PubRank

A Ichinose

Author PubWeight™ 48.98‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Distinct C-terminus of the B subunit of factor XIII in a population-associated major phenotype: the first case of complete allele-specific alternative splicing products in the coagulation and fibrinolytic systems. J Thromb Haemost 2009 1.45
2 Localization of the coagulation factor XIII A subunit gene (F13A) to chromosome bands 6p24----p25. Cytogenet Cell Genet 1988 1.41
3 Amino acid sequence of the b subunit of human factor XIII, a protein composed of ten repetitive segments. Biochemistry 1986 1.40
4 Rapid killing of human neutrophils by the potent activator phorbol 12-myristate 13-acetate (PMA) accompanied by changes different from typical apoptosis or necrosis. J Leukoc Biol 1996 1.37
5 The activation of pro-urokinase by plasma kallikrein and its inactivation by thrombin. J Biol Chem 1986 1.33
6 Amino acid sequence of the a subunit of human factor XIII. Biochemistry 1986 1.32
7 Nucleotide sequence of the gene for the b subunit of human factor XIII. Biochemistry 1990 1.21
8 Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31-32.1 and restriction fragment length polymorphism at the locus. Hum Genet 1989 1.21
9 Binding of cationic alpha-helical peptides to plasmid DNA and their gene transfer abilities into cells. J Biol Chem 1997 1.13
10 Factor XIII transglutaminase supports hematogenous tumor cell metastasis through a mechanism dependent on natural killer cell function. J Thromb Haemost 2008 1.10
11 Characterization of the gene for human plasminogen, a key proenzyme in the fibrinolytic system. J Biol Chem 1990 1.04
12 Factor XIII-mediated cross-linking of NH2-terminal peptide of alpha 2-plasmin inhibitor to fibrin. FEBS Lett 1983 0.94
13 Localization of the binding site of tissue-type plasminogen activator to fibrin. J Clin Invest 1986 0.92
14 Two genetic defects in a patient with complete deficiency of the b-subunit for coagulation factor XIII. Blood 1993 0.90
15 Structural features of the proteins participating in blood coagulation and fibrinolysis. Cold Spring Harb Symp Quant Biol 1986 0.90
16 Proteolytic activation of tissue plasminogen activator by plasma and tissue enzymes. FEBS Lett 1984 0.89
17 Comparison of the effects of various anticholinergic drugs on human isolated urinary bladder. Arch Int Pharmacodyn Ther 1996 0.89
18 Anesthetic management for a patient with Kearns-Sayre syndrome. Anesth Analg 1995 0.89
19 The gene for human protein Z is localized to chromosome 13 at band q34 and is coded by eight regular exons and one alternative exon. Biochemistry 1998 0.87
20 Fibrin-associated plasminogen activation in alpha 2-plasmin inhibitor deficiency. Blood 1983 0.86
21 Cloning of cDNAs coding for the heavy chain region and connecting region of human factor V, a blood coagulation factor with four types of internal repeats. Biochemistry 1987 0.86
22 Limulus hemocyte transglutaminase. cDNA cloning, amino acid sequence, and tissue localization. J Biol Chem 1993 0.86
23 In vitro trypanocidal activity of dibutyltin dichloride and its fatty acid derivatives. Parasitol Res 2003 0.85
24 Factor XIII: recommended terms and abbreviations. J Thromb Haemost 2006 0.84
25 Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system. Blood 1998 0.84
26 Diagnosis and classification of factor XIII deficiencies. J Thromb Haemost 2011 0.83
27 Histidine-rich glycoprotein and alpha 2-plasmin inhibitor in inhibition of plasminogen binding to fibrin. Thromb Res 1984 0.83
28 Identification of a flavivirus isolated from mosquitos in Chiang Mai Thailand. Southeast Asian J Trop Med Public Health 1999 0.83
29 Expression and release of the a and b subunits for human coagulation factor XIII in baby hamster kidney (BHK) cells. J Biochem 1996 0.83
30 Expression of fimbriae and host response in Branhamella catarrhalis respiratory infections. Microbiol Immunol 1994 0.82
31 Plasma lipoprotein(a) levels and expression of the apolipoprotein(a) gene are dependent on the nucleotide polymorphisms in its 5'-flanking region. J Clin Invest 1997 0.82
32 Possible presence of a capsule in Branhamella catarrhalis. Microbiol Immunol 1991 0.82
