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Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 4662 - 4662
Abstract Essential Thrombocythemia (ET) is an extremely rare disorder during childhood, characterized by clonal expansion of megakaryocytic and thrombocytic... 
Journal Article
Turkish Journal of Hematology, ISSN 1300-7777, 2017, Volume 34, Issue 4, pp. 360 - 361
Calreticulin (CALR) mutations were first identified exclusively in JAK2-MPL-negative essential thrombocythemia (ET) and primary myelofibrosis (PMF) at a rate... 
Essential thrombocythemia | Calreticulin | Primary myelofibrosis | MYELOPROLIFERATIVE NEOPLASMS | HEMATOLOGY | T?p | Bone marrow | Mutation | Anemia | Patients | Tumors | Letter to the Editor
Journal Article
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 5054 - 5054
Abstract Introduction: Factor XI (FXI) is a homodimeric serine protease enzyme, which is produced in the liver and circulates in the plasma complexed with high... 
Journal Article
Archives of Medical Research, ISSN 0188-4409, 04/2019, Volume 50, Issue 3, pp. 91 - 97
Diabetic nephropathy (DN) is one of the most serious microvascular complications in diabetic patients. The kruppel-like transcription factor-4 (KLF-4) affects... 
Type 2 diabetes | DNA methylation | Epigenetics | Diabetic nephropathy | Kruppel-like transcription factor-4 | KIDNEY-DISEASE | MEDICINE, RESEARCH & EXPERIMENTAL | PROMOTER | Epigenetic inheritance | Diabetics | Analysis | Genes | DNA | Diabetic nephropathies | Genetic research | Genetic aspects | Methylation | Gene expression
Journal Article
Turkish Journal of Hematology, ISSN 1300-7777, 2018, Volume 35, Issue 1, pp. 79 - 80
Factor XI (FXI) is a homodimeric serine protease, which is produced in the liver and circulates in the plasma complexed with high-molecular-weight kininogen.... 
Factor XI | Family | Mutation | ACTIVATION | HEMATOLOGY | T?p | Families & family life | Enzymes | Letters to the Editor
Journal Article
Thalassemia Reports, ISSN 2039-4357, 06/2018, Volume 8, Issue 2
The mutation detection of β thalassemia is absolutely necessary for molecular diagnosis, as well as any genetic epidemiological study. The β globin gene has 3... 
thalassemia major | Turkey | β globin mutations | Northern Iraq | Albania
Journal Article
Blood, ISSN 0006-4971, 11/2010, Volume 116, Issue 21, pp. 3171 - 3171
Abstract Abstract 3171 Introduction: The pathogenesis of thrombus formation in antiphospholipid syndrome (APS) is not clear. Therefore, it is difficult to... 
Journal Article
Postępy Higieny i Medycyny Doświadczalnej, ISSN 0032-5449, 10/2019, Volume 73, pp. 529 - 535
No-reflow phenomenon is an important complication of primary percutaneous coronary intervention. Several variants in the endothelial nitric oxide synthase... 
Journal Article
Turkish Journal of Hematology, ISSN 1300-7777, 2011, Volume 28, Issue 3, pp. 213 - 218
Journal Article
Blood, ISSN 0006-4971, 11/2006, Volume 108, Issue 11, pp. 3885 - 3885
Abstract The cytotoxic T lymphocyte associated antigen-4 (CTLA-4) is expressed on T lymphocytes, and inhibits the T cell responses. CTLA-4 A49G polymorphism... 
Journal Article
Turkish journal of haematology : official journal of Turkish Society of Haematology, ISSN 1300-7777, 02/2019, Volume 36, Issue 1, pp. 29 - 36
Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose arid elastic skin, growth and developmental... 
ATP6V0A2 | Bleeding diathesis | Cutis laxa | Wound healing | Whole exome sequencing | MULTIMERIZATION | GLYCOSYLATION | HEMATOLOGY | Congenital diseases | Intellectual disabilities | Families & family life | Genomes | Mutation | Microcephaly | Bioinformatics | Siblings
Journal Article
Turkish Journal of Haematology, ISSN 1300-7777, 03/2013, Volume 30, Issue 1, p. 8
Journal Article
Journal of Cytology, ISSN 0970-9371, 10/2018, Volume 35, Issue 4, pp. 252 - 254
Journal Article
Turkish Journal of Haematology, ISSN 1300-7777, 09/2011, Volume 28, Issue 3, p. 213
Journal Article
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