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Changes in Methionine Metabolism and Histone H3 Trimethylation Are Linked to Mitochondrial Defects in Multiple Sclerosis.
J Neurosci. 2015 Nov 11;35(45):15170-86. doi: 10.1523/JNEUROSCI.4349-14.2015.
J Neurosci. 2015.
PMID: 26558787
Free PMC article.
Erythropoietin Upregulates Brain Hemoglobin Expression and Supports Neuronal Mitochondrial Activity.
Singhal NK, Alkhayer K, Shelestak J, Clements R, Freeman E, McDonough J.
Singhal NK, et al. Among authors: alkhayer k.
Mol Neurobiol. 2018 Oct;55(10):8051-8058. doi: 10.1007/s12035-018-0971-6. Epub 2018 Mar 1.
Mol Neurobiol. 2018.
PMID: 29498007
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Neuronal Hemoglobin Expression and Its Relevance to Multiple Sclerosis Neuropathology.
Brown N, Alkhayer K, Clements R, Singhal N, Gregory R, Azzam S, Li S, Freeman E, McDonough J.
Brown N, et al. Among authors: alkhayer k.
J Mol Neurosci. 2016 May;59(1):1-17. doi: 10.1007/s12031-015-0711-6. Epub 2016 Jan 25.
J Mol Neurosci. 2016.
PMID: 26809286
Free PMC article.
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Betaine restores epigenetic control and supports neuronal mitochondria in the cuprizone mouse model of multiple sclerosis.
Singhal NK, Sternbach S, Fleming S, Alkhayer K, Shelestak J, Popescu D, Weaver A, Clements R, Wasek B, Bottiglieri T, Freeman EJ, McDonough J.
Singhal NK, et al. Among authors: alkhayer k.
Epigenetics. 2020 Aug;15(8):871-886. doi: 10.1080/15592294.2020.1735075. Epub 2020 Mar 9.
Epigenetics. 2020.
PMID: 32096676
Free PMC article.
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Efficient removal of environmental pollutants by green synthesized metal nanoparticles of Clitoriaternatea.
Sa N, Alkhayer K, Behera A.
Sa N, et al. Among authors: alkhayer k.
Heliyon. 2024 Apr 23;10(9):e29865. doi: 10.1016/j.heliyon.2024.e29865. eCollection 2024 May 15.
Heliyon. 2024.
PMID: 38707360
Free PMC article.
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Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations.
Al-Khayer K, Hagstrom S, Pauer G, Zegarra H, Sears J, Traboulsi EI.
Al-Khayer K, et al.
Am J Ophthalmol. 2004 Feb;137(2):375-7. doi: 10.1016/S0002-9394(03)00913-9.
Am J Ophthalmol. 2004.
PMID: 14962443
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A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI.
Yazdani A, et al.
Am J Ophthalmol. 2003 Nov;136(5):861-5. doi: 10.1016/s0002-9394(03)00891-2.
Am J Ophthalmol. 2003.
PMID: 14597037
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Lymphedema-distichiasis syndrome and FOXC2 gene mutation.
Traboulsi EI, Al-Khayer K, Matsumoto M, Kimak MA, Crowe S, Wilson SE, Finegold DN, Ferrell RE, Meisler DM.
Traboulsi EI, et al.
Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2.
Am J Ophthalmol. 2002.
PMID: 12383817
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