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Preview	Issue Date	Title	Author(s)
	2014	Deciphering the secret role of Sox4 gene locus during mouse cerebral corticogenesis	Ling, K.; Lee, H.; Brautigan, P.; Moore, S.; Fraser, R.; Cheah, P.; Raison, J.; Babic, M.; Lee, Y.; Daish, T.; Mattiske, D.; Mann, J.; Adelson, D.; Thomas, P.; Hahn, C.; Scott, H.; 12th Biennial Meeting of the Asian-Pacific Society for Neurochemistry (23 Aug 2014 - 26 Aug 2014 : Kaohsiung, Taiwan)
	2018	A four-gene lincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients	Beck, D.; Thoms, J.; Palu, C.; Herold, T.; Shah, A.; Olivier, J.; Boelen, L.; Huang, Y.; Chacon, D.; Brown, A.; Babic, M.; Hahn, C.; Perugini, M.; Zhou, X.; Huntly, B.; Schwarzer, A.; Klusmann, J.-H.; Berdel, W.; Wörmann, B.; Büchner, T.; et al.
	2020	RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML	Brown, A.L.; Arts, P.; Carmichael, C.L.; Babic, M.; Dobbins, J.; Chong, C.-E.; Schreiber, A.W.; Feng, J.; Phillips, K.; Wang, P.P.S.; Ha, T.; Homan, C.C.; King-Smith, S.L.; Rawlings, L.; Vakulin, C.; Dubowsky, A.; Burdett, J.; Moore, S.; McKavanagh, G.; Henry, D.; et al.
	2019	A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia	Cheah, 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.
	2020	Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome	Arts, 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.
	2020	Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis	Byrne, A.B.; Mizumoto, S.; Arts, P.; Yap, P.; Feng, J.; Schreiber, A.W.; Babic, M.; King-Smith, S.L.; Barnett, C.P.; Moore, L.; Sugahara, K.; Mutlu-Albayrak, H.; Nishimura, G.; Liebelt, J.E.; Yamada, S.; Savarirayan, R.; Scott, H.S.
	2020	Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss	Venugopal, P.; Gagliardi, L.; Forsyth, C.; Feng, J.; Phillips, K.; Babic, M.; Poplawski, N.K.; Rienhoff, H.Y.; Schreiber, A.W.; Hahn, C.N.; Brown, A.L.; Scott, H.S.
	2016	Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies	Lewinsohn, 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.
	2016	In depth analysis of the Sox4 gene locus that consists of sense and natural antisense transcripts	Ling, K.; Brautigan, P.; Moore, S.; Fraser, R.; Leong, M.; Leong, J.; Zainal Abidin, S.; Lee, H.; Cheah, P.; Raison, J.; Babic, M.; Lee, Y.; Daish, T.; Mattiske, D.; Mann, J.; Adelson, D.; Thomas, P.; Hahn, C.; Scott, H.
	2016	Derivation of an endogenous small RNA from double-stranded Sox4 sense and natural antisense transcripts in the mouse brain	Ling, K.; Brautigan, P.; Moore, S.; Fraser, R.; Cheah, P.; Raison, J.; Babic, M.; Lee, Y.; Daish, T.; Mattiske, D.; Mann, J.; Adelson, D.; Thomas, P.; Hahn, C.; Scott, H.