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Items: 1 to 50 of 121

1.

Deletion of Gb3 Synthase in Mice Resulted in the Attenuation of Bone Formation via Decrease in Osteoblasts.

Hamamura K, Hamajima K, Yo S, Mishima Y, Furukawa K, Uchikawa M, Kondo Y, Mori H, Kondo H, Tanaka K, Miyazawa K, Goto S, Togari A.

Int J Mol Sci. 2019 Sep 18;20(18). pii: E4619. doi: 10.3390/ijms20184619.

2.

Integrative genome analysis identified the KANNO blood group antigen as prion protein.

Omae Y, Ito S, Takeuchi M, Isa K, Ogasawara K, Kawabata K, Oda A, Kaito S, Tsuneyama H, Uchikawa M, Wada I, Ohto H, Tokunaga K.

Transfusion. 2019 Jul;59(7):2429-2435. doi: 10.1111/trf.15319. Epub 2019 Apr 24.

PMID:
31020675
3.

Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population.

Ushiki T, Tsuneyama H, Masuko M, Kozakai T, Kasami T, Tanaka T, Uchikawa M, Kitajima T, Kasai E, Komata T, Katagiri T, Kamimura M, Sato K, Fuse I, Ogasawara K, Nakata K.

Transfusion. 2019 Aug;59(8):2519-2522. doi: 10.1111/trf.15312. Epub 2019 Apr 16.

PMID:
30990901
4.

Newly manufactured Marukome MK-34-1 miso with angiotensin-converting enzyme inhibitory activity and its antihypertensive effects in genetic hypertensive rat models.

Tomari HS, Uchikawa M, Yamazaki A, Hirabayashi S, Yamakawa S, Kitagawa M, Yamada M, Itou S, Yamamoto T, Uehara Y.

Hypertens Res. 2019 Jun;42(6):790-800. doi: 10.1038/s41440-018-0197-z. Epub 2019 Jan 10.

PMID:
30631160
5.

A novel c.166A>T (p.Thr56Ser) mutation in GYPB*S accounting for unusual S antigen expression.

Suzuki Y, Isa K, Ogasawara K, Kikuchi Y, Yabe R, Tsuno NH, Uchikawa M, Satake M.

Vox Sang. 2019 Feb;114(2):171-173. doi: 10.1111/vox.12737. Epub 2018 Dec 6.

PMID:
30523644
6.

Evaluation of Collateral Source Characteristics With 3-Dimensional Analysis Using Micro-X-Ray Computed Tomography.

Arima Y, Hokimoto S, Tabata N, Nakagawa O, Oshima A, Matsumoto Y, Sato T, Mukunoki T, Otani J, Ishii M, Uchikawa M, Yamamoto E, Izumiya Y, Kaikita K, Ogawa H, Nishiyama K, Tsujita K.

J Am Heart Assoc. 2018 Mar 23;7(6). pii: e007800. doi: 10.1161/JAHA.117.007800.

7.

Cooperation of Sall4 and Sox8 transcription factors in the regulation of the chicken Sox3 gene during otic placode development.

Okamoto Y, Nishimura N, Matsuda K, Ranawakage DC, Kamachi Y, Kondoh H, Uchikawa M.

Dev Growth Differ. 2018 Apr;60(3):133-145. doi: 10.1111/dgd.12427. Epub 2018 Mar 8.

PMID:
29520762
8.

The B allele with a 5·8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with Bm and A1 Bm phenotypes.

Ogasawara K, Miyazaki T, Ito S, Yabe R, Uchikawa M, Enomoto T, Yokoya N, Hori Y, Kumamoto M, Watanabe S, Satake M.

Vox Sang. 2018 May;113(4):393-396. doi: 10.1111/vox.12642. Epub 2018 Feb 23.

PMID:
29473176
9.

Silent KEL alleles identified from Japanese individuals with the Ko phenotype.

Onodera T, Kawai M, Obara K, Enomoto T, Sasaki K, Osabe T, Ogasawara K, Toyoda C, Tsuneyama H, Uchikawa M, Inaba S, Satake M.

Vox Sang. 2018 Apr;113(3):290-296. doi: 10.1111/vox.12628. Epub 2017 Dec 27.

