438 results on '"Erdos, Michael R."'
Search Results
2. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
3. Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk
4. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
5. Functional interrogation of twenty type 2 diabetes-associated genes using isogenic human embryonic stem cell-derived β-like cells
6. ACE2 expression in adipose tissue is associated with cardio-metabolic risk factors and cell type composition—implications for COVID-19
7. Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing
8. Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups
9. A targeted antisense therapeutic approach for Hutchinson-Gilford progeria syndrome
10. In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice
11. Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signatures
12. Population-scale skeletal muscle single-nucleus multi-omic profiling reveals extensive context specific genetic regulation
13. Adipose tissue eQTL meta-analysis reveals the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits
14. Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle
15. New genetic loci link adipose and insulin biology to body fat distribution
16. Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity
17. Modeling islet enhancers using deep learning identifies candidate causal variants at loci associated with T2D and glycemic traits
18. Everolimus rescues multiple cellular defects in laminopathy-patient fibroblasts
19. Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants.
20. No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels
21. A genome-wide association search for type 2 diabetes genes in African Americans.
22. Inhibiting Farnesylation of Progerin Prevents the Characteristic Nuclear Blebbing of Hutchinson-Gilford Progeria Syndrome
23. Accumulation of Mutant Lamin A Causes Progressive Changes in Nuclear Architecture in Hutchinson-Gilford Progeria Syndrome
24. Genetic regulatory signatures underlying islet gene expression and type 2 diabetes
25. Bone dysplasia in Hutchinson‐Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations
26. Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 hours
27. Functional interrogation of twenty type 2 diabetes-associated genes using isogenic hESC-derived β-like cells
28. High-Throughput Screening for Evidence of Association by Using Mass Spectrometry Genotyping on DNA Pools
29. Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D
30. Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 hours
31. Functional interrogation of twenty type 2 diabetes-associated genes using isogenic hESC-derived β-like cells
32. Type 2 Diabetes: Evidence for Linkage on Chromosome 20 in 716 Finnish Affected Sib Pairs
33. Human BRCA1 Inhibits Growth in Yeast: Potential use in Diagnostic Testing
34. Human pancreatic islet microRNAs implicated in diabetes and related traits by large-scale genetic analysis
35. Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants
36. BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues
37. Human pancreatic islet microRNAs implicated in diabetes and related traits by large-scale genetic analysis
38. Super-enhancers delineate disease-associated regulatory nodes in T cells
39. Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans
40. A Progeria Mutation Reveals Functions for Lamin a in Nuclear Assembly, Architecture, and Chromosome Organization
41. A Farnesyltransferase Inhibitor Prevents Both the Onset and Late Progression of Cardiovascular Disease in a Progeria Mouse Model
42. A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants
43. A Lamin A Protein Isoform Overexpressed in Hutchinson-Gilford Progeria Syndrome Interferes with Mitosis in Progeria and Normal Cells
44. Mutant Nuclear Lamin a Leads to Progressive Alterations of Epigenetic Control in Premature Aging
45. Progressive Vascular Smooth Muscle Cell Defects in a Mouse Model of Hutchinson-Gilford Progeria Syndrome
46. SARS-CoV-2 infection induces beta cell transdifferentiation
47. Global Epigenomic Analysis of Primary Human Pancreatic Islets Provides Insights into Type 2 Diabetes Susceptibility Loci
48. Genetic reduction of mTOR extends lifespan in a mouse model of Hutchinson‐Gilford Progeria syndrome
49. Genetic effects on liver chromatin accessibility identify disease regulatory variants
50. Addendum: Biotinylation by antibody recognition—a method for proximity labeling
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