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Institution

University of Adelaide

EducationAdelaide, South Australia, Australia
About: University of Adelaide is a education organization based out in Adelaide, South Australia, Australia. It is known for research contribution in the topics: Population & Pregnancy. The organization has 27251 authors who have published 79167 publications receiving 2671128 citations. The organization is also known as: The University of Adelaide & Adelaide University.


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Journal ArticleDOI
TL;DR: The new method is considerably more powerful, detecting approximately 50% more likely helix-turn-helix sequences without an increase in false predictions.
Abstract: We present an update of our method for systematic detection and evaluation of potential helix-turn-helix DNA-binding motifs in protein sequences [Dodd, I. and Egan, J. B. (1987) J. Mol. Biol. 194, 557-564]. The new method is considerably more powerful, detecting approximately 50% more likely helix-turn-helix sequences without an increase in false predictions. This improvement is due almost entirely to the use of a much larger reference set of 91 presumed helix-turn-helix sequences. The scoring matrix derived from this reference set has been calibrated against a large protein sequence database so that the score obtained by a sequence can be used to give a practical estimation of the probability that the sequence is a helix-turn-helix motif.

528 citations

Journal ArticleDOI
TL;DR: In this article, a metamaterial-inspired microwave microfluidic sensor is proposed, where the main part of the device is a microstrip coupled complementary split-ring resonator (CSRR), and the liquid sample flowing inside the channel modifies the resonance frequency and peak attenuation of the CSRR resonance.
Abstract: A new metamaterial-inspired microwave microfluidic sensor is proposed in this paper. The main part of the device is a microstrip coupled complementary split-ring resonator (CSRR). At resonance, a strong electric field will be established along the sides of CSRR producing a very sensitive area to a change in the nearby dielectric material. A micro-channel is positioned over this area for microfluidic sensing. The liquid sample flowing inside the channel modifies the resonance frequency and peak attenuation of the CSRR resonance. The dielectric properties of the liquid sample can be estimated by establishing an empirical relation between the resonance characteristics and the sample complex permittivity. The designed microfluidic sensor requires a very small amount of sample for testing since the cross-sectional area of the sensing channel is over five orders of magnitude smaller than the square of the wavelength. The proposed microfluidic sensing concept is compatible with lab-on-a-chip platforms owing to its compactness.

527 citations

Journal ArticleDOI
TL;DR: The first attempts to study the whole transcriptome began in the early 1990s, and technological advances since the late 1990s have made transcriptomics a widespread discipline as mentioned in this paper, which has enabled the study of how gene expression changes in different organisms and has been instrumental in the understanding of human disease.
Abstract: Transcriptomics technologies are the techniques used to study an organism’s transcriptome, the sum of all of its RNA transcripts. The information content of an organism is recorded in the DNA of its genome and expressed through transcription. Here, mRNA serves as a transient intermediary molecule in the information network, whilst noncoding RNAs perform additional diverse functions. A transcriptome captures a snapshot in time of the total transcripts present in a cell. The first attempts to study the whole transcriptome began in the early 1990s, and technological advances since the late 1990s have made transcriptomics a widespread discipline. Transcriptomics has been defined by repeated technological innovations that transform the field. There are two key contemporary techniques in the field: microarrays, which quantify a set of predetermined sequences, and RNA sequencing (RNA-Seq), which uses high-throughput sequencing to capture all sequences. Measuring the expression of an organism’s genes in different tissues, conditions, or time points gives information on how genes are regulated and reveals details of an organism’s biology. It can also help to infer the functions of previously unannotated genes. Transcriptomic analysis has enabled the study of how gene expression changes in different organisms and has been instrumental in the understanding of human disease. An analysis of gene expression in its entirety allows detection of broad coordinated trends which cannot be discerned by more targeted assays.

