標(biāo)題: Titlebook: Retinal Degenerative Diseases; Joe G. Hollyfield,Robert E. Anderson,Matthew M. La Conference proceedings 2006 The Editor(s) (if applicable [打印本頁(yè)] 作者: 珍愛(ài) 時(shí)間: 2025-3-21 16:43
書(shū)目名稱Retinal Degenerative Diseases影響因子(影響力)
作者: avarice 時(shí)間: 2025-3-21 22:58 作者: 大量 時(shí)間: 2025-3-22 00:25 作者: 最初 時(shí)間: 2025-3-22 07:23
Chun-hong Xia,Haiquan Liu,Meng Wang,Debra Cheung,Alex Park,Yang Yang,Xin Du,Bo Chang,Bruce Beutler,Xnd Local Dimensions of Curriculum Internationalization?.? The Outcomes of Local and Global International Education?.? Internationalization for Local and Global Employability?.? Regional and National Cases of Lo978-94-6300-301-8作者: 不適當(dāng) 時(shí)間: 2025-3-22 09:05
Stephen P. Daiger,Suma P. Shankar,Alice B. Schindler,Lori S. Sullivan,Sara J. Bowne,Terri M. King,E.作者: BILK 時(shí)間: 2025-3-22 14:38 作者: patriarch 時(shí)間: 2025-3-22 20:16 作者: 牽連 時(shí)間: 2025-3-22 23:27 作者: motor-unit 時(shí)間: 2025-3-23 05:00 作者: 獨(dú)特性 時(shí)間: 2025-3-23 07:43
Darius M. Moshfeghi,Zhenglin Yang,Nathan D. Faulkner,Goutam Karan,Sukanya Thirumalaichary,Erik Pearsnalization in Local and Global Contexts?.? Local and Global Drivers for Change?.? Global and Local Dimensions of Curriculum Internationalization?.? The Outcomes of Local and Global International Education?.? Internationalization for Local and Global Employability?.? Regional and National Cases of Lo作者: INCUR 時(shí)間: 2025-3-23 10:27
Xinhua Shu,Brian Tulloch,Alan Lennon,Caroline Hayward,Mary O’Connell,Artur V. Cideciyan,Samuel G. Janalization in Local and Global Contexts?.? Local and Global Drivers for Change?.? Global and Local Dimensions of Curriculum Internationalization?.? The Outcomes of Local and Global International Education?.? Internationalization for Local and Global Employability?.? Regional and National Cases of Lo作者: eucalyptus 時(shí)間: 2025-3-23 17:53 作者: carotenoids 時(shí)間: 2025-3-23 19:57
Bradley J. Katz,Zhenglin Yang,Marielle Payne,Yin Lin,Yu Zhao,Erik Pearson,Shan Duan,Shin Kamaya,Goutnalization in Local and Global Contexts?.? Local and Global Drivers for Change?.? Global and Local Dimensions of Curriculum Internationalization?.? The Outcomes of Local and Global International Education?.? Internationalization for Local and Global Employability?.? Regional and National Cases of Lo作者: 皮薩 時(shí)間: 2025-3-23 22:59 作者: Inflated 時(shí)間: 2025-3-24 03:12 作者: 原諒 時(shí)間: 2025-3-24 08:33
Aileen Aherne,Avril Kennan,Paul F. Kenna,Niamh McNally,G. Jane Farrar,Pete Humphriesnalization in Local and Global Contexts?.? Local and Global Drivers for Change?.? Global and Local Dimensions of Curriculum Internationalization?.? The Outcomes of Local and Global International Education?.? Internationalization for Local and Global Employability?.? Regional and National Cases of Lo作者: Omnipotent 時(shí)間: 2025-3-24 13:27 作者: 走調(diào) 時(shí)間: 2025-3-24 18:44 作者: 硬化 時(shí)間: 2025-3-24 19:31 作者: certain 時(shí)間: 2025-3-25 00:55
RCC1-Like Domain and ORF15: Essentials in RPGR Genede (nt) ubiquitously expressed transcript which include 19 exons coding for 815 amino acids. Exon ORF15 which was identified later, encodes 567 amino acids, and was shown to be a mutation hot spot. Disease-causing mutations reported so far are localized in 5-prime exons and ORF15, while none have be作者: 合群 時(shí)間: 2025-3-25 06:17 作者: 巫婆 時(shí)間: 2025-3-25 11:21 作者: 字形刻痕 時(shí)間: 2025-3-25 13:10 作者: Ventilator 時(shí)間: 2025-3-25 18:48 作者: BULLY 時(shí)間: 2025-3-25 22:30 作者: Maximizer 時(shí)間: 2025-3-26 00:49 作者: GEM 時(shí)間: 2025-3-26 06:39
