scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.YFRNE.2020.100850 |
P698 | PubMed publication ID | 32504632 |
P2093 | author name string | Claudia Barth | |
Ann-Marie G de Lange | |||
P2860 | cites work | Microchimerism in Japanese women patients with systemic sclerosis | Q78044345 |
Feto-maternal microchimerism in connective tissue diseases | Q78516511 | ||
Changes in serum cytokine concentrations during the menopausal transition | Q79428451 | ||
Chimerism occurs in thyroid, lung, skin and lymph nodes of women with sons | Q80841841 | ||
The association of luteinizing hormone and follicle-stimulating hormone with cytokines and markers of disease activity in rheumatoid arthritis: a case-control study | Q83906110 | ||
Greater depressive symptoms, cognition, and markers of brain aging: Northern Manhattan Study | Q88617860 | ||
Role of inflammation and oxidative stress in the etiology of primary ovarian insufficiency | Q88990920 | ||
From baby brain to mommy brain: Widespread gray matter gain after giving birth | Q89918078 | ||
Common brain disorders are associated with heritable patterns of apparent aging of the brain | Q90263046 | ||
Differential effects of completed and incomplete pregnancies on the risk of Alzheimer disease | Q90321586 | ||
Modulating inflammation for cancer therapy | Q91521931 | ||
Early and late effects of maternal experience on hippocampal neurogenesis, microglia, and the circulating cytokine milieu | Q92069195 | ||
The long and short term effects of motherhood on the brain | Q92074295 | ||
Applying a Women's Health Lens to the Study of the Aging Brain | Q92105083 | ||
Pregnancy Immunogenetics and Genomics: Implications for Pregnancy-Related Complications and Autoimmune Disease | Q92225885 | ||
The Pregnancy Pickle: Evolved Immune Compensation Due to Pregnancy Underlies Sex Differences in Human Diseases | Q92757840 | ||
Decreased effector regulatory T cells and increased activated CD4+ T cells in premature ovarian insufficiency | Q93049323 | ||
Male microchimerism in the human female brain | Q21134035 | ||
Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum | Q24567463 | ||
One-year brain atrophy evident in healthy aging | Q24642943 | ||
FOXP3(+) Treg Cells and Gender Bias in Autoimmune Diseases | Q26781235 | ||
Hippocampal plasticity during the peripartum period: influence of sex steroids, stress and ageing | Q26862576 | ||
The structural biology of oestrogen metabolism | Q27009283 | ||
Fetal microchimerism in women with breast cancer | Q28251536 | ||
The genetical evolution of social behaviour. II | Q28256861 | ||
Transfer of fetal cells with multilineage potential to maternal tissue | Q28270559 | ||
A new paradigm for depression in new mothers: the central role of inflammation and how breastfeeding and anti-inflammatory treatments protect maternal mental health | Q28395601 | ||
Age-related decline of myelin proteins is highly correlated with activation of astrocytes and microglia in the rat CNS | Q28568321 | ||
Androgens alter T-cell immunity by inhibiting T-helper 1 differentiation | Q28655545 | ||
Neuroinflammatory component of gray matter pathology in multiple sclerosis | Q29398383 | ||
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | Q29417007 | ||
Brain atrophy in Alzheimer's Disease and aging | Q30251935 | ||
High consistency of regional cortical thinning in aging across multiple samples | Q30489836 | ||
Correlations of Y chromosome microchimerism with disease activity in patients with SLE: analysis of preliminary data | Q30804232 | ||
Estrogen- and progesterone-mediated structural neuroplasticity in women: evidence from neuroimaging. | Q31047972 | ||
B cell subsets in postmenopausal women and the effect of hormone replacement therapy | Q31926177 | ||
Endocrine factors modulating immune responses in pregnancy | Q33611653 | ||
Estrogen: a master regulator of bioenergetic systems in the brain and body | Q33623924 | ||
The maternal brain: an organ with peripartal plasticity | Q33634903 | ||
Onset of progressive phase is an age-dependent clinical milestone in multiple sclerosis | Q33643239 | ||
APOE predicts amyloid-beta but not tau Alzheimer pathology in cognitively normal aging | Q33695738 | ||
Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group | Q33726399 | ||
T-cell subsets (Th1 versus Th2). | Q33989214 | ||
Gender differences in autoimmune disease | Q34040802 | ||
Genetic conflicts in human pregnancy | Q34060435 | ||
50 years of hormonal contraception-time to find out, what it does to our brain | Q34071651 | ||
Gender specificity of altered human immune cytokine profiles in aging | Q34072272 | ||
