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  1. AU="Jönsson, Klas"
  2. AU="de Steenwinkel, Jurriaan E M"
  3. AU="Yadav, Kabir"
  4. AU="Sasmaz, Mahmut Unsal"
  5. AU="Solá-Sánchez, Ernesto"
  6. AU="Cinquanta, Lucrezia"
  7. AU="Drivenes, Jakob Lillemoen"
  8. AU="Martín, José Ignacio Valero"
  9. AU=Mahmood Shah Sayed Mustafa
  10. AU=Sales-Peres Silvia Helena de Carvalho
  11. AU="Boyea, Beth Lincoln"
  12. AU=Martorell-Marugan Jordi
  13. AU="Serventi, Lisa"
  14. AU=O'Shea John J AU=O'Shea John J
  15. AU="Jiang, Dahai"
  16. AU="Sheng, Chu-Qiao"
  17. AU="Rodríguez, Fausto J."
  18. AU="Sadowski, Peter"
  19. AU="Noguera, Austin"
  20. AU="Daigneault, Tina"
  21. AU="Flores-Martínez, José Juan"
  22. AU="Gan, Yu-Ling"
  23. AU=Banno Asoka AU=Banno Asoka
  24. AU="Bertolin, Kalyne"
  25. AU="Rising, James A"
  26. AU="Jackson Voelkel"
  27. AU="Arias, Marisa"
  28. AU="Le, Uyen Nguyen Phuong"
  29. AU="Shim, Yun M"
  30. AU="Ngan, Hau Lan"
  31. AU="Shah, Fawad Ali"
  32. AU="Rodriguez Chinesta, J M"
  33. AU="Reddy, Avril"
  34. AU="Vachani, Anil"
  35. AU="Lofland, Gabriela"
  36. AU="Zou, Xiaoyan"
  37. AU="Norhafizah Bt Sahril"

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  1. Buch ; Dissertation / Habilitation: Fibronectin binding proteins of Staphylococcus aureus

    Jönsson, Klas

    (Rapport / Institutionen för Mikrobiologi ; 52)

    1992  

    Verfasserangabe Klas Jönsson
    Serientitel Rapport / Institutionen för Mikrobiologi ; 52
    Rapport / Institutionen för Mikrobiologie, Sveriges Lantbruksuniversitet
    Überordnung Rapport / Institutionen för Mikrobiologie, Sveriges Lantbruksuniversitet
    Schlagwörter Staphylococcus aureus ; Fibronectin-binding protein ; Nucleotidsequenz
    Schlagwörter Nucleotide ; Nukleotidsequenz
    Umfang Getr. Zählung : Ill., graph. Darst.
    Erscheinungsort Uppsala
    Erscheinungsland Schweden
    Dokumenttyp Buch ; Dissertation / Habilitation
    Dissertation / Habilitation Uppsala, Sveriges Lantbruksuniv., Diss., 1992
    HBZ-ID HT006354290
    ISBN 91-576-4567-1 ; 978-91-576-4567-8
    Datenquelle Katalog ZB MED Ernährung, Umwelt, Agrar

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    SignaturLeihstatusStandort
    948/2226 ausleihbar (Lesesaal) Freihandmagazin (U1)

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  2. Buch ; Dissertation / Habilitation: Fibronectin-binding proteins of Staphylococcus aureus

    Jönsson, Klas

    (Rapport / Institutionen för mikrobiologi ; 52)

    1992  

    Titelvarianten Sammlung
    Verfasserangabe Klas Jönsson
    Serientitel Rapport / Institutionen för mikrobiologi ; 52
    Sprache Nicht zu entscheiden
    Umfang Getr. Zählung, graph. Darst
    Verlag Swedish Univ. of Agricultural Sciences
    Erscheinungsort Uppsala
    Dokumenttyp Buch ; Dissertation / Habilitation
    Dissertation / Habilitation Zugl. : Uppsala, Univ., Diss. : 1992
    ISBN 9157645671 ; 9789157645678
    Datenquelle Max Rubner-Institut, Bundesforschungsinstitut für Ernährung und Lebensmittel

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  3. Buch ; Dissertation / Habilitation: Fibronectin-binding proteins of Staphylococcus aureus