PMID:
29280152
10.

Nasal and otic placode specific regulation of Sox2 involves both activation by Sox-Sall4 synergism and multiple repression mechanisms.

Sugahara S, Fujimoto T, Kondoh H, Uchikawa M.

Dev Biol. 2018 Jan 1;433(1):61-74. doi: 10.1016/j.ydbio.2017.11.005. Epub 2017 Nov 11.

11.

Immunoglobulin G Fc glycans are not essential for antibody-mediated immune suppression to murine erythrocytes.

Marjoram D, Cruz-Leal Y, Bernardo L, Le NPL, Crispin M, Yu X, Uchikawa M, Lazarus AH.

Blood. 2017 Dec 28;130(26):2902-2905. doi: 10.1182/blood-2017-06-793729. Epub 2017 Nov 6. No abstract available.

PMID:
29109102
12.

Enhancer Analyses Using Chicken Embryo Electroporation.

Uchikawa M, Nishimura N, Iwafuchi-Doi M, Kondoh H.

Methods Mol Biol. 2017;1650:191-202. doi: 10.1007/978-1-4939-7216-6_12.

PMID:
28809022
13.

Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype.

Kawai M, Obara K, Onodera T, Enomoto T, Ogasawara K, Tsuneyama H, Uchikawa M, Inaba S.

Transfusion. 2017 Apr;57(4):1072-1077. doi: 10.1111/trf.13990. Epub 2017 Feb 14.

PMID:
28194794
14.

Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.

Isa K, Sasaki K, Ogasawara K, Saito M, Tsuneyama H, Yabe R, Uchikawa M, Satake M.

Vox Sang. 2016 Oct;111(3):315-319. doi: 10.1111/vox.12413. Epub 2016 May 17.

PMID:
27183894
15.

Validation of the diagnostic utility of D-dimer measurement in patients with acute aortic syndrome.

Kotani Y, Toyofuku M, Tamura T, Shimada K, Matsuura Y, Tawa H, Uchikawa M, Higashi S, Fujimoto J, Yagita K, Sato F, Atagi Y, Hamasaki T, Tsujimoto T, Chishiro T.

Eur Heart J Acute Cardiovasc Care. 2017 Apr;6(3):223-231. doi: 10.1177/2048872616652261. Epub 2016 Jun 2.

PMID:
27257263
16.

Regulation of trunk neural crest delamination by δEF1 and Sip1 in the chicken embryo.

Yasumi T, Inoue M, Maruhashi M, Kamachi Y, Higashi Y, Kondoh H, Uchikawa M.

Dev Growth Differ. 2016 Feb;58(2):205-14. doi: 10.1111/dgd.12256. Epub 2015 Dec 22.

PMID:
26691438
17.

Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3.

Isa K, Yamamuro Y, Ogasawara K, Yabe R, Ogiyama Y, Ito S, Takahashi Y, Kominato Y, Sano R, Uchikawa M.

Vox Sang. 2016 Apr;110(3):285-7. doi: 10.1111/vox.12363. Epub 2015 Nov 3.

PMID:
26529276
18.

Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expression.

Ogasawara K, Sasaki K, Isa K, Tsuneyama H, Uchikawa M, Satake M, Tadokoro K.

Vox Sang. 2016 Feb;110(2):179-84. doi: 10.1111/vox.12322. Epub 2015 Sep 4.

PMID:
26340140
19.

Molecular basis for D- Japanese: identification of novel DEL and D- alleles.

Ogasawara K, Suzuki Y, Sasaki K, Osabe T, Isa K, Tsuneyama H, Uchikawa M, Satake M, Tadokoro K.

Vox Sang. 2015 Nov;109(4):359-65. doi: 10.1111/vox.12290. Epub 2015 May 7.

PMID:
25953588
20.

A novel DO null allele with a c.268C>T (p.Gln90Stop) mutation in Japanese.

Onodera T, Tsuneyama H, Ogasawara K, Isa K, Satake M, Tadokoro K, Uchikawa M.

Vox Sang. 2015 Aug;109(2):191-3. doi: 10.1111/vox.12260. Epub 2015 Apr 10.

PMID:
25865759
21.

