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SBF1
Inherited Neuropathies
Caenorhabditis Elegans SDF-9 Enhances Insulin/Insulin-Like Signaling Through Interaction with DAF-2
Transcriptome-Wide Association Study Identifies Susceptibility Genes For
Male Infertility, Impaired Spermatogenesis, and Azoospermia in Mice Deficient for the Pseudophosphatase Sbf1
A Concise Review of Human Brain Methylome During Aging and Neurodegenerative Diseases
Genetic Investigations of Sporadic Inclusion Body Myositis and Myopathies with Structural Abnormalities and Protein Aggregates in Muscle
Understanding the Genetic Basis of Phenotype Variability in Individuals with Neurocognitive Disorders
Enrichment of Mutations in Chromatin Regulators in People with Rett Syndrome Lacking Mutations in MECP2
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
SBF1 Mutations Associated with Autosomal Recessive Axonal Neuropathy with Cranial Nerve Involvement
Specifically to Iga Increases Class Switch Recombination the Histone
Enrichment of Phosphorylated Tau (Thr181) and Functionally Interacting Molecules in Chronic Traumatic Encephalopathy Brain-Derived Extracellular Vesicles
10Th Anniversary of the Human Genome Project
Clinical and Genetic Aspects of Charcot-Marie- Tooth Disease Subtypes
Charcot&Ndash;Marie&Ndash;Tooth Disease
Identification of 22Q13 Genes Most Likely to Contribute to Phelan
“Fork and Bracket” Syndrome Expands the Spectrum of SBF1-Related Sensory Motor Polyneuropathies
Mutations in MTMR13, a New Pseudophosphatase Homologue Of
Top View
Blueprint Genetics Charcot-Marie-Tooth Neuropathy
1 C. Elegans SDF-9 Enhances Insulin/Insulin-Like Signaling
A Phylogenetic Survey of Myotubularin Genes of Eukaryotes: Distribution, Protein Structure, Evolution, and Gene Expression David Kerk, Greg BG Moorhead*
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
Key Genes Associated with Diabetes Mellitus and Hepatocellular Carcinoma T ⁎ ⁎ Gao-Min Liu , Hua-Dong Zeng, Cai-Yun Zhang, Ji-Wei Xu
Enrichment of Mutations in Chromatin Regulators in People with Rett Syndrome Lacking Mutations in MECP2
Supplementary Materials: Figure S1. the Effect of PROX1 Silencing on the Cell Cycle, the Proliferation and the Survival of CGTH
The Relative Contribution of Proximal 59 Flanking Sequence and Microsatellite Variation on Brain Vasopressin 1A Receptor (Avpr1a) Gene Expression and Behavior
Clinical and Electrophysiological Aspects of Charcot-Marie-Tooth Disease
Overlapping Molecular Pathological Themes Link Charcot–Marie–Tooth Neuropathies and Hereditary Spastic Paraplegias
B-Binding Sites Across Human Chromosome 22
A Cross-Disorder Dosage Sensitivity Map of the Human Genome
The Phosphoinositide 3-Phosphatase MTMR2 Interacts with PSD-95 and Maintains Excitatory Synapses by Modulating Endosomal Traffic
Splicing Mutation in Sbf1 Causes Nonsyndromic Male Infertility in the Rat
Knockdown of the Ribosomal Protein El38 in HEK293 Cells Changes the Translational Efficiency of Specific Genes
Charcot-Marie-Tooth
Emerging Therapies for Charcot-Marie-Tooth Inherited Neuropathies