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Year | Number of Results |
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2006 | 1 |
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Page 1
CLPP Depletion Causes Diplotene Arrest; Underlying Testis Mitochondrial Dysfunction Occurs with Accumulation of Perrault Proteins ERAL1, PEO1, and HARS2.
Cells. 2022 Dec 22;12(1):52. doi: 10.3390/cells12010052.
Cells. 2022.
PMID: 36611846
Free PMC article.
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice.
Brenner D, Sieverding K, Srinidhi J, Zellner S, Secker C, Yilmaz R, Dyckow J, Amr S, Ponomarenko A, Tunaboylu E, Douahem Y, Schlag JS, Rodríguez Martínez L, Kislinger G, Niemann C, Nalbach K, Ruf WP, Uhl J, Hollenbeck J, Schirmer L, Catanese A, Lobsiger CS, Danzer KM, Yilmazer-Hanke D, Münch C, Koch P, Freischmidt A, Fetting M, Behrends C, Parlato R, Weishaupt JH.
Brenner D, et al. Among authors: amr s.
J Exp Med. 2024 May 6;221(5):e20221190. doi: 10.1084/jem.20221190. Epub 2024 Mar 22.
J Exp Med. 2024.
PMID: 38517332
Free PMC article.
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Endogenous anti-tumorigenic nitro-fatty acids inhibit the ubiquitin-proteasome system by directly targeting the 26S proteasome.
Brat C, Huynh Phuoc HP, Awad O, Parmar BS, Hellmuth N, Heinicke U, Amr S, Grimmer J, Sürün D, Husnjak K, Carlsson M, Fahrer J, Bauer T, Krieg SC, Manolikakes G, Zacharowski K, Steinhilber D, Münch C, Maier TJ, Roos J.
Brat C, et al. Among authors: amr s.
Cell Chem Biol. 2023 Oct 19;30(10):1277-1294.e12. doi: 10.1016/j.chembiol.2023.06.017. Epub 2023 Jul 19.
Cell Chem Biol. 2023.
PMID: 37473760
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A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match.
Verheyden NA, Klostermann M, Brüggemann M, Steede HM, Scholz A, Amr S, Lichtenthaeler C, Münch C, Schmid T, Zarnack K, Krueger A.
Verheyden NA, et al. Among authors: amr s.
Nucleic Acids Res. 2024 May 23:gkae416. doi: 10.1093/nar/gkae416. Online ahead of print.
Nucleic Acids Res. 2024.
PMID: 38783381
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Adherence to antihypertensives in the United States: A comparative meta-analysis of 23 million patients.
Dean YE, Motawea KR, Shebl MA, Elawady SS, Nuhu K, Abuzuaiter B, Awayda K, Fouad AM, Tanas Y, Batista R, Elsayed A, Hassan NAIF, El-Sakka AA, Hasan W, Husain R, Lois A, Arora A, Arora A, Ayad E, Elbahaie MA, Shah J, Shady A, Chaudhuri D, Aiash H.
Dean YE, et al. Among authors: shady a.
J Clin Hypertens (Greenwich). 2024 Apr;26(4):303-313. doi: 10.1111/jch.14788. Epub 2024 Mar 15.
J Clin Hypertens (Greenwich). 2024.
PMID: 38488773
Free PMC article.
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Congenital erythropoietic porphyria: identification and expression of eight novel mutations in the uroporphyrinogen III synthase gene.
Shady AA, Colby BR, Cunha LF, Astrin KH, Bishop DF, Desnick RJ.
Shady AA, et al.
Br J Haematol. 2002 Jun;117(4):980-7. doi: 10.1046/j.1365-2141.2002.03558.x.
Br J Haematol. 2002.
PMID: 12060141
Free article.
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Uroporphyrinogen III synthase knock-in mice have the human congenital erythropoietic porphyria phenotype, including the characteristic light-induced cutaneous lesions.
Bishop DF, Johansson A, Phelps R, Shady AA, Ramirez MC, Yasuda M, Caro A, Desnick RJ.
Bishop DF, et al. Among authors: shady aa.
Am J Hum Genet. 2006 Apr;78(4):645-58. doi: 10.1086/502667. Epub 2006 Feb 9.
Am J Hum Genet. 2006.
PMID: 16532394
Free PMC article.
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