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1.Role of the BrafV637E mutation in hepatocarcinogenesis induced by treatment with diethylnitrosamine in neonatal B6C3F1 mice

作者：Masahiro Yamamoto ; Hiroki Tanaka ; Bing Xin ; Yuji Nishikawa ; Kosuke Yamazaki ; Keiko Shimizu and Katsuhiro Ogawa

刊名：Molecular Carcinogenesis

出版年：2017

2.Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses

作者：Akira Ohishi ; Gen Nishimura ; Fumiko Kato ; Hiroyuki Ono ; Kaori Maruwaka ; Mako Ago ; Hiroshi Suzumura ; Etsuko Hirose ; Yuki Uchida ; Maki Fukami and Tsutomu Ogata

刊名：American Journal of Medical Genetics Part A

出版年：2017

3.Cooperation of MLL/AF10(OM-LZ) with PTPN11 activating mutation induced monocytic leukemia with a shorter latency in a mouse bone marrow transplantation model

作者：Jen-Fen Fu ; Sung-Tzu Liang ; Ying-Jung Huang ; Kung-Hao Liang ; Tzung-Hai Yen ; Der-Cherng Liang and Lee-Yung Shih

刊名：International Journal of Cancer

出版年：2017

4.Morphological features that can predict BRAF^V600E-mutated carcinoma in paediatric thyroid cytology

作者：E. D. Rossi ; T. Bizzarro ; M. Martini ; S. Capodimonti ; T. Cenci ; G. Fadda ; F. Schmitt and L. M. Larocca

刊名：Cytopathology

出版年：2017

5.Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation - a novel phenotype of the mitochondrial disease

作者：H. Mierzewska ; M. Rydzanicz ; T. Biegański ; J. Kosinska ; M. Mierzewska-Schmidt ; A. Ługowska ; A. Pollak ; P. Stawiński ; A. Walczak ; A. Kędra ; E. Obersztyn ; E. Szczepanik and R. Płoski

刊名：Clinical Genetics

出版年：2017

6.Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual

作者：Lixin Wang ; Chunyan Huang ; Zengzhen Wei ; Jinzhe Tan ; Li Qin and Li Tian

刊名：Transfusion

出版年：2017

7.Identification and functional analysis of c.422_423InsT, a novel mutation of the HNF1A gene in a patient with diabetes

作者：Jesú ; s Miguel Magañ ; a-Cerino ; Juan P. Luna-Arias ; Marí ; a Luisa Labra-Barrios ; Bartolo Avendañ ; o-Borromeo ; Xavier Miguel Boldo-Leó ; n and Mirian Carolina Martí ; nez-Ló ; pez

刊名：Molecular Genetics & Genomic Medicine

出版年：2017

8.Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions

作者：Haishan Jiang ; Hiroshi Shimizu ; Atsushi Shiga ; Masami Tanaka ; Osamu Onodera ; Akiyoshi Kakita and Hitoshi Takahashi

刊名：Neuropathology

出版年：2017

9.Solution structure of the first RNA recognition motif domain of human spliceosomal protein SF3b49 and its mode of interaction with a SF3b145 fragment

作者：Kanako Kuwasako ; Nobukazu Nameki ; Kengo Tsuda ; Mari Takahashi ; Atsuko Sato ; Naoya Tochio ; Makoto Inoue ; Takaho Terada ; Takanori Kigawa ; Naohiro Kobayashi ; Mikako Shirouzu ; Takuhiro Ito ; Taiichi Sakamoto ; Kaori Wakamatsu ; Peter Gü ; ntert ; Seizo Takahashi ; Shigeyuki Yokoyama and Yutaka Muto

刊名：Protein Science

出版年：2017

10.Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K-AKT pathway

作者：Anna-Lena Volckmar ; Jonas Leichsenring ; Christa Flechtenmacher ; Nicole Pfarr ; Udo Siebolts ; Martina Kirchner ; Jan Budczies ; Michael Bockmayr ; Kathrin Ridinger ; Katja Lorenz ; Esther Herpel ; Aurelia Noske ; Wilko Weichert ; Frederick Klauschen ; Peter Schirmacher ; Roland Penzel ; Volker Endris and Albrecht Stenzinger

刊名：Genes, Chromosomes and Cancer

出版年：2017

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