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

Year Number of Results
1998 3
1999 1
2000 1
2001 1
2002 2
2003 1
2004 3
2005 5
2006 5
2007 6
2008 2
2009 5
2010 3
2011 12
2012 15
2013 11
2014 8
2015 7
2016 8
2017 7
2018 8
2019 13
2020 7
2021 10
2022 0
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Search Results

124 results
Results by year
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Page 1
Thymic regulatory T cells arise via two distinct developmental programs.
Owen DL, Mahmud SA, Sjaastad LE, Williams JB, Spanier JA, Simeonov DR, Ruscher R, Huang W, Proekt I, Miller CN, Hekim C, Jeschke JC, Aggarwal P, Broeckel U, LaRue RS, Henzler CM, Alegre ML, Anderson MS, August A, Marson A, Zheng Y, Williams CB, Farrar MA. Owen DL, et al. Among authors: broeckel u. Nat Immunol. 2019 Feb;20(2):195-205. doi: 10.1038/s41590-018-0289-6. Epub 2019 Jan 14. Nat Immunol. 2019. PMID: 30643267 Free PMC article.
A Platform for Generation of Chamber-Specific Cardiac Tissues and Disease Modeling.
Zhao Y, Rafatian N, Feric NT, Cox BJ, Aschar-Sobbi R, Wang EY, Aggarwal P, Zhang B, Conant G, Ronaldson-Bouchard K, Pahnke A, Protze S, Lee JH, Davenport Huyer L, Jekic D, Wickeler A, Naguib HE, Keller GM, Vunjak-Novakovic G, Broeckel U, Backx PH, Radisic M. Zhao Y, et al. Among authors: broeckel u. Cell. 2019 Feb 7;176(4):913-927.e18. doi: 10.1016/j.cell.2018.11.042. Epub 2019 Jan 24. Cell. 2019. PMID: 30686581 Free PMC article.
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.
Kraja AT, Liu C, Fetterman JL, Graff M, Have CT, Gu C, Yanek LR, Feitosa MF, Arking DE, Chasman DI, Young K, Ligthart S, Hill WD, Weiss S, Luan J, Giulianini F, Li-Gao R, Hartwig FP, Lin SJ, Wang L, Richardson TG, Yao J, Fernandez EP, Ghanbari M, Wojczynski MK, Lee WJ, Argos M, Armasu SM, Barve RA, Ryan KA, An P, Baranski TJ, Bielinski SJ, Bowden DW, Broeckel U, Christensen K, Chu AY, Corley J, Cox SR, Uitterlinden AG, Rivadeneira F, Cropp CD, Daw EW, van Heemst D, de Las Fuentes L, Gao H, Tzoulaki I, Ahluwalia TS, de Mutsert R, Emery LS, Erzurumluoglu AM, Perry JA, Fu M, Forouhi NG, Gu Z, Hai Y, Harris SE, Hemani G, Hunt SC, Irvin MR, Jonsson AE, Justice AE, Kerrison ND, Larson NB, Lin KH, Love-Gregory LD, Mathias RA, Lee JH, Nauck M, Noordam R, Ong KK, Pankow J, Patki A, Pattie A, Petersmann A, Qi Q, Ribel-Madsen R, Rohde R, Sandow K, Schnurr TM, Sofer T, Starr JM, Taylor AM, Teumer A, Timpson NJ, de Haan HG, Wang Y, Weeke PE, Williams C, Wu H, Yang W, Zeng D, Witte DR, Weir BS, Wareham NJ, Vestergaard H, Turner ST, Torp-Pedersen C, Stergiakouli E, Sheu WH, Rosendaal FR, Ikram MA, Franco OH, Ridker PM, Perls TT, Pedersen O, Nohr EA, Newman AB, Linneberg A, Langenberg C, Kilpeläinen TO, Kardia SLR, Jørgensen ME, Jørgensen T, Sørensen TIA, Homuth G, Hansen T, Goodarzi MO, Deary IJ, Christensen C, Chen YI, Chakravarti A, Brandslund I, Bonnelykke K, Taylor KD, Wilson JG, Rodriguez S, Davies G, Horta BL, Thyagarajan B, Rao DC, Grarup N, Davila-Roman VG, Hudson G, Guo X, Arnett DK, Hayward C, Vaidya D, Mook-Kanamori DO, Tiwari HK, Levy D, Loos RJF, Dehghan A, Elliott P, Malik AN, Scott RA, Becker DM, de Andrade M, Province MA, Meigs JB, Rotter JI, North KE. Kraja AT, et al. Among authors: broeckel u. Am J Hum Genet. 2019 Jan 3;104(1):112-138. doi: 10.1016/j.ajhg.2018.12.001. Epub 2018 Dec 27. Am J Hum Genet. 2019. PMID: 30595373 Free PMC article.
Genetic determinants of hypertension: an update.
Harrison M, Maresso K, Broeckel U. Harrison M, et al. Among authors: broeckel u. Curr Hypertens Rep. 2008 Dec;10(6):488-95. doi: 10.1007/s11906-008-0091-1. Curr Hypertens Rep. 2008. PMID: 18959837 Review.
The ENTPD1 promoter polymorphism -860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk.
Maloney JP, Branchford BR, Brodsky GL, Cosmic MS, Calabrese DW, Aquilante CL, Maloney KW, Gonzalez JR, Zhang W, Moreau KL, Wiggins KL, Smith NL, Broeckel U, Di Paola J. Maloney JP, et al. Among authors: broeckel u. FASEB J. 2017 Jul;31(7):2771-2784. doi: 10.1096/fj.201600344R. Epub 2017 Mar 16. FASEB J. 2017. PMID: 28302652 Free PMC article.
Genes for left ventricular hypertrophy.
Arnett DK, de las Fuentes L, Broeckel U. Arnett DK, et al. Among authors: broeckel u. Curr Hypertens Rep. 2004 Feb;6(1):36-41. doi: 10.1007/s11906-004-0009-5. Curr Hypertens Rep. 2004. PMID: 14972088 Review.
Toward the etiologies of congenital heart diseases.
Pelech AN, Broeckel U. Pelech AN, et al. Among authors: broeckel u. Clin Perinatol. 2005 Dec;32(4):825-44, vii. doi: 10.1016/j.clp.2005.09.005. Clin Perinatol. 2005. PMID: 16325664 Review.
Incorporating G6PD genotyping to identify patients with G6PD deficiency.
Morris SA, Crews KR, Hayden RT, Takemoto CM, Yang W, Baker DK, Broeckel U, Relling MV, Haidar CE. Morris SA, et al. Among authors: broeckel u. Pharmacogenet Genomics. 2021 Oct 22. doi: 10.1097/FPC.0000000000000456. Online ahead of print. Pharmacogenet Genomics. 2021. PMID: 34693927
The future of genetic case-control studies.
Schork NJ, Fallin D, Thiel B, Xu X, Broeckel U, Jacob HJ, Cohen D. Schork NJ, et al. Among authors: broeckel u. Adv Genet. 2001;42:191-212. doi: 10.1016/s0065-2660(01)42023-2. Adv Genet. 2001. PMID: 11037322 Review.
124 results