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Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique.

作者信息

Kaufman B A, White P S, Steinbrueck T, Donis-Keller H, Brodeur G M

机构信息

Department of Neurological Surgery, Washington University School of Medicine, Saint Louis, MO 63110.

出版信息

Hum Genet. 1994 Oct;94(4):418-22. doi: 10.1007/BF00201604.

DOI:10.1007/BF00201604
PMID:7927340
Abstract

We identified two informative polymorphisms in the transcribed 3' untranslated region of the tumor necrosis factor receptor 2 (TNFR2) gene using the polymerase chain reaction (PCR) with the single-strand conformation polymorphism (SSCP) technique. These polymorphisms demonstrated Mendelian inheritance and were useful for linkage analysis. TNFR2 was very closely linked to the pronatriodilatin gene (PND), and the TNFR2 SSCP polymorphisms were much more informative than the restriction fragment length polymorphisms currently available for the PND locus. In addition, we have demonstrated that genotyping could be performed with DNA obtained from paraffin-embedded tissue.

摘要

相似文献

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2
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本文引用的文献

1
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity.1号染色体上皮肤恶性黑色素瘤-发育异常痣(CMM/DN)位点的进一步证据以及遗传异质性的证据。
Am J Hum Genet. 1993 Mar;52(3):537-50.
2
A complex single strand conformational polymorphism (SSCP) in the tumor necrosis factor receptor 2 (TNFR2) gene on chromosome 1p36.2.位于1号染色体p36.2区域的肿瘤坏死因子受体2(TNFR2)基因中存在一种复杂的单链构象多态性(SSCP)。
Hum Mol Genet. 1993 Jun;2(6):824. doi: 10.1093/hmg/2.6.824-a.
3
Use of the single-strand conformation polymorphism technique to detect loss of heterozygosity in neuroblastoma.
运用单链构象多态性技术检测神经母细胞瘤中的杂合性缺失。
Genes Chromosomes Cancer. 1993 Jun;7(2):102-8. doi: 10.1002/gcc.2870070207.
4
Analysis of DNA extracted from formalin-fixed, paraffin-embedded tissues by enzymatic amplification and hybridization with sequence-specific oligonucleotides.通过酶促扩增及与序列特异性寡核苷酸杂交对从福尔马林固定、石蜡包埋组织中提取的DNA进行分析。
Biochem Biophys Res Commun. 1987 Feb 13;142(3):710-6. doi: 10.1016/0006-291x(87)91472-0.
5
Immunomodulatory properties of recombinant murine and human tumor necrosis factor.重组鼠源和人源肿瘤坏死因子的免疫调节特性
Cancer Res. 1988 Feb 1;48(3):544-50.
6
BglII dimorphism at the human atrial natriuretic peptide (ANP) gene locus.人心房钠尿肽(ANP)基因位点的BglII二态性。
Nucleic Acids Res. 1986 Jun 25;14(12):5121. doi: 10.1093/nar/14.12.5121.
7
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.可通过聚合酶链反应进行分型的大量人类DNA多态性类别。
Am J Hum Genet. 1989 Mar;44(3):388-96.
8
Human atrial natriuretic peptides (ANP) gene locus: BglI RFLP.人类心钠素(ANP)基因位点:BglI限制性片段长度多态性
Nucleic Acids Res. 1986 Nov 25;14(22):9223. doi: 10.1093/nar/14.22.9223.
9
TaqI polymorphism at the 3' end of the human pronatriodilatin gene (hPND).人类心钠素原基因(hPND)3' 端的TaqI多态性
Nucleic Acids Res. 1986 Nov 11;14(21):8697. doi: 10.1093/nar/14.21.8697.
10
XhoI polymorphism at the human pronatriodilatin (hPND) gene locus.人利钠素原(hPND)基因位点的XhoI多态性
Nucleic Acids Res. 1986 Nov 11;14(21):8696. doi: 10.1093/nar/14.21.8696.