百科全书
发表于 2025-3-30 10:25:09
Progressive Pathways in Age-Related Macular Degeneration, photoreceptor cell loss. No current therapy halts vision loss. Numerous genetic and/or environmental factors likely contribute to the initiating events leading to AMD. Progressive events from cellular dysfunction and tissue destruction result in the histopathological features of AMD including druse
cipher
发表于 2025-3-30 15:56:52
http://reply.papertrans.cn/83/8293/829206/829206_52.png
SNEER
发表于 2025-3-30 19:50:32
http://reply.papertrans.cn/83/8293/829206/829206_53.png
Arthritis
发表于 2025-3-30 21:48:00
Retinal and Choroidal Alterations Following Photodynamic Therapy,d by age-related macular degeneration (AMD), presumed ocular histoplasmosis syndrome (POHS) and myopic maculopathy (No Authors, 1999; Bressler, 2001; No Authors, 2001). The basic mechanism of PDT is the light activation of photosensitizing agent based on its absorption profile. PDT involves two cruc
CANON
发表于 2025-3-31 04:30:17
Usher Syndrome: Correlation between Visual Field Size and Maximal ERG Response B-Wave Amplitude,field) and objective measurements [(e.g., the electroretinogram (ERG)]. The ERG provides essential information on the amount and quality of functioning retina left. The a-wave of the full-field flash maximal ERG response reflects the combined activity of rod and cone photoreceptors, whereas the b-wa
Axillary
发表于 2025-3-31 05:31:01
The Cellular Function of the Usher Gene Product Myosin VIIa is Specified by Its Ligands,Charles Usher (Usher, 1914), is the most common hereditary form of combined blind-and deafness (~ 50% of cases in the developed countries). USH designates a group of clinically and genetically heterogeneous disorders with hearing loss and retinitis pigmentosa (RP). Three different USH types (USH1, 2
逃避现实
发表于 2025-3-31 12:52:46
Mouse Models for Usher Syndrome 1b,SH1 being the most severe. Children with USH1 are born profoundly deaf, and then begin to lose their sight as a result of retinitis pigmentosa usually in their second decade of life. Mutations in at least seven different genes can cause USHI. Four of these have now been identified. The most common f
justify
发表于 2025-3-31 14:02:35
http://reply.papertrans.cn/83/8293/829206/829206_58.png
原谅
发表于 2025-3-31 20:08:12
Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP,these two genes, contrastingthe similar approaches to identifying the genes and mutations with the dissimilar strategies for functional analysis. In microcosm, this serves as a reminder that retinal disease genes associated with similar clinical phenotypes may have very different biological roles.
神圣将军
发表于 2025-4-1 01:43:35
http://reply.papertrans.cn/83/8293/829206/829206_60.png