Literature DB >> 25856206

Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21).

Nicolas Duployez1, Jean-Baptiste Micol2,3, Nicolas Boissel4, Arnaud Petit5, Sandrine Geffroy1, Maxime Bucci1, Hélène Lapillonne6, Aline Renneville1, Guy Leverger5, Norbert Ifrah7, Hervé Dombret4, Omar Abdel-Wahab3, Eric Jourdan8, Claude Preudhomme1.   

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Year:  2015        PMID: 25856206     DOI: 10.3109/10428194.2015.1037754

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


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  8 in total

Review 1.  Aberrant histone modifications induced by mutant ASXL1 in myeloid neoplasms.

Authors:  Shuhei Asada; Toshio Kitamura
Journal:  Int J Hematol       Date:  2018-12-05       Impact factor: 2.490

2.  Comprehensive mutational profiling of core binding factor acute myeloid leukemia.

Authors:  Nicolas Duployez; Alice Marceau-Renaut; Nicolas Boissel; Arnaud Petit; Maxime Bucci; Sandrine Geffroy; Hélène Lapillonne; Aline Renneville; Christine Ragu; Martin Figeac; Karine Celli-Lebras; Catherine Lacombe; Jean-Baptiste Micol; Omar Abdel-Wahab; Pascale Cornillet; Norbert Ifrah; Hervé Dombret; Guy Leverger; Eric Jourdan; Claude Preudhomme
Journal:  Blood       Date:  2016-03-15       Impact factor: 22.113

Review 3.  The Role of Additional Sex Combs-Like Proteins in Cancer.

Authors:  Jean-Baptiste Micol; Omar Abdel-Wahab
Journal:  Cold Spring Harb Perspect Med       Date:  2016-10-03       Impact factor: 6.915

4.  Identification of a novel PDGFRA point mutation at p.P6L as a potential molecular target of imatinib in an eosinophilia patient showing genetic heterogeneity.

Authors:  Miaomiao Zhao; Qiuling Wu; Linghui Xia; Min Zhang; Jianqing Yang; Yaya Li; Shichun Tu; Yadan Wang
Journal:  Cancer Biol Ther       Date:  2018-10-25       Impact factor: 4.742

5.  Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.

Authors:  Fang Fu; Ru Li; Ting-Ying Lei; Dan Wang; Xin Yang; Jin Han; Min Pan; Li Zhen; Jian Li; Fa-Tao Li; Xiang-Yi Jing; Dong-Zhi Li; Can Liao
Journal:  Hum Genet       Date:  2020-07-21       Impact factor: 4.132

6.  De novo dominant ASXL3 mutations alter H2A deubiquitination and transcription in Bainbridge-Ropers syndrome.

Authors:  Anshika Srivastava; K C Ritesh; Yao-Chang Tsan; Rosy Liao; Fengyun Su; Xuhong Cao; Mark C Hannibal; Catherine E Keegan; Arul M Chinnaiyan; Donna M Martin; Stephanie L Bielas
Journal:  Hum Mol Genet       Date:  2015-12-08       Impact factor: 6.150

7.  Understanding the phenotypic spectrum of ASXL-related disease: Ten cases and a review of the literature.

Authors:  Vishnu Anand Cuddapah; Holly A Dubbs; Laura Adang; Steven L Kugler; Elizabeth M McCormick; Zarazuela Zolkipli-Cunningham; Xilma R Ortiz-González; Shana McCormack; Elaine Zackai; Daniel J Licht; Marni J Falk; Eric D Marsh
Journal:  Am J Med Genet A       Date:  2021-03-10       Impact factor: 2.578

8.  Genomic complexity and dynamics of clonal evolution in childhood acute myeloid leukemia studied with whole-exome sequencing.

Authors:  Riccardo Masetti; Ilaria Castelli; Annalisa Astolfi; Salvatore Nicola Bertuccio; Valentina Indio; Marco Togni; Tamara Belotti; Salvatore Serravalle; Giuseppe Tarantino; Marco Zecca; Martina Pigazzi; Giuseppe Basso; Andrea Pession; Franco Locatelli
Journal:  Oncotarget       Date:  2016-08-30
  8 in total

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