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JaLCDOI 10.18926/AMO/56178
FullText URL 72_4_401.pdf
Author Wada, Nozomu| Ikeda, Fusao| Mori, Chizuru| Takaguchi, Koichi| Fujioka, Shin-ichi| Kobashi, Haruhiko| Morimoto, Yoichi| Kariyama, Kazuya| Sakaguchi, Kosaku| Hashimoto, Noriaki| Moriya, Akio| Kawaguchi, Mitsuhiko| Miyatake, Hirokazu| Hagihara, Hiroaki| Kubota, Junichi| Takayama, Hiroki| Takeuchi, Yasuto| Yasunaka, Tetsuya| Takaki, Akinobu| Iwasaki, Yoshiaki| Okada, Hiroyuki|
Abstract Daclatasvir (DCV) + asunaprevir (ASV) combination therapy has become available for patients with hepatitis C virus (HCV) serogroup 1 infection. We studied the efficacy of this therapy by focusing on the factors associated with sustained virological responses (SVR) including resistance-associated variants (RAVs) and mixed infection of different HCV genotypes. We enrolled 951 HCV serogroup 1-positive patients who received this combination therapy at our hospital or affiliated hospitals. The presence of RAVs in non-structural (NS) regions 3 and 5A was analyzed by direct sequencing. HCV genotypes were determined by PCR with genotype-specific primers targeting HCV core and NS5B regions. SVR was achieved in 91.1% of patients. Female sex, age > 70 years, and RAVs were significantly associated with non-SVR (p<0.01 for all). Propensity score-matching results among the patients without RAVs regarding sex, age, and fibrosis revealed that mixed HCV infection determined by HCV NS5B genotyping showed significantly lower SVR rates than 1B-mono infection (p=0.02). Female sex and RAVs were significant factors associated with treatment failure of this combination therapy for patients with HCV serogroup 1 infection. Mixed HCV infection other than 1B-mono infection would be useful for predicting treatment failure.
Keywords mixed genotype daclatasvir asunaprevir HCV serogrouping 1 infection
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-08
Volume volume72
Issue issue4
Publisher Okayama University Medical School
Start Page 401
End Page 406
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30140089
JaLCDOI 10.18926/AMO/56177
FullText URL 72_4_395.pdf
Author Hishii, Shuhei| Miyatake, Nobuyuki| Nishi, Hiroyuki| Katayama, Akihiko| Ujike, Kazuhiro| Koumoto, Kiichi| Hashimoto, Hiroo|
Abstract We explored the relationship between sedentary behavior and the health-related quality of life (HRQOL) in patients on chronic hemodialysis. A total of 60 outpatients, aged 71.1±12.0 years, were enrolled in this cross-sectional study. Sedentary behavior was measured using a tri-accelerometer and HRQOL was evaluated by the Euro-QOL questionnaire (EQ-5D). The relationship between the patients’ sedentary behavior and HRQOL was evaluated by simple and multiple correlation analyses. The relative sedentary behavior (%) for total days was 73.7±12.9% and the EQ-5D scores were 0.688±0.233. Relative sedentary behavior (%) was negatively correlated with EQ-5D scores for total days, hemodialysis days and non-hemodialysis days. The relative light-intensity physical activity (LPA) (%) and relative moderately vigorous-intensity physical activity (MVPA) (%) were correlated with EQ-5D scores. Multiple regression showed that the relative sedentary behavior (%) had a clinical impact on EQ-5D scores after adjusting for confounding factors for total, hemodialysis and non-hemodialysis days. Sedentary behavior is closely linked to HRQOL, and reducing sedentary behavior may be beneficial to improve the HRQOL of patients on chronic hemodialysis.
Keywords physical activity sedentary behavior health-related quality of life HRQOL hemodialysis
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-08
Volume volume72
Issue issue4
Publisher Okayama University Medical School
Start Page 395
End Page 400
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30140088
JaLCDOI 10.18926/AMO/56176
FullText URL 72_4_387.pdf
Author Hada, Kumiko| Kuse, Emiko| Nakatsuka, Mikiya|
Abstract To elucidate the psychiatric characteristics of mothers and the supportive behavior of their partners during late pregnancy, 131 mothers who gave birth at 2 general hospitals in City A between August 2009 and September 2010 (control group: n=90; recurrent pregnancy loss (RPL) group: n=41) completed a self-administered questionnaire on four separate occasions: during late pregnancy, during hospitalization, at 1-month postpartum, and at 3-months postpartum. The RPL group had significantly (p=0.03) lower anxiety regarding potential change in their appearance than the controls, but were more likely to worry about losing their baby (58% vs. 38%) (p=0.021). At 3-months postpartum, the RPL group reported having had more stress during pregnancy than the controls (49% vs. 31%; p=0.041). There were no significant differences in state or trait anxiety (State-Trait Anxiety Inventory) between the 2 groups at any of the four measurements. However, state anxiety decreased significantly throughout the hospitalization for controls (p <0.001), but did not decrease significantly for the RPL group until 3 months postpartum (p<0.05). RPL participants who expressed high satisfaction with their partners’ supportive behavior received significantly greater psychological support than did participants with low satisfaction. Healthcare professionals should attempt to support both members of RPL couples.
