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Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
Kim HG, Rosenfeld JA, Scott DA, Bénédicte G, Labonne JD, Brown J, McGuire M, Mahida S, Naidu S, Gutierrez J, Lesca G, des Portes V, Bruel AL, Sorlin A, Xia F, Capri Y, Muller E, McKnight D, Torti E, Rüschendorf F, Hummel O, Islam Z, Kolatkar PR, Layman LC, Ryu D, Kong IK, Madan-Khetarpal S, Kim CH. Kim HG, et al. Among authors: islam z. Mol Autism. 2019 Oct 22;10:35. doi: 10.1186/s13229-019-0286-0. eCollection 2019. Mol Autism. 2019. PMID: 31649809 Free PMC article.
Sox2: A Regulatory Factor in Tumorigenesis and Metastasis.
Chaudhary S, Islam Z, Mishra V, Rawat S, Ashraf GM, Kolatkar PR. Chaudhary S, et al. Among authors: islam z. Curr Protein Pept Sci. 2019;20(6):495-504. doi: 10.2174/1389203720666190325102255. Curr Protein Pept Sci. 2019. PMID: 30907312 Review.
Novel engineered nanobodies specific for N-terminal region of alpha-synuclein recognize Lewy-body pathology and inhibit in-vitro seeded aggregation and toxicity.
Hmila I, Vaikath NN, Majbour NK, Erskine D, Sudhakaran IP, Gupta V, Ghanem SS, Islam Z, Emara MM, Abdesselem HB, Kolatkar PR, Achappa DK, Vinardell T, El-Agnaf OMA. Hmila I, et al. Among authors: islam z. FEBS J. 2022 Aug;289(15):4657-4673. doi: 10.1111/febs.16376. Epub 2022 Feb 25. FEBS J. 2022. PMID: 35090199 Free PMC article.
Pyridoxine non-responsive p.R336C mutation alters the molecular properties of cystathionine beta-synthase leading to severe homocystinuria phenotype.
Al-Sadeq DW, Thanassoulas A, Islam Z, Kolatkar P, Al-Dewik N, Safieh-Garabedian B, Nasrallah GK, Nomikos M. Al-Sadeq DW, et al. Among authors: islam z. Biochim Biophys Acta Gen Subj. 2022 Jul;1866(7):130148. doi: 10.1016/j.bbagen.2022.130148. Epub 2022 Apr 10. Biochim Biophys Acta Gen Subj. 2022. PMID: 35417765 Free article. No abstract available.
495 results