Lack of evidence of foetal microchimerism in female Spanish patients with systemic sclerosis | Q73003135 | ||
Antiinflammatory effects of estrogen on microglial activation | Q73027691 | ||
The immune response during the luteal phase of the ovarian cycle: a Th2-type response? | Q73134957 | ||
Immune effects of hormone replacement therapy in post-menopausal women | Q73559562 | ||
Serum interleukin-6, soluble interleukin-6 receptor and soluble gp130 exhibit different patterns of age- and menopause-related changes | Q73617563 | ||
The evaluation of determinants of early postpartum low mood: the importance of parity and inter-pregnancy interval | Q73807298 | ||
Th2-oriented profile of male offspring T cells present in women with systemic sclerosis and reactive with maternal major histocompatibility complex antigens | Q77628805 | ||
Inflammation in Alzheimer disease-a brief review of the basic science and clinical literature | Q37982377 | ||
Androgen in postmenopausal women | Q37997227 | ||
History of oral contraceptive drugs and their use worldwide | Q38079343 | ||
Childbirths and risk of female predominant and other autoimmune diseases in a population-based Danish cohort. | Q38437632 | ||
Parity and the risk of autoimmune thyroid disease: a community-based study. | Q38442358 | ||
Perimenopause as a neurological transition state | Q38501586 | ||
A possible role of estrone produced in adipose tissues in modulating postmenopausal bone density | Q38531711 | ||
Neuroplasticity in the maternal hippocampus: Relation to cognition and effects of repeated stress | Q38539991 | ||
Sex differences in Alzheimer risk: Brain imaging of endocrine vs chronologic aging | Q38601642 | ||
Immunological implications of pregnancy-induced microchimerism. | Q38686693 | ||
Multiparity improves outcomes after cerebral ischemia in female mice despite features of increased metabovascular risk | Q38711384 | ||
Inflammatory markers in late pregnancy in association with postpartum depression-A nested case-control study | Q38747140 | ||
Associations between specific autoimmune diseases and subsequent dementia: retrospective record-linkage cohort study, UK. | Q38751838 | ||
Defeating Alzheimer's disease and other dementias: a priority for European science and society | Q38778638 | ||
Estrogens, Neuroinflammation, and Neurodegeneration. | Q38838452 | ||
The importance of studying sex differences in disease: The example of multiple sclerosis | Q39015338 | ||
Pregnancy leads to long-lasting changes in human brain structure | Q39089403 | ||
An examination of changes in maternal neuroimmune function during pregnancy and the postpartum period | Q39153376 | ||
A survey of neuroimmune changes in pregnant and postpartum female rats | Q39337538 | ||
The unique immunological and microbial aspects of pregnancy | Q39382358 | ||
Claudin-5 as a novel estrogen target in vascular endothelium | Q39775405 | ||
Hormonal contraception and the development of autoimmunity: A review of the literature | Q40039972 | ||
Hormone therapy, timing of initiation, and cognition in women aged older than 60 years: the REMEMBER pilot study. | Q40335153 | ||
Significant fetal-maternal hemorrhage after termination of pregnancy: implications for development of fetal cell microchimerism. | Q40717942 | ||
Lifelong estrogen exposure and cognitive performance in elderly women | Q41618550 | ||
Th1-type immunity is incompatible with successful pregnancy | Q41632972 | ||
Estrogen use, APOE, and cognitive decline: evidence of gene-environment interaction | Q41737310 | ||
Interferon-gamma-producing T cells, pregnancy, and postpartum relapses of multiple sclerosis. | Q43462697 | ||
Hormonal and reproductive risk factors for development of systemic lupus erythematosus: results of a population-based, case-control study | Q43505242 | ||
Cytokine pattern in postmenopause | Q43911039 | ||
Does the use of hormonal contraceptives cause microstructural changes in cerebral white matter? Preliminary results of a DTI and tractography study. | Q44021001 | ||
Estradiol in vivo regulation of brain mitochondrial proteome. | Q44224743 | ||
Cumulative estrogen exposure, number of menstrual cycles, and Alzheimer's risk in a cohort of British women | Q44274296 | ||
Trends in incidence and mortality in rheumatoid arthritis in Rochester, Minnesota, over a forty-year period | Q44506234 | ||
Human thymocytes secrete luteinizing hormone: an autocrine regulator of T-cell proliferation | Q44995482 | ||
The effect of different doses of micronized 17beta-estradiol on C-reactive protein, interleukin-6, and lipids in older women | Q45042716 | ||
