Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Igor A. Lisukov"'
Publikováno v:
Сахарный диабет, Vol 17, Iss 2, Pp 20-28 (2014)
Diabetes mellitus (DM) is characterised by relative or absolute insulin deficiency. The currently available treatment methods for DM cannot provide normal blood glucose level without hypo- or hyperglycaemia episodes, thus failing to completely preven
Externí odkaz:
https://doaj.org/article/5fea63dcb79f4622be035a7dd28afd1c
Publikováno v:
Сахарный диабет, Vol 17, Iss 2, Pp 20-28 (2014)
Diabetes mellitus (DM) is characterised by relative or absolute insulin deficiency. The currently available treatment methods for DM cannot provide normal blood glucose level without hypo- or hyperglycaemia episodes, thus failing to completely preven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad1615c2716da7e5abc7185877a0fbe
https://doi.org/10.14341/dm2014220-28
https://doi.org/10.14341/dm2014220-28
Autor:
Alexandra A. Sipol, Elena V. Babenko, Dimitry I. Yakunin, Zhanna Chubukina, Alexander Popov, Natalya V. Pronkina, Vyacheslav I. Borisov, Svetlana A. Lugovskaya, Andrea J. Illingworth, Tatyana V. Glazanova, Elena Boyakova, Igor A. Lisukov, E V Naumova, Alexander D. Kulagin, Leonid Saveliev
Publikováno v:
Hematology. 20:31-38
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal stem cell disorder characterized by partial or absolute deficiency of glycophosphatidyl-inositol (GPI) anchor-linked surface proteins on blood cells. A lack of precise diagnostic standar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e22bfdc86bb1bbfc524493daf103669
https://doi.org/10.1179/1607845414y.0000000162
https://doi.org/10.1179/1607845414y.0000000162
Autor:
Vladimir Y. Melnichenko, Igor A. Lisukov, Andrei A. Novik, Yury L. Shevchenko, Sergei V. Shamanski, Oleg A. Rykavicin, Boris V. Afanasiev, Denis A. Fedorenko, Gary I. Gorodokin, Aleksey N. Kuznetsov, Alexander D. Kulagin, Tatyana Ionova, Roman Ivanov, Vladimir A. Kozlov
Publikováno v:
Experimental Hematology. 36:922-928
High-dose immunosuppressive therapy (HDIT) with autologous hematopoietic stem cell transplantation (auto-HSCT) is a new and promising approach to the treatment of multiple sclerosis (MS) patients because currently there are no effective treatment met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf437364d721b2ed323f9cde00840068
https://doi.org/10.1016/j.exphem.2008.03.001
https://doi.org/10.1016/j.exphem.2008.03.001
Autor:
Masahara Nobuyoshi, Igor A. Lisukov, Hideo Tanaka, Naihui Huang, Maged S. Mahmoud, Michio M. Kawano
Publikováno v:
Blood. 87:4311-4315
Recent phenotypic analysis of plasma cells showed that normal plasma cells do express the B-cell lineage-specific molecule CD19, but their malignant counterpart (myeloma cells) are CD19-. To clarify the meaning of loss of CD19 antigen on myeloma cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfe1770cba8c59aeb832328880c02ae5
https://doi.org/10.1182/blood.v87.10.4311.bloodjournal87104311
https://doi.org/10.1182/blood.v87.10.4311.bloodjournal87104311
Publikováno v:
Blood. 87:3375-3383
By using two-color phenotypic analysis with fluorescein isothiocyanate- anti-CD38 and phycoerythrin-anti-CD19 antibodies, we found that pre-B cells (CD38+CD19+) signifcantly decreased depending on the number of plasma cells (CD38++CD19+) in the bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b589b381ab9ef60dac9bce2ff8fd2ab5
