result 254 件
| FullText URL | fulltext.pdf |
|---|---|
| Author | Omichi, Ryotaro| Yoshimura, Hidekane| Shibata, Seiji B.| Vandenberghe, Luk H.| Smith, Richard J.H.| |
| Keywords | AAV2 adeno-associated virus deafness dual vectors gene therapy hair cells hearing loss injection tropism viral vectors |
| Published Date | 2020-05-13 |
| Publication Title | Molecular Therapy - Methods & Clinical Development |
| Volume | volume17 |
| Publisher | Cell Press |
| Start Page | 1167 |
| End Page | 1177 |
| ISSN | 23290501 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| Copyright Holders | © 2020 The Author(s). |
| File Version | publisher |
| PubMed ID | 32518805 |
| DOI | 10.1016/j.omtm.2020.05.007 |
| Web of Science KeyUT | 000540906400104 |
| Related Url | isVersionOf https://doi.org/10.1016/j.omtm.2020.05.007 |
| FullText URL | fulltext.pdf |
|---|---|
| Author | Morita, Daichi| Takahashi, Eizo| Morita, Masatomo| Ohnishi, Makoto| Mizuno, Tamaki| Miyoshi, Shin‐ichi| Dutta, Devarati| Ramamurthy, Thandavarayan| Chowdhury, Goutam| Mukhopadhyay, Asish K.| Okamoto, Keinosuke| |
| Keywords | antibiotic resistance diarrhea genome sequence genomic island integron Vibrio cholerae |
| Note | This is the peer reviewed version of the following article: Daichi Morita et. al. Genomic characterization of antibiotic resistance‐encoding genes in clinical isolates of Vibrio cholerae non‐O1/non‐O139 strains from Kolkata, India: generation of novel types of genomic islands containing plural antibiotic resistance genes. Microbiology and Immunology 64(6) 435-444 (2020), which has been published in final form at https://doi.org/10.1111/1348-0421.12790. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.| |
| Published Date | 2020-03-28 |
| Publication Title | Microbiology and Immunology |
| Volume | volume64 |
| Issue | issue6 |
| Publisher | Wiley |
| Start Page | 435 |
| End Page | 444 |
| ISSN | 03855600 |
| NCID | AA00738350 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| File Version | author |
| PubMed ID | 32222116 |
| DOI | 10.1111/1348-0421.12790 |
| Web of Science KeyUT | 000527073000001 |
| Related Url | isVersonOf https://doi.org/10.1111/1348-0421.12790 |
| FullText URL | MGM_fulltext.pdf MGM_Fig1.tif MGM_Fig2.tif MGM_Fig3.tiff MGM_SuppleFig1.tif MGM_SuppleFig2.tif |
|---|---|
| Author | Akiyama, Tomoyuki| Kubota, Takuo| Ozono, Keiichi| Michigami, Toshimi| Kobayashi, Daisuke| Takeyari, Shinji| Sugiyama, Yuichiro| Noda, Masahiro| Harada, Daisuke| Namba, Noriyuki| Suzuki, Atsushi| Utoyama, Maiko| Kitanaka, Sachiko| Uematsu, Mitsugu| Mitani, Yusuke| Matsunami, Kunihiro| Takishima, Shigeru| Ogawa, Erika| Kobayashi, Katsuhiro| |
| Keywords | Asfotase alfa Liquid chromatography Vitamin B6 Diagnostic marker Therapeutic monitoring |
| Published Date | 2018-07-17 |
| Publication Title | Molecular Genetics and Metabolism |
| Volume | volume125 |
| Issue | issue1-2 |
| Publisher | Elsevier |
| Start Page | 174 |
| End Page | 180 |
| ISSN | 10967192 |
| NCID | AA11158931 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| File Version | author |
| PubMed ID | 30049651 |
| DOI | 10.1016/j.ymgme.2018.07.006 |
| Web of Science KeyUT | 000447682900022 |
| Related Url | isVersionOf https://doi.org/10.1016/j.ymgme.2018.07.006 |
| JaLCDOI | 10.18926/AMO/58276 |
|---|---|
| FullText URL | 74_2_165.pdf |
| Author | Umemura, Hiroshi| Miura, Katsuhiro | Naruse, Hiromu| Hatta, Yoshihiro| Takei, Masami| Nakayama, Tomohiro| |
| Abstract | Hereditary hemorrhagic telangiectasia (HHT; also known as Osler-Weber-Rendu disease) is an autosomal dominant genetic disorder that causes frequent epistaxis, mucocutaneous telangiectasia, and visceral arteriovenous malformations. Four genes (ENG, ACVRL1, SMAD4, and GDF2) have been identified as pathogenic in HHT. We describe the case of a 50-year-old Japanese man highly suspected of having HHT due to recurrent epistaxis, mucocutaneous telangiectasia, and a family history. Genomic analysis revealed a novel missense mutation of c.100T>A, p.Cys34Ser in the patient’s ACVRL1 gene. We used 6 freeware programs to perform an in silico analysis of this mutation. The results demonstrated the mutation’s high pathogenicity. |
