標題: Titlebook: Degenerative Retinal Diseases; Matthew M. LaVail,Joe G. Hollyfield,Robert E. Ande Book 1997 Springer Science+Business Media New York 1997 [打印本頁] 作者: 拿著錫 時間: 2025-3-21 16:40
書目名稱Degenerative Retinal Diseases影響因子(影響力)
書目名稱Degenerative Retinal Diseases影響因子(影響力)學科排名
書目名稱Degenerative Retinal Diseases網(wǎng)絡公開度
書目名稱Degenerative Retinal Diseases網(wǎng)絡公開度學科排名
書目名稱Degenerative Retinal Diseases被引頻次
書目名稱Degenerative Retinal Diseases被引頻次學科排名
書目名稱Degenerative Retinal Diseases年度引用
書目名稱Degenerative Retinal Diseases年度引用學科排名
書目名稱Degenerative Retinal Diseases讀者反饋
書目名稱Degenerative Retinal Diseases讀者反饋學科排名
作者: 龍卷風 時間: 2025-3-21 23:18 作者: 導師 時間: 2025-3-22 01:17
https://doi.org/10.1007/978-1-4615-5933-7cell; cell death; cloning; eye; gene therapy; genetics; macular degeneration; retina作者: HACK 時間: 2025-3-22 06:12
978-1-4613-7718-4Springer Science+Business Media New York 1997作者: 斷斷續(xù)續(xù) 時間: 2025-3-22 11:45
Theorie der Wirkungen organischer K?rpersence of drusen and basal laminar deposits (BLD) in the macula. Drusen are extracellular deposits which form between the retinal pigment epithelial (RPE) basal lamina and the inner collagenous zone of Bruch’s membrane. Although the relationship between macular drusen and the development of AMD has b作者: 向下五度才偏 時間: 2025-3-22 16:00 作者: 向下五度才偏 時間: 2025-3-22 17:16 作者: fringe 時間: 2025-3-23 01:14
https://doi.org/10.1007/978-3-8349-4458-0lectroretinogram (ERG), in which the amplitude of a-wave is normal and larger than that of b-wave (1). We previously reported that CSNB cases with negative ERG can be divided into two types, complete or incomplete, based on the difference in rod visual functions, cone mediated ERGs, ERG oscillatory 作者: 蘆筍 時間: 2025-3-23 02:55
https://doi.org/10.1007/978-3-658-06298-9lor vision disturbance, macular degeneration and abnormalities on cone mediated electroretinogram (ERG) (1–4). This eye disease is distinguishable from the autosomal form by a family pedigree in which affected males appear on the maternal side without male to male transmission. Two XLCD families, wi作者: 背帶 時間: 2025-3-23 06:08
Entscheidungsvorbereitung für den Chefitis pigmentosa (RP) who did not have foveal cysts. Their serum was examined for the presence of antibodies that immunoreacted with retinal proteins. Twenty-seven of 30 patients with bilateral cystoid edema and retinal degeneration had serum anti-retinal protein antibody activity, compared to 3/50 h作者: emulsify 時間: 2025-3-23 12:46
https://doi.org/10.1007/978-3-658-29967-5lental vascularized mass due to maldeveloped retina, followed by complications of cataracts and corneal opacities leading to bulbar atrophies in adult. Some patients have psychomotor retardation and progressive hearing loss as part of a multisystem syndromic disorder. This vitreoretinal dysplastic d作者: forbid 時間: 2025-3-23 15:37
Die polumschaltbaren Maschinen, (15-30%) in the age group of >75 years (Bressler., Klein., Vingerling., Mitchell.) will significantly increase, causing enormous social and financial problems for the community. In spite of the significance of the problem, to date the pathogenesis of AMD remains unknown and the disease is essential作者: 我要沮喪 時間: 2025-3-23 18:58
Die polumschaltbaren Maschinen,ntralis. Iodoacetate (IA) was administered by subretinal injection in the area centralis. Subretinal delivery involved injection of IA into the subretinal space of a 4 mm diameter retinal bleb, using a dose of 0.1, 1, 1.6, 2 or 5 μg IA/bleb. IA was dissolved in 50 μl of BSS or a viscous hyaluronate 作者: 陳腐思想 時間: 2025-3-23 22:58
