MSCRAMM-MEDIATED ADHERENCE OF MICROORGANISMS TO HOST TISSUES

Bacterial Adherence: Adhesin-Receptor Interactions Mediating the Attachment of Bacteria to Mucosal Surfaces

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Multiple β1 chain integrins are receptors for invasin, a protein that promotes bacterial penetration into mammalian cells

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Fibronectin binding mediated by a novel class of surface organelles on Escherichia coll

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Identification of invasin: A protein that allows enteric bacteria to penetrate cultured mammalian cells

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Effect of plasminogen activator (urokinase), plasmin, and thrombin on glycoprotein and collagenous components of basement membrane.

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Fibronectin binds to Staphylococcus aureus

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Conservation of a hexapeptide sequence in the anchor region of surface proteins from Gram‐positive cocci

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Serotypes, hemolysin production, and receptor recognition of Escherichia coli strains associated with neonatal sepsis and meningitis

Korhonen, T. K., Valtonen, M., Parkkinen, J., Väisänen-Rhen, V., Finne, J., Ørskov, F., Ørskov, I., Svenson, S. B., & Mäkelä, P. H. (1985) · Infection and Immunity · doi:10.1128/iai.48.2.486-491.1985 · Cited by 360

Malaria circumsporozoite protein binds to heparan sulfate proteoglycans associated with the surface membrane of hepatocytes.

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Antibodies to the conserved cytoplasmic domain of the integrin beta 1 subunit react with proteins in vertebrates, invertebrates, and fungi.

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Biogenesis and Functionality of Sortase-Assembled Pili in Gram-Positive Bacteria

Chang, C., Ramirez, N. A., Bhat, A. H., Nguyen, M. T., Kumari, P., Ton-That, H., Das, A., & Ton‐That, H. (2024) · Annual Review of Microbiology · doi:10.1146/annurev-micro-112123-100908 · Cited by 11

Purification, characterization, and crystallization of the adhesive domain of SdrD from Staphylococcus aureus

Zhang, L., Xiang, H., Gao, J., Hu, J., Miao, S., Wang, L., Deng, X., & Li, S. (2009) · Protein Expression and Purification · doi:10.1016/j.pep.2009.09.007 · Cited by 11

Dysregulation of the endothelium followingStaphylococcus aureusinfection

Kerrigan, S. W., & McDonnell, C. J. (2015) · Biochemical Society Transactions · doi:10.1042/bst20140309 · Cited by 11

Immunization Against Staphylococcus aureus Infections

Barie, P. S., Narayan, M., & Sawyer, R. G. (2018) · Surgical Infections · doi:10.1089/sur.2018.263 · Cited by 11

Streptococcus pneumoniae binds collagens and C1q via the SSURE repeats of the PfbB adhesin

Gaetano, G. V. D., Coppolino, F., Lentini, G., Famà, A., Cullotta, C., Raffaele, I., Motta, C., Teti, G., Speziale, P., Pietrocola, G., et al. (2022) · Molecular Microbiology · doi:10.1111/mmi.14920 · Cited by 11

Solution structure of a bacterial immunoglobulin‐like domain of the outer membrane protein ( L ig B ) from L eptospira

Mei, S., Zhang, J., Zhang, X., & Tu, X. (2014) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.24723 · Cited by 11

Mycobacterial laminin-binding histone-like protein mediates collagen-dependent cytoadherence

Dias, A. A., Raze, D., de Lima, C. S., Marques, M. A. M., Drobecq, H., Debrie, A., Ribeiro-Guimarães, M. L., Biet, F., & Pessolani, M. C. V. (2012) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/s0074-02762012000900025 · Cited by 11

Quantification of Staphylococcus aureus Adhesion to Equine Bone Surfaces Passivated with Plasmalyte™ and Hyperimmune Plasma

Bauer, S. M., Santschi, E. M., Fialkowski, J. P., Clayton, M. K., & Proctor, R. A. (2004) · Veterinary Surgery · doi:10.1111/j.1532-950x.2004.04054.x · Cited by 11

Strategies to prevent infections associated with cardiovascular implantable electronic devices

Palraj, R., Farid, S., & Sohail, M. R. (2017) · Expert Review of Medical Devices · doi:10.1080/17434440.2017.1322506 · Cited by 11

The role of the msaABCR operon in implant-associated chronic osteomyelitis in Staphylococcus aureus USA300 LAC