| Keywords | ACVRL1 hereditary hemorrhagic telangiectasia in silico analysis missense mutation Osler-Weber- Rendu disease |
| Amo Type | Case Report |
| Publication Title | Acta Medica Okayama |
| Published Date | 2020-04 |
| Volume | volume74 |
| Issue | issue2 |
| Publisher | Okayama University Medical School |
| Start Page | 165 |
| End Page | 169 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2020 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 32341592 |
| Web of Science KeyUT | 000528278500011 |
| NAID | 120006839455 |
| FullText URL | fulltext.pdf |
|---|---|
| Author | Kin, Kyohei| Yasuhara, Takao| Kameda, Masahiro| Date, Isao| |
| Keywords | animal model alpha-synuclein DJ-1 neurotoxin Parkin Parkinson's disease pesticide PINK1 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine 6-hydroxydopamine |
| Published Date | 2019-10-30 |
| Publication Title | International Journal of Molecular Sciences |
| Volume | volume20 |
| Issue | issue21 |
| Publisher | MDPI |
| Start Page | E5402 |
| ISSN | 1422-0067 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| Copyright Holders | © 2019 by the authors. |
| File Version | publisher |
| PubMed ID | 31671557 |
| DOI | 10.3390/ijms20215402 |
| Web of Science KeyUT | 000498946100160 |
| Related Url | isVersionOf https://doi.org/10.3390/ijms20215402 |
| FullText URL | NCN7_5_288.pdf Fig.pdf |
|---|---|
| Author | Nakano, Yumiko| Tsunoda, Keiichiro| Yamashita, Toru| Mitsui, Jun| Sato, Kota| Takemoto, Mami| Hishikawa, Nozomi| Ohta, Yasuyuki| Toda, Tatsushi| Tsuji, Shoji| Abe, Koji| |
| Keywords | anti-cholinesterase drug the CHRNE gene congenital myasthenic syndrome late presentation mimicking seronegative myasthenia gravis |
| Note | "This is the peer reviewed version of the following article: Yumiko Nakano et. al. Late presented congenital myasthenic syndrome with novel compound heterozygous CHRNE mutations mimicking seronegative myasthenia gravis. Neurology and Clinical Neuroscience (2019) 7(5) 288-290, which has been published in final form at https://doi.org/10.1111/ncn3.12317. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions."| |
| Published Date | 2019-06-29 |
| Publication Title | Neurology and Clinical Neuroscience |
| Volume | volume7 |
| Issue | issue5 |
| Publisher | Wiley |
| Start Page | 288 |
| End Page | 290 |
| ISSN | 2049-4173 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| File Version | author |
| DOI | 10.1111/ncn3.12317 |
| Web of Science KeyUT | 000476042100001 |
| Related Url | isVersionOf https://doi.org/10.1111/ncn3.12317 |
| FullText URL | fulltext.pdf |
|---|---|
| Author | Iwata, Yasunori| Satou, Kenji| Furuichi, Kengo| Yoneda, Ikuko| Matsumura, Takuhiro| Yutani, Masahiro| Fujinaga, Yukako| Hase, Atsushi| Morita, Hidetoshi| Ohta, Toshiko| Senda, Yasuko| Sakai-Takemori, Yukiko| Wada, Taizo| Fujita, Shinichi| Miyake, Taito| Yasuda, Haruka| Sakai, Norihiko| Kitajima, Shinji| Toyama, Tadashi| Shinozaki, Yasuyuki| Sagara, Akihiro| Miyagawa, Taro| Hara, Akinori| Shimizu, Miho| Kamikawa, Yasutaka| Ikeo, Kazuho| Shichino, Shigeyuki| Ueha, Satoshi| Nakajima, Takuya| Matsushima, Kouji| Kaneko, Shuichi| Wada, Takashi| |
| Keywords | Bloodstream infection Cna MRSA Whole genome sequencing |
| Published Date | 2019-11-15 |
| Publication Title | International Journal of Infectious Diseases |
| Volume | volume91 |
| Publisher | Elsevier |
| Start Page | 22 |
| End Page | 31 |
| ISSN | 12019712 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| Copyright Holders | © 2019 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. |
