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PCDHA4
Supplementary Table 1: Adhesion Genes Data Set
Structural Determinants of Adhesion by Protocadherin-19 and Implications for Its Role in Epilepsy Sharon Cooper Cedarville University,
[email protected]
Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology
Protocadherin Family: Diversity, Structure, and Function Hirofumi Morishita1 and Takeshi Yagi2
Enhancer Hubs and Loop Collisions Identified from Single-Allele Topologies
An Epigenetic Reprogramming Strategy to Resensitize
Thousands of Cpgs Show DNA Methylation Differences in ACPA-Positive Individuals
Using an Atlas of Gene Regulation Across 44 Human Tissues to Inform Complex Disease- and Trait-Associated Variation
Comparing the Effects of Vitamin E Tocotrienol-Rich Fraction Supplementation and Α-Tocopherol Supplementation on Gene Expression in Healthy Older Adults
Full Text (PDF)
Mutations on Protein Function
Molecular Sciences High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorder
Genomics of Ovarian Cancer Progression Reveals Diverse Metastatic Trajectories Including Intraepithelial Metastasis to the Fallopian Tube
Gwas Meta-Analysis of Intelligence 1
Remote Memory and Cortical Synaptic Plasticity Require Neuronal CCCTC-Binding Factor (CTCF)
Name Aliases Binding Partner Physiology / Oncology References
The Genetic Architecture of the Human Thalamus and Its Overlap with Ten
A CATH Domain Functional Family Based Approach to Identify
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Genome-Wide Methylation Profiling of the Different Stages of Hepatitis B Virus-Related Hepatocellular Carcinoma Development in P
G-Protocadherin Structural Diversity and Functional Implications
Genome-Wide CNV Investigation Suggests a Role for Cadherin, Wnt, and P53 Pathways in Primary Open-Angle Glaucoma Valeria Lo Faro1,2, Jacoline B
PCDHA4 Rabbit Polyclonal Antibody – TA341926 | Origene
Antisense Lncrna Transcription Drives Stochastic Protocadherin Α Promoter Choice
Agglomerative Epigenetic Aberrations Are a Common Event in Human Breast Cancer
A Webservice Aided by Deep Learning to Mine Pubmed for Addiction-Related Genes
Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
Suppementary Table 9. Predicted Targets of Hsa-Mir-181A by Targetscan 6.2
Detection of Genomic Alterations Caused by Low-Dose Γ-Irradiation in Human Normal Fibroblast Cells
WO 2014/100434 Al 26 June 2014 (26.06.2014) W P O P C T
Analysis of Whole Exome Sequencing in Severe Mental Illness Hints at Selection of Brain Development and Immune Related Genes
Genome-Wide Allele-Specific Methylation Is Enriched at Gene
The Aryl Hydrocarbon Receptor Pathway: a Key Component of the Microrna-Mediated AML Signalisome
BMC Research Notes Biomed Central
Differential and Spatial Expression Meta-Analysis of Genes
Usbiological Datasheet
1 a Gene Ontology Approach to Autism Spectrum Disorders