    Jönsson, Klas

    (Rapport / Institutionen för mikrobiologi ; 52)

    1992  

    Titelvarianten Sammlung
    Verfasserangabe Klas Jönsson
    Serientitel Rapport / Institutionen för mikrobiologi ; 52
    Sprache Nicht zu entscheiden
    Umfang Getr. Zählung, graph. Darst
    Verlag Swedish Univ. of Agricultural Sciences
    Erscheinungsort Uppsala
    Dokumenttyp Buch ; Dissertation / Habilitation
    Dissertation / Habilitation Zugl. : Uppsala, Univ., Diss. : 1992
    ISBN 9157645671 ; 9789157645678
    Datenquelle Bibliothek der Tierärztlichen Hochschule Hannover

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  4. Buch ; Dissertation / Habilitation: Fibronectin-binding proteins of staphylococcus aureus

    Jönsson, Klas

    (Rapport / Sveriges lantbruksuniversitet, Institutionen för mikrobiologi = : Report / Swedish University of Agricultural Sciences, Department of Microbiology, ; 52)

    1992  

    Verfasserangabe Klas Jönsson
    Serientitel Rapport / Sveriges lantbruksuniversitet, Institutionen för mikrobiologi = : Report / Swedish University of Agricultural Sciences, Department of Microbiology, ; 52
    Schlagwörter Biological Sciences
    Sprache Englisch
    Umfang 1 v. (various pagings) :, ill. ;, 24 cm.
    Verlag Swedish University of Agricultural Sciences, Dept. of Microbiology ; c 1992
    Erscheinungsort Uppsala
    Dokumenttyp Buch ; Dissertation / Habilitation
    Dissertation / Habilitation Thesis (Ph. D.) -- Sveriges lantbruksuniversitet, (1992?)
    Anmerkung Abstract inserted.
    ISBN 9157645671 ; 9789157645678
    Datenquelle NAL Katalog (AGRICOLA)

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  5. Artikel ; Online: Production, crystallization and preliminary X-ray diffraction analysis of the allergen Can f 2 from Canis familiaris.

    Madhurantakam, Chaithanya / Nilsson, Ola B / Jönsson, Klas / Grönlund, Hans / Achour, Adnane

    Acta crystallographica. Section F, Structural biology and crystallization communications

    2009  Band 65, Heft Pt 5, Seite(n) 467–471

    Abstract: The allergen Can f 2 from dog (Canis familiaris) present in saliva, dander and fur is an important cause of allergic sensitization worldwide. Here, the production, isolation, crystallization and preliminary X-ray diffraction analysis of two crystal forms ...

    Abstract The allergen Can f 2 from dog (Canis familiaris) present in saliva, dander and fur is an important cause of allergic sensitization worldwide. Here, the production, isolation, crystallization and preliminary X-ray diffraction analysis of two crystal forms of recombinant Can f 2 are reported. The first crystal form belonged to space group C222, with unit-cell parameters a = 68.7, b = 77.3, c = 65.1 A, and diffracted to 1.55 A resolution, while the second crystal form belonged to space group C2, with unit-cell parameters a = 75.7, b = 48.3, c = 68.7 A, beta = 126.5 degrees , and diffracted to 2.1 A resolution. Preliminary data analysis indicated the presence of a single molecule in the asymmetric unit for both crystal forms.
    Mesh-Begriff(e) Allergens/chemistry ; Allergens/genetics ; Allergens/metabolism ; Amino Acid Sequence ; Animals ; Antigens, Plant ; Cloning, Molecular ; Crystallization ; Crystallography, X-Ray ; Dogs ; Molecular Sequence Data
    Chemische Substanzen Allergens ; Antigens, Plant ; allergen Can f 2
    Sprache Englisch
    Erscheinungsdatum 2009-04-24
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1744-3091
    ISSN (online) 1744-3091
    DOI 10.1107/S1744309109010884
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel: Molecular cloning and characterization of two Helicobacter pylori genes coding for plasminogen-binding proteins.

