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MCFD2
Familial Multiple Coagulation Factor Deficiencies
Alterations of Genetic Variants and Transcriptomic Features of Response to Tamoxifen in the Breast Cancer Cell Line
Analysis of Newly Detected Mutations in the MCFD2 Gene Giving Rise to Combined Deficiency of Coagulation Factors V and VIII
Combined Factor V and Factor VIII Deficiency in a Thai Patient
MCFD2 Antibody
A Peripheral Blood Gene Expression Signature to Diagnose Subclinical Acute Rejection
Rabbit Anti-MCFD2 Antibody-SL18724R
Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Genotypes of Patients with Combined Factor V and VIII Deficiency
Familial Multiple Coagulation Factor Deficiencies
Crystal Structure of the LMAN1-CRD/MCFD2 Transport Receptor Complex Provides Insight Into Combined Deficiency of Factor V and Factor VIII
Combined Deficiency of Factor V and Factor VIII Is Due to Mutations In
A Network Inference Approach to Understanding Musculoskeletal
Gnomad Lof Supplement
Molecular Profiling of Liver Sinusoidal Endothelial Cells in Comparison To
The Genetic Program of Pancreatic Β-Cell Replication in Vivo
Haemophilia A: from Mutation Analysis to New Therapies
Top View
Blueprint Genetics Bleeding Disorder/Coagulopathy Panel
Ep 2270226 B1
Structural Basis for the Cooperative Interplay Between the Two Causative Gene Products of Combined Factor V and Factor VIII Deficiency
Mouse Mcfd2 Knockout Project (CRISPR/Cas9)
Supporting Information
Indian Journal of Human Genetics Now Indexed with Volume 13, Issue 3, September-December 2007
Global Analyses of Chromosome 17 and 18 Genes of Lung Telocytes
Combining Genome Wide Association Studies and Differential Gene
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Improved Secretion of Glycoproteins Using an N-Glycan-Restricted Passport Sequence Tag Recognized by Cargo Receptor
Unraveling the Molecular Mechanism Underlying ALS-Linked Astrocyte
Rare Congenital Bleeding Disorders
Enrichment of Neural-Related Genes in Human Mesenchymal Stem Cells from Neuroblastoma Patients
Antioxidants Reduce Endoplasmic Reticulum Stress and Improve Protein Secretion
Mouse Mcfd2 Conditional Knockout Project (CRISPR/Cas9)
1 Introduction 1.1 General Introduction……………………………………………………………
Supplemental Table 2: UC Vs. NL Gene List Gene Name Symbol
Primepcr™Assay Validation Report