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1دورية أكاديمية
المؤلفون: Aminetou Taleb Brahim, Mariem Taleb, Harouna Soumaré, Sidi Mohamed Ghaber, Aminetou Mohamed, Ali Ould Mohamed Salem Boukhary
المصدر: Frontiers in Bioscience-Scholar, Vol 16, Iss 2, p 11 (2024)
مصطلحات موضوعية: sickle cell disease, fetal hemoglobin, bcl11a gene, single nucleotide polymorphisms, mauritania, Biology (General), QH301-705.5, Biochemistry, QD415-436
وصف الملف: electronic resource
العلاقة: https://www.imrpress.com/journal/FBS/16/2/10.31083/j.fbs1602011Test; https://doaj.org/toc/1945-0516Test
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2دورية أكاديمية
المؤلفون: Rahyssa Rodrigues Sales, Bárbara Lisboa Nogueira, Jéssica Abdo Gonçalves Tosatti, Karina Braga Gomes, Marcelo Rizzatti Luizon
المصدر: Frontiers in Pharmacology, Vol 12 (2022)
مصطلحات موضوعية: BCL11A gene, fetal hemoglobin (HbF), genetic polymorphisms, hydroxyurea (HU) therapy, pathway analysis, pharmacogenetics, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fphar.2021.779497/fullTest; https://doaj.org/toc/1663-9812Test
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3دورية أكاديمية
المؤلفون: Ety, Subarna Sayed, Farjana Akther Noor, Mohabbat Hossain, Suprovath Kumar Sarker, Syed Saleheen Qadri, Kaiissar Mannoor
المصدر: Science Proceedings Series; Vol 2 No 1 (2020): Science Proceedings Series; 66-71 ; 2663-9467 ; 2663-9459
مصطلحات موضوعية: Hemoglobin E/beta-thalassemia, clinical phenotypes, BCL11A Gene, SNPs, fetal hemoglobin
وصف الملف: application/pdf
العلاقة: https://readersinsight.net/SPS/article/view/1291/968Test; https://readersinsight.net/SPS/article/view/1291Test
الإتاحة: https://doi.org/10.31580/sps.v2i1.1291Test
https://readersinsight.net/SPS/article/view/1291Test -
4دورية أكاديمية
المؤلفون: Paramee Phanrahan, Supawadee Yamsri, Nattiya Teawtrakul, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Supan Fucharoen
المصدر: Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
مصطلحات موضوعية: Non-transfusion dependent thalassemia, HBS1L-MYB gene, BCL11A gene, KLF1 gene, Gγ-XmnI polymorphism, Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
العلاقة: https://www.mjhid.org/index.php/mjhid/article/view/3916Test; https://doaj.org/toc/2035-3006Test
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المؤلفون: Rahyssa Rodrigues Sales (11982134), Bárbara Lisboa Nogueira (11982137), Jéssica Abdo Gonçalves Tosatti (11982140), Karina Braga Gomes (10356182), Marcelo Rizzatti Luizon (10460093)
مصطلحات موضوعية: Pharmacology, Basic Pharmacology, Clinical Pharmacology and Therapeutics, Clinical Pharmacy and Pharmacy Practice, Pharmaceutical Sciences, Pharmacogenomics, Toxicology (incl. Clinical Toxicology), Pharmacology and Pharmaceutical Sciences not elsewhere classified, BCL11A gene, fetal hemoglobin (HbF), genetic polymorphisms, hydroxyurea (HU) therapy, pathway analysis, pharmacogenetics, sickle cell anemia (SCA), systematic review
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6دورية أكاديمية
المؤلفون: Reeves, Reilly
المصدر: Honors Theses
مصطلحات موضوعية: BCL11A Gene, 3D Printing, Hypotonia
وصف الملف: application/pdf
العلاقة: https://scholarsjunction.msstate.edu/honorstheses/63Test; https://scholarsjunction.msstate.edu/cgi/viewcontent.cgi?article=1062&context=honorsthesesTest
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المؤلفون: Supawadee Yamsri, Supan Fucharoen, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Nattiya Teawtrakul, Paramee Phanrahan
المصدر: Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