Sahukhal, G. S., Tucci, M. A., Benghuzzi, H., Wilson, G. A., & Elasri, M. O. (2020) · BMC Microbiology · doi:10.1186/s12866-020-01964-8 · Cited by 11

Complicated Urinary Tract Infections due to Catheters

O’May, G. A., Jacobsen, S. M., Stickler, D. J., Mobley, H. L. T., & Shirtliff, M. E. (2008) · Springer series on biofilms · doi:10.1007/978-3-540-68119-9_6 · Cited by 13

Genotypic screening of atypical Staphylococcus aureus strains isolated from clinical samples for presence of selected adhesin genes

Wiśniewska, K., Garbacz, K., & Piechowicz, L. (2008) · Médecine et Maladies Infectieuses · doi:10.1016/j.medmal.2008.06.003 · Cited by 11

Tolerance of staphylococci to bactericidal antibiotics

Vaudaux, P. E., & Lew, D. P. (2006) · Injury · doi:10.1016/j.injury.2006.04.004 · Cited by 11

Molecular detection of adhesins genes and biofilm formation in methicillin resistant Staphylococcus aureus

Békir, K. (2012) · African Journal of Microbiology Research · doi:10.5897/ajmr11.1191 · Cited by 11

Associations of pathogen‐specific and host‐specific characteristics with disease outcome in patients with Staphylococcus aureus bacteremic pneumonia

Sharma‐Kuinkel, B. K., Tkaczyk, C., Bonnell, J. C., Yu, L., Tovchigrechko, A., Tabor, D. E., Park, L. P., Ruffin, F., Esser, M. T., Sellman, B. R., et al. (2019) · Clinical & Translational Immunology · doi:10.1002/cti2.1070 · Cited by 11

Identification of a Collagen Type I Adhesin of Bacteroides fragilis

Galvão, B. P. G. V., Weber, B. W., Rafudeen, M. S., Ferreira, E. D. O., Patrick, S., & Abratt, V. R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091141 · Cited by 11

Untitled work

(2003) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 11

Integrins as a bridge between bacteria and cells: key targets for therapeutic wound healing

Dong, Y., Lu, Z., & Chong, Y. (2024) · Burns & Trauma · doi:10.1093/burnst/tkae022 · Cited by 11

Quantum Dots-Based Nano-Coatings for Inhibition of Microbial Biofilms: A Mini Review

Priyadarshini, E., Rawat, K., & Bohidar, H. B. (2018) · InTech eBooks · doi:10.5772/intechopen.70785 · Cited by 10

Complete genome sequence of Ilumatobacter coccineum YM16-304T

Fujinami, S., Takarada, H., Kasai, H., Sekine, M., Omata, S., Harada, T., Fukai, R., Hosoyama, A., Horikawa, H., Kato, Y., et al. (2013) · Standards in Genomic Sciences · doi:10.4056/sigs.4007734 · Cited by 10

Distribution of pathogenic factors in Staphylococcus aureus strains isolated from intra-mammary infections in cattle and buffaloes

Singh, R. S., Kumar, R., & Yadav, B. R. (2011) · Cited by 10

Nanometric Considerations in Biofilm Formation

Fernandez-Moure, J. S., Mydłowska, A., Shin, C. S., Vella, M. A., & Kaplan, L. J. (2019) · Surgical Infections · doi:10.1089/sur.2018.237 · Cited by 10

An Introduction to the World of Microbiology and Biofilmology

Percival, S. L., Thomas, J. G., & Williams, D. W. (2010) · CRC Press eBooks · doi:10.1201/9781420079944-c1 · Cited by 10

Pathogenicity Factors in Group C and G Streptococci

Chhatwal, G. S., McMillan, D. J., & Talay, S. R. (2014) · ASM Press eBooks · doi:10.1128/9781555816513.ch17 · Cited by 10

Involvement of extracellular matrix proteins in the course of experimental paracoccidioidomycosis

González, A., Gómez, B. L., Muñoz, C., Aristizabal, B. H., Restrepo, Á., Hamilton, A. J., & Cano, L. E. (2008) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2008.00411.x · Cited by 10

The pathogenesis of Staphylococcus aureus in the trauma patient and potential future therapies

Villavicencio, R. T., & Wall, M. J. (1996) · The American Journal of Surgery · doi:10.1016/s0002-9610(96)00102-x · Cited by 10

