نتایج جستجو برای: familial mds

تعداد نتایج: 63422  

2005
A G Nikitin

Group classification of systems of two coupled nonlinear reaction-diffusion equation with a diagonal diffusion matrix is carried out. Symmetries of diffusion systems with singular diffusion matrix and additional first order derivative terms are described.

Journal: :CoRR 2010
Martianus Frederic Ezerman Somphong Jitman San Ling

Assuming the validity of the MDS Conjecture, the weight distribution of all MDS codes is known. Using a recently-established characterization of asymmetric quantum error-correcting codes, linear MDS codes can be used to construct asymmetric quantum MDS codes with dz ≥ dx ≥ 2 for all possible values of length n for which linear MDS codes over Fq are known to exist.

Journal: :IEEE Transactions on Information Theory 2008

Journal: :Molecular Cytogenetics 2021

Abstract Background Central diabetes insipidus (CDI) is a rare complication of myelodysplastic syndrome (MDS). Although the cytogenetic features patients with MDS and CDI are not clear, in acute myeloid leukemia (AML) associated chromosome 7 and/or 3 anomalies. Case presentation In this report, we describe two concurrent CDI, one them, was first manifestation. One patient had monosomy on metaph...

2015
Ulrike E Maske Markus A Busch Frank Jacobi Katja Beesdo-Baum Ingeburg Seiffert Hans-Ulrich Wittchen Steffi Riedel-Heller Ulfert Hapke

BACKGROUND Prevalence estimates for depression vary considerably by the type of assessment instrument, and there is limited information on their overlap in population-based samples. Our aim was to compare the Patient Health Questionnaire-9 (PHQ-9) with the Composite International Diagnostic Interview (CIDI) as measures for current major depressive syndrome (MDS) in a large population-based samp...

2017
Toshio Asayama Hideto Tamura Mariko Ishibashi Yasuko Kuribayashi-Hamada Asaka Onodera-Kondo Namiko Okuyama Akiko Yamada Masumi Shimizu Keiichi Moriya Hidemi Takahashi Koiti Inokuchi

T-cell immunoglobulin mucin-3 (Tim-3), an inhibitory immune checkpoint receptor, is highly expressed on acute myeloid leukemia cells and its ligand galectin-9 is reported to drive leukemic progression by binding with Tim-3. However, it remains unclear whether the Tim-3-galectin-9 pathway is associated with the pathophysiology of myelodysplastic syndromes (MDS). Thus, we investigated the express...

2013
Bettina Kárai Eszter Szánthó János Kappelmayer Zsuzsa Hevessy

BACKGROUND Confirming diagnosis of myelodysplastic syndromes (MDS) is often challenging. Standard diagnostic methods are cytomorphology (CM) and cytogenetics. Multiparameter flow cytometry (MFC) is upcoming in MDS diagnostic work up, comparability and investigator experiences are critical. Myeloid nuclear differentiation antigen (MNDA) in myelomonocytic cells might be expressed more weakly in p...

Journal: :Blood 2010
Miriam Miesner Claudia Haferlach Ulrike Bacher Tamara Weiss Katja Macijewski Alexander Kohlmann Hans-Ulrich Klein Martin Dugas Wolfgang Kern Susanne Schnittger Torsten Haferlach

The World Health Organization classification of acute myeloid leukemia (AML) is hierarchically structured and integrates genetics, data on patients' history, and multilineage dysplasia (MLD). The category "AML with myelodysplastic syndrome (MDS)-related changes" (AML-MRC) is separated from "AML not otherwise specified" (AML-NOS) by presence of MLD, MDS-related cytogenetics, or history of MDS or...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Wendy W Pang John V Pluvinage Elizabeth A Price Kunju Sridhar Daniel A Arber Peter L Greenberg Stanley L Schrier Christopher Y Park Irving L Weissman

Myelodysplastic syndromes (MDS) are a group of disorders characterized by variable cytopenias and ineffective hematopoiesis. Hematopoietic stem cells (HSCs) and myeloid progenitors in MDS have not been extensively characterized. We transplanted purified human HSCs from MDS samples into immunodeficient mice and show that HSCs are the disease-initiating cells in MDS. We identify a recurrent loss ...

Journal: :iranian journal of public health 0
shirin ferdowsi 1. dept. of hematology, iranian blood transfusion organization , tehran, iran. reza shirkoohi 2. dept. of molecular genetics, cancer research center, cancer institute, imam khomeini hospital complex, tehran university of medical sciences , tehran, iran. gholamreza toogeh 3. dept. of hematology-oncology and bmt research center, imam khomeini hospital complex, tehran university of medical sciences , tehran, iran.

the myelodysplastic syndrome (mds) is a highly heterogenous disorder and karyotype analysis is helpful for diagnostic and prognostic estimation. deletion in long arm chromosome 6 (6q del) as a sole abnormality is a rare event in mds. this is the first case report of del (6q) as the only observed diagnostic change in iran. we also reviewed the literature of this cytogenetic lesion.

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