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Academic literature on the topic 'Is91'

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Published: 7 July 2024

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Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Journal articles on the topic "Is91":

1

Xu, De-Qi, John O. Cisar, Nicholas Ambulos, Donald H. Burr, and Dennis J. Kopecko. "Molecular Cloning and Characterization of Genes for Shigella sonnei Form I O Polysaccharide: Proposed Biosynthetic Pathway and Stable Expression in a Live Salmonella Vaccine Vector." Infection and Immunity 70, no. 8 (August 2002): 4414–23. http://dx.doi.org/10.1128/iai.70.8.4414-4423.2002.

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ABSTRACT The gene region for biosynthesis of Shigella sonnei form I O polysaccharide (O-Ps) and flanking sequences, totaling >18 kb, was characterized by deletion analysis to define a minimal construct for development of Salmonella-based live vaccine vector strains. Lipopolysaccharide (LPS) expression and DNA sequence studies of plasmid deletion derivatives indicated form I O-Ps expression from a 12.3-kb region containing a putative promoter and 10 contiguous open reading frames (ORFs), one of which is the transposase of IS630. A detailed biosynthetic pathway, consistent with the predicted functions of eight of the nine essential ORFs and the form I O-Ps structure, is proposed. Further sequencing identified partial IS elements (i.e., IS91 and IS630) and wzz upstream of the form I coding region and a fragment of aqpZ and additional full or partial IS elements (i.e., IS629, IS91, and IS911) downstream of this region. The stability of plasmid-based form I O-Ps expression was greater from low-copy vectors than from high-copy vectors and was enhanced by deletion of the downstream IS91 from plasmid inserts. Both core-linked (i.e., LPS) and non-core-linked (i.e., capsule-like) surface expression of form I O-Ps were detected by Western blotting and silver staining of polyacrylamide gel electrophoresis-separated Shigella and Escherichia coli extracts. However, salmonellae, which have a core that is chemically dissimilar to that of shigellae, expressed only non-core-linked surface-associated form I O-Ps. Finally, attenuated Salmonella enterica serovar Typhi live vaccine vector candidates, containing minimal-sized form I operon constructs, elicited immune protection in mice against virulent S. sonnei challenge, thereby supporting the promise of live, oral vaccines for the prevention of shigellosis.
2

Turner, Sally A., Shelley N. Luck, Harry Sakellaris, Kumar Rajakumar, and Ben Adler. "Nested Deletions of the SRL Pathogenicity Island ofShigella flexneri 2a." Journal of Bacteriology 183, no. 19 (October 1, 2001): 5535–43. http://dx.doi.org/10.1128/jb.183.19.5535-5543.2001.

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ABSTRACT In this study, we determined the boundaries of a 99-kb deletable element of Shigella flexneri 2a strain YSH6000. The element, designated the multiple-antibiotic resistance deletable element (MRDE), had recently been found to contain a 66-kb pathogenicity island (PAI)-like element (designated the SRL PAI) which carries the Shigella resistance locus (SRL), encoding resistance determinants to streptomycin, ampicillin, chloramphenicol, and tetracycline. The YSH6000 MRDE was found to be flanked by two identical IS91 elements present at the S. flexneri homologs of the Escherichia coli genesputA and mdoA on NotI fragment D. Sequence data from two YSH6000-derived MRDE deletants, YSH6000T and S2430, revealed that deletion of the MRDE occurred between the two flanking IS91 elements, resulting in a single IS91 element spanning the two original IS91 loci. Selection for the loss of tetracycline resistance confirmed that the MRDE deletion occurred reproducibly from the same chromosomal site and also showed that the SRL PAI and the SRL itself were capable of independent deletion from the chromosome, thus revealing a unique set of nested deletions. The excision frequency of the SRL PAI was estimated to be 10−5 per cell in the wild type, and mutation of a P4-like integrase gene (int) at the left end of the SRL PAI revealed that int mediates precise deletion of the PAI.
3

Schlör, Stefan, Sabine Riedl, Julia Blaß, and Joachim Reidl. "Genetic Rearrangements of the Regions Adjacent to Genes Encoding Heat-Labile Enterotoxins (eltAB) of EnterotoxigenicEscherichia coli Strains." Applied and Environmental Microbiology 66, no. 1 (January 1, 2000): 352–58. http://dx.doi.org/10.1128/aem.66.1.352-358.2000.