Conference proceedings 2006ng in the field. THe topics in this volume explore the etiology, cellular mechanisms, epidemiology, genetics, models and potential therapeutic measures for the blinding diseases of retinitis pigmentosa and age-related macular degeneration..作者: attenuate 時(shí)間: 2025-3-26 09:15 作者: 有雜色 時(shí)間: 2025-3-26 15:50 作者: 季雨 時(shí)間: 2025-3-26 18:35
A First Locus for Isolated Autosomal Recessive Optic Atrophy (ROA1) Maps to Chromosome 8q21-q22f DOA has been demonstrated. Three loci have been reported: OPA1 [3q28–q29; MIM 165500], OPA4 [18q12.2–q12.3; MIM 605293, and OPA5 (22q12.1–q13.1).. OPA1 which accounts for about 90% of DOA is due to mutations in the Msp1 protein [MIM 605290].作者: dapper 時(shí)間: 2025-3-27 01:01
Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by IMPDH1 Mutationshose patients that have been identified to date. The two mutations originally identified in large RP10 families in 2002 were Arg224Pro and Asp226Asn substitutions, and since then several additional mutations have been identified in RP families and individual patients (Kennan ., 2002; Bowne ., 2002; Daiger ., 2003; Grover ., 2004).作者: ureter 時(shí)間: 2025-3-27 03:49
Biochemical Function of the LCA Linked Protien, Aryl Hydrocarbon Receptor Interacting Protein Like-1CA is characterized by severely impaired vision and a weak or absent electroretinogram evident within the first year of life. To date, seven genes have been independently linked to LCA.. The majority of mutations implicated in the causation of LCA are genetically consistent with recessively inherited loss-of-function pathogenesis mechanisms..作者: 一回合 時(shí)間: 2025-3-27 06:13
field. THe topics in this volume explore the etiology, cellular mechanisms, epidemiology, genetics, models and potential therapeutic measures for the blinding diseases of retinitis pigmentosa and age-related macular degeneration..978-1-4899-9772-2978-0-387-32442-5作者: BILIO 時(shí)間: 2025-3-27 13:20
Bietti Crystalline Corneoretinal Dystrophy Associated with , Gene Mutationsparate Japanese patients with BCD and conclude that mutations in the . gene are the major cause of BCD. The IVS6-8_c.810del/insGC mutation is found at a higher frequency in the Asian populations suggesting a founder effect.作者: 喚起 時(shí)間: 2025-3-27 14:02
Annexins in Bruch’s Memberane and Drusenrom the cytosol to the exterior of cells across the plasma membrane by an unknown mehanism. When located extracellular, some annexins have been shown to function as receptors for other extracellular proteins: annexin II binds to tenascin and tissue plasminogen activator, while annexin V binds to collagen (Kojima, 1997).作者: 玷污 時(shí)間: 2025-3-27 21:49
Genetic Factors Modifying Clinical Expression of Autosomal Dominant RPeffects. One way to reduce the complexity is to focus on individuals who share a dominant mutation identical by descent, thus eliminating variability in the underlying mutation and variation in . to the mutation. A further simplification is to limit analysis to a single, extended family, which may r作者: 衰弱的心 時(shí)間: 2025-3-28 00:55
