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1. Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluids

3. Journal update monthly top five

6. Evaluating gene-disease relationships in motile ciliopathies: an international ClinGen and BEAT-PCD ERS CRC collaboration.

7. Journal update monthly top five

8. Axonemal structures reveal mechanoregulatory and disease mechanisms

9. Update on primary ciliary dyskinesia

10. Proceedings of the 4th BEAT-PCD Conference and 5th PCD Training School

12. The network dependency of religious and secular belief

17. Studies on the coupling of opioid and cannabinoid receptors to adenylyl cyclase

18. Journal update monthly top five

19. TUBB4Bvariants specifically impact ciliary function, causing a ciliopathic spectrum

21. Journal update monthly top five

22. High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations

27. Proceedings of the 2nd BEAT-PCD conference and 3rd PCD training school: part 1

28. Journal update monthly top five

29. Journal update monthly top five

36. The COVID-19 emergency response assessment study: a prospective longitudinal survey of frontline doctors in the UK and Ireland

37. Psychological distress and trauma during the COVID-19 pandemic: survey of doctors practising anaesthesia, intensive care medicine, and emergency medicine in the United Kingdom and Republic of Ireland

42. Dysfunctional Bronchial Cilia Are a Feature of Chronic Obstructive Pulmonary Disease (COPD)

43. Psychological distress and trauma during the COVID-19 pandemic: survey of doctors practising anaesthesia, intensive care medicine, and emergency medicine in the United Kingdom and Republic of Ireland

47. Psychological distress during the acceleration phase of the COVID-19 pandemic: a survey of doctors practising in emergency medicine, anaesthesia and intensive care medicine in the UK and Ireland

48. Higher throughput drug screening for rare respiratory diseases: readthrough therapy in primary ciliary dyskinesia

50. Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects

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