17beta-estradiol differentially regulates blood-brain barrier permeability in young and aging female rats. | Q45096375 | ||
Brain magnetic resonance imaging findings in patients with systemic sclerosis | Q46220666 | ||
Parity and Risk of Thyroid Autoimmunity Based on the NHANES (2001-2002, 2007-2008, 2009-2010, and 2011-2012). | Q46240152 | ||
Motherhood and the hormones of pregnancy modify concentrations of hippocampal neuronal dendritic spines | Q46590660 | ||
Decrease in hippocampal neurogenesis during pregnancy: a link to immunity | Q46637809 | ||
Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery | Q46760489 | ||
Opposite effects of microchimerism on breast and colon cancer | Q46884475 | ||
Pregnancy-associated progenitor cells differentiate and mature into neurons in the maternal brain. | Q34131118 | ||
Wired for reproduction: organization and development of sexually dimorphic circuits in the mammalian forebrain | Q34132322 | ||
Continuous versus cyclic progesterone exposure differentially regulates hippocampal gene expression and functional profiles | Q34185639 | ||
A dominant negative ERβ splice variant determines the effectiveness of early or late estrogen therapy after ovariectomy in rats | Q34201028 | ||
Epigenetic regulation of estrogen-dependent memory | Q34243105 | ||
Pregnancy and pregnancy-associated hormones alter immune responses and disease pathogenesis | Q34260259 | ||
Microchimeric fetal cells play a role in maternal wound healing after pregnancy | Q34352689 | ||
Estrogen regulation of glucose metabolism and mitochondrial function: therapeutic implications for prevention of Alzheimer's disease | Q34360055 | ||
Microchimerism in recurrent miscarriage | Q34455664 | ||
Dose and temporal pattern of estrogen exposure determines neuroprotective outcome in hippocampal neurons: therapeutic implications | Q34558386 | ||
Hormonal changes in the menopause transition | Q34644005 | ||
Androgens and estrogens modulate the immune and inflammatory responses in rheumatoid arthritis | Q34735562 | ||
Estrogen anti-inflammatory activity in brain: a therapeutic opportunity for menopause and neurodegenerative diseases | Q34784469 | ||
Inflammation and pregnancy: the role of the immune system at the implantation site | Q34806659 | ||
The HRT controversy: observational studies and RCTs fall in line | Q34975284 | ||
The plasticity of human maternal brain: longitudinal changes in brain anatomy during the early postpartum period | Q35053878 | ||
Follicle-stimulating hormone stimulates TNF production from immune cells to enhance osteoblast and osteoclast formation | Q35075554 | ||
What is normal in normal aging? Effects of aging, amyloid and Alzheimer's disease on the cerebral cortex and the hippocampus | Q35129501 | ||
Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci | Q35168836 | ||
How immune mechanisms are affected by pregnancy | Q35172870 | ||
C terminus of Hsc70-interacting protein (CHIP)-mediated degradation of hippocampal estrogen receptor-alpha and the critical period hypothesis of estrogen neuroprotection | Q35198156 | ||
Sex hormones modulate brain damage in multiple sclerosis: MRI evidence | Q35485697 | ||
White matter hyperintensities on brain magnetic resonance in systemic sclerosis | Q35555552 | ||
Estrogen and cognition: applying preclinical findings to clinical perspectives | Q35591832 | ||
Antigenic challenge in the etiology of autoimmune disease in women | Q35622496 | ||
Onset timing, thoughts of self-harm, and diagnoses in postpartum women with screen-positive depression findings. | Q35632995 | ||
The adaptation of the blood-brain barrier to vascular endothelial growth factor and placental growth factor during pregnancy | Q35647966 | ||
Estrogens in the nervous system: mechanisms and nonreproductive functions | Q35672515 | ||
Hormone concentrations throughout uncomplicated pregnancies: a longitudinal study | Q36067573 | ||
White matter injury and microglia/macrophage polarization are strongly linked with age-related long-term deficits in neurological function after stroke. | Q36113123 | ||
Progesterone and autoimmune disease | Q36202227 | ||
Preliminary evidence that long-term estrogen use reduces white matter loss in aging | Q36296643 | ||
Menopausal hot flashes and white matter hyperintensities | Q36355611 | ||
Sex differences in the causes and consequences of white matter hyperintensities | Q46939985 | ||
Add Alzheimer's disease to the list of autoimmune diseases | Q47624527 | ||
Kynurenic acid is reduced in females and oral contraceptive users: Implications for depression | Q47722395 | ||
