Perinatal Natural History of the Ts1Cje Mouse Model of Down Syndrome: Growth Restriction, Early Mortality, Heart Defects, and Delayed Development.

The Ts1Cje model of Down syndrome is of particular interest for perinatal studies because affected males are fertile. This permits affected pups to be carried in wild-type females, which is similar to human pregnancies. Here we describe the early natural history and growth profiles of Ts1Cje embryos...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:	PLoS ONE
المؤلفون الرئيسيون:	Millie A Ferrés, Diana W Bianchi, Ashley E Siegel, Roderick T Bronson, Gordon S Huggins, Faycal Guedj
التنسيق:	مقال
اللغة:	الإنجليزية
منشور في:	Public Library of Science (PLoS) 2016-01-01
الوصول للمادة أونلاين:	http://europepmc.org/articles/PMC5145234?pdf=render

مواد مشابهة

Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome
حسب: Nadine M. Aziz, وآخرون
منشور في: (2018-06-01)

Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome
حسب: Kai-Leng Tan, وآخرون
منشور في: (2014-12-01)

DYSREGULATION OF REST DURING BRAIN DEVELOPMENT OF THE TS1CJE MOUSE MODEL FOR DOWN SYNDROME
حسب: Chong-Teik Lim, وآخرون
منشور في: (2023-10-01)

Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model.
حسب: Usman Bala, وآخرون
منشور في: (2018-01-01)

Phenotype microarrays reveal metabolic dysregulations of neurospheres derived from embryonic Ts1Cje mouse model of Down syndrome.
حسب: Eryse Amira Seth, وآخرون
منشور في: (2020-01-01)

Unbalanced dendritic inhibition of CA1 neurons drives spatial-memory deficits in the Ts2Cje Down syndrome model
حسب: Sergio Valbuena, وآخرون
منشور في: (2019-11-01)

CJE-PCHF: Chinese Joint Entity and Relation Extraction Model Based on Progressive Contrastive Learning and Heterogeneous Feature Fusion
حسب: Meng He, وآخرون
منشور في: (2024-10-01)

Perinatal IV Aluminum and Developmental Delay
حسب: J Gordon Millichap
منشور في: (1997-06-01)

Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome
حسب: Dong P. Liu, وآخرون
منشور في: (2003-12-01)

Synaptic Vesicle Recycling Is Unaffected in the Ts65Dn Mouse Model of Down Syndrome.
حسب: Jamie R K Marland, وآخرون
منشور في: (2016-01-01)

Increased hippocampal epigenetic age in the Ts65Dn mouse model of Down Syndrome
حسب: Francesco Ravaioli, وآخرون
منشور في: (2024-05-01)

Hypocellularity in the murine model for Down Syndrome Ts65Dn is not affected by adult neurogenesis
حسب: Rosa eLópez-Hidalgo, وآخرون
منشور في: (2016-03-01)

Frequency, Family and Social Aspects of TS
حسب: J Gordon Millichap
منشور في: (1994-03-01)

Airport Cluster Delay Prediction Based on TS-BiLSTM-Attention
حسب: Xiujie Wei, وآخرون
منشور في: (2023-06-01)

[Letter to the editor] PCR prescreen for genotyping the Ts65Dn mouse model of Down syndrome
حسب: Hernan Lorenzi, وآخرون
منشور في: (2010-01-01)

Glutamatergic synaptic deficits in the prefrontal cortex of the Ts65Dn mouse model for Down syndrome
حسب: Aurore Thomazeau, وآخرون
منشور في: (2023-09-01)

Ts66Yah, a mouse model of Down syndrome with improved construct and face validity
حسب: Arnaud Duchon, وآخرون
منشور في: (2022-12-01)

Fin-TS and Fix-TS on fractional quaternion delayed neural networks with uncertainty via establishing a new Caputo derivative inequality approach
حسب: Qiong Wu, وآخرون
منشور في: (2022-06-01)

Bioinformatic characterization of differential proteins in the hippocampus of Ts65Dn: A mouse model of down syndrome
حسب: Zhang Bin, وآخرون
منشور في: (2014-01-01)

