Cargando…

Comprehensive maternal serum proteomics identifies the cytoskeletal proteins as non-invasive biomarkers in prenatal diagnosis of congenital heart defects

Congenital heart defects (CHDs) are the most common group of major birth defects. Presently there are no clinically used biomarkers for prenatally detecting CHDs. Here, we performed a comprehensive maternal serum proteomics assessment, combined with immunoassays, for the discovery of non-invasive bi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chen, Lizhu, Gu, Hui, Li, Jun, Yang, Ze-Yu, Sun, Xiao, Zhang, Li, Shan, Liping, Wu, Lina, Wei, Xiaowei, Zhao, Yili, Ma, Wei, Zhang, Henan, Cao, Songying, Huang, Tianchu, Miao, Jianing, Yuan, Zhengwei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2016
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707500/ https://www.ncbi.nlm.nih.gov/pubmed/26750556 http://dx.doi.org/10.1038/srep19248

Ejemplares similares

Identification of PCSK9 as a novel serum biomarker for the prenatal diagnosis of neural tube defects using iTRAQ quantitative proteomics
por: An, Dong, et al.
Publicado: (2015)

Application potential of bone marrow mesenchymal stem cell (BMSCs) based tissue-engineering for spinal cord defect repair in rat fetuses with spina bifida aperta
por: Li, Xiaoshuai, et al.
Publicado: (2016)

Nuclear factor I-C disrupts cellular homeostasis between autophagy and apoptosis via miR-200b-Ambra1 in neural tube defects
por: Huang, Wanqi, et al.
Publicado: (2021)

Intra‐amniotic mesenchymal stem cell therapy improves the amniotic fluid microenvironment in rat spina bifida aperta fetuses
por: Wei, Xiaowei, et al.
Publicado: (2022)

Congenital perineal hamartomas with rectal duplication: A case report
por: Zhang, Yixin, et al.
Publicado: (2023)

Prenatal diagnosis of congenital heart defects: echocardiography
por: Sun, Heather Y.
Publicado: (2021)

Actin cytoskeletal defects in immunodeficiency
por: Moulding, Dale A, et al.
Publicado: (2013)

Epidemiological Aspects, Prenatal Screening and Diagnosis of Congenital Heart Defects in Beijing
por: Zhang, Yanchun, et al.
Publicado: (2021)

Intra-amniotic transplantation of brain-derived neurotrophic factor-modified mesenchymal stem cells treatment for rat fetuses with spina bifida aperta
por: Ma, Wei, et al.
Publicado: (2022)

Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis
por: Yang, Jiaomei, et al.
Publicado: (2015)

Defects of microtubule cytoskeletal organization in NOA human testes
por: Wu, Xiaolong, et al.
Publicado: (2022)

The current state of prenatal detection of genetic conditions in congenital heart defects
por: Findley, Tina O., et al.
Publicado: (2021)

Proteomic analysis of metabolic, cytoskeletal and stress response proteins in human heart failure
por: Li, Weiming, et al.
Publicado: (2012)

Prenatal Diagnosis of a Fetus with Congenital Heart Defect and Ring Chromosome 14
por: Sánchez, Javier, et al.
Publicado: (2012)

Associated factors for prenatally diagnosed fetal congenital heart diseases
por: Ruan, Yanping, et al.
Publicado: (2023)

Defects in Cytoskeletal Signaling Pathways, Arrhythmia, and Sudden Cardiac Death
por: Smith, Sakima, et al.
Publicado: (2012)

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects
por: Musfee, Fadi I., et al.
Publicado: (2021)

TRIM4 is associated with neural tube defects based on genome-wide DNA methylation analysis
por: Zhang, Henan, et al.
Publicado: (2019)

Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects
por: Liu, Jingjing, et al.
Publicado: (2022)

Prenatal ultrasound diagnosis of congenital infantile fibrosarcoma and congenital hemangioma: Three case reports
por: Liang, Ru-Na, et al.
Publicado: (2023)

Prenatal Diagnosis of a Congenital Postaxial Longitudinal Limb Defect: A Case Report
por: Pauleta, Joana, et al.
Publicado: (2010)

Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study
por: Bakker, Marian K, et al.
Publicado: (2019)

Utility of Fetal Cardiovascular Magnetic Resonance for Prenatal Diagnosis of Complex Congenital Heart Defects
por: Salehi, Daniel, et al.
Publicado: (2021)

ILEE: Algorithms and toolbox for unguided and accurate quantitative analysis of cytoskeletal images
por: Li, Pai, et al.
Publicado: (2022)

Artificial Intelligence in Prenatal Ultrasound Diagnosis
por: He, Fujiao, et al.
Publicado: (2021)

Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
por: Ross, Jacob A., et al.
Publicado: (2019)

Molecular Defects in Friedreich’s Ataxia: Convergence of Oxidative Stress and Cytoskeletal Abnormalities
por: Smith, Frances M., et al.
Publicado: (2020)

Prenatal Management Strategy for Immune-Associated Congenital Heart Block in Fetuses
por: Liao, Hongyu, et al.
Publicado: (2021)

Intra-Amniotic Delivery of CRMP4 siRNA Improves Mesenchymal Stem Cell Therapy in a Rat Spina Bifida Model
por: Wei, Xiaowei, et al.
Publicado: (2020)

Content and Quality of Information Websites About Congenital Heart Defects Following a Prenatal Diagnosis
por: Carlsson, Tommy, et al.
Publicado: (2015)

Experiences of informational needs and received information following a prenatal diagnosis of congenital heart defect
por: Carlsson, Tommy, et al.
Publicado: (2016)

Prenatal diagnosis of congenital anomalies
por: Todros, T, et al.
Publicado: (2001)

Epidemiology, prenatal diagnosis, and neonatal outcomes of congenital heart defects in eastern China: a hospital-based multicenter study
por: Zhang, Xiaohui, et al.
Publicado: (2020)

Dictyostelium mutants lacking the cytoskeletal protein coronin are defective in cytokinesis and cell motility
Publicado: (1993)

Proteomic and Microscopic Strategies towards the Analysis of the Cytoskeletal Networks in Major Neuropsychiatric Disorders
por: Coumans, Joëlle V. F., et al.
Publicado: (2016)

Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting
por: Yi, Tong, et al.
Publicado: (2022)

SELDI-TOF-MS Proteomic Profiling of Serum, Urine, and Amniotic Fluid in Neural Tube Defects
por: Liu, Zhenjiang, et al.
Publicado: (2014)

IAG Regulates the Expression of Cytoskeletal Protein-Encoding Genes in Shrimp Testis
por: Lv, Qian, et al.
Publicado: (2023)

Risk factors of malnutrition in Chinese children with congenital heart defect
por: Zhang, Mingjie, et al.
Publicado: (2020)

Information following a Diagnosis of Congenital Heart Defect: Experiences among Parents to Prenatally Diagnosed Children
por: Carlsson, Tommy, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_vbpot6bc9ti6h46umfe4t1jv0g