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  1. Article ; Online: Reproductive immunology issue one: cellular and molecular biology.

    Croy, B Anne

    Cellular & molecular immunology

    2014  Volume 11, Issue 5, Page(s) 405–406

    MeSH term(s) Allergy and Immunology/trends ; Animals ; Cell Biology/trends ; Endocrine System/immunology ; Female ; Genitalia/immunology ; Humans ; Killer Cells, Natural/immunology ; Male ; Molecular Biology/trends ; Placental Circulation ; Pregnancy ; Reproduction/immunology ; Reproductive Medicine/trends ; Trophoblasts/immunology
    Language English
    Publishing date 2014-07-28
    Publishing country China
    Document type Editorial ; Introductory Journal Article
    ZDB-ID 2435097-7
    ISSN 2042-0226 ; 1672-7681
    ISSN (online) 2042-0226
    ISSN 1672-7681
    DOI 10.1038/cmi.2014.64
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Reproductive immunology issue 2: cellular and molecular biology.

    Croy, B Anne

    Cellular & molecular immunology

    2014  Volume 11, Issue 6, Page(s) 503–505

    MeSH term(s) Abortion, Habitual/immunology ; Allergy and Immunology ; Animals ; Cell Biology ; Female ; Gene Expression Regulation, Developmental ; Humans ; Immune Tolerance ; MicroRNAs/genetics ; Molecular Biology ; Pregnancy/immunology ; Reproductive Medicine
    Chemical Substances MicroRNAs
    Language English
    Publishing date 2014-09-29
    Publishing country China
    Document type Editorial ; Introductory Journal Article
    ZDB-ID 2435097-7
    ISSN 2042-0226 ; 1672-7681
    ISSN (online) 2042-0226
    ISSN 1672-7681
    DOI 10.1038/cmi.2014.98
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Uterine natural killer cell partnerships in early mouse decidua basalis.

    Felker, Allison M / Croy, B Anne

    Journal of leukocyte biology

    2016  Volume 100, Issue 4, Page(s) 645–655

    Abstract: The decidua basalis of developing mouse implantation sites is highly enriched in ... ...

    Abstract The decidua basalis of developing mouse implantation sites is highly enriched in CD45
    MeSH term(s) Animals ; Apoptosis ; Decidua/immunology ; Female ; Gestational Age ; Immunological Synapses ; Killer Cells, Natural/chemistry ; Killer Cells, Natural/immunology ; Leukocyte Common Antigens/analysis ; Leukocytes/chemistry ; Leukocytes/immunology ; Mice ; Mice, Inbred C57BL ; NK Cell Lectin-Like Receptor Subfamily A/analysis ; Platelet Endothelial Cell Adhesion Molecule-1/analysis ; Pregnancy ; Receptors, Mitogen/analysis
    Chemical Substances Dolichos biflorus lectin receptor ; Klra3 protein, mouse ; NK Cell Lectin-Like Receptor Subfamily A ; Platelet Endothelial Cell Adhesion Molecule-1 ; Receptors, Mitogen ; Leukocyte Common Antigens (EC 3.1.3.48) ; Ptprc protein, mouse (EC 3.1.3.48)
    Language English
    Publishing date 2016-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605722-6
    ISSN 1938-3673 ; 0741-5400
    ISSN (online) 1938-3673
    ISSN 0741-5400
    DOI 10.1189/jlb.1HI0515-226R
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  4. Article ; Online: The Elsevier trophoblast research award lecture: Impacts of placental growth factor and preeclampsia on brain development, behaviour, and cognition.

    Rätsep, Matthew T / Hickman, Andrew F / Croy, B Anne

    Placenta

    2016  Volume 48 Suppl 1, Page(s) S40–S46

    Abstract: Preeclampsia (PE) is a significant gestational disorder affecting 3-5% of all human pregnancies. In many PE pregnancies, maternal plasma is deficient in placental growth factor (PGF), a placentally-produced angiokine. Beyond immediate fetal risks ... ...

