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1. Modulation of FGF pathway signaling and vascular differentiation using designed oligomeric assemblies

2. Meningioma transcriptomic landscape demonstrates novel subtypes with regional associated biology and patient outcome

3. Chromatin context-dependent regulation and epigenetic manipulation of prime editing

5. Multiplex single-cell chemical genomics reveals the kinase dependence of the response to targeted therapy

6. Reversible, tunable epigenetic silencing of TCF1 generates flexibility in the T cell memory decision

7. Proteostasis governs differential temperature sensitivity across embryonic cell types

8. Single-cell census of human tooth development enables generation of human enamel

9. Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project

11. Machine learning dissection of human accelerated regions in primate neurodevelopment

12. Results of genetic analysis of 11 341 participants enrolled in the My Life, Our Future hemophilia genotyping initiative in the United States

15. 3030 – THE EPIGENETIC REGULATOR LANDSCAPE OF STEMNESS NETWORKS IN ACUTE MYELOID LEUKEMIA

16. Benchmarked approaches for reconstruction of in vitro cell lineages and in silico models of C. elegans and M. musculus developmental trees

17. Adaptations in Hippo-Yap signaling and myofibroblast fate underlie scar-free ear appendage wound healing in spiny mice

18. Benchmarked approaches for reconstruction of in vitro cell lineages and in silico models of C. elegans and M. musculus developmental trees

21. Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signatures

23. High-Throughput Single-Cell Sequencing with Linear Amplification

26. A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens

29. Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History

31. Cicero Predicts cis-Regulatory DNA Interactions from Single-Cell Chromatin Accessibility Data

32. A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility

33. Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution

34. Low Pass Genomes of 141,431 Chinese Reveal Patterns of Viral Infection, Novel Phenotypic Associations, and the Genetic History of China

36. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

39. Activation of a cryptic splice site in the mitochondrial elongation factor GFM1 causes combined OXPHOS deficiency

40. Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort

44. Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study

46. Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis Lungs

47. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

48. Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3

49. De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay

50. MAT2A Mutations Predispose Individuals to Thoracic Aortic Aneurysms

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