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ABSTRACT One of the most common bacterially mediated diarrheal infections is caused by enterotoxigenic Escherichia coli (ETEC) strains. ETEC-derived plasmids are responsible for the distribution of the genes encoding the main toxins, namely, the heat-labile and heat-stable enterotoxins. The origins and transfer modes (intra- or interplasmid) of the toxin-encoding genes have not been characterized in detail. In this study, we investigated the DNA regions located near the heat-labile enterotoxin-encoding genes (eltAB) of several clinical isolates. It was found that the eltAB region is flanked by conserved 236- and 280-bp regions, followed by highly variable DNA sequences which consist mainly of partial insertion sequence (IS) elements. Furthermore, we demonstrated that rearrangements of the eltAB region of one particular isolate, which harbors an IS91R sequence next toeltAB, could be produced by a recA-independent but IS91 sequence-dependent mechanism. Possible mechanisms of dissemination of IS element-associated enterotoxin-encoding genes are discussed.
4

del Pilar Garcillan-Barcia, M., Irantzu Bernales, M. Victoria Mendiola, and Fernando de la Cruz. "Single-stranded DNA intermediates in IS91 rolling-circle transposition." Molecular Microbiology 39, no. 2 (January 2001): 494–502. http://dx.doi.org/10.1046/j.1365-2958.2001.02261.x.

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5

Mendiola, M. V., I. Bernales, and F. de la Cruz. "Differential roles of the transposon termini in IS91 transposition." Proceedings of the National Academy of Sciences 91, no. 5 (March 1, 1994): 1922–26. http://dx.doi.org/10.1073/pnas.91.5.1922.

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6

Diaz-Aroca, E., M. V. Mendiola, J. C. Zabala, and F. de la Cruz. "Transposition of IS91 does not generate a target duplication." Journal of Bacteriology 169, no. 1 (1987): 442–43. http://dx.doi.org/10.1128/jb.169.1.442-443.1987.

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7

Schleinitz, Kathleen M., Tatiana Vallaeys, and Sabine Kleinsteuber. "Structural Characterization of ISCR8, ISCR22, and ISCR23, Subgroups of IS91-Like Insertion Elements." Antimicrobial Agents and Chemotherapy 54, no. 10 (July 12, 2010): 4321–28. http://dx.doi.org/10.1128/aac.00006-10.

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ABSTRACT Analysis of ISCR8 (ISPps1) revealed that this group of insertion elements has to be subdivided into three subgroups: ISCR8, ISCR22, and ISCR23. The distinction of three subgroups is supported by phylogenetic analysis of the transposase open reading frames (ORFs). Comparison of over 20 complete and partial ISCR8/22/23 elements identified oriIS candidate sequences for all groups and a terIS candidate sequence for ISCR8. The oriIS sequences, their distance to the transposase ORFs, and the sequence of this intervening region are group specific, further supporting the definition of two new ISCR elements. ISCR8/22/23 have a very broad host range, including Gram-positive and Gram-negative bacteria, among which are several (opportunistic) pathogens. The IS often resides on plasmids or in the vicinity of other mobile elements and is mostly associated with genes for the degradation of halo- or nitro-aromatics. However, in one case ISCR8 was found in the neighborhood of an antibiotic resistance determinant in Klebsiella pneumoniae. ISCR8 resembles other IS91 family elements in mediating genetic rearrangements by homologous recombination between two copies. In Delftia acidovorans this led to the loss of the genes encoding dichlorprop cleavage. In conclusion, this study shows that ISCR8 could be a fully functional and active member of the IS91 family of insertion elements.
8

Mendiola, M. V., Y. Jubete, and F. de la Cruz. "DNA sequence of IS91 and identification of the transposase gene." Journal of Bacteriology 174, no. 4 (1992): 1345–51. http://dx.doi.org/10.1128/jb.174.4.1345-1351.1992.

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Garcillán-Barcia, M. Pilar, and Fernando Cruz. "Distribution of IS91 family insertion sequences in bacterial genomes: evolutionary implications." FEMS Microbiology Ecology 42, no. 2 (November 2002): 303–13. http://dx.doi.org/10.1111/j.1574-6941.2002.tb01020.x.

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GARCILLANBARCIA, M. "Distribution of IS91 family insertion sequences in bacterial genomes: evolutionary implications." FEMS Microbiology Ecology 42, no. 2 (November 2002): 303–13. http://dx.doi.org/10.1016/s0168-6496(02)00340-9.