Keywords recurrent pregnancy loss persistent anxiety supportive behavior of partner psychological support
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-08
Volume volume72
Issue issue4
Publisher Okayama University Medical School
Start Page 387
End Page 394
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30140087
JaLCDOI 10.18926/AMO/56171
FullText URL 72_4_359.pdf
Author Mitsui, Takashi| Tani, Kazumasa| Maki, Jota| Eguchi, Takeshi| Tamada, Shoko| Eto, Eriko| Hayata, Kei| Masuyama, Hisashi|
Abstract Abnormal glucose metabolism during pregnancy is an established risk factor for preeclampsia (PE). Disruption of the balance between placental angiogenic factors is linked to PE pathophysiology. We examined whether hypoxia-induced factor-1α (HIF-1α) and protein kinase Cβ (PKCβ) are involved in the regulation of placental angiogenic factors under high-glucose conditions in vitro. The human choriocarcinoma cell lines BeWo and JEG-3, and the human trophoblast cell line HTR-8/SVneo were cultured with 10 and 25 mmol/L glucose [control glucose group (CG) and high-glucose group (HG), respectively]. We examined the changes in HIF-1α, soluble fms-like tyrosine kinase-1 (sFlt-1), placental growth factor (PlGF), and vascular endothelial growth factor (VEGF) expression in the CG and HG by real-time PCR and ELISA. PKC activation was also measured by ELISA. The expressions of HIF-1α, sFlt-1, PlGF, and VEGF were significantly higher in the HG than in the CG. PKC activity was significantly increased in the HG. High glucose affected the expression of angiogenic factors in choriocarcinoma cells via the PKCβ and HIF-1α pathways, suggesting their involvement in PE pathogenesis.
Keywords high-glucose condition preeclampsia protein kinase C
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-08
Volume volume72
Issue issue4
Publisher Okayama University Medical School
Start Page 359
End Page 367
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30140083
JaLCDOI 10.18926/AMO/56170
FullText URL 72_4_351.pdf
Author Goto, Shinichiro| Nosaka, Nobuyuki| Yorifuji, Takashi| Wada, Tomoaki| Fujii, Yosuke| Yashiro, Masato| Washio, Yosuke| Hasegawa, Kosei| Tsukahara, Hirokazu| Morishima, Tsuneo|
Abstract We studied the etiology of pediatric acute encephalitis/encephalopathy (pAEE) using epidemiological data obtained from a nationwide survey in Japan. Two-step questionnaires were sent to the pediatric departments of hospitals throughout the country in 2007, querying the number of the cases during 2005-2006 as the first step, and asking for the details of clinical information as the second step. In all, 636 children with pAEE (age ≤ 15 years) were enrolled. For the known etiology of pAEE (63.5% of the total cases), 26 microbes and 2 clinical entities were listed, but the etiology of 36.5% remained unknown. Influenza virus (26.7%), exanthem subitum (12.3%), and rotavirus (4.1%) were the most common, and the incidence of pAEE peaked at the age of 1 year. This trend was common among all etiologies. Among the neurological symptoms observed at the onset of pAEE, seizures were observed more often in patients aged ≤ 3 years, although abnormal speech and behavior were also common in older children. Undesirable outcomes (death and neurological sequelae) occurred at high rates in patients with any known etiology other than mycoplasma. In conclusion, these findings provide comprehensive insight into pAEE in Japan.