    Jönsson, Klas / Guo, Betty P / Monstein, Hans-Jürg / Mekalanos, John J / Kronvall, Göran

    Proceedings of the National Academy of Sciences of the United States of America

    2004  Band 101, Heft 7, Seite(n) 1852–1857

    Abstract: Helicobacter pylori binds a number of host cell proteins, including the plasma protein plasminogen, which is the proenzyme of the serine protease plasmin. Two H. pylori plasminogen-binding proteins have been described; however, no genes were identified. ... ...

    Abstract Helicobacter pylori binds a number of host cell proteins, including the plasma protein plasminogen, which is the proenzyme of the serine protease plasmin. Two H. pylori plasminogen-binding proteins have been described; however, no genes were identified. Here we report the use of a phage display library to clone two genes from the H. pylori CCUG 17874 genome that mediate binding to plasminogen. DNA sequence analysis of one of these genes revealed 96.6% homology with H. pylori 26695 HP0508. A subsequent database search revealed that the amino acid sequence of a lysine-rich C-terminal segment of HP0508 is identical to the C terminus of HP0863. Recombinant proteins expressed from HP0508 and HP0863 bound plasminogen specifically and in a lysine-dependent manner. We designate these genes pgbA and pgbB, respectively. These proteins are expressed by a variety of H. pylori strains, have surface-exposed domains, and do not inhibit plasminogen activation. These results indicate that pgbA and pgbB may allow H. pylori to coat its exterior with plasminogen, which subsequently can be activated to plasmin. The surface acquisition of protease activity may enhance the virulence of H. pylori.
    Mesh-Begriff(e) Amino Acid Sequence ; Bacterial Proteins/chemistry ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Carrier Proteins/chemistry ; Carrier Proteins/genetics ; Carrier Proteins/metabolism ; Cloning, Molecular ; Computational Biology ; Fibrinolysin/metabolism ; Genes, Bacterial/genetics ; Helicobacter pylori/genetics ; Lysine/metabolism ; Molecular Sequence Data ; Plasminogen/metabolism ; Protein Binding ; Recombinant Proteins/chemistry ; Recombinant Proteins/genetics ; Recombinant Proteins/metabolism
    Chemische Substanzen Bacterial Proteins ; Carrier Proteins ; Recombinant Proteins ; plasminogen-binding protein, bacteria ; Plasminogen (9001-91-6) ; Fibrinolysin (EC 3.4.21.7) ; Lysine (K3Z4F929H6)
    Sprache Englisch
    Erscheinungsdatum 2004-02-09
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.0307329101
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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    Verfügbar in ZB MED Köln/Königswinter

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  7. Artikel ; Online: Plasmablasts generated during repeated dengue infection are virus glycoprotein-specific and bind to multiple virus serotypes.

    Xu, Meihui / Hadinoto, Vey / Appanna, Ramapraba / Joensson, Klas / Toh, Ying Xiu / Balakrishnan, Thavamalar / Ong, Swee Hoe / Warter, Lucile / Leo, Yee Sin / Wang, Cheng-I / Fink, Katja

    Journal of immunology (Baltimore, Md. : 1950)

    2012  Band 189, Heft 12, Seite(n) 5877–5885

    Abstract: Dengue virus immune protection is specific to the serotype encountered and is thought to persist throughout one's lifetime. Many serotype cross-reactive memory B cells isolated from humans with previous dengue infection are specific for the nonstructural ...

