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CCM2
Identification of Cis-Regulatory Sequence
Transcriptome-Wide Profiling of Cerebral Cavernous Malformations
Mir-17-92 Fine-Tunes MYC Expression and Function to Ensure
CCM1 and CCM2 Variants in Patients with Cerebral Cavernous
Cerebral Cavernous Malformations: from Genes to Proteins to Disease
A Focus on Genetic Features of Cerebral Cavernous Malformations and Brain Arteriovenous Malformations Pathogenesis
Human Social Genomics in the Multi-Ethnic Study of Atherosclerosis
Phylogenetic Analysis of Harmonin Homology Domains
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance
Cisplatin Treatment of Testicular Cancer Patients Introduces Long-Term Changes in the Epigenome Cecilie Bucher-Johannessen1, Christian M
CCM2 Molecular Signaling Pathway Arianne J
Single-Cell Transcriptome Analysis Reveals Mesenchymal Stem Cells In
Report Mutations in a Gene Encoding a Novel Protein Containing A
Using Hidden Markov Models to Investigate G- Quadruplex Motifs in Genomic Sequences
Wasin Vol. 9 N. 4 2558.Pmd
CCM2–CCM3 Interaction Stabilizes Their Protein Expression and Permits Endothelial Network Formation
Primate Specific Retrotransposons, Svas, in the Evolution of Networks That Alter Brain Function
Detection, Validation, and Downstream Analysis of Allelic Variation in Gene Expression
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Detection, Validation, and Downstream Analysis of Allelic Variation in Gene Expression Daniel C
Identification of Genomic Targets of Transcription Factor Aebp1 and Its Role in Survival of Glioma Cells
CCM2 Deficient Endothelial Cells Undergo a Mechano-Dependent Reprogramming Into Senescence Associated Secretory Phenotype Used to Recruit Endothelial and Immune Cells
Mapping Endothelial-Cell Diversity in Cerebral Cavernous Malformations
CCM) Patients: an Overall View from Genes to Endothelial Cells
First Interchromosomal Insertion in a Patient with Cerebral and Spinal Cavernous Malformations Robin A
CCM2 Gene CCM2 Scaffold Protein
An Rnai Screen in Mammalian Embryos
Simultaneous Discovery of Candidate Imprinted Genes and Imprinting
Nuclear Genetic Regulation of the Human Mitochondrial Transcriptome