Differential expression of two alternatively spliced mrnas for the XP21 glycerol kinase gene suggest specific and divergent functions

被引：0
|
作者：
Ohira, RH
Dipple, KM
McCabe, ERB
机构：
[1] Univ Calif Los Angeles, Dept Human Genet, David Geffen Sch Med, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Dept Pediat, David Geffen Sch Med, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA USA
来源：
JOURNAL OF INVESTIGATIVE MEDICINE | 2003年 / 51卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
47
引用
收藏
页码：S99 / S99
页数：1
相关论文
共 13 条
  • [1] Differential expression of two alternatively spliced mRNAs for the Xp21 glycerol kinase gene suggest specific and divergent functions.
    Ohira, RH
    Dipple, KM
    McCabe, ERB
    JOURNAL OF INVESTIGATIVE MEDICINE, 2003, 51 : S119 - S119
  • [2] Human glycerol kinase (GK): Tissue-specific expression patterns of two alternatively spliced mRNAs from the Xp2l GK gene
    Ohira, RH
    Dipple, KM
    McCabe, ERB
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 331 - 331
  • [3] ISOLATION OF THE HUMAN XP21 GLYCEROL KINASE GENE BY POSITIONAL CLONING
    WALKER, AP
    MUSCATELLI, F
    MONACO, AP
    HUMAN MOLECULAR GENETICS, 1993, 2 (02) : 107 - 114
  • [4] GENOMIC SCANNING FOR EXPRESSED SEQUENCES IN XP21 IDENTIFIES THE GLYCEROL KINASE GENE
    GUO, WW
    WORLEY, K
    ADAMS, V
    MASON, J
    SYLVESTERJACKSON, D
    ZHANG, YH
    TOWBIN, JA
    FOGT, DD
    MADU, S
    WHEELER, DA
    MCCABE, ERB
    NATURE GENETICS, 1993, 4 (04) : 367 - 372
  • [5] COMPLEX GLYCEROL KINASE-DEFICIENCY - GENOMIC MAPPING IN XP21 USING DNA FROM PATIENTS WITH THIS CONTIGUOUS GENE SYNDROME
    MCCABE, ERB
    TOWBIN, JA
    BALLABIO, A
    CHAMBERLAIN, J
    BURGHES, A
    KLEIN, CJ
    FOX, JE
    PILLERS, DA
    RIZZO, WB
    VANDENENGH, G
    TRASK, BJ
    PEDIATRIC RESEARCH, 1990, 27 (04) : A134 - A134
  • [6] Complex Glycerol Kinase Deficiency (Xp21 Deletion Syndrome): A Case Report of a Contiguous Gene Disorder Necessitating Creative Anesthetic Planning
    Rossell, Baptiste
    Godart, Juliette
    Petyt, Caroline
    Veyckemans, Francis
    A & A PRACTICE, 2020, 14 (10): : e01294
  • [7] A novel Xp21 contiguous gene deletion associated with Duchenne muscular dystrophy, glycerol kinase deficiency, congenital adrenal hypoplasia and non-specific mental retardation
    Baert, S
    Drouin-Garraud, V
    Leturcq, F
    Marret, P
    Forget, C
    Frebourg, T
    Saugier-Veber, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 559 - 559
  • [8] Contiguous gene deletion syndrome in Xp21:: The association between glycerol kinase deficiency congenital suprarenal hypoplasia and Duchenne's muscular dystrophy
    Pantoja-Martinez, J.
    Martinez-Castellano, F.
    Tarazona-Casany, I.
    Buesa-Ibanez, E.
    Ardid-Encinar, M.
    Esparza-Sanchez, M. A.
    Arzo, J. Bonet
    REVISTA DE NEUROLOGIA, 2007, 44 (10) : 606 - 609
  • [9] Clinical heterogeneity and molecular findings in five Polish patients with glycerol kinase deficiency: investigation of two splice site mutations with computerized splice junction analysis and Xp21 gene-specific mRNA analysis
    Hellerud, C
    Adamowicz, M
    Jurkiewicz, D
    Taybert, J
    Kubalska, J
    Ciara, E
    Popowska, E
    Ellis, JR
    Lindstedt, S
    Pronicka, E
    MOLECULAR GENETICS AND METABOLISM, 2003, 79 (03) : 149 - 159
  • [10] Expression and differential intracellular localization of two major forms of human 8-oxoguanine DNA glycosylase encoded by alternatively spliced OGG1 mRNAs
    Nishioka, K
    Ohtsubo, T
    Oda, H
    Fujiwara, T
    Kang, DC
    Sugimachi, K
    Nakabeppu, Y
    MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (05) : 1637 - 1652
12