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CCBE1
Proteolytic Activation Defines Distinct Lymphangiogenic Mechanisms for VEGFC and VEGFD
Study of the Requirement of the CCBE1 Growth Factor in the Generation of Cardiac Myocytes from Hes Cells
Mutations in CCBE1 Cause Generalized Lymph Vessel Dysplasia
Prioritization of Genes Involved in Endothelial Cell Apoptosis by Their Implication in Lymphedema Using an Analysis of Associative Gene Networks with Andsystem Olga V
Genetic Epidemiology of Hypertension in Populations
Mouse Ccbe1 Conditional Knockout Project (CRISPR/Cas9)
Loss of ADAMTS3 Activity Causes Hennekam Lymphangiectasia–Lymphedema Syndrome 3 Pascal Brouillard1,‡, Laura Dupont2,‡, Raphael Helaers1, Richard Coulie1, George E
CCBE1 Mutation in Two Siblings, One Manifesting Lymphedema-Cholestasis Syndrome, and the Other, Fetal Hydrops
Comprehensive Analysis Reveals Novel Gene Signature in Head and Neck Squamous Cell Carcinoma: Predicting Is Associated with Poor Prognosis in Patients
Differentially Expressed Genes in Aneurysm Tissue Compared With
Defective Synaptic Connectivity and Axonal Neuropathology in a Human
Collagen and Calcium-Binding EGF Domains 1 Is Frequently Inactivated in Ovarian Cancer by Aberrant Promoter Hypermethylation and Modulates Cell Migration and Survival
CCBE1 Enhances Lymphangiogenesis Via ADAMTS3-Mediated VEGF-C Processing
Expression Profile of SYNE3 and Bioinformatic Analysis of Its
Efficient Activation
Gene-Expression Differences in Peripheral Blood Between Lithium Responders and Non-Responders in the Lithium Treatment-Moderate Dose Use Study (Litmus)
Universidade De Lisboa Faculdade De Farmácia Assessment of the Role Of
Genomic Landscape and Mutational Spectrum of ADAMTS Family Genes in Mendelian Disorders Based on Gene Evidence Review for Variant Interpretation
Top View
Pathway-Focused Gene Interaction Analysis Reveals the Regulation Of
Ccbe1 Regulates Vegfc-Mediated Induction of Vegfr3 Signaling During Embryonic Lymphangiogenesis Ludovic Le Guen1,*, Terhi Karpanen2, Dörte Schulte2, Nicole C
TWEAK-Fn14 Signaling Activates Myofibroblasts to Drive Progression
CCBE1 Is Mutated in a Form of Recessively Inherited Generalised
Specific Fibroblast Subpopulations and Neuronal Structures Provide Local
Genome-Wide Association Study of Comorbid Depressive Syndrome and Alcohol Dependence Alexis C
Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, in Silico Analysis
CCBE1 Gene Collagen and Calcium Binding EGF Domains 1
The Proteolytic Activation of Vascular Endothelial Growth Factorc
A Novel Mutation in CELSR1 Is Associated with Hereditary Lymphedema M
Aberrant Expression of Collagen Family Genes in the Brain Regions Developing Under Agonistic Interactions in Male Mice
Convergent Genome-Wide Association Study Results
Crawford Et Al. 1 Expanding the Genotypic Spectrum of CCBE1
Hennekam Syndrome
Proteolytic Cleavages in the VEGF Family: Generating Diversity Among Angiogenic Vegfs, Essential for the Activation of Lymphangiogenic Vegfs
GENOME-WIDE ASSOCIATION STUDIES of CHILDHOOD BONE HEALTH by Kelly Amanda Johnson BS, University of Maryland, College Park, 2014
Progesterone Receptor Transcriptome and Cistrome in Decidualized Human Endometrial Stromal Cells
BMC Research Notes Biomed Central