Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rubaiya Gulshan"'
Autor:
Md. Rayhan Mahmud, Sanjida Khanam Tamanna, Sharmin Akter, Lincon Mazumder, Sumona Akter, Md. Rakibul Hasan, Mrityunjoy Acharjee, Israt Zahan Esti, Md. Saidul Islam, Md. Maksudur Rahman Shihab, Md. Nahian, Rubaiya Gulshan, Sadia Naser, Anna Maria Pirttilä
Publikováno v:
Gut Microbes, Vol 16, Iss 1 (2024)
Phages are the most diversified and dominant members of the gut virobiota. They play a crucial role in shaping the structure and function of the gut microbial community and consequently the health of humans and animals. Phages are found mainly in the
Externí odkaz:
https://doaj.org/article/fc586c2df0f64278aedae480a0c0f0bb
Autor:
Md Jubayer Hossain, Md Wahidul Islam, Ummi Rukaiya Munni, Rubaiya Gulshan, Sumaiya Akter Mukta, Md Sharif Miah, Sabia Sultana, Mousumi Karmakar, Jannatul Ferdous, Mohammad Ariful Islam
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Thalassemia is one of the most common autosomal recessive hereditary blood disorders worldwide, especially in developing countries, including Bangladesh. Thus, this study aimed to determine HRQoL and its determinants of thalassemia patients
Externí odkaz:
https://doaj.org/article/c977c2c4cd134edd94cff157899aa2d1
Autor:
Md. Jubayer Hossain, Md. Wahidul Islam, Ummi Rukaiya Munni, Rubaiya Gulshan, Sumaiya Akter Mukta, Sharif Miah, Sabia Sultana, Mousumi Karmakar, Jannatul Ferdous, Mohammad Ariful Islam
Background One of the most common autosomal recessive hereditary blood disorders in the world, especially in developing countries like Bangladesh. Patients suffering from this disease face physical, emotional, and social problems that lessen their he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5aa85da480268f79dd54ca9c6ac8456
https://doi.org/10.21203/rs.3.rs-2528887/v1
https://doi.org/10.21203/rs.3.rs-2528887/v1
Autor:
Jubayer Hossain, Syeda Tasneem Towhid, Sabia Sultana, Sumaiya Akter Mukta, Rubaiya Gulshan, Sharif Miah
BackgroundThalassemia is the most common congenital single-gene condition. It is marked by a lack of or reduced synthesis of either the alpha- or beta-globin chains and passed down from parents to offspring. This study aimed to determine how healthy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf6e6f23017903bac74228788cc556e8
https://doi.org/10.1101/2022.09.19.22280125
https://doi.org/10.1101/2022.09.19.22280125