Exclusion of ABCA-1 as a candidate gene for canine Scott syndrome.
作者信息
Brooks M B, Catalfamo J L, Etter K, Brisbin A, Bustamante C D
出版信息
J Thromb Haemost. 2008 Sep;6(9):1608-10. doi: 10.1111/j.1538-7836.2008.03068.x.
Abstract
摘要
相似文献
1
Exclusion of ABCA-1 as a candidate gene for canine Scott syndrome.排除ABCA - 1作为犬类斯科特综合征候选基因的可能性。
J Thromb Haemost. 2008 Sep;6(9):1608-10. doi: 10.1111/j.1538-7836.2008.03068.x.
2
3
An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease.一个 ABCA4 功能丧失突变导致犬类形式的斯特格病。
PLoS Genet. 2019 Mar 19;15(3):e1007873. doi: 10.1371/journal.pgen.1007873. eCollection 2019 Mar.
4
The ABCA subclass of mammalian transporters.
Biochim Biophys Acta. 1999 Dec 6;1461(2):395-404. doi: 10.1016/s0005-2736(99)00170-4.
5
A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.一个犬类的芳基硫酸酯酶 G (ARSG) 突变导致的芳基硫酸酯酶缺乏与神经元蜡样脂褐质沉积症有关。
Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14775-80. doi: 10.1073/pnas.0914206107. Epub 2010 Aug 2.
6
7
A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome.ABCA1基因中的一种新型错义突变导致斯科特综合征患者的蛋白质转运改变和磷脂酰丝氨酸易位减少。
Blood. 2005 Jul 15;106(2):542-9. doi: 10.1182/blood-2004-05-2056. Epub 2005 Mar 24.
8
9
Identification of genetic variation and haplotype structure of the canine ABCA4 gene for retinal disease association studies.鉴定与犬类视网膜疾病相关的 ABCA4 基因的遗传变异和单倍型结构。
Mol Genet Genomics. 2010 Oct;284(4):243-50. doi: 10.1007/s00438-010-0560-5. Epub 2010 Jul 27.
10
Expression and role of PGP, BCRP, MRP1 and MRP3 in multidrug resistance of canine mammary cancer cells.PGP、BCRP、MRP1 和 MRP3 在犬乳腺癌细胞多药耐药中的表达及作用。
BMC Vet Res. 2013 Jun 17;9:119. doi: 10.1186/1746-6148-9-119.
本文引用的文献
1
Calcium-diacylglycerol guanine nucleotide exchange factor I gene mutations associated with loss of function in canine platelets.与犬血小板功能丧失相关的钙 - 二酰甘油鸟嘌呤核苷酸交换因子I基因突变
Transl Res. 2007 Aug;150(2):81-92. doi: 10.1016/j.trsl.2007.03.006. Epub 2007 May 25.
2
ABCA1, from pathology to membrane function.ABCA1，从病理学到膜功能
Pflugers Arch. 2007 Feb;453(5):569-79. doi: 10.1007/s00424-006-0108-z. Epub 2006 Jul 21.
3
Molecular defects in the ABCA1 pathway affect platelet function.
Pathophysiol Haemost Thromb. 2006;35(1-2):166-74. doi: 10.1159/000093563.
4
Flow cytometric measurement of platelet-leukocyte aggregates: a possible target to monitor platelet function?血小板-白细胞聚集体的流式细胞术检测：监测血小板功能的一个可能靶点？
Semin Thromb Hemost. 2005;31(4):400-3. doi: 10.1055/s-2005-916673.
5
A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome.ABCA1基因中的一种新型错义突变导致斯科特综合征患者的蛋白质转运改变和磷脂酰丝氨酸易位减少。
Blood. 2005 Jul 15;106(2):542-9. doi: 10.1182/blood-2004-05-2056. Epub 2005 Mar 24.
6
Surface exposure of phosphatidylserine in pathological cells.病理细胞中磷脂酰丝氨酸的表面暴露。
Cell Mol Life Sci. 2005 May;62(9):971-88. doi: 10.1007/s00018-005-4527-3.
7
Chromosome-specific microsatellite multiplex sets for linkage studies in the domestic dog.用于家犬连锁研究的染色体特异性微卫星多重试剂盒。
Genomics. 2004 Sep;84(3):550-4. doi: 10.1016/j.ygeno.2004.06.006.
8
Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease).家族性高密度脂蛋白缺乏症（丹吉尔病）中血小板活化受损。
J Biol Chem. 2004 Aug 6;279(32):34032-7. doi: 10.1074/jbc.M405174200. Epub 2004 May 25.
9
The ABCA1 transporter modulates late endocytic trafficking: insights from the correction of the genetic defect in Tangier disease.ABCA1转运蛋白调节晚期内吞运输：来自丹吉尔病基因缺陷纠正的见解。
J Biol Chem. 2004 Apr 9;279(15):15571-8. doi: 10.1074/jbc.M314160200. Epub 2004 Jan 27.
10
Phospholipid flip-flop in biogenic membranes: what is needed to connect opposite sides.生物膜中的磷脂翻转：连接膜两侧需要什么。
Semin Cell Dev Biol. 2002 Jun;13(3):163-70. doi: 10.1016/s1084-9521(02)00044-7.
Zotero 插件