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3. The efficacy and safety of modified bortezomib‐lenalidomide‐dexamethasone in transplant‐eligible patients with newly diagnosed multiple myeloma. (28th November 2019)

4. The longest reported sibling survivors of a severe form of congenital myasthenic syndrome with the ALG14 pathogenic variant. Issue 4 (31st December 2021)

5. Investigation of the cumulative number of chromosome aberrations induced by three consecutive CT examinations in eight patients. (28th October 2019)

6. Improved harvest and fixation methodology for isolated human peripheral blood mononuclear cells in cytokinesis-block micronucleus assay. (1st February 2021)

7. Dose–response curves for analyzing of dicentric chromosomes and chromosome translocations following doses of 1000 mGy or less, based on irradiated peripheral blood samples from five healthy individuals. (13th October 2017)

8. Analysis of chromosome translocation frequency after a single CT scan in adults. (21st June 2016)

9. Xq26.1‐26.2 gain identified on array comparative genomic hybridization in bilateral periventricular nodular heterotopia with overlying polymicrogyria. (23rd July 2014)

10. Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling. Issue 10 (26th July 2018)