Search

Search Constraints

You searched for: Author/Creator Hayashi, Yasuhide

Search Results

1. Acute myeloid leukaemia with myelodysplastic features in children: a report of Japanese Paediatric Leukaemia/Lymphoma Study Group. (8th July 2014)

2. ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1‐RUNX1T1 and associated with a better prognosis. Issue 5 (14th February 2017)

3. C/EBPβ induces B‐cell acute lymphoblastic leukemia and cooperates with BLNK mutations. Issue 12 (23rd October 2021)

4. Characteristics of genetic alterations of peripheral T‐cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG). (13th July 2021)

5. Characterization of genetic lesions in rhabdomyosarcoma using a high‐density single nucleotide polymorphism array. Issue 7 (23rd May 2013)

6. Clinical and biological features of paediatric acute myeloid leukaemia (AML) with primary induction failure in the Japanese Paediatric Leukaemia/Lymphoma Study Group AML‐05 study. (19th February 2019)

7. Clinical features and prognostic impact of PRDM16 expression in adult acute myeloid leukemia. Issue 11 (11th August 2017)

8. CSF3R and CALR mutations in paediatric myeloid disorders and the association of CSF3R mutations with translocations, including t(8; 21). (9th April 2015)

9. Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1‐RUNX1T1 transcripts. (13th June 2021)

10. Gene alterations involving the CRLF2‐JAK pathway and recurrent gene deletions in Down syndrome‐associated acute lymphoblastic leukemia in Japan. Issue 11 (16th July 2014)