    Abstract Preeclampsia (PE) is a significant gestational disorder affecting 3-5% of all human pregnancies. In many PE pregnancies, maternal plasma is deficient in placental growth factor (PGF), a placentally-produced angiokine. Beyond immediate fetal risks associated with acute termination of the pregnancy, offspring of PE pregnancies (PE-F1) have higher long-term risks for hypertension, stroke, and cognitive impairment compared to F1s from uncomplicated pregnancies. At present, mechanisms that explain PE-F1 gains in postpartum risks are poorly understood. Our laboratory found that mice genetically-deleted for Pgf have altered fetal and adult brain vascular development. This is accompanied by sexually dimorphic alterations in anatomic structure in the adult Pgf
    Language English
    Publishing date 2016-12
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 603951-0
    ISSN 1532-3102 ; 0143-4004
    ISSN (online) 1532-3102
    ISSN 0143-4004
    DOI 10.1016/j.placenta.2016.02.001
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    Zs.A 1578: Show issues Location:
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  5. Article ; Online: Preeclampsia may influence offspring neuroanatomy and cognitive function: a role for placental growth factor†.

    Kay, Vanessa R / Rätsep, Matthew T / Figueiró-Filho, Ernesto A / Croy, B Anne

    Biology of reproduction

    2019  Volume 101, Issue 2, Page(s) 271–283

    Abstract: Preeclampsia (PE) is a common pregnancy complication affecting 3-5% of women. Preeclampsia is diagnosed clinically as new-onset hypertension with associated end organ damage after 20 weeks of gestation. Despite being diagnosed as a maternal syndrome, ... ...

    Abstract Preeclampsia (PE) is a common pregnancy complication affecting 3-5% of women. Preeclampsia is diagnosed clinically as new-onset hypertension with associated end organ damage after 20 weeks of gestation. Despite being diagnosed as a maternal syndrome, fetal experience of PE is a developmental insult with lifelong cognitive consequences. These cognitive alterations are associated with distorted neuroanatomy and cerebrovasculature, including a higher risk of stroke. The pathophysiology of a PE pregnancy is complex, with many factors potentially able to affect fetal development. Deficient pro-angiogenic factor expression is one aspect that may impair fetal vascularization, alter brain structure, and affect future cognition. Of the pro-angiogenic growth factors, placental growth factor (PGF) is strongly linked to PE. Concentrations of PGF are inappropriately low in maternal blood both before and during a PE gestation. Fetal concentrations of PGF appear to mirror maternal circulating concentrations. Using Pgf-/- mice that may model effects of PE on offspring, we demonstrated altered central nervous system vascularization, neuroanatomy, and behavior. Overall, we propose that development of the fetal brain is impaired in PE, making the offspring of preeclamptic pregnancies a unique cohort with greater risk of altered cognition and cerebrovasculature. These individuals may benefit from early interventions, either pharmacological or environmental. The early neonatal period may be a promising window for intervention while the developing brain retains plasticity.
    MeSH term(s) Animals ; Child ; Child Development ; Cognition/physiology ; Female ; Humans ; Nervous System/growth & development ; Nervous System/pathology ; Placenta Growth Factor/genetics ; Placenta Growth Factor/metabolism ; Pre-Eclampsia/pathology ; Pregnancy
    Chemical Substances Placenta Growth Factor (144589-93-5)
    Language English
    Publishing date 2019-06-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1118-6
    ISSN 1529-7268 ; 0006-3363
    ISSN (online) 1529-7268
    ISSN 0006-3363
    DOI 10.1093/biolre/ioz095
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 551: Show issues Location:
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  6. Article ; Online: Influences of placental growth factor on mouse retinal vascular development.