https://doi.org/10.1007/3-540-35017-9 inherited retinal dystrophies both in different animal species and in human. In dogs, different types of retinal dystrophies have been described affecting primarily the photoreceptors and/or pigment epithelium. A recessively inherited retinal dystrophy has been reported in a strain of Swedish Briar作者: languid 時間: 2025-3-24 03:09
https://doi.org/10.1007/3-540-35017-9tic trait in autosomal recessive (ar), autosomal dominant (ad) and X-linked fashions. While it had long been suspected that RP initially involves the photoreceptor cells, it was not until defects in photoreceptor-specific gene products were identified in patients with adRP (2) or arRP (3,4) that thi作者: 微枝末節(jié) 時間: 2025-3-24 09:39 作者: META 時間: 2025-3-24 11:32 作者: 高腳酒杯 時間: 2025-3-24 16:13 作者: BOLUS 時間: 2025-3-24 19:28
https://doi.org/10.1007/978-3-322-98658-0s investigations, has long been considered to be the primary pathology leading to retinal degeneration in this mutant (1–3). Light microscopic and ultrastructural studies of the developing photoreceptors of these animals have determined that the phagocytic defect is first evident around postnatal da作者: 相一致 時間: 2025-3-25 01:27
https://doi.org/10.1007/978-3-322-98658-0omeres of retinoid-deprived flies. In .. the visual system recovers quickly upon retinoid replacement even after prolonged deprivation. Importantly, photoreceptors do not degenerate. Total deprivation of all retinoids including retinoic acid is possible in . Thus deprivation of vitamin A chromophore作者: 公豬 時間: 2025-3-25 06:48
Die Aufgaben des Wissenschaftsrates mice are the two major vertebrate organisms for these analyses, the invertebrate .. provides a compelling alternative model system to study hereditary retinal degeneration. The invertebrate and vertebrate photoreceptor cells are dramatically different in both structure and organization, their visua作者: Collected 時間: 2025-3-25 07:59
https://doi.org/10.1007/978-3-662-39475-5pressed genes, for example the rhodopsin gene, have been identified as primary genetic defects. Using transgenic . as a model system, we investigated whether mutations in distinct amino acids which are conserved within the cytoplasmic domains throughout the rhodopsin family, namely Leu81, Asn86 or G作者: 嚙齒動物 時間: 2025-3-25 11:47
Development of a Model for Macular Degeneration, (15-30%) in the age group of >75 years (Bressler., Klein., Vingerling., Mitchell.) will significantly increase, causing enormous social and financial problems for the community. In spite of the significance of the problem, to date the pathogenesis of AMD remains unknown and the disease is essentially untreatable.作者: Spirometry 時間: 2025-3-25 17:20 作者: 恩惠 時間: 2025-3-25 21:10 作者: 硬化 時間: 2025-3-26 02:54
,Histochemical Comparison of Ocular “Drusen” in Monkey and Human,een established in a number of studies (1–4), relatively little is known about their composition or origin. Thorough characterization of these age-related deposits has been hampered by a paucity of suitable human donor tissues and the lack of an appropriate animal model of the disease.作者: 不能仁慈 時間: 2025-3-26 06:11 作者: Notorious 時間: 2025-3-26 11:08
Structures of the Oligosaccharides of Rhodopsin from Normal and Rcs Rats,ver, in either the amounts or structures of the rhodopsin oligosaccharide chains from young or adult control rats and RCS rats, although some differences were detected in the relative distribution of some oligosaccharide isomers.作者: incite 時間: 2025-3-26 14:28
Schlafmittel und Inhalationsan?stheticaARMD have been described, and end-stage histopathological descriptions of ARMD are available, little is known about the cellular mechanisms associated with the normal maintenance and turnover of Bruch’s membrane, the events that lead to drusen formation, or the cause of subretinal neovascularization and atrophy of the RPE and choriocapillaris.作者: 小畫像 時間: 2025-3-26 20:10 作者: vitreous-humor 時間: 2025-3-27 01:02