Keywords childhood encephalitis encephalopathy etiology Japan pAEE
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-08
Volume volume72
Issue issue4
Publisher Okayama University Medical School
Start Page 351
End Page 357
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30140082
JaLCDOI 10.18926/AMO/56167
FullText URL 72_4_331.pdf
Author Miyahara, Kanae| Kuroda, Masahiro| Yoshimura, Yuuki| Aoyama, Hideki| Oita, Masataka| Sugianto, Irfan| Matsuzaki, Hidenobu| Ihara, Hiroki| Katayama, Norihisa| Katsui, Kuniaki| Kanazawa, Susumu| Asaumi, Junichi|
Abstract We used image-processing software to analyze the setup errors at the skin surface position of breast cancer patients (n=66) who underwent post-operative whole breast irradiation at our hospital in 2014-2015. The sixty-six digital reconstructed radiographs (DRR) were created at the treatment planning for each patient. The lineacgraphies (n=377) were taken after the patients’ setup during radiotherapy. The lineacgraphies and DRR were superimposed at the skin surface position for each patient with the image-processing software. We measured the deviations of the isocenters for the nipple-lung (X) direction and craniocaudal (Y) direction and the deviation of the rotation angle of the XY axes between the lineacgraphy and DRR on the superimposed images. The systematic error (μ, Σ) and random error (σ) were calculated from the X and Y deviations and rotation angle deviation. The μ of X, Y, and rotation angle were 0.01 mm, −1.2 mm, and 0.05°, respectively. The Σ of X, Y, and rotation angle were 1.8 mm, 1.5 mm, and 0.9°, respectively. The σ of X, Y, and rotation angle were 2.0 mm, 1.5 mm, and 1.0°, respectively. Our analyses thus revealed that evaluations using image-processing software at the skin surface position in routine breast radiotherapy result in sufficiently small setup errors.
Keywords breast cancer radiotherapy position verification skin surface image processing software
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-08
Volume volume72
Issue issue4
Publisher Okayama University Medical School
Start Page 331
End Page 336
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 30140079
FullText URL MicroBio_Res_215_29.pdf table_S1.pdf Fig.pdf
Author Sing’ombe Ombiro Geofrey| Sawai, Taku| Noutoshi, Yoshiteru| Nishina, Yuta| Matsui, Hidenori| Yamamoto, Mikihiro| Toyoda, Kazuhiro| Ichinose, Yuki|
Keywords Bactericide Ralhibitins Ralstonia solanacearum Lead compounds
Note This is an Accepted Manuscript of an article published by Elsevier| This fulltext will be available in June 2019|
Published Date 2018-10
Publication Title Microbiological Research
Volume volume215
Publisher Elsevier
Start Page 29
End Page 35
ISSN 0944-5013
NCID AA11017780
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version author
DOI 10.1016/j.micres.2018.06.005
Web of Science KeyUT 000446291000005
Related Url isVersionOf https://doi.org/10.1016/j.micres.2018.06.005
Title Alternative Effects of Upstream Disturbances on Supersonic Flowfield with Transverse Injection
FullText URL TransJSASS_64_4_244.pdf
Author 河内 俊憲| 浦本 翔平| 升谷 五郎|
Keywords Scramjet Combustor Wall Injection Spatial Correlation Turbulence Very Large Scale Motion Stereoscopic PIV
Published Date 2016-08-05
Publication Title 日本航空宇宙学会論文集
Volume volume64
Issue issue4
Publisher 日本航空宇宙学会
Start Page 244
End Page 252
ISSN 13446460
NCID AA11307372
Content Type Journal Article
language Japanese
OAI-PMH Set 岡山大学
File Version publisher
DOI 10.2322/jjsass.64.244
Related Url isVersionOf https://doi.org/10.2322/jjsass.64.244
FullText URL Stem_Cells_International_7530942.pdf
Author Eguchi, Takanori| Kuboki, Takuo|
Published Date 2016-06-12
Publication Title Stem cells international
Volume volume2016
Publisher SAGE-Hindawi Access to Research
Start Page 7530942
ISSN 1687-966X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version publisher
PubMed ID 27382371
DOI 10.1155/2016/7530942
Web of Science KeyUT 000378772000001
Related Url isVersionOf https://doi.org/10.1155/2016/7530942
FullText URL PlosOne_2018_e0191109.pdf