Reproductive factors and risk of systemic lupus erythematosus: nationwide cohort study in Denmark | Q47846590 | ||
Multiparity-induced enhancement of hippocampal neurogenesis and spatial memory depends on ovarian hormone status in middle age. | Q48165955 | ||
Immune cell circulating subsets are affected by gonadal function | Q48201151 | ||
Microglia and Alzheimer's disease | Q48301324 | ||
The maternal 'baby brain' revisited | Q48337951 | ||
Systemic sclerosis: brain abnormalities revealed by conventional magnetic resonance imaging and magnetization transfer imaging | Q48598100 | ||
Differential longitudinal changes in cortical thickness, surface area and volume across the adult life span: regions of accelerating and decelerating change. | Q48706099 | ||
Selective sparing of brain tissue in postmenopausal women receiving hormone replacement therapy | Q48884485 | ||
Progesterone attenuates demyelination and microglial reaction in the lysolecithin-injured spinal cord | Q50436940 | ||
Fetal progenitor cells naturally transferred through pregnancy participate in inflammation and angiogenesis during wound healing. | Q50510648 | ||
Pregnancy persistently affects memory T cell populations. | Q50610830 | ||
Fetal microchimerism in the maternal mouse brain: a novel population of fetal progenitor or stem cells able to cross the blood-brain barrier? | Q50758919 | ||
Long-term prospective study of the influence of estrone levels on events in postmenopausal women with or at high risk for coronary artery disease. | Q51355481 | ||
3 Tesla MRI detects accelerated hippocampal volume reduction in postmenopausal women. | Q51526355 | ||
Pregnancy allows the transfer and differentiation of fetal lymphoid progenitors into functional T and B cells in mothers. | Q51720614 | ||
Lack of association between thyroid autoantibodies and parity in a population study argues against microchimerism as a trigger of thyroid autoimmunity. | Q51826332 | ||
White matter hyperintensities in the forties: their prevalence and topography in an epidemiological sample aged 44-48. | Q51886805 | ||
Incidence of AD may decline in the early 90s for men, later for women: The Cache County study. | Q51960492 | ||
Effect of hormone replacement therapy on post-menopausal changes of lymphocytes and T cell subsets. | Q52025730 | ||
Reproductive period, endogenous estrogen exposure and dementia incidence among women in Latin America and China; A 10/66 population-based cohort study. | Q52681403 | ||
Pregnancy is associated with a lower risk of onset and a better prognosis in multiple sclerosis. | Q52880959 | ||
The discrepancy between observational studies and randomized trials of menopausal hormone therapy: did expectations shape experience? | Q52957319 | ||
Senile plaques stimulate microglia to release a neurotoxin found in Alzheimer brain | Q53201329 | ||
Endogenous estrogen levels and Alzheimer's disease among postmenopausal women. | Q53233390 | ||
The number of pregnancies is a risk factor for Alzheimer's disease. | Q53282854 | ||
Brain Aging and APOE ε4 Interact to Reveal Potential Neuronal Compensation in Healthy Older Adults. | Q53418756 | ||
Microchimerism and HLA-compatible relationships of pregnancy in scleroderma. | Q53782517 | ||
A gender gap in autoimmunity. | Q55032884 | ||
Androgen-Induced Immunosuppression. | Q55357541 | ||
Sex differences in autoimmune disease | Q55970264 | ||
Executive summary of the Stages of Reproductive Aging Workshop + 10: addressing the unfinished agenda of staging reproductive aging | Q56995376 | ||
Women's Pregnancy Life History and Alzheimer's Risk: Can Immunoregulation Explain the Link? | Q57174073 | ||
Inflammation: Bridging Age, Menopause and APOEε4 Genotype to Alzheimer's Disease | Q57816569 | ||
Sex Hormones in Acquired Immunity and Autoimmune Disease | Q58583865 | ||
Exercise and the Aging Brain: Considerations for Sex Differences | Q60045415 | ||
Increased Alzheimer's risk during the menopause transition: A 3-year longitudinal brain imaging study | Q60303191 | ||
Sex differences in Alzheimer disease — the gateway to precision medicine | Q60637417 | ||
Global, regional, and national burden of Alzheimer's disease and other dementias, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016 | Q60641769 | ||
Cross-Sectional and Longitudinal MRI Brain Scans Reveal Accelerated Brain Aging in Multiple Sclerosis | Q64078909 | ||
Autoimmune Disease in Women: Endocrine Transition and Risk Across the Lifespan | Q64081204 | ||
Progesterone-Related Immune Modulation of Pregnancy and Labor | Q64102042 | ||
Study of MRI brain findings and carotid US features in systemic sclerosis patients, relationship with disease parameters | Q64111768 | ||
