Browsing "University Library" by Author Feng, J.

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PreviewIssue DateTitleAuthor(s)
2014A case of Aromatase deficiency due to a novel CYP19A1 mutationGagliardi, L.; Scott, H.; Feng, J.; Torpy, D.
2019A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemiaCheah, J.J.C.; Brown, A.L.; Schreiber, A.W.; Feng, J.; Babic, M.; Moore, S.; Young, C.C.; Fine, M.; Phillips, K.; Guandalini, M.; Wilson, P.; Poplawski, N.; Hahn, C.N.; Scott, H.S.
2017A novel, somatic, transforming mutation in the extracellular domain of epidermal growth factor receptor identified in myeloproliferative neoplasmCasolari, D.; Nguyen, T.; Butcher, C.; Iarossi, D.; Hahn, C.; Bray, S.; Neufing, P.; Parker, W.; Feng, J.; Maung, K.; Wee, A.; Vidovic, L.; Kok, C.; Bardy, P.; Branford, S.; Lewis, I.; Lane, S.; Scott, H.; Ross, D.; D'Andrea, R.
2015A tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant cloneHahn, C.; Ross, D.; Feng, J.; Beligaswatte, A.; Hiwase, D.; Parker, W.; Ho, M.; Zawitkowski, M.; Ambler, K.; Cheetham, G.; Lee, Y.; Babic, M.; Butcher, C.; Engler, G.; Brown, A.; D'Andrea, R.; Lewis, I.; Schreiber, A.; To, L.; Scott, H.
2018A template guided approach to generating cell permeable inhibitors of Staphylococcus aureus biotin protein ligasePaparella, A.; Feng, J.; Blanco-Rodriguez, B.; Feng, Z.; Phetsang, W.; Blaskovich, M.; Cooper, M.; Booker, G.; Polyak, S.; Abell, A.
2014ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasiaGagliardi, L.; Schreiber, A.; Hahn, C.; Feng, J.; Cranston, T.; Boon, H.; Hotu, C.; Oftedal, B.; Cutfield, R.; Adelson, D.; Braund, W.; Gordon, R.; Rees, D.; Grossman, A.; Torpy, D.; Scott, H.
2016Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implicationsGagliardi, L.; Burt, M.; Feng, J.; Poplawski, N.; Scott, H.
2016Biotin protein ligase is a target for new antibacterialsFeng, J.; Paparella, A.S.; Booker, G.W.; Polyak, S.W.; Abell, A.D.
2016Ectrodactyly and lethal pulmonary acinar dysplasia associated with homozygous FGFR2 mutations identified by exome sequencingBarnett, C.; Nataren, N.; Klingler-Hoffmann, M.; Schwarz, Q.; Chong, C.; Lee, Y.; Bruno, D.; Lipsett, J.; Mcphee, A.; Schreiber, A.; Feng, J.; Hahn, C.; Scott, H.
2009Granular lightweight fill composed of sand and tire scrapDeng, A.; Feng, J.; Zhang, X.; Yu, X.; Fu, H.; Zhang, J.; GeoHunan International Conference (2009 : Changsha, Hunan, China)
2018Halogenation of biotin protein ligase inhibitors improves whole cell activity against Staphylococcus aureusPaparella, A.S.; Lee, K.J.; Hayes, A.J.; Feng, J.; Feng, Z.; Cini, D.; Deshmukh, S.; Booker, G.W.; Wilce, M.C.; Polyak, S.W.; Abell, A.D.
2019Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6Byrne, A.B.; Arts, P.; Polyak, S.W.; Feng, J.; Schreiber, A.W.; Kassahn, K.S.; Hahn, C.N.; Mordaunt, D.A.; Fletcher, J.M.; Lipsett, J.; Bratkovic, D.; Booker, G.W.; Smith, N.J.; Scott, H.S.
2018Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk diseaseBranford, S.; Wang, P.; Yeung, D.T.; Thomson, D.; Purins, A.; Wadham, C.; Shahrin, N.H.; Marum, J.E.; Nataren, N.; Parker, W.T.; Geoghegan, J.; Feng, J.; Shanmuganathan, N.; Mueller, M.C.; Dietz, C.; Stangl, D.; Donaldson, Z.; Altamura, H.; Georgievski, J.; Braley, J.; et al.
2012Isoform specific regulation of divalent metal (ion) transporter (DMT1) by proteasomal degradationGarrick, M.; Zhao, L.; Roth, J.; Jiang, H.; Feng, J.; Foot, N.; Dalton, H.; Kumar, S.; Garrick, L.
2013Modeling mechanical response of cemented EPS-backfillDeng, A.; Feng, J.; Congress on Stability and Performance of Slopes and Embankments (2013 : San Diego)
2009Modeling of a pilot-scale trickle bed reactor for the catalytic oxidation of phenolWu, Q.; Hu, X.; Yue, P.; Feng, J.; Chen, X.; Zhang, H.; Qiao, S.
2016New series of BPL inhibitors to probe the ribose-binding pocket of Staphylococcus aureus biotin protein ligaseFeng, J.; Paparella, A.; Tieu, W.; Heim, D.; Clark, S.; Hayes, A.; Booker, G.; Polyak, S.; Abell, A.
2016Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignanciesLewinsohn, M.; Brown, A.L.; Weinel, L.M.; Phung, C.; Rafidi, G.; Lee, M.K.; Schreiber, A.W.; Feng, J.; Babic, M.; Chong, C.E.; Lee, Y.; Yong, A.; Suthers, G.K.; Poplawski, N.; Altree, M.; Phillips, K.; Jaensch, L.; Fine, M.; D'Andrea, R.J.; Lewis, I.D.; et al.
2020Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndromeArts, P.; Garland, J.; Byrne, A.B.; Hardy, T.S.E.; Babic, M.; Feng, J.; Wang, P.; Ha, T.; King-Smith, S.L.; Schreiber, A.W.; Crawford, A.; Manton, N.; Moore, L.; Barnett, C.P.; Scott, H.S.
2009Photo Fenton degradation of high concentration Orange II (2 mM) using catalysts containing Fe: A comparative studyFeng, J.; Hu, X.; Yue, P.; Qiao, S.