Zobrazeno 1 - 10 of 55 pro vyhledávání: '"Mariam Anees"'
1
Akademický článek
In Silico, In Vitro, and In Vivo Evaluation of Caffeine-Coated Nanoparticles as a Promising Therapeutic Avenue for AML through NF-Kappa B and TRAIL Pathways Modulation
Autor: Muhammad Hamid Siddique, Sidra Bukhari, Inam Ullah Khan, Asiya Essa, Zain Ali, Usama Sabir, Omiya Ayoub, Haleema Saadia, Muhammad Yaseen, Aneesa Sultan, Iram Murtaza, Philip G. Kerr, Mashooq Ahmad Bhat, Mariam Anees
Publikováno v: Pharmaceuticals, Vol 16, Iss 12, p 1742 (2023)
Background: Advancements in nanoscience have led to a profound paradigm shift in the therapeutic applications of medicinally important natural drugs. The goal of this research is to develop a nano-natural product for efficient cancer treatment. Metho
Externí odkaz: https://doaj.org/article/f005c72e86c54cc5936d00379a31da5c
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2
Akademický článek
Naphthoquinones from Handroanthus impetiginosus promote skin wound healing through Sirt3 regulation
Autor: Fayyaz Ahmad, Shaheen Bibi, Mincheol Kang, Mariam Anees, Muhammad Ansar, Muhammad Rizwan Alam, Sun Kim, Hussain Wahedi
Publikováno v: Iranian Journal of Basic Medical Sciences, Vol 23, Iss 9, Pp 1139-1145 (2020)
Objective(s): Lapachone is a natural naphthoquinone-derived compound found in Tabebuia avellanedae. It is well-known for its analgesic, anti-inflammatory, anti-microbial, diuretic, and anti-cancerous effects. However, the wound-healing effects of thi
Externí odkaz: https://doaj.org/article/b80ed5c743dd432dad7eadb529a02269
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3
Akademický článek
Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta
Autor: Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Chuen Khor, Jia Nee Foo, Mariam Anees
Publikováno v: Journal of Biomedical Science, Vol 25, Iss 1, Pp 1-10 (2018)
Abstract Introduction Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disease with skeletal fragility and variable extra-skeletal manifestations. To date several point mutations in 18 different genes causing different types
Externí odkaz: https://doaj.org/article/4ee6f9ae808548d895c5a582c1faddf4
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4
Akademický článek
Data of expression status of miR- 29a and its putative target mitochondrial apoptosis regulatory gene DRP1 upon miR-15a and miR-214 inhibition
Autor: Muhammad Ishtiaq Jan, Riaz Anwar Khan, Abdul Malik, Tahir Ali, Muhammad Bilal, Long Bo, Abdul Sajid, Naseeb Urehman, Nayyar Waseem, Javed Nawab, Murad Ali, Abdul Majeed, Hamid Ahmad, Sohail Aslam, Sadia Hamera, Aneesa Sultan, Mariam Anees, Qamar Javed, Iram Murtaza
Publikováno v: Data in Brief, Vol 16, Iss , Pp 1000-1004 (2018)
Data is about the mitochondrial apoptosis regulatory framework genes PUMA, DRP1 (apoptotic), and ARC (anti-apoptotic) analysis after the employment of their controlling miRNAs inhibitors. The data represents putative conserved targeting of seed regio
Externí odkaz: https://doaj.org/article/7a5ee20075584ce685e7803fae833029
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5
Akademický článek
A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family
Autor: Mehran Kausar, Elaine Guo Yan Chew, Hazrat Ullah, Mariam Anees, Chiea Chuen Khor, Jia Nee Foo, Outi Makitie, Saima Siddiqi
Publikováno v: Frontiers in Genetics, Vol 10 (2019)
We report on three new patients with spondyloocular syndrome (SOS) in a consanguineous Pakistani family. All three patients present progressive generalized osteoporosis, short stature, recurrent fractures, hearing loss and visual impairments. WES rev
Externí odkaz: https://doaj.org/article/2e3d2cc6bcaa44dd9215eebeea2e4742
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6
Akademický článek
Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta
Autor: Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Chuen Khor, Jia Nee Foo, Mariam Anees
Publikováno v: Journal of Biomedical Science, Vol 26, Iss 1, Pp 1-1 (2019)
In the original publication of this article [1], there are two errors in the article which the cDNA position of the pathogenic variant WNT1 p.Gly324Cys should be c.970G>T instead of c.1168G>T.
Externí odkaz: https://doaj.org/article/8bc113d60241444b8a77e0f421d618c8
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