Zobrazeno 1 - 10
of 1 264
pro vyhledávání: '"ARMS-PCR"'
Publikováno v:
Arab Gulf Journal of Scientific Research, 2023, Vol. 42, Issue 3, pp. 714-721.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/AGJSR-01-2023-0016
Autor:
Ayesha Afzal, Harooma Jamshaid, Yasmin Badshah, Maria Shabbir, Janeen H. Trembley, Sameen Zafar, Ghulam Murtaza Kamal, Tayyaba Afsar, Fohad Mabood Husain, Suhail Razak
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background Chronic myeloid leukaemia (CML) is a type of blood cancer that begins in the hematopoietic stem cells. It is primarily characterized by a specific chromosomal aberration, the Philadelphia chromosome. While the fusion gene is a maj
Externí odkaz:
https://doaj.org/article/88f3ec3131af4cbc841ca8ca1519d148
Publikováno v:
Journal of Hebei University of Science and Technology, Vol 45, Iss 5, Pp 497-507 (2024)
In order to achieve its nucleotide polymorphism (SNP) accurate typing, this paper establishes a molecular diagnostic technique based on fluorescent quantitative PCR for accurate genotyping of the nucleotide polymorphism (SNP) at the rs755555 locus of
Externí odkaz:
https://doaj.org/article/3713bb9608a14ed08ed06097dfab7be9
Autor:
Tayyaba Hussain, Yasmin Badshah, Maria Shabbir, Fizzah Abid, Ghulam Murtaza Kamal, Amna Fayyaz, Janeen H. Trembley, Tayyaba Afsar, Fohad Mabood Husain, Suhail Razak
Publikováno v:
Cancer Cell International, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Hepatocellular carcinoma (HCC) is a global health concern. Due to late diagnosis and limited therapeutic strategies, HCC based mortality rate is exponentially increasing globally. Genetic predisposition is a non-avoidable intrinsi
Externí odkaz:
https://doaj.org/article/5e3038e4338b4b46ac0340cab2e1ca94
Genotyping single point mutations in rd1 and rd8 mice using melting curve analysis of qPCR fragments
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract PCR is tolerant to single nucleotide mismatches. Therefore, genotyping of point mutations by PCR requires special conditions for the amplification of allele-specific PCR fragments. MS-PCR (mutagenically separated PCR) is an improved version
Externí odkaz:
https://doaj.org/article/7f5088d57eff44bcbd82ac0d94c6c0fa
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract The parallel rise in obesity and male infertility in modern societies necessitates the identification of susceptibility genes underlying these interconnected health issues. In our study, we conducted a comprehensive search in the OMIM databa
Externí odkaz:
https://doaj.org/article/f42e578b13ba459383b6026b4cd2541b
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 32, Iss 1, Pp 7416-7427 (2024)
Introduction: The TP53 gene on the short arm of chromosome 17p, which is known as a tumor suppressor gene, encodes the transcription factor p53, and this factor controls cell cycle progression. This study was done to assess the association of TP53 (r
Externí odkaz:
https://doaj.org/article/d908d435b5664ab98c7f078dbe8488c0
Autor:
Atiyeh Mellati, Samaneh Soltani, Tohid Kazemi, Nooshin Ahmadzadeh, Maryam Akhtari, Elham Madreseh, Ahmadreza Jamshidi, Elham Farhadi, Mahdi Mahmoudi
Publikováno v:
BMC Rheumatology, Vol 8, Iss 1, Pp 1-8 (2024)
Abstract Background Through investigating genetic variations, it has been demonstrated that single nucleotide polymorphisms (SNPs) in the IL-23 receptor (IL23R) gene have a critical role in the pathophysiology of ankylosing spondylitis (AS). Here, we
Externí odkaz:
https://doaj.org/article/69ae0f6a2f744b5b9b19ca07f71c5bd0
Autor:
Saeied Malekzadeh, Sara Ghaffarian
Publikováno v:
Iranian South Medical Journal, Vol 26, Iss 3, Pp 155-166 (2024)
Background: The MisMatch Repair (MMR) system is a conserved system with a key role in genetic stability and replication integrity. The MLH1 gene is one of the four main components of the MMR complex. This study was conducted to assess the association
Externí odkaz:
https://doaj.org/article/efe4cc4cda9a4a569f11a48ff57a7a24
Autor:
Maryam Nawab, Syeda Kiran Riaz, Eiman Ismail, Alfar Ahamed, Aaysha Tariq, Muhammad Faraz Arshad Malik, Naeem F. Qusty, Farkad Bantun, Petr Slama, Massab Umair, Shafiul Haque, D. Katterine Bonilla-Aldana, Alfonso J. Rodriguez-Morales
Publikováno v:
Annals of Clinical Microbiology and Antimicrobials, Vol 23, Iss 1, Pp 1-9 (2024)
Abstract Global impact of COVID-19 pandemic has heightened the urgency for efficient virus detection and identification of variants such as the Q57H mutation. Early and efficient detection of SARS-CoV-2 among densely populated developing countries is
Externí odkaz:
https://doaj.org/article/a250d108a6de473faed6707169a9f910