center of Molecular Immunology. PO Box 16040,
   Havana 11600, Cuba. E-mail: mauro@ict.cim.sld.cu
   Department of Tumor Cell Biology. Danish Cancer Society,
   DK-2100 Copenhagen, Denmark.
TI Human Anti-ganglioside IgG Antibody Response Induced
   by in vitro Immunization with Liposomes Containing 
   GM3(NeuGc) Ganglioside
DE ganglioside
DE human antibody
DE in vitro immunization
SO Biotecnologia Aplicada 1999;16:246-248
AB A new in vitro immunization system of human peripheral
   blood lymphocytes using liposomes containing
   gangliosides, is described. Purified human B lymphocytes
   were cultured in the CD40 system in the presence of
   liposomes containing different concentrations of
   GM3(NeuGc) ganglioside, ranging from 1 to 1000 ng/mL.
   After an initial primary in vitro immunization period (3
   4 days), antigen-stimulated B cells and autologous
   activated CD4+ T lymphocytes previously activated with an
   anti-CD3 monoclonal antibody were cultured in the
   presence of staphylococcal enterotoxin A. Human antibody
   production was measured by an anti-ganglioside ELISA
   after 4 and 8 days of culture. Specific antibody
   responses against GM3(NeuGc) of IgM and IgG isotypes were
   induced after 4 days in culture, and a predominant
   antigen-specific IgG antibody production was observed 8
   days after antigenic stimulation.
CC Article on Techniques
CC Language: Spanish

AU Gerardo Guillen
IN Centro de Ingenieria Genetica y Biotecnologia.
   Ave. 31 entre 158 y 190, Cubanacan, Playa. AP 6162,
   CP 10600, Cuba. Telf: (53-7) 21 6221;
   Fax: (53-7) 21 4764; E-mail: gerardo.guillen@cigb.edu.cu
TI XI Congreso Internacional de Virologia
SO Biotecnologia Aplicada 1999;16:249-252
CC Report
CC Language: Spanish

AU Gerardo Guillen
IN Centro de Ingenieria Genetica y Biotecnologia.
   Ave. 31 entre 158 y 190, Cubanacan, Playa. AP 6162,
   CP 10600, Cuba. Telf: (53-7) 21 6221;
   Fax: (53-7) 21 4764; E-mail: gerardo.guillen@cigb.edu.cu
TI IX Congreso Internacional de Bacteriologia y Micologia
SO Biotecnologia Aplicada 1999;16:253-255
CC Report
CC Language: Spanish

AU Maria L Genta, Hugo D Genta
IN Laboratorio de Tecnologia de Alimentos,
   Facultad de Bioquimica, Quimica y Farmacia.
   Instituto de Ingenieria Quimica.
   Facultad de Ciencias Exactas y Tecnologia.
   Universidad Nacional de Tucuman.
   Ave. Independencia 1800, 4000 San Miguel de Tucuman,
   Argentina. Telf: (54-381) 436 4093 (Interno 222);
   Fax: (54-381) 436 3004;
   E-mail: nalvarez@herrera.unt.edu.ar
TI La bioindustria en Japon
SO Biotecnologia Aplicada 1999;16:257-260
CC Focus
CC Language: Spanish

AU Jorge Bacallao, Josefina Lugo
IN Dpto. Computacion y Biometria.
   Instituto Superior de Ciencias Medicas.
   Calle 146 No. 3102, La Habana 11600, Cuba.
   E-mail: bacallao@comput.giron.sld.cu
   Dpto. Ensayos Clinicos.
   Instituto Nacional de Oncologia y Radiobiologia.
   Ciudad de La Habana, Cuba.
TI Use of prior Knowledge in Randomized Clinical Trials
   with a Binary Response Variable
DE beta-binomial distribution
DE binary response
DE clinical trials
DE non-Bayesian methods
SO Biotecnologia Aplicada 1999;16:261-263
AB When testing a new drug, the researcher faces the ethical
   and technical problem of incorporating the existing
   knowledge derived from previous trials, from a
   meta-analysis or simply from his subjective judgement.
   This paper proposes a non-Bayesian method based on the
   beta-binomial distribution, which can be used in the
   clinical trial of a drug or treatment when the response
   variable is dichotomous. The method consists in the
   modeling of the previous knowledge by means of the beta
   distribution in the assessment of both toxicity and
   efficacy, and a statistical test of efficacy, which
   depends on a parameter of the beta-binomial distribution.
CC Focus
CC Language: Spanish

