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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1994 1
1997 2
2002 1
2003 2
2004 1
2006 1
2009 1
2010 1
2012 2
2013 2
2014 5
2015 5
2016 6
2017 7
2018 7
2019 7
2020 8
2021 5
2022 5
2023 2
2024 2

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61 results

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Page 1
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.
Frésard L, Smail C, Ferraro NM, Teran NA, Li X, Smith KS, Bonner D, Kernohan KD, Marwaha S, Zappala Z, Balliu B, Davis JR, Liu B, Prybol CJ, Kohler JN, Zastrow DB, Reuter CM, Fisk DG, Grove ME, Davidson JM, Hartley T, Joshi R, Strober BJ, Utiramerur S; Undiagnosed Diseases Network; Care4Rare Canada Consortium; Lind L, Ingelsson E, Battle A, Bejerano G, Bernstein JA, Ashley EA, Boycott KM, Merker JD, Wheeler MT, Montgomery SB. Frésard L, et al. Nat Med. 2019 Jun;25(6):911-919. doi: 10.1038/s41591-019-0457-8. Epub 2019 Jun 3. Nat Med. 2019. PMID: 31160820 Free PMC article.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Braun DA, et al. Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14. Nat Genet. 2017. PMID: 28805828 Free PMC article.
Rivaroxaban for Stroke Prevention after Embolic Stroke of Undetermined Source.
Hart RG, Sharma M, Mundl H, Kasner SE, Bangdiwala SI, Berkowitz SD, Swaminathan B, Lavados P, Wang Y, Wang Y, Davalos A, Shamalov N, Mikulik R, Cunha L, Lindgren A, Arauz A, Lang W, Czlonkowska A, Eckstein J, Gagliardi RJ, Amarenco P, Ameriso SF, Tatlisumak T, Veltkamp R, Hankey GJ, Toni D, Bereczki D, Uchiyama S, Ntaios G, Yoon BW, Brouns R, Endres M, Muir KW, Bornstein N, Ozturk S, O'Donnell MJ, De Vries Basson MM, Pare G, Pater C, Kirsch B, Sheridan P, Peters G, Weitz JI, Peacock WF, Shoamanesh A, Benavente OR, Joyner C, Themeles E, Connolly SJ; NAVIGATE ESUS Investigators. Hart RG, et al. N Engl J Med. 2018 Jun 7;378(23):2191-2201. doi: 10.1056/NEJMoa1802686. Epub 2018 May 16. N Engl J Med. 2018. PMID: 29766772 Free article. Clinical Trial.
"Dolichoectatic Vertebrobasilar Artery Aneurysms".
Rezai Jahromi B, Niemelä M. Rezai Jahromi B, et al. Neurosurg Clin N Am. 2022 Oct;33(4):419-429. doi: 10.1016/j.nec.2022.06.003. Epub 2022 Sep 11. Neurosurg Clin N Am. 2022. PMID: 36229129 Review.
Correction to: Transient expression of human serum albumin (HSA) in tobacco leaves.
Sedaghati B, Haddad R, Bandehpour M. Sedaghati B, et al. Mol Biol Rep. 2020 Sep;47(9):7179. doi: 10.1007/s11033-020-05724-9. Mol Biol Rep. 2020. PMID: 32894434
The article 'Transient expression of human serum albumin (HSA) in tobacco leaves' written by Behnam Sedaghati, Raheem Haddad, and Mojgan Bandehpour, was originally published online on 8th July 2020 with Open Access under a Creative Commons Attribution (CC BY) license 4.0. …
The article 'Transient expression of human serum albumin (HSA) in tobacco leaves' written by Behnam Sedaghati, Raheem Haddad, and Moj …
Conformational selection in the flaviviral NS2B-NS3 protease.
Behnam MAM, Klein CDP. Behnam MAM, et al. Biochimie. 2020 Jul;174:117-125. doi: 10.1016/j.biochi.2020.04.014. Epub 2020 Apr 23. Biochimie. 2020. PMID: 32335227
The structural changes of NS3 are mediated by conserved residues and reveal a subpocket, which we denote as subpocket B, extending beyond the catalytic aspartate 75 towards the allosteric binding site, providing a unique connection between the orthosteric and allosteric si …
The structural changes of NS3 are mediated by conserved residues and reveal a subpocket, which we denote as subpocket B, extending be …
Evidence for a folded conformation of methionine- and leucine-enkephalin in a membrane environment.
Behnam BA, Deber CM. Behnam BA, et al. J Biol Chem. 1984 Dec 10;259(23):14935-40. J Biol Chem. 1984. PMID: 6501322 Free article.
These combined results, in conjunction with studies on the specific interactions of enkephalin substituents with the micelles (Deber, C. M., and Behnam, B. A., (1984) Proc. Natl. Acad. Sci. U. S. A. 81, 61-65) suggest that enkephalin folds into an intramolecularly H …
These combined results, in conjunction with studies on the specific interactions of enkephalin substituents with the micelles (Deber, C. M., …
61 results