Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Norioki Ohno"'
Publikováno v:
Clinical and Experimental Immunology. 190:268-279
Summary Regulatory T cells (Tregs) control immune responses by suppressing various inflammatory cells. Tregs in newborn babies may play an important role in preventing excessive immune responses during their environmental change. We examined the numb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8936f8f0bc19b8df5b62f56b6dbe0d1d
https://doi.org/10.1111/cei.13008
https://doi.org/10.1111/cei.13008
Autor:
Yasuhiko Sera, Syuhei Karakawa, Teruyuki Kajiume, Masao Kobayashi, Nobutsune Ishikawa, Norioki Ohno
Publikováno v:
Stem Cell Discovery. :25-30
The Polycomb group protein Bmi1 is a constituent of the Polycomb repressive complex 1, and it is an important molecule for the regulation of the self-renewal of hematopoietic stem cells. In the field of clinical hematology, there are reports that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bff9dd99bc03e939424d70f39192ec1e
https://doi.org/10.4236/scd.2012.22004
https://doi.org/10.4236/scd.2012.22004
Autor:
Yoshihiro Takihara, Tomoki Kawai, Norioki Ohno, Ryuta Nishikomori, Satoshi Okada, Masao Kobayashi, Motoaki Ohtsubo, Miyuki Tsumura, Yoko Mizoguchi, Shin'ichiro Yasunaga, Takemasa Sakaguchi, Shuhei Karakawa
Publikováno v:
Journal of Clinical Immunology. 31:762-772
X-linked ectodermal dysplasia with immunodeficiency (XL-ED-ID) is caused by hypomorphic mutations in NEMO, which encodes nuclear factor-kappaB (NF-κB) essential modulator. We identified a novel mutation, 769-1 G>C, at the splicing acceptor site of e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9e8801f405ca222964688268f67f3ee
https://doi.org/10.1007/s10875-011-9560-4
https://doi.org/10.1007/s10875-011-9560-4
Autor:
Teruyuki Kajiume, Keiichi Hara, Norioki Ohno, Tomoaki Yoshida, Masao Kobayashi, Hiroshi Kawaguchi
Publikováno v:
Pediatric Hematology and Oncology. 26:375-380
Kasabach-Merritt syndrome is a life-threatening congenital disorder characterized by an enlarging hemangioma, thrombocytopenia, and consumption coagulopathy. We report the case of a one-month male infant who presented with a large cutaneous tumor in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::718418ba8ae38407d0295fcb5a8df901
https://doi.org/10.1080/08880010902976643
https://doi.org/10.1080/08880010902976643
Publikováno v:
Stem cells and development. 18(8)
Human umbilical cord blood (CB) has been used successfully in stem cell transplantation. A subpopulation of CD34(+) cells expresses chemokine receptor CXCR4 which is critical for bone marrow engraftment in human hematopoietic stem cells. Here, we dem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cf9488b9a3c564ba12da40575b23059
https://pubmed.ncbi.nlm.nih.gov/19113880
https://pubmed.ncbi.nlm.nih.gov/19113880
Publikováno v:
Experimental hematology. 37(7)
Objective The Polycomb -group ( PcG ) genes regulate global gene expression in many biological processes, including hematopoiesis, by manipulating specific target genes. It is known that various PcG genes regulate self-renewal of hematopoietic stem c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b9188d916bc36441d6106b7a6644165
https://pubmed.ncbi.nlm.nih.gov/19409954
https://pubmed.ncbi.nlm.nih.gov/19409954
Publikováno v:
Platelets. 23:399-400
EDTA-dependent pseudothrombocytopenia (PTCP) is characterised by a low platelet count caused by autoantibodies in the serum reacting with EDTA-anticoagulated blood. EDTA-dependent PTCP is caused by a factor that retains EDTA anticoagulation activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33008804b90fe0d757afcab1ab00da68
https://doi.org/10.3109/09537104.2011.624210
https://doi.org/10.3109/09537104.2011.624210
Publikováno v:
Blood. 120:4724-4724
Abstract 4724 Erythropoietin (EPO), which is used to treat anemic immature neonates, is thought to be effective for treating neonatal hypoxic encephalopathy by stimulating nervous system cells or vascular stem cells. On stem cells, CXCR4 is an import
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab39e46839003fccc6edfe7c6403064d
https://doi.org/10.1182/blood.v120.21.4724.4724
https://doi.org/10.1182/blood.v120.21.4724.4724
Autor:
Ryuta Nishikomori, Tomoki Kawai, Motoaki Ohtsubo, Norioki Ohno, Masao Kobayashi, Shin'ichiro Yasunaga, Shuhei Karakawa, Yoshihiro Takihara, Miyuki Tsumura, Satoshi Okada, Yoko Mizoguchi
Publikováno v:
Blood. 116:1732-1732
Abstract 1732 X-linked ectodermal dysplasia with immunodeficiency (XL-EDA-ID) is caused by hypomorphic mutations in the nuclear factor κB (NF-κB) essential modulator (NEMO) gene, also called IKBKG, and these mutations impair but do not abolish NF-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::504bbd67352493c39395607061f33ff5
https://doi.org/10.1182/blood.v116.21.1732.1732
https://doi.org/10.1182/blood.v116.21.1732.1732
Publikováno v:
Blood. 112:1721-1721
Human umbilical cord blood (CB) is rich source of hematopoietic stem cells (HSCs) and provides an attractive alternative to bone marrow or mobilized peripheral blood transplantation. However, major disadvantage of CB transplantation is the relatively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b28aded0e0d6764808262910600953be
https://doi.org/10.1182/blood.v112.11.1721.1721
https://doi.org/10.1182/blood.v112.11.1721.1721