由人触珠蛋白（HP）cDNA探针pULB1148检测到的TaqI限制性片段长度多态性。 - Suppr | 超能文献

A TaqI RFLP detected by the human haptoglobin (HP) cDNA probe, pULB1148.

作者信息

Hyland V J

机构信息

Department of Histopathology, Adelaide Children's Hospital, SA, Australia.

出版信息

Nucleic Acids Res. 1988 Aug 25;16(16):8203. doi: 10.1093/nar/16.16.8203.

DOI:10.1093/nar/16.16.8203

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC338545/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6896/338545/900b2fe470c4/nar00158-0440-a.jpg

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

A TaqI RFLP detected by the human haptoglobin (HP) cDNA probe, pULB1148.由人触珠蛋白（HP）cDNA探针pULB1148检测到的TaqI限制性片段长度多态性。

Nucleic Acids Res. 1988 Aug 25;16(16):8203. doi: 10.1093/nar/16.16.8203.

2

An AvaII polymorphism in the haptoglobin alpha gene (HPA).触珠蛋白α基因（HPA）中的AvaII多态性。

Nucleic Acids Res. 1989 Jun 26;17(12):4906. doi: 10.1093/nar/17.12.4906.

3

A TaqI RFLP detected by the probe VK45C6 [D16S131] at 16p13.11.由位于16p13.11的探针VK45C6 [D16S131]检测到的TaqI限制性片段长度多态性。

Nucleic Acids Res. 1989 Aug 11;17(15):6430. doi: 10.1093/nar/17.15.6430.

4

Detection of two TaqI polymorphisms in the VTR region of the human HRAS1 oncogene.

Cytogenet Cell Genet. 1986;43(3-4):174-80. doi: 10.1159/000132317.

5

A TaqI RFLP detecting single copy fragment (G80) from chromosome 7 p13-p15 (D7S373).一种检测来自7号染色体p13 - p15（D7S373）单拷贝片段（G80）的TaqI限制性片段长度多态性

Nucleic Acids Res. 1987 Sep 25;15(18):7653. doi: 10.1093/nar/15.18.7653.

6

A new TaqI polymorphism detected by the cDNA encoding amyloid beta protein of Alzheimer's disease.通过阿尔茨海默病淀粉样β蛋白的cDNA检测到一种新的TaqI多态性。

Nucleic Acids Res. 1987 Nov 11;15(21):9103. doi: 10.1093/nar/15.21.9103.

7

A PvuII RFLP detected in the human prion protein (PrP) gene.在人类朊病毒蛋白（PrP）基因中检测到一种PvuII限制性片段长度多态性。

Nucleic Acids Res. 1987 Apr 10;15(7):3191. doi: 10.1093/nar/15.7.3191.

8

Human TaqI RFLP recognized by neurofilament gene probes.神经丝基因探针识别的人类TaqI限制性片段长度多态性

Nucleic Acids Res. 1988 May 11;16(9):4183. doi: 10.1093/nar/16.9.4183.

9

RFLP for TaqI at the human neurofilament (NF-L) gene locus.人类神经丝蛋白（NF-L）基因位点TaqI的限制性片段长度多态性

Nucleic Acids Res. 1988 May 11;16(9):4184. doi: 10.1093/nar/16.9.4184.

10

XmnI RFLP at 5q13 detected by a 0.49 kb Xmn I fragment of human hexosaminidase (HEXB) cDNA.通过人己糖胺酶（HEXB）cDNA的0.49 kb XmnI片段检测到5q13处的XmnI限制性片段长度多态性。

Nucleic Acids Res. 1988 Aug 25;16(16):8198. doi: 10.1093/nar/16.16.8198.

引用本文的文献

1

A novel I247T missense mutation in the haptoglobin 2 beta-chain decreases the expression of the protein and is associated with ahaptoglobinemia.触珠蛋白2β链中的一种新型I247T错义突变会降低该蛋白的表达，并与无触珠蛋白血症相关。

Hum Genet. 2004 Apr;114(5):499-502. doi: 10.1007/s00439-004-1098-6. Epub 2004 Mar 4.

2

The haptoglobin-gene deletion responsible for anhaptoglobinemia.导致无结合珠蛋白血症的结合珠蛋白基因缺失。

Am J Hum Genet. 1998 Feb;62(2):245-52. doi: 10.1086/301701.

本文引用的文献

1

Molecular cloning of human haptoglobin cDNA: evidence for a single mRNA coding for alpha 2 and beta chains.人触珠蛋白cDNA的分子克隆：编码α2和β链的单一信使核糖核酸的证据

EMBO J. 1983;2(6):1003-7. doi: 10.1002/j.1460-2075.1983.tb01534.x.