Literature DB >> 22430633

Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees.

A Buijs, M Poot, S van der Crabben, B van der Zwaag, E van Binsbergen, M J van Roosmalen, M Tavakoli-Yaraki, O de Weerdt, H K Nieuwenhuis, M van Gijn, W P Kloosterman.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2012        PMID： 22430633     DOI： 10.1038/leu.2012.79

Source DB:  PubMed          Journal:  Leukemia        ISSN： 0887-6924            Impact factor:   11.528


× No keyword cloud information.
  9 in total

1.  Gene Fusion due to Chromosome Misconnection May Seriously Affect Your Health.

Authors:  Martin Poot
Journal:  Mol Syndromol       Date:  2015-03-26

Review 2.  Role of RUNX1 in hematological malignancies.

Authors:  Raman Sood; Yasuhiko Kamikubo; Paul Liu
Journal:  Blood       Date:  2017-02-08       Impact factor: 22.113

3.  Don't Mess with RUNX1.

Authors:  M Poot
Journal:  Mol Syndromol       Date:  2012-09-27

Review 4.  Familial myelodysplastic syndrome/acute leukemia syndromes: a review and utility for translational investigations.

Authors:  Allison H West; Lucy A Godley; Jane E Churpek
Journal:  Ann N Y Acad Sci       Date:  2014-01-27       Impact factor: 5.691

5.  Gene of the issue: RUNX1 mutations and inherited bleeding.

Authors:  Neil V Morgan; Martina E Daly
Journal:  Platelets       Date:  2017-02-17       Impact factor: 3.862

6.  High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing.

Authors:  Anh Nhi Tran; Fulya Taylan; Vasilios Zachariadis; Ingegerd Ivanov Öfverholm; Anna Lindstrand; Francesco Vezzi; Britta Lötstedt; Magnus Nordenskjöld; Ann Nordgren; Daniel Nilsson; Gisela Barbany
Journal:  PLoS One       Date:  2018-03-12       Impact factor: 3.240

7.  RUNX1 upregulation via disruption of long-range transcriptional control by a novel t(5;21)(q13;q22) translocation in acute myeloid leukemia.

Authors:  Chi-Keung Cheng; Terry H Y Wong; Thomas S K Wan; Angela Z Wang; Natalie P H Chan; Nelson C N Chan; Chi-Kong Li; Margaret H L Ng
Journal:  Mol Cancer       Date:  2018-08-29       Impact factor: 27.401

8.  RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.

Authors:  Anna L Brown; Peer Arts; Catherine L Carmichael; Milena Babic; Julia Dobbins; Chan-Eng Chong; Andreas W Schreiber; Jinghua Feng; Kerry Phillips; Paul P S Wang; Thuong Ha; Claire C Homan; Sarah L King-Smith; Lesley Rawlings; Cassandra Vakulin; Andrew Dubowsky; Jessica Burdett; Sarah Moore; Grace McKavanagh; Denae Henry; Amanda Wells; Belinda Mercorella; Mario Nicola; Jeffrey Suttle; Ella Wilkins; Xiao-Chun Li; Joelle Michaud; Peter Brautigan; Ping Cannon; Meryl Altree; Louise Jaensch; Miriam Fine; Carolyn Butcher; Richard J D'Andrea; Ian D Lewis; Devendra K Hiwase; Elli Papaemmanuil; Marshall S Horwitz; Georges Natsoulis; Hugh Y Rienhoff; Nigel Patton; Sally Mapp; Rachel Susman; Susan Morgan; Julian Cooney; Mark Currie; Uday Popat; Tilmann Bochtler; Shai Izraeli; Kenneth Bradstock; Lucy A Godley; Alwin Krämer; Stefan Fröhling; Andrew H Wei; Cecily Forsyth; Helen Mar Fan; Nicola K Poplawski; Christopher N Hahn; Hamish S Scott
Journal:  Blood Adv       Date:  2020-03-24

9.  RUNX1 haploinsufficiency results in granulocyte colony-stimulating factor hypersensitivity.

Authors:  D W L Chin; M Sakurai; G S S Nah; L Du; B Jacob; T Yokomizo; T Matsumura; T Suda; G Huang; X-Y Fu; Y Ito; H Nakajima; M Osato
Journal:  Blood Cancer J       Date:  2016-01-08       Impact factor: 11.037
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.