Scientific Publications

Search by Keyword(s)
Found 3 results

Filters: Author is Azam, M  [Clear All Filters]

Search Results

  • Showing 1-3 of 3 Results
2015
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.Roosing, S., Hofree M., Kim S., Scott E., Copeland B., Romani M., Silhavy JL, Rosti RO, Schroth J., Mazza T., Miccinilli E., Zaki MS, Swoboda KJ, Milisa-Drautz J., Dobyns WB, Mikati M., İncecik F., Azam M., Borgatti R., Romaniello R., et al. eLife, 2015/05/30, Volume 4, (2015) Read More / View Supplemental Materials
Abstract
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.Akizu, N., Cantagrel V., Zaki MS, Al-Gazali L., Wang X., Rosti RO, Dikoglu E., Gelot AB, Rosti B., Vaux KK, Scott EM, Silhavy JL, Schroth J., Copeland B., Schaffer AE, Gordts PL, Esko JD, Buschman MD, Field SJ, Napolitano G., et al. Nature genetics, 2015/04/06, (2015) Read More / View Supplemental Materials
Abstract
2009
Lin28 promotes transformation and is associated with advanced human malignancies.Viswanathan, SR, Powers JT, Einhorn W., Hoshida Y., Ng TL, Toffanin S., O'Sullivan M., Lu J., Phillips LA, Lockhart VL, Shah SP, Tanwar PS, Mermel CH, Beroukhim R., Azam M., Teixeira J., Meyerson M., Hughes TP, Llovet JM, Radich J., et al. Nature genetics, 2009/07/01, Volume 41, Issue 7, p.843-8, (2009) Read More / View Supplemental Materials
Abstract
  • Showing 1-3 of 3 Results