https://doi.org/10.1007/978-3-658-06298-9ecognized entity of XLCD associated with the Mizuo-Nakamura phenomenon in which the tapetal-like reflex disappeared after long dark adaptation (3). DNA analysis of XLCD families has also been reported, and the causative gene (COD1) has been localized to the short arm of the X-chromosome (5–7).作者: 衰弱的心 時間: 2025-3-27 03:35 作者: 身體萌芽 時間: 2025-3-27 08:11
,TIMP-3 Accumulation in Bruch’s Membrane and Drusen in Eyes From Normal and Age-Related Macular DegeARMD have been described, and end-stage histopathological descriptions of ARMD are available, little is known about the cellular mechanisms associated with the normal maintenance and turnover of Bruch’s membrane, the events that lead to drusen formation, or the cause of subretinal neovascularization and atrophy of the RPE and choriocapillaris.作者: 得體 時間: 2025-3-27 11:08
Photoreceptor Rosettes in Age-Related Macular Degeneration Donor Tissues,ptors. Vision loss occurs gradually over the course of many years. The wet form is less common but results in a more acute visual loss, which involves newly formed blood vessels below the macula that leak fluid and blood into the macular area.作者: PANT 時間: 2025-3-27 15:55 作者: cacophony 時間: 2025-3-27 21:28
Autoimmune Retinopathy,the cystoid edema present in RP patients that is absent in controls and in patients with RP without cystoid edema. The significance of the antibodies to retinal proteins in the pathophysiology of the disease process is currently under study.作者: integral 時間: 2025-3-28 00:33
Norrie Disease in Japan,. Some patients have psychomotor retardation and progressive hearing loss as part of a multisystem syndromic disorder. This vitreoretinal dysplastic disease is transmitted as a simple X-linked pattern of inheritance, so that hemizygous males are affected whereas heterozygous females remain asymptomatic..作者: 分離 時間: 2025-3-28 05:05
Theorie der Wirkungen organischer K?rpereen established in a number of studies (1–4), relatively little is known about their composition or origin. Thorough characterization of these age-related deposits has been hampered by a paucity of suitable human donor tissues and the lack of an appropriate animal model of the disease.作者: Substitution 時間: 2025-3-28 08:12
https://doi.org/10.1007/978-3-8349-4458-0potentials, degree of refractive errors, and family survey (2). It has been concluded that complete and incomplete types are different clinical entities, having demonstrated several explicit differences between the two CSNB types (3,4).作者: follicular-unit 時間: 2025-3-28 12:26 作者: Tincture 時間: 2025-3-28 18:15 作者: cogitate 時間: 2025-3-28 19:24 作者: 態(tài)學 時間: 2025-3-28 23:56 作者: irreducible 時間: 2025-3-29 05:51
Matthew M. LaVail,Joe G. Hollyfield,Robert E. Ande作者: Eructation 時間: 2025-3-29 09:34
Subretinal Iodoacetate,space and promoted a localized IA effect. Subretinal IA dissolved in BSS caused less severe and less consistent PR degeneration. Healon? or BSS alone did not induce PR damage. Thus, a model with PR-lacking area centralis has been created by subretinal injection of IA with a viscous solution. This mo作者: EXTOL 時間: 2025-3-29 11:47
Hereditary Retinal Dystrophy of Swedish Briard Dogs,is and direct sequencing of PCR products to screen the coding region as well as most splice donor and acceptor sites for mutations in a small kinship of dogs consisting of six offspring of an affected Swedish Briard dog. Our analysis revealed various sequence polymorphisms in all genes except arrest作者: N防腐劑 時間: 2025-3-29 17:56
