المؤلفون: Bhagyalaxmi Das, Bishnu Prasad Dash, Dharma Niranjan Mishra, Rabindra Kumar Jena

المصدر: National Journal of Laboratory Medicine, Vol 12, Iss 2, Pp PO11-PO13 (2023)

مصطلحات موضوعية: anaemia, haemoglobin variants, beta-globin gene, Microbiology, QR1-502, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://njlm.net/article_fulltext.aspx?issn=0973-709x&year=2023&month=April&volume=12&issue=2&page=PO11%20-%20PO13&id=2713; https://doaj.org/toc/2277-8551; https://doaj.org/toc/2455-6882

URL الوصول: https://doaj.org/article/2d3c97495b04459dac6ef44306bdc572

المؤلفون: Karaer, Kadri, ÅžahinoÄŸlu, Bahtiyar, ÅžahinoÄŸlu, Esra Pekpak, Gürler, Abdullah I., Kirat, Emre, Karaer, Derya

مصطلحات موضوعية: Thalassemia, Beta-Globin gene, Mutations, Turkey, Prenatal-Diagnosis, Region, Hemoglobinopathies, University

Relation: Gazi Medical Journal; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.12996/gmj.2023.12; https://hdl.handle.net/11499/50439; 34; 63; 67; WOS:000908834300012

الاتاحة: https://hdl.handle.net/11499/50439
https://doi.org/10.12996/gmj.2023.12

المؤلفون: Mehrzad S, Keshtmand Z

المصدر: Fiyz̤, Vol 24, Iss 2, Pp 219-226 (2020)

مصطلحات موضوعية: thalassemia, snapshot, beta-globin gene, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://feyz.kaums.ac.ir/article-1-3927-en.html; https://doaj.org/toc/1029-7855; https://doaj.org/toc/2008-9821

URL الوصول: https://doaj.org/article/6b367476c1c94fb1ab36d1da06e17ce6

المؤلفون: Uçar, Havva, Eren, Esin, Aslan, Vedat, Kurtoğlu, Erdal, Yılmaz, Necat, Kurtoğlu, Ayşegül Uğur

المساهمون: Başka Kurum

مصطلحات موضوعية: HbF, Talasemi İntermedia, Beta globin gen delesyonu, Thalassemia Intermedia, Beta globin gene deletion

وصف الملف: application/pdf

Relation: Selçuk Genel Tıp Dergisi; Makale - Uluslararası Hakemli Dergi - Başka Kurum Yazarı; Kurtoğlu, A. U., Uçar, H., Eren, E., Aslan, V., Kurtoğlu, E., Yılmaz, N., (2021). Periferik Kanında %100 HbF Bulunan Talasemi İntermedia Olgusu. Genel Tıp Dergisi, 31 (2), 180-181.; https://hdl.handle.net/20.500.12395/43835; 31; 180; 181

الاتاحة: https://hdl.handle.net/20.500.12395/43835

المؤلفون: Ayşegül Uğur Kurtoğlu, Havva Uçar, Esin Eren, Vedat Aslan, Erdal Kurtoğlu, Necat Yılmaz

المصدر: Genel Tıp Dergisi, Vol 31, Iss 2, Pp 180-181 (2021)

مصطلحات موضوعية: hbf, talasemi i̇ntermedia, beta globin gen delesyonu, thalassemia intermedia, beta globin gene deletion, Medicine (General), R5-920

Relation: https://dergipark.org.tr/tr/download/article-file/1851246; https://doaj.org/toc/2602-3741; https://doaj.org/article/7e8730e48fbb484096efb15862df4ae2

الاتاحة: https://doi.org/10.15321/GenelTipDer.2021.310
https://doaj.org/article/7e8730e48fbb484096efb15862df4ae2

المؤلفون: Nasrollah SALEH-GOHARI, Kolsoum SAEIDI, Sima ZIAADINI-DASHTKHAKI

المصدر: Iranian Journal of Public Health, Vol 49, Iss 4 (2020)

مصطلحات موضوعية: Beta-thalassemia, Beta-globin gene, Haplotype, Iran, Public aspects of medicine, RA1-1270

وصف الملف: electronic resource

Relation: https://ijph.tums.ac.ir/index.php/ijph/article/view/11924; https://doaj.org/toc/2251-6085; https://doaj.org/toc/2251-6093

URL الوصول: https://doaj.org/article/f43fba7f31bb407781aff7e960770ad3

المؤلفون: Wu, X. M., He, X. R., Liu, Fahui, Jiang, X. C., Wang, P., Zhang, J. Y., Jiang, J.