PREVESICAL ABSCESS SECONDARY TO PUBIS SYMPHYSIS SEPTIC ARTHRITIS

Lorenzo, G., Meseguer, M. A., del Rio, P., nchez, J. S., & Rafael, L. (2000) · The Pediatric Infectious Disease Journal · doi:10.1097/00006454-200009000-00021 · Cited by 10

Binding of a peptide from a Streptococcus dysgalactiae MSCRAMM to the N‐terminal F1 module pair of human fibronectin involves both modules

Schwarz‐Linek, U., Plevin, M. J., Pickford, A. R., Höök, M., Campbell, I. D., & Potts, J. R. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)02418-8 · Cited by 10

The effect of culture conditions on the in-vitro adherence of methicillin-resistant Staphylococcus aureus

van Wamel, W. J. B., Vandenbroucke‐Grauls, C. M. J. E., Verhoef, J., & Fluit, A. C. (1998) · Journal of Medical Microbiology · doi:10.1099/00222615-47-8-705 · Cited by 10

Mixed-charge glycopolypeptides as antibacterial coatings with long-term activity

Yang, F., Shi, J. Y., Wei, Y., Gao, Q., Shen, J., Yin, L., & Tang, H. (2024) · Chinese Chemical Letters · doi:10.1016/j.cclet.2024.109746 · Cited by 9

Patient-specific effects of soluble factors from Staphylococcus aureus and Staphylococcus epidermidis biofilms on osteogenic differentiation of primary human osteoblasts

Tübel, J., Maier, E., Jegen, M., Marthen, C., Obermeier, A., Haug, A. T., Schneider, J., & Burgkart, R. (2021) · Scientific Reports · doi:10.1038/s41598-021-96719-4 · Cited by 9

Characterization of the Secreted Acid Phosphatase SapS Reveals a Novel Virulence Factor of Staphylococcus aureus That Contributes to Survival and Virulence in Mice

Ahmad-Mansour, N., Elhawy, M. I., Huc-Brandt, S., Youssouf, N., Pätzold, L., Martin, M., Wadood, N. A., Aljohmani, A., Morsli, M., Krasteva‐Christ, G., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232214031 · Cited by 9

Technology landscape and a short patentometric review for antibiofilm technologies

Speziali, M. G., Lívio, D. F., Tarabal, V. S., & Granjeiro, P. A. (2022) · World Patent Information · doi:10.1016/j.wpi.2022.102158 · Cited by 9

Inhibition of bacterial biofilms by the snake venom proteome

Khan, N. A., Amorim, F. G., Dunbar, J. P., Leonard, D., Redureau, D., Quinton, L., Dugon, M. M., & Boyd, A. (2023) · Biotechnology Reports · doi:10.1016/j.btre.2023.e00810 · Cited by 9

Disruption of Staphylococcus epidermidis biofilm formation using a targeted cationic peptide

Hofmann, C. M., Bednar, K. J., Anderson, J. M., & Marchant, R. E. (2012) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.33273 · Cited by 9

On-Off Kinetics of Engagement of FNI Modules of Soluble Fibronectin by β-Strand Addition

Ma, W., Ma, H., & Mosher, D. F. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124941 · Cited by 9

Distinct virulent network between healthcare- and community-associated Staphylococcus aureus based on proteomic analysis

He, L., Meng, H., Liu, Q., Hu, M., Wang, Y., Chen, X., Liu, X., & Li, M. (2018) · Clinical Proteomics · doi:10.1186/s12014-017-9178-5 · Cited by 9

Structural insights into the intermolecular interaction of the adhesin SdrC in the pathogenicity of Staphylococcus aureus

Wang, J., Zhang, M., Wang, M., Zang, J., Zhang, X., & Hang, T. (2021) · Acta Crystallographica Section F Structural Biology Communications · doi:10.1107/s2053230x21000741 · Cited by 9

Low Concentration of the Neutrophil Proteases Cathepsin G, Cathepsin B, Proteinase-3 and Metalloproteinase-9 Induce Biofilm Formation in Non-Biofilm-Forming Staphylococcus epidermidis Isolates

Gómez-Alonso, I. S., Martínez-García, S., Cabrera, G. B., Juárez, E., Sarabia, C., Herrera, M. T., Gómez‐Chávez, F., Sánchez‐Torres, L. E., Rodríguez–Martínez, S., Cancino-Diaz, M. E., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094992 · Cited by 9

