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mutation*

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Bibliographies

15

1 Significance of FLT3-tyrosine kinase domain mutation as a prognostic factor for acute myeloid leukemia

2 Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse

3 Usefulness of BCOR gene mutation as a prognostic factor in acute myeloid leukemia with intermediate cytogenetic prognosis

4 A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers

5 Respiratory syncytial virus (RSV) SH and G proteins are not essential for viral replication in vitro: clinical evaluation and molecular characterization of a cold-passaged, attenuated RSV subgroup B mutant

6 A Saccharomyces cerevisiae mutant with increased virulence

7 Mutations, mutation rates, and evolution at the hypervariable VNTR loci of Yersinia pestis

8 PTEN mutations do not cause nuclear beta-catenin accumulation in endometrial carcinomas

9 Dmp1 is haplo-insufficient for tumor suppression and modifies the frequencies of Arf and p53 mutations in Myc-induced lymphomas

10 High frequency of resistant viruses harboring different mutations in amantadine-treated children with influenza

11 Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity

12 A common human skin tumour is caused by activating mutations in beta-catenin

13 Paired-end mapping reveals extensive structural variation in the human genome

14 Understanding human glycosylation disorders: biochemistry leads the charge

15 INK4a/ARF mutations accelerate lymphomagenesis and promote chemoresistance by disabling p53