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FHL5
Aneuploidy: Using Genetic Instability to Preserve a Haploid Genome?
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University of Florida Thesis Or Dissertation Formatting
Syntaxin Binding Mechanism and Disease-Causing Mutations In
De Novo Transcriptome Sequencing and Gene Expression Profiling With/Without B-Chromosome Plants of Lilium Amabile Doori Park, Jong-Hwa Kim, Nam-Soo Kim
Primepcr™Assay Validation Report
Identification of a Deletion in Stxbp2
Genome-Wide Characterization of Genetic Variants and Putative
Expression Profiling Associates Blood and Brain Glucocorticoid Receptor
Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors
Computational Simulations to Predict Creatine Kinase-Associated Factors: Protein-Protein Interaction Studies of Brain and Muscle Types of Creatine Kinases
10Th Anniversary of the Human Genome Project
Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells
Abnormal Sperm in Mice with Targeted Deletion of the Act (Activator of Camp-Responsive Element Modulator in Testis) Gene
Fhl5/Act, a CREM-Binding Transcriptional Activator Required for Normal Sperm Maturation and Morphology, Is Not Essential for Testicular Gene Expression
Genetic Analysis of Chromosome Replication Timing
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
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Genome-Wide Sequencing for the Identification of Rearrangements
Expression Profiling Associates Blood and Brain Glucocorticoid Receptor Signaling with Trauma-Related Individual Differences in Both Sexes
Genome‐Wide Association Study Identifies Risk Loci for Cluster
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Four and a Half LIM Domains Protein 1 Can Be As a Double-Edged Sword in Cancer Progression
Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells Marjorie Côte,1,2 Mickaël M
Fhl5/Act, a CREM-Binding Transcriptional Activator Required for Normal Sperm Maturation and Morphology, Is Not Essential for Testicular Gene Expression
Syntaxin Binding Mechanism and Disease-Causing Mutations
Transcriptomic Comparison of Human and Mouse Brain Microvessels Hannah W
Identification of Novel Biomarkers and Candidate Drug in Ovarian Cancer
Disrupted Apical Exocytosis of Cargo Vesicles Causes Enteropathy in FHL5 Patients with Munc18-2 Mutations
Genome-Wide Meta-Analysis Identifies New Susceptibility Loci for Migraine
Cell Base Assays to Investigate the Functional Relevance of HLH Genetic Variants
Leveraging Genome-Wide Association Studies Data to Inform the Biology Behind the Genetic Risk for Mitral Valve Prolapse Mengyao Yu
Supplementary Information
Subtypes of Familial Hemophagocytic Lymphohistiocytosis in Japan Based on Genetic and Functional Analyses of Cytotoxic T Lymphocytes
GWAS-Driven Pathway Analyses and Functional Validation Suggest GLIS1 As