Blood group B gene is barely expressed in in vitro erythroid culture of Bm-derived CD34+ cells without an erythroid cell-specific regulatory element.

Sano R, Nogawa M, Nakajima T, Takahashi Y, Takahashi K, Kubo R, Kominato Y, Yokohama A, Tsukada J, Yamao H, Kishida T, Ogasawara K, Uchikawa M.

Vox Sang. 2015 Apr;108(3):302-9. doi: 10.1111/vox.12220. Epub 2014 Dec 18.

PMID:
25523606
22.

A 3.0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype.

Sano R, Kuboya E, Nakajima T, Takahashi Y, Takahashi K, Kubo R, Kominato Y, Takeshita H, Yamao H, Kishida T, Isa K, Ogasawara K, Uchikawa M.

Vox Sang. 2015 Apr;108(3):310-3. doi: 10.1111/vox.12216. Epub 2014 Dec 18.

PMID:
25523382
23.

A new ABCG2 null allele with a 27-kb deletion including the promoter region causing the Jr(a-) phenotype.

Ogasawara K, Osabe T, Suzuki Y, Tsuneyama H, Isa K, Kawai M, Obara K, Ogiyama Y, Ito S, Uchikawa M, Satake M, Tadokoro K.

Transfusion. 2015 Jun;55(6 Pt 2):1467-71. doi: 10.1111/trf.12969. Epub 2014 Dec 18.

PMID:
25522810
24.

Sixteen additional enhancers associated with the chicken Sox2 locus outside the central 50-kb region.

Okamoto R, Uchikawa M, Kondoh H.

Dev Growth Differ. 2015 Jan;57(1):24-39. doi: 10.1111/dgd.12185. Epub 2014 Nov 28.

PMID:
25431100
25.

Production of human monoclonal anti-Jk3, recognising an epitope including the Jk(a) /Jk(b) polymorphic site of the Kidd glycoprotein.

Toyoda C, Suzuki Y, Tsuneyama H, Onodera T, Masuno A, Yabe R, Ogasawara K, Okuda M, Nakajima K, Uchikawa M.

Transfus Med. 2014 Oct;24(5):286-91. doi: 10.1111/tme.12146. Epub 2014 Sep 2.

PMID:
25180691
26.

Antibody-mediated immune suppression of erythrocyte alloimmunization can occur independently from red cell clearance or epitope masking in a murine model.

Yu H, Stowell SR, Bernardo L, Hendrickson JE, Zimring JC, Amash A, Uchikawa M, Lazarus AH.

J Immunol. 2014 Sep 15;193(6):2902-10. doi: 10.4049/jimmunol.1302287. Epub 2014 Aug 13.

27.

Novel swine model of transfusion-related acute lung injury.

Okazaki H, Ishikawa O, Iijima T, Kohira T, Teranishi M, Kawasaki S, Saito A, Mikami Y, Sugiura A, Hashimoto S, Shimada E, Uchikawa M, Matsuhashi M, Tsuno NH, Tanaka M, Kiyokawa N, Fujimoto J, Nagase T, Tadokoro K, Takahashi K.

Transfusion. 2014 Dec;54(12):3097-107. doi: 10.1111/trf.12766. Epub 2014 Jun 26.

PMID:
24965098
28.

ABO chimerism with a minor allele detected by the peptide nucleic acid-mediated polymerase chain reaction clamping method.

Sano R, Takahashi Y, Nakajima T, Yoshii M, Kubo R, Takahashi K, Kominato Y, Takeshita H, Yasuda T, Tsuneyama H, Uchikawa M, Isa K, Ogasawara K.

Blood Transfus. 2014 Jul;12(3):431-4. doi: 10.2450/2014.0162-13. Epub 2014 Jan 2. No abstract available.

29.

JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype.

Onodera T, Sasaki K, Tsuneyama H, Isa K, Ogasawara K, Satake M, Tadokoro K, Uchikawa M.

Vox Sang. 2014 May;106(4):382-4.

PMID:
24877238
30.

Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with phenotypes A3 and B3, respectively.

Takahashi Y, Isa K, Sano R, Nakajima T, Kubo R, Takahashi K, Kominato Y, Michino J, Masuno A, Tsuneyama H, Ito S, Ogasawara K, Uchikawa M.

