Khalil A - Search Results

1

A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases.

Khalil A, Tanos R, El-Hachem N, Kurban M, Bouvagnet P, Bitar F, Nemer G. Khalil A, et al. Sci Rep. 2017 May 3;7(1):1416. doi: 10.1038/s41598-017-01641-3. Sci Rep. 2017. PMID: 28469241 Free PMC article.

2

AutoDock and AutoDockTools for Protein-Ligand Docking: Beta-Site Amyloid Precursor Protein Cleaving Enzyme 1(BACE1) as a Case Study.

El-Hachem N, Haibe-Kains B, Khalil A, Kobeissy FH, Nemer G. El-Hachem N, et al. Among authors: khalil a. Methods Mol Biol. 2017;1598:391-403. doi: 10.1007/978-1-4939-6952-4_20. Methods Mol Biol. 2017. PMID: 28508374

3

TBX2 subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detection.

Khalil AA, Sivakumar S, Lucas FAS, McDowell T, Lang W, Tabata K, Fujimoto J, Yatabe Y, Spira A, Scheet P, Nemer G, Kadara H. Khalil AA, et al. Oncotarget. 2017 Aug 4;8(40):68230-68241. doi: 10.18632/oncotarget.19938. eCollection 2017 Sep 15. Oncotarget. 2017. PMID: 28978111 Free PMC article.

4

A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations.

Khalil A, Al-Haddad C, Hariri H, Shibbani K, Bitar F, Kurban M, Nemer G, Arabi M. Khalil A, et al. Front Cardiovasc Med. 2017 Sep 20;4:58. doi: 10.3389/fcvm.2017.00058. eCollection 2017. Front Cardiovasc Med. 2017. PMID: 28979898 Free PMC article.

5

Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes.

Khalil A, Dekmak B, Boulos F, Kantrowitz J, Spira A, Fujimoto J, Kadara H, El-Hachem N, Nemer G. Khalil A, et al. Front Oncol. 2018 Oct 30;8:482. doi: 10.3389/fonc.2018.00482. eCollection 2018. Front Oncol. 2018. PMID: 30425966 Free PMC article.

6

Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis.

Hariri H, Kurban M, Al-Haddad C, Fahed AC, Poladian S, Khalil A, Abbas O, Arabi M, Bitar F, Nemer G. Hariri H, et al. Among authors: khalil a. J Dermatol Sci. 2018 Dec;92(3):237-244. doi: 10.1016/j.jdermsci.2018.11.003. Epub 2018 Nov 10. J Dermatol Sci. 2018. PMID: 30514661

7

Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases.

Refaat MM, Hassanieh S, Ballout JA, Zakka P, Hotait M, Khalil A, Bitar F, Arabi M, Arnaout S, Skouri H, Abchee A, Abi-Saleh B, Khoury M, Massouras A, Nemer G. Refaat MM, et al. Among authors: khalil a. BMC Med Genomics. 2019 Feb 14;12(1):33. doi: 10.1186/s12920-019-0478-7. BMC Med Genomics. 2019. PMID: 30764827 Free PMC article.

8

Epigenetic Suppression of the T-box Subfamily 2 (TBX2) in Human Non-Small Cell Lung Cancer.

Nehme E, Rahal Z, Sinjab A, Khalil A, Chami H, Nemer G, Kadara H. Nehme E, et al. Among authors: khalil a. Int J Mol Sci. 2019 Mar 7;20(5):1159. doi: 10.3390/ijms20051159. Int J Mol Sci. 2019. PMID: 30866410 Free PMC article.

9

A Cautious Note on Thalidomide Usage in Cancer Treatment: Genetic Profiling of the TBX2 Sub-Family Gene Expression is Required.

Nemer G, Khalil A. Nemer G, et al. Among authors: khalil a. Drug Res (Stuttg). 2019 Sep;69(9):512-518. doi: 10.1055/a-0873-3529. Epub 2019 Apr 1. Drug Res (Stuttg). 2019. PMID: 30934098 Review.

10

Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF.

Khalil A, Karroum SB, Barake R, Dunya G, Abou-Rizk S, Kamar A, Nemer G, Bassim M. Khalil A, et al. BMC Med Genet. 2020 Jan 2;21(1):1. doi: 10.1186/s12881-019-0942-4. BMC Med Genet. 2020. PMID: 31898538 Free PMC article.

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