نتایج جستجو برای: myeloproliferative disorder

تعداد نتایج: 601334  

Journal: :Human molecular genetics 1998
D Smedley R Hamoudi J Clark W Warren M Abdul-Rauf G Somers D Venter K Fagan C Cooper J Shipley

A recently described atypical myeloproliferative disorder is invariably associated with reciprocal translocations involving 8p11-12. The most common rearrangement is a t(8;13)(p11;q11-12). Here we determine that this translocation results in the fusion of the fibroblast growth factor receptor 1 gene (FGFR1), a member of the receptor tyrosine kinase family at 8p11, to a novel gene at 13q11-12 de...

Journal: :International journal of medical science and clinical research studies 2022

Mastocytosis is one of eight subcategories neoplasms. Classification Myeloproliferative Tumors Lymphoid Tissues and hematopoietics 2008 the World Health Organization; a heterogeneous group myeloproliferative diseases that distinguished by excessive proliferation mast cells morphologically immunophenotypically atypical, in addition to accumulation these or more organs tissues, including skin, bo...

Journal: :Ecography 2016
F Mazel T J Davies L Gallien J Renaud M Groussin T Münkemüller W Thuiller

During the last decades, describing, analysing and understanding the phylogenetic structure of species assemblages has been a central theme in both community ecology and macro-ecology. Among the wide variety of phylogenetic structure metrics, three have been predominant in the literature: Faith's phylogenetic diversity (PDFaith), which represents the sum of the branch lengths of the phylogeneti...

2008
Athanasios Tragiannidis Zoe Dorothea Pana Theodotis Papageorgiou Emmanuel Hatzipantelis Maria Hatzistilianou Fani Athanassiadou

This is the report of a newborn with Down syndrome diagnosed with transient myeloproliferative disorder (TMD) that required chemotherapy on the first day of life. Children with Down syndrome have a 10- to 20-fold increased risk of developing TMD. TMD is characterized by an uncontrolled proliferation of myeloblasts in the infant's peripheral blood and bone marrow. In most instances, this unique ...

Journal: :Haematologica 2011
Damla Olcaydu Elisa Rumi Ashot Harutyunyan Francesco Passamonti Daniela Pietra Cristiana Pascutto Tiina Berg Roland Jäger Emma Hammond Mario Cazzola Robert Kralovics

BACKGROUND Myeloproliferative neoplasms constitute a group of diverse chronic myeloid malignancies that share pathogenic features such as acquired mutations in the JAK2, TET2, CBL and MPL genes. There are recent reports that a JAK2 gene haplotype (GGCC or 46/1) confers susceptibility to JAK2 mutation-positive myeloproliferative neoplasms. The aim of this study was to examine the role of the JAK...

Journal: :international journal of hematology-oncology and stem cell research 0
mehrdad payandeh medical biology research center, kermanshah university of medical sciences, kermanshah, iran. farhad shaveisi zadeh department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences and health services, tehran mohammad erfan zare medical biology research center, kermanshah university of medical sciences, kermanshah, iran; studen kamran mansouri medical biology research center, kermanshah university of medical sciences, kermanshah, iran; depart reza khodarahmi medical biology research center, kermanshah university of medical sciences, kermanshah, iran; depart saeed alimoradi paramedical faculty, kermanshah university of medical sciences, kermanshah, iran

introduction: the myeloproliferative neoplasms (mpns) are a heterogeneous group of diseases characterized by excessive production of blood cells by  hematopoietic precursors. typically, they include polycythemia vera (pv), essential thrombocythemia (et), idiopathic myelofibrosis(imf), and chronic myeloid leukemia (cml). philadelphia chromosome is the final diagnostic test for cml. recently, jak...

A Ghasemi, A Ghotaslou, B Chahardouli, F Nadali, S Abbasian, S Rostami,

Background Myeloproliferative disorders are a group of diseases characterized by increased proliferation of myeloid lineage. In addition to JAK2V617F mutation, several mutations in the c-MPL gene were described in patients with Philadelphia-negative chronic myeloproliferative disorders that could be important in the pathogenesis of diseases. The aim of present study was to investigate the fre...

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