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
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 14, Iss 4 (2015)
Interleukin-8 (IL-8) is a well-known inflammatory chemokine and suggested to be involved in the development of acne vulgaris. This study investigates IL-8 plasma levels in acne patients and healthy controls and the molecular basis for the regulation
Externí odkaz:
https://doaj.org/article/4db7c2ea934b4eb5bd16fbbea53e03bb
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:
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
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
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
Autor:
Humayoon Shafique Satti
Publikováno v:
Blood Advances, Vol 1, Iss , Pp 44-45 (2017)
Externí odkaz:
https://doaj.org/article/75a59344b5b34cb28185fb32f2cde005
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants
Autor:
Tahir N. Khan, Chunyu Liu, Shahar Bano, Zaineb Akram, Muhammad Farhan, Sughra Wahid, Feng Zhang, Tariq Ghafoor, Jianqiu Xiao, Humayoon Shafique Satti, Muhammad Ajmal, Sobia Shafique
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
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 is necessa