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Yifang Hu
Researcher at Walter and Eliza Hall Institute of Medical Research
Publications - 35
Citations - 25473
Yifang Hu is an academic researcher from Walter and Eliza Hall Institute of Medical Research. The author has contributed to research in topics: Haematopoiesis & Cellular differentiation. The author has an hindex of 23, co-authored 34 publications receiving 16561 citations. Previous affiliations of Yifang Hu include University of Melbourne.
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Journal ArticleDOI
c-Maf-dependent Treg cell control of intestinal TH17 cells and IgA establishes host-microbiota homeostasis.
Christian Neumann,Jonas Blume,Jonas Blume,Urmi Roy,Peggy P Teh,Peggy P Teh,Ajithkumar Vasanthakumar,Ajithkumar Vasanthakumar,Alexander Beller,Yang Liao,Yang Liao,Frederik Heinrich,Teresita L. Arenzana,Jason A. Hackney,Celine Eidenschenk,Eric J. C. Gálvez,Christina Stehle,Gitta Anne Heinz,Patrick Maschmeyer,Tom Sidwell,Tom Sidwell,Yifang Hu,Yifang Hu,Derk Amsen,Chiara Romagnani,Hyun-Dong Chang,Andrey Kruglov,Mir-Farzin Mashreghi,Wei Shi,Wei Shi,Till Strowig,Sascha Rutz,Axel Kallies,Axel Kallies,Alexander Scheffold +34 more
TL;DR: It is demonstrated that intestinal Treg cells upregulate the transcription factor c-Maf in response to specific signals from the gut microenvironment to establish host–microbiota homeostasis.
Journal ArticleDOI
Fas-mediated neutrophil apoptosis is accelerated by Bid, Bak, and Bax and inhibited by Bcl-2 and Mcl-1
Ben A. Croker,Joanne A. O’Donnell,Cameron J. Nowell,Donald Metcalf,Grant Dewson,Kirsteen J. Campbell,Kelly L. Rogers,Yifang Hu,Gordon K. Smyth,Jian-Guo Zhang,Michael T. White,Kurt Lackovic,Louise H. Cengia,Lorraine A. O'Reilly,Philippe Bouillet,Suzanne Cory,Andreas Strasser,Andrew W. Roberts,Andrew W. Roberts +18 more
TL;DR: Monitoring the rate of change in neutrophil viability associated with activation of the Fas-triggered death receptor pathway using real-time cell imaging shows that the Bcl-2-related proteins Bid, Bax, and Bak accelerate neutrophils apoptosis but are not essential for cell death.
Journal ArticleDOI
Haemopedia: An Expression Atlas of Murine Hematopoietic Cells.
Carolyn A. de Graaf,Carolyn A. de Graaf,Jarny Choi,Jarny Choi,Tracey M. Baldwin,Jessica E. Bolden,Jessica E. Bolden,Kirsten A. Fairfax,Kirsten A. Fairfax,Aaron J. Robinson,Aaron J. Robinson,Christine Biben,Christine Biben,Clare Morgan,Clare Morgan,Kerry A. Ramsay,Ashley P. Ng,Ashley P. Ng,Maria Kauppi,Maria Kauppi,Elizabeth A. Kruse,Elizabeth A. Kruse,Tobias Sargeant,Tobias Sargeant,Nick Seidenman,Angela D'Amico,Marthe C. D'Ombrain,Marthe C. D'Ombrain,Erin C. Lucas,Sandra Koernig,Adriana Baz Morelli,Michael J. Wilson,Steven K. Dower,Brenda Williams,Brenda Williams,Shen Y. Heazlewood,Shen Y. Heazlewood,Yifang Hu,Susan K. Nilsson,Susan K. Nilsson,Li Wu,Li Wu,Gordon K. Smyth,Gordon K. Smyth,Warren S. Alexander,Warren S. Alexander,Douglas J. Hilton,Douglas J. Hilton +47 more
TL;DR: Haemopedia, an atlas of murine gene-expression data containing 54 hematopoietic cell types, covering all the mature lineages in he matopoiesis is presented, showing that lineage branching and maturation during hematoiesi can be reconstructed using the expression patterns of small sets of genes.
Journal ArticleDOI
Pax5 loss imposes a reversible differentiation block in B-progenitor acute lymphoblastic leukemia
Grace Jie Liu,Grace Jie Liu,Luisa Cimmino,Luisa Cimmino,Julian Jude,Yifang Hu,Matthew T. Witkowski,Matthew T. Witkowski,Mark D. McKenzie,Mark D. McKenzie,Mutlu Kartal-Kaess,Mutlu Kartal-Kaess,Sarah A. Best,Sarah A. Best,Laura Tuohey,Laura Tuohey,Yang Liao,Yang Liao,Wei Shi,Wei Shi,Charles G. Mullighan,Michael A. Farrar,Stewart L Nutt,Stewart L Nutt,Gordon K. Smyth,Gordon K. Smyth,Johannes Zuber,Ross A. Dickins,Ross A. Dickins +28 more
TL;DR: In this model, restoring endogenous Pax5 expression in established B-ALL triggers immunophenotypic maturation and durable disease remission by engaging a transcriptional program reminiscent of normal B-cell differentiation by impairing a differentiation program that can be re-engaged despite the presence of additional oncogenic lesions.
Journal ArticleDOI
The use of miRNA microarrays for the analysis of cancer samples with global miRNA decrease
Di Wu,Yifang Hu,Stephen Tong,Bryan R.G. Williams,Gordon K. Smyth,Gordon K. Smyth,Michael P. Gantier +6 more
TL;DR: This work analyzed the miRNA profiles of samples with global miRNA decreases using Affymetrix miRNA microarrays following the inducible genetic deletion of Dicer1 and suggested that the use of cyclic loess based on non-miRNA small RNAs can help to improve the sensitivity and specificity of miRNA profiling in cancer samples withglobal miRNA decrease.