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Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 31, 2019
Validation of the Boston University staging system in AL amyloidosisRoss Tomlinson, Nicholas Matigian, Peter Mollee
Respiratory Medicine|October 1, 2020
Management of isoniazid-monoresistant tuberculosis (Hr-TB) in Queensland, Australia: a retrospective case seriesMalcolm Wilson, Bridget O'Connor, Nicholas Matigian, et al.
Biology|June 28, 2023
Induction of Reactive Bone Stromal Fibroblasts in 3D Models of Prostate Cancer Bone MetastasesLouisa C E Windus, Nicholas Matigian, Vicky M Avery
BMC Bioinformatics|March 1, 2017
MINT: a multivariate integrative method to identify reproducible molecular signatures across independent experiments and platformsFlorian Rohart, Aida Eslami, Nicholas Matigian, et al.
Scientific Reports|August 16, 2017
Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitorsSusitha Premarathne, Mariyam Murtaza, Nicholas Matigian, et al.
Frontiers in Oncology|January 27, 2022
Spatial Profiling Identifies Prognostic Features of Response to Adjuvant Therapy in Triple Negative Breast Cancer (TNBC)Arutha Kulasinghe, James Monkman, Esha T Shah, et al.
Genomics Data|October 21, 2015
Transcriptional ontogeny of first trimester human fetal and placental mesenchymal stem cells: Gestational age versus nicheJennifer M Ryan, Nicholas Matigian, Rebecca A Pelekanos, et al.
Genomics Data|October 21, 2015
Multipotent human stromal cells isolated from cord blood, term placenta and adult bone marrow show distinct differences in gene expression patternNicholas Matigian, Gary Brooke, Faten Zaibak, et al.
Annals of the Rheumatic Diseases|February 1, 2019
IL-23 favours outgrowth of spondyloarthritis-associated pathobionts and suppresses host support for homeostatic microbiotaLinda M Rehaume, Nicholas Matigian, Ahmed M Mehdi, et al.
Disease Models & Mechanisms|December 25, 2012
A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutationsGreger Abrahamsen, Yongjun Fan, Nicholas Matigian, et al.
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