المصدر: Computational and Structural Biotechnology Journal. 20:2986-3003

مصطلحات موضوعية: Molecular Biology, Molekylärbiologi, Gene therapy, ex vivo, retroviral vectors, stem cells, clinical, approvals, severe combined immunodeficiency, chronic granulomatous-disease, beta-globin gene, t-cell therapy, inactivating lentiviral vector, cord, blood transplantation, bone-marrow, ciltacabtagene autoleucel, packaging signal, Biochemistry & Molecular Biology, Biotechnology & Applied Microbiology

URL الوصول: https://gup.ub.gu.se/publication/320224

المؤلفون: Md Tarikul Islam, Suprovath Kumar Sarkar, Nusrat Sultana, Mst. Noorjahan Begum, Golam Sarower Bhuyan, Shezote Talukder, A. K. M. Muraduzzaman, Md Alauddin, Mohammad Sazzadul Islam, Pritha Promita Biswas, Aparna Biswas, Syeda Kashfi Qadri, Tahmina Shirin, Bilquis Banu, Salma Sadya, Manzoor Hussain, Golam Sarwardi, Waqar Ahmed Khan, Mohammad Abdul Mannan, Hossain Uddin Shekhar, Emran Kabir Chowdhury, Abu Ashfaqur Sajib, Sharif Akhteruzzaman, Syed Saleheen Qadri, Firdausi Qadri, Kaiissar Mannoor

المصدر: BMC Genetics, Vol 19, Iss 1, Pp 1-12 (2018)

مصطلحات موضوعية: Beta-globin gene, Mutational hot-spot, Beta-thalassemia, High resolution melting curve, Carrier screening, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12863-017-0594-3; https://doaj.org/toc/1471-2156

URL الوصول: https://doaj.org/article/41573a4d652e45bbb16515209ff766eb

المؤلفون: Mohammad Bagher Hashemi-Soteh, Seyed Saeed Mousavi, Alireza Tafazoli

المصدر: Journal of Biomedical Science, Vol 24, Iss 1, Pp 1-5 (2017)

مصطلحات موضوعية: Beta-thalassemia, Beta-globin gene, Haplotypes, Prenatal diagnosis, Mazandaran, Medicine

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12929-017-0396-y; https://doaj.org/toc/1423-0127

URL الوصول: https://doaj.org/article/d3416d9e46784c5488f8845a08086c53

المؤلفون: Wittaya Jomoui, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Nga Thi Nguyen, Hoa Van Nguyen, Supan Fucharoen

المصدر: Annals of Human Biology, Vol 44, Iss 8, Pp 747-750 (2017)

مصطلحات موضوعية: haemoglobin variant, beta globin gene haplotype, phylogenetic tree, Biology (General), QH301-705.5, Human anatomy, QM1-695, Physiology, QP1-981

وصف الملف: electronic resource

Relation: https://doaj.org/toc/0301-4460; https://doaj.org/toc/1464-5033

URL الوصول: https://doaj.org/article/d97225f3672c4e71a2403771173818ad

المؤلفون: Çevirici, Hatice, Acıpayam, Can, Yenilmez, Ebru Dündar, Belen, Fatma Burcu, Pekpak, Esra, Yaman, Yöntem, Tuli, Abdullah

مصطلحات موضوعية: Beta Globin Gene Mutation, Beta Thalassemia, Children, Syrian Immigrants, Beta Talasemi, Beta Globin Gen Mutasyonu, Suriye’li Göçmenler, Çocuk

وصف الملف: application/pdf

Relation: Turkish Journal of Biochemistry; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Çevirici, H., Acıpayam, C., Yenilmez, E. D., Belen, F. B., Pekpak, E. . Tuli, A. (2019). Investigation of beta globin gene mutations in Syrian refugee patients with thalassemia major. Turkish Journal of Biochemistry, 44(2), 126-129. http://doi.org/ 10.1515/tjb-2018-0492; http://doi.org/ 10.1515/tjb-2018-0492; https://hdl.handle.net/20.500.12511/4664; 44; 126; 129; Q4

