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Your search keyword '"Ho, Lena"' showing total 188 results

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1. Inhibition of IL-11 signalling extends mammalian healthspan and lifespan

5. A high-resolution map of human RNA translation

6. Mast cell activation in lungs during SARS-CoV-2 infection associated with lung pathology and severe COVID-19

7. PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP production

8. Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy

12. Correction: PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP production

13. Comprehensive methylome map of lineage commitment from haematopoietic progenitors

16. Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assembly

19. Viral proteases activate the CARD8 inflammasome in the human cardiovascular system

21. ZAKα-driven ribotoxic stress response activates the human NLRP1 inflammasome

25. C5orf42 is the major gene responsible for OFD syndrome type VI

26. Human NLRP1 is activated by ZAKɑ-driven ribotoxic stress response

28. Erratum: Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy (The American Journal of Human Genetics (2021) 108(7) (1301–1317), (S0002929721001877), (10.1016/j.ajhg.2021.05.003))

32. Signatures of mast cell activation are associated with severe COVID-19

34. Loss of C2orf69 defines a fatal auto-inflammatory mitochondriopathy in Humans and Zebrafish

35. Dominant-negative NFKBIA mutation promotes IL-1β production causing hepatic disease with severe immunodeficiency

36. BRAWNIN: A sORF-encoded Peptide Essential for Vertebrate Mitochondrial Complex III Assembly

44. Proteomic and Bioinformatic Analysis of mSWI/SNF (BAF) Complexes Reveals Extensive Roles in Human Malignancy

47. C5orf42 is the major gene responsible for OFD syndrome type VI

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