User profiles for "author:Katsuyoshi Takata"
Katsuyoshi Takata新潟大学医学部分子病理学 Verified email at bccrc.ca Cited by 5925 |
IgG4‐related disease: historical overview and pathology of hematological disorders
Y Sato, K Notohara, M Kojima, K Takata… - Pathology …, 2010 - Wiley Online Library
IgG4‐related diseases comprise a recently recognized systemic syndrome characterized by
mass‐forming lesions in mainly exocrine tissue that consist of lymphoplasmacytic infiltrates …
mass‐forming lesions in mainly exocrine tissue that consist of lymphoplasmacytic infiltrates …
Pathology of follicular lymphoma
K Takata, T Miyata-Takata, Y Sato… - Journal of Clinical and …, 2014 - jstage.jst.go.jp
Follicular lymphoma (FL) is a heterogeneous disease, and there are many different
subgroups, such as in terms of age of onset, involved organ (especially extranodal sites …
subgroups, such as in terms of age of onset, involved organ (especially extranodal sites …
Ocular adnexal IgG4‐related disease has uniform clinicopathology
Y Sato, K Ohshima, K Ichimura, M Sato… - Pathology …, 2008 - Wiley Online Library
IgG4‐related disease is a recently proposed clinical entity with several unique
clinicopathological features. Ocular adnexal IgG4‐related disease, however, has not well …
clinicopathological features. Ocular adnexal IgG4‐related disease, however, has not well …
[HTML][HTML] Double-hit gene expression signature defines a distinct subgroup of germinal center B-cell-like diffuse large B-cell lymphoma
D Ennishi, A Jiang, M Boyle, B Collinge… - Journal of Clinical …, 2019 - ncbi.nlm.nih.gov
Purpose High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements
(HGBL-DH/TH) has a poor outcome after standard chemoimmunotherapy. We sought to …
(HGBL-DH/TH) has a poor outcome after standard chemoimmunotherapy. We sought to …
[HTML][HTML] Systemic IgG4-related lymphadenopathy: a clinical and pathologic comparison to multicentric Castleman's disease
Y Sato, M Kojima, K Takata, T Morito, H Asaoku… - Modern Pathology, 2009 - Elsevier
IgG4-related disease sometimes involves regional and/or systemic lymph nodes, and often
clinically and/or histologically mimics multicentric Castleman's disease or malignant …
clinically and/or histologically mimics multicentric Castleman's disease or malignant …
Molecular and genetic characterization of MHC deficiency identifies EZH2 as therapeutic target for enhancing immune recognition
D Ennishi, K Takata, W Béguelin, G Duns, A Mottok… - Cancer discovery, 2019 - AACR
We performed a genomic, transcriptomic, and immunophenotypic study of 347 patients with
diffuse large B-cell lymphoma (DLBCL) to uncover the molecular basis underlying acquired …
diffuse large B-cell lymphoma (DLBCL) to uncover the molecular basis underlying acquired …
Primary gastrointestinal follicular lymphoma involving the duodenal second portion is a distinct entity: a multicenter, retrospective analysis in Japan
K Takata, H Okada, N Ohmiya, S Nakamura… - Cancer …, 2011 - Wiley Online Library
We conducted a multicenter, retrospective study to determine the anatomical distribution and
prognostic factors of gastrointestinal (GI) follicular lymphoma (FL). This study included 125 …
prognostic factors of gastrointestinal (GI) follicular lymphoma (FL). This study included 125 …
Single-cell transcriptome analysis reveals disease-defining T-cell subsets in the tumor microenvironment of classic Hodgkin lymphoma
T Aoki, LC Chong, K Takata, K Milne, M Hav… - Cancer discovery, 2020 - AACR
Hodgkin lymphoma is characterized by an extensively dominant tumor microenvironment
(TME) composed of different types of noncancerous immune cells with rare malignant cells …
(TME) composed of different types of noncancerous immune cells with rare malignant cells …
Combinatorial treatment rescues tumour-microenvironment-mediated attenuation of MALT1 inhibitors in B-cell lymphomas
Activated B-cell-like diffuse large B-cell lymphomas (ABC-DLBCLs) are characterized by
constitutive activation of nuclear factor κB driven by the B-cell receptor (BCR) and Toll-like …
constitutive activation of nuclear factor κB driven by the B-cell receptor (BCR) and Toll-like …
[HTML][HTML] Interleukin-1 loop model for pathogenesis of Langerhans cell histiocytosis
I Murakami, M Matsushita, T Iwasaki… - Cell Communication and …, 2015 - Springer
We propose Langerhans cell histiocytosis (LCH) is an inflammatory process that is
prolonged by mutations. We hypothesize that Merkel cell polyomavirus (MCPyV) infection …
prolonged by mutations. We hypothesize that Merkel cell polyomavirus (MCPyV) infection …