| scholarly article | Q13442814 |
| P2093 | author name string | J R Scott | |
| V A Fischetti | |||
| K F Jones | |||
| P2860 | cites work | Persistence of type-specific antibodies in man following infection with group A streptococci | Q33970090 |
| Current knowledge of type-specific M antigens of group A streptococci | Q33972503 | ||
| STUDIES ON THE BIOLOGY OF STREPTOCOCCUS : I. ANTIGENIC RELATIONSHIPS BETWEEN STRAINS OF STREPTOCOCCUS HAEMOLYTICUS | Q34019938 | ||
| TYPE-SPECIFIC ANTIGENS, M AND T, OF MATT AND GLOSSY VARIANTS OF GROUP A HEMOLYTIC STREPTOCOCCI | Q34019948 | ||
| Lysis of grouped and ungrouped streptococci by lysozyme | Q34161494 | ||
| Streptococcal M protein: alpha-helical coiled-coil structure and arrangement on the cell surface | Q35451738 | ||
| THE LYSIS OF CELL WALLS OF GROUP A STREPTOCOCCI BY STREPTOMYCES ALBUS ENZYME TREATED WITH DIISOPROPYL FLUOROPHOSPHATE. CHARACTERISTICS OF THE LYTIC REACTION AND THE SOLUBLE CELL WALL FRAGMENTS. | Q36267466 | ||
| Group a streptococcal antigens cross-reactive with myocardium. Purification of heart-reactive antibody and isolation and characterization of the streptococcal antigen | Q36335754 | ||
| Tropomyosin-like seven residue periodicity in three immunologically distinct streptococal M proteins and its implications for the antiphagocytic property of the molecule | Q36343372 | ||
| Gonococcal pilus subunit size heterogeneity correlates with transitions in colony piliation phenotype, not with changes in colony opacity | Q36348176 | ||
| Streptococcal M6 protein expressed in Escherichia coli. Localization, purification, and comparison with streptococcal-derived M protein | Q36348692 | ||
| The multiple molecular structure of the M proteins of group A streptococci | Q36379227 | ||
| Immunochemical analysis of intact M protein secreted from cell wall-less streptococci | Q36422079 | ||
| Amino acid sequence and physicochemical similarities between streptococcal M protein and mammalian tropomyosin | Q37339264 | ||
| Pilus genes of Neisseria gonorrheae: chromosomal organization and DNA sequence | Q37570924 | ||
| Repeating covalent structure of streptococcal M protein | Q37590018 | ||
| Presence of two distinct regions in the coiled-coil structure of the streptococcal Pep M5 protein: relationship to mammalian coiled-coil proteins and implications to its biological properties | Q37677979 | ||
| Relationship of M protein genes in group A streptococci | Q37680923 | ||
| Lysis of Streptococcus mutans cells with mutanolysin, a lytic enzyme prepared from a culture liquor of Streptomyces globisporus 1829 | Q40565906 | ||
| Purification and properties of M protein extracted from group A streptococci with pepsin: covalent structure of the amino terminal region of type 24 M antigen | Q40774064 | ||
| Electron microscopic studies on streptococci. I. M antigen | Q41521427 | ||
| Location of variable and conserved epitopes among the multiple serotypes of streptococcal M protein | Q42746939 | ||
| Preparation and properties of a protein (R antigen) occurring in streptococci of group A, type 28 and in certain streptococci of other serological groups | Q42821099 | ||
| Studies on the bacteriophages of hemolytic streptococci. II. Antigens released from the streptococcal cell wall by a phage-associated lysin | Q42823062 | ||
| A rapid, sensitive method for detection of alkaline phosphatase-conjugated anti-antibody on Western blots. | Q50925449 | ||
| Genomic rearrangements correlated with antigenic variation inTrypanosoma brucei | Q59013171 | ||
| Structural identification of the antibody-binding sites of Hong Kong influenza haemagglutinin and their involvement in antigenic variation | Q59062494 | ||
| Pilus expression in Neisseria gonorrhoeae involves chromosomal rearrangement | Q64451909 | ||
| Requirements for the opsonic activity of human IgG directed to type 6 group A streptococci: net basic charge and intact Fc region | Q70237635 | ||
| The complete amino acid sequence of a biologically active 197-residue fragment of M protein isolated from type 5 group A streptococci | Q70332693 | ||
| Studies on group A streptococcal M-proteins: purification of type 5 M-protein and comparison of its amino terminal sequence with two immunologically unrelated M-protein molecules | Q72124240 | ||
| Expression of Streptococcal M Protein inEscherichia coli | Q72707030 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1384-1401 | |
| P577 | publication date | 1985-06-01 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Size variation of the M protein in group A streptococci | |
| P478 | volume | 161 |
| Q37010316 | A highly conserved region present in transcripts encoding heterologous M proteins of group A streptococci. |
| Q46623194 | A host factor absent from Lactococcus lactis subspecies lactis MG1363 is required for conjugative transposition |
