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TFPT
Location Analysis of Estrogen Receptor Target Promoters Reveals That
Subterranean Mammals Show Convergent Regression in Ocular Genes and Enhancers, Along with Adaptation to Tunneling
Biological Models of Colorectal Cancer Metastasis and Tumor Suppression
Heterozygous Deletions of Noncoding Parts of the PRPF31 Gene Cause Retinitis Pigmentosa Via Reduced Gene Expression
The Cytogenetics of Hematologic Neoplasms 1 5
Atypical Chromosome Abnormalities in Acute Myeloid Leukemia Type M4
Text-Based Analysis of Genes, Proteins, Aging, and Cancer
A Study Into the Evolutionary Divergence of the Core Promoter Elements of PRPF31 and TFPT
Initiation of Antiviral B Cell Immunity Relies on Innate Signals from Spatially Positioned NKT Cells
Global Analysis of SUMO-Binding Proteins Identifies Sumoylation As a Key Regulator of the INO80 Chromatin Remodeling Complex
Unifying the Genomics-Based Classes of Cancer Fusion Gene Partners: Large Cancer Fusion Genes Are Evolutionarily Conserved
(TCF3) (NM 003200) Human Recombinant Protein Product Data
A Study Into the Evolutionary Divergence of the Core Promoter Elements of PRPF31 and TFPT
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
UNIVERSITY of CALIFORNIA, SAN DIEGO Measuring
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Global Analysis of Sumo-Binding Proteins Identifies Sumoylation
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
Top View
Correspondence on Lovell Et Al.: Identification of Chicken Genes Previously Assumed to Be Evolutionarily Lost
A Study Into the Evolutionary Divergence of the Core Promoter
A Novel Approach to Identification of Diagnostic Markers In
Protein-Protein and Protein-DNA Interactions of the Human C2H2 Zinc Finger Proteins
Atlas Journal
Mouse Tfpt Conditional Knockout Project (CRISPR/Cas9)
Atlas Journal
A 112 Kb Deletion in Chromosome 19Q13.42 Leads to Retinitis Pigmentosa
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Lineage-Specific Programming Target Genes Defines Potential for Th1
American Society of Human Genetics 67Th Annual Meeting October 17–21, 2017 in Orlando, Florida
Molecular Genetics of Ocular Diseases
Experimental Acute Exposure to Thirdhand Smoke and Changes in the Human Nasal Epithelial Transcriptome a Randomized Clinical Trial
Genes on Bovine Chromosome 18 Associated with Bilateral Convergent Strabismus with Exophthalmos in German Brown Cattle
Kb Genomic Deletion on 19Q13.42 in Autosomal-Dominant Retinitis Pigmentosa with Incomplete Penetrance
Human TCF3 Blocking Peptide (CDBP2927) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: a Novel Genomic Rearrangement
Wo2018/191558