| 1 | Precursor of H-type II histo-blood group antigen and subterminal sialic acids on gangliosides are significantly implicated in cell entry and infection by a porcine P[11] rotavirus | 4.1 | 2 | Citations (PDF) |
| 2 | Infection Studies with Airway Organoids from Carollia perspicillata Indicate That the Respiratory Epithelium Is Not a Barrier for Interspecies Transmission of Influenza Viruses. | 2.4 | 21 | Citations (PDF) |
| 3 | Canine Distemper Virus Alters Defense Responses in an Ex Vivo Model of Pulmonary Infection | 2.3 | 6 | Citations (PDF) |
| 4 | Infection of porcine enteroids and 2D differentiated intestinal epithelial cells with rotavirus A to study cell tropism and polarized immune response | 4.1 | 17 | Citations (PDF) |
| 5 | Overcoming the Barrier of the Respiratory Epithelium during Canine Distemper Virus Infection. | 3.3 | 15 | Citations (PDF) |
| 6 | Primary harbour seal (Phoca vitulina) airway epithelial cells show high susceptibility to infection by a seal-derived influenza A virus (H5N8) | 1.3 | 3 | Citations (PDF) |
| 7 | Phenotypic and Transcriptional Changes of Pulmonary Immune Responses in Dogs Following Canine Distemper Virus Infection | 3.3 | 7 | Citations (PDF) |
| 8 | Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV) | 3.6 | 22 | Citations (PDF) |
| 9 | Time-dependent viral interference between influenza virus and coronavirus in the infection of differentiated porcine airway epithelial cells | 3.6 | 24 | Citations (PDF) |
| 10 | Infection of bovine well-differentiated airway epithelial cells by Pasteurella multocida: actions and counteractions in the bacteria–host interactions | 2.2 | 11 | Citations (PDF) |
| 11 | Surveillance of European Domestic Pig Populations Identifies an Emerging Reservoir of Potentially Zoonotic Swine Influenza A Viruses | 12.5 | 121 | Citations (PDF) |
| 12 | The Cell Tropism of Porcine Respiratory Coronavirus for Airway Epithelial Cells Is Determined by the Expression of Porcine Aminopeptidase N | 2.3 | 15 | Citations (PDF) |
| 13 | Avian Influenza A Virus Infects Swine Airway Epithelial Cells without Prior Adaptation | 2.3 | 22 | Citations (PDF) |
| 14 | SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease InhibitorCell, 2020, 181, 271-280.e8 | 24.4 | 15,101 | Citations (PDF) |
| 15 | Trypsin promotes porcine deltacoronavirus mediating cell-to-cell fusion in a cell type-dependent manner | 4.1 | 41 | Citations (PDF) |
| 16 | Fusogenicity of the Ghana Virus (Henipavirus: Ghanaian bat henipavirus) Fusion Protein is Controlled by the Cytoplasmic Domain of the Attachment Glycoprotein | 2.3 | 16 | Citations (PDF) |
| 17 | Viral Coinfection Replaces Effects of Suilysin on Streptococcus suis Adherence to and Invasion of Respiratory Epithelial Cells Grown under Air-Liquid Interface Conditions. | 2.0 | 16 | Citations (PDF) |
| 18 | Infection Studies in Pigs and Porcine Airway Epithelial Cells Reveal an Evolution of A(H1N1)pdm09 Influenza A Viruses Toward Lower Virulence | 2.3 | 15 | Citations (PDF) |
| 19 | Highly Pathogenic Avian Influenza A(H5N8) Virus in Gray Seals, Baltic Sea. | 2.9 | 74 | Citations (PDF) |
| 20 | A newly developed tetraplex real-time RT-PCR for simultaneous screening of influenza virus types A, B, C and D | 2.3 | 39 | Citations (PDF) |
| 21 | Sialic acid-dependent interaction of group B streptococci with influenza virus-infected cells reveals a novel adherence and invasion mechanism | 0.7 | 9 | Citations (PDF) |
| 22 | People also looked at | 2.9 | 17 | Citations (PDF) |
| 23 | Increased virulence of a PB2/HA mutant of an avian H9N2 influenza strain after three passages in porcine differentiated airway epithelial cells | 1.6 | 6 | Citations (PDF) |