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Journal articles Dissertations / Theses Books

Dissertations / Theses on the topic "Is91":

1

Fauconnier, Aurélien. "Étude des modalités de transposition des séquences d'insertion bactériennes des familles IS91-ISCR." Electronic Thesis or Diss., Limoges, 2023. http://www.theses.fr/2023LIMO0101.

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Les éléments de la famille IS91/ISCR constituent une famille hautement associée à des gènes de virulence et de résistance aux antibiotiques. Cette famille d'IS atypique code une transposase HUH médiant les évènements de transposition en utilisant un mécanisme de transposition en cercle roulant. Contrairement aux autres membres de la famille, IS91 contient un petit ORF codant potentiellement pour un polypeptide de 121 acides aminés, Orf121, en amont du gène de la transposase, tnpA. La première partie de ce travail a consisté à une étude in silico de deux éléments de la famille IS91, IS91 et IS1294b présentent des séquences conservées au niveau de la transposase et des régions terIS et oriIS. La deuxième partie du travail a été expérimentale concernant la régulation et l’efficacité de la transposition. Nous avons montré que i) la transcription du gène tnpA provient principalement du promoteur Porf121 et que la transcription des deux gènes est couplée, ii) l'expression de la protéine Orf121 en cis ou en trans a un effet inhibiteur sur la transposition in vivo de IS91, iii) Orf121 est nécessaire à la reconnaissance et au clivage précis de l'extrémité terIS91 pour limiter la mobilisation de l’ADN adjacent. En ce qui concerne la transposition de IS91, nous avons montré que seuls les intermédiaires circulaires ADN simple brin peuvent être insérés dans une nouvelle séquence cible et avons identifié deux doigts de zinc essentiels pour l’activité de la transposition, appelés ZF1 impliquant les cystéines 41, 68, 73, 76 et ZF2 impliquant les cystéines, 53, 58, 360 et 363. Enfin, nous avons démontré que les transposases des éléments de la famille IS91 (IS91, ISKnp22) et de la famille ISCR (ISCR1) sont capables de se mobiliser et de reconnaitre et cliver l’extrémité oriIS de IS91, ISCR1 et ISCR2 et l’extrémité terIS de IS91 et ISCR2
The IS91/ISCR family is highly associated with virulence and antibiotic resistance genes. This atypical IS family encodes a HUH transposase mediating transposition events using a rolling circle transposition mechanism. Unlike the other members of the family, IS91 contains a small ORF potentially encoding a 121 amino acid polypeptide, Orf121, upstream of the transposase gene, tnpA. The first part of this work consisted of an in silico study of two members of the IS91 family, IS91 and IS1294b, that have conserved sequences of the transposase and terIS and oriIS regions. The second part of this work was experimental and focused on the transposition efficiency and regulation. We have shown that i) transcription of the tnpA gene originates mainly from the Porf121 promoter and that transcription of the two genes is coupled, ii) expression of the Orf121 protein in cis or in trans has an inhibitory effect on in vivo transposition of IS91, iii) Orf121 is required for recognition and precise cleavage of the terIS91 end to limit mobilization of the adjacent DNA. With regard to IS91 transposition, we showed that only single-stranded circular DNA intermediates can be inserted into a new target sequence and identified two zinc fingers essential for the transposase activity, called ZF1 involving cysteines 41, 68, 73 and 76 and ZF2 involving cysteines 53, 58, 360 and 363. Finally, we demonstrated that transposases from the IS91 family (IS91, ISKnp22) and the ISCR family (ISCR1) are able to mobilize and recognize and cleave the oriIS end of IS91, ISCR1 and ISCR2 and the terIS end of IS91 and ISCR2
2

Oliveira, Luisa Abruzzi de. "Análise transcricional dos genes ISA1, NFS1 e ISU1 de Eucalyptus grandis sob estresse." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2008. http://hdl.handle.net/10183/15492.

