FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

EM Taylor

Research Profile

Chemicals & Drugs

Disorders

Genes & Molecular Sequences

Amino Acid Sequences

Physiology

Phenomena

Ultraviolet Rays

Anatomy

Concepts & Ideas

Living Beings

Schizosaccharomyces

Co-author Network

Publications

TOP 3
EM Taylor; Alice C Copsey; JJ Hudson; Susanne Vidot; Alan Lehmann
Identification of the proteins, including MAGEG1, that make up the human SMC5-6 protein complex.
Bernard C Broughton; Mark Berneburg; Heather Fawcett; EM Taylor; Colin F Arlett; Tiziana Nardo; Miria Stefanini; Emory Menefee; Vera H Price; S Queille; Alain Sarasin; E Bohnert; Jean Krutmann; R Davidson; Kenneth H Kraemer; Alan Lehmann
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
EM Taylor; J S Moghraby; J H Lees; B Smit; P B Moens; Alan Lehmann
Characterization of a novel human SMC heterodimer homologous to the Schizosaccharomyces pombe Rad18/Spr18 complex.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of EM Taylor (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2008: EM Taylor; Alice C Copsey; JJ Hudson; Susanne Vidot; Alan Lehmann
Identification of the proteins, including MAGEG1, that make up the human SMC5-6 protein complex.
Molecular and cellular biology 2008;28(4):1197-206.
2001: Bernard C Broughton; Mark Berneburg; Heather Fawcett; EM Taylor; Colin F Arlett; Tiziana Nardo; Miria Stefanini; Emory Menefee; Vera H Price; S Queille; Alain Sarasin; E Bohnert; Jean Krutmann; R Davidson; Kenneth H Kraemer; Alan Lehmann
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
Human molecular genetics 2001;10(22):2539-47.
2001: EM Taylor; J S Moghraby; J H Lees; B Smit; P B Moens; Alan Lehmann
Characterization of a novel human SMC heterodimer homologous to the Schizosaccharomyces pombe Rad18/Spr18 complex.
Molecular biology of the cell 2001;12(6):1583-94.
2000: Mark Berneburg; Peter H Clingen; SA Harcourt; Jillian E Lowe; EM Taylor; Michael H L Green; Jean Krutmann; Colin F Arlett; Alan Lehmann
The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
Cancer research 2000;60(2):431-8.
1998: Antony M Carr; EM Taylor
1st MRC Human Genetics Symposium: maintenance of genomic stability.
Biochimica et biophysica acta 1998;1378(3):R55-8.
1998: EM Taylor; Alan Lehmann
Conservation of eukaryotic DNA repair mechanisms.
International journal of radiation biology 1998;74(3):277-86.
1997: G Flaggs; AW Plug; K M Dunks; Kirsten E Mundt; J C Ford; M R Quiggle; EM Taylor; Christoph H Westphal; Terry Ashley; MF Hoekstra; Antony M Carr
Atm-dependent interactions of a mammalian chk1 homolog with meiotic chromosomes.
Current biology : CB 1997;7(12):977-86.
1997: EM Taylor; Bernard C Broughton; Elena Botta; Miria Stefanini; Alain Sarasin; Nicolaas G J Jaspers; Heather Fawcett; SA Harcourt; Colin F Arlett; Alan Lehmann
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(16):8658-63.