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SMCHD1
Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of Cpg Island Methylation on The
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Myopia in African Americans Is Significantly Linked to Chromosome 7P15.2-14.2
Mechanisms Underlying Phenotypic Heterogeneity in Simplex Autism Spectrum Disorders
A Quantitative Telomeric Chromatin Isolation Protocol Identifies Different Telomeric States
Conservation and Innovation in the DUX4-Family Gene Network
SMCHD1 Polyclonal Antibody Purified Rabbit Polyclonal Antibody (Pab) Catalog # AP57717
Remotely Acting SMCHD1 Gene Regulatory Elements: in Silico Prediction and Identification of Potential Regulatory Variants in Patients with FSHD Mary B
Role of the Chromosome Architectural Factor SMCHD1 in X-Chromosome Inactivation, Gene Regulation, and Disease in Humans
(SMCHD1) Regulates Gene Expression
Double SMCHD1 Variants in FSHD2: the Synergistic Effect of Two SMCHD1 Variants on D4Z4 Hypomethylation and Disease Penetrance in FSHD2
Smchd1 (NM 028887) Mouse Untagged Clone Product Data
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Facioscapulohumeral Muscular Dystrophy (FSHD) Molecular Diagnosis: from Traditional Technology to the NGS Era
Relating SMCHD1 Structure to Its Function in Epigenetic Silencing
SMCHD1 Antibody Order 021-34695924
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PRC1 Collaborates with SMCHD1 to Fold the X-Chromosome and Spread
Mouse Smchd1 Conditional Knockout Project (CRISPR/Cas9)
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Gordon, C. T. Et Al. (2017) De Novo Mutations in SMCHD1 Cause Bosma Arhinia Microphthalmia Syndrome and Abrogate Nasal Development
CLIA Laboratory Testing for Facioscapulohumeral Dystrophy a Retrospective Analysis
Computational Studies of the Genome Dynamics of Mammalian Transposable Elements and Their Relationships to Genes
The Effects of the DNA Demethylating Reagent, 5-Azacytidine on SMCHD1 Genomic Localization S
The FSHD2 Gene SMCHD1 Is a Modifier of Disease Severity in Families Affected by FSHD1
Contribution of Genetic and Epigenetic Changes to Escape from X-Chromosome Inactivation
Genome-Wide Binding and Mechanistic Analyses of Smchd1-Mediated Epigenetic Regulation
1 SMCHD1 Mutation Spectrum for Facioscapulohumeral Muscular
Epigenetic Regulator Smchd1 Functions As a Tumor Suppressor
Chromosome Inactivation
Does DNA Methylation Matter in FSHD?
Smchd1 Underlies the Formation of H3k9me3 Blocks on the Inactive X Chromosome in Mice
Smchd1 Is a Maternal Effect Gene Required for Genomic Imprinting
Identification of Two Novel SMCHD1 Sequence Variants in Families with FSHD-Like Muscular Dystrophy
SMCHD1 Has Separable Roles in Chromatin Architecture and Gene Silencing That Could Be Targeted in Disease
Role of the Chromosome Architectural Factor SMCHD1 in X Chromosome
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
Identification of SMCHD1 Domains for Nuclear Localization, Homo-Dimerization, and Protein Cleavage Yosuke Hiramuki and Stephen J