FURTHER EVIDENCE FOR A POST-TRANSLATIONAL PHENOMENON IN THE INTERACTION OF ALPHA-THALASSEMIA WITH SICKLE-CELL TRAIT

被引：5

作者：

RAHBAR, S

NOZARI, G

CHILLAR, R

WALLACE, RB

机构：

[1] MARTIN LUTHER KING JR GEN HOSP,LOS ANGELES,CA 90059

[2] CITY HOPE NATL MED CTR,BECKMAN RES INT,DUARTE,CA 91010

来源：

HEMOGLOBIN | 1988年 / 12卷 / 01期

关键词：

D O I：

10.3109/03630268808996885

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：71 / 76

页数：6

共 20 条

[1]

ABRAHAM E C, 1976, Hemoglobin, V1, P27, DOI 10.3109/03630267609031020

[2] DIFFERENCES IN AFFINITY OF VARIANT BETA-CHAINS FOR ALPHA-CHAINS - POSSIBLE EXPLANATION FOR VARIATION IN PERCENTAGES OF BETA-CHAIN VARIANTS IN HETEROZYGOTES [J].

ABRAHAM, EC ;

HUISMAN, THJ .

HEMOGLOBIN, 1977, 1 (08) :861-873

[3] ALPHA-THALASSEMIA-2 AND THE VARIABILITY OF HEMATOLOGICAL VALUES IN CHILDREN WITH SICKLE-CELL-ANEMIA [J].

ALTAY, C ;

GRAVELY, ME ;

JOSEPH, BR ;

WILLIAMS, DF .

PEDIATRIC RESEARCH, 1981, 15 (08) :1093-1096

[4] ELECTROSTATIC INTERACTIONS IN THE ASSEMBLY OF HEMOGLOBIN [J].

BUNN, HF ;

MCDONALD, MJ .

NATURE, 1983, 306 (5942) :498-500

[5]

BUNN HF, 1987, BLOOD, V69, P1

[6] DETECTION OF SICKLE-CELL BETA-S-GLOBIN ALLELE BY HYBRIDIZATION WITH SYNTHETIC OLIGONUCLEOTIDES [J].

CONNER, BJ ;

REYES, AA ;

MORIN, C ;

ITAKURA, K ;

TEPLITZ, RL ;

WALLACE, RB .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (01) :278-282

[7] ALPHA-GLOBIN GENE ORGANIZATION IN BLACKS PRECLUDES THE SEVERE FORM OF ALPHA-THALASSEMIA [J].

DOZY, AM ;

KAN, YW ;

EMBURY, SH ;

MENTZER, WC ;

WANG, WC ;

LUBIN, B ;

DAVIS, JR ;

KOENIG, HM .

NATURE, 1979, 280 (5723) :605-607

[8]

EMBURY SH, 1982, N ENGL J MED, V306, P280

[9]

Goossens M, 1981, Methods Enzymol, V76, P805

[10] PERCENTAGES OF ABNORMAL-HEMOGLOBINS IN ADULTS WITH A HETEROZYGOSITY FOR AN ALPHA-CHAIN AND OR A BETA-CHAIN VARIANT [J].

HUISMAN, THJ .

AMERICAN JOURNAL OF HEMATOLOGY, 1983, 14 (04) :393-404

← 1 2 →