10
results
for author:"Parsons D.W."
in Literature Citations
| SMAD4 gene mutations are associated with poor prognosis in pancreatic cancer. Blackford A., Serrano O.K., Wolfgang C.L., Parmigiani G., Jones S., Zhang X., Parsons D.W., Lin J.C., Leary R.J., Eshleman J.R. et al. Clin. Cancer Res. 15:4674-4679(2009) · Mapped (3) |
| Genetic mutations associated with cigarette smoking in pancreatic cancer. Blackford A., Parmigiani G., Kensler T.W., Wolfgang C., Jones S., Zhang X., Parsons D.W., Lin J.C., Leary R.J., Eshleman J.R. et al. Cancer Res. 69:3681-3688(2009) · Mapped (508) |
| Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. Jones S., Hruban R.H., Kamiyama M., Borges M., Zhang X., Parsons D.W., Lin J.C., Palmisano E., Brune K., Jaffee E.M. et al. Science 324:217-217(2009) · Mapped (2) |
| IDH1 and IDH2 mutations in gliomas. Yan H., Parsons D.W., Jin G., McLendon R., Rasheed B.A., Yuan W., Kos I., Batinic-Haberle I., Jones S., Riggins G.J. et al. N. Engl. J. Med. 360:765-773(2009) · Mapped (15) |
| An integrated genomic analysis of human glioblastoma multiforme. Parsons D.W., Jones S., Zhang X., Lin J.C.-H., Leary R.J., Angenendt P., Mankoo P., Carter H., Siu I.-M., Gallia G.L. et al. |
| 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. |
| Mutational analysis of the tyrosine phosphatome in colorectal cancers. Wang Z., Shen D., Parsons D.W., Bardelli A., Sager J., Szabo S., Ptak J., Silliman N., Peters B.A., van der Heijden M.S. et al. Science 304:1164-1166(2004) · UniProtKB (1) |
| Three classes of genes mutated in colorectal cancers with chromosomal instability. Wang Z., Cummins J.M., Shen D., Cahill D.P., Jallepalli P.V., Wang T.-L., Parsons D.W., Traverso G., Awad M., Silliman N. et al. |
| The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy. Monani U.R., Sendtner M., Coovert D.D., Parsons D.W., Andreassi C., Le T.T., Jablonka S., Schrank B., Rossoll W., Rossol W. et al. Hum. Mol. Genet. 9:333-339(2000) · Mapped (9) |
| Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number. Parsons D.W., McAndrew P.E., Iannaccone S.T., Mendell J.R., Burghes A.H., Prior T.W. Am. J. Hum. Genet. 63:1712-1723(1998) · UniProtKB (1) |
