Mirza Jawad Ul Hasnain
Overview
Explore the profile of Mirza Jawad Ul Hasnain including associated specialties, affiliations and a list of published articles.
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6
Citations
56
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Recent Articles
1.
Babar M, Ali A, Abbas S, Hasnain M, Babar N, Babar H, et al.
Iran J Public Health
. 2023 Feb;
51(9):2048-2059.
PMID: 36743378
Background: Retinitis pigmentosa (RP) belongs to pigmentary retinopathies, a generic name for all retinal dystrophies with a major phenotypical and genotypical variation, characterized by progressive reduction of photo-receptor functionality of...
2.
Makhdoom M, Maqbool A, Muhammad H, Makhdoom S, Ashraf H, Hasnain M, et al.
Cell Mol Biol (Noisy-le-grand)
. 2022 Dec;
68(7):40-45.
PMID: 36495521
Parthenium hysterophorus has been used to cure cancer, fever, malaria, diarrhea, dysentery, and neurologic disorders. This study evaluates the anti-diabetic effects of methanolic extract of P. hysterophorus (MEPH) in alloxan-induced...
3.
Pervez M, Hasnain M, Abbas S, Moustafa M, Aslam N, Shah S
Biomed Res Int
. 2022 Oct;
2022:3457806.
PMID: 36212714
Background: Next-generation sequencing methods have been developed and proposed to investigate any query in genomics or clinical activity involving DNA. Technical advancement in these sequencing methods has enhanced sequencing volume...
4.
Hasnain M, Amin F, Ghani A, Ahmad S, Rahman Z, Aslam T, et al.
IEEE/ACM Trans Comput Biol Bioinform
. 2021 Oct;
19(6):3715-3724.
PMID: 34613918
Parkinson's disease is the second most common progressive neurodegenerative movement disorder. Mutations in retromer complex subunit and VPS35 represent the second most common cause of late-onset familial Parkinson's disease. The...
5.
Anwar T, Hasnain M, Sarwar A, Kanwal H, Afzal B, Babar M, et al.
Pak J Pharm Sci
. 2020 Mar;
33(1(Supplementary)):287-294.
PMID: 32122860
The PHLPP (Pleckstrin homology domain leucine-rich repeat protein phosphatases) is a newly discovered group of genes which includes PHLPP1 and PHLPP2 and plays an integral part in several cellular processes...
6.
Hasnain M, Shoaib M, Qadri S, Afzal B, Anwar T, Abbas S, et al.
PLoS One
. 2020 Jan;
15(1):e0225368.
PMID: 31971949
Single Nucleotide Polymorphisms (SNPs) are the most common candidate mutations in human beings that play a vital role in the genetic basis of certain diseases. Previous studies revealed that Solute...