Vox Sang. 2014 Aug;107(2):171-80. doi: 10.1111/vox.12136. Epub 2014 Mar 6.

PMID:
24602004
31.

Regulation of mesodermal precursor production by low-level expression of B1 Sox genes in the caudal lateral epiblast.

Yoshida M, Uchikawa M, Rizzoti K, Lovell-Badge R, Takemoto T, Kondoh H.

Mech Dev. 2014 May;132:59-68. doi: 10.1016/j.mod.2014.01.003. Epub 2014 Feb 6.

32.

Anti-KANNO: a novel alloantibody against a red cell antigen of high frequency.

Kawabata K, Uchikawa M, Ohto H, Yasuda H, Tsuneyama H, Tsuchida H, Ito S.

Transfus Med Rev. 2014 Jan;28(1):23-8. doi: 10.1016/j.tmrv.2013.12.001. Epub 2013 Dec 16.

PMID:
24485899
33.

Novel alleles of Lan- in Japanese populations.

Tanaka M, Yamamuro Y, Takahashi J, Ogasawara K, Osabe T, Tsuneyama H, Enomoto T, Watanabe S, Uchikawa M, Tadokoro K, Tani Y.

Transfusion. 2014 May;54(5):1438-9. doi: 10.1111/trf.12540. Epub 2014 Jan 9. No abstract available.

PMID:
24400966
34.

Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype.

Takahashi Y, Isa K, Sano R, Nakajima T, Kubo R, Takahashi K, Kominato Y, Tsuneyama H, Ogasawara K, Uchikawa M.

Vox Sang. 2014 Feb;106(2):167-75. doi: 10.1111/vox.12077. Epub 2013 Sep 2.

PMID:
23992526
35.

Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.

Lomas-Francis C, Vege S, Velliquette RW, Fuchisawa A, Uchikawa M, Tani Y, Moro H, Debnath AK, Westhoff CM.

Transfusion. 2013 Nov;53(11 Suppl 2):2887-91. doi: 10.1111/trf.12377. Epub 2013 Aug 22.

PMID:
23968329
36.

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.

Nakajima T, Sano R, Takahashi Y, Kubo R, Takahashi K, Kominato Y, Tsukada J, Takeshita H, Yasuda T, Uchikawa M, Isa K, Ogasawara K.

Transfusion. 2013 Nov;53(11 Suppl 2):2917-27. doi: 10.1111/trf.12181. Epub 2013 Apr 8.

PMID:
23560502
37.

TLR4-MD-2 complex is negatively regulated by an endogenous ligand, globotetraosylceramide.

Kondo Y, Ikeda K, Tokuda N, Nishitani C, Ohto U, Akashi-Takamura S, Ito Y, Uchikawa M, Kuroki Y, Taguchi R, Miyake K, Zhang Q, Furukawa K, Furukawa K.

Proc Natl Acad Sci U S A. 2013 Mar 19;110(12):4714-9. doi: 10.1073/pnas.1218508110. Epub 2013 Mar 5.

38.

Progression of neurogenesis in the inner ear requires inhibition of Sox2 transcription by neurogenin1 and neurod1.

Evsen L, Sugahara S, Uchikawa M, Kondoh H, Wu DK.

J Neurosci. 2013 Feb 27;33(9):3879-90. doi: 10.1523/JNEUROSCI.4030-12.2013.

39.

Expression of ABO blood-group genes is dependent upon an erythroid cell-specific regulatory element that is deleted in persons with the B(m) phenotype.

Sano R, Nakajima T, Takahashi K, Kubo R, Kominato Y, Tsukada J, Takeshita H, Yasuda T, Ito K, Maruhashi T, Yokohama A, Isa K, Ogasawara K, Uchikawa M.

Blood. 2012 May 31;119(22):5301-10. doi: 10.1182/blood-2011-10-387167. Epub 2012 Mar 9.

PMID:
22408256
40.

The prosensory function of Sox2 in the chicken inner ear relies on the direct regulation of Atoh1.

Neves J, Uchikawa M, Bigas A, Giraldez F.

PLoS One. 2012;7(1):e30871. doi: 10.1371/journal.pone.0030871. Epub 2012 Jan 23.

