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1. An immunohistochemical atlas of necroptotic pathway expression

2. CaMKK2 as an emerging treatment target for bipolar disorder

4. A common human MLKL polymorphism confers resistance to negative regulation by phosphorylation

13. Conformational interconversion of MLKL and disengagement from RIPK3 precede cell death by necroptosis

19. Nanobodies identify an activated state of the TRIB2 pseudokinase

20. A common humanMLKLpolymorphism confers resistance to negative regulation by phosphorylation

21. Giving Children Space: A Phenomenological Exploration of Student Experiences in Space Science Inquiry

24. The intracellular domains of the EphB6 and EphA10 receptor tyrosine pseudokinases function as dynamic signalling hubs

26. Membrane permeabilization is mediated by distinct epitopes in mouse and human orthologs of the necroptosis effector, MLKL

28. Modifying the resolving cysteine affects the structure and hydrogen peroxide reactivity of peroxiredoxin 2

29. Mechanism of NanR gene repression and allosteric induction of bacterial sialic acid metabolism

30. A toolbox for imaging RIPK1, RIPK3 and MLKL in mouse and human cells

31. Structure–Function Studies of the Antibiotic Target l,l-Diaminopimelate Aminotransferase from Verrucomicrobium spinosum Reveal an Unusual Oligomeric Structure

33. Mechanism of NanR gene repression and allosteric induction of bacterial sialic acid metabolism

35. The basis for non-canonical ROK family function in the N-acetylmannosamine kinase from the pathogen Staphylococcus aureus

38. Structure–Function Studies of the Antibiotic Target l,l-Diaminopimelate Aminotransferase from Verrucomicrobium spinosumReveal an Unusual Oligomeric Structure

39. Functional and solution structure studies of amino sugar deacetylase and deaminase enzymes from Staphylococcus aureus.

40. Inhibitors identify an auxiliary role for mTOR signalling in necroptosis execution downstream of MLKL activation.

41. Large Scale Genomic Investigation of Pediatric Cholestasis Reveals a Novel Hepatorenal Ciliopathy Caused by PSKH1 Mutations.

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