    Abstract Dengue virus immune protection is specific to the serotype encountered and is thought to persist throughout one's lifetime. Many serotype cross-reactive memory B cells isolated from humans with previous dengue infection are specific for the nonstructural and the prM structural viral proteins, and they can enhance infection in vitro. However, plasmablasts circulating in enormous numbers during acute secondary infection have not been studied. In this study, we analyzed single plasmablasts from two patients by sorting the cells for Ig sequence analysis and for recombinant expression of Abs. In contrast to memory B cells, most plasmablast-derived Abs bound to the structural E protein of dengue, and protection experiments in mice revealed that virus serotypes encountered during past infections were neutralized more efficiently than were the serotypes of the current infection. Together with genetic analyses, we show evidence that plasmablasts in dengue patients are a polyclonal pool of activated E protein-specific memory B cells and that their specificity is not representative of the serum Abs secreted by long-lived plasma cells in the memory phase. These results contribute to the understanding of the phenomenon of original antigenic sin in dengue.
    Mesh-Begriff(e) Adult ; Animals ; Binding Sites, Antibody ; Capsid Proteins/immunology ; Capsid Proteins/metabolism ; Cell Differentiation/immunology ; Dengue/classification ; Dengue/immunology ; Dengue/virology ; Dengue Virus/classification ; Dengue Virus/immunology ; Epitopes, B-Lymphocyte/immunology ; Epitopes, B-Lymphocyte/metabolism ; Humans ; Immunologic Memory ; Mice ; Plasma Cells/immunology ; Plasma Cells/metabolism ; Plasma Cells/virology ; Protein Binding/immunology ; Recurrence ; Serotyping ; Viral Envelope Proteins/immunology ; Viral Envelope Proteins/metabolism ; Virion/immunology ; Virion/metabolism ; Young Adult
    Chemische Substanzen Capsid Proteins ; Epitopes, B-Lymphocyte ; Viral Envelope Proteins
    Sprache Englisch
    Erscheinungsdatum 2012-12-15
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3056-9
    ISSN 1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
    ISSN (online) 1550-6606
    ISSN 0022-1767 ; 1048-3233 ; 1047-7381
    DOI 10.4049/jimmunol.1201688
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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    Verfügbar in ZB MED Köln/Königswinter

    Ud II Zs.37: Hefte anzeigen Standort:
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    bis Jg. 2021: Bestellungen von Artikeln über das Online-Bestellformular
    ab Jg. 2022: Lesesaal (EG)
    Zs.MG 28: Hefte anzeigen

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  8. Artikel ; Online: Toll-like receptor 4 promoter polymorphisms: common TLR4 variants may protect against severe urinary tract infection.

    Ragnarsdóttir, Bryndís / Jönsson, Klas / Urbano, Alexander / Grönberg-Hernandez, Jenny / Lutay, Nataliya / Tammi, Martti / Gustafsson, Mattias / Lundstedt, Ann-Charlotte / Leijonhufvud, Irene / Karpman, Diana / Wullt, Björn / Truedsson, Lennart / Jodal, Ulf / Andersson, Björn / Svanborg, Catharina

    PloS one

    2010  Band 5, Heft 5, Seite(n) e10734

    Abstract: Background: Polymorphisms affecting Toll-like receptor (TLR) structure appear to be rare, as would be expected due to their essential coordinator role in innate immunity. Here, we assess variation in TLR4 expression, rather than structure, as a ... ...

    Abstract Background: Polymorphisms affecting Toll-like receptor (TLR) structure appear to be rare, as would be expected due to their essential coordinator role in innate immunity. Here, we assess variation in TLR4 expression, rather than structure, as a mechanism to diversify innate immune responses.
    Methodology/principal findings: We sequenced the TLR4 promoter (4,3 kb) in Swedish blood donors. Since TLR4 plays a vital role in susceptibility to urinary tract infection (UTI), promoter sequences were obtained from children with mild or severe disease. We performed a case-control study of pediatric patients with asymptomatic bacteriuria (ABU) or those prone to recurrent acute pyelonephritis (APN). Promoter activity of the single SNPs or multiple allelic changes corresponding to the genotype patterns (GPs) was tested. We then conducted a replication study in an independent cohort of adult patients with a history of childhood APN. Last, in vivo effects of the different GPs were examined after therapeutic intravesical inoculation of 19 patients with Escherichia coli 83972. We identified in total eight TLR4 promoter sequence variants in the Swedish control population, forming 19 haplotypes and 29 genotype patterns, some with effects on promoter activity. Compared to symptomatic patients and healthy controls, ABU patients had fewer genotype patterns, and their promoter sequence variants reduced TLR4 expression in response to infection. The ABU associated GPs also reduced innate immune responses in patients who were subjected to therapeutic urinary E. coli tract inoculation.
    Conclusions: The results suggest that genetic variation in the TLR4 promoter may be an essential, largely overlooked mechanism to influence TLR4 expression and UTI susceptibility.
    Mesh-Begriff(e) Adolescent ; Bacteriuria/complications ; Bacteriuria/genetics ; Case-Control Studies ; Child ; Child, Preschool ; Female ; Follow-Up Studies ; Genetic Predisposition to Disease ; Haplotypes/genetics ; Humans ; Immunity, Innate/genetics ; Infant ; Male ; Polymorphism, Single Nucleotide/genetics ; Promoter Regions, Genetic/genetics ; Sweden ; Toll-Like Receptor 4/genetics ; Transcription, Genetic ; Urinary Tract Infections/genetics ; Urinary Tract Infections/pathology ; Urinary Tract Infections/prevention & control ; Urinary Tract Infections/therapy ; Young Adult
    Chemische Substanzen TLR4 protein, human ; Toll-Like Receptor 4
    Sprache Englisch
    Erscheinungsdatum 2010-05-20
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0010734
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Pathogen specific, IRF3-dependent signaling and innate resistance to human kidney infection.

