Zakariyah A - Search Results

1

Association of Genetic Variant FVIII Gene and Factor VIII: A Pilot Study Among Hemophilia A Female Relatives in Saudi Arabia.

Almohammadi AT, Radhwi O, AlAhwal H, Barefah A, Bahashwan S, Ashankyty IM, Almashjari M, Ayaz R, Al-Marzouki A, Zaher GF, Hussain H, Samman AA, Zakariyah A. Almohammadi AT, et al. Among authors: zakariyah a. Cureus. 2023 Jul 17;15(7):e42038. doi: 10.7759/cureus.42038. eCollection 2023 Jul. Cureus. 2023. PMID: 37593302 Free PMC article.

2

Identification of cystic fibrosis transmembrane conductance regulator gene (CFTR) variants: A retrospective study on the western and southern regions of Saudi Arabia.

Almaghamsi T, Attiyah WB, Bahasan M, Alotaibi BA, AlAhmadi SF, Hanbazazh M, Zakariyah A, Saleem RA, AlAnezi MK, Hawsawi Y. Almaghamsi T, et al. Among authors: zakariyah a. Saudi Med J. 2023 Oct;44(10):987-994. doi: 10.15537/smj.2023.44.10.20230290. Saudi Med J. 2023. PMID: 37777263 Free PMC article.

3

Medical Students' Perception of Pathology in Saudi Arabia.

Hanbazazh M, Khashab RM, Ameen NK, Alghamdi MA, Aldawsari LS, Altoukhi SM, Samargandy S, Zakariyah A. Hanbazazh M, et al. Among authors: zakariyah a. Int J Surg Pathol. 2024 Feb 6:10668969241226708. doi: 10.1177/10668969241226708. Online ahead of print. Int J Surg Pathol. 2024. PMID: 38321866

4

The Prevalence of Risk Factors Among Children Diagnosed With Attention-Deficit/Hyperactivity Disorder, Aged 4-17 Years: A Cross-Sectional Study.

Zakariyah AF. Zakariyah AF. Cureus. 2023 Nov 21;15(11):e49161. doi: 10.7759/cureus.49161. eCollection 2023 Nov. Cureus. 2023. PMID: 38130565 Free PMC article.

5

Combinatorial Utilization of Murine Embryonic Stem Cells and In Vivo Models to Study Human Congenital Heart Disease.

Zakariyah A, Rajgara R, Shelton M, Blais A, Skerjanc IS, Burgon PG. Zakariyah A, et al. Curr Protoc Stem Cell Biol. 2019 Feb;48(1):e75. doi: 10.1002/cpsc.75. Epub 2018 Dec 12. Curr Protoc Stem Cell Biol. 2019. PMID: 30548532

6

In Vitro Modeling of Congenital Heart Defects Associated with an NKX2-5 Mutation Revealed a Dysregulation in BMP/Notch-Mediated Signaling.

Zakariyah AF, Rajgara RF, Horner E, Cattin ME, Blais A, Skerjanc IS, Burgon PG. Zakariyah AF, et al. Stem Cells. 2018 Apr;36(4):514-526. doi: 10.1002/stem.2766. Epub 2018 Jan 9. Stem Cells. 2018. PMID: 29282804

7

Congenital heart defect causing mutation in Nkx2.5 displays in vivo functional deficit.

Zakariyah AF, Rajgara RF, Veinot JP, Skerjanc IS, Burgon PG. Zakariyah AF, et al. J Mol Cell Cardiol. 2017 Apr;105:89-98. doi: 10.1016/j.yjmcc.2017.03.003. Epub 2017 Mar 14. J Mol Cell Cardiol. 2017. PMID: 28302382

8

Testosterone enhances cardiomyogenesis in stem cells and recruits the androgen receptor to the MEF2C and HCN4 genes.

Al Madhoun AS, Voronova A, Ryan T, Zakariyah A, McIntire C, Gibson L, Shelton M, Ruel M, Skerjanc IS. Al Madhoun AS, et al. Among authors: zakariyah a. J Mol Cell Cardiol. 2013 Jul;60:164-71. doi: 10.1016/j.yjmcc.2013.04.003. Epub 2013 Apr 15. J Mol Cell Cardiol. 2013. PMID: 23598283

9

TMED2/p24β1 is expressed in all gestational stages of human placentas and in choriocarcinoma cell lines.

Zakariyah A, Hou W, Slim R, Jerome-Majewska L. Zakariyah A, et al. Placenta. 2012 Mar;33(3):214-9. doi: 10.1016/j.placenta.2011.12.009. Epub 2011 Dec 31. Placenta. 2012. PMID: 22212250

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