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Os agrupamentos de ferro-enxofre (Fe-S) são grupos prostéticos necessários para a manutenção da vida, pois estão envolvidos em diversos processos incluindo a transferência de elétrons, reações metabólicas, sinalização e regulação da expressão gênica. As plantas realizam fotossíntese e respiração, dois processos que requerem proteínas Fe-S, sendo os únicos organismos em que a síntese destas proteínas é compartimentalizada. Diversos fatores afetam o desenvolvimento das plantas, entre eles, a temperatura baixa, fator limitante à produtividade e à distribuição geográfica das plantas, incluindo Eucalyptus grandis, uma espécie com grande importância econômica. Neste trabalho foi realizada uma análise transcricional dos genes NFS1, ISA1 e ISU1 de E. grandis após diferentes estúmlos por meio de PCR quantitativa (qRT-PCR) e microarranjos. Após o tratamento de plântulas de E. grandis com frio, foram realizados experimentos de qRT-PCR. Os resultados foram normalizados com os genes constitutivos codificadores da histona H2B e da ribonucleoproteína L23A. Considerando tal normalização, ISU1 aumentou sua expressão em 0,6 e 1,7 vezes, NFS1 apresentou um aumento de 6 e 8 vezes, enquanto ISA1 apresentou um aumento de 69 a 114 vezes em relação à condição controle. Utilizando-se a técnica de microarranjos, foi analisada a diferença de expressão entre folhas e xilema de árvores maduras de E. grandis. O gene NFS1 apresentou maior expressão nas folhas do que em xilema, porém os genes ISA1 e ISU1 apresentaram um padrão de expressão equivalente entre os dois tipos de tecidos. Esses resultados sugerem que (i) os genes NFS1 e ISA1 podem estar relacionados à resposta celular ao estresse causado por frio; e que (ii) os aumentos na expressão devem-se, provavelmente, ao metabolismo de enxofre e à indução de enzimas antioxidantes. Foi também realizado um experimento de curva de tempo com a submissão de plântulas de E. grandis ao resfriamento, objetivando-se verificar em que momento esses genes começam a ter suas expressões aumentadas. O gene ISU1 apresentou maior expressão gênica nas primeiras duas horas de tratamento, caindo drasticamente logo após este período. O gene ISA1, que havia apresentado a maior expressão relativa no experimento anterior, não apresentou diferença significativa no padrão de expressão durante as 16 horas de resfriamento, assim como o gene NFS1. Esses resultados indicam que as proteínas Fe-S, frente ao resfriamento, estão possivelmente envolvidas na recuperação das plantas após tal estresse.
Iron-sulfur (Fe-S) clusters are prosthetic groups required for the maintenance of life because they are involved in various vital processes, including electron transfers, metabolic reactions, signaling and regulation of gene expression. Plants perform photosynthesis and respiration, two processes that require Fe-S proteins, and are the only organisms in which the synthesis of these proteins is compartmentalized. Several factors and stresses affect the development of plants including low temperature, which is a productivity-limiting factor and restricts plants to certain geographical distributions, including Eucalyptus grandis, a species with significant economic importance. The aim of this study is to perform an analysis of E. grandis NFS1 and ISA1 gene expressions after different stimuli through quantitative PCR (qRT-PCR) and microarrays. qRT-PCR experiment were conducted on plants submitted to a cold treatment. The results were normalized with the housekeeping genes encoding histone H2B and ribonucleoprotein L23A. Considering such normalizations, ISU1 increased the expression 0.6 and 1-fold, NFS1 showed a 6 and 8-fold increase in comparison with the control condition, while ISA1 gene increased 69 and 114-fold. Using microarrays, the difference in expression between leaves and xylem of E. grandis was analyzed. The NFS1 gene showed higher expression in leaves than in xylem, but the ISA1and ISU1 showed equivalent pattern of expression in both types of tissues. These results suggest that (i) NFS1 and ISA1 genes are related to the cellular response to the stress caused by chilling, and that (ii) the increased expression should be probably due to the metabolism of sulfur and to the induction of antioxidative enzymes. A time-course experiment was also conducted during the cold stress of E. grandis plants to look at which moment these genes begin to increase their expressions. The ISU1 gene showed higher expression in the first 2 hours of treatment, and than decreased severally after this period. The ISA1 gene, which had shown the highest expression in the previous experiment, did not show significant differences in the pattern of expression during the 16 hours of chilling treatment, as well as the NFS1 gene. These results indicate that Fe-S proteins, in response to low temperature, are possibly involved in the recovery of the plants after this stress.
3

Salmanian, Mazda. "Inverse multiplexing of IS95 traffic for video transmission." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0027/MQ27025.pdf.

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Salmanian, Mazda Carleton University Dissertation Engineering Systems and Computer. "Inverse multiplexing of IS95 traffic for video transmission." Ottawa, 1997.