525 citations

Journal ArticleDOI
Derrek P. Hibar1, Lars T. Westlye2, Lars T. Westlye3, Nhat Trung Doan2, Nhat Trung Doan3, Neda Jahanshad1, Joshua W. Cheung1, Christopher R.K. Ching1, Amelia Versace4, Amy C. Bilderbeck5, Anne Uhlmann6, Benson Mwangi7, Bernd Kramer8, Bronwyn Overs9, Cecilie B. Hartberg2, Christoph Abé10, Danai Dima11, Danai Dima12, Dominik Grotegerd13, Emma Sprooten14, Erlend Bøen, Esther Jiménez15, Fleur M. Howells6, G. Delvecchio, Henk Temmingh6, J Starke6, Jorge R. C. Almeida16, Jose Manuel Goikolea15, Josselin Houenou17, L M Beard18, Lisa Rauer8, Lucija Abramovic19, M Bonnin15, M F Ponteduro12, Maria Keil20, Maria M. Rive21, Nailin Yao22, Nailin Yao23, Nefize Yalin12, Pablo Najt24, P. G. P. Rosa25, Ronny Redlich13, Sarah Trost20, Saskia P. Hagenaars26, Scott C. Fears27, Scott C. Fears28, Silvia Alonso-Lana, T.G.M. van Erp29, Thomas Nickson26, Tiffany M. Chaim-Avancini25, Timothy B. Meier30, Timothy B. Meier31, Torbjørn Elvsåshagen2, Torbjørn Elvsåshagen3, Unn K. Haukvik2, Won Hee Lee14, Aart H. Schene32, Adrian J. Lloyd33, Allan H. Young12, Allison C. Nugent34, Anders M. Dale35, Andrea Pfennig36, Andrew M. McIntosh26, Beny Lafer25, Bernhard T. Baune37, C J Ekman10, Carlos A. Zarate34, Carrie E. Bearden38, Carrie E. Bearden27, Chantal Henry39, Chantal Henry17, Christian Simhandl, Colm McDonald24, C Bourne5, C Bourne40, Dan J. Stein6, Daniel H. Wolf18, Dara M. Cannon24, David C. Glahn22, David C. Glahn23, Dick J. Veltman41, Edith Pomarol-Clotet, Eduard Vieta15, Erick J. Canales-Rodríguez, Fabiano G. Nery25, Fabiano G. Nery42, Fábio L.S. Duran25, Geraldo F. Busatto25, Gloria Roberts43, Godfrey D. Pearlson22, Godfrey D. Pearlson23, Guy M. Goodwin5, Harald Kugel13, Heather C. Whalley26, Henricus G. Ruhé5, Jair C. Soares7, Janice M. Fullerton43, Janice M. Fullerton9, Janusz K. Rybakowski44, Jonathan Savitz31, Khallil T. Chaim25, M. Fatjó-Vilas, Márcio Gerhardt Soeiro-de-Souza25, Marco P. Boks19, Marcus V. Zanetti25, Maria Concepcion Garcia Otaduy25, Maristela S. Schaufelberger25, Martin Alda45, Martin Ingvar46, Martin Ingvar10, Mary L. Phillips4, Matthew J. Kempton12, Michael Bauer36, Mikael Landén47, Mikael Landén10, Natalia Lawrence48, N.E.M. van Haren19, Neil Horn6, Nelson B. Freimer38, Oliver Gruber8, Peter R. Schofield9, Peter R. Schofield43, Philip B. Mitchell43, René S. Kahn19, Rhoshel K. Lenroot9, Rhoshel K. Lenroot43, Rodrigo Machado-Vieira25, Rodrigo Machado-Vieira34, Roel A. Ophoff19, Roel A. Ophoff38, Salvador Sarró, Sophia Frangou14, Theodore D. Satterthwaite18, Tomas Hajek34, Tomas Hajek45, Udo Dannlowski13, Ulrik Fredrik Malt2, Ulrik Fredrik Malt3, Volker Arolt13, Wagner F. Gattaz25, Wayne C. Drevets49, Xavier Caseras50, Ingrid Agartz2, Paul M. Thompson1, Ole A. Andreassen2, Ole A. Andreassen3 
University of Southern California1, University of Oslo2, Oslo University Hospital3, University of Pittsburgh4, Oxford Health NHS Foundation Trust5, University of Cape Town6, University of Texas Health Science Center at Houston7, Heidelberg University8, Neuroscience Research Australia9, Karolinska Institutet10, City University London11, King's College London12, University of Münster13, Icahn School of Medicine at Mount Sinai14, University of Barcelona15, Brown University16, French Institute of Health and Medical Research17, University of Pennsylvania18, Utrecht University19, University of Göttingen20, University of Amsterdam21, Hartford Hospital22, Yale University23, National University of Ireland, Galway24, University of São Paulo25, University of Edinburgh26, University of California, Los Angeles27, West Los Angeles College28, University of California, Irvine29, Medical College of Wisconsin30, McGovern Institute for Brain Research31, Radboud University Nijmegen32, Northumberland, Tyne and Wear NHS Foundation Trust33, National Institutes of Health34, University of California, San Diego35, Dresden University of Technology36, University of Adelaide37, Semel Institute for Neuroscience and Human Behavior38, Pasteur Institute39, University of Birmingham40, VU University Medical Center41, University of Cincinnati Academic Health Center42, University of New South Wales43, Poznan University of Medical Sciences44, Dalhousie University45, Karolinska University Hospital46, University of Gothenburg47, University of Exeter48, Janssen Pharmaceutica49, Cardiff University50
TL;DR: The largest study to date of cortical gray matter thickness and surface area measures from brain magnetic resonance imaging scans of bipolar disorder patients is performed, revealing previously undetected associations and providing an extensive analysis of potential confounding variables in neuroimaging studies of BD.
Abstract: Despite decades of research, the pathophysiology of bipolar disorder (BD) is still not well understood. Structural brain differences have been associated with BD, but results from neuroimaging studies have been inconsistent. To address this, we performed the largest study to date of cortical gray matter thickness and surface area measures from brain magnetic resonance imaging scans of 6503 individuals including 1837 unrelated adults with BD and 2582 unrelated healthy controls for group differences while also examining the effects of commonly prescribed medications, age of illness onset, history of psychosis, mood state, age and sex differences on cortical regions. In BD, cortical gray matter was thinner in frontal, temporal and parietal regions of both brain hemispheres. BD had the strongest effects on left pars opercularis (Cohen's d=-0.293; P=1.71 × 10-21), left fusiform gyrus (d=-0.288; P=8.25 × 10-21) and left rostral middle frontal cortex (d=-0.276; P=2.99 × 10-19). Longer duration of illness (after accounting for age at the time of scanning) was associated with reduced cortical thickness in frontal, medial parietal and occipital regions. We found that several commonly prescribed medications, including lithium, antiepileptic and antipsychotic treatment showed significant associations with cortical thickness and surface area, even after accounting for patients who received multiple medications. We found evidence of reduced cortical surface area associated with a history of psychosis but no associations with mood state at the time of scanning. Our analysis revealed previously undetected associations and provides an extensive analysis of potential confounding variables in neuroimaging studies of BD.

