Brooke Gardiner
Brooke Gardiner
Genomic Service Coordinator, University of Queensland
Потвърден имейл адрес: uq.edu.au
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes
AV Biankin, N Waddell, KS Kassahn, MC Gingras, LB Muthuswamy, ...
Nature 491 (7424), 399-405, 2012
Stem cell transcriptome profiling via massive-scale mRNA sequencing
N Cloonan, ARR Forrest, G Kolle, B Gardiner, GJ Faulkner, MK Brown, ...
Nature methods 5 (7), 613-619, 2008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation
ME Dinger, PP Amaral, TR Mercer, KC Pang, SJ Bruce, BB Gardiner, ...
Genome research 18 (9), 1433-1445, 2008
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ...
Nature 526 (7571), 112-117, 2015
Brief report: intestinal dysbiosis in ankylosing spondylitis
ME Costello, F Ciccia, D Willner, N Warrington, PC Robinson, B Gardiner, ...
Arthritis & rheumatology 67 (3), 686-691, 2015
MicroRNAs and their isomiRs function cooperatively to target common biological pathways
N Cloonan, S Wani, Q Xu, J Gu, K Lea, S Heater, C Barbacioru, ...
Genome biology 12 (12), 1-20, 2011
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells
MR Tallack, T Whitington, WS Yuen, EN Wainwright, JR Keys, ...
Genome research 20 (8), 1052-1063, 2010
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ...
The American Journal of Human Genetics 93 (5), 915-925, 2013
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60
AM McInerney-Leo, M Schmidts, CR Cortés, PJ Leo, B Gener, ...
The American Journal of Human Genetics 93 (3), 515-523, 2013
Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy
M Schmidts, J Vodopiutz, S Christou-Savina, CR Cortés, ...
The American Journal of Human Genetics 93 (5), 932-944, 2013
Reduced mucin sulfonation and impaired intestinal barrier function in the hyposulfataemic NaS1 null mouse
PA Dawson, S Huxley, B Gardiner, T Tran, JL McAuley, S Grimmond, ...
Gut 58 (7), 910-919, 2009
Transcriptional analysis of early lineage commitment in human embryonic stem cells
AL Laslett, S Grimmond, B Gardiner, L Stamp, A Lin, SM Hawes, ...
BMC developmental biology 7 (1), 1-18, 2007
Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptome
TR Mercer, ME Dinger, CP Bracken, G Kolle, JM Szubert, DJ Korbie, ...
Genome research 20 (12), 1639-1650, 2010
Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6
DB Sparrow, A McInerney-Leo, ZS Gucev, B Gardiner, M Marshall, PJ Leo, ...
Human molecular genetics 22 (8), 1625-1631, 2013
Dynamic transcription programs during ES cell differentiation towards mesoderm in serum versus serum-freeBMP4 culture
SJ Bruce, BB Gardiner, LJ Burke, MM Gongora, SM Grimmond, ...
BMC genomics 8 (1), 1-26, 2007
Temporal and spatial transcriptional programs in murine kidney development
G Challen, B Gardiner, G Caruana, X Kostoulias, G Martinez, M Crowe, ...
Physiological genomics 23 (2), 159-171, 2005
Osteonectin/SPARC induction by ectopic β3 integrin in human radial growth phase primary melanoma cells
RA Sturm, K Satyamoorthy, F Meier, BB Gardiner, DJ Smit, B Vaidya, ...
Cancer research 62 (1), 226-232, 2002
Profiling gene expression induced by protease-activated receptor 2 (PAR2) activation in human kidney cells
JY Suen, B Gardiner, S Grimmond, DP Fairlie
PLoS One 5 (11), e13809, 2010
Inhibition of melanin synthesis by cystamine in human melanoma cells
L Qiu, M Zhang, I Tonks, G Kay, PG Parsons, RA Sturm, B Gardiner
Journal of investigative dermatology 114 (1), 21-27, 2000
Osteonectin downregulates E‐cadherin, induces osteopontin and focal adhesion kinase activity stimulating an invasive melanoma phenotype
DJ Smit, BB Gardiner, RA Sturm
International journal of cancer 121 (12), 2653-2660, 2007
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Статии 1–20