Christopher Francis HigginsFRSEFRSAFMedSci (born 24 June 1955) is a British molecular biologist, geneticist, academic and scientific advisor. He was the Vice-Chancellor of Durham University from 2007 to 2014. He took early retirement on 30 September 2014, following a discussion at Senate on limiting the powers of the Vice Chancellor.[5] He was previously the director of the MRC Clinical Sciences Centre and Head of Division in the Faculty of Medicine at Imperial College London.
In April 2007, he was appointed Vice-Chancellor of Durham University. He succeeded Sir Kenneth Calman and became the University's 23rd Vice-Chancellor.[8] He took early retirement on 30 September 2014, following a discussion at Senate on limiting the powers of the Vice Chancellor.[5]
Higgins is not currently married, although he has been married twice. He has five daughters, two from his first marriage and three from the second.[6]
References
1 2 "HIGGINS, Prof. Christopher Francis"(Who's Who 2013, A & C Black, an imprint of Bloomsbury Publishing plc, 2013; online edn, Oxford University Press).(subscription required)
↑ Van Veen, H. W.; Callaghan, R.; Soceneantu, L.; Sardini, A.; Konings, W. N.; Higgins, C. F. (1998). "A bacterial antibiotic-resistance gene that complements the human multidrug-resistance P-glycoprotein gene". Nature. 391 (6664): 291–295. Bibcode:1998Natur.391..291V. doi:10.1038/34669. PMID9440694. S2CID205003632.
↑ Hyde, S. C.; Gill, D. R.; Higgins, C. F.; Trezise, A. E. O.; MacVinish, L. J.; Cuthbert, A. W.; Ratcliff, R.; Evans, M. J.; Colledge, W. H. (1993). "Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy". Nature. 362 (6417): 250–255. Bibcode:1993Natur.362..250H. doi:10.1038/362250a0. PMID7681548. S2CID4273074.
↑ Valverde, M. A.; Díaz, M.; Sepúlveda, F. V.; Gill, D. R.; Hyde, S. C.; Higgins, C. F. (1992). "Volume-regulated chloride channels associated with the human multidrug-resistance P-glycoprotein". Nature. 355 (6363): 830–833. Bibcode:1992Natur.355..830V. doi:10.1038/355830a0. PMID1371598. S2CID4275168.
↑ Hyde, S. C.; Emsley, P.; Hartshorn, M. J.; Mimmack, M. M.; Gileadi, U.; Pearce, S. R.; Gallagher, M. P.; Gill, D. R.; Hubbard, R. E.; Higgins, C. F. (1990). "Structural model of ATP-binding proteing associated with cystic fibrosis, multidrug resistance and bacterial transport". Nature. 346 (6282): 362–365. Bibcode:1990Natur.346..362H. doi:10.1038/346362a0. PMID1973824. S2CID1364720.
↑ Higgins, C. F.; Hiles, I. D.; Salmond, G. P. C.; Gill, D. R.; Downie, J. A.; Evans, I. J.; Holland, I. B.; Gray, L.; Buckel, S. D.; Bell, A. W.; Hermodson, M. A. (1986). "A family of related ATP-binding subunits coupled to many distinct biological processes in bacteria". Nature. 323 (6087): 448–450. Bibcode:1986Natur.323..448H. doi:10.1038/323448a0. PMID3762694. S2CID4255180.
↑ Higgins, C. F.; Haag, P. D.; Nikaido, K.; Ardeshir, F.; Garcia, G.; Ames, G. F. (1982). "Complete nucleotide sequence and identification of membrane components of the histidine transport operon of S. Typhimurium". Nature. 298 (5876): 723–727. Bibcode:1982Natur.298..723H. doi:10.1038/298723a0. PMID7050725. S2CID4266380.
↑ Tame, J. R.; Murshudov, G. N.; Dodson, E. J.; Neil, T. K.; Dodson, G. G.; Higgins, C. F.; Wilkinson, A. J. (1994). "The structural basis of sequence-independent peptide binding by OppA protein". Science. 264 (5165): 1578–1581. Bibcode:1994Sci...264.1578T. doi:10.1126/science.8202710. PMID8202710.
↑ Owen-Hughes, T. A.; Pavitt, G. D.; Santos, D. S.; Sidebotham, J. M.; Hulton, C. S.; Hinton, J. C.; Higgins, C. F. (1992). "The chromatin-associated protein H-NS interacts with curved DNA to influence DNA topology and gene expression". Cell. 71 (2): 255–265. doi:10.1016/0092-8674(92)90354-F. PMID1423593. S2CID33653978.
↑ Gill, D. R.; Hyde, S. C.; Higgins, C. F.; Valverde, M. A.; Mintenig, G. M.; Sepúlveda, F. V. (1992). "Separation of drug transport and chloride channel functions of the human multidrug resistance P-glycoprotein". Cell. 71 (1): 23–32. doi:10.1016/0092-8674(92)90263-C. PMID1382860. S2CID10797659.
↑ Hulton, C. S.; Seirafi, A.; Hinton, J. C.; Sidebotham, J. M.; Waddell, L.; Pavitt, G. D.; Owen-Hughes, T.; Spassky, A.; Buc, H.; Higgins, C. F. (1990). "Histone-like protein H1 (H-NS), DNA supercoiling, and gene expression in bacteria". Cell. 63 (3): 631–642. doi:10.1016/0092-8674(90)90458-Q. PMID2171779. S2CID44501388.
↑ Higgins, C. F.; Dorman, C. J.; Stirling, D. A.; Waddell, L.; Booth, I. R.; May, G.; Bremer, E. (1988). "A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. Typhimurium and E. Coli". Cell. 52 (4): 569–584. doi:10.1016/0092-8674(88)90470-9. PMID2830029. S2CID43197280.
↑ Newbury, S. F.; Smith, N. H.; Higgins, C. F. (1987). "Differential mRNA stability controls relative gene expression within a polycistronic operon". Cell. 51 (6): 1131–1143. doi:10.1016/0092-8674(87)90599-X. PMID2446776. S2CID2227781.
↑ Newbury, S. F.; Smith, N. H.; Robinson, E. C.; Hiles, I. D.; Higgins, C. F. (1987). "Stabilization of translationally active mRNA by prokaryotic REP sequences". Cell. 48 (2): 297–310. doi:10.1016/0092-8674(87)90433-8. PMID2433046. S2CID43061195.
↑ Stern, M. J.; Ames, G. F.; Smith, N. H.; Robinson, E. C.; Higgins, C. F. (1984). "Repetitive extragenic palindromic sequences: A major component of the bacterial genome". Cell. 37 (3): 1015–1026. doi:10.1016/0092-8674(84)90436-7. PMID6378385. S2CID34493605.
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