Dave Tang
Dave Tang
Verified email at postman.riken.jp - Homepage
Title
Cited by
Cited by
Year
An atlas of human long non-coding RNAs with accurate 5′ ends
CC Hon, JA Ramilowski, J Harshbarger, N Bertin, OJL Rackham, J Gough, ...
Nature 543 (7644), 199-204, 2017
5712017
Site-specific DICER and DROSHA RNA products control the DNA-damage response
S Francia, F Michelini, A Saxena, D Tang, M De Hoon, V Anelli, M Mione, ...
Nature 488 (7410), 231-235, 2012
4082012
A genome wide survey of SNP variation reveals the genetic structure of sheep breeds
JW Kijas, D Townley, BP Dalrymple, MP Heaton, JF Maddox, A McGrath, ...
PloS one 4 (3), e4668, 2009
3122009
Analysis of early nephron patterning reveals a role for distal RV proliferation in fusion to the ureteric tip via a cap mesenchyme-derived connecting segment
K Georgas, B Rumballe, MT Valerius, HS Chiu, RD Thiagarajan, ...
Developmental biology 332 (2), 273-286, 2009
2042009
Identification of anchor genes during kidney development defines ontological relationships, molecular subcompartments and regulatory pathways
RD Thiagarajan, KM Georgas, BA Rumballe, E Lesieur, HS Chiu, ...
PloS one 6 (2), e17286, 2011
712011
RNA-MATE: a recursive mapping strategy for high-throughput RNA-sequencing data
N Cloonan, Q Xu, GJ Faulkner, DF Taylor, DTP Tang, G Kolle, ...
Bioinformatics 25 (19), 2615-2616, 2009
622009
Suppression of artifacts and barcode bias in high-throughput transcriptome analyses utilizing template switching
DTP Tang, C Plessy, M Salimullah, AM Suzuki, R Calligaris, S Gustincich, ...
Nucleic acids research 41 (3), e44-e44, 2013
522013
The rare and undiagnosed diseases diagnostic service–application of massively parallel sequencing in a state-wide clinical service
G Baynam, N Pachter, F McKenzie, S Townshend, J Slee, C Kiraly-Borri, ...
Orphanet journal of rare diseases 11 (1), 1-7, 2016
392016
Refining transcriptional programs in kidney development by integration of deep RNA-sequencing and array-based spatial profiling
RD Thiagarajan, N Cloonan, BB Gardiner, TR Mercer, G Kolle, ...
BMC genomics 12 (1), 1-16, 2011
302011
CCL2 enhances pluripotency of human induced pluripotent stem cells by activating hypoxia related genes
Y Hasegawa, D Tang, N Takahashi, Y Hayashizaki, ARR Forrest, ...
Scientific reports 4 (1), 1-10, 2014
252014
Analysis of the complement and molecular evolution of tRNA genes in cow
DTP Tang, EA Glazov, SM McWilliam, WC Barris, BP Dalrymple
BMC genomics 10 (1), 1-13, 2009
242009
Comparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiation
HS Chiu, JC Szucsik, KM Georgas, JL Jones, BA Rumballe, D Tang, ...
Developmental biology 344 (2), 1071-1087, 2010
212010
Reference genotype and exome data from an Australian Aboriginal population for health-based research
D Tang, D Anderson, RW Francis, G Syn, SE Jamieson, T Lassmann, ...
Scientific data 3 (1), 1-7, 2016
182016
piRNAs warrant investigation in Rett Syndrome: an omics perspective
A Saxena, D Tang, P Carninci
Disease markers 33 (5), 261-275, 2012
182012
High expression of insulin receptor on tumour‐associated blood vessels in invasive bladder cancer predicts poor overall and progression‐free survival
F Roudnicky, LC Dieterich, C Poyet, L Buser, P Wild, D Tang, ...
The Journal of pathology 242 (2), 193-205, 2017
152017
Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene
MB Abraham, D Li, D Tang, SM O’Connell, F McKenzie, EM Lim, ...
International journal of pediatric endocrinology 2017 (1), 1-9, 2017
142017
A novel, homozygous mutation in desert hedgehog (DHH) in a 46, XY patient with dysgenetic testes presenting with primary amenorrhoea: a case report
KM Rothacker, KL Ayers, D Tang, K Joshi, JA Van Den Bergen, ...
International journal of pediatric endocrinology 2018 (1), 1-9, 2018
72018
International Sheep Genomics, C., 2009. A genome wide survey of SNP variation reveals the genetic structure of sheep breeds
JW Kijas, D Townley, BP Dalrymple, MP Heaton, JF Maddox, A McGrath, ...
PloS one 4, e4668, 0
7
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number‐dependent manner
M Bertuzzi, D Tang, R Calligaris, C Vlachouli, S Finaurini, R Sanges, ...
Human mutation 41 (4), 807-824, 2020
22020
Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians
D Tang, M Fakiola, G Syn, D Anderson, HJ Cordell, ESH Scaman, E Davis, ...
Scientific reports 8 (1), 1-13, 2018
22018
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Articles 1–20