7 results for author:"Barber T.D." in Literature citations
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| Somatic mutations in CCK2R alter receptor activity that promote oncogenic phenotypes. Willard M.D., Lajiness M.E., Wulur I.H., Feng B., Swearingen M.L., Uhlik M.T., Kinzler K.W., Velculescu V.E., Sjoblom T., Markowitz S.D. et al. Mol. Cancer Res. 10:739-749(2012) · Mapped (6) |
| Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers. Barber T.D., McManus K., Yuen K.W., Reis M., Parmigiani G., Shen D., Barrett I., Nouhi Y., Spencer F., Markowitz S. et al. Proc. Natl. Acad. Sci. U.S.A. 105:3443-3448(2008) · Mapped (29) |
| The consensus coding sequences of human breast and colorectal cancers. Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J., Silliman N. et al. |
| Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcoma. Barber T.D., Barber M.C., Tomescu O., Barr F.G., Ruben S., Friedman T.B. Genomics 79:278-284(2002) · Mapped (7) |
| Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Liang Y., Wang A., Belyantseva I.A., Anderson D.W., Probst F.J., Barber T.D., Miller W., Touchman J.W., Jin L., Sullivan S.L. et al. |
| PAX3 gene structure, alternative splicing and evolution. Barber T.D., Barber M.C., Cloutier T.E., Friedman T.B. Gene 237:311-319(1999) · Mapped (5) |
| Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. Liang Y., Wang A., Probst F.J., Arhya I.N., Barber T.D., Chen K.S., Deshmukh D., Dolan D.F., Hinnant J.T., Carter L.E. et al. Am. J. Hum. Genet. 62:904-915(1998) · Mapped (15) |