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MAL (gene)
Illegitimate DNA Integration in Mammalian Cells
The Human Genome Project
Genetics As Explanation: Limits to the Human Genome Project’ (2006, 2009)
Connecting Myelin-Related and Synaptic Dysfunction In
A New Entrez Database Transitioning from Locuslink to Entrez
ALK, the Chromosome 2 Gene Locus Altered by the T(2;5) in Non
Genetic Nomenclature Zhiliang Hu Iowa State University,
[email protected]
Viral Component of the Human Genome V
Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse Janan T
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
The Proteins of Keratoconus: a Literature Review Exploring Their Contribution to the Pathophysiology of the Disease
An Evaluation of Cancer Subtypes and Glioma Stem Cell Characterisation Unifying Tumour Transcriptomic Features with Cell Line Expression and Chromatin Accessibility
MAL Antibody / Myelin and Lymphocyte Protein (RQ6195)
Chromosomal Abnormalities and Mental Illness
Identification and Interaction Analysis of Molecular Markers in Pancreatic
Rabbit Anti-MAL/FITC Conjugated Antibody-SL4693R-FITC
Ancient Genomics of Modern Humans: the First Decade
The Micromechanics of DNA
Top View
Catalogue of Gene Symbols for Wheat
Supporting Disease Candidate Gene Discovery Based on Phenotype Mining
Characterization of an Unusual and Complex Chromosome 2 1 Rearrangement Using Somatic Cell Genetics and Cloned DNA Probes
Chromosome Mapping of the Genes That Control Differentiation And
Mapping Our Genes-Genome Projects: How Big? How Fast? (1988)
High-Depth African Genomes Inform Human Migration and Health
Structure and Function of the Human Genome
Tobacco Smoking Induces Metabolic Reprogramming of Renal Cell Carcinoma
Standard Genetic Nomenclature Zhiliang Hu Iowa State University,
[email protected]
Review the Human Genome Project Maynard V
What Can the Y Chromosome Tell Us About the Origin of Modern Humans?
In Silico Characterization of Genetic Alterations Associated with Mal De Meleda
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force
Molecular Characterization of a Complex Small Supernumerary Marker Chromosome Derived from Chromosome 18P: an Addition to the Li
The MAL Protein, an Integral Component of Specialized Membranes, in Normal Cells and Cancer
Mal-Light: Enhancing Lysine Malonylation Sites Prediction Problem Using Evolutionary-Based Features
Table of Contents List of Investigators
Genetic Linkage of Meleda Disease to Chromosome 8Qter
Human MAL Blocking Peptide (CDBP2924) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Nested Retrotransposition in the East Asian Mouse Genome Causes the Classical Nonagouti Mutation
Anti-MAL Monoclonal Antibody (DCABH-12260) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use