    Kay, Vanessa R / Tayade, Chandrakant / Carmeliet, Peter / Croy, B Anne

    Developmental dynamics : an official publication of the American Association of Anatomists

    2017  Volume 246, Issue 9, Page(s) 700–712

    Abstract: Background: Placental growth factor (PGF) is important for wound-healing and vascular collaterogenesis. PGF deficiency is associated with preeclampsia, a hypertensive disease of human pregnancy. Offspring born to preeclamptic mothers display cognitive ... ...

    Abstract Background: Placental growth factor (PGF) is important for wound-healing and vascular collaterogenesis. PGF deficiency is associated with preeclampsia, a hypertensive disease of human pregnancy. Offspring born to preeclamptic mothers display cognitive impairments and brain vascular and neurostructural deviations. Low PGF production during development may contribute to alterations in offspring cerebrovascular beds. Retina is a readily accessible part of the central nervous system with a well-described pattern of vascular development in mice. Impacts of PGF deficiency were addressed during mouse retinal vascularization.
    Results: Retinal vessels were compared between Pgf
    Conclusions: Overall, PGF has a role in retinal vascular angiogenesis and vessel organization during development but does not affect retinal vessel adaptations in adult females during pregnancy. Developmental Dynamics 246:700-712, 2017. © 2017 Wiley Periodicals, Inc.
    Language English
    Publishing date 2017-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1102541-4
    ISSN 1097-0177 ; 1058-8388
    ISSN (online) 1097-0177
    ISSN 1058-8388
    DOI 10.1002/dvdy.24540
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  7. Article ; Online: Adult Pgf

    Kay, Vanessa R / Cahill, Lindsay S / Hanif, Anas / Sled, John G / Carmeliet, Peter / Tayade, Chandrakant / Croy, B Anne

    Scientific reports

    2019  Volume 9, Issue 1, Page(s) 9285

    Abstract: Offspring of preeclamptic pregnancies have cognitive alterations. Placental growth factor (PGF), is low in preeclampsia; reduced levels may affect brain development. PGF-null mice differ from normal congenic controls in cerebrovasculature, neuroanatomy ... ...

    Abstract Offspring of preeclamptic pregnancies have cognitive alterations. Placental growth factor (PGF), is low in preeclampsia; reduced levels may affect brain development. PGF-null mice differ from normal congenic controls in cerebrovasculature, neuroanatomy and behavior. Using brain imaging and behavioral testing, we asked whether developmentally asynchronous (i.e. neonatal) PGF supplementation alters the vascular, neuroanatomic and/or behavioral status of Pgf
    MeSH term(s) Animals ; Animals, Newborn ; Anxiety/genetics ; Behavior, Animal ; Body Weight ; Brain/diagnostic imaging ; Brain/growth & development ; Cerebrum/anatomy & histology ; Contrast Media ; Depression/genetics ; Female ; Gadolinium ; Magnetic Resonance Imaging ; Male ; Maze Learning ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Microscopy, Fluorescence ; Perfusion ; Placenta Growth Factor/genetics ; Placenta Growth Factor/therapeutic use ; Recombinant Proteins/therapeutic use ; Retinal Vessels/anatomy & histology ; Sex Factors ; Vascular Endothelial Growth Factor A/metabolism ; X-Ray Microtomography
    Chemical Substances Contrast Media ; Pgf protein, mouse ; Recombinant Proteins ; Vascular Endothelial Growth Factor A ; Placenta Growth Factor (144589-93-5) ; Gadolinium (AU0V1LM3JT)
    Language English
    Publishing date 2019-06-26
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-019-45824-6
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  8. Article: Using ultrasonography to define fetal-maternal relationships: moving from humans to mice.

    Zhang, Jianhong / Croy, B Anne

    Comparative medicine

    2009  Volume 59, Issue 6, Page(s) 527–533

    Abstract: Ultrasound scanning is a noninvasive, accurate, and cost-effective method to create images of the female reproductive tract clinically and in research. Ultrasonography is particularly valuable for studying the dynamic relationships among mother, placenta, ...

