Three RFLPs are detected by an alpha spectrin genomic clone.
作者信息
Hoffman N, Stanislovitis P, Watkins P C, Klinger K W, Linnenbach A J, Forget B G
出版信息
Nucleic Acids Res. 1987 Jun 11;15(11):4696. doi: 10.1093/nar/15.11.4696.
Abstract
摘要
相似文献
1
Three RFLPs are detected by an alpha spectrin genomic clone.通过一个α血影蛋白基因组克隆检测到三种限制性片段长度多态性。
Nucleic Acids Res. 1987 Jun 11;15(11):4696. doi: 10.1093/nar/15.11.4696.
2
Xba I polymorphisms in the 5' region of human erythrocyte alpha spectrin gene (Spna).人类红细胞α-血影蛋白基因（Spna）5'区域的Xba I多态性
Nucleic Acids Res. 1988 Nov 25;16(22):10950. doi: 10.1093/nar/16.22.10950.
3
Mapping of alpha-spectrin on distal mouse chromosome 1.α-血影蛋白在小鼠1号染色体远端的定位
Cytogenet Cell Genet. 1987;45(1):52-4. doi: 10.1159/000132424.
4
Isolation and characterization of cDNA clones for human erythrocyte beta-spectrin.人红细胞β-血影蛋白cDNA克隆的分离与鉴定
Proc Natl Acad Sci U S A. 1987 Nov;84(21):7468-72. doi: 10.1073/pnas.84.21.7468.
5
RFLPs associated with pMC1, an anonymous single copy clone from the short arm of chromosome 19 [HGM8 assignment no. D19S14].与pMC1相关的限制性片段长度多态性，pMC1是来自19号染色体短臂的一个匿名单拷贝克隆[人类基因定位第8版编号：D19S14]。
Nucleic Acids Res. 1987 Jan 12;15(1):378. doi: 10.1093/nar/15.1.378.
6
Cloning of a portion of the chromosomal gene for human erythrocyte alpha-spectrin by using a synthetic gene fragment.利用合成基因片段克隆人红细胞α-血影蛋白部分染色体基因
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2397-401. doi: 10.1073/pnas.83.8.2397.
7
A StuI RFLP in the human beta-spectrin gene (SPTB).人类β-血影蛋白基因（SPTB）中的一种斯图I限制性片段长度多态性
Nucleic Acids Res. 1991 May 11;19(9):2515. doi: 10.1093/nar/19.9.2515.
8
The gelsolin (GSN) cDNA clone, from 9q32-34, identifies BclI and StuI RFLPs.来自9q32 - 34的凝溶胶蛋白（GSN）cDNA克隆可识别BclI和StuI限制性片段长度多态性。
Nucleic Acids Res. 1989 Jun 12;17(11):4425. doi: 10.1093/nar/17.11.4425.
9
Two linked RFLPs at chromosomal band 1p32.位于染色体1p32带的两个连锁限制性片段长度多态性
Nucleic Acids Res. 1989 Aug 11;17(15):6427. doi: 10.1093/nar/17.15.6427.
10
Identification and mapping of RFLPs for human tissue factor (HTF) to chromosome 1p.人类组织因子（HTF）的限制性片段长度多态性（RFLP）的鉴定及其在1号染色体短臂上的定位。
Nucleic Acids Res. 1987 Nov 11;15(21):9098. doi: 10.1093/nar/15.21.9098.
引用本文的文献
1
2
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.在一个显性遗传性球形红细胞增多症家系中，红细胞带3基因的无义突变与mRNA积累减少相关。
J Clin Invest. 1996 Jan 15;97(2):373-80. doi: 10.1172/JCI118425.
3
A TaqI polymorphism in the human erythroid beta spectrin gene.
Hum Genet. 1995 Mar;95(3):365-6. doi: 10.1007/BF00225212.
4
Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).血影蛋白αI结构域的两种致椭圆红细胞增多的αI/74变体。血影蛋白库洛兹（GGT----GTT；αI 40位甘氨酸----缬氨酸）和血影蛋白里昂（CTT----TTT；αI 43位亮氨酸---苯丙氨酸）。
J Clin Invest. 1990 Aug;86(2):548-54. doi: 10.1172/JCI114743.
5
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele.有证据表明，SpαI/65遗传性椭圆形红细胞增多症的表达由一个与同源α-血影蛋白等位基因相关的遗传因素复合而成。
Hum Genet. 1990 Oct;85(6):627-30. doi: 10.1007/BF00193587.
6
Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.SpαV/41：αIV-αV结构域连接处常见的血影蛋白多态性。与位于反式的α-血影蛋白变体导致的遗传性椭圆形红细胞增多症的表达水平相关。
J Clin Invest. 1991 Jun;87(6):2169-77. doi: 10.1172/JCI115250.
7
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.与αI/74遗传性椭圆形红细胞增多症相关的β-血影蛋白基因点突变。对血影蛋白二聚体自我缔合机制的影响。
J Clin Invest. 1990 Sep;86(3):909-16. doi: 10.1172/JCI114792.
8
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.α-血影蛋白第28密码子的四种不同突变与遗传性椭圆形红细胞增多症中结构和功能异常的血影蛋白αI/74相关。
J Clin Invest. 1991 Sep;88(3):743-9. doi: 10.1172/JCI115371.
9
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.遗传性椭圆形红细胞增多症和热异形红细胞症中常见的一种血影蛋白α I 46 - 50a - kD肽异常与远离蛋白水解切割位点的突变有关。血影蛋白三螺旋模型功能重要性的证据。
J Clin Invest. 1992 Mar;89(3):892-8. doi: 10.1172/JCI115669.
10
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin.意大利南部的αI/65遗传性椭圆形红细胞增多症：源于非洲的证据。
Hum Genet. 1992 Jul;89(5):553-6. doi: 10.1007/BF00219183.
本文引用的文献
1
Cloning of a portion of the chromosomal gene for human erythrocyte alpha-spectrin by using a synthetic gene fragment.利用合成基因片段克隆人红细胞α-血影蛋白部分染色体基因
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2397-401. doi: 10.1073/pnas.83.8.2397.
2
The alpha-spectrin gene is on chromosome 1 in mouse and man.α-血影蛋白基因在小鼠和人类中都位于1号染色体上。
Proc Natl Acad Sci U S A. 1985 Jun;82(11):3790-3. doi: 10.1073/pnas.82.11.3790.
Zotero 插件