THE RISE AND FALL OF POSITIONAL CLONING

被引:80
作者
BALLABIO, A [1 ]
机构
[1] BAYLOR COLL MED, CTR HUMAN GENOME, HOUSTON, TX 77030 USA
关键词
D O I
10.1038/ng0493-277
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:277 / 279
页数:3
相关论文
共 53 条
[1]   SEQUENCE IDENTIFICATION OF 2,375 HUMAN BRAIN GENES [J].
ADAMS, MD ;
DUBNICK, M ;
KERLAVAGE, AR ;
MORENO, R ;
KELLEY, JM ;
UTTERBACK, TR ;
NAGLE, JW ;
FIELDS, C ;
VENTER, JC .
NATURE, 1992, 355 (6361) :632-634
[2]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[3]   CLONING OF THE ESSENTIAL MYOTONIC-DYSTROPHY REGION AND MAPPING OF THE PUTATIVE DEFECT [J].
ASLANIDIS, C ;
JANSEN, G ;
AMEMIYA, C ;
SHUTLER, G ;
MAHADEVAN, M ;
TSILFIDIS, C ;
CHEN, C ;
ALLEMAN, J ;
WORMSKAMP, NGM ;
VOOIJS, M ;
BUXTON, J ;
JOHNSON, K ;
SMEETS, HJM ;
LENNON, GG ;
CARRANO, AV ;
KORNELUK, RG ;
WIERINGA, B ;
DEJONG, PJ .
NATURE, 1992, 355 (6360) :548-551
[4]   THE LOWE OCULOCEREBRORENAL SYNDROME GENE ENCODES A PROTEIN HIGHLY HOMOLOGOUS TO INOSITOL POLYPHOSPHATE-5-PHOSPHATASE [J].
ATTREE, O ;
OLIVOS, IM ;
OKABE, I ;
BAILEY, LC ;
NELSON, DL ;
LEWIS, RA ;
MCINNES, RR ;
NUSSBAUM, RL .
NATURE, 1992, 358 (6383) :239-242
[5]   AN EXONIC MUTATION IN THE HUP2 PAIRED DOMAIN GENE CAUSES WAARDENBURG SYNDROME [J].
BALDWIN, CT ;
HOTH, CF ;
AMOS, JA ;
DASILVA, EO ;
MILUNSKY, A .
NATURE, 1992, 355 (6361) :637-638
[6]   ISOLATION OF A CANDIDATE GENE FOR NORRIE DISEASE BY POSITIONAL CLONING [J].
BERGER, W ;
MEINDL, A ;
VANDEPOL, TJR ;
CREMERS, FPM ;
ROPERS, HH ;
DOERNER, C ;
MONACO, A ;
BERGEN, AAB ;
LEBO, R ;
WARBURG, M ;
ZERGOLLERN, L ;
LORENZ, B ;
GAL, A ;
BLEEKERWAGEMAKERS, EM ;
MEITINGER, T .
NATURE GENETICS, 1992, 1 (03) :199-203
[7]   MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER [J].
BROOK, JD ;
MCCURRACH, ME ;
HARLEY, HG ;
BUCKLER, AJ ;
CHURCH, D ;
ABURATANI, H ;
HUNTER, K ;
STANTON, VP ;
THIRION, JP ;
HUDSON, T ;
SOHN, R ;
ZEMELMAN, B ;
SNELL, RG ;
RUNDLE, SA ;
CROW, S ;
DAVIES, J ;
SHELBOURNE, P ;
BUXTON, J ;
JONES, C ;
JUVONEN, V ;
JOHNSON, K ;
HARPER, PS ;
SHAW, DJ ;
HOUSMAN, DE .
CELL, 1992, 68 (04) :799-808
[8]   DETECTION OF AN UNSTABLE FRAGMENT OF DNA SPECIFIC TO INDIVIDUALS WITH MYOTONIC-DYSTROPHY [J].
BUXTON, J ;
SHELBOURNE, P ;
DAVIES, J ;
JONES, C ;
VANTONGEREN, T ;
ASLANIDIS, C ;
DEJONG, P ;
JANSEN, G ;
ANVRET, M ;
RILEY, B ;
WILLIAMSON, R ;
JOHNSON, K .
NATURE, 1992, 355 (6360) :547-548
[9]   A MAJOR SEGMENT OF THE NEUROFIBROMATOSIS TYPE-1 GENE - CDNA SEQUENCE, GENOMIC STRUCTURE, AND POINT MUTATIONS [J].
CAWTHON, RM ;
WEISS, R ;
XU, GF ;
VISKOCHIL, D ;
CULVER, M ;
STEVENS, J ;
ROBERTSON, M ;
DUNN, D ;
GESTELAND, R ;
OCONNELL, P ;
WHITE, R .
CELL, 1990, 62 (01) :193-201
[10]   ISOLATION OF A CANDIDATE GENE FOR MENKES DISEASE THAT ENCODES A POTENTIAL HEAVY-METAL BINDING-PROTEIN [J].
CHELLY, J ;
TUMER, Z ;
TONNESEN, T ;
PETTERSON, A ;
ISHIKAWABRUSH, Y ;
TOMMERUP, N ;
HORN, N ;
MONACO, AP .
NATURE GENETICS, 1993, 3 (01) :14-19