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CD3EAP
Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant In
NRF1) Coordinates Changes in the Transcriptional and Chromatin Landscape Affecting Development and Progression of Invasive Breast Cancer
Human Social Genomics in the Multi-Ethnic Study of Atherosclerosis
CREB-Dependent Transcription in Astrocytes: Signalling Pathways, Gene Profiles and Neuroprotective Role in Brain Injury
Association of Chromosome 19 to Lung Cancer Genotypes and Phenotypes
Supporting Information
Extensive Cargo Identification Reveals Distinct Biological Roles of the 12 Importin Pathways Makoto Kimura1,*, Yuriko Morinaka1
Recessive Mutations in POLR1C Cause a Leukodystrophy by Impairing Biogenesis of RNA Polymerase III Isabelle Thiffault
Recessive Mutations in POLR1C Cause a Leukodystrophy by Impairing Biogenesis of RNA Polymerase III
Cryo-EM Structures of Human RNA Polymerase I
Offenmüller Et Al. Risk Loci in ALL Gene Location SNP Group And
1 Dynamics of Re-Constitution of the Human Nuclear Proteome After Cell
Identifying Novel Putative Genes Linked to Stuttering in Highly Multiplex
Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1
Felipe Fidalgo De Carvalho
S41598-019-41896-6.Pdf
Systematic Bromodomain Protein Screens Identify Homologous Recombination and R-Loop Suppression Pathways Involved in Genome Integrity
Identificação De Mutações Germinativas Em Pacientes Com Câncer Papilífero Familiar De Tireoide Através De Análise De Exoma
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