    Abstract Ultrasound scanning is a noninvasive, accurate, and cost-effective method to create images of the female reproductive tract clinically and in research. Ultrasonography is particularly valuable for studying the dynamic relationships among mother, placenta, and fetus during pregnancy because this modality does not disturb the ongoing course of gestation. Importantly, the complex vascular changes in the mother induced by pregnancy and the vascular system generated to support placental function can be assessed quantitatively and functionally by ultrasonography. Many mouse models are available that address aspects of human placental function and dysfunction, but high-quality microultrasound technology suitable for use in pregnant mice has become widely available only recently. This technical advance now enables real-time recording of maternal-fetal interactions in pregnant rodents. The ability to perform microultrasonic analyses of parameters such as uterine arterial remodeling, hemodynamic changes, placental development, and fetal growth in mice now permits research that uses the same imaging platform as that for human patients. This capability will enhance the translation of information derived from rodent studies to the clinic.
    MeSH term(s) Animals ; Female ; Humans ; Maternal-Fetal Exchange ; Mice ; Pregnancy ; Ultrasonography, Doppler ; Ultrasonography, Prenatal
    Language English
    Publishing date 2009-12-25
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2006425-1
    ISSN 1532-0820 ; 0023-6764
    ISSN 1532-0820 ; 0023-6764
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Using Ultrasonography to Define Fetal-Maternal Relationships: Moving from Humans to Mice

    Zhang, Jianhong / Croy, B. Anne

    Comparative medicine. 2009 Dec., v. 59, no. 6

    2009  

    Abstract: Ultrasound scanning is a noninvasive, accurate, and cost-effective method to create images of the female reproductive tract clinically and in research. Ultrasonography is particularly valuable for studying the dynamic relationships among mother, placenta, ...

    Abstract Ultrasound scanning is a noninvasive, accurate, and cost-effective method to create images of the female reproductive tract clinically and in research. Ultrasonography is particularly valuable for studying the dynamic relationships among mother, placenta, and fetus during pregnancy because this modality does not disturb the ongoing course of gestation. Importantly, the complex vascular changes in the mother induced by pregnancy and the vascular system generated to support placental function can be assessed quantitatively and functionally by ultrasonography. Many mouse models are available that address aspects of human placental function and dysfunction, but high-quality microultrasound technology suitable for use in pregnant mice has become widely available only recently. This technical advance now enables real-time recording of maternal-fetal interactions in pregnant rodents. The ability to perform microultrasonic analyses of parameters such as uterine arterial remodeling, hemodynamic changes, placental development, and fetal growth in mice now permits research that uses the same imaging platform as that for human patients. This capability will enhance the translation of information derived from rodent studies to the clinic.
    Keywords dams (mothers) ; fetus ; pregnancy ; placenta ; blood vessels ; hemodynamics ; fetal development ; ultrasonography ; mice ; animal models
    Language English
    Dates of publication 2009-12
    Size p. 527-533.
    Document type Article
    ISSN 1532-0820
    Database NAL-Catalogue (AGRICOLA)

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  10. Article ; Online: Maternal-fetal immunology.

    Croy, B Anne / Murphy, Shawn P

    Immunological investigations

    2008  Volume 37, Issue 5, Page(s) 389–394

    MeSH term(s) Animals ; Female ; Humans ; Maternal-Fetal Exchange/immunology ; Pregnancy/immunology ; Pregnancy Complications/immunology ; Trophoblasts/cytology ; Trophoblasts/immunology ; Trophoblasts/metabolism ; Uterus/blood supply ; Uterus/growth & development ; Uterus/immunology
    Language English
    Publishing date 2008
    Publishing country England
    Document type Introductory Journal Article
    ZDB-ID 632565-8
    ISSN 1532-4311 ; 0882-0139
    ISSN (online) 1532-4311
    ISSN 0882-0139
    DOI 10.1080/08820130802191631
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