BORRBangladesh Open Research Repository
SearchSubmitAboutContact
BORRResearch for a Better Bangladesh.
AboutSubmit PaperContactTermsPolicyGitHub

© 2026 Bangladesh Open Research Repository.

Filters

Sort By

Sort by dateSort by citations
Year Range
to
Clear all filters

All Papers

16+ results
Field: Myeloproliferative Neoplasms: Diagnosis and Treatment

Aberrant activation of the PI3K/mTOR pathway promotes resistance to sorafenib in AML

Verified

Oscar Lindblad, Eugenia Cordero, Alexandre Puissant, L Macaulay et al.

Journal: Oncogene
Year: 2016
Citations: 130

Therapy directed against oncogenic FLT3 has been shown to induce response in patients with acute myeloid leukemia (AML), but these responses are almost always transient. To address the mechanism of FLT3 inhibitor resistance, we generated two resistant AML cell lines by sustained treatment with the F...

Health SciencesMedicineHematologyOpen Access
Read Source

Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry

Verified

Melanie J. Percy, Mary Frances McMullin, Simon N. Jowitt, Michael F. Potter et al.

Journal: BloodYear: 2003Citations: 90

The Chuvash form of polycythemia is an autosomal recessive disorder common to a large number of families in central Russia. Affected individuals have been reported to be homozygous for an Arg200Trp mutation in the von Hippel-Lindau (VHL) gene. We have screened 78 patients with erythrocytosis and fou...

Life SciencesBiochemistry, Genetics and Molecular BiologyCancer ResearchOpen Access
Read Source

A comparison of two nomenclature systems for primary systemic vasculitis

Verified

Ian N Bruce, A. L. Bell

Journal: Lara D. VeekenYear: 1997Citations: 56

Recently, two new systems have been proposed for the nomenclature of primary vasculitides: the 1990 American College of Rheumatology (ACR) classification criteria and the 1992 Chapel Hill Consensus Conference (CHCC) definitions. We compared these two systems in the same cohort of patients with prima...

Health SciencesMedicinePulmonary and Respiratory MedicineOpen Access
Read Source

Hydroxyurea and blood transfusion therapy for Sickle cell disease in South Asia: inconsistent treatment of a neglected disease

Verified

Thamal Darshana, David C. Rees, Anuja Premawardhena

Journal: Orphanet Journal of Rare DiseasesYear: 2021Citations: 17

BACKGROUND: Hydroxyurea and blood transfusion therapies remain the main therapeutic strategies for Sickle cell disease. Preliminary data suggest substantial variation and inconsistencies in practice of these two therapeutic modalities in South Asia. In this systematic review we searched Medline, Coc...

Health SciencesMedicineGeneticsOpen Access
Read Source

Polycythaemia-inducing mutations in the erythropoietin receptor (EPOR): mechanism and function as elucidated by epidermal growth factor receptor-EPOR chimeras

Verified

Mor Gross, Nathalie Ben‐Califa, Mary Frances McMullin, Melanie J. Percy et al.

Journal: British Journal of HaematologyYear: 2014Citations: 15

Primary familial and congenital polycythaemia (PFCP) is a disease characterized by increased red blood cell mass, and can be associated with mutations in the intracellular region of the erythropoietin (EPO) receptor (EPOR). Here we explore the mechanisms by which EPOR mutations induce PFCP, using an...

Health SciencesMedicineHematologyOpen Access
Read Source

A prognostication system based on clinical parameters and [18F]-FDG PET/CT in patients with newly diagnosed multiple myeloma

Verified

Junlong Li, Xiao Zhang, Chunxia Qin, Xun Sun et al.

Journal: European Journal of Nuclear Medicine and Molecular ImagingYear: 2022Citations: 14

Purpose This study aimed to assess prognosis of patients with newly diagnosed multiple myeloma (NDMM) by combining [ 18 F]-FDG positron emission tomography (PET)/CT parameters and clinical indices. Methods Clinical data and PET/CT parameters of 133 NDMM patients were retrospectively analyzed for ass...

Health SciencesMedicineHematology
Read Source

Clinical profile and demographic characteristics of moderate and severe hemophilia patients in a tertiary care hospital of Bangladesh

Verified

Mohammed Nadimul Islam, Akhil Ranjon Biswas, Humayra Nazneen, Nobendu Chowdhury et al.

Journal: Orphanet Journal of Rare DiseasesYear: 2022Citations: 12

BACKGROUND: Hemophilia is one of the commonest inherited bleeding disorders which may lead to chronic bleeding tendencies and life-long disabilities if not properly managed. Knowing the pattern of the disease aids in the prevention of disability and improvement of quality of life in hemophilia. Howe...

Health SciencesMedicineHematologyOpen Access
Read Source

Clinico-Pathological Study on Haemophilia: An Analysis of 50 Cases

Verified

M A Uddin, MJ Rahman, MM Rahman, SA Sultana et al.

