Literature DB >> 11243240

Recurrent ATM mutations in T-PLL on diverse haplotypes: no support for their germline origin.

T Stankovic, A M Taylor, M R Yuille, I Vorechovsky.   

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Year:  2001        PMID： 11243240     DOI： 10.1182/blood.v97.5.1517

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  4 in total

1.  Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomy.

Authors:  Daniel Nowak; Emilie Le Toriellec; Marc-Henri Stern; Norihiko Kawamata; Tadayuki Akagi; Martin J Dyer; Wolf-Karsten Hofmann; Seishi Ogawa; H Phillip Koeffler
Journal:  Haematologica       Date:  2009-03-10       Impact factor: 9.941

Review 2.  ATM, radiation, and the risk of second primary breast cancer.

Authors:  Jonine L Bernstein; Patrick Concannon
Journal:  Int J Radiat Biol       Date:  2017-07-27       Impact factor: 2.694

3.  Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma.

Authors:  Nicole Y Fang; Timothy C Greiner; Dennis D Weisenburger; Wing C Chan; Julie M Vose; Lynette M Smith; James O Armitage; R Aeryn Mayer; Brian L Pike; Francis S Collins; Joseph G Hacia
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-15       Impact factor: 11.205

4.  SAMHD1 is recurrently mutated in T-cell prolymphocytic leukemia.

Authors:  Patricia Johansson; Ludger Klein-Hitpass; Axel Choidas; Peter Habenberger; Bijan Mahboubi; Baek Kim; Anke Bergmann; René Scholtysik; Martina Brauser; Anna Lollies; Reiner Siebert; Thorsten Zenz; Ulrich Dührsen; Ralf Küppers; Jan Dürig
Journal:  Blood Cancer J       Date:  2018-01-19       Impact factor: 11.037
  4 in total

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