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SETBP1
Sleeping Beauty Transposon Mutagenesis Identifies Genes That
A Yeast Phenomic Model for the Influence of Warburg Metabolism on Genetic Buffering of Doxorubicin Sean M
A Set of Regulatory Genes Co-Expressed in Embryonic Human Brain Is Implicated in Disrupted Speech Development
Blueprint Genetics Comprehensive Growth Disorders / Skeletal
Report 99517
Oncoscore: a Novel, Internet-Based Tool to Assess the Oncogenic Potential of Genes
Title: a Yeast Phenomic Model for the Influence of Warburg Metabolism on Genetic
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
Downregulation of SETBP1 Promoted Non-Small Cell Lung Cancer Progression by Inducing Cellular EMT and Disordered Immune Status
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
SETBP1 Overexpression Is a Novel Leukemogenic Mechanism That Predicts Adverse Outcome in Elderly Patients with Acute Myeloid Leukemia
FOXP2 and Language Alterations in Psychiatric Pathology Salud Mental, Vol
Transcriptome Profiling Reveals the Complexity of Pirfenidone Effects in IPF
Alternative Splicing and Cancer: a Systematic Review
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Overlapping SETBP1 Gain-Of-Function Mutations in Schinzel-Giedion Syndrome and Hematologic Malignancies
SETBP1 Dysregulation in Congenital Disorders and Myeloid Neoplasms
Rare Disease Database.)
Top View
SETBP1 Gene SET Binding Protein 1
Multivariate Analysis Identifies Eight Novel Loci Associated with Meat
The Pathophysiology of Spinal Bulbar Muscular Atrophy: a Longitudinal Analysis of Mouse Muscle and Spinal Cord
Clinical Delineation of SETBP1 Haploinsufficiency Disorder
18Q Deletions from 18Q11.2 to 18Q21.2
Setbp1 and Ets2-Erg
High-Throughput Discovery of Novel Developmental Phenotypes
Comprehensive Genetic Test Menu
Rabbit Anti-SETBP1/FITC Conjugated Antibody
52 Genetic Loci Influencing Myocardial&Nbsp
SETBP1 Induces Transcription of a Network of Development Genes by Acting As an Epigenetic Hub
(Gly870ser) Variant in a Patient with Schinzel-Giedion Syndrome