Statistical correlation between pharyngitis and temporomandibular joint disease

Jeon, Y.-D., Lee, J., Cho, B., Rotaru, H., Kim, J. C., & Kim, S. (2005) · Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology · doi:10.1016/j.tripleo.2004.10.007 · Cited by 9

Adhesion of Streptococcus gallolyticus strains to extracellular matrix proteins

Vanrobaeys, M., Haesebrouck, F., Ducatelle, R., & Herdt, P. D. (2000) · Veterinary Microbiology · doi:10.1016/s0378-1135(00)00180-2 · Cited by 9

Effect of pH, salt and chemical rinses on bacterial attachment to extracellular matrix proteins

Zulfakar, S. S., White, J. D., Ross, T., & Tamplin, M. L. (2013) · Food Microbiology · doi:10.1016/j.fm.2013.01.010 · Cited by 9

Microbial exposure early in life regulates airway inflammation in mice after infection with Streptococcus pneumoniae with enhancement of local resistance

Yasuda, Y., Matsumura, Y., Kasahara, K., Ouji, N., Sugiura, S., Mikasa, K., & Kita, E. (2009) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00193.2009 · Cited by 9

Steered molecular dynamics study reveals insights into the function of the repetitive B region of collagen- and fibrinogen-binding MSCRAMMs

Beulin, D. S. J., & Ponnuraj, K. (2016) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2016.1152566 · Cited by 9

The Safety of Probiotics in Foods in Europe and Its Legislation

Vankerckhoven, V., Swings, J., Vancanneyt, M., Goossens, H., Ouwehand, A. C., Lähteenmäki, A., & Huys, G. R. B. (2005) · CRC Press eBooks · doi:10.1201/9781420027570.ch18 · Cited by 9

Assessment of Cpa, Scl1 and Scl2 in clinical group A streptococcus isolates and patients from north India: an evaluation of the host pathogen interaction

Chaudhary, P., Kumar, R., Sagar, V., Sarkar, S., Singh, R., Ghosh, S., Singh, S., & Chakraborti, A. (2017) · Research in Microbiology · doi:10.1016/j.resmic.2017.09.002 · Cited by 9

Learning From Controversy: Contemporary Surgical Management of Aortic Valve Endocarditis

Nappi, F., Singh, S. S. A., & Timofeeva, I. (2020) · Clinical Medicine Insights Cardiology · doi:10.1177/1179546820960729 · Cited by 9

Staphylococcal Enterotoxins and Toxic Shock Syndrome Toxin‐1 and Their Association among Bacteremic and Infective Endocarditis Patients in Egypt

Elsherif, H. M., Helal, Z. H., El‐Ansary, M. R., Fahmy, Z. A., Eltayeb, W. N., Radwan, S., & Aboshanab, K. M. (2020) · BioMed Research International · doi:10.1155/2020/6981095 · Cited by 9

The Staphylococcus aureus Map protein is an immunomodulator that interferes with T cell–mediated responses

Lee, L. Y., Miyamoto, Y., McIntyre, B. W., Höök, M., McCrea, K. W., McDevitt, D., & Brown, E. L. (2002) · Journal of Clinical Investigation · doi:10.1172/jci200216318 · Cited by 9

Staphylococcus aureus infection of human primary keratinocytes

Aufiero, B. M., Duanmu, Z., Guo, M., Meduri, N. B., Falkow, S., & Murakawa, G. J. (2004) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2004.08.009 · Cited by 9

Staphylococcal Infections

Orscheln, R. C., Shinefield, H. R., & Geme, J. W. S. (2006) · Elsevier eBooks · doi:10.1016/b0-72-160537-0/50019-0 · Cited by 10

In silico testing to identify compounds that inhibit ClfA and ClfB binding to the host for the formulation of future drugs against Staphylococcus aureus colonization and infection

Singh, S. K., Bhattacharjee, M., Unni, B., Kashyap, R. S., Malik, A., Akhtar, S., & Fatima, S. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1422500 · Cited by 11

How does Staphylococcus aureus successfully colonize the nasal cavity

Chen, P., Ma, Y., & Xiao, Y. (2025) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2025.2486171 · Cited by 8

Antibacterial and antibiofilm efficacies of calamansi essential oil on Staphylococcus aureus and its application in chicken preservation

Zhu, S., Zhang, H., Yang, M., Chen, Y., Hao, Y., Liu, L., & Kang, J. (2025) · Food Control · doi:10.1016/j.foodcont.2025.111556 · Cited by 8