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5

Zegarra, Rodríguez Demóstenes. "Diseño del equipamiento de conmutación de una red celular CDMA/IS95/1X." Bachelor's thesis, Pontificia Universidad Católica del Perú, 2006. http://tesis.pucp.edu.pe/repositorio/handle/123456789/1084.

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El presente trabajo de tesis se ha sido realizado con la finalidad de exponer los principales conceptos que se deben tener en consideración al afrontar el problema de dimensionar la etapa de conmutación dentro de una red celular llegando a determinar la solución conceptual y su posterior ejecución, para mayor claridad se presentan casos prácticos de dimensionamiento y el desarrollo de un proyecto. Por consiguiente y con la finalidad de brindar un concepto teórico general, en el capítulo 1, se presenta el esquema de una red celular CDMA mostrando los principales equipos que componen esta red, describiendo las funciones fundamentales, capacidades y elementos internos de los principales equipos. En el marco teórico, capítulo 2, se describen los principales conceptos referentes a tráfico telefónico y la descripción de los parámetros que indican el estado de una red celular, con el objetivo de caracterizar el comportamiento de llamadas de los usuarios y por ende de la misma red. En el capítulo 3 se muestra la aplicación de los conceptos teóricos en casos prácticos de dimensionamiento de tráfico, determinación de estructura de la red y control de la capacidad de equipos. El objetivo es que tomando en consideración todas las reglas de dimensionamiento y parámetros de control de calidad, en cada uno de los tres casos expuestos en este capítulo, se debe plantear para cada caso una solución de ingeniería factible de aplicar. Teniendo ya planteada la solución de un problema se debe ejecutar, por lo que en el capítulo 4 se ha descrito las principales consideraciones que se deben tener en la ejecución de un proyecto, como ejemplo, y para un mejor entendimiento, se ha tomado al segundo caso del capítulo 3. Finalmente el Capítulo 5 muestra muy brevemente un análisis de los costos involucrados en el caso 1 del capítulo 3.
Tesis
6

HAREN, LAURENCE. "Relations structure/fonction des facteurs proteiques exprimes par l'element transposable bacterien is911." Toulouse 3, 1998. http://www.theses.fr/1998TOU30232.

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La sequence d'insertion is911 est composee de deux cadres de lecture partiellement chevauchants et encadres par de courtes extremites inversement repetees. Sa transposase est produite suite a un decalage de phase traductionnel programme peu avant la fin du premier cadre de lecture. Ce mode de synthese lui permet : (i) d'associer la synthese de la transposase (orfab) a celle du produit du premier cadre de lecture (orfa), un facteur regulateur qui stimule sa transposition intermoleculaire ; (ii) d'assembler deux domaines fonctionnels distincts, un domaine de liaison specifique aux extremites code par le premier cadre de lecture et un domaine catalytique code par le second cadre de lecture, sur un seul polypeptide. Le domaine catalytique a ete defini sur la base de sa structure predite etroitement homologue a celle du cur catalytique des integrases retrovirales. Nous avons confirme cette homologie au niveau fonctionnel. Nous avons egalement decele une thermosensibilite intrinseque de l'activite de la transposase, confirmee par l'obtention de mutants thermoresistants. Orfab et orfa partagent une region n-terminale comportant un motif helice-tour-helice (hth) putatif suivi d'un motif leucine-zipper (lz). La sequence du lz differe cependant dans les deux proteines. La caracterisation fine de ce motif suggere qu'il est structuralement et fonctionnellement homologue aux lzs des facteurs de transcription eucaryotes. Il est implique dans l'homo- et l'heteromultimerisation d'orfab et d'orfa. Il pourrait permettre une dimerisation du motif hth adjacent, requise pour une fixation efficace aux extremites du transposon, et intervenir dans la fonction regulatrice d'orfa en permettant la fixation de multimeres hybrides orfa/orfab. Deux autres regions sont egalement impliquees dans l'oligomerisation de la transposase : une region situee directement en aval du lz et probablement impliquee dans le pontage proteique des extremites, et une region contenue dans le domaine catalytique.
7

Gueguen, Erwan. "Étude de la thermosensibilité de transposition de la séquence d'insertion bactérienne IS911." Toulouse 3, 2006. http://www.theses.fr/2006TOU30183.

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Inglis, Neil Fraser. "Studies on a 40kDa protein antigen of IS901/902-positive Mycobacterium avium." Thesis, University of Edinburgh, 1998. http://hdl.handle.net/1842/21315.

