Detalhe da pesquisa
1.
Identification of Four Novel Candidate Genes for Non-syndromic Intellectual Disability in Pakistani Families.
Biochem Genet
; 2023 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37985543
2.
The molecular genetics of human appendicular skeleton.
Mol Genet Genomics
; 297(5): 1195-1214, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35907958
3.
Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein-truncating mutations of ASPM.
Biotechnol Appl Biochem
; 69(6): 2296-2303, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34826358
4.
A novel protein truncating mutation in L2HGDH causes L-2-hydroxyglutaric aciduria in a consanguineous Pakistani family.
Metab Brain Dis
; 37(1): 243-252, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34719772
5.
A Novel Distachionate from Breynia distachia Treats Inflammations by Modulating COX-2 and Inflammatory Cytokines in Rat Liver Tissue.
Molecules
; 27(8)2022 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35458792
6.
Preparation and Characterization of Controlled-Release Floating Bilayer Tablets of Esomeprazole and Clarithromycin.
Molecules
; 27(10)2022 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35630719
7.
Preparation of Losartan Potassium Controlled Release Matrices and In-Vitro Investigation Using Rate Controlling Agents.
Molecules
; 27(3)2022 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35164127
8.
Synthesis of Starch-Grafted Polymethyl Methacrylate via Free Radical Polymerization Reaction and Its Application for the Uptake of Methylene Blue.
Molecules
; 27(18)2022 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36144579
9.
Pharmacological Properties of 4', 5, 7-Trihydroxyflavone (Apigenin) and Its Impact on Cell Signaling Pathways.
Molecules
; 27(13)2022 Jul 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35807549
10.
Alopecia-mental retardation syndrome: Molecular genetics of a rare neuro-dermal disorder.
Ann Hum Genet
; 85(5): 147-154, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33881165
11.
The molecular genetics of UV-Sensitive syndrome: A rare dermal anomaly.
J Pak Med Assoc
; 71(10): 2391-2396, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34974577
12.
A Parallel Architecture for the Partitioning Around Medoids (PAM) Algorithm for Scalable Multi-Core Processor Implementation with Applications in Healthcare.
Sensors (Basel)
; 18(12)2018 Nov 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30477277
13.
Current updates on genetic spectrum of usher syndrome.
Nucleosides Nucleotides Nucleic Acids
; : 1-24, 2024 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38718411
14.
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly.
Genes (Basel)
; 14(4)2023 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37107627
15.
Genetic basis of ß-thalassemia in families of pashtun ethnicity in Dera Ismail Khan district of Khyber Pakhtun-Khwa province, Pakistan.
Expert Rev Hematol
; 16(9): 693-699, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37491848
16.
Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms.
Front Neurol
; 14: 1168307, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37305761
17.
A Study on the Adoption of Blockchain for IoT Devices in Supply Chain.
Comput Intell Neurosci
; 2022: 9228982, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35909824
18.
Preparation and In Vitro Evaluation of Controlled-Release Matrices of Losartan Potassium Using Ethocel Grade 10 and Carbopol 934P NF as Rate-Controlling Polymers.
Polymers (Basel)
; 14(15)2022 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35893957
19.
In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 Gene.
Genes (Basel)
; 13(4)2022 04 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35456478
20.
In Silico Analysis of the L-2-Hydroxyglutarate Dehydrogenase Gene Mutations and Their Biological Impact on Disease Etiology.
Genes (Basel)
; 13(4)2022 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35456504