33 Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domain. Blood 1996 0.81
34 Flow cytometric studies of the D antigen of various Rh phenotypes with particular reference to Du and Del. Transfusion 1990 0.81
35 Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation. Blood 2001 0.81
36 Regulation of human protein Z gene expression by liver-enriched transcription factor HNF-4alpha and ubiquitous factor Sp1. J Thromb Haemost 2007 0.81
37 Attachment of Moraxella catarrhalis occurs to the positively charged domains of pharyngeal epithelial cells. Microb Pathog 2000 0.80
38 Use of autologous plasmin during vitrectomy for diabetic maculopathy. Eur J Ophthalmol 2006 0.80
39 Limulus hemocyte transglutaminase. Its purification and characterization, and identification of the intracellular substrates. J Biol Chem 1993 0.80
40 Castalagin from Anogeissus leiocarpus mediates the killing of Leishmania in vitro. Parasitol Res 2008 0.79
41 Neutrophil response to Pseudomonas aeruginosa in respiratory infection. Microbiol Immunol 1993 0.79
42 Transcriptional regulation of cell type-specific expression of the TATA-less A subunit gene for human coagulation factor XIII. J Biol Chem 1999 0.79
43 Reversible cross-linking of alpha 2-plasmin inhibitor to fibrinogen by fibrin-stabilizing factor. Biochim Biophys Acta 1982 0.79
44 A collaborative study to establish the 1st International Standard for factor XIII plasma. J Thromb Haemost 2007 0.78
45 Plasma lipoprotein(a) levels are high in patients with central retinal artery occlusion. Thromb Res 1998 0.78
46 Efficacy of autologous plasmin for idiopathic macular hole surgery. Eur J Ophthalmol 2005 0.78
47 As many as 12 cases with haemorrhagic acquired factor XIII deficiency due to its inhibitors were recently found in Japan. Thromb Haemost 2011 0.78
48 Expression and induction by IL-6 of the normal and variant genes for human plasminogen. Biochem Biophys Res Commun 1997 0.78
49 Novel deletion and insertion mutations cause splicing defects, leading to severe reduction in mRNA levels of the A subunit in severe factor XIII deficiency. Thromb Haemost 1998 0.78
50 Impaired protein folding, dimer formation, and heterotetramer assembly cause intra- and extracellular instability of a Y283C mutant of the A subunit for coagulation factor XIII. Biochemistry 2001 0.77
51 Molecular and cellular basis of deficiency of the b subunit for factor XIII secondary to a Cys430-Phe mutation in the seventh Sushi domain. J Clin Invest 1995 0.77
52 Possible roles of transglutaminases in Alzheimer's disease. Dement Geriatr Cogn Disord 1998 0.76
53 Common mutation of plasminogen detected in three Asian populations by an amplification refractory mutation system and rapid automated capillary electrophoresis. Thromb Haemost 1999 0.76
54 Novel Y283C mutation of the A subunit for coagulation factor XIII: molecular modelling predicts its impaired protein folding and dimer formation. Br J Haematol 2001 0.76
55 Anti-factor XIII A subunit (FXIII-A) autoantibodies block FXIII-A2 B2 assembly and steal FXIII-A from native FXIII-A2 B2. J Thromb Haemost 2015 0.76
56 Characterization of the 5'-flanking regions of plasminogen-related genes A and B. FEBS Lett 1997 0.75
57 Expression of plasminogen-related gene B varies among normal tissues and increases in cancer tissues. FEBS Lett 1999 0.75
58 [Deficiency of A or B subunit for coagulation factor XIII]. Ryoikibetsu Shokogun Shirizu 1998 0.75
59 Hageman factor (factor XII) in cerebrovascular diseases. Nihon Ketsueki Gakkai Zasshi 1985 0.75
60 Proteosomal degradation of naturally recurring R260C missense and exon-IV deletion mutants of factor XIII A-subunit expressed in mammalian cells. Haemophilia 2012 0.75
61 Lipoprotein(a) concentration and molecular weight of apolipoprotein(a) in patients with cerebrovascular disease and diabetes mellitus. Thromb Res 1997 0.75
62 Genetic diagnosis of dysplasminogenemia: detection of an Ala601-Thr mutation in 118 out of 125 families and identification of a new Asp676-Asn mutation. Thromb Haemost 1996 0.75
63 A scanning electron microscopic observation of detached dental calculus on cementum surface. J Nihon Univ Sch Dent 1982 0.75