| File Version | publisher |
| PubMed ID | 31740408 |
| DOI | 10.1016/j.ijid.2019.11.003 |
| Web of Science KeyUT | 000510867100004 |
| Related Url | isVersionOf https://doi.org/10.1016/j.ijid.2019.11.003 |
| FullText URL | fulltext.pdf |
|---|---|
| Author | Yokoi, Katsuyuki| Nakajima, Yoko| Shinkai, Yasuko| Sano, Yoshimi| Imamura, Mototaka| Akiyama, Tomoyuki| Yoshikawa, Tetsushi| Ito, Tetsuya| Kurahashi, Hiroki| |
| Keywords | ALPL Dominant-negative mutations Hypophosphatasia Premature loss of deciduous |
| Published Date | 2019-12-31 |
| Publication Title | Molecular Genetics and Metabolism Reports |
| Volume | volume21 |
| Publisher | Elsevier |
| Start Page | 100515 |
| ISSN | 22144269 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| Copyright Holders | © 2019 The Authors. Published by Elsevier Inc. |
| File Version | publisher |
| PubMed ID | 31641588 |
| DOI | 10.1016/j.ymgmr.2019.100515 |
| Web of Science KeyUT | 000500718300013 |
| Related Url | isVersionOf https://doi.org/10.1016/j.ymgmr.2019.100515 |
| FullText URL | fulltext.pdf |
|---|---|
| Author | Noguchi, Hirofumi| Miyagi-Shiohira, Chika| Nakashima, Yoshiki| Kinjo, Takao| Kobayashi, Naoya| Saitoh, Issei| Watanabe, Masami| Shapiro, A. M. James| Kin, Tatsuya| |
| Keywords | induced tissue-specific progenitor cells iTP induced tissue-specific stem cells iTS induced pluripotent stem cells iPSCs reprogramming factors pancreas |
| Published Date | 2019-06-14 |
| Publication Title | Molecular Therapy - Methods and Clinical Development |
| Volume | volume13 |
| Publisher | Cell Press |
| Start Page | 243 |
| End Page | 252 |
| ISSN | 2329-0501 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| Copyright Holders | © 2019 The Author(s). |
| File Version | publisher |
| PubMed ID | 30828587 |
| DOI | 10.1016/j.omtm.2019.01.011 |
| Web of Science KeyUT | 000471284200022 |
| Related Url | isVersionOf https://doi.org/10.1016/j.omtm.2019.01.011 |
| FullText URL | NeurobiolDis_50_209.pdf |
|---|---|
| Author | Ohmori, Iori| Ouchida, Mamoru| Kobayashi, Katsuhiro| Jitsumori, Yoshimi| Mori, Akiko| Michiue, Hiroyuki| Nishiki, Teiichi| Ohtsuka, Yoko| Matsui, Hideki| |
| Note | CACNA1A variants contribute to severity of seizures in Dravet syndrome| |
| Published Date | 2013-02 |
| Publication Title | Neurobiology of disease |
| Volume | volume50 |
| Publisher | Academic Press |
| Start Page | 209 |
| End Page | 217 |
| ISSN | 09699961 |
| NCID | AA11645502 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| File Version | author |
| PubMed ID | 23103419 |
| DOI | 10.1016/j.nbd.2012.10.016 |
| Web of Science KeyUT | 000313758100023 |
| Related Url | isVersionOf https://doi.org/10.1016/j.nbd.2012.10.016 |
| JaLCDOI | 10.18926/AMO/56940 |
|---|---|
| FullText URL | 73_4_367.pdf |
| Author | Mifune-Morioka, Tomoyo| A. Uchida, Haruhito| Fukushima, Kazuhiko| Watanabe, Mayu| Ouchi, Chihiro| Mise, Koki| Kawakita, Chieko| Kano, Yuzuki| Onishi, Akifumi| Toma, Kishio| Eguchi, Jun| Wada, Nozomu| Ikeda, Fusao| Sasaki, Erika| Suganami, Yu| Kishida, Masayuki| Sugiyama, Hitoshi| Okada, Hiroyuki| Wada, Jun| |
| Abstract | Eight years prior to her present admission, a 61-year-old Japanese woman was diagnosed with autoimmune hepatitis, slowly progressive insulin-dependent diabetes mellitus, and chronic thyroiditis; she had been treated with oral prednisolone (PSL). After she suddenly discontinued PSL, she newly developed systemic lupus erythematosus. A combination therapy of oral PSL and intravenous cyclophosphamide resulted in remission. She was finally diagnosed with autoimmune polyglandular syndrome (APS) type 3 (3A ,3B, 3D), complicated with four different autoimmune diseases. Since patients with type 3 APS may present many manifestations over a long period of time, they should be carefully monitored. |
