小鼠突变型严重联合免疫缺陷（scid）位于第16号染色体上。 - Suppr

Suppr

超能文献

The mouse mutation severe combined immune deficiency (scid) is on chromosome 16.

作者信息

Bosma G C, Davisson M T, Ruetsch N R, Sweet H O, Shultz L D, Bosma M J

机构信息

Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111.

出版信息

Immunogenetics. 1989;29(1):54-7. doi: 10.1007/BF02341614.

DOI:10.1007/BF02341614

PMID:2908877

Abstract

摘要

相似文献

The mouse mutation severe combined immune deficiency (scid) is on chromosome 16.小鼠突变型严重联合免疫缺陷（scid）位于第16号染色体上。

Immunogenetics. 1989;29(1):54-7. doi: 10.1007/BF02341614.

The scid mouse mutant.

Curr Top Microbiol Immunol. 1988;137:197-202. doi: 10.1007/978-3-642-50059-6_29.

The scid mutation: occurrence and effect.

Curr Top Microbiol Immunol. 1989;152:3-9. doi: 10.1007/978-3-642-74974-2_1.

Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice.CBA/N小鼠X连锁免疫缺陷突变（xid）的定位

J Immunol. 1980 Apr;124(4):1875-7.

Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes.X连锁无丙种球蛋白血症与X连锁免疫缺陷基因的共定位。

Science. 1993 Jul 16;261(5119):355-8. doi: 10.1126/science.8332900.

The SCID mouse mutant: definition, characterization, and potential uses.严重联合免疫缺陷小鼠突变体：定义、特征及潜在用途。

Annu Rev Immunol. 1991;9:323-50. doi: 10.1146/annurev.iy.09.040191.001543.

Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice.免疫缺陷XID小鼠中布鲁顿酪氨酸激酶独特区域的突变

Science. 1993 Jul 16;261(5119):358-61. doi: 10.1126/science.8332901.

A high-resolution linkage map of the tight skin 2 (Tsk2) locus: a mouse model for scleroderma (SSc) and other cutaneous fibrotic diseases.紧密皮肤2（Tsk2）位点的高分辨率连锁图谱：硬皮病（SSc）和其他皮肤纤维化疾病的小鼠模型。

Mamm Genome. 1996 Aug;7(8):610-2. doi: 10.1007/s003359900181.

The fld mutation maps near to but distinct from the Apob locus on mouse chromosome 12.fld突变定位于小鼠12号染色体上靠近载脂蛋白B（Apob）基因座但与之不同的位置。

Mamm Genome. 1996 Jul;7(7):555-7. doi: 10.1007/s003359900166.

The scid mutation in mice causes a general defect in DNA repair.小鼠中的严重联合免疫缺陷（scid）突变会导致DNA修复出现普遍缺陷。

Nature. 1990 Oct 4;347(6292):479-82. doi: 10.1038/347479a0.

引用本文的文献

Cytotoxic effector functions of T cells are not required for protective immunity against fatal Rickettsia typhi infection in a murine model of infection: Role of TH1 and TH17 cytokines in protection and pathology.在鼠伤寒立克次体感染的小鼠模型中，针对致命性鼠伤寒立克次体感染的保护性免疫不需要T细胞的细胞毒性效应功能：TH1和TH17细胞因子在保护和病理过程中的作用。

PLoS Negl Trop Dis. 2017 Feb 21;11(2):e0005404. doi: 10.1371/journal.pntd.0005404. eCollection 2017 Feb.

Liver Necrosis and Lethal Systemic Inflammation in a Murine Model of Rickettsia typhi Infection: Role of Neutrophils, Macrophages and NK Cells.鼠伤寒立克次体感染小鼠模型中的肝坏死和致死性全身炎症：中性粒细胞、巨噬细胞和自然杀伤细胞的作用

PLoS Negl Trop Dis. 2016 Aug 22;10(8):e0004935. doi: 10.1371/journal.pntd.0004935. eCollection 2016 Aug.

Transcription factor zinc finger and BTB domain 1 is essential for lymphocyte development.转录因子锌指和 BTB 结构域蛋白 1 对于淋巴细胞发育是必需的。

J Immunol. 2012 Aug 1;189(3):1253-64. doi: 10.4049/jimmunol.1200623. Epub 2012 Jun 29.

Can humanized mice reflect the complex pathobiology of HIV-associated neurocognitive disorders?人源化小鼠能否反映与 HIV 相关的神经认知障碍的复杂病理生物学？

J Neuroimmune Pharmacol. 2012 Jun;7(2):352-62. doi: 10.1007/s11481-011-9335-y. Epub 2012 Jan 7.

Key genomic changes necessary for an in vivo lethal mouse marburgvirus variant selection process.体内致死性马尔堡病毒变异株选择过程所需的关键基因组变化。

J Virol. 2011 Apr;85(8):3905-17. doi: 10.1128/JVI.02372-10. Epub 2011 Feb 2.