https://doi.org/10.1182/blood.v87.8.3375.bloodjournal8783375
https://doi.org/10.1182/blood.v87.8.3375.bloodjournal8783375
Autor:
Maged S. Mahmoud, Keiichiro Mihara, Naihui Huang, Michio M. Kawano, Takako Tsujimoto, Yuka Harada, Atsushi Kuramoto, Igor A. Lisukov
Publikováno v:
British Journal of Haematology. 92:184-191
In the peripheral blood (PB) we detected so-called early plasma cells that might already be committed to entering the bone marrow (BM). By two-colour staining with FITC-anti-CD38 antibody, their intensity (CD38++) of expression of CD38 antigen was be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf16f7cab9807e6e6eb71a9af737bfce
https://doi.org/10.1046/j.1365-2141.1996.300835.x
https://doi.org/10.1046/j.1365-2141.1996.300835.x
Autor:
Igor A. Lisukov, Ekaterina Ya. Shevela, Alexander D. Kulagin, Elena R. Chernykh, Vera V. Sergeevicheva, Irina Kruchkova, D. S. Sergeevichev, Vladimir A. Kozlov, A. V. Gilevich
Publikováno v:
Case Reports in Medicine
Case Reports in Medicine, Vol 2012 (2012)
Case Reports in Medicine, Vol 2012 (2012)
Pure red cell aplasia (PRCA) is a rare complication in recipients of allogenic stem cell from ABO incompatible donors. It is characterized by reticulocytopenia and by an absence of red cell cell precursors in the bone marrow. Despite close isohemaggl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cf9b79ef19d7dd6d596af0e754176e4
http://europepmc.org/articles/PMC3385157
http://europepmc.org/articles/PMC3385157
Autor:
Inna V. Markova, Igor A. Lisukov, Elena Vinogradova, Tatyana Chagorova, T P Zagoskina, AD Kulagin, Anna Unzhekova, Alexey Maschan, Yuriy Schatochin, Boris V. Afanasyev, Michael Maschan, Elena Kuznetsova, Kudrat Abdulkadyrov, Julia Sedlova, Alexander Rumyantsev, I.L. Davydkin, K D Kaplanov, Galina Salogub, Aryslan Akhmadeev, Shamardina Av, Tatyana Schelekhova, Nina Tsvetaeva, Tatyana Schneider, Lidiya Kovaleva, Elena Volodicheva, Tatyana Sycheva, Olimpiada Kanjukova, Marina Savinova, Maria Ivanova, Svetlana Osynikhina, Elena Karyagina
Publikováno v:
Blood. 126:4642-4642
Study objectives The aim of the study was to evaluate disease characteristics and treatment practices of ITP in Russia. Materials and methods The ITP Registry was a multicenter, prospective, observational cohort study. The observation period for each
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb360906e7e88fc7f4dedad0dd8ef8f6
https://doi.org/10.1182/blood.v126.23.4642.4642
https://doi.org/10.1182/blood.v126.23.4642.4642
Autor:
Elena Vinogradova, Andrey Zaritskiy, Tatyana Schneider, Alexey Maschan, A. D. Kulagin, S.P. Yakupova, Tatiana Krinitsina, T S Kaporskaya, Andrey Gavrilenko, Yulia Bogdanova, Elena Shilova, Bulat Bakirov, Igor A. Lisukov, Svetlana Volkova, Viktoria Ustyantseva, Natalia Kosacheva, Boris V. Afanasyev, Sergey Meresiy, Kudrat Abdulkadyrov, Valentina Ivanova, Alexander Rumyantsev, Tatiana Kazankova, Yuriy V. Shatokhin, Ludmila Anchukova
Publikováno v:
Blood. 124:5163-5163
Background: Paroxysmal nocturnal hemoglobinuria is a rare clonal hematopoietic stem cell disease that can lead to life-threatening complications including thrombotic events (TE), chronic kidney disease (CKD) and pulmonary hypertension. In 2011 the In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::910d59eac2ef9326e0eabf5c94a32a55
https://doi.org/10.1182/blood.v124.21.5163.5163
https://doi.org/10.1182/blood.v124.21.5163.5163