OLIGODENDROCYTES EXPRESS A NORMAL PHENOTYPE IN CARBONIC-ANHYDRASE II-DEFICIENT MICE

被引：31

作者：

GHANDOUR, MS ^{[1
]}

SKOFF, RP ^{[1
]}

VENTA, PJ ^{[1
]}

TASHIAN, RE ^{[1
]}

机构：

[1] UNIV MICHIGAN,DEPT HUMAN GENET,ANN ARBOR,MI 48109

来源：

JOURNAL OF NEUROSCIENCE RESEARCH | 1989年 / 23卷 / 02期

关键词：

D O I：

10.1002/jnr.490230208

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

引用

页码：180 / 190

页数：11

共 33 条

[21] N-ETHYL-N-NITROSOUREA INDUCED NULL MUTATION AT THE MOUSE CAR-2 LOCUS - AN ANIMAL-MODEL FOR HUMAN CARBONIC ANHYDRASE-II DEFICIENCY SYNDROME [J].

LEWIS, SE ;

ERICKSON, RP ;

BARNETT, LB ;

VENTA, PJ ;

TASHIAN, RE .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (06) :1962-1966

[22]

LEWIS SE, 1986, GENETIC TOXICOLOGY E, P359

[23]

Lindskog S, 1971, ENZYMES, P587

[24]

Maniatis T., 1982, MOL CLONING

[25]

Norton W, 1984, ADV NEUROCHEM, V5, P1

[26]

SCHLABACH MR, 1975, J BIOL CHEM, V250, P2182

[27] CARBONIC ANHYDRASE-II DEFICIENCY IN 12 FAMILIES WITH THE AUTOSOMAL RECESSIVE SYNDROME OF OSTEOPETROSIS WITH RENAL TUBULAR-ACIDOSIS AND CEREBRAL CALCIFICATION [J].

SLY, WS ;

WHYTE, MP ;

SUNDARAM, V ;

TASHIAN, RE ;

HEWETTEMMETT, D ;

GUIBAUD, P ;

VAINSEL, M ;

BALUARTE, HJ ;

GRUSKIN, A ;

ALMOSAWI, M ;

SAKATI, N ;

OHLSSON, A .

NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (03) :139-145

[28] CARBONIC ANHYDRASE-II DEFICIENCY IDENTIFIED AS THE PRIMARY DEFECT IN THE AUTOSOMAL RECESSIVE SYNDROME OF OSTEOPETROSIS WITH RENAL TUBULAR-ACIDOSIS AND CEREBRAL CALCIFICATION [J].

SLY, WS ;

HEWETTEMMETT, D ;

WHYTE, MP ;

YU, YSL ;

TASHIAN, RE .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (09) :2752-2756

[29]

TASHIAN RE, 1982, ISOZYMES CURRENT TOP, V7, P79

[30]

TASHIAN RE, 1984, ANN NY ACAD SCI, V429, P1

← 1 2 3 4 →