الرئيسية › دليل الباحثين › Salem Abbès
Salem Abbès
الانتماء : Tunis University · Institut Pasteur de Tunis · Tunis El Manar University
- 59منشورات (انتماء تونسي)
- 83مجموع المنشورات
- 1839الاستشهادات
- 22مؤشر h
الملف البحثي
لدى Salem Abbès 59 منشور(ات) مفهرسة (1995–2026). تُنشر أعماله أساسًا في «Cellular Physiology and Biochemistry»، «Hemoglobin» و«Hematology». أكثر مقالاته استشهادًا هو «Haplotype Diversity and Linkage Disequilibrium at Human G6PD : Recent Origin of Alleles That Confer Malarial Resistance» (2001)، وقد استُشهد به 630 مرة. 2 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا، ألمانيا، السعودية.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Hemoglobinopathies and Related Disorders
- Blood groups and transfusion
- Erythrocyte Function and Pathophysiology
- Iron Metabolism and Disorders
- Neonatal Health and Biochemistry
المنشورات (59)
- Mutation Spectrum of Hemoglobinopathies in Tunisia
- Cord Blood-Based Neonatal Screening for Hemoglobinopathies in Northern Tunisia
- Implication of rs1026611 in the MCP-1 Gene and V64I of CCR2 in Stroke among SCA Tunisian Patients: A Brief Study
- P1549: NOVEL SLC4A1 GENE MUTATIONS IN HEREDITARY SPHEROCYTOSIS BAND 3 PROTEIN-DEFICIENT TUNISIAN PATIENTS
- Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency
- Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians
- Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions
- EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients
- Retentissement psychosocial et scolaire de la bêta-thalassémie majeure en Tunisie
- Hb Moscva [β24(B6)Gly→Asp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient
- hOCT1 gene expression predict for optimal response to Imatinib in Tunisian patients with chronic myeloid leukemia
- Molecular study of ABCB1 gene and its correlation with imatinib response in chronic myeloid leukemia
- Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene
- Les modèles explicatifs de causalité de la beta-thalassémie majeure
- P53 activation inhibits all types of hematopoietic progenitors and all stages of megakaryopoiesis
- Triggering of Suicidal Erythrocyte Death by Regorafenib
- TET2-mediated 5-hydroxymethylcytosine induces genetic instability and mutagenesis
- Association of genetic variation inIKZF1, ARID5B, CDKN2A, andCEBPEwith the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence
- Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance
- rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients
- Regulatory network analysis of microRNAs and genes in imatinib-resistant chronic myeloid leukemia
- Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
- Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients
- Embelin-Induced Phosphatidylserine Translocation in the Erythrocyte Cell Membrane
- Enhanced Eryptosis Following Exposure to Carnosic Acid
- Triggering of Suicidal Erythrocyte Death by Topotecan
- Saquinavir Induced Suicidal Death of Human Erythrocytes
- Enhanced Eryptosis Following Exposure to Lopinavir
- Stimulation of Eryptosis by Narasin
- Zopolrestat Induced Suicidal Death of Human Erythrocytes
- Efavirenz Induced Suicidal Death of Human Erythrocytes
- Triggering of Suicidal Erythrocyte Death by the Antibiotic Ionophore Nigericin
- Ritonavir‐Induced Suicidal Death of Human Erythrocytes
- Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene
- rs11886868 and rs4671393 ofBCL11Aassociated with HbF level variation and modulate clinical events among sickle cell anemia patients
- Polymorphisms in XPC, XPD and XPG DNA repair genes and leukemia risk in a Tunisian population
- Rare hemoglobin variants in T unisian population
- Haplotype Map of Sickle Cell Anemia in Tunisia
- The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer
- Early Complication in Sickle Cell Anemia Children due toA(TA)nTAAPolymorphism at the Promoter ofUGT1A1Gene
- Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among Sickle Cell Aneamia patients
- Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia
- Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population
- Two new class III G6PD variants [G6PD Tunis (c.920A > C: p.307Gln > Pro) and G6PD Nefza (c.968T > C: p.323 Leu > Pro)] and overview of the spectrum of mutations in Tunisia
- Three new mutations account for the prevalence of glucose 6 phosphate deshydrogenase (G6PD) deficiency in Tunisia
- Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian βSChromosomes
- Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia
- KIT mutation detection in Tunisian patients with newly diagnosed myelogenous leukemia: prevalence and prognostic significance
- Enseigner l’évolution du vivant dans un contexte concordiste
- Red cells exchanges in sickle cells disease lead to a selective reduction of erythrocytes‐derived blood microparticles
- Influence of genetic polymorphisms of xenobiotic metabolizing enzymes on the risk of developing leukemia in a Tunisian population
- Molecular characterization of a discrete hemoglobinopathy upon investigation for a lung hydatic cyst in an old Tunisian patient
- Erythrocytapheresis in Sickle Cell Disease Lead to An Elective Reduction of Erythrocytes-Derived Blood Microparticles
- Overcoming the Effect of the Socio-cultural Context: Impact of Teaching Evolution in Tunisia
- Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia
- Contribution to the Description of the β‐Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity
- MOLECULAR SPECTRUM OFα-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH
- Haplotype Diversity and Linkage Disequilibrium at Human G6PD : Recent Origin of Alleles That Confer Malarial Resistance
- Two Fetal Hemoglobin Variants Affecting the Same Residue: HB F-Emirates [Gγ59(E3)LYS→GLU] and HB F-Sacromonte [Gγ59(E3)LYS→GLN]
مجلات النشر
- Cellular Physiology and Biochemistry × 11
- Hemoglobin × 5
- Hematology × 3
- Cancer Chemotherapy and Pharmacology × 2
- International Journal of Laboratory Hematology × 2
- Basic & Clinical Pharmacology & Toxicology × 2
المنشورات حسب السنة
- 20261
- 20251
- 20222
- 20212
- 20201
- 20192
- 20181
- 20174
- 20169
- 201512
التعاون العلمي
المؤسسات الشريكة : Faculté de médecine de Tunis · Hôpital Charles-Nicolle · University of Tübingen · Inserm · Institut Gustave Roussy
بلدان المؤلفين المشاركين : فرنسا · ألمانيا · السعودية
المؤلفون المشاركون
- Samia Menif
- Dorra Chaouachi
- Imen Moumni
- Leila Chaouch
- Imen Darragi
- Kaïs Douzi
- Ghada Bouguerra
- Miniar Kalai
- Imen Boudrigua
- Inès Safra
- Amine Zoraï
- Raouf Hafsia
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