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You searched for: Author/Creator Yoshida, Kenichi

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

5. 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)

7. Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells. Issue 1 (December 2017)

8. Characteristic and complementary chiral recognition ability of four recently developed immobilized chiral stationary phases based on amylose and cellulose phenyl carbamates and benzoates. Issue 7 (12th April 2022)

9. Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study. Issue 9 (17th July 2020)

10. Clonal evidence for the development of neuroblastoma with extensive copy‐neutral loss of heterozygosity arising in a mature teratoma. Issue 7 (6th May 2021)