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Age‐Associated Decline in Resistance toBabesia microtiIs Genetically Determined
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archinte.158.19.2149openalex-snapshot
Human Babesiosis in New York State
inferredcites →https://doi.org/10.1016/0014-4894(82)90065-0openalex-snapshot
Babesia microti: Infectivity of parasites from ticks for hamsters and white-footed mice
inferredcites →https://doi.org/10.1016/0047-6374(83)90036-2openalex-snapshot
The effect of age on the infection and immunoresponsiveness of mice to Babesia microti
inferredcites →https://doi.org/10.1016/s0952-7915(97)80152-5openalex-snapshot
Innate immunity: impact on the adaptive immune response
inferredcites →https://doi.org/10.1046/j.1365-3024.2001.00402.xopenalex-snapshot
The age‐related immunity in cattle to Babesia bovis infection involves the rapid induction of interleukin‐12, interferon‐γ and inducible nitric oxide synthase mRNA expression in the spleen
inferredcites →https://doi.org/10.1056/nejm199807163390304openalex-snapshot
Persistent Parasitemia after Acute Babesiosis
inferredcites →https://doi.org/10.1086/319742openalex-snapshot
Severe Babesiosis in Long Island: Review of 34 Cases and Their Complications
inferredcites →https://doi.org/10.1093/intimm/3.5.467openalex-snapshot
Treatment of murine CD5− B cells with anti-lg, but not LPS, induces surface CD5: two B-cell activation pathways
inferredcites →https://doi.org/10.1097/00007890-198403000-00024openalex-snapshot
BALB.D2-Mlsa-A new congenic mouse strain
inferredcites →https://doi.org/10.1128/iai.37.3.1127-1131.1982openalex-snapshot
Age resistance in bovine babesiosis: role of blood factors in resistance to Babesia bovis
inferredcites →https://doi.org/10.1128/iai.67.8.4143-4148.1999openalex-snapshot
Roles of CD4+T Cells and Gamma Interferon in Protective Immunity againstBabesia microtiInfection in Mice
inferredcites →https://doi.org/10.1128/iai.69.12.7955-7958.2001openalex-snapshot
Innate Resistance toBabesiaInfection Is Influenced by Genetic Background and Gender
inferredcites →https://doi.org/10.1128/iai.70.9.5304-5306.2002openalex-snapshot
Cellular Immunity, but Not Gamma Interferon, Is Essential for Resolution ofBabesia microtiInfection in BALB/c Mice
inferredcites →https://doi.org/10.1128/jcm.35.2.450-454.1997openalex-snapshot
Human babesiosis in Taiwan: asymptomatic infection with a Babesia microti-like organism in a Taiwanese woman
inferredcites →https://doi.org/10.1128/jcm.40.7.2431-2436.2002openalex-snapshot
Seroprevalence ofBabesiaInfections in Humans Exposed to Ticks in Midwestern Germany
inferredcites →https://doi.org/10.1542/peds.89.6.1045openalex-snapshot
Babesiosis: An Underdiagnosed Disease of Children
inferredcites →https://doi.org/10.2307/3283623openalex-snapshot
Infection of Immunodeficient Mice with a Mouse-Adapted Substrain of the Gray Strain of Babesia microti
inferredcites →https://doi.org/10.2307/3283793openalex-snapshot
Detection of Canine Erythrocytes Infected with Babesia gibsoni by Flow Cytometry
inferredcites →https://doi.org/10.3201/eid0902.020271openalex-snapshot
Endemic Babesiosis in Another Eastern State: New Jersey
inferredcites →https://doi.org/10.4269/ajtmh.1980.29.507openalex-snapshot
Thymus Dependence of Resistance to Infection with Babesia microti of Human Origin in Mice
inferredcites →https://doi.org/10.4269/ajtmh.1980.29.738openalex-snapshot
Babesiosis in Post-Splenectomy Hosts
inferredcites →https://doi.org/10.4269/ajtmh.2003.68.431openalex-snapshot
INCREASING HEALTH BURDEN OF HUMAN BABESIOSIS IN ENDEMIC SITES
inferredcites →https://doi.org/10.7326/0003-4819-107-6-944_1openalex-snapshot
Babesiosis and Infection with Human Immunodeficiency Virus (HIV)
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.4839235openalex-extracted
Persistence Human Babesiosis with Low-Grade Parasitemia, Challenges for Clinical Diagnosis and Management
inferred← citeshttps://doi.org/10.1002/ccr3.2301openalex-snapshot
Splenic infarction in babesiosis: A rare presentation
inferred← citeshttps://doi.org/10.1002/ccr3.4744openalex-snapshot
The unusual case of babesiosis causing disseminated intravascular coagulation with hemophagocytic lymphohistiocytosis
inferred← citeshttps://doi.org/10.1007/s00436-016-5128-9openalex-snapshot
High prevalence of Babesia microti ‘Munich’ type in small mammals from an Ixodes persulcatus/Ixodes trianguliceps sympatric area in the Omsk region, Russia
inferred← citeshttps://doi.org/10.1007/s00580-022-03328-2openalex-snapshot
Hematological approaches of canines naturally infected by Babesia spp. and Hepatozoon spp.