Journal: Journal of Bangladesh College of Physicians and SurgeonsYear: 1970Citations: 12

A prospective study was carried out on the patients presenting with history of recurrent joint swelling and wound bleeding in outpatient department of Haematology, Bangabandhu Sheikh Mujib Medical University (BSMMU) and Armed Forces Institute of Pathology (AFIP), Dhaka Cantonment from January 2000 t...

Health SciencesMedicineHematologyOpen Access
Read Source

Phase distribution of chronic myeloid leukemia in Bangladesh

Verified

Md. Abdul Mottalib, Tanvira Afroze Sultana, Md. Ibrahim Khalil, Siew Hua Gan et al.

Journal: BMC Research NotesYear: 2014Citations: 11

BACKGROUND: Here, we report the phase distribution of chronic myeloid leukemia (CML), defined based on the World Health Organization criteria, among 63 patients in Bangladesh. All patients were diagnosed based on complete blood count, bone marrow examination including bone marrow aspiration and reve...

Health SciencesMedicineHematologyOpen Access
Read Source

Prognostic Impact of <b><i>NPM1</i></b> Mutations in Serbian Adult Patients with Acute Myeloid Leukemia

Verified

Miloš Kuzmanović, Nataša Tos̆ić, Nataša Čolović, Teodora Karan-Djurašević et al.

Journal: Acta HaematologicaYear: 2012Citations: 11

Based on current findings, the presence of NPM1 mutations in acute myeloid leukemia (AML) patients is associated with an increased probability of complete remission (CR) and better overall survival (OS). We determined the incidence and prognostic relevance of NPM1 mutations, their association with F...

Health SciencesMedicineHematology
Read Source

Vascular defects in gain‐of‐function fps/festransgenic mice correlate with PDGF‐ and VEGF‐induced activation of mutant Fps/Fes kinase in endothelial cells

Verified

Waheed Sangrar, Jeffrey Mewburn, Sandra G. Vincent, John T. Fisher et al.

Journal: Journal of Thrombosis and HaemostasisYear: 2004Citations: 11

Background Fps/Fes is a cytoplasmic tyrosine kinase that is abundantly expressed in the myeloid, endothelial, epithelial, neuronal and platelet lineages. Genetic manipulation in mice has uncovered potential roles for this kinase in hematopoiesis, innate immunity, inflammation and angiogenesis. Objec...

Life SciencesBiochemistry, Genetics and Molecular BiologyMolecular BiologyOpen Access
Read Source

Identification of Potential Key Genes and Regulatory Markers in Essential Thrombocythemia Through Integrated Bioinformatics Analysis and Clinical Validation

Verified

Jie Wang, Yun Wu, Md. Nazim Uddin, Rong Chen et al.

Journal: Pharmacogenomics and Personalized MedicineYear: 2021Citations: 10

Introduction: Essential thrombocytosis (ET) is a group of myeloproliferative neoplasms characterized by abnormal proliferation of platelet and megakaryocytes. Research on potential key genes and novel regulatory markers in essential thrombocythemia (ET) is still limited. Methods: Downloading array p...

Health SciencesMedicineGeneticsOpen Access
Read Source

Primary Familial and Congenital Polycythemia

Verified

Celeste Bento, Mary Frances McMullin, Melanie J. Percy, Holger Cario

Year: 2016Citations: 10

Clinical characteristics Primary familial and congenital polycythemia (PFCP) is characterized by isolated erythrocytosis in an individual with a normal-sized spleen and absence of disorders causing secondary erythrocytosis. Clinical manifestations relate to the erythrocytosis and can include plethor...

Health SciencesMedicineGenetics
Read Source

High efficacy of Azacitidine plus HAG in acute myeloid leukemia: an open-label, single-arm, multi-center, phase 2 study

Verified

Jun Li, Qi Han, Yanqing Huang, Yanhui Wei et al.

Journal: Blood Cancer JournalYear: 2022Citations: 9

Acute myeloid leukemia (AML) is a heterogeneous hematologic malignancy with high mortality and poor outcome, especially for elderly/un fi t (age ≥ 60 years or un fi t patients who are ineligible to receive intensive chemotherapy) with adverse genetic and molecular abnormalities in the newly diagnosed ...

Health SciencesMedicineHematologyOpen Access
Read Source

Hydroxyurea treatment is associated with reduced degree of oxidative perturbation in children and adolescents with sickle cell anemia

Verified

Caian L. Vinhaes, Rozana Teixeira, Jay A. S. Monteiro-Júnior, Rafael Tibúrcio et al.

Journal: Scientific ReportsYear: 2020Citations: 9

Sickle cell anemia (SCA) is the most common inherited hemolytic anemia worldwide. Here, we performed an exploratory study to investigate the systemic oxidative stress in children and adolescents with SCA. Additionally, we evaluated the potential impact of hydroxyurea therapy on the status of oxidati...

Health SciencesMedicineGeneticsOpen Access
Read Source
PreviousPage 1 of 2+Next