Search

Search Constraints

You searched for: Author/Creator Ogawa, Seishi

Search Results

1. A Cryptic NUP214-ABL1 Fusion in B-cell Precursor Acute Lymphoblastic Leukemia. Issue 6 (August 2018)

2. A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India. Issue 1 (26th September 2019)

3. A Possible Association Between a Nucleotide‐Binding Domain LRR‐Containing Protein Family PYD‐Containing Protein 1 Mutation and an Autoinflammatory Disease Involving Liver Cirrhosis. Issue 4 (27th May 2021)

4. A robust molecular pattern for myelodysplastic syndromes in two independent cohorts investigated by next‐generation sequencing can be revealed by comparative bioinformatic analyses. (12th June 2014)

5. Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome. Issue 2 (16th November 2020)

6. Adult T‐cell leukemia cells are characterized by abnormalities of Helios expression that promote T cell growth. Issue 8 (19th May 2013)

7. Alteration of the immune environment in bone marrow from children with recurrent B cell precursor acute lymphoblastic leukemia. Issue 1 (29th November 2021)

8. An eltrombopag‐induced remission of bone‐marrow aplasia accompanied by marked leukoerythroblastosis and splenomegaly. (28th June 2022)

9. 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)

10. ATRT-11. PREVALENCE OF GERMLINE VARIANTS IN SMARCB1 INCLUDING SOMATIC MOSAICISM IN AT/RT AND OTHER RHABDOID TUMORS. (4th December 2020)