inferred← citeshttps://doi.org/10.1007/s10522-007-9106-6openalex-snapshot
Outcome and immune responses after Brucella abortus infection in young adult and aged mice
inferred← citeshttps://doi.org/10.1016/b978-012369391-4/50054-0openalex-snapshot
Murine Models of Infectious Diseases in the Aged
inferred← citeshttps://doi.org/10.1016/j.arr.2011.12.006openalex-snapshot
Dietary restriction in rats and mice: A meta-analysis and review of the evidence for genotype-dependent effects on lifespan
inferred← citeshttps://doi.org/10.1016/j.exger.2005.11.003openalex-snapshot
Age-related changes in cell surface and senescence markers in the spleen of DBA/2 mice: A flow cytometric analysis
inferred← citeshttps://doi.org/10.1016/j.exppara.2008.08.008openalex-snapshot
Babesia rodhaini: The protective effect of pyruvate kinase deficiency in mice
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.05.015openalex-snapshot
Caloric restriction and the aging process: a critique
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e39960openalex-snapshot
Persistent human babesiosis with low-grade parasitemia, challenges for clinical diagnosis and management
inferred← citeshttps://doi.org/10.1016/j.ijpara.2018.06.006openalex-snapshot
Investigating disease severity in an animal model of concurrent babesiosis and Lyme disease
inferred← citeshttps://doi.org/10.1016/j.mad.2008.01.009openalex-snapshot
Mucosal adjuvant activity of flagellin in aged mice
inferred← citeshttps://doi.org/10.1016/j.onehlt.2022.100443openalex-snapshot
Tick-borne diseases in Egypt: A one health perspective
inferred← citeshttps://doi.org/10.1016/j.onehlt.2023.100547openalex-snapshot
Human-biting ticks and zoonotic tick-borne pathogens in North Africa: diversity, distribution, and trans-Mediterranean public health challenges
inferred← citeshttps://doi.org/10.1016/j.pt.2022.11.003openalex-snapshot
Animal models of the immunology and pathogenesis of human babesiosis
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2016.10.008openalex-snapshot
Seroprevalence of Babesia bovis , B. bigemina , Trypanosoma evansi , and Anaplasma marginale antibodies in cattle in southern Egypt
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2018.07.005openalex-snapshot
Distribution and risk factors associated with Babesia spp. infection in hunting dogs from Southern Italy
inferred← citeshttps://doi.org/10.1017/s0031182011000400openalex-snapshot
Investigating the persistence of tick-borne pathogens via the R 0 model
inferred← citeshttps://doi.org/10.1063/1.4954196openalex-snapshot
Insulator-based dielectrophoretic diagnostic tool for babesiosis
inferred← citeshttps://doi.org/10.1080/14787210.2020.1752193openalex-snapshot
Management strategies for human babesiosis
inferred← citeshttps://doi.org/10.1086/496891openalex-snapshot
Babesia microtiandBorrelia burgdorferiFollow Independent Courses of Infection in Mice
inferred← citeshttps://doi.org/10.1086/525852openalex-snapshot
Persistent and Relapsing Babesiosis in Immunocompromised Patients
inferred← citeshttps://doi.org/10.1089/vbz.2020.2754openalex-snapshot
Using Data Surveillance to Understand the Rising Incidence of Babesiosis in the United States, 2011–2018
inferred← citeshttps://doi.org/10.1097/01.shk.0000144134.03598.c5openalex-snapshot
GENETIC DETERMINANTS INFLUENCING THE RESPONSE TO INJURY, INFLAMMATION, AND SEPSIS
inferred← citeshttps://doi.org/10.1097/ipc.0b013e31809fe523openalex-snapshot
Babesiosis, Significance of Spleen Function Illustrated by Postsplenectomy Course in 3 Cases
inferred← citeshttps://doi.org/10.1111/cmi.13350openalex-snapshot
Pathogenesis ofBorrelia burgdorferiandBabesia microtiin TLR4‐Competent and TLR4 ‐dysfunctional C3H mice
inferred← citeshttps://doi.org/10.1111/j.1537-2995.2005.00609.xopenalex-snapshot
Demonstrable parasitemia among Connecticut blood donors with antibodies to Babesia microti
inferred← citeshttps://doi.org/10.1111/j.1537-2995.2009.02429.xopenalex-snapshot
CONFERENCE REPORT: Transfusion‐transmitted babesiosis in the United States: summary of a workshop
inferred← citeshttps://doi.org/10.1111/mec.16819openalex-snapshot
