Search

Your search keyword '"Justin Cotney"' showing total 61 results

Search Constraints

Start Over You searched for: Author "Justin Cotney" Remove constraint Author: "Justin Cotney"
61 results on '"Justin Cotney"'

Search Results

1. Enhanced osteogenic potential of iPSC-derived mesenchymal progenitor cells following genome editing of GWAS variants in the RUNX1 gene

2. Rare variants analyses suggest novel cleft genes in the African population

3. A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

4. Integrative analysis of transcriptome dynamics during human craniofacial development identifies candidate disease genes

5. Integration of multimodal data in the developing tooth reveals candidate regulatory loci driving human odontogenic phenotypes

7. Zebrafish models of alx-linked frontonasal dysplasia reveal a role for Alx1 and Alx3 in the anterior segment and vasculature of the developing eye

8. ALX1‐related frontonasal dysplasia results from defective neural crest cell development and migration

9. Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate

10. High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development

11. RNA-Seq profiling of spinal cord motor neurons from a presymptomatic SOD1 ALS mouse.

12. Specific ZNF274 binding interference atSNORD116activates the maternal transcripts in Prader-Willi syndrome neurons

13. 'Integration of multimodal data in the developing tooth reveals candidate dental disease genes'

14. A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

15. Integrative analysis of transcriptomics in human craniofacial development reveals novel candidate disease genes

16. Evidence against tetrapod-wide digit identities and for a limited frame shift in bird wings

17. A bipartite boundary element restricts UBE3A imprinting to mature neurons

18. Identification of enamel knot gene signature within the developing mouse molar

19. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation

20. Massively parallel discovery of human-specific substitutions that alter enhancer activity

21. ALX1‐related frontonasal dysplasia results from defective neural crest cell development and migration

22. Epigenomic and Transcriptomic Dynamics During Human Heart Organogenesis

23. An

24. Investigating global gene expression changes in a murine model of cherubism

25. Sarcomere Function Inhibits Cardiomyocyte Replication and Promotes Polyploidization Through a DNA Damage Response that Limits In vivo Cell Engraftment

26. An Irf6-Esrp1/2 regulatory axis controls midface morphogenesis in vertebrates

27. High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development

28. Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications

29. Massively parallel discovery of human-specific substitutions that alter neurodevelopmental enhancer activity

30. Massively parallel disruption of enhancers active during human corticogenesis

31. Integrative approaches generate insights into the architecture of non-syndromic cleft lip ± cleft palate

32. Sarcomere function activates a p53-dependent DNA damage response that promotes polyploidization and limits in vivo cell engraftment

33. Multi-focal control of mitochondrial gene expression by oncogenic MYC provides potential therapeutic targets in cancer

34. BIOLOGICAL SCIENCES: Genetics

35. The marked diversity of unique cortical enhancers enables neuron-specific tools by Enhancer-Driven Gene Expression

36. High Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development

37. Evolutionary changes in promoter and enhancer activity during human corticogenesis

38. High Resolution Epigenomic Atlas of Early Human Craniofacial Development

39. The genomic landscape of cohesin-associated chromatin interactions

40. Mitochondrial Stress Engages E2F1 Apoptotic Signaling to Cause Deafness

41. Core human mitochondrial transcription apparatus is a regulated two-component system in vitro

42. Elucidation of separate, but collaborative functions of the rRNA methyltransferase-related human mitochondrial transcription factors B1 and B2 in mitochondrial biogenesis reveals new insight into maternally inherited deafness

43. Human Mitochondrial Ribosomal Protein MRPL12 Interacts Directly with Mitochondrial RNA Polymerase to Modulate Mitochondrial Gene Expression

44. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

45. Evidence for an Early Gene Duplication Event in the Evolution of the Mitochondrial Transcription Factor B Family and Maintenance of rRNA Methyltransferase Activity in Human mtTFB1 and mtTFB2

46. The Evolution of Lineage-Specific Regulatory Activities in the Human Embryonic Limb

47. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

48. Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO

49. Abstract 1256: Multi-focal control of mitochondrial gene expression by oncogenic MYC provides effective therapeutic targets in cancer

50. RNA-Seq profiling of spinal cord motor neurons from a presymptomatic SOD1 ALS mouse

Catalog

Books, media, physical & digital resources