書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases影響因子(影響力)學科排名
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases網(wǎng)絡公開度
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases網(wǎng)絡公開度學科排名
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases被引頻次
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases被引頻次學科排名
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases年度引用
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases年度引用學科排名
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases讀者反饋
書目名稱Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases讀者反饋學科排名
作者: 挖掘 時間: 2025-3-21 22:13
https://doi.org/10.1007/978-3-662-26337-2n APP and PS1 have been described. Second, in rare families with PS1 mutations, there are mutation-bearing individuals who may have escaped clinical disease. Third, some APP mutations alter the sequence of Aβ and lead to severe angiopathy with hemorrhage, rather than the plaques and tangles of AD. F作者: 該得 時間: 2025-3-22 02:18 作者: Outwit 時間: 2025-3-22 07:04 作者: 過于平凡 時間: 2025-3-22 11:37 作者: Fillet,Filet 時間: 2025-3-22 16:05 作者: Fillet,Filet 時間: 2025-3-22 17:37 作者: 小隔間 時間: 2025-3-22 23:27 作者: 泛濫 時間: 2025-3-23 02:14
,Early Onset Familial Alzheimer’s Disease: Is a Mutation Predictive of Pathology?,n APP and PS1 have been described. Second, in rare families with PS1 mutations, there are mutation-bearing individuals who may have escaped clinical disease. Third, some APP mutations alter the sequence of Aβ and lead to severe angiopathy with hemorrhage, rather than the plaques and tangles of AD. F作者: Urgency 時間: 2025-3-23 07:41 作者: hardheaded 時間: 2025-3-23 10:57
,Variable Phenotype of Alzheimer’s Disease with Spastic Paraparesis,been made since the earliest clinical reports of FAD: namely, that a number of AD families have been reported in which some individuals have SP. In 1997, the key observation was made that PS1 mutations were associated with the presence of SP, suggesting that there was a complex relationship between 作者: Estrogen 時間: 2025-3-23 15:10 作者: 擴音器 時間: 2025-3-23 21:08 作者: Geyser 時間: 2025-3-24 00:46 作者: 爭吵 時間: 2025-3-24 05:21 作者: 刺耳 時間: 2025-3-24 06:56 作者: 輕率的你 時間: 2025-3-24 11:07
Frontotemporal Dementias: Genotypes and Phenotypes,作者: reperfusion 時間: 2025-3-24 17:22
,Phenotype/genotype correlations in Parkinson’s disease,作者: 兇猛 時間: 2025-3-24 21:26 作者: monogamy 時間: 2025-3-25 02:48 作者: 過分自信 時間: 2025-3-25 06:22 作者: 兒童 時間: 2025-3-25 08:37 作者: 抱狗不敢前 時間: 2025-3-25 11:41 作者: 得意人 時間: 2025-3-25 16:03 作者: integral 時間: 2025-3-25 20:59 作者: 鐵砧 時間: 2025-3-26 02:07
https://doi.org/10.1007/978-3-642-92051-6ormalities of protein metabolism. Distinctive features have been identified that assist in the recognition of specific diseases or specific types of abnormalities of protein metabolism that are shared by several neurodegenerative disorders. Identification of the earliest manifestations of the phenot作者: 障礙物 時間: 2025-3-26 07:39 作者: 填滿 時間: 2025-3-26 08:41 作者: 清楚說話 時間: 2025-3-26 16:31 作者: assent 時間: 2025-3-26 17:02 作者: 小丑 時間: 2025-3-26 23:39
Die Matrixmethode mit variablen Stoffwerten,nts who carry PSEN mutations and have Alzheimer‘s disease with a variety of other clinical phenotypes including spastic paraplegia, seizures, myoclonus, parkinsonism, epilepsy and amyloid angiopathy. Remarkably, three of the studied families have frontotemporal dementia (FTD). The mutations associat作者: 悲觀 時間: 2025-3-27 03:14 作者: opportune 時間: 2025-3-27 07:32
https://doi.org/10.1007/978-3-642-90834-7ng that phenotype to known disease mechanisms, including genetic variations and pathology. This approach has been particularly difficult with frontotemporal dementias (FTD), because of the diversity and continuous evolution of its behavioral, language and cognitive symptoms. Recent systematic clinic作者: Exaggerate 時間: 2025-3-27 13:15
978-3-642-06395-4Springer-Verlag Berlin Heidelberg 2005作者: GEST 時間: 2025-3-27 17:28 作者: heirloom 時間: 2025-3-27 18:11