Living with chronic infection: Persistent immunomodulation during avirulent haemoparasitic infection in a wild rodent
inferred← citeshttps://doi.org/10.1111/trf.12098openalex-snapshot
Development of a real‐time polymerase chain reaction assay for sensitive detection and quantitation of Babesia microti infection
inferred← citeshttps://doi.org/10.1111/trf.14889openalex-snapshot
Minimal infectious dose and dynamics of Babesia microti parasitemia in a murine model
inferred← citeshttps://doi.org/10.1128/cmr.00022-10openalex-snapshot
Transfusion-Transmitted Babesia spp.: Bull's-Eye on Babesia microti
inferred← citeshttps://doi.org/10.1128/iai.01560-05openalex-snapshot
Babesia microti Primarily Invades Mature Erythrocytes in Mice
inferred← citeshttps://doi.org/10.1146/annurev-ento-112408-085446openalex-snapshot
Update on Powassan Virus: Emergence of a North American Tick-Borne Flavivirus
inferred← citeshttps://doi.org/10.1155/2015/405263openalex-snapshot
Babesiain a Nonsplenectomized Patient Requiring Exchange Transfusion
inferred← citeshttps://doi.org/10.1159/000358017openalex-snapshot
Emerging Pathogens - How Safe is Blood?
inferred← citeshttps://doi.org/10.1182/bloodadvances.2018026468openalex-snapshot
Robust adaptive immune response against Babesia microti infection marked by low parasitemia in a murine model of sickle cell disease
inferred← citeshttps://doi.org/10.1186/s12941-017-0179-zopenalex-snapshot
Hematologic manifestations of babesiosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0052746openalex-snapshot
Dried Whole Plant Artemisia annua as an Antimalarial Therapy
inferred← citeshttps://doi.org/10.1371/journal.pone.0137731openalex-snapshot
Vertical Transmission of Babesia microti in BALB/c Mice: Preliminary Report
inferred← citeshttps://doi.org/10.21037/lcm-21-2openalex-snapshot
Artemisia annua and artemisinins are ineffective against human Babesia microti and six Candida sp
inferred← citeshttps://doi.org/10.3389/fcimb.2017.00238openalex-snapshot
Translational Rodent Models for Research on Parasitic Protozoa—A Review of Confounders and Possibilities
inferred← citeshttps://doi.org/10.3389/fcimb.2021.685239openalex-snapshot
Lessons Learned for Pathogenesis, Immunology, and Disease of Erythrocytic Parasites: Plasmodium and Babesia
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02891openalex-snapshot
Age-Related Differential Stimulation of Immune Response by Babesia microti and Borrelia burgdorferi During Acute Phase of Infection Affects Disease Severity
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00085openalex-snapshot
Babesia microti Infection Changes Host Spleen Architecture and Is Cleared by a Th1 Immune Response
inferred← citeshttps://doi.org/10.3389/fmicb.2021.697669openalex-snapshot
Babesia microti: Pathogen Genomics, Genetic Variability, Immunodominant Antigens, and Pathogenesis
inferred← citeshttps://doi.org/10.3389/fmicb.2022.862894openalex-snapshot
Babesia microti Infection Inhibits Melanoma Growth by Activating Macrophages in Mice
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1799424openalex-snapshot
Molecular epidemiology of Babesia microti in southern Zhejiang: an integrated survey of humans, rodent reservoirs, and tick vectors (2020–2023)
inferred← citeshttps://doi.org/10.3390/pathogens11111309openalex-snapshot
Transmission Cycle of Tick-Borne Infections and Co-Infections, Animal Models and Diseases
inferred← citeshttps://doi.org/10.3390/pathogens13020123openalex-snapshot
Immune Mediators Important for a Protective Secondary Response to Babesia microti
inferred← citeshttps://doi.org/10.3390/pathogens8030102openalex-snapshot
Persistence of Babesia microti Infection in Humans
inferred← citeshttps://doi.org/10.3390/pathogens8030117openalex-snapshot
Babesia microti—Borrelia burgdorferi Coinfection
inferred← citeshttps://doi.org/10.4269/ajtmh.17-0146openalex-snapshot
Risk Factors for Severe Infection, Hospitalization, and Prolonged Antimicrobial Therapy in Patients with Babesiosis
inferred← citeshttps://doi.org/10.4303/jnd/235688openalex-snapshot
What Could Be a Primary Cause of Multiple Sclerosis: Is It an Autoimmunity Triggered by Chronic Protozoan Infection?
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