| 24 | The Hemagglutinin of Bat-Associated Influenza Viruses Is Activated by TMPRSS2 for pH-Dependent Entry into Bat but Not Human Cells | 1.6 | 23 | Citations (PDF) |
| 25 | The differentiated airway epithelium infected by influenza viruses maintains the barrier function despite a dramatic loss of ciliated cells | 2.8 | 105 | Citations (PDF) |
| 26 | Efficient suilysin-mediated invasion and apoptosis in porcine respiratory epithelial cells after streptococcal infection under air-liquid interface conditions | 2.8 | 44 | Citations (PDF) |
| 27 | Mycoplasma hyopneumoniae does not affect the interferon-related anti-viral response but predisposes the pig to a higher level of inflammation following swine influenza virus infection | 2.2 | 17 | Citations (PDF) |
| 28 | Recombinant mumps viruses expressing the batMuV fusion glycoprotein are highly fusion active and neurovirulent | 2.2 | 5 | Citations (PDF) |
| 29 | Porcine epidemic diarrhea virus inhibits dsRNA-induced interferon-β production in porcine intestinal epithelial cells by blockade of the RIG-I-mediated pathway | 2.3 | 67 | Citations (PDF) |
| 30 | Porcine aminopeptidase N mediated polarized infection by porcine epidemic diarrhea virus in target cells | 1.7 | 36 | Citations (PDF) |
| 31 | Functional properties and genetic relatedness of the fusion and hemagglutinin-neuraminidase proteins of a mumps virus-like bat virus. | 2.6 | 17 | Citations (PDF) |
| 32 | Analysis of Ebola Virus Entry Into Macrophages. | 2.3 | 54 | Citations (PDF) |
| 33 | Precision-cut intestinal slices as a culture system to analyze the infection of differentiated intestinal epithelial cells by avian influenza viruses | 1.0 | 13 | Citations (PDF) |
| 34 | Sialic acid-dependent interactions between influenza viruses and Streptococcus suis affect the infection of porcine tracheal cells | 2.2 | 28 | Citations (PDF) |
| 35 | The cell receptor level is reduced during persistent infection with influenza C virus | 1.1 | 7 | Citations (PDF) |
| 36 | A lysine-methionine exchange in a coronavirus surface protein transforms a retention motif into an endocytosis signal | 1.3 | 3 | Citations (PDF) |
| 37 | Differences in the tissue tropism to chicken oviduct epithelial cells between avian coronavirus IBV strains QX and B1648 are not related to the sialic acid binding properties of their spike proteins | 2.2 | 37 | Citations (PDF) |
| 38 | Characterization of African bat henipavirus GH-M74a glycoproteins | 2.2 | 27 | Citations (PDF) |
| 39 | Attachment protein G of an African bat henipavirus is differentially restricted in chiropteran and nonchiropteran cells. | 2.6 | 14 | Citations (PDF) |
| 40 | Three viruses of the bovine respiratory disease complex apply different strategies to initiate infection | 2.2 | 67 | Citations (PDF) |
| 41 | Innate immune response to a H3N2 subtype swine influenza virus in newborn porcine trachea cells, alveolar macrophages, and precision-cut lung slices | 2.2 | 50 | Citations (PDF) |
| 42 | Infection of differentiated airway epithelial cells from caprine lungs by viruses of the bovine respiratory disease complex | 1.6 | 10 | Citations (PDF) |
| 43 | Characterization of the Sialic Acid Binding Activity of Influenza A Viruses Using Soluble Variants of the H7 and H9 Hemagglutinins | 1.6 | 22 | Citations (PDF) |
| 44 | Phages bearing affinity peptides to severe acute respiratory syndromes-associated coronavirus differentiate this virus from other viruses | 2.2 | 8 | Citations (PDF) |
| 45 | Replication characteristics of swine influenza viruses in precision-cut lung slices reflect the virulence properties of the viruses | 2.2 | 38 | Citations (PDF) |
