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Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease.
Bokhari HA, Shaik NA, Banaganapalli B, Nasser KK, Ageel HI, Al Shamrani AS, Rashidi OM, Al Ghubayshi OY, Shaik J, Ahmad A, Alrayes NM, Al-Aama JY, Elango R, Saadah OI. Bokhari HA, et al. Among authors: nasser kk. Saudi J Biol Sci. 2020 Jun;27(6):1494-1502. doi: 10.1016/j.sjbs.2020.04.011. Epub 2020 Apr 14. Saudi J Biol Sci. 2020. PMID: 32489286 Free PMC article.
Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects.
Gaboon NEA, Banaganapalli B, Nasser K, Razeeth M, Alsaedi MS, Rashidi OM, Abdelwehab LS, Alahmadi TS, Safdar OY, Shaik J, Choudhry HMZ, Al-Numan HH, Khan MI, Al-Aama JY, Elango R, Shaik NA. Gaboon NEA, et al. Saudi J Biol Sci. 2020 Jan;27(1):324-334. doi: 10.1016/j.sjbs.2019.10.001. Epub 2019 Oct 18. Saudi J Biol Sci. 2020. PMID: 31889854 Free PMC article.
SHH Signaling as a Key Player in Endometrial Cancer: Unveiling the Correlation with Good Prognosis, Low Proliferation, and Anti-Tumor Immune Milieu.
Snijesh VP, Krishnamurthy S, Bhardwaj V, Punya KM, Niranjana Murthy AS, Almutadares M, Habhab WT, Nasser KK, Banaganapalli B, Shaik NA, Albaqami WF. Snijesh VP, et al. Among authors: nasser kk. Int J Mol Sci. 2024 Sep 27;25(19):10443. doi: 10.3390/ijms251910443. Int J Mol Sci. 2024. PMID: 39408773 Free PMC article.
Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects.
Alsafwani RS, Nasser KK, Shinawi T, Banaganapalli B, ElSokary HA, Zaher ZF, Shaik NA, Abdelmohsen G, Al-Aama JY, Shapiro AJ, O Al-Radi O, Elango R, Alahmadi T. Alsafwani RS, et al. Among authors: nasser kk. Front Med (Lausanne). 2021 Sep 13;8:724826. doi: 10.3389/fmed.2021.724826. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34589502 Free PMC article.
21 results