| Q36231622 | A major surface protein on group A streptococci is a glyceraldehyde-3-phosphate-dehydrogenase with multiple binding activity |
| Q37007120 | A method for allelic replacement that uses the conjugative transposon Tn916: deletion of the emm6.1 allele in Streptococcus pyogenes JRS4. |
| Q68355340 | A secreted receptor related to M1 protein of Streptococcus pyogenes binds to fibrinogen, IgG, and albumin |
| Q33585717 | An intermediate in transposition of the conjugative transposon Tn916. |
| Q37017639 | Analysis by gel electrophoresis, Western blot, and peptide mapping of protein A heterogeneity in Staphylococcus aureus strains |
| Q67479912 | Analysis of pneumococcal PspA microheterogeneity in SDS polyacrylamide gels and the association of PspA with the cell membrane |
| Q35533677 | Anaplasma marginale major surface protein 3 is encoded by a polymorphic, multigene family |
| Q92964432 | B cell superantigens in the human intestinal microbiota |
| Q37016911 | Biological and immunochemical identity of M protein on group G streptococci with M protein on group A streptococci |
| Q35623001 | Cell wall anchoring of the Streptococcus pyogenes M6 protein in various lactic acid bacteria. |
| Q67974091 | Chemotactic response of equine polymorphonuclear leucocytes to Streptococcus equi |
| Q37055410 | Common themes in microbial pathogenicity |
| Q36353164 | Conversion of an M- group A streptococcus to M+ by transfer of a plasmid containing an M6 gene |
| Q36712396 | DNA sequence of the serum opacity factor of group A streptococci: identification of a fibronectin-binding repeat domain. |
| Q37193737 | Defining Staphylococcus epidermidis cell wall proteins |
| Q33762432 | Deletion of repeats in the alpha C protein enhances the pathogenicity of group B streptococci in immune mice. |
| Q40146546 | Delivery and expression of a heterologous antigen on the surface of streptococci |
| Q59359640 | Development of Phage Lysins as Novel Therapeutics: A Historical Perspective |
| Q34269341 | Differentiation between two biologically distinct classes of group A streptococci by limited substitutions of amino acids within the shared region of M protein-like molecules |
| Q45345430 | E-cadherin is the receptor for internalin, a surface protein required for entry of L. monocytogenes into epithelial cells |
| Q40780228 | Evidence for two distinct classes of streptococcal M protein and their relationship to rheumatic fever |
| Q40152490 | Expression of protein F, the fibronectin-binding protein of Streptococcus pyogenes JRS4, in heterologous streptococcal and enterococcal strains promotes their adherence to respiratory epithelial cells |
| Q35381699 | Expression of the Arp protein, a member of the M protein family, is not sufficient to inhibit phagocytosis of Streptococcus pyogenes |
| Q39529596 | Generation and surface localization of intact M protein in Streptococcus pyogenes are dependent on sagA. |
| Q38331955 | Genetic diversity among the T-protein genes of group A streptococci. |
| Q36997329 | Heparin-inhibitable basement membrane-binding protein of Streptococcus pyogenes |
| Q40746320 | Heptad motifs within the distal subdomain of the coiled-coil rod region of M protein from rheumatic fever and nephritis associated serotypes of group A streptococci are distinct from each other: nucleotide sequence of the M57 gene and relation of th |
| Q37029644 | Homologous regions within M protein genes in group A streptococci of different serotypes |
| Q43694162 | Homology of glucosyltransferase gene and protein sequences from Streptococcus sobrinus and Streptococcus mutans |
| Q39824807 | Hyaluronate capsule and surface M protein in resistance to opsonization of group A streptococci |
| Q36184493 | Identification of a divergent M protein gene and an M protein-related gene family in Streptococcus pyogenes serotype 49 |
| Q34373919 | Identification of a gene that regulates expression of M protein, the major virulence determinant of group A streptococci |
| Q36357079 | Identification of an endogenous membrane anchor-cleaving enzyme for group A streptococcal M protein. Its implication for the attachment of surface proteins in gram-positive bacteria |
| Q37233872 | Identification of the innate human immune response to surface-exposed proteins of coagulase-negative staphylococci |
| Q40151753 | Identification of two proteins associated with virulence of Streptococcus suis type 2. |
| Q40193823 | Immunologic and genetic comparison of Streptococcus equi isolates from the United States and Europe |
| Q36505180 | In vivo efficacy of a chimeric peptide derived from the conserved region of the M protein against group C and G streptococci |
| Q45235700 | Isolated DNA repeat region from fcrA76, the Fc-binding protein gene from an M-type 76 strain of group A streptococci, encodes a protein with Fc-binding activity |