| Keywords | autoimmune polyglandular syndrome type 3 systemic lupus erythematosus autoimmune hepatitis slowly progressive insulin-dependent diabetes mellitus chronic thyroiditis |
| Amo Type | Case Report |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-08 |
| Volume | volume73 |
| Issue | issue4 |
| Publisher | Okayama University Medical School |
| Start Page | 367 |
| End Page | 372 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31439961 |
| JaLCDOI | 10.18926/AMO/56933 |
|---|---|
| FullText URL | 73_4_315.pdf |
| Author | Ono, Shintaro| Nakayama, Masaaki| Tachibana, Masato| Abu Saleh Muhammad Shahriar| Heling, Wang| Takashiba, Shogo| Ohara, Naoya| |
| Abstract | The periodontal pathogen Porphyromonas gingivalis shows colonial pigmentation on blood agar and produces gingipains (Kgp, RgpA, and RgpB), cysteine proteases involved in an organism’s virulence and pigmentation. We showed previously that deletion of the PGN_0300 gene abolished the pigmentation activity and reduced the proteolytic activity of gingipains. The role of the PGN_0297 gene, which consists of an operon with the PGN_0300 gene, is unclear. Herein we examined the effect of PGN_0297 gene deletion on the pigmentation and proteolytic activities and transcriptional levels of gingipains. A PGN_0297 gene deletion mutant (ΔPGN_0297) did not exhibit the pigmentation. The proteolytic activity of the gingipains was decreased in the culture supernatant and on the cell surface of ΔPGN_0297. The mutant ΔPGN_0297 failed to attenuate Akt phosphorylation at Thr308 and Ser473, but both phosphorylations were attenuated in the wild-type and its complementation strain. The deletion of PGN_0297 gene did not substantially affect the transcriptional levels of the gingipain genes kgp, rgpA, and rgpB. Taken together, these results indicate that PGN_0297 is closely involved in the secretion and maturation of gingipains. |
| Keywords | periodontitis Porphyromonas gingivalis gingipain C-terminal domain secretion system |
| Amo Type | Original Article |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-08 |
| Volume | volume73 |
| Issue | issue4 |
| Publisher | Okayama University Medical School |
| Start Page | 315 |
| End Page | 323 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31439954 |
| JaLCDOI | 10.18926/AMO/56930 |
|---|---|
| FullText URL | 73_4_285.pdf |
| Author | Otani, Yoshihiro| Ichikawa, Tomotsugu| Kurozumi, Kazuhiko| Date, Isao| |
| Abstract | Gliomas are characterized as highly diffuse infiltrating tumors, and currently available treatments such as surgery, radiation and chemotherapy are unfeasible or show limited efficacy against these tumors. Recent genetic and epigenetic analyses of glioma have revealed increasing evidence of the role of driver genetic alterations in glioma development and led to the identification of prognostic factors. Despite these findings, the survival rates of glioma patients remain low, and alternative treatments and novel targets are needed. Recent studies identified neural stem cells as the possible origin of gliomas, and some evidence has revealed shared functions and mechanisms between glioma cells and neurons, also supporting their similarity. The cytoskeleton plays important roles in the migration of normal cells as well as cancer cells. Recent reports have described a role for microtubules, a component of the cytoskeleton, in glioma invasion. Notably, several factors that regulate microtubule functions, such as microtubule-associated proteins, plus-end tracking proteins, or motor proteins, are upregulated in glioma tissues compared with normal tissue, and upregulation of these factors is associated with high invasiveness of glioma cells. In this review, we describe the mechanism of microtubules in glioma invasion and discuss the possibility of microtubule-targeted therapy to inhibit glioma invasion. |
| Keywords | glioma cytoskeletons invasion microtubules |
