Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Yu NE"'
Autor:
Daniel Allen, Orli Knop, Bryan Itkowitz, Nechama Kalter, Michael Rosenberg, Ortal Iancu, Katia Beider, Yu Nee Lee, Arnon Nagler, Raz Somech, Ayal Hendel
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract RAG2-SCID is a primary immunodeficiency caused by mutations in Recombination-activating gene 2 (RAG2), a gene intimately involved in the process of lymphocyte maturation and function. ex-vivo manipulation of a patient’s own hematopoietic s
Externí odkaz:
https://doaj.org/article/c083e55eea434c40b1934e6fc7cf4b59
Publikováno v:
Zhongguo linchuang yanjiu, Vol 36, Iss 8, Pp 1170-1174 (2023)
ObjectiveTo investigate the diagnostic value of trimethylamine N-Oxide （TMAO） and serum amyloid A （SAA） levels in peripheral blood of patients with chronic cerebral hypoperfusion （CCH）. MethodsThe patients attending the Department of Neur
Externí odkaz:
https://doaj.org/article/fd97228911aa473ab4a8c863b87197a8
Autor:
Ortal Iancu, Daniel Allen, Orli Knop, Yonathan Zehavi, Dor Breier, Adaya Arbiv, Atar Lev, Yu Nee Lee, Katia Beider, Arnon Nagler, Raz Somech, Ayal Hendel
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 31, Iss , Pp 105-121 (2023)
Severe combined immunodeficiency (SCID) is a group of disorders caused by mutations in genes involved in the process of lymphocyte maturation and function. CRISPR-Cas9 gene editing of the patient’s own hematopoietic stem and progenitor cells (HSPCs
Externí odkaz:
https://doaj.org/article/ae155571bbed4c078012ef702c2c303a
Autor:
Yu Ne Gong
Publikováno v:
Applied Mechanics and Materials. :6305-6308
Applying vitual reality technique to train athletes can carry out analysis and evaluation of movement, and innovation,and improve the technology content of sports training and make the athletes quickly master the movement technology and maintain a go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcb8b903feb490665cbf57cc6f2217f4
https://doi.org/10.4028/www.scientific.net/amm.644-650.6305
https://doi.org/10.4028/www.scientific.net/amm.644-650.6305
Publikováno v:
Türk Biyokimya Dergisi, Vol 48, Iss 1, Pp 32-38 (2022)
To explore the correlations of B cell-activating factor (BAFF), aquaporin-4 antibody (AQP4-Ab) and brain-derived neurotrophic factor (BDNF) with the severity of neuromyelitis optica spectrum disorder (NMOSD).
Externí odkaz:
https://doaj.org/article/c5bb848baa3640c796db914c84f5f689
Autor:
Ifat Geron, Angela Maria Savino, Hila Fishman, Noa Tal, John Brown, Virginia A. Turati, Chela James, Jolanda Sarno, Michal Hameiri-Grossman, Yu Nee Lee, Avigail Rein, Hillary Maniriho, Yehudit Birger, Anna Zemlyansky, Inna Muler, Kara L. Davis, Victoria Marcu-Malina, Nicole Mattson, Oren Parnas, Rabea Wagener, Ute Fischer, João T. Barata, Catriona H. M. Jamieson, Markus Müschen, Chun-Wei Chen, Arndt Borkhardt, Ilan Richard Kirsch, Arnon Nagler, Tariq Enver, Shai Izraeli
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-12 (2022)
Activating mutations in Interleukin-7 receptor alpha (IL7Ra) have been reported in B-cell precursor acute lymphoblastic leukaemia (BCP-ALL) but its role in leukaemogenesis is not clear. Here, the authors show that activation of IL7Ra in primary human
Externí odkaz:
https://doaj.org/article/38d90d34ce264d24b343a4ddcc158487
Autor:
Shirly Frizinsky, Erez Rechavi, Ortal Barel, Yu Nee Lee, Amos J. Simon, Atar Lev, Tali Stauber, Etai Adam, Raz Somech
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundDuring the process of generating diverse T and B cell receptor (TCR and BCR, respectively) repertoires, double-strand DNA breaks are produced. Subsequently, these breaks are corrected by a complex system led by the non-homologous end-joinin
Externí odkaz:
https://doaj.org/article/4b302d93034d4c11abf8ea09476eb014
Autor:
Lael Werner, Yu Nee Lee, Erez Rechavi, Atar Lev, Baruch Yerushalmi, Galina Ling, Neil Shah, Holm H. Uhlig, Batia Weiss, Raz Somech, Scott B. Snapper, Dror S. Shouval
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Patients with loss-of-function mutations in IL10 or IL10 receptor (IL10R) genes develop severe, medical-refractory, infantile-onset inflammatory bowel disease (IBD). We have previously reported significant alterations in innate and adaptive immune re
Externí odkaz:
https://doaj.org/article/73bb68229dc247a8a67ae3b9349d8ec7
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