Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 212

1.

Role of Dach1 revealed using a novel inner ear-specific Dach1-knockdown mouse model.

Miwa T, Minoda R, Ishikawa Y, Kajii T, Orita Y, Ohyama T.

Biol Open. 2019 Aug 20;8(8). pii: bio043612. doi: 10.1242/bio.043612.

2.

Addition of a β1-Blocker to Milrinone Treatment Improves Cardiac Function in Patients with Acute Heart Failure and Rapid Atrial Fibrillation.

Kobayashi S, Myoren T, Kajii T, Kohno M, Nanno T, Ishiguchi H, Nishimura S, Fukuda M, Hino A, Fujimura T, Ono M, Uchinoumi H, Tateishi H, Mochizuki M, Oda T, Okuda S, Yoshiga Y, Kawano R, Yano M.

Cardiology. 2019;142(4):195-202. doi: 10.1159/000499400. Epub 2019 May 28.

3.

Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism.

Kajii TS, Oka A, Saito F, Mitsui J, Iida J.

Bone. 2019 May;122:193-198. doi: 10.1016/j.bone.2019.03.004. Epub 2019 Mar 5.

PMID:
30849546
4.
5.

PLXNA2 identified as a candidate gene by genome-wide association analysis for mandibular prognathism in human chondrocytes.

Kajii TS, Oka A, Hatta M, Yamazaki J, Yamashita J, Iida J.

Biomed Rep. 2018 Sep;9(3):253-258. doi: 10.3892/br.2018.1128. Epub 2018 Jul 11.

6.

Distal radial arterial hypertrophy after transradial intervention: A serial intravascular ultrasound study.

Wakeyama T, Ogawa H, Iwami T, Tanaka M, Harada N, Hiratsuka A, Nakashima T, Kato T, Kinoshita N, Takenaka H, Nakamura Y, Fujii S, Kajii T, Yano M.

J Cardiol. 2018 Dec;72(6):501-505. doi: 10.1016/j.jjcc.2018.05.008. Epub 2018 Sep 13.

PMID:
30219614
7.

Osseous changes of the mandibular condyle affect backward-rotation of the mandibular ramus in Angle Class II orthodontic patients with idiopathic condylar resorption of the temporomandibular joint.

Kajii TS, Fujita T, Sakaguchi Y, Shimada K.

Cranio. 2019 Jul;37(4):264-271. doi: 10.1080/08869634.2017.1421446. Epub 2018 Jan 23.

PMID:
29359644
8.

Genome-wide association study for mandibular prognathism using microsatellite and pooled DNA method.

Saito F, Kajii TS, Oka A, Ikuno K, Iida J.

Am J Orthod Dentofacial Orthop. 2017 Sep;152(3):382-388. doi: 10.1016/j.ajodo.2017.01.021.

PMID:
28863919
9.

Cutaneous plasmacytosis successfully treated with narrowband ultraviolet B irradiation therapy.

Yanaba K, Kajii T, Matsuzaki H, Umezawa Y, Nakagawa H.

J Dermatol. 2016 Feb;43(2):229-30. doi: 10.1111/1346-8138.13164. Epub 2015 Oct 13. No abstract available.

PMID:
26458290
10.

Microsatellite genome-wide association study for mandibular prognathism.

Ikuno K, Kajii TS, Oka A, Inoko H, Ishikawa H, Iida J.

Am J Orthod Dentofacial Orthop. 2014 Jun;145(6):757-62. doi: 10.1016/j.ajodo.2014.01.022.

PMID:
24880846
11.

TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.

Ochiai H, Miyamoto T, Kanai A, Hosoba K, Sakuma T, Kudo Y, Asami K, Ogawa A, Watanabe A, Kajii T, Yamamoto T, Matsuura S.

Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1461-6. doi: 10.1073/pnas.1317008111. Epub 2013 Dec 16.

12.

Quantitative evaluation of myofibroblast apoptosis during wound healing in rat palate after post-operative administration of basic fibroblast growth factor (bFGF).

Hata Y, Ishikawa H, Ueki T, Kajii TS, Tamaoki S, Tsuruga E, Sawa Y, Taniguchi K.