https://doi.org/10.1007/b137738Parkinson; Parkinson‘s disease; Proteinopathies; amyloid precursor protein; frontotemporal dementia phen作者: puzzle 時間: 2025-3-27 23:59
Neurodegenerative Disorders as Proteinopathies: Phenotypic Relationships,ormalities of protein metabolism. Distinctive features have been identified that assist in the recognition of specific diseases or specific types of abnormalities of protein metabolism that are shared by several neurodegenerative disorders. Identification of the earliest manifestations of the phenot作者: 商談 時間: 2025-3-28 05:08 作者: Repatriate 時間: 2025-3-28 09:05
,Early Onset Familial Alzheimer’s Disease: Is a Mutation Predictive of Pathology?,(PS2) and amyloid protein precursor (APP). Although many different mutations have been recorded for each gene, in most cases the clinical picture is typical of AD, with earlier onset than in sporadic AD. The question of whether mutations in these genes invariably predict AD pathology is the subject 作者: 暖昧關(guān)系 時間: 2025-3-28 10:29 作者: GRATE 時間: 2025-3-28 18:37
,Variable Phenotype of Alzheimer’s Disease with Spastic Paraparesis,enilin 2 (PS2) genes, show considerable phenotypic variability. Monogenic diseases typically exhibit variations in biological features, such as age of onset, severity, and multiple clinical and cellular phenotypes. This variation can be due to specific alleles of the disease gene, environmental effe作者: incision 時間: 2025-3-28 22:25
Presenilin Mutations: Variations in the Behavioral Phenotype with an Emphasis on the Frontotemporalnts who carry PSEN mutations and have Alzheimer‘s disease with a variety of other clinical phenotypes including spastic paraplegia, seizures, myoclonus, parkinsonism, epilepsy and amyloid angiopathy. Remarkably, three of the studied families have frontotemporal dementia (FTD). The mutations associat作者: Etching 時間: 2025-3-29 00:51 作者: seduce 時間: 2025-3-29 03:52
Variations of the Phenotype in Frontotemporal Dementias,ng that phenotype to known disease mechanisms, including genetic variations and pathology. This approach has been particularly difficult with frontotemporal dementias (FTD), because of the diversity and continuous evolution of its behavioral, language and cognitive symptoms. Recent systematic clinic作者: separate 時間: 2025-3-29 09:38
Christopher G. Provatidis with test data.? At each point, the exercise is to understand what the possibilities are based only on the information available at that point of the hypothesis testing and data collection processes...This interesting read for the upcoming residents and medical student educates on presenting comple作者: saturated-fat 時間: 2025-3-29 13:43
Dynamic Co-located VM Detection and Membership Update for Residency Aware Inter-VM Communication in eeper, a dynamic event driven co-located VM detection and membership update approach for residency aware inter-VM communication. CoKeeper responses faster than polling based methods since the membership updates are immediately visible after the events of VM existence changes. Experimental results sh作者: 襲擊 時間: 2025-3-29 16:40 作者: Lumbar-Stenosis 時間: 2025-3-29 22:54 作者: 狂熱文化 時間: 2025-3-30 02:58
text, Leibnitz and the Seventeenth-Century Revolution, writes that “the monad … is nothing but a 1 représentation (in both senses of the French word) of Leibniz’s personality in metaphysical symbols; and there was, under contemporary circumstances, no need 2 to ‘introduce’ this concept apart from ‘p作者: 聽寫 時間: 2025-3-30 05:11
Unraveling of Lipid Raft Organization in Cell Plasma Membranes by Single-Molecule Imaging of Gangliesults reveal the first direct evidence that GPI-anchored receptors and gangliosides interact in a cholesterol-dependent manner. Furthermore, they demonstrate that gangliosides continually move in and out of rafts that contain CD59 in an extremely dynamic manner and at a much higher frequency than e