64 Anatomical evaluation of facial nerve pathways and dissection of "premasseter space" for rhytidectomy in Asians. Aesthetic Plast Surg 2012 0.75
65 [Plasminogen and apolipoproteins A]. Nihon Naika Gakkai Zasshi 1997 0.75
66 Multiple novel transcripts for apolipoprotein(a)-related gene II generated by alternative splicing in tissue- and cell type-specific manners. J Biochem 1998 0.75
67 Scanning electron microscopic observations of deposits formed over the surface of dental restorative materials in the oral cavity--short-period observations of pellicles. J Nihon Univ Sch Dent 1984 0.75
68 Therapeutic importance of transplantation of a vascularised free flap for an oromandibular injury with infection and severe scar contracture. Br J Oral Maxillofac Surg 2003 0.75
69 Cellular differentiation and death in a renaissance castle. Cell Death Differ 2003 0.75
70 A case of acquired FXIII deficiency with severe bleeding symptoms. Haemophilia 2012 0.75
71 Effect of dibutyltin(IV) on the ultrastructure of African Trypanosoma spp. Parasitol Res 2003 0.75
72 [Plasma factor XII (Hageman factor) in disease states (author's transl)]. Rinsho Ketsueki 1981 0.75
73 [The management of the intracranial hemorrhage in hemophilia and the related diseases (author's transl)]. Rinsho Shinkeigaku 1981 0.75
74 [Reactions of alpha 2 plasmin inhibitor to plasmin and fibrin; its significance in fibrinolysis inhibition and hemostasis]. Rinsho Byori 1982 0.75
75 [A case of acquired systemic anhidrosis and the relationship to autoimmune diseases]. Nihon Naika Gakkai Zasshi 1991 0.75
76 Modulating effects of mucoregulating drugs on the attachment of Haemophilus influenzae. Microb Pathog 2001 0.75
77 A founder effect is proposed for factor XIII B subunit deficiency caused by the insertion of triplet AAC in exon III encoding the second Sushi domain. Thromb Haemost 1998 0.75
78 Ala601-Thr type dysplasminogenaemia genetically diagnosed in patients with retinochoroidal vascular disorders. Br J Haematol 1997 0.75
79 ["Fibrinogen Kawaguchi": a hereditary dysfibrinogenemia characterized by defective release of fibrinopeptide A associated with altered polymerization of fibrin monomers]. Nihon Ketsueki Gakkai Zasshi 1985 0.75
80 [Transglutaminase and apoptosis]. Seikagaku 2000 0.75
81 The initiation of fibrinolysis in alpha 2-plasmin inhibitor deficient plasma. Role of fibrin. Thromb Res 1986 0.75
82 An additional Glu30Lys substitution in the Gla domain of the protein Z gene is not a common polymorphism but a rare mutation, which would cause its deficiency. J Thromb Haemost 2005 0.75
83 [Molecular and genetic basis of deficiency and molecular abnormality of coagulation factor XIII]. Tanpakushitsu Kakusan Koso 1988 0.75
84 Electron microscopic examination of Aedes albopictus clone C6/36 cells infected with dengue virus 2 at elevated incubation temperature. Acta Virol 1998 0.75
85 Presence of two plasminogen alleles in normal populations. Thromb Haemost 1998 0.75
86 [Molecular pathology of the b subunit deficiency for factor XIII]. Rinsho Byori 1997 0.75
87 [Effect of carboxy-PTIO (NO scavenger) on rabbit vascular smooth muscle]. J Smooth Muscle Res 1995 0.75
88 Anatomical and neurochemical peculiarities of the pika retina: basis for lack of circadian rhythm of core temperature. Neurosci Lett 1999 0.75
89 No Val34Leu polymorphism of the gene for factor XIIIA subunit was detected by ARMS-RACE method in three Asian populations. J Thromb Haemost 2003 0.75
90 [Disseminated intravascular coagulation (DIC); findings in 40 patients (author's transl)]. Nihon Naika Gakkai Zasshi 1981 0.75
91 [Case of systemic lupus erythematosus associated with disseminated intravascular coagulation (DIC); with special reference to the relation between autoimmune phenomena and coagulation-fibrinolysis reactions]. Nihon Naika Gakkai Zasshi 1983 0.75
92 Cerebral thrombosis in a haemophiliac. Thromb Haemost 1981 0.75
93 Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines. Haemophilia 2013 0.75
94 Neutrophil response to nontypable Haemophilus influenzae in respiratory infections. Microbiol Immunol 1993 0.75
95 [Quantitative and qualitative assessment of plasma fibrinogen in patients with cerebral thrombosis (author's transl)]. Rinsho Shinkeigaku 1982 0.75