| Q36204811 | Isolation and characterization of the cell-associated region of group A streptococcal M6 protein |
| Q35089527 | Lipid-modified surface protein antigens expressing size variation within the species Mycoplasma hyorhinis |
| Q45107208 | Many group A streptococcal strains express two different immunoglobulin-binding proteins, encoded by closely linked genes: characterization of the proteins expressed by four strains of different M-type |
| Q34202889 | Molecular analysis of group A Streptococcus type emm18 isolates temporally associated with acute rheumatic fever outbreaks in Salt Lake City, Utah |
| Q40161025 | Molecular analysis of the M protein of Streptococcus equi and cloning and expression of the M protein gene in Escherichia coli |
| Q39534301 | Molecular aspects of the phagocytosis resistance of group A streptococci |
| Q36188393 | Molecular evolution of streptococcal M protein: cloning and nucleotide sequence of the type 24 M protein gene and relation to other genes of Streptococcus pyogenes |
| Q36996853 | Molecular size variations in an immunoprotective protein complex among isolates of Anaplasma marginale |
| Q36144820 | Mry, a trans-acting positive regulator of the M protein gene of Streptococcus pyogenes with similarity to the receptor proteins of two-component regulatory systems |
| Q43820098 | Nucleotide sequence of a variant protein A ofStaphylococcus aureus suggests molecular heterogeneity among strains |
| Q40148538 | Nucleotide sequences of two adjacent M or M-like protein genes of group A streptococci: different RNA transcript levels and identification of a unique immunoglobulin A-binding protein |
| Q44533419 | Peripheral blood mononuclear cells proliferation and Th1/Th2 cytokine production in response to streptococcal M protein in psoriatic patients |
| Q34708961 | PlyC: a multimeric bacteriophage lysin |
| Q24609957 | Prevention and elimination of upper respiratory colonization of mice by group A streptococci by using a bacteriophage lytic enzyme |
| Q79257590 | Reduced IFN-gamma responses associated with HLA-DR15 presentation of streptococcal cell wall proteins to dermal Th-1 cells in psoriasis |
| Q33752582 | Reduced virulence of group A streptococcal Tn916 mutants that do not produce streptolysin S |
| Q34006146 | Restoration of Mga function to a Streptococcus pyogenes strain (M Type 50) that is virulent in mice |
| Q36963706 | Role of M protein in adherence of group A streptococci |
| Q33598757 | Role of M protein in pharyngeal colonization by group A streptococci in rats |
| Q35545719 | Role of putative virulence factors of Streptococcus pyogenes in mouse models of long-term throat colonization and pneumonia. |
| Q71834322 | Role of the conserved C‐repeat region of the M protein of Streptococcus pyogenes |
| Q35842081 | Sequence TTKF ↓ QE defines the site of proteolytic cleavage in Mhp683 protein, a novel glycosaminoglycan and cilium adhesin of Mycoplasma hyopneumoniae |
| Q43250963 | Shr is a broad-spectrum surface receptor that contributes to adherence and virulence in group A streptococcus |
| Q47196403 | Size variation in group A streptococcal M protein is generated by homologous recombination between intragenic repeats |
| Q74263575 | Skin T cell proliferative response to M protein and other cell wall and membrane proteins of group A streptococci in chronic plaque psoriasis |
| Q33665979 | Spontaneous M6 protein size mutants of group A streptococci display variation in antigenic and opsonogenic epitopes |
| Q42938486 | Streptococcal M protein size mutants occur at high frequency within a single strain |
| Q30382858 | Streptococcal M protein: molecular design and biological behavior. |
| Q36274895 | Streptococcus pyogenes type 12 M protein gene regulation by upstream sequences |
| Q39938842 | The presence of conjugative transposon Tn916 in the recipient strain does not impede transfer of a second copy of the element |
| Q33761318 | The specificity patterns of human immunoglobulin G antibodies in serum differ from those in autologous secretions |
| Q36126783 | Transfer of Tn916 between Lactococcus lactis subsp. lactis strains is nontranspositional: evidence for a chromosomal fertility function in strain MG1363 |
| Q35100210 | Ultrastructural localization of the fibrinogen-binding domain of streptococcal M protein. |
| Q39563595 | Use of the lactococcal nisA promoter to regulate gene expression in gram-positive bacteria: comparison of induction level and promoter strength. |
| Q43520964 | Variable number of tandem repeat sequences act as regulatory elements in Mycobacterium tuberculosis. |
| Q46327094 | Virulence and antigenicity of the szp-gene deleted Streptococcus equi ssp. zooepidemicus mutant in mice |
| Q40270053 | Virulence of two Streptococcus pyogenes strains (types M1 and M3) associated with toxic-shock-like syndrome depends on an intact mry-like gene |
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