Mediterranean Journal of Hematology and Infectious Diseasesمصطلحات موضوعية: Thalassemia, HBS1L-MYB gene, BCL11A gene, KLF1, Single-nucleotide polymorphism, HBG2, 03 medical and health sciences, 0302 clinical medicine, hemic and lymphatic diseases, Gene expression, Medicine, Gene, KLF1 gene, Non-transfusion dependent thalassemia, Gγ-XmnI polymorphism, lcsh:RC633-647.5, business.industry, lcsh:Diseases of the blood and blood-forming organs, Hematology, medicine.disease, Phenotype, Infectious Diseases, 030220 oncology & carcinogenesis, Immunology, Hemoglobin E, Original Article, business, 030215 immunology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe5d7f39823c779c98d413f4cce5e23Test
https://doi.org/10.4084/mjhid.2019.038Test -
8دورية أكاديمية
المؤلفون: Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Kalai, Miniar, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem
المساهمون: Laboratoire d'hématologie moléculaire et cellulaire (LR11IPT07), Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Université de Tunis El Manar (UTM), LR11IPT07
المصدر: ISSN: 1024-5332.
مصطلحات موضوعية: Sickle cell anemia, BCL11A gene, HbF, MESH: Adult, MESH: Anemia, Sickle Cell/blood, MESH: Male, MESH: Nuclear Proteins/genetics, MESH: Polymorphism, Single Nucleotide, MESH: Retrospective Studies, Sickle Cell/genetics, MESH: Carrier Proteins/genetics, MESH: Female, MESH: Fetal Hemoglobin/genetics, MESH: Fetal Hemoglobin/metabolism, MESH: Gene Frequency, MESH: Genotype, MESH: Humans, [SDV]Life Sciences [q-bio], [SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27077760; pasteur-01374983; https://riip.hal.science/pasteur-01374983Test; PUBMED: 27077760
الإتاحة: https://doi.org/10.1080/10245332.2015.1107275Test
https://riip.hal.science/pasteur-01374983Test -
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المؤلفون: Imen Moumni, Leila Chaouch, Imen Boudrigua, Dorra Chaouachi, Miniar Kalai, Houyem Ouragini, Raouf Hafsia, Salem Abbes, Imen Darragi
المساهمون: Laboratoire d'hématologie moléculaire et cellulaire (LR11IPT07), Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Université de Tunis El Manar (UTM), LR11IPT07
المصدر: Hematology
Hematology, Maney Publishing, 2016, 21 (7), pp.425-429. ⟨10.1080/10245332.2015.1107275⟩مصطلحات موضوعية: 0301 basic medicine, Male, [SDV]Life Sciences [q-bio], BCL11A gene, MESH: Genotype, 0302 clinical medicine, Gene Frequency, hemic and lymphatic diseases, Genotype, MESH: Anemia, Sickle Cell/blood, Fetal Hemoglobin, education.field_of_study, MESH: Anemia, Sickle Cell/genetics, MESH: Polymorphism, Single Nucleotide, Nuclear Proteins, [SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology, Hematology, Phenotype, Sickle cell anemia, 3. Good health, 030220 oncology & carcinogenesis, Female, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Population, MESH: Nuclear Proteins/genetics, MESH: Fetal Hemoglobin/genetics, Anemia, Sickle Cell, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, MESH: Carrier Proteins/genetics, Fetal hemoglobin, medicine, MESH: Fetal Hemoglobin/metabolism, MESH: Gene Frequency, Humans, education, Allele frequency, Genotyping, Gene, Retrospective Studies, MESH: Humans, HbF, MESH: Adult, MESH: Retrospective Studies, medicine.disease, MESH: Male, Repressor Proteins, 030104 developmental biology, Immunology, Carrier Proteins, MESH: Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21277295c1491fa73ad821a294d0762aTest
https://hal-riip.archives-ouvertes.fr/pasteur-01374983Test -
10رسالة جامعية