Muhammad Muzammal - Search Results

Year	Number of Results
2018	1
2019	1
2021	5
2022	14
2023	4
2024	0

1

A Review on the Modification of Cellulose and Its Applications.

Aziz T, Farid A, Haq F, Kiran M, Ullah A, Zhang K, Li C, Ghazanfar S, Sun H, Ullah R, Ali A, Muzammal M, Shah M, Akhtar N, Selim S, Hagagy N, Samy M, Al Jaouni SK. Aziz T, et al. Among authors: muzammal m. Polymers (Basel). 2022 Aug 5;14(15):3206. doi: 10.3390/polym14153206. Polymers (Basel). 2022. PMID: 35956720 Free PMC article. Review.

2

The molecular genetics of UV-Sensitive syndrome: A rare dermal anomaly.

Muzammal M, Ali MZ, Ahmad S, Huma S; Rizwan; Ahmad S, Abbasi AA, Khan S, Khan MA. Muzammal M, et al. J Pak Med Assoc. 2021 Oct;71(10):2391-2396. doi: 10.47391/JPMA.03-476. J Pak Med Assoc. 2021. PMID: 34974577 Free article. Review.

3

Alopecia-mental retardation syndrome: Molecular genetics of a rare neuro-dermal disorder.

Muzammal M, Ahmad S, Ali MZ, Khan MA. Muzammal M, et al. Ann Hum Genet. 2021 Sep;85(5):147-154. doi: 10.1111/ahg.12425. Epub 2021 Apr 21. Ann Hum Genet. 2021. PMID: 33881165 Review.

4

The molecular genetics of human appendicular skeleton.

Ahmad S, Ali MZ, Muzammal M, Mir FA, Khan MA. Ahmad S, et al. Among authors: muzammal m. Mol Genet Genomics. 2022 Sep;297(5):1195-1214. doi: 10.1007/s00438-022-01930-1. Epub 2022 Jul 30. Mol Genet Genomics. 2022. PMID: 35907958

5

Pharmacological Properties of 4', 5, 7-Trihydroxyflavone (Apigenin) and Its Impact on Cell Signaling Pathways.

Abid R, Ghazanfar S, Farid A, Sulaman SM, Idrees M, Amen RA, Muzammal M, Shahzad MK, Mohamed MO, Khaled AA, Safir W, Ghori I, Elasbali AM, Alharbi B. Abid R, et al. Among authors: muzammal m. Molecules. 2022 Jul 4;27(13):4304. doi: 10.3390/molecules27134304. Molecules. 2022. PMID: 35807549 Free PMC article. Review.

6

Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly.

Ahmad S, Ali MZ, Muzammal M, Khan AU, Ikram M, Muurinen M, Hussain S, Loid P, Khan MA, Mäkitie O. Ahmad S, et al. Among authors: muzammal m. Genes (Basel). 2023 Apr 5;14(4):869. doi: 10.3390/genes14040869. Genes (Basel). 2023. PMID: 37107627 Free PMC article.

7

A novel protein truncating mutation in L2HGDH causes L-2-hydroxyglutaric aciduria in a consanguineous Pakistani family.

Muzammal M, Ali MZ, Brugger B, Blatterer J, Ahmad S, Taj S, Shah SK, Khan S, Enzinger C, Petek E, Wagner K, Khan MA, Windpassinger C. Muzammal M, et al. Metab Brain Dis. 2022 Jan;37(1):243-252. doi: 10.1007/s11011-021-00832-2. Epub 2021 Nov 1. Metab Brain Dis. 2022. PMID: 34719772 Free PMC article.

8

In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 Gene.

Ali MZ, Farid A, Ahmad S, Muzammal M, Mohaini MA, Alsalman AJ, Al Hawaj MA, Alhashem YN, Alsaleh AA, Almusalami EM, Maryam M, Khan MA. Ali MZ, et al. Among authors: muzammal m. Genes (Basel). 2022 Apr 11;13(4):672. doi: 10.3390/genes13040672. Genes (Basel). 2022. PMID: 35456478 Free PMC article.

9

Preparation and Characterization of Controlled-Release Floating Bilayer Tablets of Esomeprazole and Clarithromycin.

Israr M, Pugliese N, Farid A, Ghazanfar S, Di Cerbo A, Muzammal M, Alamri AS, Basheeruddin Asdaq SM, Ahmad A, Khan KA. Israr M, et al. Among authors: muzammal m. Molecules. 2022 May 18;27(10):3242. doi: 10.3390/molecules27103242. Molecules. 2022. PMID: 35630719 Free PMC article.

10

In Silico Analysis of the L-2-Hydroxyglutarate Dehydrogenase Gene Mutations and Their Biological Impact on Disease Etiology.

Muzammal M, Di Cerbo A, Almusalami EM, Farid A, Khan MA, Ghazanfar S, Al Mohaini M, Alsalman AJ, Alhashem YN, Al Hawaj MA, Alsaleh AA. Muzammal M, et al. Genes (Basel). 2022 Apr 15;13(4):698. doi: 10.3390/genes13040698. Genes (Basel). 2022. PMID: 35456504 Free PMC article.

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