Cortical thickness variation of the maternal brain in the first 6 months postpartum: associations with parental self-efficacy. | Q64960202 | ||
Hormonal changes and mood in the puerperium | Q67766975 | ||
The immunological pregnancy protective effect of progesterone is manifested via controlling cytokine production | Q71344081 | ||
Effect of pregnancy and hormonal changes on the activity of rheumatoid arthritis | Q71750740 | ||
Subset-specific effects of sex hormones and pituitary gonadotropins on human lymphocyte proliferation in vitro | Q72210255 | ||
A universal menopausal syndrome? | Q36369113 | ||
White Matter Lipids as a Ketogenic Fuel Supply in Aging Female Brain: Implications for Alzheimer's Disease. | Q36437623 | ||
The otherness of self: microchimerism in health and disease | Q36450729 | ||
Fetal microchimerism and maternal health: a review and evolutionary analysis of cooperation and conflict beyond the womb | Q36461785 | ||
Parity and All-cause Mortality in Women and Men: A Dose-Response Meta-Analysis of Cohort Studies | Q36499602 | ||
Menopause leads to elevated expression of macrophage-associated genes in the aging frontal cortex: rat and human studies identify strikingly similar changes. | Q36572180 | ||
Relationship Between Clinical and Immunological Features with Magnetic Resonance Imaging Abnormalities in Female Patients with Neuropsychiatric Systemic Lupus Erythematosus | Q36720077 | ||
Estrogen action in neuroprotection and brain inflammation. | Q36721776 | ||
Reproductive and menopausal factors and risk of systemic lupus erythematosus in women | Q36773713 | ||
Very old women at highest risk of dementia and Alzheimer's disease: incidence data from the Kungsholmen Project, Stockholm. | Q36843772 | ||
Microchimerism in the human brain: more questions than answers | Q36846218 | ||
Sex differences in Alzheimer's disease and other dementias | Q36893692 | ||
Estrogen and CD4+ T cells | Q36925326 | ||
Reproduction-induced neuroplasticity: natural behavioural and neuronal alterations associated with the production and care of offspring | Q37081752 | ||
Postmenopausal hormone therapy and regional brain volumes: the WHIMS-MRI Study | Q37180441 | ||
Longitudinal pattern of regional brain volume change differentiates normal aging from MCI. | Q37213702 | ||
Sub-threshold depressive symptoms and brain structure: A magnetic resonance imaging study within the Whitehall II cohort | Q37255464 | ||
Essential role of estrogen for improvements in vascular endothelial function with endurance exercise in postmenopausal women | Q37275947 | ||
Effects of hormone therapy on brain structure: A randomized controlled trial | Q37280188 | ||
Number of children is associated with neuropathology of Alzheimer's disease in women | Q37283496 | ||
Early decline in glucose transport and metabolism precedes shift to ketogenic system in female aging and Alzheimer's mouse brain: implication for bioenergetic intervention | Q37296893 | ||
In-vivo Dynamics of the Human Hippocampus across the Menstrual Cycle | Q37319113 | ||
Th1 and Th2 responses: what are they? | Q37350671 | ||
Multimodal population brain imaging in the UK Biobank prospective epidemiological study | Q37378043 | ||
Interbirth intervals: Intrafamilial, intragenomic and intrasomatic conflict | Q37566670 | ||
Higher risk of progression to dementia in mild cognitive impairment cases who revert to normal | Q37593256 | ||
The implications of autoimmunity and pregnancy | Q37661793 | ||
Influence of different estrogens on neuroplasticity and cognition in the hippocampus | Q37681138 | ||
The role of pregnancy-associated hormones in the development and function of regulatory B cells | Q37689363 | ||
Contribution of systemic inflammation to chronic neurodegeneration | Q37774280 | ||
Fetal microchimerism as an explanation of disease | Q37823203 | ||
Molecular mechanisms involved in the regulation of neuritogenesis by estradiol: Recent advances. | Q37942434 | ||
Alzheimer's disease, autoimmunity and inflammation. The good, the bad and the ugly | Q37945426 | ||
Menopause in patients with autoimmune diseases | Q37961466 | ||
Immunology and the menstrual cycle. | Q37966543 | ||
P304 | page(s) | 100850 | |
P577 | publication date | 2020-06-03 | |
P1433 | published in | Frontiers in Neuroendocrinology | Q15716620 |
P1476 | title | Towards an understanding of women's brain aging: the immunology of pregnancy and menopause |
Q98243020 | The maternal brain: Region-specific patterns of brain aging are traceable decades after childbirth | cites work | P2860 |
Search more.