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Year Number of Results
2000 1
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2014 1
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2019 5
2020 4
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Page 1
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis.
Delamare M, Le Roy A, Pacault M, Schmitt L, Garrec C, Maaziz N, Myllykoski M, Rimbert A, Karaghiannis V, Aral B, Catherwood M, Airaud F, Mansour-Hendili L, Hoogewijs D, Peroni E, Idriss S, Lesieur V, Caillaud A, Si-Tayeb K, Chariau C, Gaignerie A, Rab M, Haferlach T, Meggendorfer M, Bézieau S, Benetti A, Casadevall N, Hirsch P, Rose C, Wemeau M, Galacteros F, Cassinat B, Bellosillo B, Bento C, Van Wijk R, Petrides PE, Randi ML, McMullin MF, Koivunen P, Girodon F, Gardie B; ECYT-3 consortium. Delamare M, et al. Haematologica. 2023 Nov 1;108(11):3068-3085. doi: 10.3324/haematol.2023.282913. Haematologica. 2023. PMID: 37317877 Free PMC article.
Identification of Variants Associated With Rare Hematological Disorder Erythrocytosis Using Targeted Next-Generation Sequencing Analysis.
Kristan A, Pajič T, Maver A, Režen T, Kunej T, Količ R, Vuga A, Fink M, Žula Š, Podgornik H, Anžej Doma S, Preložnik Zupan I, Rozman D, Debeljak N. Kristan A, et al. Among authors: debeljak n. Front Genet. 2021 Jul 19;12:689868. doi: 10.3389/fgene.2021.689868. eCollection 2021. Front Genet. 2021. PMID: 34349782 Free PMC article.
STAT5 as a Key Protein of Erythropoietin Signalization.
Tóthová Z, Tomc J, Debeljak N, Solár P. Tóthová Z, et al. Among authors: debeljak n. Int J Mol Sci. 2021 Jul 1;22(13):7109. doi: 10.3390/ijms22137109. Int J Mol Sci. 2021. PMID: 34281163 Free PMC article. Review.
37 results