Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Kuiying Ma"'
Autor:
Kuiying Ma, Xuan Wang, Linjie Wu, Lingling Yu, Jinhui Ye, Xueling Li, Lili Geng, Zhongyu Shi, Huihui Yang, Xijuan Zhang, Yongjian Zhang, Shuchang Wu, Pengfei Yuan, Yingchi Zhang, Fang Dong, Sha Hao, Linping Hu, Wensheng Wei, Riguo Fang, Tao Cheng
Publikováno v:
iScience, Vol 26, Iss 12, Pp 108561- (2023)
Summary: Hematopoietic stem cell (HSC) surface markers improve the understanding of cell identity and function. Here, we report that human HSCs can be distinguished by their expression of the CEA Cell Adhesion Molecule 5 (CEACAM5, CD66e), which serve
Externí odkaz:
https://doaj.org/article/bf358c0bcb274e3fab860398a9c72498
Autor:
Kuiying Ma, Tingting Bai, Pengfei Hu, Ming Zhao, Zhi Xiu, Surilige, Dalintai, Qingshan Zhang, Quan Wan
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
ObjectiveTo investigate the effects of Sanwei sandalwood decoction on improving function of the intestinal flora in doxorubicin-induced heart failure in rats.Materials and methodsThirty Sprague–Dawley rats were screened and randomly assigned into a
Externí odkaz:
https://doaj.org/article/2f27328a9927413aa514aa005d19dd49
Autor:
Yue Chen, Mei Mei, Peng Zhang, Kuiying Ma, Guangqi Song, Xin Ma, Tianchuang Zhao, Bo Tang, Hongsheng Ouyang, Guangpeng Li, Ziyi Li
Publikováno v:
Cellular Physiology and Biochemistry, Vol 32, Iss 3, Pp 523-532 (2013)
Background: Microorganisms and higher plants possess their own omega-3 and omega-6 polyunsaturated fatty acid (PUFAs) biosynthetic pathways. The n-6 fatty acid desaturase gene fad-2 codes for the n-6 desaturase enzyme that coverts oleic acid (OA 18:1
Externí odkaz:
https://doaj.org/article/d0ee4d0bda3c4f5380b39c933c4f3802
Publikováno v:
Environmental Toxicology. 38:1405-1419
Autor:
Isabelle André, Kuiying Ma, Laura E. Simons, Chloé Couzin, Jean-Sébastien Diana, Ranjita Devi Moirangthem, Elisa Magrin, Alessandra Magnani, Marina Cavazzana
Publikováno v:
Bone Marrow Transplantation. 54:749-755
Prolonged T-cell immunodeficiency following HLA- incompatible hematopoietic stem cell transplantation (HSCT) represents a major obstacle hampering the more widespread use of this approach. Strategies to fasten T-cell reconstitution in this setting ar
Autor:
Isabelle André, Laura Simons, Kuiying Ma, Ranjita Devi Moirangthem, Jean-Sébastien Diana, Elisa Magrin, Chloé Couzin, Alessandra Magnani, Chantal Lagresle-Peyrou, Marina Cavazzana
Publikováno v:
Bone Marrow Transplantation. 57:851-851
Autor:
Yongjian Zhang, Dong Wei, Pengfei Yuan, Xijuan Zhang, Chao Li, Penghui Xia, Kuiying Ma, Huihui Yang, Lingling Yu, Riguo Fang, Zhongyu Shi, Wei Zhang
Publikováno v:
Blood. 138:3820-3820
Hematopoietic stem cells (HSCs) serve as the origin of the hematopoietic system, with the ability to differentiate into all blood cell lineages and self-renewal to sustain the hematopoiesis throughout life. Hematopoietic stem cell transplantation (HS
Autor:
Chao Li, Riguo Fang, Wei Zhang, Lingling Yu, Kuiying Ma, Zhongyu Shi, Pengfei Yuan, Xijuan Zhang, Huihui Yang, Yongjian Zhang, Penghui Xia, Dong Wei
Publikováno v:
Blood. 138:2156-2156
Gene-modified hematopoietic stem cells (HSCs) therapy has demonstrated remarkable success for the treatment of inherited blood disorders. As the origin of hematologic hierarchy, HSCs play an essential role in sustaining life-long hematopoiesis. HSCs
Autor:
David Fenard, Ornellie Bernadin, Anais Girard-Gagnepain, Camille Lévy, Chantal Lagresle-Peyrou, Kuiying Ma, Rana Mhaidly, Hanem Sadek, Marina Cavazzana, Fouzia Amirache, Caroline Costa, Ranjita Devi Moirangthem, Isabelle André, François-Loïc Cosset, Els Verhoeyen, Christian Reimann, Didier Nègre, Agata Cieslak, Vahid Asnafi
Publikováno v:
Blood Advances
Blood Advances, The American Society of Hematology, 2019, 3 (3), pp.461-475. ⟨10.1182/bloodadvances.2018027508⟩
Blood Advances, 2019, 3 (3), pp.461-475. ⟨10.1182/bloodadvances.2018027508⟩
Blood Advances, The American Society of Hematology, 2019, 3 (3), pp.461-475. ⟨10.1182/bloodadvances.2018027508⟩
Blood Advances, 2019, 3 (3), pp.461-475. ⟨10.1182/bloodadvances.2018027508⟩
T cells represent a valuable tool for treating cancers and infectious and inherited diseases; however, they are mainly short-lived in vivo. T-cell therapies would strongly benefit from gene transfer into long-lived persisting naive T cells or T-cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc71d6d3ddfc5a388ab66cb716a918bb
https://hal.archives-ouvertes.fr/hal-02365989
https://hal.archives-ouvertes.fr/hal-02365989
Publikováno v:
Journal of Allergy and Clinical Immunology