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Ceroid, lipofuscin and the ceroid-lipofuscinoses (Batten disease).

作者信息

Jolly R D, Dalefield R R, Palmer D N

机构信息

Department of Veterinary Pathology and Public Health, Massey University, Palmerston North, New Zealand.

出版信息

J Inherit Metab Dis. 1993;16(2):280-3. doi: 10.1007/BF00710265.

DOI:10.1007/BF00710265
PMID:8411981
Abstract
摘要

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1
Ceroid, lipofuscin and the ceroid-lipofuscinoses (Batten disease).脂褐素、脂褐质与脂褐质沉积症（巴滕病）
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2
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Proc Finn Dent Soc. 1990;86(2):99-102.
3
Lipofuscin and ceroid pigments in aging and brain pathology. A review. I. Biochemical and morphological properties.衰老与脑病理学中的脂褐素和类蜡样色素。综述。I. 生化与形态学特性
Rom J Neurol Psychiatry. 1995 Apr-Jun;33(2):121-36.
4
Lectin histochemical study of lipopigments with special regard to neuronal ceroid-lipofuscinosis. Results with concanavalin A.脂褐素的凝集素组织化学研究，特别关注神经元蜡样脂褐质沉积症。伴刀豆球蛋白A的研究结果。
Histochemistry. 1989;93(2):197-205. doi: 10.1007/BF00315975.
5
Neuronal ceroid lipofuscinosis with prominent accumulation of ceroid lipofuscin in the myocardium.神经元蜡样脂褐质沉积症伴蜡样脂褐质在心肌中显著蓄积。
J Inherit Metab Dis. 1995;18(3):359-60. doi: 10.1007/BF00710432.
6
You say lipofuscin, we say ceroid: defining autofluorescent storage material.你说脂褐素，我们说类蜡质：定义自发荧光储存物质。
Neurobiol Aging. 2006 Apr;27(4):576-88. doi: 10.1016/j.neurobiolaging.2005.12.006. Epub 2006 Feb 7.
7
Lectin histochemistry in brains with juvenile form of neuronal ceroid-lipofuscinosis (Batten disease).患有青少年型神经元蜡样脂褐质沉积症（巴滕病）的大脑中的凝集素组织化学
Acta Neuropathol. 1990;80(3):274-9. doi: 10.1007/BF00294645.
8
An autopsy case of adult neuronal ceroid lipofuscinosis.一例成人神经元蜡样脂褐质沉积症的尸检病例。
Jpn J Psychiatry Neurol. 1986 Dec;40(4):693-700. doi: 10.1111/j.1440-1819.1986.tb03186.x.
9
Immunoreactivity of ceroid lipofuscin storage pigment in Batten disease with monoclonal antibodies to the amyloid beta-protein.用针对β-淀粉样蛋白的单克隆抗体检测巴滕病中蜡样脂褐质储存色素的免疫反应性。
N Engl J Med. 1989 Jan 26;320(4):256-7. doi: 10.1056/nejm198901263200421.
10
Autofluorescent ceroid/lipofuscin.自体荧光脂褐质
Methods Mol Biol. 1998;108:217-27. doi: 10.1385/0-89603-472-0:217.

