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SETD5
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity Received: 11 November 2016 Audrey E
Elucidating Biological Roles of Novel Murine Genes in Hearing Impairment in Africa
Stanford University
SET Domain Containing Protein 5 (SETD5) Enhances Tumor Cell
A Sleeping Beauty Transposon-Mediated Screen Identifies Murine Susceptibility Genes for Adenomatous Polyposis Coli (Apc)-Dependent Intestinal Tumorigenesis
Supplemental Table 3 Two-Class Paired Significance Analysis of Microarrays Comparing Gene Expression Between Paired
Genes Essential for Embryonic Stem Cells Are Associated with Neurodevelopmental Disorders
Setd5 Haploinsufficiency Alters Neuronal Network Connectivity And
SUPPLEMENTARY DATA Page Supplementary Text …………………………………………………………………………………
Setd5 Is Essential for Mammalian Development and the Co-Transcriptional Regulation of Histone Acetylation Anna B
HDAC3 Complex Determines Enhancer Activation for Adipogenesis
Thesis, I Have Studied Rare Monogenic Novel Neurodevelopmental Disorders Associated with ID
Loss-Of-Function Variants of SETD5 Cause Intellectual Disability and the Core Phenotype of Microdeletion 3P25.3 Syndrome
A Deep Transcriptome Meta-Analysis Reveals Sex-Based Molecular Differences in Multiple Sclerosis
3P25 Deletions
216141 2 En Bookbackmatter 461..490
De Novo SETD5 Loss-Of-Function Variant As a Cause for Intellectual Disability in a 10-Year Old Boy with an Aberrant Blind Ending Bronchus
Read FY20 Uniform Guidance Audit
Top View
The Functions of SETD5 and Mir-221 in Embryonic Stem Cell Differentiation
Genetic Variants Associated with Quantitative Glucose Homeostasis
Comparative Analysis of the Autism‑Related Variants Between Different Autistic Children in a Family Pedigree
Transposon Mutagenesis Identifies Chromatin Modifiers Cooperating
Prmcrispra Enhcrispre Patent Application Publication Nov
Sensory Neuropathy Affects Cardiac Mirna Expression Network Targeting
MRNA Transcription, Translation, and Defects in Developmental Cognitive and Behavioral Disorders
Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: an Exome Sequencing Study
Isoform Transcriptome of Developing Human Brain Provides New Insights
Contribution of Retrotransposition to Developmental Disorders
Mouse Screen Reveals Multiple New Genes Underlying Mouse and Human Hearing Loss
Generation Sequencing Analysis of 1000 Individuals With
Nmp4 Restricts Bone Marrow Osteoprogenitors And
Haploinsufficiency of the Intellectual Disability-Gene SETD5 Disturbs 1
Studying the Phenotypic Variability of Neurodevelopmental Disorders with Drosophila Melanogaster
Issue 83 of the Genetics Society Newsletter
A Novel Mutation in a Common Pathogenic Gene (SETD5) Associated with Intellectual Disability: a Case Report