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The work presented in this thesis was undertaken as part of a larger research initiative in the field of ruminant paratuberculosis (Johne's disease). One of the group's main research objectives was the identification and characterisation of subspecies-specific genes and proteins of the two members of the Mycobacterium avium complex (MAC) known to have a causal role in ruminant paratuberculosis, namely Mycobacterium avium spp. paratuberculosis (M. a. paratuberculosis) and IS901/902-positive strains of Mycobacterium avium (M. avium). A protein antigen of 40kDa (p40) was identified in an IS901/902-positive strain of M. avium, but could not be detected in M. a. paratuberculosis, IS901/902-negative M avium, or in any of 13 other species of Mycobacterium tested. Examination of 19 further MAC field isolates confirmed the absolute association between p40 and IS901/902, suggesting that p40 is a novel, subspecies-specific protein which may potentially be of value as a diagnostic antigen. Soluble p40 antigen was precipitated from cleared cell lysates and purified to homogeneity using a series of chromatographic separations. Chemical cleavage and Edman degradation of the purified p40 antigen provided both amino-terminal and internal amino acid sequence data which showed no sequence identity with any protein sequence currently in the OWL database. Translations of IS901/902 in all six reading frames revealed amino acid sequences which confirmed that the genomic insertion sequence does not encode the p40 antigen. A second protein of 30kDa (p30) was purified simultaneously, and analysis of the first 10 amino-terminal amino acid residues revealed up to 90% sequence identity with the mature secretory antigens of the "antigen 85 complex" of 8 other species of Mycobacterium. Experiments were designed to ascertain whether the p40 antigen was expressed in vivo and to assess whether any immune response to the p40 could be exploited in the development of an immune-based assay to differentiate between animals infected with M. a. paratuberculosis, and others infected with IS901/902-positive status of M. avium.
9

Williams, David Ross. "The stability of insertion sequence IS1 in Escherichia coli." Thesis, Queen's University Belfast, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317123.

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Rhodes, Glenn. "Insertion sequence 1 (IS1) in freshwater and associated sediments." Thesis, University of Liverpool, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364117.

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Books on the topic "Is91":

1

Theodore, Houghton John, Intergovernmental Panel on Climate Change. Working Group I., and Intergovernmental Panel on Climate Change. Response Strategies Work Group., eds. Climate change, 1994: Radiative forcing of climate change and an evaluation of the IPCC IS92 emission scenarios. Cambridge [England]: Cambridge University Press, 1995.

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BERNDT & MITCHUM. Cogn Neuropsychol Iss1&2 V5. Taylor & Francis Group, 1995.

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co, Missouri Star Quilt. Block Vol 9 Iss1: Idea Book. Missouri Star Quilt Co, 2022.

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Cook-Lynn, Elizabeth, and Assn Amer Ind Res. Wicazo Sa Review Vol12 Iss1 Pb. University of Minnesota Press, 1997.

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NA. Microbio: Intro Alc& Microbio Photo ATL& Iss1. Addison Wesley Publishing Company, 2007.

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Cook-Lynn, Elizabeth, and Assn Amer Ind. Wicazo Sa Review Vol 14 Iss1 Pb. University of Minnesota Press, 1999.

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NA. Microbio Intro & Current Iss1& Emerg& Stem Pkg. Addison Wesley Publishing Company, 2006.

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NA. Biology Concept & Conn& Curr Iss1& 2& Card Pkg. Addison Wesley Publishing Company, 2005.

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NA. Microbio Alter Editn W/Disease& Curr Iss1 Pk. Addison Wesley Publishing Company, 2006.

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Klug. Genetics: Molec Persp&sp03 Iss1 Nyt&eval Pk. Pearson Education, Limited, 2003.

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Book chapters on the topic "Is91":

1

Chiaravalli, Anna Maria. "Islet 1 (ISL1)." In Encyclopedia of Pathology, 1–2. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-28845-1_5087-1.

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Chiaravalli, Anna Maria. "Islet 1 (ISL1)." In Endocrine Pathology, 451–52. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-62345-6_5087.

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Chandler, Michael, and David J. Galas. "Studies on the Transposition of IS1." In Plasmids in Bacteria, 53–77. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2447-8_7.

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Krol, M. S. "Implications for Atmospheric Composition and Climate of IS92 Emissions Scenarios." In Non-CO2 Greenhouse Gases: Why and How to Control?, 247–52. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0982-6_28.

