C GPD - Search Results

1

Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.

S UK, Sankar S, Younes S, D TK, Ahmad MN, Okashah SS, Kamaraj B, Al-Subaie AM, C GPD, Zayed H. S UK, et al. Among authors: c gpd. Molecules. 2020 Nov 26;25(23):5543. doi: 10.3390/molecules25235543. Molecules. 2020. PMID: 33255942 Free PMC article.

2

Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approach.

B R, C GP. B R, et al. PLoS One. 2011;6(9):e24607. doi: 10.1371/journal.pone.0024607. Epub 2011 Sep 13. PLoS One. 2011. PMID: 21931771 Free PMC article.

3

Mechanism of artemisinin resistance for malaria PfATP6 L263 mutations and discovering potential antimalarials: An integrated computational approach.

N N, C GP, Chakraborty C, V K, D TK, V B, R S, Lu A, Ge Z, Zhu H. N N, et al. Sci Rep. 2016 Jul 29;6:30106. doi: 10.1038/srep30106. Sci Rep. 2016. PMID: 27471101 Free PMC article.

4

Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach.

P S, D KT, Tanwar H, R S, C GPD, Zayed H. P S, et al. Among authors: c gpd. J Cell Biochem. 2017 Jul;118(7):1900-1910. doi: 10.1002/jcb.25920. Epub 2017 Mar 27. J Cell Biochem. 2017. PMID: 28145583

5

Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I.

Mosaeilhy A, Mohamed MM, C GPD, El Abd HSA, Gamal R, Zaki OK, Zayed H. Mosaeilhy A, et al. Among authors: c gpd. Metab Brain Dis. 2017 Oct;32(5):1417-1426. doi: 10.1007/s11011-017-0006-4. Epub 2017 Apr 7. Metab Brain Dis. 2017. PMID: 28389991

6

Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.

P S, D TK, C GPD, R S, Zayed H. P S, et al. Among authors: c gpd. PLoS One. 2017 Apr 14;12(4):e0174953. doi: 10.1371/journal.pone.0174953. eCollection 2017. PLoS One. 2017. PMID: 28410371 Free PMC article.

7

Substitution impact of highly conserved arginine residue at position 75 in GJB1 gene in association with X-linked Charcot-Marie-tooth disease: A computational study.

Agrahari AK, Kumar A, R S, Zayed H, C GPD. Agrahari AK, et al. Among authors: c gpd. J Theor Biol. 2018 Jan 21;437:305-317. doi: 10.1016/j.jtbi.2017.10.028. Epub 2017 Oct 28. J Theor Biol. 2018. PMID: 29111421

8

An integrative bioinformatics pipeline to demonstrate the alteration of the interaction between the ALDH2*2 allele with NAD⁺ and Disulfiram.

J CP, D TK, P S, R S, W CEJ, C GPD, Zayed H. J CP, et al. Among authors: c gpd. J Cell Biochem. 2019 Oct;120(10):17030-17041. doi: 10.1002/jcb.28964. Epub 2019 May 19. J Cell Biochem. 2019. PMID: 31104322

9

Bladder neoplasms and NF-κB: an unfathomed association.

Walter CEJ, Durairajan S, Periyandavan K, C GPD, G DJD, A HRV, Johnson T, Zayed H. Walter CEJ, et al. Among authors: c gpd. Expert Rev Mol Diagn. 2020 May;20(5):497-508. doi: 10.1080/14737159.2020.1743688. Epub 2020 Apr 12. Expert Rev Mol Diagn. 2020. PMID: 32228251 Review.

10

First hybrid complete genome of Aeromonas veronii reveals chromosome-mediated novel structural variant mcr-3.30 from a human clinical sample.

Ragupathi NKD, Sethuvel DPM, Anandan S, Murugan D, Asokan K, Neethi Mohan RG, Vasudevan K, D TK, C GPD, Veeraraghavan B. Ragupathi NKD, et al. Among authors: c gpd. Access Microbiol. 2020 Feb 17;2(4):acmi000103. doi: 10.1099/acmi.0.000103. eCollection 2020. Access Microbiol. 2020. PMID: 33005867 Free PMC article.

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