2q13—an IPO Revival

被引:0
|
作者
Yang W. [1 ]
机构
[1] Walter Yang is Research Director at BioCentury,
关键词
D O I
10.1038/nbt.2663
中图分类号
学科分类号
摘要
[No abstract available]
引用
收藏
页码:672 / 672
相关论文
共 50 条
  • [41] Gray matter deficits in bipolar disorder are associated with genetic variability at interleukin-1 beta gene (2q13)
    Papiol, S.
    Molina, V.
    Desco, M.
    Rosa, A.
    Reig, S.
    Sanz, J.
    Palomo, T.
    Fananas, L.
    GENES BRAIN AND BEHAVIOR, 2008, 7 (07) : 796 - 801
  • [42] Prenatal diagnosis of 2q13 duplications: The crucial role of the family survey in genetic counseling on novel copy number variations
    Bellil, Hela
    Molina-Gomes, Denise
    Quibel, Thibaud
    Roy, Sophie
    Dard, Rodolphe
    Vialard, Francois
    Herve, Berenice
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2020, 63 (08)
  • [43] Genetic Variation at Chromosome 2q13 and Its Potential Influence on Endometriosis Susceptibility Through Effects on the IL-1 Family
    Gajbhiye, Rahul
    McKinnon, Brett
    Mortlock, Sally
    Mueller, Michael
    Montgomery, Grant
    REPRODUCTIVE SCIENCES, 2018, 25 (09) : 1307 - 1317
  • [44] Genetic variation at the interleukin-1 cluster (2Q13) is associated with morphological brain abnormalities both in schizophrenia and bipolar disorder
    Papiol, S
    Molina, V
    Desco, M
    Rosa, A
    Reig, S
    Sanz, J
    Palomo, T
    Fañanás, L
    SCHIZOPHRENIA RESEARCH, 2006, 81 : 61 - 62
  • [45] 房间隔缺损合并肾积水的2q13微缺失1例并文献复习
    于艳
    杨彦
    李晓光
    陈琦
    陈云鹏
    中华围产医学杂志, 2023, 26 (12)
  • [46] Genetic Variation at Chromosome 2q13 and Its Potential Influence on Endometriosis Susceptibility Through Effects on the IL-1 Family
    Rahul Gajbhiye
    Brett McKinnon
    Sally Mortlock
    Michael Mueller
    Grant Montgomery
    Reproductive Sciences, 2018, 25 : 1307 - 1317
  • [47] CONTRIBUTION OF GENETIC VARIABILITY IN INTERLEUKIN-1 CLUSTER (2Q13) TO THE RISK OF FUNCTIONAL PSYCHOSIS AND ITS ASSOCIATED BRAIN ABNORMALITIES
    Papiol, Sergi
    Molina, Vicente
    Fatjo-Vilas, Mar
    Monfort, Ana
    Rosa, Araceli
    Arias, Barbara
    Sanz, Javier
    Calama, J.
    Hernandez, A. I.
    Martin, C.
    Fananas, Lourdes
    SCHIZOPHRENIA RESEARCH, 2010, 117 (2-3) : 345 - 345
  • [48] Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies
    Jaiswal, Sushi Kumar
    Kumar, Ashok
    Ali, Akhtar
    Rai, Amit Kumar
    GENE, 2015, 559 (01) : 94 - 98
  • [49] Genomic analysis of 280 kb of DNA sequence from human chromosome 2q13 surrounding an ancestral chromosome fusion site.
    Fan, Y
    Linardopoulou, L
    Friedman, C
    Trask, BJ
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 179 - 179
  • [50] Pontine Tegmental Cap Dysplasia With a 2q13 Microdeletion Involving the NPHP1 Gene: Insights Into Malformations of the Mid-Hindbrain
    Macferran, Kimberly M.
    Buchmann, Robert F.
    Ramakrishnaiah, Raghu
    Griebel, May L.
    Sanger, Warren G.
    Saronwala, Anirudh
    Schaefer, G. Bradley
    SEMINARS IN PEDIATRIC NEUROLOGY, 2010, 17 (01) : 69 - 74