Disease-Associated Variants of the Rod-derived Cone Viability Factor (RdCVF) in Leber Congenital Amaetic heterogeneity of LCA has been accepted for a long time but it turned out to be largely higher than all odds. So far, 11genes have been mapped on human chromosomes and eight identified. .) the retinal specific guanylate cyclase gene (GUCY2D, retGC1; 17p13.1; LCA1; MIM 600179), .) the gene encodi作者: 漫不經(jīng)心 時(shí)間: 2025-3-28 02:42 作者: Customary 時(shí)間: 2025-3-28 06:50 作者: 多余 時(shí)間: 2025-3-28 12:34 作者: 豐滿中國(guó) 時(shí)間: 2025-3-28 16:09 作者: 津貼 時(shí)間: 2025-3-28 20:51
Biochemical Characterisation of the , Gene Associated with Late-Onset Retinal Degenerationnting for 50–60% of new blind registration in western countries (Green and Enger, 1993; Seddon, 2001). It is characterised by a late-onset degeneration of the retinal macula and represents the advanced stage of a more common disorder, age-related maculopathy. There are two clinical subtypes of AMD, 作者: COWER 時(shí)間: 2025-3-29 01:04
Bietti Crystalline Corneoretinal Dystrophy Associated with , Gene Mutations yellowish, glistening retinal crystals, choroidal sclerosis, and crystalline deposits in the peripheral cornea. Recent studies have demonstrated that the . gene which encodes a CYP450 family protein is the causative gene of the disease. We have identified a homozygous mutation in the . gene in 8 se作者: 大罵 時(shí)間: 2025-3-29 04:15 作者: collateral 時(shí)間: 2025-3-29 09:17 作者: obstinate 時(shí)間: 2025-3-29 13:28 作者: 撫育 時(shí)間: 2025-3-29 15:42
Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by IMPDH1 Mutationsesis, have been shown to cause the RP10 form of autosomal dominant retinitis pigmentosa (RP). This form of RP is generally early-onset and severe in those patients that have been identified to date. The two mutations originally identified in large RP10 families in 2002 were Arg224Pro and Asp226Asn s作者: 愛(ài)花花兒憤怒 時(shí)間: 2025-3-29 19:51
Biochemical Function of the LCA Linked Protien, Aryl Hydrocarbon Receptor Interacting Protein Like-1ited. LCA is the most rapid and severe form of congenital blindness, and it represents approximately 5% of all inherited retinopathies.. Clinically, LCA is characterized by severely impaired vision and a weak or absent electroretinogram evident within the first year of life. To date, seven genes hav作者: Habituate 時(shí)間: 2025-3-30 02:40
Characterization of Mouse Mutants with Abnormal RPE Cellsouter segments of the photoreceptor cells, removing metabolic wastes, transporting nutrients and maintaining visual cycle. RPE defects have been found in various human retinal disorders, such as age-related macular degeneration (Zarbin, 1998), Best disease (Petrukhin et al., 1998; Marmorstein et al.作者: 減震 時(shí)間: 2025-3-30 07:41 作者: vanquish 時(shí)間: 2025-3-30 09:16 作者: 可行 時(shí)間: 2025-3-30 12:48
http://image.papertrans.cn/r/image/829212.jpg作者: APEX 時(shí)間: 2025-3-30 19:06 作者: 疏忽 時(shí)間: 2025-3-30 21:22 作者: 比目魚(yú) 時(shí)間: 2025-3-31 02:00 作者: 新奇 時(shí)間: 2025-3-31 05:44 作者: Integrate 時(shí)間: 2025-3-31 10:30 作者: MULTI 時(shí)間: 2025-3-31 16:29
Darius M. Moshfeghi,Zhenglin Yang,Nathan D. Faulkner,Goutam Karan,Sukanya Thirumalaichary,Erik Pearsfacets of the theme. It reminds us that, while internationalization is strongly connected to the globalization of society, at the same time it is deeply embedded in local political, economic and social structures, systems and cultures.?.The increasing attention given to internationalization by insti作者: 字形刻痕 時(shí)間: 2025-3-31 19:07 作者: 彈藥 時(shí)間: 2025-3-31 23:23
