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

Year Number of Results
2002 1
2003 1
2004 1
2005 2
2007 2
2008 2
2009 6
2010 3
2011 4
2012 10
2013 9
2014 7
2015 8
2016 7
2017 10
2018 8
2019 13
2020 10
2021 3
2022 10
2023 12
2024 3

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120 results

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The following term was not found in PubMed: Meza-Gastelum
Page 1
G-quadruplex structures mark human regulatory chromatin.
Hänsel-Hertsch R, Beraldi D, Lensing SV, Marsico G, Zyner K, Parry A, Di Antonio M, Pike J, Kimura H, Narita M, Tannahill D, Balasubramanian S. Hänsel-Hertsch R, et al. Among authors: di antonio m. Nat Genet. 2016 Oct;48(10):1267-72. doi: 10.1038/ng.3662. Epub 2016 Sep 12. Nat Genet. 2016. PMID: 27618450
Asthma: Differential Diagnosis and Comorbidities.
Ullmann N, Mirra V, Di Marco A, Pavone M, Porcaro F, Negro V, Onofri A, Cutrera R. Ullmann N, et al. Among authors: di marco a. Front Pediatr. 2018 Oct 3;6:276. doi: 10.3389/fped.2018.00276. eCollection 2018. Front Pediatr. 2018. PMID: 30338252 Free PMC article. Review.
Exercise-Induced Bronchospasm and Allergy.
Caggiano S, Cutrera R, Di Marco A, Turchetta A. Caggiano S, et al. Among authors: di marco a. Front Pediatr. 2017 Jun 8;5:131. doi: 10.3389/fped.2017.00131. eCollection 2017. Front Pediatr. 2017. PMID: 28642859 Free PMC article. Review.
Replication-induced DNA secondary structures drive fork uncoupling and breakage.
Williams SL, Casas-Delucchi CS, Raguseo F, Guneri D, Li Y, Minamino M, Fletcher EE, Yeeles JT, Keyser UF, Waller ZA, Di Antonio M, Coster G. Williams SL, et al. Among authors: di antonio m. EMBO J. 2023 Nov 15;42(22):e114334. doi: 10.15252/embj.2023114334. Epub 2023 Oct 2. EMBO J. 2023. PMID: 37781931 Free PMC article.
Difficult and Severe Asthma in Children.
Porcaro F, Ullmann N, Allegorico A, Di Marco A, Cutrera R. Porcaro F, et al. Among authors: di marco a. Children (Basel). 2020 Dec 10;7(12):286. doi: 10.3390/children7120286. Children (Basel). 2020. PMID: 33322016 Free PMC article. Review.
Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Quaio CRDC, Moreira CM, Novo-Filho GM, Sacramento-Bobotis PR, Groenner Penna M, Perazzio SF, Dutra AP, da Silva RA, Santos MNP, de Arruda VYN, Freitas VG, Pereira VC, Pintao MC, Fornari ARDS, Buzolin AL, Oku AY, Burger M, Ramalho RF, Marco Antonio DS, E Ferreira EN, Pereira OJE, Cantagalli VD, Trindade ACG, de Sousa RRF, Reys Furuzawa C, Verzini F, Matalhana SD, Romano N, Paixão D, Olivati C, Spolador GM, Maciel GAR, Rocha VZ, Miguelez J, de Carvalho MHB, de Souza AWS, Andrade LEC, Chauffaille ML, Perazzio ADSB, Catelani ALPM, Mitne-Neto M, Kim CA, Baratela WADR. Quaio CRDC, et al. Among authors: marco antonio ds. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):955-964. doi: 10.1002/ajmg.c.31860. Epub 2020 Nov 30. Am J Med Genet C Semin Med Genet. 2020. PMID: 33258288
The Origin and Evolution of Maternal Genes.
Marco A. Marco A. Results Probl Cell Differ. 2017;63:483-494. doi: 10.1007/978-3-319-60855-6_20. Results Probl Cell Differ. 2017. PMID: 28779330 Review.
ECG, December 2019.
Ribes F, Marco A, Sánchez A. Ribes F, et al. Among authors: marco a. Rev Esp Cardiol (Engl Ed). 2019 Dec;72(12):1079. doi: 10.1016/j.rec.2019.05.013. Rev Esp Cardiol (Engl Ed). 2019. PMID: 31779965 English, Spanish. No abstract available.
120 results