From expressed sequence tags to peroxisome biogenesis disorder genes

被引：14

作者：

Dodt, G

Braverman, N

Valle, D

Gould, SJ

机构：

[1] JOHNS HOPKINS UNIV, SCH MED, DEPT BIOL CHEM, BALTIMORE, MD 21205 USA

[2] JOHNS HOPKINS UNIV, SCH MED, DEPT CELL BIOL, BALTIMORE, MD 21205 USA

[3] JOHNS HOPKINS UNIV, SCH MED, DEPT ANAT, BALTIMORE, MD 21205 USA

[4] JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA

[5] JOHNS HOPKINS UNIV, SCH MED, HOWARD HUGHES MED INST, BALTIMORE, MD 21205 USA

来源：

PEROXISOMES: BIOLOGY AND ROLE IN TOXICOLOGY AND DISEASE | 1996年 / 804卷

关键词：

D O I：

10.1111/j.1749-6632.1996.tb18641.x

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：516 / 523

页数：8

共 30 条

[1] RAPID CDNA SEQUENCING (EXPRESSED SEQUENCE TAGS) FROM A DIRECTIONALLY CLONED HUMAN INFANT BRAIN CDNA LIBRARY [J].

ADAMS, MD ;

SOARES, MB ;

KERLAVAGE, AR ;

FIELDS, C ;

VENTER, JC .

NATURE GENETICS, 1993, 4 (04) :373-386

[2] BASIC LOCAL ALIGNMENT SEARCH TOOL [J].

ALTSCHUL, SF ;

GISH, W ;

MILLER, W ;

MYERS, EW ;

LIPMAN, DJ .

JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410

[3]

BRAVERMAN N, 1995, UNPUB J CELL BIOL

[4] GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS [J].

BRUL, S ;

WESTERVELD, A ;

STRIJLAND, A ;

WANDERS, RJA ;

SCHRAM, AW ;

HEYMANS, HSA ;

SCHUTGENS, RBH ;

VANDENBOSCH, H ;

TAGER, JM .

JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) :1710-1715

[5] MUTATIONS IN THE PTS1 RECEPTOR GENE, PXR1, DEFINE COMPLEMENTATION GROUP-2 OF THE PEROXISOME BIOGENESIS DISORDERS [J].

DODT, G ;

BRAVERMAN, N ;

WONG, C ;

MOSER, A ;

MOSER, HW ;

WATKINS, P ;

VALLE, D ;

GOULD, SJ .

NATURE GENETICS, 1995, 9 (02) :115-125

[6]

ELGERSMA Y, 1993, GENETICS, V135, P731

[7] ISOLATION OF PEROXISOME-DEFICIENT MUTANTS OF SACCHAROMYCES-CEREVISIAE [J].

ERDMANN, R ;

VEENHUIS, M ;

MERTENS, D ;

KUNAU, WH .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5419-5423

[8] THE HUMAN MUTATOR GENE HOMOLOG MSH2 AND ITS ASSOCIATION WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].

FISHEL, R ;

LESCOE, MK ;

RAO, MRS ;

COPELAND, NG ;

JENKINS, NA ;

GARBER, J ;

KANE, M ;

KOLODNER, R .

CELL, 1993, 75 (05) :1027-1038

[9] RESTORATION OF PEROXISOME BIOGENESIS IN A PEROXISOME-DEFICIENT MAMMALIAN-CELL LINE BY EXPRESSION OF EITHER THE 35-KDA OR THE 70-KDA PEROXISOMAL MEMBRANE-PROTEINS [J].

GARTNER, J ;

OBIE, C ;

WATKINS, P ;

VALLE, D .

JOURNAL OF INHERITED METABOLIC DISEASE, 1994, 17 (03) :327-329

[10] DEVELOPMENT OF THE YEAST PICHIA-PASTORIS AS A MODEL ORGANISM FOR A GENETIC AND MOLECULAR ANALYSIS OF PEROXISOME ASSEMBLY [J].

GOULD, SJ ;

MCCOLLUM, D ;

SPONG, AP ;

HEYMAN, JA ;

SUBRAMANI, S .

YEAST, 1992, 8 (08) :613-628

← 1 2 3 →