الاتاحة: https://hdl.handle.net/20.500.12511/4664
http://doi.org/ 10.1515/tjb-2018-0492
https://doi.org/10.1515/tjb-2018-0492

المؤلفون: Çevirici, Hatice, Acıpayam, Can, Belen, Fatma Burcu, Pekpak, Esra, Yaman, Yöntem, Dündar Yenilmez, Ebru, Tuli, Abdullah

المساهمون: Çukurova Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, orcid:0000-0002-5519-3773, https://orcid.org/0000-0002- 6379-224X, Dündar Yenilmez, Ebru, Tuli, Abdullah

مصطلحات موضوعية: Beta thalassemia, Beta globin gene mutation, Syrian immigrants, Children

وصف الملف: application/pdf

Relation: Turk J Biochem; Makale - Ulusal Hakemli Dergi - Başka Kurum Yazarı; https://hdl.handle.net/20.500.12605/22853; 44; 126; 129

الاتاحة: https://hdl.handle.net/20.500.12605/22853

المؤلفون: Suresh Babu, T. V., Kabekkodu, Shama Prasada, Satyamoorthy, K., Shantaram, Manjula

المصدر: Open Access archive

مصطلحات موضوعية: beta-globin gene, Beta-thalassemia, DNA sequencing, HBB, Kodagu population

Relation: https://impressions.manipal.edu/open-access-archive/8422

الاتاحة: https://impressions.manipal.edu/open-access-archive/8422
https://doi.org/10.51248/.v43i01.2686

المؤلفون: Judith Barbara Zaugg, Pelin Sahlén, Robin Andersson, Meritxell Alberich-Jorda, Wouter de Laat, Bart Deplancke, Jorge Ferrer, Susanne Mandrup, Gioacchino Natoli, Dariusz Plewczynski, Alvaro Rada-Iglesias, Salvatore Spicuglia

المساهمون: European Molecular Biology Laboratory (EMBL), Royal Institute of Technology, IT University of Copenhagen (ITU), Medicine Charles University and General Faculty Hospital in Prague, University Medical Center [Utrecht], School of Life Sciences [Lausanne], Ecole Polytechnique Fédérale de Lausanne (EPFL), Barcelona Institute of Science and Technology (BIST), University of Southern Denmark (SDU), IRCCS Istituto Nazionale dei Tumori [Milano], University of Warsaw (UW), University of Cantabria, Theories and Approaches of Genomic Complexity (TAGC), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), European Project: 286079,EC:FP7:PEOPLE,FP7-PEOPLE-2011-IAPP,AIRFORS(2012), European Commission

المصدر: Nature Structural and Molecular Biology
Nature Structural and Molecular Biology, 2022, 29 (12), pp.1148-1158. ⟨10.1038/s41594-022-00896-3⟩

مصطلحات موضوعية: Epigenomics, variants, super-enhancers, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Genomics, single-cell, burkitt-lymphoma, dissection, Structural Biology, beta-globin gene, expression, chromatin, identification, Molecular Biology, shadow enhancers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d0b4372497b4a9eba825116792bd6d2
https://hdl.handle.net/20.500.11755/82992d1f-37df-4124-a419-3600b62706cf

المؤلفون: Amin Lutful Kabir, Nishat Mahzabin, Khaza Amirul Islam, Kazi Mohammad Kamrul Islam, Nusrat Jahan, Md. Arif-Ur Rahman, Md. Akhlak-Ul Islam

المصدر: Haematology Journal of Bangladesh. 5:57-60

مصطلحات موضوعية: Genetics, Beta globin gene, Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::921d1bc916bc3c4cea5fbe434c4d5441
https://doi.org/10.37545/haematoljbd202177

المؤلفون: Türkgenç, Burcu, Şanlıdağ, Burçin, Eker, Amber, Giray, Aslı, Kütük, Özgür, Yakıcıer, Cengiz, Tolun, Aslıhan

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı., orcid:0000-0002-9802-0880, Temel, Şehime Gülsün, AAG-8385-2021, 6507885442

