PMC Links for Books (Select 1469674) - PMC

Select item 82556881.

Cdan1 Is Essential for Primitive Erythropoiesis

Sharon Noy-Lotan, Orly Dgany, Nathaly Marcoux, Ayelet Atkins, Gary M. Kupfer, Linette Bosques, Christine Gottschalk, Orna Steinberg-Shemer, Benny Motro, Hannah Tamary

Front Physiol. 2021; 12: 685242. Published online 2021 Jun 21. doi: 10.3389/fphys.2021.685242

PMCID:: PMC8255688

Abstract Article PDF–2.9M

Select item 70924932.

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

Grace Swickley, Yehoshua Bloch, Lidor Malka, Adi Meiri, Sharon Noy-Lotan, Amiel Yanai, Hannah Tamary, Benny Motro

BMC Mol Cell Biol. 2020; 21: 18. Published online 2020 Mar 23. doi: 10.1186/s12860-020-00258-1

PMCID:: PMC7092493

Abstract Article PDF–2.9M

Select item 66691463.

Stem cell transplantation for congenital dyserythropoietic anemia: an analysis from the European Society for Blood and Marrow Transplantation

Maurizio Miano, Dirk-Jan Eikema, Mahmoud Aljurf, Pieter J. van’t Veer, Gülyüz Öztürk, Matthias Wölfl, Frans Smiers, Angsar Schulz, Gerard Socié, Kim Vettenranta, Cristina Diaz de Heredia, Marco Zecca, Johan Maertens, Montserrat Rovira, Jorge Sierra, Duygu Uckan-Cetinkaya, Elena Skorobogatova, Ali Bülent Antmen, Jean-Hugues Dalle, Miroslaw Markiewicz, Rose Marie Hamladji, Vassiliki Kitra-Roussou, Giorgio La Nasa, Gergely Kriván, Amal Al-Seiraihy, Stefano Giardino, Antonio Maria Risitano, Regis Peffault de Latour, Carlo Dufour

Haematologica. 2019 Aug; 104(8): e335–e339. doi: 10.3324/haematol.2018.206623

PMCID:: PMC6669146

Article PDF–718K

Select item 65391984.

Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

Roberta Russo, Roberta Marra, Immacolata Andolfo, Gianluca De Rosa, Barbara Eleni Rosato, Francesco Manna, Antonella Gambale, Maddalena Raia, Sule Unal, Susanna Barella, Achille Iolascon

Front Physiol. 2019; 10: 621. Published online 2019 May 22. doi: 10.3389/fphys.2019.00621

Correction in:: Front Physiol. 2020; 11: 940.

PMCID:: PMC6539198

Abstract Article PDF–1.3M

Select item 55418655.

Recommendations regarding splenectomy in hereditary hemolytic anemias

Achille Iolascon, Immacolata Andolfo, Wilma Barcellini, Francesco Corcione, Loïc Garçon, Lucia De Franceschi, Claudio Pignata, Giovanna Graziadei, Dagmar Pospisilova, David C. Rees, Mariane de Montalembert, Stefano Rivella, Antonella Gambale, Roberta Russo, Leticia Ribeiro, Jules Vives-Corrons, Patricia Aguilar Martinez, Antonis Kattamis, Beatrice Gulbis, Maria Domenica Cappellini, Irene Roberts, Hannah Tamary

Haematologica. 2017 Aug; 102(8): 1304–1313. Prepublished online 2017 May 26. doi: 10.3324/haematol.2016.161166

PMCID:: PMC5541865

Abstract Article PDF–334K

Select item 37620946.

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I

Christian Babbs, Nigel A. Roberts, Luis Sanchez-Pulido, Simon J. McGowan, Momin R. Ahmed, Jill M. Brown, Mohamed A. Sabry, WGS500 Consortium, David R. Bentley, Gil A. McVean, Peter Donnelly, Opher Gileadi, Chris P. Ponting, Douglas R. Higgs, Veronica J. Buckle

Haematologica. 2013 Sep; 98(9): 1383–1387. doi: 10.3324/haematol.2013.089490

PMCID:: PMC3762094

Abstract Article PDF–343K

Select item 33433387.

Codanin-1, mutated in the anaemic disease CDAI, regulates Asf1 function in S-phase histone supply

Katrine Ask, Zuzana Jasencakova, Patrice Menard, Yunpeng Feng, Geneviève Almouzni, Anja Groth

EMBO J. 2012 Apr 18; 31(8): 2013–2023. Published online 2012 Mar 9. doi: 10.1038/emboj.2012.55

Correction in:: EMBO J. 2012 Jul 18; 31(14): 3229.

PMCID:: PMC3343338

Abstract Article PDF–1.2M

Select item 3785958.

Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

Orly Dgany, Nili Avidan, Jean Delaunay, Tatyana Krasnov, Lea Shalmon, Hanna Shalev, Tal Eidelitz-Markus, Joseph Kapelushnik, Daniel Cattan, Alexandre Pariente, Michel Tulliez, Aurore Crétien, Pierre-Olivier Schischmanoff, Achille Iolascon, Eithan Fibach, Ariel Koren, Jochen Rössler, Martine Le Merrer, Isaac Yaniv, Rina Zaizov, Edna Ben-Asher, Tsvyia Olender, Doron Lancet, Jacques S. Beckmann, Hannah Tamary

Am J Hum Genet. 2002 Dec; 71(6): 1467–1474. Published online 2002 Nov 14. doi: 10.1086/344781

PMCID:: PMC378595

Abstract Article PDF–1.0M

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