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NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variants.
Michelini S, Ricci M, Serrani R, Barati S, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Basha SH, Priya S, Dautaj A, Dundar M, Krajcovic J, Bertelli M. Michelini S, et al. Among authors: dundar m. Mol Genet Genomic Med. 2021 Jan;9(1):e1529. doi: 10.1002/mgg3.1529. Epub 2020 Nov 28. Mol Genet Genomic Med. 2021. PMID: 33247628 Free PMC article.
Genetic tests for low- and middle-income countries: a literature review.
Maltese PE, Poplavskaia E, Malyutkina I, Sirocco F, Bonizzato A, Capodicasa N, Nicoulina SY, Salmina A, Aksutina N, Dundar M, Beccari T, Cecchin S, Bertelli M. Maltese PE, et al. Among authors: dundar m. Genet Mol Res. 2017 Feb 8;16(1). doi: 10.4238/gmr16019466. Genet Mol Res. 2017. PMID: 28198508 Free article. Review.
Genetic background, nutrition and obesity: a review.
Vettori A, Pompucci G, Paolini B, Del Ciondolo I, Bressan S, Dundar M, Kenanoğlu S, Unfer V, Bertelli M; Geneob Project. Vettori A, et al. Among authors: dundar m. Eur Rev Med Pharmacol Sci. 2019 Feb;23(4):1751-1761. doi: 10.26355/eurrev_201902_17137. Eur Rev Med Pharmacol Sci. 2019. PMID: 30840300 Free article. Review.
The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.
Dundar A, Bayramov R, Onal MG, Akkus M, Dogan ME, Kenanoglu S, Cerrah Gunes M, Kazimli U, Ozbek MN, Ercan O, Yildirim R, Celmeli G, Parlak M, Dundar I, Hatipoglu N, Unluhizarci K, Akalin H, Ozkul Y, Saatci C, Dundar M. Dundar A, et al. Among authors: dundar i, dundar m. Mol Biol Rep. 2019 Aug;46(4):3677-3690. doi: 10.1007/s11033-019-04809-4. Epub 2019 Apr 20. Mol Biol Rep. 2019. PMID: 31006099
Two rare PROX1 variants in patients with lymphedema.
Ricci M, Amato B, Barati S, Compagna R, Veselenyiova D, Kenanoglu S, Stuppia L, Beccari T, Baglivo M, Kurti D, Krajcovic J, Serrani R, Dundar M, Basha SH, Chiurazzi P, Bertelli M. Ricci M, et al. Among authors: dundar m. Mol Genet Genomic Med. 2020 Oct;8(10):e1424. doi: 10.1002/mgg3.1424. Epub 2020 Aug 5. Mol Genet Genomic Med. 2020. PMID: 32757260 Free PMC article.
Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes.
Ricci M, Compagna R, Amato B, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Basha SH, Serrani R, Miggiano GAD, Aquilanti B, Matera G, Marceddu G, Velluti V, Gagliardi L, Dundar M, Krajcovic J, Bertelli M. Ricci M, et al. Among authors: dundar m. Int J Genomics. 2020 Aug 25;2020:3781791. doi: 10.1155/2020/3781791. eCollection 2020. Int J Genomics. 2020. PMID: 32908855 Free PMC article.
TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema.
Michelini S, Ricci M, Veselenyiova D, Kenanoglu S, Kurti D, Baglivo M, Fiorentino A, Basha SH, Priya S, Serrani R, Krajcovic J, Dundar M, Dautaj A, Bertelli M. Michelini S, et al. Among authors: dundar m. Int J Mol Sci. 2020 Sep 16;21(18):6780. doi: 10.3390/ijms21186780. Int J Mol Sci. 2020. PMID: 32947856 Free PMC article.
Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants.
Michelini S, Ricci M, Serrani R, Stuppia L, Beccari T, Veselenyiova D, Kenanoglu S, Barati S, Kurti D, Baglivo M, Basha SH, Krajcovic J, Dundar M, Bertelli M. Michelini S, et al. Among authors: dundar m. Lymphat Res Biol. 2021 Apr;19(2):129-133. doi: 10.1089/lrb.2020.0030. Epub 2020 Sep 22. Lymphat Res Biol. 2021. PMID: 32960152 Review.
287 results