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1.
[Assembly and secretion of mutant fibrinogens with variant gamma-chain C terminal region (gamma313-gamma345)].
Rinsho Byori
; 58(8): 772-8, 2010 Aug.
Artículo
en Japonés
| MEDLINE | ID: mdl-20860169
2.
[Functional analysis of heterozygous plasma dysfibrinogens derived from two families of gammaArg275Cys and three families of gammaArg275His, and haplotype analysis for these families].
Rinsho Byori
; 57(7): 651-8, 2009 Jul.
Artículo
en Japonés
| MEDLINE | ID: mdl-19708534
3.
[Analysis of antibody reactivity for FDP D-dimer fragments by Western blotting].
Rinsho Byori
; 56(6): 449-54, 2008 Jun.
Artículo
en Japonés
| MEDLINE | ID: mdl-18646629
4.
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.
Clin Chim Acta
; 412(1-2): 53-8, 2011 Jan 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-20849840
5.
In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A>G causing abnormal RNA splicing.
Clin Chim Acta
; 411(17-18): 1325-9, 2010 Sep 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-20580695
6.
Analysis of plasmin generation and clot lysis of plasma fibrinogen purified from a heterozygous dysfibrinogenemia, BbetaGly15Cys (Hamamatsu II).
Blood Coagul Fibrinolysis
; 20(8): 726-32, 2009 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-19809304
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