On the public citation graph
Short communication: Differential immunoglobulin transfer during mastitis challenge by pathogen-specific components
0 signed · 62 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00281-009-0160-9openalex-snapshot
Immune and non-immune functions of the (not so) neonatal Fc receptor, FcRn
inferredcites →https://doi.org/10.1016/0165-2427(80)90012-4openalex-snapshot
IgA, IgG1, IgG2, IgM, and BSA in serum and mammary secretion throughout lactation
inferredcites →https://doi.org/10.1016/0165-2427(83)90056-9openalex-snapshot
Bovine immunoglobulins: An augmented review
inferredcites →https://doi.org/10.1016/0304-4165(77)90149-0openalex-snapshot
Kinetic analysis of the binding of immunoglobulins IgG1 and IgG2 to bovine mammary cells
inferredcites →https://doi.org/10.1016/j.acthis.2009.09.005openalex-snapshot
Cellular localization of aquaporins along the secretory pathway of the lactating bovine mammary gland: An immunohistochemical study
inferredcites →https://doi.org/10.1016/j.biocel.2009.12.012openalex-snapshot
Transporters, channels, or simple diffusion? Dogmas, atypical roles and complexity in transport systems
inferredcites →https://doi.org/10.1016/j.domaniend.2003.09.003openalex-snapshot
Short-term changes of mRNA expression of various inflammatory factors and milk proteins in mammary tissue during LPS-induced mastitis
inferredcites →https://doi.org/10.1016/s0749-0720(02)00073-7openalex-snapshot
Immunity and mastitis Some new ideas for an old disease
inferredcites →https://doi.org/10.1017/s002202990400007xopenalex-snapshot
Milk L -lactate concentration is increased during mastitis
inferredcites →https://doi.org/10.1017/s0022029905001135openalex-snapshot
Expression of the neonatal Fc receptor (FcRn) in the bovine mammary gland
inferredcites →https://doi.org/10.1051/vetres:2008034openalex-snapshot
Staphylococcus aureuslipoteichoic acid triggers inflammation in the lactating bovine mammary gland
inferredcites →https://doi.org/10.1099/00222615-40-2-79openalex-snapshot
Virulence factors involved in the pathogenesis of bovine intramammary infections due to Staphylococcus aureus
inferredcites →https://doi.org/10.17221/1877-vetmedopenalex-snapshot
Dose-dependent immune response in milk cells and mammary tissue after intramammary administration of lipopolysaccharide in dairy cows
inferredcites →https://doi.org/10.3168/jds.2010-3931openalex-snapshot
Lipopolysaccharide and lipoteichoic acid induce different immune responses in the bovine mammary gland
inferredcites →https://doi.org/10.3168/jds.2010-4092openalex-snapshot
Lipopolysaccharide challenge of the mammary gland in bovine induced a transient glandular shift to anaerobic metabolism
inferredcites →https://doi.org/10.3168/jds.2012-5410openalex-snapshot
Concomitant lipopolysaccharide-induced transfer of blood-derived components including immunoglobulins into milk
inferredcites →https://doi.org/10.3168/jds.s0022-0302(83)81868-2openalex-snapshot
Variation in Serum Immunoglobulins in Canadian Holstein-Friesians
inferredcites →https://doi.org/10.3168/jds.s0022-0302(83)82063-3openalex-snapshot
Physiological and Pathological Factors Influencing Bovine Immunoglobulin G1 Concentration in Milk
inferredcites →https://doi.org/10.3168/jds.s0022-0302(88)79779-9openalex-snapshot
Physiological and Pathological Factors Influencing Bovine Immunoglobulin G2 Concentration in Milk
inferredcites →https://doi.org/10.4049/jimmunol.118.2.461openalex-snapshot
The Nature of the Local Immune System of the Bovine Mammary Gland
inferredcites →https://doi.org/10.5167/uzh-98234openalex-snapshot
Concomitant LPS induced transfer of blood derived components including imunoglobulins into milk
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3938712openalex-extracted
Taurine Protects Blood-Milk Barrier Integrity Via Limiting Inflammatory Response in Streptococcus Uberis Infections
inferred← citeshttps://doi.org/10.1007/s10911-013-9309-1openalex-snapshot
The Role of Tight Junctions in Mammary Gland Function
inferred← citeshttps://doi.org/10.1007/s11259-025-10646-7openalex-snapshot
Deciphering the colostral-immunity transfer: from mammary gland to neonates small intestine
inferred← citeshttps://doi.org/10.1016/j.animal.2024.101082openalex-snapshot
Intramammary administration of lipopolysaccharides at parturition enhances immunoglobulin concentration in goat colostrum
inferred← citeshttps://doi.org/10.1016/j.animal.2025.101487openalex-snapshot
Review: Mammary gland physiology and modulation during colostrogenesis in dairy goats
inferred← citeshttps://doi.org/10.1016/j.etap.2019.103203openalex-snapshot
Species-specific models in toxicology: in vitro epithelial barriers
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.108371openalex-snapshot
Taurine protects blood-milk barrier integrity via limiting inflammatory response in Streptococcus uberis infections
inferred← citeshttps://doi.org/10.1016/j.jprot.2020.103763openalex-snapshot
Impact of Staphylococcus aureus infection on the late lactation goat milk proteome: New perspectives for monitoring and understanding mastitis in dairy goats
inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103743openalex-snapshot
Effects of chronic Staphylococcus aureus infection on immunological parameters and functionality of macrophages isolated from bovine mammary secretions
inferred← citeshttps://doi.org/10.1071/an21236openalex-snapshot
Effect of Coxiella burnetii infection on milk constituents and cow behaviour
inferred← citeshttps://doi.org/10.1093/jas/skac287openalex-snapshot
Implications of placentation type on species-specific colostrum properties in mammals
inferred← citeshttps://doi.org/10.1111/jpn.12843openalex-snapshot
Inflammatory and metabolic responses to an intramammary lipopolysaccharide challenge in early lactating cows supplemented with conjugated linoleic acid
inferred← citeshttps://doi.org/10.1186/s13028-017-0306-zopenalex-snapshot
Experimentally induced subclinical mastitis: are lipopolysaccharide and lipoteichoic acid eliciting similar pain responses?
