Cargando…

Interacting impact of maternal inflammatory response and stress on the amygdala transcriptome of pigs

Changes at the molecular level capacitate the plasticity displayed by the brain in response to stress stimuli. Weaning stress can trigger molecular changes that influence the physiology of the offspring. Likewise, maternal immune activation (MIA) during gestation has been associated with behavior di...

Descripción completa

Detalles Bibliográficos
Autores principales:	Keever-Keigher, Marissa R, Zhang, Pan, Bolt, Courtni R, Rymut, Haley E, Antonson, Adrienne M, Caputo, Megan P, Houser, Alexandra K, Hernandez, Alvaro G, Southey, Bruce R, Rund, Laurie A, Johnson, Rodney W, Rodriguez-Zas, Sandra L
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Neurogenetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496236/ https://www.ncbi.nlm.nih.gov/pubmed/33856433 http://dx.doi.org/10.1093/g3journal/jkab113

Ejemplares similares

Lasting and Sex-Dependent Impact of Maternal Immune Activation on Molecular Pathways of the Amygdala
por: Keever, Marissa R., et al.
Publicado: (2020)

Long-Lasting Impact of Maternal Immune Activation and Interaction With a Second Immune Challenge on Pig Behavior
por: Rymut, Haley E., et al.
Publicado: (2020)

Impact of Weaning and Maternal Immune Activation on the Metabolism of Pigs
por: Southey, Bruce R., et al.
Publicado: (2021)

The Combined Effect of Weaning Stress and Immune Activation during Pig Gestation on Serum Cytokine and Analyte Concentrations
por: Rymut, Haley E., et al.
Publicado: (2021)

Biochemistry and Immune Biomarkers Indicate Interacting Effects of Pre- and Postnatal Stressors in Pigs across Sexes
por: Rymut, Haley E., et al.
Publicado: (2021)

Terpenoid Backbone Biosynthesis among Pig Hippocampal Pathways Impacted by Stressors
por: Rymut, Haley E., et al.
Publicado: (2022)

Hippocampal Changes Elicited by Metabolic and Inflammatory Stressors following Prenatal Maternal Infection
por: Rodriguez-Zas, Sandra L., et al.
Publicado: (2022)

Prefrontal Cortex Response to Prenatal Insult and Postnatal Opioid Exposure
por: Rymut, Haley E., et al.
Publicado: (2022)

Acetylcholine signaling genes are required for cocaine-stimulated egg laying in Caenorhabditis elegans
por: Emerson, Soren, et al.
Publicado: (2021)

The neural G protein Gα(o) tagged with GFP at an internal loop is functional in Caenorhabditis elegans
por: Kumar, Santosh, et al.
Publicado: (2021)

Effects of maternal immune activation in porcine transcript isoforms of neuropeptide and receptor genes
por: Southey, Bruce R., et al.
Publicado: (2021)

Social defeat stress induces genome-wide 5mC and 5hmC alterations in the mouse brain
por: Kuehner, Janise N, et al.
Publicado: (2023)

FXN gene methylation determines carrier status in Friedreich ataxia
por: Lam, Christina, et al.
Publicado: (2023)

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis
por: Fridman, V, et al.
Publicado: (2015)

Frontotemporal dementia presentation in patients with heterozygous p.H157Y variant of TREM2
por: Ogonowski, Natalia, et al.
Publicado: (2023)

Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation
por: Ragoussis, Vassilis, et al.
Publicado: (2022)

Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive
por: Vogt, Guido, et al.
Publicado: (2022)

Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies
por: Pérez-Palma, Eduardo, et al.
Publicado: (2017)

Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)
por: Wang, Kun, et al.
Publicado: (2018)

Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3
por: Garcia‐Moreno, Hector, et al.
Publicado: (2022)

Prenatal and postnatal challenges affect the hypothalamic molecular pathways that regulate hormonal levels
por: Rodriguez-Zas, Sandra L., et al.
Publicado: (2023)

Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia
por: Klein, Christopher J, et al.
Publicado: (2013)

Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation
por: Liu, Yo-Tsen, et al.
Publicado: (2014)

Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis
por: Fratta, Pietro, et al.
Publicado: (2014)

Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy
por: Tucci, Arianna, et al.
Publicado: (2014)

Rare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients
por: Kuhn, Marius, et al.
Publicado: (2016)

Genetic neurological channelopathies: molecular genetics and clinical phenotypes
por: Spillane, J, et al.
Publicado: (2016)

Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series
por: Lynch, David S, et al.
Publicado: (2016)

A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy
por: Legati, Andrea, et al.
Publicado: (2017)

TBK1 mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisation
por: Pozzi, Laura, et al.
Publicado: (2017)

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses
por: Addis, Laura, et al.
Publicado: (2018)

Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development
por: Juneja, Manisha, et al.
Publicado: (2019)

Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial
por: Ohsawa, Yutaka, et al.
Publicado: (2019)

Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era
por: Lynch, David S, et al.
Publicado: (2019)

Integrative network and brain expression analysis reveals mechanistic modules in ataxia
por: Eidhof, Ilse, et al.
Publicado: (2019)

Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan
por: Yoshimura, Akiko, et al.
Publicado: (2019)

Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation
por: Tulli, Susanna, et al.
Publicado: (2019)

Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia
por: Chelban, Viorica, et al.
Publicado: (2017)

Intermediate C9orf72 alleles in neurological disorders: does size really matter?
por: Ng, Adeline S L, et al.
Publicado: (2017)

Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk
por: Bobbili, Dheeraj Reddy, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_gvhg7enhh8dpc0k60f870vm9e5