525 citations

Journal ArticleDOI
TL;DR: The feasibility of using stem cell‐mediated tissue engineering to treat periodontal diseases is demonstrated and it is demonstrated that PDLSCs were capable of regeneratingperiodontal tissues, leading to a favorable treatment for periodontitis.
Abstract: Periodontitis is a periodontal tissue infectious disease and the most common cause for tooth loss in adults. It has been linked to many systemic disorders, such as coronary artery disease, stroke, and diabetes. At present, there is no ideal therapeutic approach to cure periodontitis and achieve optimal periodontal tissue regeneration. In this study, we explored the potential of using autologous periodontal ligament stem cells (PDLSCs) to treat periodontal defects in a porcine model of periodontitis. The periodontal lesion was generated in the first molars area of miniature pigs by the surgical removal of bone and subsequent silk ligament suture around the cervical portion of the tooth. Autologous PDLSCs were obtained from extracted teeth of the miniature pigs and then expanded ex vivo to enrich PDLSC numbers. When transplanted into the surgically created periodontal defect areas, PDLSCs were capable of regenerating periodontal tissues, leading to a favorable treatment for periodontitis. This study demonstrates the feasibility of using stem cell-mediated tissue engineering to treat periodontal diseases.

524 citations


Authors

Showing all 27579 results

NameH-indexPapersCitations
Martin White1962038232387
Nicholas G. Martin1921770161952
David W. Johnson1602714140778
Nicholas J. Talley158157190197
Mark E. Cooper1581463124887
Xiang Zhang1541733117576
John E. Morley154137797021
Howard I. Scher151944101737
Christopher M. Dobson1501008105475
A. Artamonov1501858119791
Timothy P. Hughes14583191357
Christopher Hill1441562128098
Shi-Zhang Qiao14252380888
Paul Jackson141137293464
H. A. Neal1411903115480
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023127
2022597
20215,501
20205,342
20194,803
20184,443