T.S. Eliot in Translations: Exploring T.S. Eliot’s Afterlives
حسب: Lise Chenal
منشور في: (2022-12-01)

Perinatal results of restricted intrauterine growth. Cienfuegos, 2022
حسب: Cristóbal Jorge Torres González, وآخرون
منشور في: (2023-11-01)

Adaptation, Development, and Validation of the Spiritual Community and Togetherness Scale (SCoTS)
حسب: Christopher R. Dabbs, وآخرون
منشور في: (2025-01-01)

Perinatal risk for delayed abdominal delivery
حسب: V E Radzinsky, وآخرون
منشور في: (2017-12-01)

Mitigation of tropospheric delay induced errors in TS-InSAR ground deformation monitoring
حسب: Shipeng Guo, وآخرون
منشور في: (2024-12-01)

Developmental deglutition and intrinsic tongue muscle maturation phenotypes in the Ts65Dn mouse model of Down syndrome
حسب: Tiffany J. Glass, وآخرون
منشور في: (2024-12-01)

Neuroanatomical alterations and synaptic plasticity impairment in the perirhinal cortex of the Ts65Dn mouse model of Down syndrome
حسب: Vincenzo Roncacé, وآخرون
منشور في: (2017-10-01)

CoCoNuTs are a diverse subclass of Type IV restriction systems predicted to target RNA
حسب: Ryan T Bell, وآخرون
منشور في: (2024-05-01)

Ultrasound in Prediction of Perinatal Outcomes in Fetuses with Restriction of Intrauterine Growth
حسب: Azhar K Abdul-Hameed, وآخرون
منشور في: (2023-01-01)

Expressive Language Delay Related to Chromosome 7 Defect
حسب: J Gordon Millichap
منشور في: (2005-11-01)

Removing the orientational degeneracy of the TS defect in 4H–SiC by electric fields and strain
حسب: Maximilian Rühl, وآخرون
منشور في: (2021-01-01)

Effects of neonatal neural progenitor cell implantation on adult neuroanatomy and cognition in the Ts65Dn model of Down syndrome.
حسب: Angela L Rachubinski, وآخرون
منشور في: (2012-01-01)

Pattern-restricted one-cycle permutations with a pattern-restricted cycle form
حسب: Kassie Archer, وآخرون
منشور في: (2024-10-01)

Ripples and Fast Ripples as Markers for Epileptogenic Zone in TS Complex
حسب: J Gordon Millichap, وآخرون
منشور في: (2014-12-01)

Joint TS Beamforming and Hybrid TS-PS Receiving Design for SWIPT Systems
حسب: Shiqi Wang, وآخرون
منشور في: (2021-01-01)

PREVENTION OF UNFAVOURABLE PERINATAL OUTCOMES OF PLACENTAL INSUFFICIENCY AND INTRAUTERINE GROWTH RESTRICTION
حسب: P. V. Budanov, وآخرون
منشور في: (2016-12-01)

Evidence of Energy Metabolism Alterations in Cultured Neonatal Astrocytes Derived from the Ts65Dn Mouse Model of Down Syndrome
حسب: Bruna L. Zampieri, وآخرون
منشور في: (2022-01-01)

Physical Training Chronically Stimulates the Motor Neuron Cell Nucleus in the Ts65Dn Mouse, a Model of Down Syndrome
حسب: Chiara Rita Inguscio, وآخرون
منشور في: (2023-05-01)

Neonatal therapy with clenbuterol and salmeterol restores spinogenesis and dendritic complexity in the dentate gyrus of the Ts65Dn model of Down syndrome
حسب: Marco Emili, وآخرون
منشور في: (2020-07-01)

Heart rate and blood pressure in male Ts65Dn mice: a model to investigate cardiovascular responses in Down syndrome
حسب: Lara R. DeRuisseau, وآخرون
منشور في: (2019-09-01)

Maternal choline supplementation improves spatial learning and adult hippocampal neurogenesis in the Ts65Dn mouse model of Down syndrome
حسب: Ramon Velazquez, وآخرون
منشور في: (2013-10-01)