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TTC28
PARSANA-DISSERTATION-2020.Pdf
DNA Breakpoint Assay Reveals a Majority of Gross Duplications Occur in Tandem Reducing VUS Classifications in Breast Cancer Predisposition Genes
(P -Value<0.05, Fold Change≥1.4), 4 Vs. 0 Gy Irradiation
Macrophage Activation JUNB Is a Key Transcriptional Modulator Of
Accelerating Matchmaking of Novel Dysmorphology Syndromes Through Clinical and Genomic Characterization of a Large Cohort
A Novel Predictive and Prognostic Scoring for Progressive Meningioma
Gene Ontology Functional Annotations and Pleiotropy
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Mapping of Craniofacial Traits in Outbred Mice Identifies Major Developmental Genes Involved in Shape Determination
Downregulation of SNRPG Induces Cell Cycle Arrest and Sensitizes Human Glioblastoma Cells to Temozolomide by Targeting Myc Through a P53-Dependent Signaling Pathway
FISH Oracle 2: a Web Server for Integrative Visualization of Genomic Data in Cancer Research Malte Mader1,2, Ronald Simon2 and Stefan Kurtz1*
Identification of Microrna-Associated-Cerna
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
PRODUCT SPECIFICATION Product Datasheet
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Screening for Novel Hexanucleotide Repeat Expansions at ALS- and FTD-Associated Loci
Top View
L1 Retrotransposition Is a Common Feature of Mammalian Hepatocarcinogenesis
Frequent L1 Retrotranspositions Originating from TTC28 in Colorectal Cancer
Detection of Subclonal L1 Transductions in Colorectal Cancer
Single-Cell Transcriptional Dynamics and Origins of Neuronal Diversity in the Developing Mouse Neocortex
Comprehensive Analysis of Differentially Expressed Lncrnas As Diagnostic and Prognostic Markers for Colorectal Cancer
Analysis of the Whole Genome Sequence
Novel Low Frequency Variants for Polycystic Ovary Syndrome
Retrotransposition in Colorectal Cancer
LINE-1 Retrotransposon-Mediated DNA Transductions in Endometriosis Associated Ovarian Cancers
Microdeletion Del(22)(Q12.2) Encompassing the Facial Development-Associated Gene, MN1 (Meningioma 1) in a Child with Pierre-Robi
Nanopore Sequencing Enables Comprehensive Transposable Element Epigenomic Profiling
15) 8:106 DOI 10.1186/S13039-015-0205-9
Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease
Exome Sequencing of Fetal Anomaly Syndromes: Novel Phenotype–Genotype Discoveries
Microrna Binding Microrna Binding Probe Set Entrez Gene Gene
Novel Promoters and Coding First Exons in DLG2
GWAS Reveals Loci Associated with Velopharyngeal Dysfunction
Comprehensive Molecular Characterization of Human Colon and Rectal Cancer