Search Results - "KAJII, T"

BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells by Izumi, H, Matsumoto, Y, Ikeuchi, T, Saya, H, Kajii, T, Matsuura, S

“…BubR1 is a critical component of the mitotic checkpoint that delays the onset of anaphase until all chromosomes have established bipolar attachment to the…”
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Histological study of the nasal septal cartilage in BALB/c-bm/bm mouse which spontaneously induces malocclusion by Takahashi, K., Kajii, T. S., Tsukamoto, Y., Saito, F., Wada, S., Sugawara-Kato, Y., Iida, J.

“…Takahashi K., Kajii T. S., Tsukamoto Y., Saito F., Wada S., Sugawara‐Kato Y., Iida J. Histological study of the nasal septal cartilage in BALB/c‐bm/bm mouse…”
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Morphological evaluation of cranial and maxillary shape differences of the brachymorphic mouse with spontaneous malocclusion using three-dimensional micro-computed tomography by Saito, F, Kajii, TS, Sugawara-Kato, Y, Tsukamoto, Y, Arai, Y, Hirabayashi, Y, Fujimori, O, Iida, J

“…To cite this article: 
Saito F, Kajii TS, Sugawara‐Kato Y, Tsukamoto Y, Arai Y, Hirabayashi Y, Fujimori O, Iida J: 
Morphological evaluation of cranial and…”
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Interleukin-1  levels, pain intensity, and tooth movement using two different magnitudes of continuous orthodontic force by Luppanapornlarp, S., Kajii, T. S., Surarit, R., Iida, J.

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Fibroblast-specific common fragile sites induced by aphidicolin by MURANO, I, KUWANO, A, KAJII, T

“…The distribution and frequency of aphidicolin-induced common fragile sites were studied in chromosomes of cultured skin fibroblasts and PHA-stimulated…”
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Heterozygous TGFBR2 mutations in Marfan syndrome by Kajii, Tadashi, Matsumoto, Naomichi, Morisaki, Takayuki, Morisaki, Hiroko, Collod-Beroud, Gwenaëlle, Ihara, Makoto, Mizuguchi, Takeshi, Claustres, Mireille, Varret, Mathilde, Jondeau, Guillaume, Boileau, Catherine, Yoshiura, Koh-ichiro, Junien, Claudine, Kishino, Tatsuya, Akiyama, Takushi, Kinoshita, Akira, Ohta, Tohru, Abifadel, Marianne, Harada, Naoki, Nakamura, Yusuke, Furukawa, Yoichi, Niikawa, Norio, Allard, Delphine

“…Marfan syndrome is an extracellular matrix disorder with cardinal manifestations in the eye, skeleton and cardiovascular systems associated with defects in the…”
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Human adenylate kinase deficiency associated with hemolytic anemia. A single base substitution affecting solubility and catalytic activity of the cytosolic adenylate kinase by MATSUURA, S, IGARASHI, M, TANIZAWA, Y, YAMADA, M, KISHI, F, KAJII, T, FUJII, H, MIWA, S, SAKURAI, M, NAKAZAWA, A

“…Adenylate kinase deficiency in the erythrocyte is a rare genetic disorder associated with hemolytic anemia. To determine the molecular basis of this disorder,…”
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Synergistic effect of aphidicolin and ethanol on the induction of common fragile sites by KUWANO, A, KAJII, T

“…The effect of ethanol on the frequency of aphidicolin-induced common fragile sites was studied using lymphocyte cultures from two normal women. Aphidicolin was…”
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Mapping basigin (BSG), a member of the immunoglobulin superfamily, to 19p13.3 by Kaname, T, Miyauchi, T, Kuwano, A, Matsuda, Y, Muramatsu, T, Kajii, T

“…Basigin is a novel member of the immunoglobulin superfamily ubiquitously expressed in various tissues. We mapped the basigin gene at 19p13.3, using a 1.6-kb…”
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Double targets sign in ultrasonic diagnosis of intussuscepted Meckel diverticulum by ITAGAKI, A, UCHIDA, M, UEKI, K, KAJII, T

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Anatomic and chromosomal anomalies in 639 spontaneous abortuses by Kajii, T, Ferrier, A, Niikawa, N, Takahara, H, Ohama, K, Avirachan, S

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High-resolution banding in chromosomes of B lymphoblastoid cells and cultured skin fibroblasts by Kuwano, A, Kajii, T

“…High-resolution banded chromosomes were obtained in Epstein-Barr virus-transformed lymphoblastoid cells and cultured skin fibroblasts by aphidicolin…”
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Hairy throat: a dominant trait affecting seven members of a family by Tsukahara, M, Kajii, T

“…Hypertrichosis was noted on a confined area of skin in the midline of the throat, just cranial to the laryngeal prominence, in three males and four females…”
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Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome by Matsuura, Shinya, Matsumoto, Yoshiyuki, Morishima, Ken-ichi, Izumi, Hideki, Matsumoto, Hiroshi, Ito, Emi, Tsutsui, Keisuke, Kobayashi, Junya, Tauchi, Hiroshi, Kajiwara, Yoshinori, Hama, Seiji, Kurisu, Kaoru, Tahara, Hidetoshi, Oshimura, Mitsuo, Komatsu, Kenshi, Ikeuchi, Tatsuro, Kajii, Tadashi

“…Cancer‐prone syndrome of premature chromatid separation (PCS syndrome) with mosaic variegated aneuploidy (MVA) is a rare autosomal recessive disorder…”
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Isolation of human herpesvirus-6 from an infant with Kawasaki disease by Hagiwara, K, Yoshida, T, Komura, H, Kishi, F, Kajii, T

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Discordance for anomalous pancreaticobiliary ductal junction and congenital biliary dilatation in a set of monozygotic twins by Uchida, M, Tsukahara, M, Fuji, T, Fujihara, T, Ueki, K, Kajii, T

“…A pair of monozygotic twins, 2-year-old Japanese girls, discordant for both anomalous pancreaticobiliary ductal junction and congenital biliary dilatation, are…”
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The origin of mosaic down syndrome: four cases with chromosome markers by NIKAWA, N, KAJII, T

“…Four children, a girl and three boys, with diploid/trisomic mosaic Down syndrome were studied for the mechanism of origin of mosaics, using Q- and R-banding…”
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Normal values for 24-h urinary protein excretion: total and low molecular weight proteins with a sex-related difference by Kawakami, H, Murakami, T, Kajii, T

“…Urinary excretion of total and low molecular weight (LMW) (less than 40,000) proteins for a 24-h period was determined in 60 normal individuals, 30 men and 30…”
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Pachygyria, joint contractures, and facial abnormalities: a new lethal syndrome by Tsukahara, M, Sugio, Y, Kajii, T, Takahashi, M, Hirota, M, Kato, H

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BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plkl activity in interphase cells by IZUMI, H, MATSUMOTO, Y, IKEUCHI, T, SAYA, H, KAJII, T, MATSUURA, S

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