Acta Odontol Scand. 2013 Nov;71(6):1501-7. doi: 10.3109/00016357.2013.773370. Epub 2013 Feb 28.

PMID:
23445304
13.

Oxygen saturation and electromyographic changes in masseter muscle during experimental chewing of gum with harder texture.

Horikoshi E, Ishikawa H, Yoshida T, Tamaoki S, Kajii TS.

Acta Odontol Scand. 2013 Nov;71(6):1378-85. doi: 10.3109/00016357.2013.764006. Epub 2013 Feb 4.

PMID:
23374088
14.

Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.

Ichikawa M, Arai Y, Haruta M, Furukawa S, Ariga T, Kajii T, Kaneko Y.

Genes Chromosomes Cancer. 2013 Mar;52(3):274-86. doi: 10.1002/gcc.22027. Epub 2012 Dec 8.

PMID:
23225212
15.

Postnatal treatment factors affecting craniofacial morphology of unilateral cleft lip and palate (UCLP) patients in a Japanese population.

Alam MK, Iida J, Sato Y, Kajii TS.

Br J Oral Maxillofac Surg. 2013 Dec;51(8):e205-10. doi: 10.1016/j.bjoms.2012.10.001. Epub 2012 Oct 23.

PMID:
23099108
16.

Histological study of the nasal septal cartilage in BALB/c-bm/bm mouse which spontaneously induces malocclusion.

Takahashi K, Kajii TS, Tsukamoto Y, Saito F, Wada S, Sugawara-Kato Y, Iida J.

Orthod Craniofac Res. 2012 May;15(2):84-91. doi: 10.1111/j.1601-6343.2011.01538.x. Epub 2012 Mar 27.

PMID:
22515184
17.

Congenital and postnatal factors inducing malocclusions in Japanese unilateral cleft lip and palate patients-determination using logistic regression analysis.

Kajii TS, Alam MK, Mikoya T, Oyama A, Koshikawa-Matsuno M, Sugawara-Kato Y, Sato Y, Iida J.

Cleft Palate Craniofac J. 2013 Jul;50(4):466-72. doi: 10.1597/11-150. Epub 2012 Mar 12.

PMID:
22409625
18.

Morphological evaluation of cranial and maxillary shape differences of the brachymorphic mouse with spontaneous malocclusion using three-dimensional micro-computed tomography.

Saito F, Kajii TS, Sugawara-Kato Y, Tsukamoto Y, Arai Y, Hirabayashi Y, Fujimori O, Iida J.

Orthod Craniofac Res. 2011 May;14(2):100-6. doi: 10.1111/j.1601-6343.2011.01513.x. Epub 2011 Mar 15.

PMID:
21457459
19.

Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.

Miyamoto T, Porazinski S, Wang H, Borovina A, Ciruna B, Shimizu A, Kajii T, Kikuchi A, Furutani-Seiki M, Matsuura S.

Hum Mol Genet. 2011 May 15;20(10):2058-70. doi: 10.1093/hmg/ddr090. Epub 2011 Mar 9.

PMID:
21389084
20.

Relationship between degree of malocclusion and occlusal interference in mice that spontaneously develop anterior transverse crossbite.

Tsukamoto Y, Kajii TS, Sugawara-Kato Y, Hirabayashi Y, Fujimori O, Iida J.

Am J Orthod Dentofacial Orthop. 2010 Dec;138(6):710.e1-5; discussion 710-1. doi: 10.1016/j.ajodo.2010.03.028.

PMID:
21130324
21.

Three-dimensional craniomaxillary characteristics of the mouse with spontaneous malocclusion using micro-computed tomography.

Saito F, Kajii TS, Sugawara-Kato Y, Tsukamoto Y, Arai Y, Hirabayashi Y, Fujimori O, Iida J.

Eur J Orthod. 2011 Feb;33(1):43-9. doi: 10.1093/ejo/cjq023. Epub 2010 Jul 27.

22.

Interleukin-1beta levels, pain intensity, and tooth movement using two different magnitudes of continuous orthodontic force.

Luppanapornlarp S, Kajii TS, Surarit R, Iida J.

Eur J Orthod. 2010 Oct;32(5):596-601. doi: 10.1093/ejo/cjp158. Epub 2010 Jun 9.