مصطلحات موضوعية: Genetics & heredity, 3 ' UTR, Cerebellar atrophy, Polyadenylation, SCAR16, STUB1, Messenger-RNA polyadenylation, Beta-globin gene, Thalassemia, Mutation, Cleavage, Sequence, Site, 3' untranslated regions, Brain, Cerebellar ataxia, DNA mutational analysis, Genetic variation, Humans, Magnetic resonance imaging, Pedigree, Poly A, Ubiquitin-protein ligases, Protein, Tetratricopeptide Repeat, Spinocerebellar Ataxias, Hemoglobin A, Messenger RNA, Polyadenylic acid, STUB1 protein

وصف الملف: application/pdf

Relation: 114Z829; Makale - Uluslararası Hakemli Dergi; Human Mutation; Yurt dışı; Yurt içi; Sanayi; Türkgenç, B. vd. (2018). ''STUB1 polyadenylation signal variant AACAAA does not affect polyadenylation but decreases STUB1 translation causing SCAR16''. Human Mutation, 39(10), 1344-1348.; https://doi.org/10.1002/humu.23601; http://hdl.handle.net/11452/30371; 000444948000004; 2-s2.0-85052532576; 1344; 1348; 39; 10

الاتاحة: http://hdl.handle.net/11452/30371
https://doi.org/10.1002/humu.23601
https://onlinelibrary.wiley.com/doi/10.1002/humu.23601

المؤلفون: Elmi, Elmi, Nasrul, Ellyza, Syukur, Sumaryati, Susanah, Susi

المصدر: American Scientific Research Journal for Engineering, Technology, and Sciences (ASRJETS); Vol 38 No 2 (2017); 18-22 ; 2313-4402 ; 2313-4410

مصطلحات موضوعية: Beta-globin gene, thalassaemia, gene mutation, anemia

وصف الملف: application/pdf

Relation: http://asrjetsjournal.org/index.php/American_Scientific_Journal/article/view/3245/1332; http://asrjetsjournal.org/index.php/American_Scientific_Journal/article/view/3245

الاتاحة: http://asrjetsjournal.org/index.php/American_Scientific_Journal/article/view/3245

المؤلفون: Fattori, André, Kimura, Elza Miyuki, Albuquerque, Dulcinéia Martins de, Ogo, Satie Hatsushika, Stoppa, Graziela Renata, Martins, Juliana Touquinha, Lima, Carmen Silvia Passos, Saad, Sara Terezinha Ollala, Costa, Fernando Ferreira, Sonati, Maria de Fátima

المصدر: Genetics and Molecular Biology. January 2006 29(2)

مصطلحات موضوعية: polycythemia, erythrocytosis, Hb Coimbra, beta-globin gene

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000200002

المؤلفون: Diclehan Oral, Veysiye Hülya Üzel, Mehmet Akif Çürük, Selda Şimşek, Murat Söker, Selahaddin Tekes

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı, Tekeş, Selahaddin, Oral, Diclehan, Söker, Murat, Uzel, Veysiye Hülya

مصطلحات موضوعية: Turkey, HBB:c.208G > A, Clinical Biochemistry, Trait, Prenatal-Diagnosis, Biology, Güneydoğu Anadolu Bölgesi, Biochemistry, Beta-thalassemia, beta-thalassemia, β-talasemi, Disease, Variant, Molecular Biology, Genetics, HBB:c.34G > A, c.208G > A [HBB], Biochemistry (medical), c.208G>A [HBB], Sickle-Cell-Anemia, c.34G>A [HBB], Hemoglobinopathies, Thalassemia, Beta globin gene, southeastern Anatolia region, c.34G > A [HBB], Southeastern Anatolia region

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fdeb65ece4400a20264343b1d1b73b1
https://doi.org/10.1515/tjb-2020-0546

المؤلفون: Mohammad Bagher Hashemi Soteh, Haleh Akhavan Niaki, Mehrnoosh Kowsarian, Aily Aliasgharian, Ali Banihashemi

المصدر: Journal of Mazandaran University of Medical Sciences, Vol 18, Iss 67, Pp 17-25 (2008)

مصطلحات موضوعية: Beta thalassemia, frequency mutations, beta-globin gene, ARMS- PCR, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://www.mazums.ac.ir/index.php?digital_library&do=downloadPdf&sid=684; https://doaj.org/toc/1735-9260; https://doaj.org/toc/1735-9279

URL الوصول: https://doaj.org/article/672ea74079464082b8e8ea9f97c51cd0