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Chandler, Michael, Olivier Fayet, Philippe Rousseau, Bao Ton Hoang, and Guy Duval-Valentin. "Copy-out-Paste-in Transposition of IS911: A Major Transposition Pathway." In Mobile DNA III, 591–607. Washington, DC, USA: ASM Press, 2015. http://dx.doi.org/10.1128/9781555819217.ch27.

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"IS91 Rolling-Circle Transposition." In Mobile DNA II, 891–904. American Society of Microbiology, 2002. http://dx.doi.org/10.1128/9781555817954.ch37.

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"Transposition of IS911." In Mobile DNA II, 367–83. American Society of Microbiology, 2002. http://dx.doi.org/10.1128/9781555817954.ch16.

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"INTELLIGENCE SCHOOL 9 (IS9)." In MI9, 137–50. Yale University Press, 2020. http://dx.doi.org/10.2307/j.ctv15pjxb4.16.

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"IS9(WEA) WESTERN EUROPE." In MI9, 251–59. Yale University Press, 2020. http://dx.doi.org/10.2307/j.ctv15pjxb4.23.

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"14 IS9(WEA) Western Europe." In MI9, 251–59. Yale University Press, 2020. http://dx.doi.org/10.12987/9780300255928-020.

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Conference papers on the topic "Is91":

1

Manchanda, Ranjit. "Abstract IS01: Brca testing in high-risk populations." In Abstracts: 10th Biennial Ovarian Cancer Research Symposium; September 8-9, 2014; Seattle, WA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1557-3265.ovcasymp14-is01.

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Xun Liu and M. C. Papaefthymiou. "Design of a high-throughput low-power IS95 Viterbi decoder." In Proceedings of 39th Design Automation Conference. IEEE, 2002. http://dx.doi.org/10.1109/dac.2002.1012633.

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Liu, Xun, and Marios C. Papaefthymiou. "Design of a high-throughput low-power IS95 Viterbi decoder." In the 39th conference. New York, New York, USA: ACM Press, 2002. http://dx.doi.org/10.1145/513918.513988.

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"The New Infrasound Station of South America, IS01-Pilcaniyeu, Argentina." In International Congress of the Brazilian Geophysical Society&Expogef. Brazilian Geophysical Society, 2021. http://dx.doi.org/10.22564/17cisbgf2021.350.

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Lim, Billy L., Bryan Hosack, and Paul Vogt. "A web service-oriented approach to teaching CS/IS1." In the 41st ACM technical symposium. New York, New York, USA: ACM Press, 2010. http://dx.doi.org/10.1145/1734263.1734309.

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Waguespack, Leslie J. "An IS1 workbench for ACM information system curriculum '81." In the twentieth SIGCSE technical symposium. New York, New York, USA: ACM Press, 1989. http://dx.doi.org/10.1145/65293.71194.

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Jaiswal, Aruna, Elizabeth Williamson, Bhavita Patel, Gayathri Srinivasan, Kimi Kong, Carrie Lomelino, Satya Narayan, and Robert Hromas. "Abstract 1758: Splicing component ISY1 interacts with APE1 and regulates base excision repair." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-1758.

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Jaiswal, Aruna, Elizabeth Williamson, Bhavita Patel, Gayathri Srinivasan, Kimi Kong, Carrie Lomelino, Satya Narayan, and Robert Hromas. "Abstract 1758: Splicing component ISY1 interacts with APE1 and regulates base excision repair." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-1758.

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Bodelon, Clara, J. Keith Killian, Joshua N. Sampson, Holly Stevenson, William F. Anderson, Rayna Matsuno, Louise A. Brinton, Jolanta Lissowska, Mark E. Sherman, and Nicolas Wentzensen. "Abstract IS01: METHYLATION PROFILING OF OVARIAN CANCER TO STUDY ETIOLOGIC AND PROGNOSTIC HETEROGENEITY AND TO DEVELOP A MOLECULAR CLASSIFIER." In Abstracts: 11th Biennial Ovarian Cancer Research Symposium; September 12-13, 2016; Seattle, WA. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1557-3265.ovcasymp16-is01.

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Maciejewska, Izabela. "Computer-assisted audit tools in relation with international standard on quality control 1 (ISQ1): (Based on experiences from polish small audit practices)." In 2015 10th Iberian Conference on Information Systems and Technologies (CISTI). IEEE, 2015. http://dx.doi.org/10.1109/cisti.2015.7170617.

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To the bibliography