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SH2B1
Microdeletions in 16P11.2 and 13Q31.3 Associated with Developmental Delay and Generalized Overgrowth
Crucial Role of the SH2B1 PH Domain for the Control of Energy Balance
Crucial Role of the SH2B1 PH Domain for the Control of Energy Balance
Insight Into the Brain-Specific Alpha Isoform of the Scaffold Protein SH2B1 and Its Rare Obesity-Associated Variants
Genome-Wide DNA Methylation Analysis Reveals Epigenetic Pattern of SH2B1 in Chinese Monozygotic Twins Discordant for Autism Spectrum Disorder
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Multifaceted Genome-Wide Study Identifies Novel Regulatory Loci For
Neuronal SH2B1 Is Essential for Controlling Energy and Glucose Homeostasis
Leptin Receptor-Expressing Neuron Sh2b1 Supports Sympathetic Nervous System and Protects Against Obesity and Metabolic Disease
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16P11.2 Microdeletions Including the SH2B1 Gene." ABOUT US Am J Med Genet
Data-Driven and Knowledge-Driven Computational Models of Angiogenesis in Application to Peripheral Arterial Disease
SH2B1 Enhances Insulin Sensitivity by Both Stimulating the Insulin Receptor and Inhibiting Tyrosine Dephosphorylation of IRS Proteins
Recurrent 200-Kb Deletions of 16P11.2 That Include the SH2B1 Gene Are Associated with Developmental Delay and Obesity Ruxandra Bachmann-Gagescu, MD,1,2 Heather C
Autism Multiplex Family with 16P11.2P12.2 Microduplication Syndrome in Monozygotic Twins and Distal 16P11.2 Deletion in Their Brother
Implication of SH2B1 Gene Polymorphism Studies in Gestational Diabetes Mellitus in Saudi Pregnant Women
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
Role of the Adaptor Protein LNK in Normal and Malignant Hematopoiesis
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Negative Regulation of Cytokine Signalling in the Myeloid Lineage
Characterizing Gene-Gene Interactions in a Statistical Epistasis Network of Twelve Candidate Genes for Obesity Rishika De1, Ting Hu2, Jason H
Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLC1 and SH2B1
Enhancer Regulation for Induced WNT3A Expression During Neuronal
Large, Rare Chromosomal Deletions Associated with Severe Early-Onset Obesity
SH2B1 Enhances Insulin Sensitivity by Both Stimulating the Insulin Receptor and Inhibiting Tyrosine Dephosphorylation of Insulin Receptor Substrate Proteins David L
Human SH2B1 Mutations Are Associated with Maladaptive Behaviors and Obesity Michael E
Distal Chromosome 16P11.2 Duplications Containing SH2B1 In
Genetics of Obesity: What Genetic Association Studies Have Taught Us About the Biology of Obesity and Its Complications
16P11.2 Microdeletions
Polymorphisms in Sh2b1 and Spns1 Loci Are Associated with Triglyceride Levels in a Healthy Population in Northern Sweden