    Fischer, Hans / Lutay, Nataliya / Ragnarsdóttir, Bryndís / Yadav, Manisha / Jönsson, Klas / Urbano, Alexander / Al Hadad, Ahmed / Rämisch, Sebastian / Storm, Petter / Dobrindt, Ulrich / Salvador, Ellaine / Karpman, Diana / Jodal, Ulf / Svanborg, Catharina

    PLoS pathogens

    2010  Band 6, Heft 9, Seite(n) e1001109

    Abstract: The mucosal immune system identifies and fights invading pathogens, while allowing non-pathogenic organisms to persist. Mechanisms of pathogen/non-pathogen discrimination are poorly understood, as is the contribution of human genetic variation in disease ...

    Abstract The mucosal immune system identifies and fights invading pathogens, while allowing non-pathogenic organisms to persist. Mechanisms of pathogen/non-pathogen discrimination are poorly understood, as is the contribution of human genetic variation in disease susceptibility. We describe here a new, IRF3-dependent signaling pathway that is critical for distinguishing pathogens from normal flora at the mucosal barrier. Following uropathogenic E. coli infection, Irf3(-/-) mice showed a pathogen-specific increase in acute mortality, bacterial burden, abscess formation and renal damage compared to wild type mice. TLR4 signaling was initiated after ceramide release from glycosphingolipid receptors, through TRAM, CREB, Fos and Jun phosphorylation and p38 MAPK-dependent mechanisms, resulting in nuclear translocation of IRF3 and activation of IRF3/IFNβ-dependent antibacterial effector mechanisms. This TLR4/IRF3 pathway of pathogen discrimination was activated by ceramide and by P-fimbriated E. coli, which use ceramide-anchored glycosphingolipid receptors. Relevance of this pathway for human disease was supported by polymorphic IRF3 promoter sequences, differing between children with severe, symptomatic kidney infection and children who were asymptomatic bacterial carriers. IRF3 promoter activity was reduced by the disease-associated genotype, consistent with the pathology in Irf3(-/-) mice. Host susceptibility to common infections like UTI may thus be strongly influenced by single gene modifications affecting the innate immune response.
    Mesh-Begriff(e) Adult ; Animals ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Blotting, Western ; Case-Control Studies ; Cell Nucleus/metabolism ; Ceramides/metabolism ; Child ; Escherichia coli/pathogenicity ; Escherichia coli Infections/etiology ; Escherichia coli Infections/mortality ; Escherichia coli Infections/prevention & control ; Fimbriae, Bacterial ; Gene Expression Profiling ; Humans ; Immunity, Innate/physiology ; Interferon Regulatory Factor-3/genetics ; Interferon Regulatory Factor-3/metabolism ; Interferon Regulatory Factor-3/physiology ; Kidney/metabolism ; Kidney/pathology ; Kidney/virology ; Kidney Neoplasms/etiology ; Kidney Neoplasms/mortality ; Kidney Neoplasms/prevention & control ; Lung Neoplasms/etiology ; Lung Neoplasms/mortality ; Lung Neoplasms/prevention & control ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Oligonucleotide Array Sequence Analysis ; Phosphorylation ; Polymorphism, Genetic/genetics ; Promoter Regions, Genetic/genetics ; Prospective Studies ; Protein Transport ; Pyelonephritis/etiology ; Pyelonephritis/mortality ; Pyelonephritis/pathology ; RNA, Messenger/genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Signal Transduction ; Toll-Like Receptor 4/genetics ; Toll-Like Receptor 4/metabolism ; Tumor Cells, Cultured ; Urinary Tract Infections/etiology ; Urinary Tract Infections/mortality ; Urinary Tract Infections/prevention & control
    Chemische Substanzen Biomarkers, Tumor ; Ceramides ; IRF3 protein, human ; Interferon Regulatory Factor-3 ; Irf3 protein, mouse ; RNA, Messenger ; Toll-Like Receptor 4
    Sprache Englisch
    Erscheinungsdatum 2010-09-23
    Erscheinungsland United States
    Dokumenttyp Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2205412-1
    ISSN 1553-7374 ; 1553-7366
    ISSN (online) 1553-7374
    ISSN 1553-7366
    DOI 10.1371/journal.ppat.1001109
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: Identification of viral agents associated with diarrhea in young children during a winter season in Beijing, China.