Author Eguchi, Takanori| Sogawa, Chiharu| Okusha, Yuka| Uchibe, Kenta| Iinuma, Ryosuke| Ono, Kisho| Nakano, Keisuke| Murakami, Jun| Itoh, Manabu| Arai, Kazuya| Fujiwara, Toshifumi| Namba, Yuri| Murata, Yoshiki| Ohyama, Kazumi| Shimomura, Manami| Okamura, Hirohiko| Takigawa, Masaharu| Nakatsura, Tetsuya| Kozaki, Kenichi| Okamoto, Kuniaki| Calderwood, Stuart K.|
Published Date 2018-02-07
Publication Title PlosOne
Volume volume13
Issue issue2
Publisher Public Library Science
Start Page e0191109
ISSN 19326203
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version publisher
PubMed ID 29415026
DOI 10.1371/journal.pone.0191109
Web of Science KeyUT 000424325300015
Related Url isVersionOf https://doi.org/10.1371/journal.pone.0191109
FullText URL J_Cell_Biochem_116_10_2146.pdf
Author Eguchi , Taka| Prince, Thomas| Wegiel, Barbara| Calderwood, Stuart K.|
Keywords CANCER FINGER-1 INVASION MYELOID NUCLEAR BODY SUMO ZINC
Published Date 2015-04-21
Publication Title Journal of cellular biochemistry
Volume volume116
Issue issue10
Publisher Wiley
Start Page 2146
End Page 2154
ISSN 0730-2312
NCID AA1052210X
Content Type Journal Article
language Japanese
OAI-PMH Set 岡山大学
File Version author
PubMed ID 25903835
DOI 10.1002/jcb.25203
Web of Science KeyUT 000359809400004
Related Url isVersionOf https://doi.org/10.1002/jcb.25203
FullText URL J_Cell_Biochem_201805_27040.pdf
Author Okusha, Yuka| Eguchi, Takanori| Sogawa, Chiharu| Okui, Tatsuo| Nakano, Keisuke| Okamoto, Kuniaki| Kozaki, Ken‐Ichi|
Keywords PEX domain cancer metastasis non-proteolytic MMP nuclear MMP tumor stroma
Published Date 2018-05-15
Publication Title Journal of Cellular Biochemistry
Volume volume119
Issue issue9
Publisher Wiley
Start Page 7363
End Page 7376
ISSN 1097-4644
NCID AA1052210X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 29761931
DOI 10.1002/jcb.27040
Web of Science KeyUT 000445187800024
Related Url isVersionOf https://doi.org/10.1002/jcb.27040
FullText URL Mol_Cell_Biol_28_7_2391.pdf
Author Eguchi, Takanori| Kubota, Satoshi| Kawata, Kazumi| Mukudai, Yoshiki| Uehara, Junji| Ohgawara, Toshihiro| Ibaragi, Soichiro| Sasaki, Akira| Kuboki, Takuo| Takigawa, Masaharu|
Published Date 2008-04
Publication Title Molecular and Cellular Biology
Volume volume28
Issue issue7
Publisher American Society for Microbiology
Start Page 2391
End Page 2413
ISSN 0270-7306
NCID AA10620925
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version publisher
PubMed ID 18172013
DOI 10.1128/MCB.01288-07
Web of Science KeyUT 000254181400025
Related Url isVersionOf https://doi.org/10.1128/MCB.01288-07
FullText URL J_Cell_Biochem_118_1_43.pdf
Author Eguchi, Takanori| Calderwood, Stuart K.| Takigawa, Masaharu| Kubota, Satoshi| Kozaki, Ken‐ichi|
Keywords CBXs CHROMOBOX PROTEINS HEAT SHOCK FACTOR 1 HEAT SHOCK PROTEINS HETEROCHROMATIN PROTEINS HP1 HSF1 HSPs MATRIX METALLOPROTEINASE MMP3 TRANSCRIPTION
Published Date 2016-05-21
Publication Title Journal of Cellular Biochemistry
Volume volume118
Issue issue1
Publisher Wiley
Start Page 43
End Page 51
ISSN 07302312
NCID AA1052210X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 27206651
DOI 10.1002/jcb.25607
Web of Science KeyUT 000387809300005
Related Url isVersionOf https://doi.org/10.1002/jcb.25607
FullText URL J_Cell_Biochem_201805_27039.pdf
Author Ono, Kisho| Eguchi , Takanori| Sogawa, Chiharu| Calderwood, Stuart K.| Futagawa, Junya| Kasai, Tomonari| Seno, Masaharu| Okamoto, Kuniaki| Sasaki, Akira| Kozaki, Ken‐ichi|
Keywords EV proteomics exosome extracellular vesicle heat shock proteins lymph-node-metastatic oral cancer molecular chaperone
Published Date 2018-05-16
Publication Title Journal of Cellular Biochemistry
Volume volume119
Issue issue9
Publisher Wiley
Start Page 7350
End Page 7362
ISSN 07302312
NCID AA1052210X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 29768689
DOI 10.1002/jcb.27039
Web of Science KeyUT 000445187800023
Related Url isVersionOf https://doi.org/10.1002/jcb.27039
FullText URL K0005791_summary.pdf K0005791_fulltext_org.pdf K0005791_abstract_review.pdf
Author Mitsui, Takashi|
Published Date 2018-06-30
Content Type Thesis or Dissertation
