Search details
1.
A Novel Amino Acid Substitution, Fibrinogen Bßp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion.
Int J Mol Sci
; 21(24)2020 Dec 10.
Article
in English
| MEDLINE | ID: mdl-33322044
2.
Rapid ABO genotyping by high-speed droplet allele-specific PCR using crude samples.
J Clin Lab Anal
; 32(1)2018 Jan.
Article
in English
| MEDLINE | ID: mdl-28295603
3.
A Novel Mutation in the Fibrinogen Bß Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia.
Int J Mol Sci
; 18(11)2017 Nov 20.
Article
in English
| MEDLINE | ID: mdl-29156616
4.
STAT3 gene mutations and their association with pure red cell aplasia in large granular lymphocyte leukemia.
Cancer Sci
; 105(3): 342-6, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-24350896
5.
Epithelial-mesenchymal transition of A549 cells is enhanced by co-cultured with THP-1 macrophages under hypoxic conditions.
Biochem Biophys Res Commun
; 453(4): 804-9, 2014 Oct 31.
Article
in English
| MEDLINE | ID: mdl-25445593
6.
[Case with intrauterine fetus death: interphase fluorescence in situ hybridization using buccal cells is useful for examining chromosomal abnormalities when placental villus not available].
Rinsho Byori
; 60(1): 32-6, 2012 Jan.
Article
in Japanese
| MEDLINE | ID: mdl-22416454
7.
[Development of multiplex short tandem repeat (STR)-PCR for chimerism analysis in patients with hematological malignancies and comparison of chimerism in different sample sources].
Rinsho Byori
; 59(1): 24-30, 2011 Jan.
Article
in Japanese
| MEDLINE | ID: mdl-21404576
8.
Redox index of Cys-thiol residues of serum apolipoprotein E and its diagnostic potential.
Biosci Rep
; 41(8)2021 08 27.
Article
in English
| MEDLINE | ID: mdl-34286848
9.
Novel variant fibrinogen γp.C352R produced hypodysfibrinogenemia leading to a bleeding episode and failure of infertility treatment.
Int J Hematol
; 114(3): 325-333, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34117991
10.
Quantitative assessment of PTPN11 or RAS mutations at the neonatal period and during the clinical course in patients with juvenile myelomonocytic leukaemia.
Br J Haematol
; 148(4): 593-9, 2010 Feb.
Article
in English
| MEDLINE | ID: mdl-19874312
11.
Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative.
Thromb Res
; 196: 152-158, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32871307
12.
Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens.
Int J Lab Hematol
; 42(2): 190-197, 2020 Apr.
Article
in English
| MEDLINE | ID: mdl-31957968
13.
Comparison of molecular structure and fibrin polymerization between two Bß-chain N-terminal region fibrinogen variants, Bßp.G45C and Bßp.R74C.
Int J Hematol
; 112(3): 331-340, 2020 Sep.
Article
in English
| MEDLINE | ID: mdl-32562089
14.
γD318Y fibrinogen shows no fibrin polymerization due to defective "A-a" and "B-b" interactions, whereas that of γK321E fibrinogen is nearly normal.
Thromb Res
; 182: 150-158, 2019 Oct.
Article
in English
| MEDLINE | ID: mdl-31484085
15.
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.
Blood
; 115(26): 5429-31, 2010 Jul 01.
Article
in English
| MEDLINE | ID: mdl-20595524
16.
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.
Clin Chim Acta
; 448: 150-4, 2015 Aug 25.
Article
in English
| MEDLINE | ID: mdl-26148723
17.
Rapid single nucleotide polymorphism based method for hematopoietic chimerism analysis and monitoring using high-speed droplet allele-specific PCR and allele-specific quantitative PCR.
Clin Chim Acta
; 445: 101-6, 2015 May 20.
Article
in English
| MEDLINE | ID: mdl-25797898
18.
Complete measurable residual disease response after combination chemotherapy with AML-type and ALL-type regimens in pediatric B/myeloid acute bilineal leukemia.
Leuk Lymphoma
; 61(4): 967-970, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31809628
19.
Fibrin monomers derived from thrombogenic dysfibrinogenemia, Naples-type variant (BßAla68Thr), showed almost entirely normal polymerization.
Thromb Res
; 172: 1-3, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30321757
20.
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.
Clin Chim Acta
; 415: 276-8, 2013 Jan 16.
Article
in English
| MEDLINE | ID: mdl-23159843