Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Nusrat Saba"'
Autor:
Ashley S. Thompson, Nusrat Saba, Lisa J. McReynolds, Saeeda Munir, Parvez Ahmed, Sumaira Sajjad, Kristine Jones, Meredith Yeager, Frank X. Donovan, Settara C. Chandrasekharappa, Blanche P. Alter, Sharon A. Savage, Sadia Rehman
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Background Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with characteristic dysmorphology primarily caused by biallelic pathogenic germline variants in any of 22 different DNA repair genes. There are limited da
Externí odkaz:
https://doaj.org/article/e2d473ff389a43feaebabe578dd14ba9
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, 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:
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:
Saeeda Munir, Simeen Ber Rahman, Sadia Rehman, Nusrat Saba, Kehkashan Mazhar, Åsa Torinsson Naluai
Publikováno v:
International archives of allergy and immunology.
Introduction: The human leukocyte antigen (HLA) region on chromosome 6p21 is well known to carry the most important genetic factors in susceptibility to psoriasis. Different HLA alleles and haplotypes have been reported to be associated with psoriasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b03008eb03684d0afbda1319003cf9f4
https://pubmed.ncbi.nlm.nih.gov/36382644
https://pubmed.ncbi.nlm.nih.gov/36382644
Autor:
Mahpara, Zafar, Sadia, Alam, Maimoona, Sabir, Nusrat, Saba, Ahmad Ud, Din, Rafiq, Ahmad, Muhammad Rafiullah, Khan, Ali, Muhammad, Kenan Sinan, Dayisoylu
Publikováno v:
Analytical Biochemistry. 658:114926
Bacteriocins exhibited a wide spectrum of antibacterial activity against different pathogens. The aim of current study was to characterize the bacteriocins produced by Bifidobacterium spp. isolated from ruminants. The Bifidobacterium isolates were id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030f412cc42656c6e4841e5c7412d9cd
https://doi.org/10.1016/j.ab.2022.114926
https://doi.org/10.1016/j.ab.2022.114926
Autor:
Saeeda Munir, Lisa J. McReynolds, Blanche P. Alter, Frank X. Donovan, Sadia Rehman, Sharon A. Savage, Parvez Ahmed, Sumaira Sajjad, Meredith Yeager, Settara C. Chandrasekharappa, Kristine Jones, Nusrat Saba, A. Thompson
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Background Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with characteristic dysmorphology primarily caused by biallelic pathogenic germline variants in any of 22 different DNA repair genes. There are limited data on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7447a80f02ee7d87be4c206c6409f60
https://pubmed.ncbi.nlm.nih.gov/33960719
https://pubmed.ncbi.nlm.nih.gov/33960719
Autor:
Ashley S. Thompson, Nusrat Saba, Lisa J. McReynolds, Saeeda Munir, Parvez Ahmed, Sumaira Sajjad, Kristine Jones, Meredith Yeager, Frank X. Donovan, Settara C. Chandrasekharappa, Blanche P. Alter, Sharon A. Savage, Sadia Rehman
Background Fanconi anemia (FA), a cancer-prone inherited bone marrow failure syndrome associated with characteristic dysmorphology is primarily caused by autosomal recessive inheritance of pathogenic germline variants in any of 22 different DNA repai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b054f98959a2a2130c6f17c33c38e57
https://doi.org/10.21203/rs.3.rs-52108/v1
https://doi.org/10.21203/rs.3.rs-52108/v1
Autor:
Amna Noor, Sadia Rehman, Saeeda Munir, Osman Yusuf, Muhammad Saqlain, Atika Mansoor, Ghazala Kaukab Raja, Nusrat Saba
Publikováno v:
Asthma Research and Practice, Vol 4, Iss 1, Pp 1-6 (2018)
Asthma research and practice
Asthma research and practice
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 increase th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c23b3064ee8c0ed30e75945bcb78e661
http://link.springer.com/article/10.1186/s40733-018-0039-4
http://link.springer.com/article/10.1186/s40733-018-0039-4
Autor:
Saeeda Munir, Nusrat Saba, Sadia Rehman, Lubna Naseem, Madiha Naz, Parvez Ahmed, Sumaira Sajjad, Sobia Tabassum
Publikováno v:
Immunological investigations. 47(5)
FAS/FASL signaling system plays a vital role in the regulation of apoptosis, envisaged as a death process required for immune surveillance to prevent autoimmunity and tumorigenesis along with several other biological activities. Several single-nucleo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb1892411cf5feccc7cb1166f3969f72
https://pubmed.ncbi.nlm.nih.gov/29611722
https://pubmed.ncbi.nlm.nih.gov/29611722