inferred← citeshttps://doi.org/10.1186/s42523-025-00499-5openalex-snapshot
Dynamics of the milk microbial community during subacute ruminal acidosis with or without intramammary lipopolysaccharide challenge in dairy cows
inferred← citeshttps://doi.org/10.1590/1678-4162-10185openalex-snapshot
Frequency of microorganisms isolated at different stages of lactation and milk production loss associated with somatic cell count and to mastitis-causing pathogens
inferred← citeshttps://doi.org/10.17236/sat00115openalex-snapshot
Milk somatic cell count, lactate dehydrogenase activity, and immunoglobulin G concentration associated with mastitis caused by different pathogens: A field study
inferred← citeshttps://doi.org/10.17236/sat00302openalex-snapshot
Pathogen dependent effects of high amounts of oxytocin on the bloodmilk barrier integrity during mastitis in dairy cows
inferred← citeshttps://doi.org/10.2527/jas2017.1845openalex-snapshot
TRIENNIAL LACTATION SYMPOSIUM/BOLFA: Pathogen-specific immune response and changes in the blood–milk barrier of the bovine mammary gland1
inferred← citeshttps://doi.org/10.30564/vsr.v2i2.2638openalex-snapshot
Alterations in Quality Parameters of Mastitic Milk
inferred← citeshttps://doi.org/10.3168/jds.2016-10927openalex-snapshot
Short communication: Differential loss of bovine mammary epithelial barrier integrity in response to lipopolysaccharide and lipoteichoic acid
inferred← citeshttps://doi.org/10.3168/jds.2016-11093openalex-snapshot
Differential glucocorticoid-induced closure of the blood-milk barrier during lipopolysaccharide- and lipoteichoic acid-induced mastitis in dairy cows
inferred← citeshttps://doi.org/10.3168/jds.2016-11548openalex-snapshot
Supraphysiological oxytocin increases the transfer of immunoglobulins and other blood components to milk during lipopolysaccharide- and lipoteichoic acid–induced mastitis in dairy cows
inferred← citeshttps://doi.org/10.3168/jds.2017-14152openalex-snapshot
Differential somatic cell count in milk before, during, and after lipopolysaccharide- and lipoteichoic-acid-induced mastitis in dairy cows
inferred← citeshttps://doi.org/10.3168/jds.2017-14312openalex-snapshot
Selected reaction monitoring mass spectrometry of mastitis milk reveals pathogen-specific regulation of bovine host response proteins
inferred← citeshttps://doi.org/10.3168/jds.2018-15446openalex-snapshot
Undernutrition modified metabolic responses to intramammary lipopolysaccharide but had limited effects on selected inflammation indicators in early-lactation cows
inferred← citeshttps://doi.org/10.3168/jds.2019-16630openalex-snapshot
Meloxicam affects the inflammatory responses of bovine mammary epithelial cells
inferred← citeshttps://doi.org/10.3168/jds.2020-18691openalex-snapshot
Effects of local or systemic administration of meloxicam on mammary gland inflammatory responses to lipopolysaccharide-induced mastitis in dairy cows
inferred← citeshttps://doi.org/10.3168/jds.2020-18818openalex-snapshot
Nonsteroidal anti-inflammatory drugs affect the mammary epithelial barrier during inflammation
inferred← citeshttps://doi.org/10.3168/jds.2020-20029openalex-snapshot
Invited review: The role of the blood–milk barrier and its manipulation for the efficacy of the mammary immune response and milk production
inferred← citeshttps://doi.org/10.3168/jds.2021-20475openalex-snapshot
Suitability of milk lactate dehydrogenase and serum albumin for pathogen-specific mastitis detection in automatic milking systems
inferred← citeshttps://doi.org/10.3168/jds.2022-22303openalex-snapshot
Effects of hindgut acidosis on metabolism, inflammation, and production in dairy cows consuming a standard lactation diet
inferred← citeshttps://doi.org/10.3168/jds.2024-25073openalex-snapshot
Intramammary administration of lipopolysaccharides at parturition does not affect the transfer of passive immunity in goat kids
inferred← citeshttps://doi.org/10.3168/jdsc.2023-0387openalex-snapshot
Effects of oyster glycogen intramammary challenge on primiparous cow milk somatic cell counts, milk yields, and milk composition
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1031785openalex-snapshot
Immune defenses of the mammary gland epithelium of dairy ruminants
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1099623openalex-snapshot
Assessment of adaptive immune responses of dairy cows with Burkholderia contaminans-induced mastitis
inferred← citeshttps://doi.org/10.3390/ani12091059openalex-snapshot
Progress in Expression Pattern and Molecular Regulation Mechanism of LncRNA in Bovine Mastitis
inferred← citeshttps://doi.org/10.3390/ani12101228openalex-snapshot
Ethanol Extract of Artemisia Annua Prevents LPS-Induced Inflammation and Blood–Milk Barrier Disruption in Bovine Mammary Epithelial Cells
inferred← citeshttps://doi.org/10.3390/ani15111578openalex-snapshot
The Relationship Between Protein Fraction Contents and Immune Cells in Milk
inferred← citeshttps://doi.org/10.7150/ijbs.38214openalex-snapshot
LRRC75A antisense lncRNA1 knockout attenuates inflammatory responses of bovine mammary epithelial cells
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.