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PLS3
The Roles of Actin-Binding Domains 1 and 2 in the Calcium-Dependent Regulation of Actin Filament Bundling by Human Plastins
Zinc-Finger Protein 471 Suppresses Gastric Cancer Through
Clinical Studies Research
The Actin Binding Protein Plastin-3 Is Involved in the Pathogenesis of Acute Myeloid Leukemia
Human PLS3 / Plastin 3 Protein (His Tag)
Identification of Potential Prognostic Biomarkers for Tongue Squamous Cell Carcinoma
PLS3 Sequencing in Childhood-Onset Primary Osteoporosis Identifies Two Novel Disease-Causing Variants
Systems Genetics in Diversity Outbred Mice Inform BMD GWAS and Identify Determinants of Bone Strength
T-, B-And NK-Lymphoid, but Not Myeloid Cells Arise from Human
Human PLS3 / Plastin 3 Protein (His Tag)
Using Systems Genetics to Unravel the Genetics of Bone-Related Traits
Genetic Variants in the PLS3 Gene Are Associated with Osteoporotic Fractures in Postmenopausal Chinese Women
A Deep Proteome and Transcriptome Abundance Atlas of 29 Healthy Human Tissues
A Master Autoantigen-Ome Links Alternative Splicing, Female Predilection, and COVID-19 to Autoimmune Diseases
Systems Biology Analysis of the Lung Cancer‑Related Secretome
Network Mining Approach to Cancer Biomarker Discovery
Bone: Role for PLS3 in X-Linked Osteoporosis Revealed
Systems Genetics Analyses in Diversity Outbred Mice
Top View
Plastin-3 Is a Diagnostic and Prognostic Marker for Pancreatic
Retinal Genomic Fabric Remodeling After Optic Nerve Injury
2) EA7364 RADEME, Université De Lille, France
Supporting Information
Survival Motor Neuron Affects Plastin 3 Protein Levels Leading to Motor Defects
GO ID Gene Ontology Gene Symbol GO:0030552 3',5'-Camp Binding
Identification of Modifiers of Spinal Muscular Atrophy
Extensive Cellular Heterogeneity of X Inactivation Revealed by Single-Cell Allele-Specific 2 Expression in Human Fibroblasts
(PLS3) on Spinal Muscular Atrophy (SMA) by Generation of Transgenic Mouse Models
Novel PLS3 Variants in X-Linked Osteoporosis: Exploring Bone Material Properties
Patchy, Incomplete, and Heterogeneous X-Inactivation in the Human Placenta
PLS3 Expression and SMA Phenotype: a Commentary on Correlation of PLS3 Expression with Disease Severity in Children with Spinal Muscular Atrophy
X-Inactivation in Female Human Embryonic Stem Cells Is in a Nonrandom Pattern and Prone to Epigenetic Alterations
Widespread Changes in Transcriptome Profile of Human Mesenchymal
Gene Expression Comparison Between Sézary Syndrome and Lymphocytic-Variant Hypereosinophilic Syndrome Refines Biomarkers for Sézary Syndrome
Transcriptome Analysis of Microdissected Pancreatic Intraepithelial Neoplastic Lesions
Osteoporosis Caused by Mutations in PLS3: Clinical and Bone Tissue Characteristics
PLS3 Rabbit Pab
Clinical, Genetics, and Bioinformatic Characterization of Mutations Affecting an Essential Region of PLS3 in Patients with BMND18