41.

A Systematic Survey and Characterization of Enhancers that Regulate Sox3 in Neuro-Sensory Development in Comparison with Sox2 Enhancers.

Nishimura N, Kamimura Y, Ishida Y, Takemoto T, Kondoh H, Uchikawa M.

Biology (Basel). 2012 Nov 22;1(3):714-35. doi: 10.3390/biology1030714.

42.

Basigin is a receptor essential for erythrocyte invasion by Plasmodium falciparum.

Crosnier C, Bustamante LY, Bartholdson SJ, Bei AK, Theron M, Uchikawa M, Mboup S, Ndir O, Kwiatkowski DP, Duraisingh MT, Rayner JC, Wright GJ.

Nature. 2011 Nov 9;480(7378):534-7. doi: 10.1038/nature10606.

43.

Alterations of circadian clockworks during differentiation and apoptosis of rat ovarian cells.

Chu G, Yoshida K, Narahara S, Uchikawa M, Kawamura M, Yamauchi N, Xi Y, Shigeyoshi Y, Hashimoto S, Hattori MA.

Chronobiol Int. 2011 Jul;28(6):477-87. doi: 10.3109/07420528.2011.589933.

PMID:
21797776
44.

B1 and B2 Sox gene expression during neural plate development in chicken and mouse embryos: universal versus species-dependent features.

Uchikawa M, Yoshida M, Iwafuchi-Doi M, Matsuda K, Ishida Y, Takemoto T, Kondoh H.

Dev Growth Differ. 2011 Aug;53(6):761-71. doi: 10.1111/j.1440-169X.2011.01286.x. Epub 2011 Jul 18. Review.

PMID:
21762129
45.

Efficient generation of useful monoclonal antibodies reactive with globotriaosylceramide using knockout mice lacking Gb3/CD77 synthase.

Kondo Y, Tokuda N, Furukawa K, Ando R, Uchikawa M, Zhang Q, Xiaoyan F, Furukawa K.

Glycoconj J. 2011 Aug;28(6):371-84. doi: 10.1007/s10719-011-9335-4. Epub 2011 Jun 10.

PMID:
21660412
46.

Tbx6-dependent Sox2 regulation determines neural or mesodermal fate in axial stem cells.

Takemoto T, Uchikawa M, Yoshida M, Bell DM, Lovell-Badge R, Papaioannou VE, Kondoh H.

Nature. 2011 Feb 17;470(7334):394-8. doi: 10.1038/nature09729.

47.

The Pou5f1/Pou3f-dependent but SoxB-independent regulation of conserved enhancer N2 initiates Sox2 expression during epiblast to neural plate stages in vertebrates.

Iwafuchi-Doi M, Yoshida Y, Onichtchouk D, Leichsenring M, Driever W, Takemoto T, Uchikawa M, Kamachi Y, Kondoh H.

Dev Biol. 2011 Apr 15;352(2):354-66. doi: 10.1016/j.ydbio.2010.12.027. Epub 2010 Dec 23.

48.

Down-regulation of circadian clock gene period 2 in uterine endometrial stromal cells of pregnant rats during decidualization.

Uchikawa M, Kawamura M, Yamauchi N, Hattori MA.

Chronobiol Int. 2011 Feb;28(1):1-9. doi: 10.3109/07420528.2010.522289.

PMID:
21182399
49.

Collaborative study of irregular erythrocyte antibodies in Japan: results from the Japanese study group of allo-immunity and antigen diversity in Asian populations.

Takeshita A, Watanabe H, Fijihara H, Oshida M, Yurugi K, Tomoda Y, Uchikawa M, Kino S, Ohto H.

Transfus Apher Sci. 2010 Aug;43(1):3-8. doi: 10.1016/j.transci.2010.04.001. Epub 2010 Aug 2.

PMID:
20675192
50.

Regulation of Sox2 in the pre-placodal cephalic ectoderm and central nervous system by enhancer N-4.

Saigou Y, Kamimura Y, Inoue M, Kondoh H, Uchikawa M.

Dev Growth Differ. 2010 Jun;52(5):397-408. doi: 10.1111/j.1440-169X.2010.01180.x.

PMID:
20507355

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