The Vpp Mouse,r degeneration (6-9). The purpose of this chapter is to summarize a series of studies that have been carried out on one of these transgenic lines, the so-called ‘VPP’ mice (7). The available evidence indicates that the VPP mice may be a particularly useful animal model of adRP because they bear a cl作者: 離開真充足 時間: 2025-3-29 20:16 作者: 束縛 時間: 2025-3-30 01:09 作者: DAMN 時間: 2025-3-30 05:15
Defective Choroidal Angiogenesis Precedes Retinal Pigment Epithelial Phagocytic Defect in Neonatal the choroidal angiogenesis defect in mutant RCS rat pups, as well as our recent evidence indicating a reduction in the mRNA and protein for basic fibroblast growth factor (bFGF) in intact RPE of neonatal RCS rats (5). This new data is discussed in the context of previous conflicting investigations 作者: Antecedent 時間: 2025-3-30 09:09 作者: 疏忽 時間: 2025-3-30 13:23 作者: CAGE 時間: 2025-3-30 18:09
Recessive Degeneration of Photoreceptor Cells Caused by Point Mutations in the Cytoplasmic Domains ceptive cell compartment. In later states of degeneration, photoreceptor cell bodies and the extracellular interphotoreceptor space are filled with remnants of the photoreceptive membrane. Retinal degeneration is interpreted to result from alterations in rhodopsin’s cytoplasmic surface which destabi作者: chondromalacia 時間: 2025-3-30 20:57 作者: byline 時間: 2025-3-31 02:19
Zao resort hotel in the beautiful Mt. Zao region of northern Japan. This meeting was held on the occasion of the tenth anniversary of Makoto Tarnai as Pro- fessor and Chairman of Ophthalmology at Tohoku Medical School. One afternoon of the meeting contained a special symposium in honor of Professor Tarnai, wh978-1-4613-7718-4978-1-4615-5933-7作者: NOVA 時間: 2025-3-31 06:16
Die polumschaltbaren Maschinen,space and promoted a localized IA effect. Subretinal IA dissolved in BSS caused less severe and less consistent PR degeneration. Healon? or BSS alone did not induce PR damage. Thus, a model with PR-lacking area centralis has been created by subretinal injection of IA with a viscous solution. This mo作者: Glycogen 時間: 2025-3-31 12:31 作者: 符合國情 時間: 2025-3-31 14:29
https://doi.org/10.1007/3-540-35017-9r degeneration (6-9). The purpose of this chapter is to summarize a series of studies that have been carried out on one of these transgenic lines, the so-called ‘VPP’ mice (7). The available evidence indicates that the VPP mice may be a particularly useful animal model of adRP because they bear a cl作者: nitric-oxide 時間: 2025-3-31 18:13 作者: GNAW 時間: 2025-4-1 01:37 作者: prediabetes 時間: 2025-4-1 05:16 作者: 凝結(jié)劑 時間: 2025-4-1 09:38 作者: Heretical 時間: 2025-4-1 13:47
Die Aufgaben des Wissenschaftsratesife cycle and ease of mutant generation. . has provided a large number of mutants that undergo light-dependent, light-enhanced, and light-independent retinal degeneration (3). These mutants are defective in both expected and novel components that are required for visual transduction and photorecepto作者: Brain-Imaging 時間: 2025-4-1 15:42
https://doi.org/10.1007/978-3-662-39475-5ceptive cell compartment. In later states of degeneration, photoreceptor cell bodies and the extracellular interphotoreceptor space are filled with remnants of the photoreceptive membrane. Retinal degeneration is interpreted to result from alterations in rhodopsin’s cytoplasmic surface which destabi作者: GULLY 時間: 2025-4-1 18:45
,Histochemical Comparison of Ocular “Drusen” in Monkey and Human,sence of drusen and basal laminar deposits (BLD) in the macula. Drusen are extracellular deposits which form between the retinal pigment epithelial (RPE) basal lamina and the inner collagenous zone of Bruch’s membrane. Although the relationship between macular drusen and the development of AMD has b
