Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Abdul Rafay Khan"'
Publikováno v:
Evolutionary Bioinformatics, Vol 18 (2022)
Background: Pharmacogenomics (PGx), forming the basis of precision medicine, has revolutionized traditional medical practice. Currently, drug responses such as drug efficacy, drug dosage, and drug adverse reactions can be anticipated based on the gen
Externí odkaz:
https://doaj.org/article/449baae271f8404dad22beda8750c302
Autor:
Ali Amar, Ayesha Afzal, Athar Hameed, Mumtaz Ahmad, Abdul Rafay Khan, Humaira Najma, Aiysha Abid, Shagufta Khaliq
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
Abstract Background Urolithiasis is a worldwide urological problem with significant contribution of genetic factors. Pakistan, which resides within the Afro-Asian stone belt, has a high reported prevalence (12%) of urolithiasis. Osteopontin (SPP1) is
Externí odkaz:
https://doaj.org/article/006824de9ca54ddbba0c1d54587e5c0f
Publikováno v:
Evolutionary Bioinformatics, Vol 14 (2018)
Background: Current advancements in next-generation sequencing technology have made possible to sequence whole genome but assembling a large number of short sequence reads is still a big challenge. In this article, we present the comparative study of
Externí odkaz:
https://doaj.org/article/3ffdf2a0e0d046749b0a3ad5f0d222ac
Publikováno v:
Molecular Biology Reports. 50:4017-4027
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b9163397dae1d4dfd051f1f64cf950b
https://doi.org/10.1007/s11033-023-08304-9
https://doi.org/10.1007/s11033-023-08304-9
Publikováno v:
2022 3rd International Conference on Innovations in Computer Science & Software Engineering (ICONICS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a62b3a14ec7f9402acbd84f55bed323
https://doi.org/10.1109/iconics56716.2022.10100591
https://doi.org/10.1109/iconics56716.2022.10100591
Autor:
Aiysha Abid, Ali Raza, Abdul Rafay Khan, Sadaf Firasat, Saba Shahid, Seema Hashmi, Mirza Naqi Zafar, Sajid Sultan, Shagufta Khaliq, Syed Adib‐ul‐Hasan Rizvi
Publikováno v:
Clinical geneticsREFERENCES.
The primary hyperoxalurias are rare disorders of glyoxylate metabolism. Accurate diagnosis is essential for therapeutic and management strategies. We conducted a molecular study on patients suffering from recurrent calcium-oxalate stones and nephroca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8174805e52c81c3e560d3516f9085d
https://pubmed.ncbi.nlm.nih.gov/36185032
https://pubmed.ncbi.nlm.nih.gov/36185032
Autor:
Abdul Rafay Khan, Ghazala Kausar
Publikováno v:
Linguistics and Literature Review. 7:1-15
Case is a morphological realization on a noun phrase (NP) to represent the NP's grammatical relationship with the main verb of the clause. With respect to case, languages, in many cases, can be broadly divided into two alignment systems, i.e., ergati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd6b773b7e3493e9b00bb163180a8d73
https://doi.org/10.32350/llr.71.01
https://doi.org/10.32350/llr.71.01
Publikováno v:
The Pharmacogenomics Journal. 20:553-562
Tacrolimus is an immunosuppressive drug widely used in kidney transplantation. Cytochrome P450 3A5 (CYP3A5) protein is involved in tacrolimus metabolism. Single nucleotide polymorphism in the CYP3A5 gene (6986A>G) results in alteration in metabolic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e41e5d1d22563688fb7830e1bed8bced
https://doi.org/10.1038/s41397-019-0144-7
https://doi.org/10.1038/s41397-019-0144-7
COVID-19 displays marked variability in the clinical course as well as regional epidemiology. Abnormalities in RAAS system especially stemming from genetic variability in ACE and ACE2 expression (including ACE I/D polymorphism) have been proposed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb068f6dd213b02d783b7fc68e44f559
https://doi.org/10.21203/rs.3.rs-259633/v1
https://doi.org/10.21203/rs.3.rs-259633/v1
Autor:
Humaira Najma, Ali Amar, Mumtaz Ahmad, Aiysha Abid, Abdul Rafay Khan, Athar Hameed, Shagufta Khaliq, Ayesha Afzal
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
Background Urolithiasis is a worldwide urological problem with significant contribution of genetic factors. Pakistan, which resides within the Afro-Asian stone belt, has a high reported prevalence (12%) of urolithiasis. Osteopontin (SPP1) is a urinar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53bc00577eb9076083bbda85a86a7ab9
https://doi.org/10.21203/rs.2.24295/v6
https://doi.org/10.21203/rs.2.24295/v6