Genomic analysis-integrated whole-exome sequencing of neuroblastomas identifies genetic mutations in axon guidance pathway

Oncotarget

Volumn 8, Issue 34, 2017, Pages 56684-56697

  Li, Yuanyuan ^a,b   Ohira, Miki ^b,c   Zhou, Yong ^d   Xiong, Teng ^d   Luo, Wen ^d   Yang, Chao ^d   Li, Xiangchun ^d   Gao, Zhibo ^d   Zhou, Rui ^d   Nakamura, Yohko ^b   Kamijo, Takehiko ^c   Kaneko, Yasuhiko ^c   Taketani, Takeshi ^e   Ueyama, Junichi ^f   Tajiri, Tatsuro ^g   Zhang, Hongyan ^d   Wang, Jian ^d,h   Yang, Huanming ^d,h   Yin, Ye ^d   Nakagawara, Akira ^a,b  

^a Division of Dermatology   (Japan)

^b CHIBA CANCER CENTER   (Japan)

^c SAITAMA CANCER CENTER   (Japan)

^d BGI SHENZHEN   (China)

^e SHIMANE UNIVERSITY FACULTY OF MEDICINE   (Japan)

^f TOTTORI UNIVERSITY   (Japan)

^g KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^h James D Watson of Institute of Genome Sciences   (China)

Author keywords

Array CGH; Familial neuroblastoma; Genomic diversity; Neuroblastoma; Whole exome sequencing

Indexed keywords

ALK GENE; ARTICLE; AXON GUIDANCE; CANCER RISK; CANCER STAGING; CHROMOSOME ABERRATION; CONTROLLED STUDY; GENE; GENE MUTATION; GENETIC HETEROGENEITY; GENOME ANALYSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; INDEL MUTATION; MAPK SIGNALING; METASTASIS; MISSENSE MUTATION; MONOZYGOTIC TWINS; MRNA EXPRESSION ASSAY; NEUROBLASTOMA; NONSENSE MUTATION; ONCOGENE N RAS; OVERALL SURVIVAL; PHYLOGENETIC TREE; RISK ASSESSMENT; SEMA6C GENE; SILENT MUTATION; SLIT1 GENE; SOMATIC MUTATION; WHOLE EXOME SEQUENCING; WNT SIGNALING;

EID: 85029055441     PISSN: None     EISSN: 19492553     Source Type: Journal    
DOI: 10.18632/oncotarget.18079     Document Type: Article

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