Insights from model systems - The yeast connection to Friedreich ataxia

被引:33
作者
Knight, SAB
Kim, R
Pain, D
Dancis, A
机构
[1] Univ Penn, Dept Med, Div Hematol Oncol, Stellar Chance Labs 1013, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Physiol, Philadelphia, PA 19104 USA
关键词
D O I
10.1086/302270
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:365 / 371
页数:7
相关论文
共 29 条
[1]  
ALLIKMETS R, 1998, AM J HUM GENET S, V63, pA26
[2]   Iron and copper transport in yeast and its relevance to human disease [J].
Askwith, C ;
Kaplan, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (04) :135-138
[3]   Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin [J].
Babcock, M ;
deSilva, D ;
Oaks, R ;
DavisKaplan, S ;
Jiralerspong, S ;
Montermini, L ;
Pandolfo, M ;
Kaplan, J .
SCIENCE, 1997, 276 (5319) :1709-1712
[4]   The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure [J].
Bidichandani, SI ;
Ashizawa, T ;
Patel, PI .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (01) :111-121
[5]  
Bidichandani SI, 1997, AM J HUM GENET, V60, P1251
[6]   A new case of multiple mitochondrial enzyme deficiencies with decreased amount of heat shock protein 60 [J].
Briones, P ;
Vilaseca, MA ;
Ribes, A ;
Vernet, A ;
Lluch, M ;
Cusi, V ;
Huckriede, A ;
Agsteribbe, E .
JOURNAL OF INHERITED METABOLIC DISEASE, 1997, 20 (04) :569-577
[7]   Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion [J].
Campuzano, V ;
Montermini, L ;
Molto, MD ;
Pianese, L ;
Cossee, M ;
Cavalcanti, F ;
Monros, E ;
Rodius, F ;
Duclos, F ;
Monticelli, A ;
Zara, F ;
Canizares, J ;
Koutnikova, H ;
Bidichandani, SI ;
Gellera, C ;
Brice, A ;
Trouillas, P ;
DeMichele, G ;
Filla, A ;
DeFrutos, R ;
Palau, F ;
Patel, PI ;
DiDonato, S ;
Mandel, JL ;
Cocozza, S ;
Koenig, M ;
Pandolfo, M .
SCIENCE, 1996, 271 (5254) :1423-1427
[8]   The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics [J].
Chomyn, A .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) :745-751
[9]   Clinical and genetic abnormalities in patients with Friedreich's ataxia [J].
Durr, A ;
Cossee, M ;
Agid, Y ;
Campuzano, V ;
Mignard, C ;
Penet, C ;
Mandel, JL ;
Brice, A ;
Koenig, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (16) :1169-1175
[10]   MOLECULAR-CLONING OF MTP70, A MITOCHONDRIAL MEMBER OF THE HSP70 FAMILY [J].
ENGMAN, DM ;
KIRCHHOFF, LV ;
DONELSON, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :5163-5168