| 46 | Highly diversified coronaviruses in neotropical bats | 2.2 | 56 | Citations (PDF) |
| 47 | Sialic Acid Binding Properties of Soluble Coronavirus Spike (S1) Proteins: Differences between Infectious Bronchitis Virus and Transmissible Gastroenteritis Virus | 2.3 | 33 | Citations (PDF) |
| 48 | Differential Sensitivity of Bat Cells to Infection by Enveloped RNA Viruses: Coronaviruses, Paramyxoviruses, Filoviruses, and Influenza Viruses | 1.6 | 94 | Citations (PDF) |
| 49 | Bats host major mammalian paramyxoviruses | 11.4 | 583 | Citations (PDF) |
| 50 | Infection of Differentiated Porcine Airway Epithelial Cells by Influenza Virus: Differential Susceptibility to Infection by Porcine and Avian Viruses | 1.6 | 54 | Citations (PDF) |
| 51 | The sialic acid binding activity of the S protein facilitates infection by porcine transmissible gastroenteritis coronavirus | 2.3 | 39 | Citations (PDF) |
| 52 | Action Mechanisms of Lithium Chloride on Cell Infection by Transmissible Gastroenteritis Coronavirus | 1.6 | 50 | Citations (PDF) |
| 53 | Cholesterol is important for a post-adsorption step in the entry process of transmissible gastroenteritis virus | 2.7 | 31 | Citations (PDF) |
| 54 | Differential sensitivity of well-differentiated avian respiratory epithelial cells to infection by different strains of infectious bronchitis virus. | 2.6 | 26 | Citations (PDF) |
| 55 | Cholesterol Dependence of Pseudorabies Herpesvirus Entry | 1.7 | 19 | Citations (PDF) |
| 56 | Comparative analysis of the sialic acid binding activity and the tropism for the respiratory epithelium of four different strains of avian infectious bronchitis virus | 1.6 | 47 | Citations (PDF) |
| 57 | Infection of the tracheal epithelium by infectious bronchitis virus is sialic acid dependent | 1.8 | 61 | Citations (PDF) |
| 58 | Importance of cholesterol-rich membrane microdomains in the interaction of the S protein of SARS-coronavirus with the cellular receptor angiotensin-converting enzyme 2 | 1.7 | 145 | Citations (PDF) |
| 59 | Importance of cholesterol for infection of cells by transmissible gastroenteritis virus | 2.1 | 66 | Citations (PDF) |
| 60 | The spike protein of infectious bronchitis virus is retained intracellularly by a tyrosine motif. | 2.6 | 32 | Citations (PDF) |
| 61 | Canine distemper virus infection requires cholesterol in the viral envelope. | 2.6 | 45 | Citations (PDF) |
| 62 | Select what you need: A comparative evaluation of the advantages and limitations of frequently used expression systems for foreign genes | 2.9 | 304 | Citations (PDF) |
| 63 | Sialic acids as receptor determinants for coronaviruses | 1.9 | 150 | Citations (PDF) |
| 64 | A Novel Sorting Signal for Intracellular Localization Is Present in the S Protein of a Porcine Coronavirus but Absent from Severe Acute Respiratory Syndrome-associated Coronavirus* | 1.4 | 51 | Citations (PDF) |
| 65 | Respiratory syncytial virus (RSV) fusion protein subunit F2, not attachment protein G, determines the specificity of RSV infection. | 2.6 | 67 | Citations (PDF) |
| 66 | Virokinin, a Bioactive Peptide of the Tachykinin Family, Is Released from the Fusion Protein of Bovine Respiratory Syncytial Virus* | 1.4 | 41 | Citations (PDF) |
| 67 | Binding of transmissible gastroenteritis coronavirus to brush border membrane sialoglycoproteins. | 2.6 | 58 | Citations (PDF) |
| 68 | Binding of transmissible gastroenteritis coronavirus to cell surface sialoglycoproteins. | 2.6 | 47 | Citations (PDF) |
| 69 | Cleavage at the furin consensus sequence RAR/KR(109) and presence of the intervening peptide of the respiratory syncytial virus fusion protein are dispensable for virus replication in cell culture. | 2.6 | 44 | Citations (PDF) |