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本文引用的文献

1
Storage bodies in the ceroid-lipofuscinoses (Batten disease): low-molecular-weight components, unusual amino acids and reconstitution of fluorescent bodies from non-fluorescent components.蜡样脂褐质沉积症（巴滕病）中的储存小体：低分子量成分、异常氨基酸以及由非荧光成分重构荧光小体
J Inherit Metab Dis. 1993;16(2):292-5. doi: 10.1007/BF00710268.
2
Morphologic studies on adult neuronal-ceroid lipofuscinosis (NCL).成人神经元蜡样脂褐质沉积症（NCL）的形态学研究。
Clin Neuropathol. 1982;1(4):151-62.
3
Ceroid-lipofuscinosis (Batten's disease). Sequential electrophysiologic and pathologic changes in the retina of the ovine model.
澳大利亚牧牛犬中晚期神经元蜡样脂褐质沉积症的 ATP13A2 错义变异。
Mol Genet Metab. 2019 May;127(1):95-106. doi: 10.1016/j.ymgme.2018.11.015. Epub 2019 Mar 27.
4
Stable Isotope Labeling Reveals Novel Insights Into Ubiquitin-Mediated Protein Aggregation With Age, Calorie Restriction, and Rapamycin Treatment.稳定同位素标记揭示了泛素介导的蛋白质聚集在衰老、热量限制和雷帕霉素处理中的新见解。
J Gerontol A Biol Sci Med Sci. 2018 Apr 17;73(5):561-570. doi: 10.1093/gerona/glx047.
5
The proteasome and the degradation of oxidized proteins: Part II - protein oxidation and proteasomal degradation.蛋白酶体与氧化蛋白的降解：第二部分 - 蛋白质氧化与蛋白酶体降解
Redox Biol. 2014;2:99-104. doi: 10.1016/j.redox.2013.12.008. Epub 2013 Dec 17.
6
A murine model of variant late infantile ceroid lipofuscinosis recapitulates behavioral and pathological phenotypes of human disease.变异型晚发性婴儿蜡样脂褐质沉积症的小鼠模型重现了人类疾病的行为和病理表型。
PLoS One. 2013 Nov 1;8(11):e78694. doi: 10.1371/journal.pone.0078694. eCollection 2013.
7
Neuronal ceroid lipofuscinosis in the Polish Owczarek Nizinny (PON) dog. A retinal study.
Doc Ophthalmol. 1995;91(1):33-47. doi: 10.1007/BF01204622.
8
Reduced phospholipase activity, peptide storage and the pathogenesis of canine neuronal ceroid-lipofuscinosis.磷脂酶活性降低、肽储存与犬神经元蜡样脂褐质沉积症的发病机制
J Inherit Metab Dis. 1993;16(2):330-4. doi: 10.1007/BF00710276.
蜡样脂褐质沉积症（巴滕病）。绵羊模型视网膜的序贯电生理和病理变化。
Invest Ophthalmol Vis Sci. 1984 Mar;25(3):294-301.
4
Neuronal ceroid-lipofuscinosis (Batten's disease): relationship to amaurotic family idiocy?神经元蜡样脂褐质沉积症（巴顿病）：与黑蒙性家族性白痴有何关系？
Pediatrics. 1969 Oct;44(4):570-83.
5
Presidential address: Studies in the neuronal ceroid-lipofuscinoses.主席致辞：神经元蜡样脂褐质沉积症的研究
J Neuropathol Exp Neurol. 1974 Jan;33(1):1-12. doi: 10.1097/00005072-197401000-00001.
6
Ceroid-lipofuscinosis (Batten's disease): pathogenesis of blindness in the ovine model.蜡样脂褐质沉积症（巴滕病）：绵羊模型中失明的发病机制。
Neuropathol Appl Neurobiol. 1985 Jul-Aug;11(4):273-90. doi: 10.1111/j.1365-2990.1985.tb00025.x.
7
Ceroid-lipofuscinosis (Batten's disease): pathogenesis and sequential neuropathological changes in the ovine model.
Neuropathol Appl Neurobiol. 1989 Jul-Aug;15(4):371-83. doi: 10.1111/j.1365-2990.1989.tb01236.x.
8
Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinoses.人及羊蜡样脂褐质沉积症中线粒体ATP合酶的二环己基碳二亚胺反应性蛋白脂质亚基的溶酶体储存。
Adv Exp Med Biol. 1989;266:211-22; discussion 223. doi: 10.1007/978-1-4899-5339-1_15.
9
Ovine ceroid lipofuscinosis. The major lipopigment protein and the lipid-binding subunit of mitochondrial ATP synthase have the same NH2-terminal sequence.绵羊蜡样脂褐质沉积症。主要脂色素蛋白与线粒体ATP合酶的脂质结合亚基具有相同的NH2末端序列。
J Biol Chem. 1989 Apr 5;264(10):5736-40.
10
The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase.存储于绵羊蜡样脂褐质病中的主要蛋白质序列与线粒体ATP合酶的二环己基碳二亚胺反应性蛋白脂质序列相同。
Biochem J. 1990 Jun 15;268(3):751-8. doi: 10.1042/bj2680751.