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1. Glucosylceramide synthase modulation ameliorates murine renal pathologies and promotes macrophage effector function in vitro

9. PURION ® processed human amnion chorion membrane allografts retain material and biological properties supportive of soft tissue repair.

10. La vejez que nunca esperamos

13. CAÇA DESPORTIVA E CONTROLE DE JAVALIS (SUS SCROFA) EM DUAS REGIÕES DO RIO GRANDE DO SUL, BRASIL: APONTAMENTOS ETNOGRÁFICOS

18. Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis

20. Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

21. Correction of cilia structure and function alleviates multi-organ pathology in Bardet–Biedl syndrome mice

22. Dehydrated human amniotic membrane regulates tenocyte expression and angiogenesis in vitro: Implications for a therapeutic treatment of tendinopathy.

23. Synthesis of N4-acetylated 3-methylcytidine phosphoramidites for RNA solid-phase synthesis.

28. Annoying presences at the Port of Santos: an ethnography about the relationships between humans, pigeons, grains and others subjects

30. Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability

34. The endoplasmic reticulum and casein-containing vesicles contribute to milk fat globule membrane formation

35. Plasma membrane, casein-containing vesicles and endoplasmic reticulum are the main contributors for milk fat globule membrane formation

37. Differences in the timing and magnitude ofPkd1gene deletion determine the severity of polycystic kidney disease in an orthologous mouse model of ADPKD

38. Reduction of ciliary length through pharmacologic or genetic inhibition of CDK5 attenuates polycystic kidney disease in a model of nephronophthisis

39. SNARE proteins and milk products secretion

40. Caractérisation des protéines SNARE potentiellement impliquées dans la sécrétion des produits du lait

41. Molecular mechanisms of caseins exocytosis: Role of the snare proteins

42. Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis

45. Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability

48. ATNFR1genotype with a protective role in familial rheumatoid arthritis

50. OUR ANCESTORS ARE HAPPY.

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