Literature DB >> 21930148

Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome.

Jacqueline Boultwood1, Andrea Pellagatti, James S Wainscoat.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 21930148     DOI: 10.1016/j.advenzreg.2011.09.008

Source DB:  PubMed          Journal:  Adv Biol Regul        ISSN: 2212-4926


× No keyword cloud information.
  15 in total

Review 1.  Emerging cellular and gene therapies for congenital anemias.

Authors:  Leif S Ludwig; Rajiv K Khajuria; Vijay G Sankaran
Journal:  Am J Med Genet C Semin Med Genet       Date:  2016-10-28       Impact factor: 3.908

2.  mRNA deadenylation and telomere disease.

Authors:  Philip J Mason; Monica Bessler
Journal:  J Clin Invest       Date:  2015-04-20       Impact factor: 14.808

Review 3.  Recent insights into inherited bone marrow failure syndromes.

Authors:  Shefali Parikh; Monica Bessler
Journal:  Curr Opin Pediatr       Date:  2012-02       Impact factor: 2.856

4.  Using induced human pluripotent stem cells to study Diamond-Blackfan anemia: an outlook on the clinical possibilities.

Authors:  Philip J Mason; Nieves Perdigones; Monica Bessler
Journal:  Expert Rev Hematol       Date:  2013-12       Impact factor: 2.929

5.  Guilty as CHARGED: p53's expanding role in disease.

Authors:  Jeanine L Van Nostrand; Laura D Attardi
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

Review 6.  Advances in genetic studies of inherited bone marrow failure syndromes and their associated malignancies.

Authors:  Qi-Hong Yu; Shu-Ye Wang; Zhanhe Wu
Journal:  Transl Pediatr       Date:  2014-10

7.  Model system identification of novel congenital heart disease gene candidates: focus on RPL13.

Authors:  Analyne M Schroeder; Massoud Allahyari; Georg Vogler; Maria A Missinato; Tanja Nielsen; Michael S Yu; Jeanne L Theis; Lars A Larsen; Preeya Goyal; Jill A Rosenfeld; Timothy J Nelson; Timothy M Olson; Alexandre R Colas; Paul Grossfeld; Rolf Bodmer
Journal:  Hum Mol Genet       Date:  2019-12-01       Impact factor: 6.150

8.  Genetics. Mysterious ribosomopathies.

Authors:  Kathleen L McCann; Susan J Baserga
Journal:  Science       Date:  2013-08-23       Impact factor: 47.728

9.  Biallelic splicing variants in the nucleolar 60S assembly factor RBM28 cause the ribosomopathy ANE syndrome.

Authors:  Carson J Bryant; Cláudia F Lorea; Hiram Larangeira de Almeida; Letícia Weinert; Leonardo Vedolin; Filippo Pinto E Vairo; Susan J Baserga
Journal:  Proc Natl Acad Sci U S A       Date:  2021-05-11       Impact factor: 11.205

Review 10.  An evolutionary approach to clonally complex hematologic disorders.

Authors:  Emily Schwenger; Ulrich Steidl
Journal:  Blood Cancer Discov       Date:  2021-04-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.