Haplotype analysis of candidate genes from a region on 19q13.3 of the human genome newly identified as highly associated with MS

被引：0
|
作者：
Booth, D
Ban, M
Bennetts, B
Heard, R
Stewart, G
机构：
[1] Childrens Hosp Westmead Sydney, Sydney, NSW, Australia
[2] Univ Cambridge, Cambridge CB2 1TN, England
来源：
JOURNAL OF THE NEUROLOGICAL SCIENCES | 2005年 / 238卷
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：S222 / S222
页数：1
相关论文
共 44 条
  • [1] The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomas
    Chou, D
    Miyashita, T
    Mohrenweiser, HW
    Ueki, K
    Kastury, K
    Druck, T
    vonDeimling, A
    Huebner, K
    Reed, JC
    Louis, DN
    [J]. CANCER GENETICS AND CYTOGENETICS, 1996, 88 (02) : 136 - 140
  • [2] Confirmation of a gene for multiple sclerosis (MS) to chromosome region 19q13.3
    Lucotte, G
    [J]. GENETIC COUNSELING, 2002, 13 (02): : 133 - 138
  • [3] CLONING OF A HIGHLY CONSERVED HUMAN PROTEIN SERINE-THREONINE PHOSPHATASE GENE FROM THE GLIOMA CANDIDATE REGION ON CHROMOSOME 19Q13.3
    YONG, WH
    UEKI, K
    CHOU, D
    REEVES, SA
    VONDEIMLING, A
    GUSELLA, JF
    MOHRENWEISER, HW
    BUCKLER, AJ
    LOUIS, DN
    [J]. GENOMICS, 1995, 29 (02) : 533 - 536
  • [4] REFINED MAPPING AND COLOCALIZATION OF THE HUMAN GENES FOR PROSTATE-SPECIFIC ANTIGEN AND PANCREATIC KALLIKREIN TO 19Q13.3
    WINQVIST, R
    HENTTU, P
    GRZESCHIK, KH
    VIHKO, P
    [J]. CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 2026 - 2026
  • [5] RFLP IDENTIFIED BY THE PROBE PKE0.6 (D19S117) AT HUMAN-CHROMOSOME 19Q13.3
    SHUTLER, G
    TSILFIDIS, C
    LEBLOND, S
    KORNELUK, RG
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (05) : 1158 - 1158
  • [6] APOE alleles modulate associations of plasma metabolites with variants from multiple genes on chromosome 19q13.3
    Nazarian, Alireza
    Loiko, Elena
    Yassine, Hussein N.
    Finch, Caleb E.
    Kulminski, Alexander M.
    [J]. FRONTIERS IN AGING NEUROSCIENCE, 2022, 14
  • [7] Precise genetic mapping and haplotype analysis of the Mucolipidosis IV candidate region on human chromosome 19p13.2-13.3.
    Acierno, JS
    Falardeau, J
    Kennedy, JC
    Leyne, M
    Bromley, MC
    Colman, M
    Sun, M
    Bove, C
    Bach, G
    Ashworth, L
    Schiripo, T
    Ma, S
    Helbling, LA
    Goldin, E
    Schiffmann, R
    Slaugenhaupt, SA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 384 - 384
  • [8] Haplotype frequencies in a sub-region of chromosome 19q13.3, related to risk and prognosis of cancer, differ dramatically between ethnic groups
    Schierup, Mikkel H.
    Mailund, Thomas
    Li, Heng
    Wang, Jun
    Tjonneland, Anne
    Vogel, Ulla
    Bolund, Lars
    Nexo, Bjorn A.
    [J]. BMC MEDICAL GENETICS, 2009, 10
  • [9] A FREQUENT HINCII POLYMORPHISM IDENTIFIED BY THE HUMAN-CHROMOSOME 19Q13.3 PROBE PKEX0.8 (D19S118)
    TSILFIDIS, C
    SHUTLER, G
    MAHADEVAN, M
    KORNELUK, RG
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (05) : 1157 - 1157
  • [10] A 3 ALLELE INSERTION POLYMORPHISM IS IDENTIFIED BY THE HUMAN-CHROMOSOME 19Q13.3 PROBE PKBE0.8 (D19S119)
    KORNELUK, RG
    TSILFIDIS, C
    SHUTLER, G
    MAHADEVAN, M
    BAILLY, J
    SURH, LC
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (05) : 1157 - 1157
12345