Grant Number 甲第5791号
Granted Date 2018-06-30
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL K0005784_abstract_review.pdf K0005784_summary.pdf K0005784_fulltext.pdf
Author Yamanari, Toshio|
Published Date 2018-06-30
Content Type Thesis or Dissertation
Grant Number 甲第5784号
Granted Date 2018-06-30
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL BBB_82_7_1172.pdf
Author Uemura, Ryota| Ogura, Mikako| Matsumaru, Chihiro| Akiyama, Tsuyoshi| Maeda, Megumi| Kimura, Yoshinobu|
Keywords Acidic PNGase FNG: free N-glycan Fuc: L-fucose Gal: D-galactose GlcNAc: N-acetyl-D-glucosamine HPLC: high-performance liquid chromatography Man: D-mannose NeuNAc2Gal2GlcNAc2Man3GlcNAc1: NeuNAcα2–6Galβ1–4GlcNAcβ1–2Manα1–6(NeuNAcα2–6Galβ1–4GlcNAcβ1–2Manα1–3)Manβ1–4GlcNAc NeuNAc2Gal2GlcNAc2Man3GlcNAc2: NeuNAcα2–6Galβ1–4GlcNAcβ1–2Manα1–6(NeuNAcα2–6Galβ1–4GlcNAcβ1–2Manα1–3)Manβ1–4GlcNAcβ1–4GlcNAc NeuNAc: N-acetylneuraminic acid PA-: pyridylamino PNGase-A: aPNGase from almond seed PNGase-Le: aPNGase from tomato (Solanum lycopersium L.) PNGase: peptide:N-glycanase PTC: plant complex type RCA120: Ricinus communis agglutinin (120 kDa) RP-HPLC: reversed-phase HPLC SF-HPLC: size-fractionation HPLC Xyl: D-xylose affinity chromatography enzyme assay free N-glycans transgenic plant
Published Date 2018-04
Publication Title Bioscience, Biotechnology, and Biochemistry
Volume volume82
Issue issue7
Publisher Taylor & Francis
Start Page 1172
End Page 1175
ISSN 09168451
NCID AA10824164
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 29658432
DOI 10.1080/09168451.2018.1459464
Web of Science KeyUT 000436822900015
Related Url isVersionOf https://doi.org/10.1080/09168451.2018.1459464
FullText URL BBB_81_7_1405.pdf
Author Tanabe, Chinatsu| Kaori, Furuta| Megumi, Maeda| Yoshinobu, Kimura|
Keywords Phyllostachys edulis antigenic N-glycans bamboo shoot plant N-glycans plant glycoproteins
Published Date 2017-05
Publication Title Bioscience, Biotechnology, and Biochemistry
Volume volume81
Issue issue7
Publisher Taylor & Francis
Start Page 1405
End Page 1408
ISSN 0916-8451
NCID AA10824164
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
File Version author
PubMed ID 28471334
DOI 10.1080/09168451.2017.1320519
Web of Science KeyUT 000402992500021
Related Url isVersionOf https://doi.org/10.1080/09168451.2017.1320519
JaLCDOI 10.18926/AMO/56074
FullText URL 72_3_283.pdf
Author Namba, Shihoko| Ikeda, Fusao| Takaguchi, Koichi| Shimomura, Yasuyuki| Yasunaka, Tetsuya| Okada, Hiroyuki|
Abstract We investigated whether a small amount of blood collected by fingertip blood sampling would be adequate in a mass examination for hepatitis virus infection in Japan. A cross-sectional survey was conducted at health fairs in Kasaoka City and Shodoshima Island, where participants took the hepatitis screening test. A total of 114 consecutive individuals who took the hepatitis screening test were enrolled. Twenty microliters of plasma was successfully obtained from all participants. Among the participants, two had positive results for HBs antigen and two were positive for anti-HCV; all four were > 60 years old and rarely visited the hospital. Thirty-three and 38 patients chronically infected with HBV and HCV, respectively, were examined for confirmatory assays at participating hospitals. All subjects with undetectable serum levels of HBs antigen and anti-HCV had undetectable levels of both markers in fingertip blood, and the levels in serum and fingertip blood were significantly correlated (p<0.01). The lower detection limit of HBs antigen was defined as 0.005 IU/ml, and the cut-off value of anti-HCV was 1.0 by using 10-μl fingertip blood samples. The fingertip blood sampling described herein may be adequate in mass examinations for hepatitis virus testing in Japan.
Keywords fingertip hepatitis test HBV HCV Japan
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2018-06
Volume volume72
Issue issue3
Publisher Okayama University Medical School
Start Page 283
End Page 287
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2018 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 29926006