| Amo Type | Review |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-08 |
| Volume | volume73 |
| Issue | issue4 |
| Publisher | Okayama University Medical School |
| Start Page | 285 |
| End Page | 297 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31439951 |
| JaLCDOI | 10.18926/AMO/56872 |
|---|---|
| FullText URL | 73_3_273.pdf |
| Author | Hayata, Kei| Masuyama, Hisashi| Eto, Eriko| Mitsui, Takashi| Tamada, Shoko| Eguchi, Takeshi| Maki, Jota| Tani, Kazumasa| Ohira, Akiko| Washio, Yosuke| Yoshimoto, Junko| Hasegawa, Kosei| |
| Abstract | Nager syndrome is a rare disease involving severe micrognathia and upper limb shortening. In this report, we describe a case in which micrognathia of the fetus was suspected based on the observation of upper limb shortening during detailed B mode and 3D/4D ultrasonographic observation, and combined fetal MRI and 3D-CT led to a prenatal diagnosis of Nager syndrome. Upon birth, because severe micrognathia caused airway obstruction and made it difficult to spread the larynx for intubation, effective ventilation could not be carried out and a tracheostomy was necessary. Since a differential diagnosis of Nager syndrome can be made based on the fact that micrognathia typically co-occurs with upper limb shortening, it is possible to diagnose the disease before birth and prepare for life-saving measures accordingly. |
| Keywords | Nager syndrome acrofacial dysostosis micrognathia jaw index SF3B4 |
| Amo Type | Case Report |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-06 |
| Volume | volume73 |
| Issue | issue3 |
| Publisher | Okayama University Medical School |
| Start Page | 273 |
| End Page | 277 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31235977 |
| JaLCDOI | 10.18926/AMO/56870 |
|---|---|
| FullText URL | 73_3_263.pdf |
| Author | Shimoyama, Yuichiro| Umegaki, Osamu| Ooi, Yukimasa| Shigemoto, Sho| Agui, Tomoyuki| Kadono, Noriko| Minami, Toshiaki| |
| Abstract | A previously healthy 40-year-old Japanese male was urgently admitted with a 2-month history of dysphagia, 30-kg weight loss, and fever. Human immunodeficiency virus (HIV) antibodies and cytomegalovirus antigenemia were positive. Pneumocystis pneumonia and cytomegalovirus pneumonia were suspected. The patient was diagnosed with acquired immune deficiency syndrome (AIDS). Cytomegalovirus antigenemia became negative 20 days after the positive result. On hospital day 41, he experienced cardiopulmonary arrest. The clinical diagnosis was fulminant type 1 diabetes mellitus. He later developed hypoglycemia and was diagnosed with adrenal insufficiency accompanied by septic shock. He died of multiple organ failure 29 h post-admission to our ICU. |
| Keywords | fulminant type 1 diabetes mellitus human immunodeficiency virus cytomegalovirus hypoglycemia |
| Amo Type | Case Report |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-06 |
| Volume | volume73 |
| Issue | issue3 |
| Publisher | Okayama University Medical School |
| Start Page | 263 |
| End Page | 267 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31235975 |
| JaLCDOI | 10.18926/AMO/56869 |
|---|---|
| FullText URL | 73_3_255.pdf |
| Author | Seki, Daisuke| Takeshita, Nobuo| Seiryu, Masahiro| Deguchi, Toru| Takano-Yamamoto, Teruko| |
| Abstract | Orthodontists need to understand the orthodontic risks associated with systemic disorders. Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant disorder with genetic and morphological variability. The risks of orthodontic treatment in ARS patients have been unclear. Here we describe the correction of an anterior open bite in a 15-year-old Japanese female ARS patient by molar intrusion using sectional archwires with miniscrew implants. An undesirable development of external apical root resorption (EARR) was observed in all intrusive force-applied posterior teeth during the patient’s orthodontic treatment, suggesting that ARS patients have a higher risk of EARR than the general population. |
