Literature DB >> 19102804

Shwachman-Diamond syndrome: implications for understanding the molecular basis of leukaemia.

Yigal Dror1.   

Abstract

Inherited bone marrow failure syndromes provide extremely useful genetic models for understanding leukaemogenesis because the initial genetic defect can be identified and the risk of leukaemia is very high. Shwachman-Diamond syndrome is one of the most common inherited bone marrow failure syndromes and an example of such a model. Here, I describe the malignant features of Shwachman-Diamond syndrome and discuss the potential molecular mechanisms that can lead to leukaemia.

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Year:  2008        PMID: 19102804     DOI: 10.1017/S1462399408000938

Source DB:  PubMed          Journal:  Expert Rev Mol Med        ISSN: 1462-3994            Impact factor:   5.600


  5 in total

Review 1.  Clinical spectrum and molecular pathophysiology of Shwachman-Diamond syndrome.

Authors:  James N Huang; Akiko Shimamura
Journal:  Curr Opin Hematol       Date:  2011-01       Impact factor: 3.284

2.  Cellular and molecular architecture of hematopoietic stem cells and progenitors in genetic models of bone marrow failure.

Authors:  Stephanie Heidemann; Brian Bursic; Sasan Zandi; Hongbing Li; Sagi Abelson; Robert J Klaassen; Sharon Abish; Meera Rayar; Vicky R Breakey; Houtan Moshiri; Santhosh Dhanraj; Richard de Borja; Adam Shlien; John E Dick; Yigal Dror
Journal:  JCI Insight       Date:  2020-02-27

3.  SBDS-Deficient Cells Have an Altered Homeostatic Equilibrium due to Translational Inefficiency Which Explains their Reduced Fitness and Provides a Logical Framework for Intervention.

Authors:  Piera Calamita; Annarita Miluzio; Arianna Russo; Elisa Pesce; Sara Ricciardi; Farhat Khanim; Cristina Cheroni; Roberta Alfieri; Marilena Mancino; Chiara Gorrini; Grazisa Rossetti; Ivana Peluso; Massimiliano Pagani; Diego L Medina; Johanna Rommens; Stefano Biffo
Journal:  PLoS Genet       Date:  2017-01-05       Impact factor: 5.917

Review 4.  Translating the Game: Ribosomes as Active Players.

Authors:  Piera Calamita; Guido Gatti; Annarita Miluzio; Alessandra Scagliola; Stefano Biffo
Journal:  Front Genet       Date:  2018-11-15       Impact factor: 4.599

Review 5.  Spectrum and risk of neoplasia in Werner syndrome: a systematic review.

Authors:  Julia M Lauper; Alison Krause; Thomas L Vaughan; Raymond J Monnat
Journal:  PLoS One       Date:  2013-04-01       Impact factor: 3.240

  5 in total

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