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Advances in hemophilia: experimental aspects and therapy.血友病的进展:实验方面与治疗
Pediatr Clin North Am. 2008 Apr;55(2):357-76, viii. doi: 10.1016/j.pcl.2008.01.010.
2
In vivo models of haemophilia - status on current knowledge of clinical phenotypes and therapeutic interventions.血友病的体内模型——当前临床表型和治疗干预知识的现状
Haemophilia. 2008 Mar;14(2):248-59. doi: 10.1111/j.1365-2516.2007.01636.x. Epub 2008 Jan 7.
3
Gender and inter-species influence on coagulation tests of rats and mice.性别和种间因素对大鼠和小鼠凝血试验的影响。
Thromb Res. 2007;120(3):415-9. doi: 10.1016/j.thromres.2006.10.012. Epub 2006 Dec 5.
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Genetic diagnosis of haemophilia and other inherited bleeding disorders.血友病及其他遗传性出血性疾病的基因诊断
Haemophilia. 2006 Jul;12 Suppl 3:82-9. doi: 10.1111/j.1365-2516.2006.01263.x.
5
Development of a rat solid tumor model for continuous low-dose-rate irradiation studies using 125I and 103Pd sources.利用¹²⁵I和¹⁰³Pd源建立用于连续低剂量率辐照研究的大鼠实体瘤模型。
Brachytherapy. 2004;3(3):159-72. doi: 10.1016/j.brachy.2004.08.004.
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Dynamic fMRI and EEG recordings during spike-wave seizures and generalized tonic-clonic seizures in WAG/Rij rats.WAG/Rij大鼠棘波-慢波发作和全身强直-阵挛发作期间的动态功能磁共振成像和脑电图记录
J Cereb Blood Flow Metab. 2004 Jun;24(6):589-99. doi: 10.1097/01.WCB.0000117688.98763.23.
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Genetic animal models for absence epilepsy: a review of the WAG/Rij strain of rats.失神癫痫的遗传动物模型:WAG/Rij大鼠品系综述
Behav Genet. 2003 Nov;33(6):635-55. doi: 10.1023/a:1026179013847.
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Current therapy for rare factor deficiencies.罕见因子缺乏症的当前治疗方法。
Haemophilia. 2001 Jan;7 Suppl 1:16-22. doi: 10.1046/j.1365-2516.2001.00100.x.
9
Hemangiomas and hemangiosarcomas in inbred laboratory mice.近交系实验小鼠中的血管瘤和血管肉瘤
Lab Anim Sci. 1995 Oct;45(5):497-502.
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Clinical pathology reference ranges of laboratory animals. Working Group II, Nonclinical Safety Evaluation Subcommittee of the Japan Pharmaceutical Manufacturers Association.实验动物的临床病理学参考范围。日本制药工业协会非临床安全性评价小组委员会第二工作组。
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近交系WAG/RijYcb大鼠的自发性凝血病

Spontaneous coagulopathy in inbred WAG/RijYcb rats.

作者信息

Booth Carmen J, Brooks Marjory B, Rockwell Sara

机构信息

Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

Comp Med. 2010 Feb;60(1):25-30.

PMID:20158945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2826081/
Abstract

Here we describe a series of cases of spontaneous coagulopathy in a colony of inbred WAG/RijYcb (WAG/RijY) rats. This strain previously had been bred at our institution without symptomatology for several decades. The index case was a 10-wk-old male rat that developed a large hematoma at a subcutaneous injection site. Clinicopathologic findings included a decreased RBC count, decreased hematocrit, decreased hemoglobin concentration, normal PT, and prolonged (50% to 70%) aPTT (52 s; reference, 15 to 33 s). Examination of additional WAG/RijY rats that died unexpectedly or had clinical signs of bleeding in the absence of experimental manipulation also revealed normal PT and prolonged aPTT. Histologic examinations of tissues from all rats were unremarkable except for severe acute focally extensive hemorrhage corresponding to the macroscopic findings of acute hemorrhage. Furthermore the aPTT in 8 clinically normal adult rats and 8 clinically normal 4-wk-old WAG/RijY littermates of both sexes was prolonged. We conclude that these WAG/RijY rats have an inherited defect in the intrinsic coagulation pathway.

摘要

在此,我们描述了近交系WAG/RijYcb(WAG/RijY)大鼠群体中一系列自发性凝血病病例。该品系此前在我们机构繁殖了数十年,未出现症状。首例病例是一只10周龄雄性大鼠,其皮下注射部位出现了一个大血肿。临床病理检查结果包括红细胞计数减少、血细胞比容降低、血红蛋白浓度降低、凝血酶原时间正常以及活化部分凝血活酶时间延长(50%至70%)(52秒;参考值为15至33秒)。对其他意外死亡或在无实验操作情况下有出血临床症状的WAG/RijY大鼠进行检查,也发现凝血酶原时间正常而活化部分凝血活酶时间延长。除了与急性出血宏观表现相对应的严重急性局灶性广泛出血外,所有大鼠组织的组织学检查均无异常。此外,8只临床正常的成年大鼠和8只临床正常的4周龄WAG/RijY同窝仔鼠(雌雄均有)的活化部分凝血活酶时间也延长。我们得出结论,这些WAG/RijY大鼠在内源性凝血途径存在遗传性缺陷。