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Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.
Hum Mol Genet. 2017 Aug 15;26(16):3031-3045. doi: 10.1093/hmg/ddx140.
Hum Mol Genet. 2017.
PMID: 28521042
Free PMC article.
Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.
Alrayes N, Mallah BA, Issa NM, Banaganapalli B, Ahmad Shaik N, Nasser KK, Alshehri BA, Bhuiyan ZA, Bdier AY, Al-Aama JY.
Alrayes N, et al. Among authors: ahmad shaik n.
Gene. 2023 Jan 30;851:146909. doi: 10.1016/j.gene.2022.146909. Epub 2022 Sep 23.
Gene. 2023.
PMID: 36162527
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Identifying significant genes and functionally enriched pathways in familial hypercholesterolemia using integrated gene co-expression network analysis.
Awan Z, Alrayes N, Khan Z, Almansouri M, Ibrahim Hussain Bima A, Almukadi H, Ibrahim Kutbi H, Jayasheela Shetty P, Ahmad Shaik N, Banaganapalli B.
Awan Z, et al. Among authors: ahmad shaik n.
Saudi J Biol Sci. 2022 May;29(5):3287-3299. doi: 10.1016/j.sjbs.2022.02.002. Epub 2022 Feb 9.
Saudi J Biol Sci. 2022.
PMID: 35844366
Free PMC article.
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Tumor necrosis factor alpha -C850T polymorphism is significantly associated with endometriosis in Asian Indian women.
Lakshmi KV, Shetty P, Vottam K, Govindhan S, Ahmad SN, Hasan Q.
Lakshmi KV, et al.
Fertil Steril. 2010 Jul;94(2):453-6. doi: 10.1016/j.fertnstert.2009.03.020. Epub 2009 Apr 25.
Fertil Steril. 2010.
PMID: 19394608
Free article.
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