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1
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Journal
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Genes and environment (Online)

Nihon Kankyō Henʼigen Gakkai. ©2006-

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2
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Article
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Effects of the Iowa and Milano mutations on apolipoprotein A-I structure and dynamics determined by hydrogen exchange and mass spectrometry.

Chetty, Palaniappan Sevugan ; Ohshiro, Maki ; Saito, Hiroyuki ; Dhanasekaran, Padmaja ; Lund-Katz, Sissel ; Mayne, Leland ; Englander, Walter ; Phillips, Michael C Chetty, Palaniappan Sevugan (correspondence author) ; Chetty, Palaniappan Sevugan (record owner)

Biochemistry, November 6, 2012, Vol.51(44), pp.8993-9001 [Peer Reviewed Journal]

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3
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Remarkable increase in fluoroquinolone-resistant Mycoplasma genitalium in Japan.

Kikuchi, Mina ; Ito, Shin ; Yasuda, Mitsuru ; Tsuchiya, Tomohiro ; Hatazaki, Kyoko ; Takanashi, Masaki ; Ezaki, Takayuki ; Deguchi, Takashi Kikuchi, Mina (correspondence author) ; Kikuchi, Mina (record owner)

The Journal of antimicrobial chemotherapy, September 2014, Vol.69(9), pp.2376-2382 [Peer Reviewed Journal]

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4
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Mutations in COQ2 in familial and sporadic multiple-system atrophy.

Mitsui, Jun Matsukawa, Takashi (record owner) ; Ishiura, Hiroyuki ; Fukuda, Yoko ; Ichikawa, Yaeko ; Date, Hidetoshi ; Ahsan, Budrul ; Nakahara, Yasuo ; Momose, Yoshio ; Takahashi, Yuji ; Iwata, Atsushi ; Goto, Jun ; Yamamoto, Yorihiro ; Komata, Makiko ; Shirahige, Katsuhiko ; Hara, Kenju ; Kakita, Akiyoshi ; Yamada, Mitsunori ; Takahashi, Hitoshi ; Onodera, Osamu ; Nishizawa, Masatoyo ; Takashima, Hiroshi ; Kuwano, Ryozo ; Watanabe, Hirohisa ; Ito, Mizuki ; Sobue, Gen ; Soma, Hiroyuki ; Yabe, Ichiro ; Sasaki, Hidenao ; Aoki, Masashi ; Ishikawa, Kinya ; Mizusawa, Hidehiro ; Kanai, Kazuaki ; Hattori, Takamichi ; Kuwabara, Satoshi ; Arai, Kimihito ; Koyano, Shigeru ; Kuroiwa, Yoshiyuki ; Hasegawa, Kazuko ; Yuasa, Tatsuhiko ; Yasui, Kenichi ; Nakashima, Kenji ; Ito, Hijiri ; Izumi, Yuishin ; Kaji, Ryuji ; Kato, Takeo ; Kusunoki, Susumu ; Osaki, Yasushi ; Horiuchi, Masahiro ; Kondo, Tomoyoshi ; Murayama, Shigeo ; Hattori, Nobutaka ; Yamamoto, Mitsutoshi ; Murata, Miho ; Satake, Wataru ; Toda, Tatsushi ; Dürr, Alexandra ; Brice, Alexis ; Filla, Alessandro ; Klockgether, Thomas ; Wüllner, Ullrich ; Nicholson, Garth ; Gilman, Sid ; Shults, Clifford W ; Tanner, Caroline M ; Kukull, Walter A ; Lee, Virginia M -Y ; Masliah, Eliezer ; Low, Phillip A ; Sandroni, Paola ; Trojanowski, John Q ; Ozelius, Laurie ; Foroud, Tatiana ; Tsuji, Shoji ; Tsuji, Shoji ; Tsuji, Shoji

The New England journal of medicine, July 18, 2013, Vol.369(3), pp.233-244 [Peer Reviewed Journal]

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5
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Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

Yu, Timothy w ; Chahrour, Maria h ; Coulter, Michael e ; Jiralerspong, Sarn ; Okamura-Ikeda, Kazuko ; Ataman, Bulent ; Schmitz-Abe, Klaus ; Harmin, David a ; Adli, Mazhar ; Malik, Athar n ; D'Gama, Alissa m ; Lim, Elaine t ; Sanders, Stephan j ; Mochida, Ganesh h ; Partlow, Jennifer n ; Sunu, Christine m ; Felie, Jillian m ; Rodriguez, Jacqueline ; Nasir, Ramzi h ; Ware, Janice ; Joseph, Robert m ; Hill, R sean ; Kwan, Benjamin y ; Al-Saffar, Muna ; Mukaddes, Nahit m ; Hashmi, Asif ; Balkhy, Soher ; Gascon, Generoso g ; Hisama, Fuki m ; Leclair, Elaine ; Poduri, Annapurna ; Oner, Ozgur ; Al-Saad, Samira ; Al-Awadi, Sadika a ; Bastaki, Laila ; Ben-Omran, Tawfeg ; Teebi, Ahmad s ; Al-Gazali, Lihadh ; Eapen, Valsamma ; Stevens, Christine r ; Rappaport, Leonard ; Gabriel, Stacey b ; Markianos, Kyriacos ; State, Matthew w ; Greenberg, Michael e ; Taniguchi, Hisaaki ; Braverman, Nancy e ; Morrow, Eric m ; Walsh, Christopher a

Neuron, Jan 23, 2013, Vol.77(2), pp.259-273 [Peer Reviewed Journal]

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6
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A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.

Al-Hamed, Mohamed H ; Al-Sabban, Essam ; Al-Mojalli, Hamad ; Al-Harbi, Naffaa ; Faqeih, Eissa ; Al Shaya, Hammad ; Alhasan, Khalid ; Al-Hissi, Safaa ; Rajab, Mohamed ; Edwards, Noel ; Al-Abbad, Abbas ; Al-Hassoun, Ibrahim ; Sayer, John A ; Meyer, Brian F Al-Hamed, Mohamed H (correspondence author) ; Al-Hamed, Mohamed H (record owner)

Journal of human genetics, July 2013, Vol.58(7), pp.480-489 [Peer Reviewed Journal]

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7
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Genetic characterization of the Miyako horse based on polymorphisms of microsatellites and mitochondrial DNA

Senju, Natsuko ; Tozaki, Teruaki ; Kakoi, Hironaga ; Almunia, Julio ; Maeda, Masami ; Matsuyama, Ryota ; Takasu, Masaki

The Journal of Veterinary Medical Science, 2017, Vol.79(1), p.218 [Peer Reviewed Journal]

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8
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Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene

Hasegawa, Kosei ; Higuchi, Yosuke ; Yamashita, Miho ; Tanaka, Hiroyuki

Clinical Pediatric Endocrinology, 2015, Vol.24(1), p.33-36 [Peer Reviewed Journal]

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9
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Article
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Myofibrillar myopaathy

Hayashi, Yukiko

Rinsho shinkeigaku = Clinical neurology, 2013, Vol.53(11), pp.1105-8 [Peer Reviewed Journal]

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10
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A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant with Nephrogenic Diabetes Insipidus

Daitsu, Takashi ; Igaki, Junko ; Goto, Masahiro ; Hasegawa, Yukihiro

Clinical Pediatric Endocrinology, 2014, Vol.23(4), p.115-117 [Peer Reviewed Journal]

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