Preventive Immunology for Livestock and Zoonotic Infectious Diseases in the One Health Era: From Mechanistic Insights to Innovative Interventions

Marzouk, E., & Alajaji, A. I. (2025) · Veterinary Sciences · doi:10.3390/vetsci12101014 · Cited by 14

PERANAN PROTEIN ADHESI MATRIKS EKSTRASELULAR DALAM PATOGENITAS BAKTERI STAPHYLOCOCCUS AUREUS

Husna, C. A. (2018) · AVERROUS Jurnal Kedokteran dan Kesehatan Malikussaleh · doi:10.29103/averrous.v4i2.1041 · Cited by 8

The crafty opponent: the defense systems of Staphylococcus aureus and response measures

Hou, H., Yang, L., Jin, Y., Chen, S., Long, J., Duan, G., & Yang, H. (2022) · Folia Microbiologica · doi:10.1007/s12223-022-00954-9 · Cited by 8

Prospecting Potential Inhibitors of Sortase A from Enterococcus faecalis: A Multidrug Resistant Bacteria, through In-silico and In-vitro Approaches

Das, S., Vijay Kumar, H. S., Pal, S. K., Srivastava, V. K., Jyoti, A., Kumar, S., & Kaushik, S. (2019) · Protein and Peptide Letters · doi:10.2174/0929866527666191227143048 · Cited by 8

Factor XIIIa Mediated Attachment of S. aureus Fibronectin-Binding Protein A (FnbA) to Fibrin: Identification of Gln103 as a Major Cross-Linking Site

Elena, S., Nuñez, L., Baker, S. M., & Matsuka, Y. V. (2006) · Biochemistry · doi:10.1021/bi0521240 · Cited by 8

Assessment of Potential Risk Factors and Related Properties of Clinical, Faecal and Dairy Bifidobacterium Isolates

Ouwehand, A. C., Saxelin, M., & Salminen, S. (2004) · Bioscience and Microflora · doi:10.12938/bifidus.23.37 · Cited by 8

Cell Wall-Anchored Surface Proteins and Lipoproteins of Gram-Positive Bacteria

Mazmanian, S. K., & Schneewind, O. (2014) · ASM Press eBooks · doi:10.1128/9781555817992.ch6 · Cited by 8

Is it feasible to control pathogen infection by competitive binding of probiotics to the host?

Fukuda, K. (2017) · Virulence · doi:10.1080/21505594.2017.1382798 · Cited by 8

Antimicrobial resistance: Biofilms, small colony variants, and intracellular bacteria

Straub, J., Baertl, S., Verheul, M., Walter, N., Wong, R. M. Y., Alt, V., & Rupp, M. (2024) · Injury · doi:10.1016/j.injury.2024.111638 · Cited by 7

Bacterial and bacterial derivatives-based drug delivery systems: a novel approach for treating central nervous system disorders

Gao, S., Li, X., & Han, B. (2024) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2024.2444364 · Cited by 7

Biofilms and antibiotic resistance profile of Enterococcus faecalis in selected dairy cattle farm environments in Bangladesh

Fahim, N. A. I., Rana, M. L., Hasan, M. F., Salam, S., Masud, R. I., Huda, N., Saha, S., & Rahman, M. T. (2025) · PLoS ONE · doi:10.1371/journal.pone.0323667 · Cited by 8

Trimeric Autotransporter DsrA Is a Major Mediator of Fibrinogen Binding in Haemophilus ducreyi

Fusco, W. G., Elkins, C. A., & Leduc, I. (2013) · Infection and Immunity · doi:10.1128/iai.00743-13 · Cited by 7

The crystal structure of the ligand‐binding region of serine‐glutamate repeat containing protein A (SgrA) of Enterococcus faecium reveals a new protein fold: functional characterization and insights into its adhesion function

Nagarajan, R., Hendrickx, A. P. A., & Ponnuraj, K. (2016) · FEBS Journal · doi:10.1111/febs.13792 · Cited by 7

Biochemical characterization of PE_PGRS61 family protein of Mycobacterium tuberculosis H37Rv reveals the binding ability to fibronectin.

