Noy-Lotan S - Search Results

1

Cdan1 Is Essential for Primitive Erythropoiesis.

Noy-Lotan S, Dgany O, Marcoux N, Atkins A, Kupfer GM, Bosques L, Gottschalk C, Steinberg-Shemer O, Motro B, Tamary H. Noy-Lotan S, et al. Front Physiol. 2021 Jun 21;12:685242. doi: 10.3389/fphys.2021.685242. eCollection 2021. Front Physiol. 2021. PMID: 34234691 Free PMC article.

2

Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated.

Noy-Lotan S, Dgany O, Lahmi R, Marcoux N, Krasnov T, Yissachar N, Ginsberg D, Motro B, Resnitzky P, Yaniv I, Kupfer GM, Tamary H. Noy-Lotan S, et al. Haematologica. 2009 May;94(5):629-37. doi: 10.3324/haematol.2008.003327. Epub 2009 Mar 31. Haematologica. 2009. PMID: 19336738 Free PMC article.

3

Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli Arabs.

Gilad O, Dgany O, Noy-Lotan S, Krasnov T, Elitzur S, Pissard S, Kventsel I, Yacobovich J, Tamary H. Gilad O, et al. Hemoglobin. 2014;38(5):319-24. doi: 10.3109/03630269.2014.954668. Epub 2014 Sep 15. Hemoglobin. 2014. PMID: 25222045

4

Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis.

Steinberg-Shemer O, Keel S, Dgany O, Walsh T, Noy-Lotan S, Krasnov T, Yacobovich J, Quarello P, Ramenghi U, King MC, Shimamura A, Tamary H. Steinberg-Shemer O, et al. J Pediatr Hematol Oncol. 2016 Oct;38(7):e260-2. doi: 10.1097/MPH.0000000000000587. J Pediatr Hematol Oncol. 2016. PMID: 27258031 Free PMC article.

5

Molecular diagnosis of α-thalassemia in a multiethnic population.

Gilad O, Shemer OS, Dgany O, Krasnov T, Nevo M, Noy-Lotan S, Rabinowicz R, Amitai N, Ben-Dor S, Yaniv I, Yacobovich J, Tamary H. Gilad O, et al. Eur J Haematol. 2017 Jun;98(6):553-562. doi: 10.1111/ejh.12866. Epub 2017 Apr 6. Eur J Haematol. 2017. PMID: 28160324

6

Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.

Steinberg-Shemer O, Ulirsch JC, Noy-Lotan S, Krasnov T, Attias D, Dgany O, Laor R, Sankaran VG, Tamary H. Steinberg-Shemer O, et al. Cold Spring Harb Mol Case Stud. 2017 Nov 21;3(6):a001941. doi: 10.1101/mcs.a001941. Print 2017 Nov. Cold Spring Harb Mol Case Stud. 2017. PMID: 28667000 Free PMC article.

7

Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.

Shefer Averbuch N, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Yacobovich J, Kuperman AA, Kattamis A, Ben Barak A, Roth-Jelinek B, Chubar E, Shabad E, Dufort G, Ellis M, Wolach O, Pazgal I, Abu Quider A, Miskin H, Tamary H. Shefer Averbuch N, et al. Eur J Haematol. 2018 Sep;101(3):297-304. doi: 10.1111/ejh.13097. Epub 2018 Jun 25. Eur J Haematol. 2018. PMID: 29786897

8

Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Steinberg-Shemer O, Goldberg TA, Yacobovich J, Levin C, Koren A, Revel-Vilk S, Ben-Ami T, Kuperman AA, Zemer VS, Toren A, Kapelushnik J, Ben-Barak A, Miskin H, Krasnov T, Noy-Lotan S, Dgany O, Tamary H. Steinberg-Shemer O, et al. Among authors: noy lotan s. Haematologica. 2020 Jul;105(7):1825-1834. doi: 10.3324/haematol.2019.222877. Epub 2019 Sep 26. Haematologica. 2020. PMID: 31558676 Free PMC article.

9

Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So Silent.

Gilad O, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Tamary H, Yacobovich J. Gilad O, et al. Among authors: noy lotan s. Acta Haematol. 2020;143(5):432-437. doi: 10.1159/000503023. Epub 2020 Jan 14. Acta Haematol. 2020. PMID: 31935715

10

Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease.

Swickley G, Bloch Y, Malka L, Meiri A, Noy-Lotan S, Yanai A, Tamary H, Motro B. Swickley G, et al. Among authors: noy lotan s. BMC Mol Cell Biol. 2020 Mar 23;21(1):18. doi: 10.1186/s12860-020-00258-1. BMC Mol Cell Biol. 2020. PMID: 32293259 Free PMC article.

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