Large granular lymphocyte leukemia

L Sokol, TP Loughran Jr - The oncologist, 2006 - academic.oup.com
Learning Objectives After completing this course, the reader will be able to: Discuss the
basic principles of molecular and cellular biology of LGL leukemia. Describe distinct clinical …

Thrombocytopenia in cancer patients

HA Liebman - Thrombosis research, 2014 - Elsevier
Thrombocytopenia is a frequent complication of cancer and its treatment. The causes of
thrombocytopenia in cancer patients can be diverse and multifactorial. Systemic …

Network model of survival signaling in large granular lymphocyte leukemia

R Zhang, MV Shah, J Yang… - Proceedings of the …, 2008 - National Acad Sciences
T cell large granular lymphocyte (T-LGL) leukemia features a clonal expansion of antigen-
primed, competent, cytotoxic T lymphocytes (CTL). To systematically understand signaling …

CD4+CD25high Foxp3+ regulatory T cells in myelodysplastic syndrome (MDS)

SY Kordasti, W Ingram, J Hayden… - Blood, The Journal …, 2007 - ashpublications.org
Foxp3+ regulatory T cells (Tregs) play a central role in maintaining immune tolerance. A
reduction in the function of Tregs is a key feature of autoimmune diseases, whereas their …

Functional characterization of CD4+ T cells in aplastic anemia

S Kordasti, J Marsh, S Al-Khan, J Jiang… - Blood, The Journal …, 2012 - ashpublications.org
The role of CD4+ T cells in the pathogenesis of aplastic anemia (AA) is not well
characterized. We investigate CD4+ T-cell subsets in AA. Sixty-three patients with acquired …

IL‐17‐producing CD4+ T cells, pro‐inflammatory cytokines and apoptosis are increased in low risk myelodysplastic syndrome

SY Kordasti, B Afzali, Z Lim, W Ingram… - British journal of …, 2009 - Wiley Online Library
Immunological responses are increasingly recognised as being important in the initiation
and progression of myelodysplastic syndrome (MDS). Indeed, autoimmune diseases …

[HTML][HTML] Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7

VB Pastor, SS Sahoo, J Boklan, GC Schwabe… - …, 2017 - pmc.ncbi.nlm.nih.gov
Familial myelodysplastic syndromes arise from haploinsufficiency of genes involved in
hematopoiesis and are primarily associated with early-onset disease. Here we describe a …

Refractory anemia with ringed sideroblasts associated with marked thrombocytosis (RARS-T), another myeloproliferative condition characterized by JAK2 V617F …

H Szpurka, R Tiu, G Murugesan, S Aboudola, ED Hsi… - Blood, 2006 - ashpublications.org
Abstract JAK2 V617F mutation recently was identified as a pathogenic factor in typical
chronic myeloproliferative diseases (CMPD). Some forms of myelodysplastic syndromes …

Evolving insights in the pathogenesis and therapy of cutaneous T‐cell lymphoma (mycosis fungoides and Sezary syndrome)

HK Wong, A Mishra, T Hake… - British journal of …, 2011 - Wiley Online Library
Cutaneous T‐cell lymphomas (CTCL) are a heterogeneous group of malignancies derived
from skin‐homing T cells. The most common forms of CTCL are Mycosis Fungoides (MF) …

[HTML][HTML] The analysis of clonal diversity and therapy responses using STAT3 mutations as a molecular marker in large granular lymphocytic leukemia

HLM Rajala, T Olson, MJ Clemente, S Lagström… - …, 2015 - ncbi.nlm.nih.gov
T-cell large granular lymphocytic leukemia and chronic lymphoproliferative disorder of
natural killer cells are intriguing entities between benign and malignant lymphoproliferation …