Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Atika, Mansoor"'
Autor:
Sajid Mansoor, Ayesha Raza Butt, Asima Bibi, Saima Mushtaq, Inayat Ullah, Fahad Alshahrani, Amjad Khan, Atika Mansoor
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0291332 (2023)
Cytokines play an important role in SARS-CoV-2 infection progression and severity. A number of inflammatory cytokines have been directly associated with disease severity including IL-6 (interleukin-6), IL-10, TNF-α (tumor necrosis factor alpha), IFN
Externí odkaz:
https://doaj.org/article/e9f5d7120ffa474eb1cfa7e79cd35160
Autor:
Asima Bibi, Sameen Abbas, Saima Mushtaq, Atika Mansoor, Ivan R. Green, Tauqeer Hussain Mallhi, Yusra Habib Khan, Amjad Khan
Publikováno v:
Medicina, Vol 59, Iss 2, p 272 (2023)
Background and Objectives: Several vaccines have been approved for the prevention of the coronavirus disease, discovered on 31 December in Wuhan, China. Pakistan procured vaccines from various countries. However, the lack of knowledge and reluctance
Externí odkaz:
https://doaj.org/article/2997a0f11a1a4e98afddf8575e944025
Autor:
Nusrat Saba, Osman Yusuf, Sadia Rehman, Saeeda Munir, Amna Noor, Muhammad Saqlain, Atika Mansoor, Ghazala Kaukab Raja
Publikováno v:
Asthma Research and Practice, Vol 4, Iss 1, Pp 1-6 (2018)
Abstract Background Genetic variations in different loci and genes are important in asthma pathogenesis. There is much importance of various immunological pathways in the IgE secretion regulation. Alterations in any main part of these pathways can in
Externí odkaz:
https://doaj.org/article/5bd48293beb74780be9326c3d437cd8d
Autor:
Nusrat Saba, Ghazala Kaukab Raja, Osman Yusuf, Sadia Rehman, Saeeda Munir, Sumaira Sajjad, Atika Mansoor
Publikováno v:
International Journal of Immunogenetics. 49:372-378
Asthma, a chronic inflammatory disorder of the lungs and airways, typically results from a combination of multiple environmental and genetic factors. Human leucocyte antigen (HLA) region on chromosome 6p21 encodes the most highly polymorphic loci in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ddb01a1a3cc12410fba0ea2d44a845a
https://doi.org/10.1111/iji.12602
https://doi.org/10.1111/iji.12602
Autor:
Celia Zazo Seco, Anna Castells-Nobau, Seol-hee Joo, Margit Schraders, Jia Nee Foo, Monique van der Voet, S. Sendhil Velan, Bonnie Nijhof, Jaap Oostrik, Erik de Vrieze, Radoslaw Katana, Atika Mansoor, Martijn Huynen, Radek Szklarczyk, Martin Oti, Lisbeth Tranebjærg, Erwin van Wijk, Jolanda M. Scheffer-de Gooyert, Saadat Siddique, Jonathan Baets, Peter de Jonghe, Syed Ali Raza Kazmi, Suresh Anand Sadananthan, Bart P. van de Warrenburg, Chiea Chuen Khor, Martin C. Göpfert, Raheel Qamar, Annette Schenck, Hannie Kremer, Saima Siddiqi
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 2, Pp 105-118 (2017)
A consanguineous family from Pakistan was ascertained to have a novel deafness-dystonia syndrome with motor regression, ichthyosis-like features and signs of sensory neuropathy. By applying a combined strategy of linkage analysis and whole-exome sequ
Externí odkaz:
https://doaj.org/article/61e74f9ef396439ebd381addcbedf971
Autor:
Aneesa Sultan, Sana Riaz, Muhammad Usman Tareen, Anwarullah, Sana Rubab, Ayesha Batool, Atika Mansoor, Saima Siddiqi
Publikováno v:
Tropical Journal of Pharmaceutical Research. 18:851-855
Purpose: To investigate the association of *2 and *17 single nucleotide polymorphisms (SNPs) of CYP2C19 gene with hypertension in Pakistani population. Methods: The study was conducted on 527 hypertensive patients and 530 unrelated healthy controls f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::199b47eddcfb6cedc7ca1f5e0a490928
https://doi.org/10.4314/tjpr.v18i4.24
https://doi.org/10.4314/tjpr.v18i4.24
Autor:
Nusrat Saba, Osman Yusuf, Sadia Rehman, Saeeda Munir, Naghman Bashir, Atika Mansoor, Ghazala Raja-Kaukab
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 14, Iss 3 (2015)
Asthma is a chronic inflammatory and remodeling disorder of the airways, in which many cells, cellular elements, and cytokines play important roles. The role of tumor necrosis factor- α (TNF-α) in asthma is unclear in Pakistani population. The aim
Externí odkaz:
https://doaj.org/article/9cb663252b9f4ff297e3f62bf8fe921c
Autor:
Madiha Kanwal, Saadia Alyas, Muhammad Afzal, Atika Mansoor, Rashda Abbasi, Flora Tassone, Sajid Malik, Kehkashan Mazhar
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0122213 (2015)
Fragile-X syndrome (FXS) is the most common form of inherited intellectual disability (ID) and affects 0.7-3.0% of intellectually compromised population of unknown etiology worldwide. It is mostly caused by repeat expansion mutations in the FMR1 at c
Externí odkaz:
https://doaj.org/article/bffefdb4a2754a9982046cbaee26164b
Autor:
Raheel Qamar, Atika Mansoor, Bushra Mirza, Kehkashan Mazhar, Shazia Micheal, Saima Siddiqi, Noor Ullah
Publikováno v:
Personalized Medicine. 16:35-49
Aim: 5,10-MTHFR-single nucleotide polymorphisms are important for normal functioning of the enzyme that plays a key role in DNA synthesis, folate metabolism and methylation reactions. Methodology & results: Male infertility association of C665T and A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee88b877d58b8a17270e059c5da8fb9e
https://doi.org/10.2217/pme-2018-0045
https://doi.org/10.2217/pme-2018-0045
Autor:
Sobia Shafique, Saima Siddiqi, Margit Schraders, Jaap Oostrik, Humaira Ayub, Ammad Bilal, Muhammad Ajmal, Celia Zazo Seco, Tim M Strom, Atika Mansoor, Kehkashan Mazhar, Syed Tahir A Shah, Alamdar Hussain, Maleeha Azam, Hannie Kremer, Raheel Qamar
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100146 (2014)
The frequency of inherited bilateral autosomal recessive non-syndromic hearing loss (ARNSHL) in Pakistan is 1.6/1000 individuals. More than 50% of the families carry mutations in GJB2 while mutations in MYO15A account for about 5% of recessive deafne
Externí odkaz:
https://doaj.org/article/0ff92de14e01459da9c0b5e21e2c36d0