Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Humayoon Shafique Satti"'
Autor:
Fatima Suhaib, Maria Khan, Humayoon Shafique Satti, Shahreen Zahid, Muhammad Kaleem, Abdul Samad Khan
Publikováno v:
Journal of Islamic International Medical College, Vol 19, Iss 3, Pp 165-171 (2024)
Objective: This study aimed to analyse the osteogenic potential of a novel experimental material comprising of nano-hydroxyapatite grafted glass fiber scaffolds using murine osteoblast MC3T3-E1 cell lines through gene expression of biomarkers for ost
Externí odkaz:
https://doaj.org/article/1aefd07644334ee8aa217cd966136546
Autor:
Afshan Noor, Fahim Akhtar, Saleem Ahmed Khan, Mehreen Ali Khan, Zaineb Akram, Ghassan Umair Shamshad, Humayoon Shafique Satti, Qamar-Un-Nisa Chaudhry, Fozia Fatima
Publikováno v:
Journal of Applied Hematology, Vol 13, Iss 4, Pp 255-262 (2022)
BACKGROUND: This study aimed to determine the association of single-nucleotide polymorphisms (SNPs) of interleukin-6 (IL-6) gene with the survival and disease status of patients after allogeneic hematopoietic stem cell transplantation. MATERIALS AND
Externí odkaz:
https://doaj.org/article/2a8e998e73fe4aa5ab0c8f373bf20400
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants
Autor:
Chunyu Liu, Muhammad Ajmal, Zaineb Akram, Tariq Ghafoor, Muhammad Farhan, Sobia Shafique, Sughra Wahid, Shahar Bano, Jianqiu Xiao, Humayoon Shafique Satti, Feng Zhang, Tahir Naeem Khan
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
Abstract Osteopetrosis is a genetically heterogenous, fatal bone disorder characterized by increased bone density. Globally, various genetic causes are reported for osteopetrosis with all forms of inheritance patterns. A precise molecular diagnosis i
Externí odkaz:
https://doaj.org/article/2bf5b2c415524ca4aafc8083fa1e385f
Autor:
Raheel Iftikhar, Qamar un Nisa Chaudhry, Tariq Mehmood Satti, Syed Kamran Mahmood, Tariq Ghafoor, Ghassan Umair Shamshad, Nighat Shahbaz, Mehreen Ali Khan, Tariq Azam Khattak, Jahanzeb Rehman, Muhammad Farhan, Saima Humayun, Humera Haq, Syeda Ammaara Anwaar Naqvi, Faiz Anwer, Humayoon Shafique Satti, Parvez Ahmed
Publikováno v:
Clinical Hematology International, Vol 2, Iss 2 (2020)
Allogeneic stem cell transplant for high-risk aplastic anemia (AA) yields inferior results using conventional cyclophosphamide (CY)-based conditioning. The use of fludarabine (Flu)-based regimens has resulted in improved outcomes in high-risk patient
Externí odkaz:
https://doaj.org/article/d351dd7dd74c441297ae6d732ecfb695
Autor:
Humayoon Shafique Satti
Publikováno v:
Blood Advances, Vol 1, Iss , Pp 44-45 (2017)
Externí odkaz:
https://doaj.org/article/75a59344b5b34cb28185fb32f2cde005
Autor:
Ayaz Khan, Shixiong Tian, Muhammad Tariq, Sheraz Khan, Muhammad Safeer, Naimat Ullah, Nazia Akbar, Iram Javed, Mahnoor Asif, Ilyas Ahmad, Shahid Ullah, Humayoon Shafique Satti, Raees Khan, Muhammad Naeem, Mahwish Ali, John Rendu, Julien Fauré, Klaus Dieterich, Xenia Latypova, Shahid Mahmood Baig, Naveed Altaf Malik, Feng Zhang, Tahir Naeem Khan, Chunyu Liu
Publikováno v:
Molecular Genetics and Genomics. 297:1601-1613
Hereditary neurological disorders (HNDs) are a clinically and genetically heterogeneous group of disorders. These disorders arise from the impaired function of the central or peripheral nervous system due to aberrant electrical impulses. More than 60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cabcb7b0d627957db87c74f7d66809
https://doi.org/10.1007/s00438-022-01945-8
https://doi.org/10.1007/s00438-022-01945-8
Autor:
Zaineb Akram, Raheel Iftikhar, Humayoon Shafique Satti, Qamar un Nisa Chaudhry, Tariq Ghafoor, Tariq Khattak, Nighat Shahbaz, Mehreen Ali Khan, Nadia Sial, Hammad Javed, Saima Humayun Toor, Maryam Khan, Memoona Khan
Publikováno v:
Blood. 140:13009-13010
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::718a599ed0097cfdd4a8df64ede0dae2
https://doi.org/10.1182/blood-2022-171042
https://doi.org/10.1182/blood-2022-171042
Autor:
Tariq Mehmood Satti, Mehreen Ali Khan, Qamar-Un-Nisa Chaudhry, Tariq Ghafoor, Nadia Sial, Zaineb Akram, Parvez Ahmed, Nighat Shahbaz, Humayoon Shafique Satti, Salman Akbar Malik, Syed Kamran Mahmood
Publikováno v:
Regenerative Engineering and Translational Medicine. 7:234-243
Mesenchymal stromal cells (MSCs) have emerged as a promising candidate for the treatment of steroid-refractory graft-versus-host disease (GVHD). In this uncontrolled, pilot clinical study, we report safety and efficacy of allogeneic bone marrow MSCs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34d1b5b8d474fcb658f4becf2802e2d0
https://doi.org/10.1007/s40883-020-00160-4
https://doi.org/10.1007/s40883-020-00160-4
Autor:
Parvez Ahmed, Mehreen Ali Khan, Zaineb Akram, Syed Kamran Mahmood, Tariq Mahmood Satti, Qamar Un Nisa Chaudhry, Nighat Shahbaz, Raheel Iftikhar, Humayoon Shafique Satti, Tariq Ghafoor
Publikováno v:
Hematology. 25:48-54
Objective: Prevalence of aplastic anemia (AA) is high in the Asian population. This study was done to explore the etiology and association of AA with various socio-economic and environmental factor...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60081271c0dcd0c8ca022349b79bcef5
https://doi.org/10.1080/16078454.2019.1711344
https://doi.org/10.1080/16078454.2019.1711344
Autor:
Tariq Ghafoor, Mehreen Ali Khan, Muhammad Farhan, Humayoon Shafique Satti, Faiz Anwer, Tariq Mehmood Satti, Parvez Ahmed, Qamar Un Nisa Chaudhry, Ghassan Umair Shamshad, Syed Kamran Mahmood, Nighat Shahbaz, Tariq Azam Khattak, Saima Humayun, Jahanzeb Rehman, Raheel Iftikhar
Publikováno v:
Biology of Blood and Marrow Transplantation. 25:2375-2382
Despite excellent transplant outcomes of aplastic anemia (AA) in developed countries, management in developing countries is challenging because of delay in the diagnosis, use of family donors for transfusions, and higher infection risk pretransplant.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d70ae2b4619b1447d9ff7f2a8641e6f7
https://doi.org/10.1016/j.bbmt.2019.07.029
https://doi.org/10.1016/j.bbmt.2019.07.029