Items where Author is "He, Xiaotong"
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Number of items: 2.
Article
Megremis, Spyridon 
ORCID: https://orcid.org/0000-0002-4082-5387
Walker, Thomas D J ORCID: https://orcid.org/0000-0003-4607-7321
He, Xiaotong ORCID: https://orcid.org/0000-0003-4017-2037
O’Sullivan, James
Ollier, William E R ORCID: https://orcid.org/0000-0001-6502-6584
Chinoy, Hector ORCID: https://orcid.org/0000-0001-6492-1288
Pendleton, Neil ORCID: https://orcid.org/0000-0003-0794-2386
et al.
ORCID: https://orcid.org/0000-0002-4082-5387
Walker, Thomas D J ORCID: https://orcid.org/0000-0003-4607-7321
He, Xiaotong ORCID: https://orcid.org/0000-0003-4017-2037
O’Sullivan, James
Ollier, William E R ORCID: https://orcid.org/0000-0001-6502-6584
Chinoy, Hector ORCID: https://orcid.org/0000-0001-6492-1288
Pendleton, Neil ORCID: https://orcid.org/0000-0003-0794-2386
et al.
Megremis, Spyridon ORCID: https://orcid.org/0000-0002-4082-5387, Walker, Thomas D J ORCID: https://orcid.org/0000-0003-4607-7321, He, Xiaotong ORCID: https://orcid.org/0000-0003-4017-2037, O’Sullivan, James, Ollier, William E R ORCID: https://orcid.org/0000-0001-6502-6584, Chinoy, Hector ORCID: https://orcid.org/0000-0001-6492-1288, Pendleton, Neil ORCID: https://orcid.org/0000-0003-0794-2386, Payton, Antony, Hampson, Lynne, Hampson, Ian and Lamb, Janine A ORCID: https://orcid.org/0000-0002-7248-0539
(2021)
Analysis of human total antibody repertoires in TIF1γ autoantibody positive dermatomyositis.
Communications Biology, 4 (1).
ISSN 2399-3642
ORCID: https://orcid.org/0000-0002-4082-5387, Walker, Thomas D J ORCID: https://orcid.org/0000-0003-4607-7321, He, Xiaotong ORCID: https://orcid.org/0000-0003-4017-2037, O’Sullivan, James, Ollier, William E R ORCID: https://orcid.org/0000-0001-6502-6584, Chinoy, Hector ORCID: https://orcid.org/0000-0001-6492-1288, Pendleton, Neil ORCID: https://orcid.org/0000-0003-0794-2386, Payton, Antony, Hampson, Lynne, Hampson, Ian and Lamb, Janine A ORCID: https://orcid.org/0000-0002-7248-0539
Slevin, Mark, Kumar, Shant, He, Xiaotong and Gaffney, John (1999) Physiological concentrations of gangliosides GM1, GM2 and GM3 differentially modify basic-fibroblast-growth-factor-induced mitogenesis and the associated signalling pathway in endothelial cells. International journal of cancer, 82 (3). pp. 412-23. ISSN 0020-7136