Chiaki Taira

发表

K. Matsuda, Toshiro Ito, T. Honda, 2012, Leukemia research.

Development of a rapid and sensitive one-step reverse transcription-nested polymerase chain reaction in a single tube using the droplet-polymerase chain reaction machine.

Yasunori Saito, A. Yamaguchi, K. Matsuda, 2015, Clinica chimica acta; international journal of clinical chemistry.

Epithelial-mesenchymal transition of A549 cells is enhanced by co-cultured with THP-1 macrophages under hypoxic conditions.

K. Matsuda, Hiroshi Yamamoto, N. Ishimine, 2014, Biochemical and biophysical research communications.

Novel high-speed droplet-allele specific-polymerase chain reaction: application in the rapid genotyping of single nucleotide polymorphisms.

A. Yamaguchi, K. Matsuda, T. Honda, 2013, Clinica chimica acta; international journal of clinical chemistry.

Quantitative assessment of PTPN11 or RAS mutations at the neonatal period and during the clinical course in patients with juvenile myelomonocytic leukaemia

H. Kanegane, K. Koike, S. Nonoyama, 2010, British journal of haematology.

Redox index of Cys-thiol residues of serum apolipoprotein E and its diagnostic potential

Y. Kawakami, K. Yamauchi, Chiaki Taira, 2021, Bioscience reports.

A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia

K. Matsuda, T. Uehara, M. Sugano, 2017, International journal of molecular sciences.

A novel frameshift mutation in the fibrinogen γC terminal region, FGG c.1169_1170 del AT, leading to hypofibrinogenemia.

K. Nagata, T. Honda, M. Sugano, 2017, Thrombosis research.

A novel high-speed droplet-polymerase chain reaction can detect human influenza virus in less than 30 min.

A. Yamaguchi, K. Matsuda, T. Honda, 2012, Clinica chimica acta; international journal of clinical chemistry.

Rapid detection of PML-RARA fusion gene by novel high-speed droplet-reverse transcriptase-polymerase chain reaction: possibility for molecular diagnosis without lagging behind the morphological analyses.

A. Yamaguchi, K. Matsuda, T. Honda, 2013, Clinica chimica acta; international journal of clinical chemistry.

Quantitative monitoring of single nucleotide mutations by allele-specific quantitative PCR can be used for the assessment of minimal residual disease in patients with hematological malignancies throughout their clinical course.

K. Matsuda, T. Honda, F. Ishida, 2011, Clinica chimica acta; international journal of clinical chemistry.

Genetic analysis of TP53 in childhood myelodysplastic syndrome and juvenile myelomonocytic leukemia.

K. Koike, Y. Nakazawa, K. Matsuda, 2011, Leukemia research.

STAT3 gene mutations and their association with pure red cell aplasia in large granular lymphocyte leukemia

Y. Kwong, H. Makishima, K. Matsuda, 2014, Cancer science.

Rapid ABO genotyping by high‐speed droplet allele‐specific PCR using crude samples

K. Matsuda, T. Uehara, T. Honda, 2018, Journal of clinical laboratory analysis.

Application of allele-specific quantitative PCR using genomic DNA to monitor minimal residual disease based on mutant gene levels following allogeneic hematopoietic stem cell transplantation in patients with hematological malignancies: comparison of mutant levels with autologous DNA percentage by sh

K. Matsuda, T. Honda, M. Sugano, 2012, Clinica chimica acta; international journal of clinical chemistry.

γD318Y fibrinogen shows no fibrin polymerization due to defective "A-a" and "B-b" interactions, whereas that of γK321E fibrinogen is nearly normal.

N. Okumura, Chiaki Taira, Y. Higuchi, 2019, Thrombosis research.

Novel variant fibrinogen γp.C352R produced hypodysfibrinogenemia leading to a bleeding episode and failure of infertility treatment

N. Okumura, Chiaki Taira, Y. Higuchi, 2021, International Journal of Hematology.

Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens

N. Okumura, Chiaki Taira, Y. Higuchi, 2020, International journal of laboratory hematology.

Complete measurable residual disease response after combination chemotherapy with AML-type and ALL-type regimens in pediatric B/myeloid acute bilineal leukemia

K. Koike, Y. Nakazawa, K. Matsuda, 2019, Leukemia & lymphoma.

Rapid single nucleotide polymorphism based method for hematopoietic chimerism analysis and monitoring using high-speed droplet allele-specific PCR and allele-specific quantitative PCR.

A. Yamaguchi, K. Matsuda, Masayuki Uehara, 2015, Clinica chimica acta; international journal of clinical chemistry.

Comparison of molecular structure and fibrin polymerization between two Bβ-chain N-terminal region fibrinogen variants, Bβp.G45C and Bβp.R74C

N. Okumura, Chiaki Taira, Y. Higuchi, 2020, International Journal of Hematology.

Fibrin monomers derived from thrombogenic dysfibrinogenemia, Naples-type variant (BβAla68Thr), showed almost entirely normal polymerization.

K. Nagata, N. Okumura, Chiaki Taira, 2018, Thrombosis research.

Long-term survival after nonintensive chemotherapy in some juvenile myelomonocytic leukemia patients with CBL mutations, and the possible presence of healthy persons with the mutations.

K. Koike, Y. Nakazawa, T. Nakahata, 2010, Blood.

Simple polymerase chain reaction for the detection of mutations and deletions in the epidermal growth factor receptor gene: applications of this method for the diagnosis of non-small-cell lung cancer.

K. Matsuda, K. Yamauchi, Chiaki Taira, 2009, Clinica chimica acta; international journal of clinical chemistry.

A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion

N. Okumura, Chiaki Taira, Y. Higuchi, 2020, International journal of molecular sciences.

Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative.

N. Okumura, Chiaki Taira, Y. Higuchi, 2020, Thrombosis research.