PMID:
20534713
23.

Monocortical mandibular bone grafting for reconstruction of alveolar cleft.

Mikoya T, Inoue N, Matsuzawa Y, Totsuka Y, Kajii TS, Hirosawa T.

Cleft Palate Craniofac J. 2010 Sep;47(5):454-68. doi: 10.1597/09-172.

PMID:
20180704
24.

BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.

Izumi H, Matsumoto Y, Ikeuchi T, Saya H, Kajii T, Matsuura S.

Oncogene. 2009 Aug 6;28(31):2806-20. doi: 10.1038/onc.2009.141. Epub 2009 Jun 8.

PMID:
19503101
25.
26.

Growth and development of the cranial base in mice that spontaneously develop anterior transverse crossbite.

Tsukamoto Y, Kajii TS, Oonishi Y, Sugawara-Kato Y, Hirabayashi Y, Iida J.

Am J Orthod Dentofacial Orthop. 2008 Nov;134(5):676-83. doi: 10.1016/j.ajodo.2006.08.025.

PMID:
18984401
27.

Predicted prevalence of Down syndrome live births in Japan, 1970-2006.

Kajii T.

Am J Med Genet A. 2008 Jun 1;146A(11):1387-8. doi: 10.1002/ajmg.a.32323. No abstract available.

PMID:
18412276
28.

Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome.

Matsuura S, Matsumoto Y, Morishima K, Izumi H, Matsumoto H, Ito E, Tsutsui K, Kobayashi J, Tauchi H, Kajiwara Y, Hama S, Kurisu K, Tahara H, Oshimura M, Komatsu K, Ikeuchi T, Kajii T.

Am J Med Genet A. 2006 Feb 15;140(4):358-67.

PMID:
16411201
29.

Elevated levels of beta-endorphin in temporomandibular joint synovial lavage fluid of patients with closed lock.

Kajii TS, Okamoto T, Yura S, Mabuchi A, Iida J.

J Orofac Pain. 2005 Winter;19(1):41-6.

PMID:
15779538
30.

ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation.

Kubota T, Furuumi H, Kamoda T, Iwasaki N, Tobita N, Fujiwara N, Goto Y, Matsui A, Sasaki H, Kajii T.

Am J Med Genet A. 2004 Sep 1;129A(3):290-3.

PMID:
15326630
31.

Agenesis of third molar germs depends on sagittal maxillary jaw dimensions in orthodontic patients in Japan.

Kajii TS, Sato Y, Kajii S, Sugawara Y, Iida J.

Angle Orthod. 2004 Jun;74(3):337-42.

PMID:
15264644
32.

Heterozygous TGFBR2 mutations in Marfan syndrome.

Mizuguchi T, Collod-Beroud G, Akiyama T, Abifadel M, Harada N, Morisaki T, Allard D, Varret M, Claustres M, Morisaki H, Ihara M, Kinoshita A, Yoshiura K, Junien C, Kajii T, Jondeau G, Ohta T, Kishino T, Furukawa Y, Nakamura Y, Niikawa N, Boileau C, Matsumoto N.

Nat Genet. 2004 Aug;36(8):855-60. Epub 2004 Jul 4.

33.

Induction of premature chromatid separation (PCS) in individuals with PCS trait and in normal controls.

Ikeuchi T, Yang ZQ, Wakamatsu K, Kajii T.

Am J Med Genet A. 2004 Jun 1;127A(2):128-32.

PMID:
15108198
34.

Premature chromatid separation (PCS) vs. premature centromere division (PCD).

Kajii T, Ikeuchi T.

Am J Med Genet A. 2004 May 1;126A(4):433-4. No abstract available.

PMID:
15098246
35.

Prenatal diagnosis of a heterozygous carrier of premature chromatid separation (PCS) trait.

Kajii T, Asamoto A.

Am J Med Genet A. 2004 May 1;126A(4):432. No abstract available.

PMID:
15098245
36.

Duplication of 8p23.2: a benign cytogenetic variant?

Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, Ida T, Yoshiura K, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N.

Am J Med Genet. 2002 Aug 15;111(3):285-8.

PMID:
12210324
37.

