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CCNL2
Brain-Specific Knock-Out of Hypoxia-Inducible Factor-1Α
Mouse Ccnl2 Conditional Knockout Project (CRISPR/Cas9)
Gene Expression Responses to DNA Damage Are Altered in Human Aging and in Werner Syndrome
Comparative Transcriptomics Reveals Similarities and Differences
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
CCNL2 (NM 030937) Human Tagged ORF Clone Product Data
Agricultural University of Athens
Analysis of Genetic Association Using Hierarchical Clustering and Cluster Validation Indices
ZBTB33 Is Mutated in Clonal Hematopoiesis and Myelodysplastic Syndromes and Impacts RNA Splicing
CDK11 Loss Induces Cell Cycle Dysfunction and Death of BRAF and NRAS Melanoma Cells
CDK11 Loss Induces Cell Cycle Dysfunction and Death of BRAF and NRAS Melanoma Cells
Mouse SNP Miner: an Annotated Database of Mouse Functional Single Nucleotide Polymorphisms Eli Reuveni*1, Vasily E Ramensky2 and Cornelius Gross1
Spatial Maps of Prostate Cancer Transcriptomes Reveal an Unexplored Landscape of Heterogeneity
Fusion Genes in Gynecologic Tumors: the Occurrence, Molecular Mechanism and Prospect for Therapy ✉ Bingfeng Lu1, Ruqi Jiang1, Bumin Xie1,Wuwu1 and Yang Zhao 1
Cell-Penetrating Peptides Predicted from CASC3, AKIP1, and AHRR Proteins
Extensive and Coordinated Transcription of Noncoding Rnas
Discovery of Synthetic Lethal and Tumor Suppressive Paralog Pairs in the Human Genome
Defining the Genomic Signature of the Parous Breast
Top View
Lsm12 Is an NAADP Receptor and a Two-Pore Channel Regulatory Protein Required for Calcium Mobilization from Acidic Organelles Ji
Supplementary Information Patients and Sample Preparation
Download Validation Data
Transcriptome Characterization by RNA Sequencing Identifies a Major Molecular and Clinical Subdivision in Chronic Lymphocytic Leukemia
Memory T Cell RNA Rearrangement Programmed by Heterogeneous Nuclear Ribonucleoprotein Hnrnpll
Genome-Wide Profiling of DNA Methylation and Gene Expression Identifies Candidate Genes for Human Diabetic Neuropathy Kai Guo1†, Stephanie A
CCNL2 Sirna (Mouse)
Supplemental Data
Supp File S2.Pdf
Literature Optimized Integration of Gene Expression for Organ-Specific Evaluation of Toxicogenomics Datasets
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Supplementary Table 1 Paired SAM Analysis of Genes Changing in Response to Letrozole Treatment (Complete List)
Identification of Key Micrornas and Target Genes for the Diagnosis of Bone Nonunion
INSTITUTO CARLOS CHAGAS Doutorado Em Biociências E Biotecnologia
Modeling Gene Regulation from Paired Expression and Chromatin Accessibility Data
Attractor Metafeatures and Their Application in Biomolecular Data Analysis
Wo 2008/153743 A2
An Integrative Transcriptomic and Methylation Approach for Identifying Differentially Expressed Circular Rnas Associated with DNA Methylation Change