14 results for author:"Taylor A.M.R." in Literature citations
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| The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage. Stewart G.S., Panier S., Townsend K., Al-Hakim A.K., Kolas N.K., Miller E.S., Nakada S., Ylanko J., Olivarius S., Mendez M. et al. Cell 136:420-434(2009) · UniProtKB (15) |
| The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4. Clements P.M., Breslin C., Deeks E.D., Byrd P.J., Ju L., Bieganowski P., Brenner C., Moreira M.-C., Taylor A.M.R., Caldecott K.W. DNA Repair 3:1493-1502(2004) · UniProtKB (3) |
| MDC1 is a mediator of the mammalian DNA damage checkpoint. Stewart G.S., Wang B., Bignell C.R., Taylor A.M.R., Elledge S.J. |
| hMRE11: genomic structure and a null mutation identified in a transcript protected from nonsense-mediated mRNA decay. Pitts S.A., Kullar H.S., Stankovic T., Stewart G.S., Last J.I.K., Bedenham T., Armstrong S.J., Piane M., Chessa L., Taylor A.M.R. et al. Hum. Mol. Genet. 10:1155-1162(2001) · UniProtKB (1) |
| The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder. Stewart G.S., Maser R.S., Stankovic T., Bressan D.A., Kaplan M.I., Jaspers N.G.J., Raams A., Byrd P.J., Petrini J.H.J., Taylor A.M.R. |
| Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia. Stankovic T., Weber P., Stewart G., Bedenham T., Murray J., Byrd P.J., Moss P.A.H., Taylor A.M.R. Lancet 353:26-29(1999) · UniProtKB (1) |
| ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. Stankovic T., Kidd A.M.J., Sutcliffe A., McGuire G.M., Robinson P., Weber P., Bedenham T., Bradwell A.R., Easton D.F., Lennox G.G. et al. Am. J. Hum. Genet. 62:334-345(1998) · UniProtKB (1) |
| Construction of a transcription map around the gene for ataxia telangiectasia; identification of at least four novel genes. Stankovic T., Byrd P.J., Cooper P.R., McConville C.M., Munroe D.J., Riley J.H., Watts G.D.J., Ambrose H., McGuire G., Smith A.D. et al. Genomics 40:267-276(1997) · UniProtKB (2) |
| Identification and analysis of expression of human VACM-1, a cullin gene family member located on chromosome 11q22-23. Byrd P.J., Stankovic T., McConville C.M., Smith A.D., Cooper P.R., Taylor A.M.R. |
| Analysis of the ATM protein in wild-type and ataxia telangiectasia cells. Lakin N.D., Weber P., Stankovic T., Rottinghaus S.T., Taylor A.M.R., Jackson S.P. Oncogene 13:2707-2716(1996) · UniProtKB (1) |
| A gene transcribed from the bidirectional ATM promoter coding for a serine rich protein: amino acid sequence, structure and expression studies. Byrd P.J., Cooper P.R., Stankovic T., Kullar H.S., Watts G.D.J., Robinson P.J., Taylor A.M.R. Hum. Mol. Genet. 5:1785-1791(1996) · UniProtKB (1) · Mapped (1) |
| Mutations revealed by sequencing the 5' half of the gene for ataxia telangiectasia. Byrd P.J., McConville C.M., Cooper P., Parkhill J., Stankovic T., McGuire G.M., Thick J.A., Taylor A.M.R. Hum. Mol. Genet. 5:145-149(1996) · UniProtKB (2) |
| Mutations associated with variant phenotypes in ataxia-telangiectasia. McConville C.M., Stankovic T., Byrd P.J., McGuire G.M., Yao Q.-Y., Lennox G.G., Taylor A.M.R. Am. J. Hum. Genet. 59:320-330(1996) · UniProtKB (1) · Mapped (8) |
| A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Savitsky K., Bar-Shira A., Gilad S., Rotman G., Ziv Y., Vanagaite L., Tagle D.A., Smith S., Uziel T., Sfez S. et al. |