Cargando…

Exonic DNA Sequencing of ERBB4 in Bipolar Disorder

The Neuregulin-ErbB4 pathway plays a crucial role in brain development and constitutes one of the most biologically plausible signaling pathways implicated in schizophrenia and, to a lesser extent, in bipolar disorder (BP). However, recent genome-wide association analyses have not provided evidence...

Descripción completa

Detalles Bibliográficos
Autores principales:	Goes, Fernando S., Rongione, Michael, Chen, Yun-Ching, Karchin, Rachel, Elhaik, Eran, Potash, James B.
Formato:	Texto
Lenguaje:	English
Publicado:	Public Library of Science 2011
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102700/ https://www.ncbi.nlm.nih.gov/pubmed/21637803 http://dx.doi.org/10.1371/journal.pone.0020242

Ejemplares similares

Systematic review of genome-wide gene expression studies of bipolar disorder
por: Seifuddin, Fayaz, et al.
Publicado: (2013)

A Hybrid Likelihood Model for Sequence-Based Disease Association Studies
por: Chen, Yun-Ching, et al.
Publicado: (2013)

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
por: Jia, Xiaoming, et al.
Publicado: (2021)

Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
por: Jia, Xiaoming, et al.
Publicado: (2021)

Targeted Sequencing of FKBP5 in Suicide Attempters with Bipolar Disorder
por: Breen, Marie E., et al.
Publicado: (2016)

Genome-Wide DNA Methylation Scan in Major Depressive Disorder
por: Sabunciyan, Sarven, et al.
Publicado: (2012)

ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy
por: Hyder, Zerin, et al.
Publicado: (2021)

Genome-wide association of mood-incongruent psychotic bipolar disorder
por: Goes, F S, et al.
Publicado: (2012)

Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder
por: Judy, Jennifer Toolan, et al.
Publicado: (2013)

Racial differences in the major clinical symptom domains of bipolar disorder
por: Li, Kevin, et al.
Publicado: (2023)

Cross-Species Analysis of Genic GC(3) Content and DNA Methylation Patterns
por: Tatarinova, Tatiana, et al.
Publicado: (2013)

Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder
por: Nishioka, Masaki, et al.
Publicado: (2021)

'Genome order index' should not be used for defining compositional constraints in nucleotide sequences - a case study of the Z-curve
por: Elhaik, Eran, et al.
Publicado: (2010)

The Missing Link of Jewish European Ancestry: Contrasting the Rhineland and the Khazarian Hypotheses
por: Elhaik, Eran
Publicado: (2013)

Empirical Distributions of F (ST) from Large-Scale Human Polymorphism Data
por: Elhaik, Eran
Publicado: (2012)

In Search of the jüdische Typus: A Proposed Benchmark to Test the Genetic Basis of Jewishness Challenges Notions of “Jewish Biomarkers”
por: Elhaik, Eran
Publicado: (2016)

A “Wear and Tear” Hypothesis to Explain Sudden Infant Death Syndrome
por: Elhaik, Eran
Publicado: (2016)

Neonatal circumcision and prematurity are associated with sudden infant death syndrome (SIDS)
por: Elhaik, Eran
Publicado: (2019)

Editorial: Population Genetics of Worldwide Jewish People
por: Elhaik, Eran
Publicado: (2017)

Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated
por: Elhaik, Eran
Publicado: (2022)

Nucleolin and ErbB2 inhibition reduces tumorigenicity of ErbB2-positive breast cancer
por: Wolfson, Eya, et al.
Publicado: (2018)

ERBB2 exon 20 insertions are rare in Brazilian non‐small cell lung cancer
por: de Oliveira Cavagna, Rodrigo, et al.
Publicado: (2022)

Validation and assessment of variant calling pipelines for next-generation sequencing
por: Pirooznia, Mehdi, et al.
Publicado: (2014)

Quantitative Phosphoproteomics Analysis of ERBB3/ERBB4 Signaling
por: Wandinger, Sebastian K., et al.
Publicado: (2016)

IsoPlotter(+): A Tool for Studying the Compositional Architecture of Genomes
por: Elhaik, Eran, et al.
Publicado: (2013)

A Comparative Study and a Phylogenetic Exploration of the Compositional Architectures of Mammalian Nuclear Genomes
por: Elhaik, Eran, et al.
Publicado: (2014)

On the Unfounded Enthusiasm for Soft Selective Sweeps III: The Supervised Machine Learning Algorithm That Isn’t
por: Elhaik, Eran, et al.
Publicado: (2021)

A Fast Algorithm for Exonic Regions Prediction in DNA Sequences
por: Saberkari, Hamidreza, et al.
Publicado: (2013)

Periodicity of DNA in exons
por: Eskesen, Stephen T, et al.
Publicado: (2004)

Investigation of the prevalence and clinical implications of ERBB2 exon 16 skipping mutations in Chinese pan-cancer patients
por: Shang, Yanhong, et al.
Publicado: (2023)

Pair Matcher (PaM): fast model-based optimization of treatment/case-control matches
por: Elhaik, Eran, et al.
Publicado: (2019)

Genomic regulatory sequences in the pathogenesis of bipolar disorder
por: Levchenko, Anastasia, et al.
Publicado: (2023)

Integrated entropy-based approach for analyzing exons and introns in DNA sequences
por: Li, Junyi, et al.
Publicado: (2019)

Sensitivity of epidermal growth factor receptor and ErbB2 exon 20 insertion mutants to Hsp90 inhibition
por: Xu, W, et al.
Publicado: (2007)

Clinical characterization of ERBB2 exon 20 insertions and heterogeneity of outcomes responding to afatinib in Chinese lung cancer patients
por: Liu, Zhefeng, et al.
Publicado: (2018)

Clinical significance of ERBB2 exon 16 skipping: analysis of a real-world retrospective observational cohort study
por: Shi, Lei, et al.
Publicado: (2020)

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
por: Maier, Robert, et al.
Publicado: (2015)

Bipolar Disorder in Children
por: Renk, Kimberly, et al.
Publicado: (2014)

HapZipper: sharing HapMap populations just got easier
por: Chanda, Pritam, et al.
Publicado: (2012)

Endocrine resistance in breast cancer: new roles for ErbB3 and ErbB4
por: Sutherland, Robert L
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_s6onvk2ob85ib52bvoosde36v9