| Keywords | Axenfeld-Rieger syndrome external apical root resorption miniscrew implant anterior open bite |
| Amo Type | Case Report |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-06 |
| Volume | volume73 |
| Issue | issue3 |
| Publisher | Okayama University Medical School |
| Start Page | 255 |
| End Page | 262 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31235974 |
| FullText URL | J_ClinMicrobiol_51_3_1040.pdf |
|---|---|
| Author | Naha, A.| Chowdhury, G.| Ghosh-Banerjee, J.| Senoh, M.| Takahashi, T.| Ley, B.| Thriemer, K.| Deen, J.| Seidlein, L. V.| Ali, S. M.| Khatib, A.| Ramamurthy, T.| Nandy, R. K.| Nair, G. B.| Takeda, Y.| Mukhopadhyay, A. K.| |
| Keywords | Vibrio cholerae ctxB Cholera PFGE |
| Note | This is an Accepted Manuscript of an article published by American Society for Microbiology| |
| Published Date | 2013-03 |
| Publication Title | Journal of Clinical Microbiology |
| Volume | volume51 |
| Issue | issue3 |
| Publisher | American Society for Microbiology |
| Start Page | 1040 |
| End Page | 1045 |
| ISSN | 00951137 |
| NCID | AA00695531 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| File Version | author |
| PubMed ID | 23325815 |
| DOI | 10.1128/JCM.03162-12 |
| Web of Science KeyUT | 000315121700055 |
| Related Url | isVersionOf https://doi.org/10.1128/JCM.03162-12 |
| FullText URL | Nucleic _Acids_Res_44_12_5658.pdf |
|---|---|
| Author | Bhupesh Kumar Thakur| Dasgupta, Nirmalya| Ta, Atri| Das, Santasabuj| |
| Published Date | 2016-04-07 |
| Publication Title | Nucleic Acids Research |
| Volume | volume44 |
| Issue | issue12 |
| Publisher | Oxford University Press |
| Start Page | 5658 |
| End Page | 5672 |
| ISSN | 03051048 |
| NCID | AA00760269 |
| Content Type | Journal Article |
| language | English |
| OAI-PMH Set | 岡山大学 |
| File Version | publisher |
| PubMed ID | 27060138 |
| DOI | 10.1093/nar/gkw189 |
| Web of Science KeyUT | 000381210900019 |
| Related Url | isVersionOf https://doi.org/10.1093/nar/gkw189 |
| JaLCDOI | 10.18926/AMO/56655 |
|---|---|
| FullText URL | 73_2_181.pdf |
| Author | Okamura, Tomoka| Washio, Yousuke| Yoshimoto, Junko| Tani, Kazumasa| Tsukahara, Hirokazu| Shimada, Akira| |
| Abstract | Most cases of transient abnormal myelopoiesis (TAM) in neonates with Down syndrome (DS) resolve spontaneously; however, DS-TAM neonates with hydrops fetalis (HF) show poor clinical outcomes. We report three infants with DS-TAM and HF who were treated with exchange transfusion (ET) followed by low-dose cytarabine (LD-CA). All of them survived without developing liver failure, acute leukemia, or other serious adverse events. Our results suggest that this combination treatment with ET and LD-CA would be safe, tolerable and effective as an novel approach for DS-TAM patients with HF. |
| Keywords | cytarabine Down syndrome exchange transfusion hydrops fetalis transient abnormal myelopoiesis |
| Amo Type | Case Report |
| Publication Title | Acta Medica Okayama |
| Published Date | 2019-04 |
| Volume | volume73 |
| Issue | issue2 |
| Publisher | Okayama University Medical School |
| Start Page | 181 |
| End Page | 188 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| Content Type | Journal Article |
| language | English |
| Copyright Holders | CopyrightⒸ 2019 by Okayama University Medical School |
| File Version | publisher |
| Refereed | True |
| PubMed ID | 31015754 |
| FullText URL | K0005801_abstract_review.pdf K0005801_fulltext.pdf K0005801_summary.pdf |
|---|---|
| Author | Haruma, Tomoko| |
| Published Date | 2018-09-27 |
| Content Type | Thesis or Dissertation |
| Grant Number | 甲第5801号 |
| Granted Date | 2018-09-27 |
| Thesis Type | Doctor of Philosophy in Medical Science |
| Grantor | 岡山大学 |
| language | English |