Maternal isodisomy for 14q21-q24 in a man with diabetes mellitus.

Kayashima T, Katahira M, Harada N, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Nakamura Y, Kajii T, Niikawa N, Kishino T.

Am J Med Genet. 2002 Jul 22;111(1):38-42.

PMID:
12124731
38.

Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1.

Miyoshi O, Yabe R, Wakui K, Fukushima Y, Koizumi S, Uchikawa M, Kajii T, Numakura C, Takahashi S, Hayasaka K, Niikawa N.

Am J Med Genet. 2001 Dec 1;104(3):250-6.

PMID:
11754053
39.

Cancer-prone syndrome of mosaic variegated aneuploidy and total premature chromatid separation: report of five infants.

Kajii T, Ikeuchi T, Yang ZQ, Nakamura Y, Tsuji Y, Yokomori K, Kawamura M, Fukuda S, Horita S, Asamoto A.

Am J Med Genet. 2001 Nov 15;104(1):57-64. Review.

PMID:
11746029
40.

Presence of third molar germs in orthodontic patients in Japan.

Kajii T, Imai T, Kajii S, Iida J.

Am J Orthod Dentofacial Orthop. 2001 Mar;119(3):245-50.

PMID:
11244418
41.

Chromosomal instability syndrome of total premature chromatid separation with mosaic variegated aneuploidy is defective in mitotic-spindle checkpoint.

Matsuura S, Ito E, Tauchi H, Komatsu K, Ikeuchi T, Kajii T.

Am J Hum Genet. 2000 Aug;67(2):483-6. Epub 2000 Jun 30.

42.

Long-term effects of prostaglandin E2 on the mineralization of a clonal osteoblastic cell line (MC3T3-E1).

Kajii T, Suzuki K, Yoshikawa M, Imai T, Matsumoto A, Nakamura S.

Arch Oral Biol. 1999 Mar;44(3):233-41.

PMID:
10217514
43.

Reply to letter to the editor by Schrander-Stumpel--"what's in a name?".

Kajii T, Niikawa N.

Am J Med Genet. 1999 Mar 19;83(3):212. No abstract available.

PMID:
10096600
44.

Mosaic variegated aneuploidy with multiple congenital abnormalities: homozygosity for total premature chromatid separation trait.

Kajii T, Kawai T, Takumi T, Misu H, Mabuchi O, Takahashi Y, Tachino M, Nihei F, Ikeuchi T.

Am J Med Genet. 1998 Jul 7;78(3):245-9.

PMID:
9677059
45.

A recurrent translocation, t(16;21)(q24;q22), associated with acute myelogenous leukemia: identification by fluorescence in situ hybridization.

Shimada M, Ohtsuka E, Shimizu T, Matsumoto T, Matsushita K, Tanimoto F, Kajii T.

Cancer Genet Cytogenet. 1997 Jul 15;96(2):102-5.

PMID:
9216714
46.

Interstitial deletion of 8p: report of two patients and review of the literature.

Tsukahara M, Murano I, Aoki Y, Kajii T, Furukawa S.

Clin Genet. 1995 Jul;48(1):41-5. Review.

PMID:
7586643
47.

Congenital heart defects in Aarskog syndrome.

Fernandez I, Tsukahara M, Mito H, Yoshii H, Uchida M, Matsuo K, Kajii T.

Am J Med Genet. 1994 May 1;50(4):318-22. Review.

PMID:
8209909
48.

Tricho-rhino-phalangeal syndrome type III.

Kajii T, Fernandez Gonzalez I, Matsuura S.

Am J Med Genet. 1994 Feb 1;49(3):349-50. No abstract available.

PMID:
8209900
49.

Mapping of the human guanosine monophosphate reductase gene (GMPR) to chromosome 6p23 by fluorescence in situ hybridization.

Murano I, Tsukahara M, Kajii T, Yoshida A.

Genomics. 1994 Jan 1;19(1):179-80. No abstract available.

PMID:
8188226
50.

Occipital horn syndrome: report of a patient and review of the literature.

Tsukahara M, Imaizumi K, Kawai S, Kajii T.

Clin Genet. 1994 Jan;45(1):32-5. Review.

PMID:
8149649

Supplemental Content

Support Center