Zobrazeno 1 - 10
of 247
pro vyhledávání: '"B Nikbin"'
Autor:
A Sarafnejad, F Siavoshi, R Safaralizadeh, S Masarat, F Khosravi, R Malekzadeh, B Nikbin, AR Salehi-Nodeh
Publikováno v:
Iranian Journal of Public Health, Vol 36, Iss 1, Pp 50-54 (2007)
Background: Flow cytometry is a rapid, sensitive, and reliable method for determination of bacterial viability. Here we assayed the capability of flow cytometry to detect Helicobacter pylori viable cells in both forms of spiral and coccoid. Methods:
Externí odkaz:
https://doaj.org/article/6c5b6ae47d6d4dc5a89069050eaae388
Autor:
M Mohyeddin Bonab, S Yazdanbakhsh, K Alimoghaddom, A Ghavamzadeh, F Hooshmand, J Lotfi, F Talebian, B Nikbin
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 2, Iss 2 (2005)
Human mesenchymal stem cell (MSC) can be isolated from bone marrow (BM) and differentiated into multiple lineages. These properties make them promising tools in cell and gene therapy. Up to now, no definite therapeutic intervention for late stages of
Externí odkaz:
https://doaj.org/article/32a4c9f3b2064ab3805b8d1f902e8a4a
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 2, Iss 2 (2005)
Mesenchyml stem cell (MSC) are receiving much attention in treatment of various diseases. The low frequency of MSCs in bone marrow (BM) necessitates their in vitro expansion prior to clinical use. We evaluated the effect of long term culture on the s
Externí odkaz:
https://doaj.org/article/45d81acf823946f7bf1c6e371299ddf6
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 2, Iss 1 (2005)
Objective: Mesenchymal stem cells (MSC) are capable of self-renewal and differentiation into various connective tissue lineages. Therefore, they have attracted a lot of attention from investigators in the context of stem cell therapies. In our study,
Externí odkaz:
https://doaj.org/article/6657c99b3d924de5a90ef04bc013b300
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 1, Iss 1 (2004)
Background: Thalassemia is probably the most common single gene disorder causing a major public health problem in the world. Currently, allogenic hematopoietic stem cell transplantation (HSCT) is the only curative therapy for thalassemia. One major l
Externí odkaz:
https://doaj.org/article/c8ede8f84bb049049b6a3078a36d4fb8
Autor:
F. Mohammadi, M. H. Niknam, M. Nafar, B. Einollahi, B. Nazari, M. Lessanpezeshki, M. A. Amirzargar, G. Solgi, B. Nikbin, A. A. Amirzargar
Publikováno v:
International Journal of Organ Transplantation Medicine, Vol 4, Iss 2, Pp 77-85 (2013)
Background: A growing body of evidence demonstrated an immune etiology as well as nonimmune mechanismsfor episodes of clinical acute rejection and long-term allograft dysfunction.Objective: To investigate the correlation of IFN-γ-producing cells and
Externí odkaz:
https://doaj.org/article/b9781ffe20414fc186594fc41d7c9fc9
Publikováno v:
Acta Medica Iranica, Vol 42, Iss 2, Pp 97-100 (2004)
Brucellosis is an infectious disease and it seems that it affects human immune system and can cause acute, subacute and chronic clinical features. Forty patients suffering from chronic brucellosis were studied for CD3+, CD4+,CD8+, CD19+, cells and CD
Externí odkaz:
https://doaj.org/article/73cf7f7b47ec4b969aaf3fabcc5d82f7
Akademický článek
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Autor:
L. Xie, Y. Cui, M. Frontczak-Baniewicz, K. Matsuno, A. Takaki, T. Ritter, H. Nakauchi, J. Wang, X. K. Li, T. Suzuki, K. Chiang, S. C. Napier, G. Pourmand, J. Rutkowska, C. Lu, L. O'Flynn, B. Paul, M. Ranjbar, H. Bakkaloglu, U. Rungpanich, M. Carin, X. He, H. Xu, A. Rydzewski, Y. Sawanobori, A. Sugioka, M. Durlik, C. Wu, M. Maksymowicz, M. Gewartowska, P. Wongprompitak, D. Shi, T. Nakano, U. Eldegez, H. Dolezyczek, Q. Li, M. EbrahimiRad, Y. Shimada, S. Goto, S. Sato, H. Kishimoto, S. Nagao, X. Cao, G. Solgi, A. Sarafnejad, A. Mehrsai, C. Lai, S. Kawamoto, S. Takahashi, M. Li, C. Yeh, Y. Zhang, B. Nikbin, K. Ozdilli, L. Hsu, K. Chen, A. Seraji, A. A. Asadpour, W. L. Olszewski, A. Amirzargar, N. Watanabe, S. Ikehara, K. Ono, J. Wright, X. Zhang, D. Yin, S. Takahara, L. Ma, G. E. Karahan, N. Ohmori, B. Kelly, H. Ohdan, N. Srisamut, H. Ueta, S. Yamazaki, C. Chen, P. Tanthuvanit, R. Abe, F. Savran Oguz, T. Goto, G. Levy, J. Mytilineos, S. Kobayashi, V. Gadi, Y. Tashiro, S. Watanabe, P. Ekpo, M. Mohammadnia, M. Morita, T. Miyagi, Y. Long, K. Mori, A. Turkmen, S. Nakamura, S. K. Geevarghese, B. Ansaripour, M. Taherimahmoudi, A. A. Amirzargar, X. Gao, Y. Jiang, M. Shi, Y. Motoi, Y. K. Caliskan, H. Hasegawa, Q. Shi, Q. Gao, Y. Tanaka, M. Nosov, C. Kekik, M. Swietek, M. Zagozda, G. Chen, J. Chen
Publikováno v:
International Immunology. 22:iv75-iv78
Autor:
'A. Aghamohammadi, A. Farhoudi, H. Hosseini Nik, Sh. Khazali, Z. Pourpak, F. Khosravi, A. Sarrafnezhad, AA. Amir-Zargar, N. Rezaei, K. Abolmaali, D. Mansouri B. Nikbin\\'
Publikováno v:
Acta Medica Iranica, Vol 42, Iss 4, Pp 272-276 (2004)
Acta Medica Iranica, Vol 42, Iss 4 (2004)
Acta Medica Iranica, Vol 42, Iss 4 (2004)
Common variable immunodeficiency (CVID) is a heterogeneous heritable disease characterized by arrest in B cell differentiation. An association between CVID and two HLA haplotypes, haplotype I (HLA-A1, HLA-B8, HLA-DR3) and haplotype II (HLA-A29, HLA-B