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653 results on '"Eric Sibley"'

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1. Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease.

3. Dual embryonic origin of the mammalian enteric nervous system

4. Contributors

5. Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease

6. Intestinal Pdx1 mediates nutrient metabolism gene networks and maternal expression is essential for perinatal growth in mice

7. The human lactase persistence-associated SNP −13910*T enables in vivo functional persistence of lactase promoter–reporter transgene expression

8. Increased HLA-DR Expression on Tissue Eosinophils in Eosinophilic Esophagitis

9. Pdx1inactivation restricted to the intestinal epithelium in mice alters duodenal gene expression in enterocytes and enteroendocrine cells

10. Microtome-Free 3-Dimensional Confocal Imaging Method for Visualization of Mouse Intestine With Subcellular-Level Resolution

11. Transient cytochalasin-D treatment induces apically administered rAAV2 across tight junctions for transduction of enterocytes

13. Spatio-temporal patterns of intestine-specific transcription factor expression during postnatal mouse gut development

14. Proteasome modulating agents induce rAAV2-mediated transgene expression in human intestinal epithelial cells

15. Transcriptional regulation of the lactase-phlorizin hydrolase promoter by PDX-1

16. Genetic Variation and Lactose Intolerance

17. Subarachnoid hemorrhage and isolated atresia of the aortic arch 1 1Clinical Communications is coordinated by Roger Barkin, MD, of HealthONE, Denver, Colorado

18. −13915*G DNA polymorphism associated with lactase persistence in Africa interacts with Oct-1

20. Expression profiling identifies novel gene targets and functions for Pdx1 in the duodenum of mature mice

21. Neonatal jaundice and liver disease

22. Contributors

23. Eotaxin and FGF enhance signaling through an Extracellular signal-related kinase (ERK)-dependent pathway in the pathogenesis of Eosinophilic Esophagitis

24. Congenital Disorders of Digestion and Absorption

26. Selenium Deficiency

27. SOS

28. Signal Transduction of Apoptosis

29. Splenic Agenesis

30. Spinal Spastic Paraplegia

31. Maternal Uniparental Disomy for Chromosome 7

32. Stress-induced Tachycardia

33. Multiple Risk Factor Syndrome

34. Myocarditis, Autoimmune

35. Supraventricular Tachycardia

36. Myogastrointestinal Encephalomyopathy

37. 3-MGA-Type I

38. Morbus Reiter

39. Miller-Dieker Syndrome

40. Mortimer’s Malady

41. Spondyloepiphyseal Dysplasia Tarda

42. MGN

43. Muscular Dystrophy, Tardive, with Contractures

44. Malignant Phenylketonuria

45. Metachromatic Leukodystrophy

46. Menkes Disease

47. Shah-Waardenburg Syndrome

48. Myo-Neuro-Gastro-Intestinal Encephalopathy

49. Sphingolipid Activator Protein Deficiency

50. Slowing of Respiration

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