14
results
for author:"Ross M.T."
in Literature Citations
| The DNA sequence and biological annotation of human chromosome 1. Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A. et al. Nature 441:315-321(2006) · UniProtKB (2,571) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,199) |
| The DNA sequence and comparative analysis of human chromosome 10. Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C. et al. Nature 429:375-381(2004) · UniProtKB (1,061) |
| The DNA sequence and analysis of human chromosome 13. Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S. et al. Nature 428:522-528(2004) · UniProtKB (460) |
| The DNA sequence and analysis of human chromosome 6. Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L., Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E. et al. Nature 425:805-811(2003) · UniProtKB (1,570) |
| An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders. Thiselton D.L., McDowall J., Brandau O., Ramser J., d'Esposito F., Bhattacharya S.S., Ross M.T., Hardcastle A.J., Meindl A. |
| The DNA sequence and comparative analysis of human chromosome 20. Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L. et al. Nature 414:865-871(2001) · UniProtKB (802) |
| Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region. Braybrook C., Warry G., Howell G., Mandryko V., Arnason A., Bjornsson A., Ross M.T., Moore G.E., Stanier P. Hum. Genet. 108:537-545(2001) · UniProtKB (2) |
| Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and ankyloglossia (CPX) critical region. Braybrook C., Warry G., Howell G., Arnason A., Bjornsson A., Moore G.E., Ross M.T., Stanier P. Genomics 72:128-136(2001) · UniProtKB (1) |
| The DNA sequence of human chromosome 22. Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K. et al. |
| A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation. Carrie A., Jun L., Bienvenu T., Vinet M.-C., McDonell N., Couvert P., Zemni R., Cardona A., Van Buggenhout G., Frints S. et al. |
| A YAC-based physical map of the mouse genome. Nusbaum C., Slonim D.K., Harris K.L., Birren B.W., Steen R.G., Stein L.D., Miller J., Dietrich W.F., Nahf R., Wang V. et al. Nat. Genet. 22:388-393(1999) · Mapped (3) |
| Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22. Walpole S.M., Hiriyana K.T., Nicolaou A., Bingham E.L., Durham J., Vaudin M., Ross M.T., Yates J.R.W., Sieving P.A., Trump D. |
| Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes. van de Vosse E., Walpole S.M., Nicolaou A., van der Bent P., Cahn A., Vaudin M., Ross M.T., Durham J., Pavitt R., Wilkinson J. et al. Genomics 49:96-102(1998) · UniProtKB (1) |