| 70 | Comparison of the sialic acid binding activity of transmissible gastroenteritis coronavirus and K99 | 2.1 | 15 | Citations (PDF) |
| 71 | A Single Amino Acid Change in the Cytoplasmic Domains of Measles Virus Glycoproteins H and F Alters Targeting, Endocytosis, and Cell Fusion in Polarized Madin-Darby Canine Kidney Cells* | 1.4 | 47 | Citations (PDF) |
| 72 | The hemagglutinin of canine distemper virus determines tropism and cytopathogenicity. | 2.6 | 171 | Citations (PDF) |
| 73 | Sialic acid binding activity of transmissible gastroenteritis coronavirus affects sedimentation behavior of virions and solubilized glycoproteins. | 2.6 | 20 | Citations (PDF) |
| 74 | Proteolytic Activation of Respiratory Syncytial Virus Fusion ProteinCLEAVAGE AT TWO FURIN CONSENSUS SEQUENCES* | 1.4 | 143 | Citations (PDF) |
| 75 | Importance of the Carboxyl-terminal FTSL Motif of Membrane Cofactor Protein for Basolateral Sorting and EndocytosisPOSITIVE AND NEGATIVE MODULATION BY SIGNALS INSIDE AND OUTSIDE THE CYTOPLASMIC TAIL* | 1.4 | 23 | Citations (PDF) |
| 76 | Polarized budding of measles virus is not determined by viral surface glycoproteins. | 2.6 | 61 | Citations (PDF) |
| 77 | Membrane Cofactor Protein (CD46) Is a Basolateral Protein That Is Not EndocytosedIMPORTANCE OF THE TETRAPEPTIDE FTSL AT THE CARBOXYL TERMINUS* | 1.4 | 48 | Citations (PDF) |
| 78 | Transfer of an Esterase-Resistant Receptor Analog to the Surface of Influenza C Virions Results in Reduced Infectivity Due to Aggregate Formation | 1.7 | 15 | Citations (PDF) |
| 79 | Two Different Cytoplasmic Tails Direct Isoforms of the Membrane Cofactor Protein (CD46) to the Basolateral Surface of Madin-Darby Canine Kidney Cells* | 1.4 | 37 | Citations (PDF) |
| 80 | Virus entry into a polarized epithelial cell line (MDCK): similarities and dissimilarities between influenza C virus and bovine coronavirus | 2.2 | 15 | Citations (PDF) |
| 81 | Membrane Cofactor Protein with Different Types of -Glycans Can Serve As Measles Virus Receptor | 1.7 | 20 | Citations (PDF) |
| 82 | Identification of a 40-kDa Cell Surface Sialoglycoprotein with the Characteristics of a Major Influenza C Virus Receptor in a Madin-Darby Canine Kidney Cell Line (∗) | 1.4 | 58 | Citations (PDF) |
| 83 | The catalytic triad of the influenza C virus glycoprotein HEF esterase: characterization by site-directed mutagenesis and functional analysis | 2.2 | 22 | Citations (PDF) |
| 84 | A Synthetic Sialic Acid Analog That Is Resistant to the Receptor-Destroying Enzyme Can Be Used by Influenza C Virus as a Receptor Determinant for Infection of Cells | 1.5 | 8 | Citations (PDF) |
| 85 | Post-translational Folding of the Influenza C Virus Glycoprotein HEF: Defective Processing in Cells Expressing the Cloned Gene | 2.2 | 14 | Citations (PDF) |
| 86 | Modification of sialic acids by 9-O-acetylation is detected in human leucocytes using the lectin property of influenza C virus. | 1.8 | 38 | Citations (PDF) |
| 87 | Persistent influenza C virus possesses distinct functional properties due to a modified HEF glycoprotein | 2.2 | 12 | Citations (PDF) |
| 88 | Binding of measles virus to membrane cofactor protein (CD46): importance of disulfide bonds and N-glycans for the receptor function. | 2.6 | 46 | Citations (PDF) |
| 89 | Structural and Functional Analysis of the Surface Protein of Human Coronavirus OC43 | 1.7 | 114 | Citations (PDF) |
| 90 | A sialic acid analogue acting as a receptor determinant for binding but not for infection by influenza C virus | 1.9 | 23 | Citations (PDF) |
| 91 | Surface glycoprotein of influenza C virus: Inactivation and restoration of the acetylesterase activity on nitrocellulose | 2.1 | 1 | Citations (PDF) |