Monu, M., & Meena, L. S. (2016) · PubMed Central · doi:10.22038/ijbms.2016.7736 · Cited by 7

Crystal Structure of an Invasivity-Associated Domain of SdrE in S. aureus

Luo, M., Zhang, X., Zhang, S., Zhang, H., Yang, W. J., Zhu, Z., Chen, K., Bai, L., Wei, J., Huang, A., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0168814 · Cited by 7

Collagen adhesin–nanoparticle interaction impairs adhesin's ligand binding mechanism

Aribam, S. D., Ogawa, Y., Shimoji, Y., Balakumar, S., & Ponnuraj, K. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.04.006 · Cited by 7

Expression, purification, crystallization and preliminary X-ray diffraction studies of the human keratin 4-binding domain of serine-rich repeat protein 1 from Streptococcus agalactiae

Sundaresan, R., Samen, U., & Ponnuraj, K. (2011) · Acta Crystallographica Section F Structural Biology and Crystallization Communications · doi:10.1107/s1744309111040413 · Cited by 7

Membrane proteins of Pseudoalteromonas tunicata during the transition from planktonic to extracellular matrix‐adherent state

Hoke, D. E., Zhang, K., Egan, S., Hatfaludi, T., Buckle, A. M., & Adler, B. (2011) · Environmental Microbiology Reports · doi:10.1111/j.1758-2229.2011.00246.x · Cited by 7

Superantigen types inStaphylococcus aureus isolated from patients with cystic fibrosis

Bania, J., Dąbrowska, A., Różalska, B., Sadowska, B., Więckowska-Szakiel, M., Korzekwa, K., Žarczyńska, A., Bystroń, J., Chrzanowska, J., & Molenda, J. (2006) · Folia Microbiologica · doi:10.1007/bf02931628 · Cited by 7

Binding of Leptospira to extracellular matrix proteins.

Chirathaworn, C., Patarakul, K., Saksit, V., & Poovorawan, Y. (2007) · PubMed · Cited by 7

Escaping ESKAPE: A chalcone perspective

Uchil, A., Murali, T. S., & Nayak, R. (2021) · Results in Chemistry · doi:10.1016/j.rechem.2021.100229 · Cited by 7

Pathogenicity Factors in Group C and G Streptococci

Turner, C. E., Bubba, L., & Efstratiou, A. (2019) · ASM Press eBooks · doi:10.1128/9781683670131.ch16 · Cited by 7

Designing Antibacterial Surfaces for Biomedical Implants

Pham, V., Bhadra, C. M., Truong, V. K., Crawford, R. J., & Ivanova, E. P. (2015) · Springer eBooks · doi:10.1007/978-3-319-18594-1_6 · Cited by 7

Role of host cell integrins in the microsporidium Encephalitozoon intestinalis adherence and infection in vitro

Leonard, C. A., & Hayman, J. R. (2017) · FEMS Microbiology Letters · doi:10.1093/femsle/fnx169 · Cited by 7

The redox potential interferes with the expression of laminin binding molecules in Bacteroides fragilis

Ferreira, E. D. O., Yates, E. A., Goldner, M., Vommaro, R. C., Filho, F. C. E. S., Petrópolis, D. B., & Domingues, R. M. C. P. (2008) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/s0074-02762008000700010 · Cited by 7

Binding of extracellular matrix proteins by lactobacilli

Štyriak, I., Žatkovič, B., & Marsálková, S. (2001) · Folia Microbiologica · doi:10.1007/bf02825894 · Cited by 7

Targeted delivery of vancomycin to Staphylococcus epidermidis biofilms using a fibrinogen‐derived peptide

Hofmann, C. M., Anderson, J. M., & Marchant, R. E. (2012) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.34166 · Cited by 7

Report of the national heart, lung and blood institute-national institute of allergy and infectious diseases working group on antimicrobial strategies and cardiothoracic surgery

Lowy, F. D., Waldhausen, J. A., Miller, M. A., Sopko, G. S., Rosenberg, Y., & Skarlatos, S. I. (2004) · American Heart Journal · doi:10.1016/j.ahj.2003.08.016 · Cited by 7

Monosaccharide inhibition of adherence by Pseudomonas aeruginosa to canine corneocytes

McEwan, N. A., Rème, C. A., Gatto, H., & Nuttall, T. J. (2008) · Veterinary Dermatology · doi:10.1111/j.1365-3164.2008.00678.x · Cited by 7

An Introduction to the World of Microbiology and Biofilmology

Percival, S., & Cutting, K. (2010) · CRC Press eBooks · doi:10.1201/9781420079944-5 · Cited by 7

Bacterial Adhesion

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