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CAP2
Partial Deletion of Chromosome 6P Causing Developmental Delay and Mild Dysmorphisms in a Child
The Capacity of Long-Term in Vitro Proliferation of Acute Myeloid
Gene Ontology Functional Annotations and Pleiotropy
Transdifferentiation of Human Mesenchymal Stem Cells
CREB-Dependent Transcription in Astrocytes: Signalling Pathways, Gene Profiles and Neuroprotective Role in Brain Injury
Agricultural University of Athens
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Rare Copy Number Variants and Congenital Heart Defects in the 22Q11.2 Deletion Syndrome
The Role of Cyclase-Associated Protein (CAP)
CAP2 Deficiency Delays Myofibril Actin Cytoskeleton Differentiation and Disturbs Skeletal Muscle Architecture and Function
A Parsimony Approach to Genome-Wide Ortholog Assignment
Deletions in Chromosome 6P22.3-P24.3, Including ATXN1, Are Associated with Developmental Delay and Autism Spectrum Disorders
Targeting MRTF/SRF in CAP2-Dependent Dilated Cardiomyopathy Delays Disease Onset
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