Mouse models with human immunity and their application in biomedical research.具有人类免疫的小鼠模型及其在生物医学研究中的应用。

J Cell Mol Med. 2009 Jun;13(6):1043-58. doi: 10.1111/j.1582-4934.2008.00347.x. Epub 2008 Apr 15.

Primary T-lymphocyte immunodeficiencies.原发性T淋巴细胞免疫缺陷

Clin Rev Allergy Immunol. 2001 Feb;20(1):3-26. doi: 10.1385/CRIAI:20:1:3.

Nonsense mutation at Tyr-4046 in the DNA-dependent protein kinase catalytic subunit of severe combined immune deficiency mice.重症联合免疫缺陷小鼠的DNA依赖性蛋白激酶催化亚基中Tyr-4046位点的无义突变。

Proc Natl Acad Sci U S A. 1997 Mar 18;94(6):2438-43. doi: 10.1073/pnas.94.6.2438.

SCID mice and the study of parasitic disease.重症联合免疫缺陷小鼠与寄生虫病研究

Clin Microbiol Rev. 1996 Apr;9(2):126-34. doi: 10.1128/CMR.9.2.126.

Identification of a nonsense mutation in the carboxyl-terminal region of DNA-dependent protein kinase catalytic subunit in the scid mouse.在严重联合免疫缺陷（scid）小鼠中DNA依赖蛋白激酶催化亚基羧基末端区域无义突变的鉴定。

Proc Natl Acad Sci U S A. 1996 Sep 17;93(19):10285-90. doi: 10.1073/pnas.93.19.10285.

本文引用的文献

[Essential lymphocytophthisis; new clinical aspect of infant pathology].[原发性淋巴细胞消耗症；婴儿病理学的新临床方面]

Ann Paediatr. 1950 Jul-Aug;175(1-2):1-32.

[Agammaglobulinemia & alymphocytosis with atrophy of lymphatic tissue].[无丙种球蛋白血症及淋巴细胞减少伴淋巴组织萎缩]

Helv Paediatr Acta. 1958 Dec;13(6):551-85.

[Familial lymphopenia with agammaglobulinemia & severe moniliasis: the essential lymphocytophthisis as a special form of early childhood agammaglobulinemia].[伴有无丙种球蛋白血症和严重念珠菌病的家族性淋巴细胞减少症：作为幼儿期无丙种球蛋白血症一种特殊形式的原发性淋巴细胞消耗症]

Helv Paediatr Acta. 1958 Oct;13(4):313-38.

A severe combined immunodeficiency mutation in the mouse.小鼠中的一种严重联合免疫缺陷突变。

Nature. 1983 Feb 10;301(5900):527-30. doi: 10.1038/301527a0.

Sequences of immunoglobulin lambda 1 genes in a lambda 1 defective mouse strain.λ1缺陷小鼠品系中免疫球蛋白λ1基因的序列

Nature. 1982 Jul 8;298(5870):184-7. doi: 10.1038/298184a0.

The primary immunodeficiencies. (2).原发性免疫缺陷病。（2）。

N Engl J Med. 1984 Aug 2;311(5):300-10. doi: 10.1056/NEJM198408023110506.

Linkage of the Igl-1 structural and regulatory genes to Akv-2 on chromosome 16.免疫球蛋白轻链-1（Igl-1）结构基因和调控基因与16号染色体上的Akv-2的连锁关系。

Immunogenetics. 1984;19(6):527-37. doi: 10.1007/BF00403444.

Induction of resting B cells to DNA synthesis by soluble monoclonal anti-immunoglobulin.可溶性单克隆抗免疫球蛋白诱导静止B细胞进行DNA合成

Eur J Immunol. 1984 Aug;14(8):753-7. doi: 10.1002/eji.1830140816.

Regional assignment of ADA and ITPA to mouse chromosome 2 (C1----ter). A demonstration of the conserved linkage of enzyme and proto-oncogene loci.腺苷脱氨酶（ADA）和次黄嘌呤-鸟嘌呤磷酸核糖转移酶（ITPA）在小鼠2号染色体（着丝粒----端粒）上的区域定位。酶基因座与原癌基因座保守连锁的证明。

J Hered. 1984 May-Jun;75(3):175-80. doi: 10.1093/oxfordjournals.jhered.a109907.

Extrachromosomal DNA substrates in pre-B cells undergo inversion or deletion at immunoglobulin V-(D)-J joining signals.前B细胞中的染色体外DNA底物在免疫球蛋白V-(D)-J连接信号处发生倒位或缺失。

Cell. 1987 Jun 19;49(6):775-83. doi: 10.1016/0092-8674(87)90615-5.

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。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验