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PUS7L
Pseudouridine Synthases Modify Human Pre-Mrna Co-Transcriptionally and Affect Splicing
Vfabstract-Booklet-2017---Nda-Removed.Pdf
Stroke Genetics and Genomics
Genomic and Transcriptomic Investigations Into the Feed Efficiency Phenotype of Beef Cattle
Computational Inferences of Mutations Driving Mesenchymal Differentiation in Glioblastoma
Identification of Novel Cellular Factors Involved in HIV-1 Latency
Tumors Normals
Investigating the Impact of Telomere Dysfunction on the Chronic Lymphocytic Leukaemia Genome
A Grainyhead-Like 2/Ovo-Like 2 Pathway Regulates Renal Epithelial Barrier Function and Lumen Expansion
Diagnóstico Molecular Do Transtorno Do Espectro Autista Através Do Sequenciamento Completo De Exoma Molecular Diagnosis Of
Mirnas Documented to Play a Role in Hematopoietic Cell Lineage. Our
Xu Jialin Thesis 2018
Gene Mapping of Monogenic Disorders and Complex Diseases Via Genome Wide Association Studies Xia Zhao Iowa State University
Pathway and Network Analysis of Transcriptomic and Genomic Data.Pdf
A Quantitative Genetic Analysis of Limb Segment Morphology in Humans and Other Primates: Genetic Variance, Morphological Integration, and Linkage Analysis
PUS7 Mutations Impair Pseudouridylation in Humans and Cause Intellectual Disability and Microcephaly
PUS7L (K-13): Sc-138566
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(12) Patent Application Publication (10) Pub. No.: US 2015/0050728A1 Benvenisty Et Al
WO 2017/069958 A2 27 April 2017 (27.04.2017) P O P C T
Pathogenic Mutation of Lrrk2 – a Mouse Model for Pre-Motor Parkinson’S Disease
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