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Bioinformatics Analysis for the Identification of Differentially Expressed Genes and Related Signaling Pathways in H
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Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
Characterized by Array CGH in a Boy with Cat-Eye Syndrome Irén Haltrich1*, Henriett Pikó2, Eszter Kiss1, Zsuzsa Tóth1, Veronika Karcagi2 and György Fekete1
Alternatively Spliced Homologous Exons Have Ancient Origins and Are Highly Expressed at the Protein Level
Chromosome 22Q11.2 Deletion Syndrome Associated with Congenital Heart Defects
Sheep Genome Functional Annotation Reveals Proximal Regulatory Elements Contributed to the Evolution of Modern Breeds
Agricultural University of Athens
Common Low Complexity Regions for SARS-Cov-2 and Human
Actin Mutations and Their Role in Disease
Transcriptomics Uncovers Substantial Variability Associated with Alterations in Manufacturing Processes of Macrophage Cell Therapy Products Olga L
Identification of Novel Regulatory Genes in Acetaminophen
Mapping Axon Initial Segment Structure and Function by Multiplexed Proximity Biotinylation
MICAL3 (3A6): Sc-517049
Multi-Pronged Human Protein Mimicry by SARS-Cov-2 Reveals
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Molecular Sciences High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorder
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Retroviral Envelope Gene Captures and Syncytin Exaptation For
Expanding the Universe of Retinal Disease Gene Interactions Network
HBV DNA Integration and Clonal Hepatocyte Expansion in Chronic Hepatitis B Patients Considered Immune Tolerant
Transcriptome Analysis of Differentially Expressed Genes
Structure-Function Studies of MICAL, the Unusual Multidomain Flavoenzyme Involved in Actin Cytoskeleton Dynamics
Identification of Long Non-Coding RNA Signatures for Squamous Cell Carcinomas and Adenocarcinomas
Allelic Expression Analysis of the Osteoarthritis Susceptibility Locus That Maps to MICAL3
US 2020/0078401 A1 VIJAYANAND Et Al
Clinical Variability of the 22Q11.2 Duplication Syndrome
A De Novo Ssmc (22) Characterized by High-Resolution Chromosome Microarray Analysis in a Chinese Boy with Cat-Eye Syndrome
PRODUCT SPECIFICATION Product Datasheet
MICAL3 CRISPR/Cas9 KO Plasmid (M): Sc-431461
Facilitating Identification of Minimal Protein Binding Domains by Cross
Allelic Expression Analysis of the Osteoarthritis Susceptibility Locus
Kb Triplication in the Cat Eye Syndrome Critical Region Causes Anorectal, Renal and Preauricular Anomalies in a Three-Generation Family
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22Q11.2 Deletion Syndrome
Heterozygous Gene Truncation Delineates the Human Haploinsufficient Genome
Supplementary Table 1. a Full List of Cancer Genes