Microarray Analysis of Differentially Expressed Fetal Genes in Placental Tissue Derived from Early and Late Onset Severe Pre-eclampsia von Nishizawa, H, Pryor-Koishi, K, Kato, T, Kowa, H, Kurahashi, H, Udagawa, Y

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Intact attentional orienting towards inverted faces revealed by both manual responses and eye-movement measurement in individuals with Williams syndrome von Hirai, M., Muramatsu, Y., Mizuno, S., Kurahashi, N., Kurahashi, H., Nakamura, M.

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Contribution of fetal ANXA5 gene promoter polymorphisms to the onset of pre-eclampsia von Ota, S, Miyamura, H, Nishizawa, H, Inagaki, H, Inagaki, A, Inuzuka, H, Suzuki, M, Miyazaki, J, Sekiya, T, Udagawa, Y, Kurahashi, H

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Upregulation of HtrA4 in the placentas of patients with severe pre-eclampsia von Inagaki, A, Nishizawa, H, Ota, S, Suzuki, M, Inuzuka, H, Miyamura, H, Sekiya, T, Kurahashi, H, Udagawa, Y

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Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia von Taniguchi‐Ikeda, M., Morisada, N., Inagaki, H., Ouchi, Y., Takami, Y., Tachikawa, M., Satake, W., Kobayashi, K., Tsuneishi, S., Takada, S., Yamaguchi, H., Nagase, H., Nozu, K., Okamoto, N., Nishio, H., Toda, T., Morioka, I., Wada, H., Kurahashi, H., Iijima, K.

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Long AT-rich palindromes and the constitutional t(11;22) breakpoint von KURAHASHI, Hiroki, EMANUEL, Beverly S

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Molecular phylogeny of the blowfly genus Chrysomya von SINGH, B., KURAHASHI, H., WELLS, J. D.

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The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements von Kurahashi, H, Inagaki, H, Ohye, T, Kogo, H, Tsutsumi, M, Kato, T, Tong, M, Emanuel, BS

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Calcium channel inhibition accelerates polycystic kidney disease progression in the Cy/+ rat von Nagao, S., Nishii, K., Yoshihara, D., Kurahashi, H., Nagaoka, K., Yamashita, T., Takahashi, H., Yamaguchi, T., Calvet, J.P., Wallace, D.P.

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Correlation of axillary osmidrosis to a SNP in the ABCC11 gene determined by the Smart Amplification Process (SmartAmp) method von Inoue, Y, Mori, T, Toyoda, Y, Sakurai, A, Ishikawa, T, Mitani, Y, Hayashizaki, Y, Yoshimura, Y, Kurahashi, H, Sakai, Y

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Nine-year follow-up in a child with chromosomal integration of human herpesvirus 6 transmitted from an unrelated donor through the Japan Marrow Donor Program von Yagasaki, H., Shichino, H., Shimizu, N., Ohye, T., Kurahashi, H., Yoshikawa, T., Takahashi, S.

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Virological analysis of inherited chromosomally integrated human herpesvirus‐6 in three hematopoietic stem cell transplant patients von Miura, H., Kawamura, Y., Kudo, K., Ihira, M., Ohye, T., Kurahashi, H., Kawashima, N., Miyamura, K., Yoshida, N., Kato, K., Takahashi, Y., Kojima, S., Yoshikawa, T.

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Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures von KURAHASHI, H, WANG, J.-W, YASUMOTO, S, OGAWA, A, KANEKO, S, HIROSE, S, ISHII, A, KOJIMA, T, WAKAI, S, KIZAWA, T, FUJIMOTO, Y, KIKKAWA, K, YOSHIMURA, K, INOUE, T

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Overproduction of the follistatin‐related gene protein in the placenta and maternal serum of women with pre‐eclampsia von Pryor‐Koishi, K, Nishizawa, H, Kato, T, Kogo, H, Murakami, T, Tsuchida, K, Kurahashi, H, Udagawa, Y

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P-039 Parthenogenetic chimeras may be the cause of the development of a case of 46, XX/46, XY chimeras complicated by severe oligozoospermia von Ikeda, S, Koyama, N, Kinoshita, K, Miyoshi, J, Masuda, H, Kurahashi, H

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Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats von Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae, Kato, Takema, Emanuel, Beverly S, Kurahashi, Hiroki

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A rare synaptonemal complex protein 3 gene variant in unexplained female infertility von Nishiyama, S, Kishi, T, Kato, T, Suzuki, M, Bolor, H, Nishizawa, H, Iwata, N, Udagawa, Y, Kurahashi, H

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Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22) von KURAHASHI, H, SHAIKH, T. H, PING HU, ROE, B. A, EMANUEL, B. S, BUDARF, M. L

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Two different forms of palindrome resolution in the human genome: deletion or translocation von Kato, Takema, Inagaki, Hidehito, Kogo, Hiroshi, Ohye, Tamae, Yamada, Kouji, Emanuel, Beverly S., Kurahashi, Hiroki

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W233 POLYMORPHISMS IN THE ANNEXIN A5 GENE PROMOTER IN JAPANESE WOMEN WITH PREECLAMPSIA von Miyamura, H., Nishizawa, H., Ota, S., Suzuki, M., Inagaki, A., Inuzuka, H., Nishiyama, S., Kurahashi, H., Udagawa, Y.

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