    Liu, Chunyan / Grillner, Lena / Jonsson, Klas / Linde, Annika / Shen, Kunling / Lindell, Annika Tiveljung / Wirgart, Benita Zweygberg / Johansen, Kari

    Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology

    2005  Band 35, Heft 1, Seite(n) 69–72

    Abstract: Background: Viral diarrhea remains a major cause of childhood morbidity and mortality worldwide. Although rotavirus was extensively studied in China, few comprehensive studies of all viral agents related to diarrhea in children have been conducted.: ... ...

    Abstract Background: Viral diarrhea remains a major cause of childhood morbidity and mortality worldwide. Although rotavirus was extensively studied in China, few comprehensive studies of all viral agents related to diarrhea in children have been conducted.
    Objectives: Our study was performed to investigate the role of enteric viruses in acute diarrhea in our country and to evaluate methods that could be used in routine diagnostics.
    Study design: One hundred stool samples were collected from children under 5 years of age seeking medical care for acute diarrhea during the winter season 2000/2001 in Beijing Children's Hospital. All specimens were initially screened microscopically for leucocytes/red blood cells. Samples with negative results were analyzed for virus presence using commercial EIAs and/or in-house RT-PCRs.
    Results: At least one viral agent was found in 67% of the specimens. The frequency of rotavirus, astrovirus, norovirus and enteric adenovirus was 59%, 8%, 6% and 2%, respectively. Dual infections were found in 9.0% (6/67) of the positive samples. The results from rotavirus and astrovirus EIAs were concordant with those of rotavirus and astrovirus RT-PCRs.
    Conclusions: Enteric viruses play an important role in pediatric diarrhea during the winter season in China. A combination of microscopic examination of stool samples with specific EIA assays to detect virus antigen in stool specimens may be suitable for routine diagnostics.
    Mesh-Begriff(e) Adenoviruses, Human/classification ; Adenoviruses, Human/genetics ; Adenoviruses, Human/isolation & purification ; Child, Preschool ; China/epidemiology ; Diarrhea/epidemiology ; Diarrhea/virology ; Female ; Humans ; Immunoenzyme Techniques ; Infant ; Male ; Mamastrovirus/classification ; Mamastrovirus/genetics ; Mamastrovirus/isolation & purification ; Norovirus/classification ; Norovirus/genetics ; Norovirus/isolation & purification ; RNA, Viral/analysis ; RNA, Viral/isolation & purification ; Reverse Transcriptase Polymerase Chain Reaction ; Rotavirus/classification ; Rotavirus/genetics ; Rotavirus/isolation & purification ; Seasons ; Virus Diseases/epidemiology ; Virus Diseases/virology ; Viruses/classification ; Viruses/genetics ; Viruses/isolation & purification
    Chemische Substanzen RNA, Viral
    Schlagwörter covid19
    Sprache Englisch
    Erscheinungsdatum 2005-07-05
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1446080-4
    ISSN 1873-5967 ; 1386-6532
    ISSN (online) 1873-5967
    ISSN 1386-6532
    DOI 10.1016/j.jcv.2005.04.007
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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