| 92 | Bovine coronavirus uses N-acetyl-9-O-acetylneuraminic acid as a receptor determinant to initiate the infection of cultured cells | 2.2 | 101 | Citations (PDF) |
| 93 | Neuraminidase treatment of avian infectious bronchitis coronavirus reveals a hemagglutinating activity that is dependent on sialic acid-containing receptors on erythrocytes | 1.7 | 71 | Citations (PDF) |
| 94 | A single point mutation of the influenza C virus glycoprotein (HEF) changes the viral receptor-binding activity | 1.7 | 35 | Citations (PDF) |
| 95 | A synthetic sialic acid analogue is recognized by influenza C virus as a receptor determinant but is resistant to the receptor-destroying enzyme. | 1.4 | 47 | Citations (PDF) |
| 96 | Isolated HE-protein from hemagglutinating encephalomyelitis virus and bovine coronavirus has receptor-destroying and receptor-binding activity | 1.7 | 95 | Citations (PDF) |
| 97 | Monoclonal antibodies differentiate between the haemagglutinating and the receptor-destroying activities of bovine coronavirus | 2.2 | 18 | Citations (PDF) |
| 98 | High level transient expression of the murine coronavirus haemagglutinin-esterase | 2.2 | 19 | Citations (PDF) |
| 99 | The S protein of bovine coronavirus is a hemagglutinin recognizing 9-O-acetylated sialic acid as a receptor determinant. | 2.6 | 181 | Citations (PDF) |
| 100 | The hemagglutinating glycoproteins of influenza B and C viruses are acylated with different fatty acids | 1.7 | 49 | Citations (PDF) |
| 101 | Hemagglutinating encephalomyelitis virus attaches to -acetyl-9--acetylneuraminic acid-containing receptors on erythrocytes: comparison with bovine coronavirus and influenza C virus | 2.1 | 60 | Citations (PDF) |
| 102 | Isolation and Characterization of Sialate 9(4)-O-Acetylesterase from Influenza C Virus | 1.3 | 33 | Citations (PDF) |
| 103 | Analysis of functional epitopes on the glycoprotein of influenza C virus | 2.1 | 1 | Citations (PDF) |
| 104 | The Glycoprotein of Influenza C Virus Is the Haemagglutinin, Esterase and Fusion Factor | 2.2 | 93 | Citations (PDF) |
| 105 | N-Acetyl-9-0-acetylneuraminic Acid, the Receptor Determinant for Influenza C Virus, is a Differentiation Marker on Chicken Erythrocytes | 1.3 | 43 | Citations (PDF) |
| 106 | The surface receptor is a major determinant of the cell tropism of influenza C virus | 1.7 | 71 | Citations (PDF) |
| 107 | Influenza C virus uses 9-O-acetyl-N-acetylneuraminic acid as a high affinity receptor determinant for attachment to cells. | 1.4 | 281 | Citations (PDF) |
| 108 | The receptor‐destroying enzyme of influenza C virus is neuraminate‐O‐acetylesterase. | 5.4 | 218 | Citations (PDF) |
| 109 | Neuraminic acid is involved in the binding of influenza C virus to erythrocytes | 1.7 | 41 | Citations (PDF) |
| 110 | Rat α macroglobulin inhibits hemagglutination by influenza C virus | 2.1 | 22 | Citations (PDF) |
| 111 | Posttranslational modification and intracellular transport of mumps virus glycoproteins. | 2.6 | 27 | Citations (PDF) |
| 112 | Synthesis of mumps virus polypeptides in infected vero cells | 1.7 | 48 | Citations (PDF) |
| 113 | Isolation and structural analysis of influenza C virion glycoproteins | 1.7 | 74 | Citations (PDF) |
| 114 | Gene products of influenza C virus | 1.2 | 16 | Citations (PDF) |
| 115 | A precursor glycoprotein in influenza C virus | 1.7 | 67 | Citations (PDF) |
| 116 | Carbohydrate components of influenza C virions. | 2.6 | 21 | Citations (PDF) |
| 117 | Efficient replication of avian, porcine and human influenza A viruses in well-differentiated bovine airway epithelial cells | 4.1 | 3 | Citations (PDF) |
