Literature DB >> 23239956

Don't Mess with RUNX1.

M Poot.   

Abstract

Entities:  

Year:  2012        PMID： 23239956      PMCID： PMC3507267          DOI： 10.1159/000342878

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN： 1661-8769


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  14 in total

1.  SIFT: Predicting amino acid changes that affect protein function.

Authors:  Pauline C Ng; Steven Henikoff
Journal:  Nucleic Acids Res       Date:  2003-07-01       Impact factor: 16.971

Review 2.  Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.

Authors:  M Poot; J J van der Smagt; E H Brilstra; T Bourgeron
Journal:  Cytogenet Genome Res       Date:  2011-11-12       Impact factor: 1.636

3.  Chromosome studies in human leukemia. II. Chronic granulocytic leukemia.

Authors:  P C NOWELL; D A HUNGERFORD
Journal:  J Natl Cancer Inst       Date:  1961-11       Impact factor: 13.506

4.  Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline.

Authors:  Wigard P Kloosterman; Victor Guryev; Mark van Roosmalen; Karen J Duran; Ewart de Bruijn; Saskia C M Bakker; Tom Letteboer; Bernadette van Nesselrooij; Ron Hochstenbach; Martin Poot; Edwin Cuppen
Journal:  Hum Mol Genet       Date:  2011-02-24       Impact factor: 6.150

Review 5.  Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.

Authors:  R Hochstenbach; J E Buizer-Voskamp; J A S Vorstman; R A Ophoff
Journal:  Cytogenet Genome Res       Date:  2011-11-02       Impact factor: 1.636

6.  Whole-exome sequencing of pediatric acute lymphoblastic leukemia.

Authors:  H Lilljebjörn; M Rissler; C Lassen; J Heldrup; M Behrendtz; F Mitelman; B Johansson; T Fioretos
Journal:  Leukemia       Date:  2011-11-18       Impact factor: 11.528

7.  A method and server for predicting damaging missense mutations.

Authors:  Ivan A Adzhubei; Steffen Schmidt; Leonid Peshkin; Vasily E Ramensky; Anna Gerasimova; Peer Bork; Alexey S Kondrashov; Shamil R Sunyaev
Journal:  Nat Methods       Date:  2010-04       Impact factor: 28.547

8.  Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

Authors:  T R Golub; G F Barker; S K Bohlander; S W Hiebert; D C Ward; P Bray-Ward; E Morgan; S C Raimondi; J D Rowley; D G Gilliland
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-23       Impact factor: 11.205

Review 9.  The impact of translocations and gene fusions on cancer causation.

Authors:  Felix Mitelman; Bertil Johansson; Fredrik Mertens
Journal:  Nat Rev Cancer       Date:  2007-03-15       Impact factor: 60.716

10.  A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia.

Authors:  Fady M Mikhail; Lionel Coignet; Nadia Hatem; Zeinab I Mourad; Hala M Farawela; Dalal M El Kaffash; Nahla Farahat; Giuseppina Nucifora
Journal:  Genes Chromosomes Cancer       Date:  2004-02       Impact factor: 5.006
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