標題: Titlebook: Advances in Vision Research, Volume II; Genetic Eye Research Gyan Prakash,Takeshi Iwata Book 2019 This is a U.S. government work and not un [打印本頁] 作者: cucumber 時間: 2025-3-21 16:38
書目名稱Advances in Vision Research, Volume II影響因子(影響力)
書目名稱Advances in Vision Research, Volume II影響因子(影響力)學(xué)科排名
書目名稱Advances in Vision Research, Volume II網(wǎng)絡(luò)公開度
書目名稱Advances in Vision Research, Volume II網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Advances in Vision Research, Volume II被引頻次
書目名稱Advances in Vision Research, Volume II被引頻次學(xué)科排名
書目名稱Advances in Vision Research, Volume II年度引用
書目名稱Advances in Vision Research, Volume II年度引用學(xué)科排名
書目名稱Advances in Vision Research, Volume II讀者反饋
書目名稱Advances in Vision Research, Volume II讀者反饋學(xué)科排名
作者: Ostrich 時間: 2025-3-21 21:28 作者: Constitution 時間: 2025-3-22 02:33 作者: 關(guān)心 時間: 2025-3-22 08:36 作者: PET-scan 時間: 2025-3-22 12:20
Emerging Market Companies as Globalizers,e world. 15% identify as Māori and 7% as Pacific peoples, and the spectrum of inherited eye disease encountered in this population varies from that seen in those identifying as NZ European. Keratoconus is more common, while primary open-angle glaucoma is rare. A number of founder pathogenic variants作者: apiary 時間: 2025-3-22 13:29 作者: dyspareunia 時間: 2025-3-22 18:57
Lloyd Motz,Jefferson Hane Weaveror molecular research is considerable, with heritable factors linked in both common and uncommon diseases such as primary open-angle glaucoma, primary angle-closure glaucoma, diabetic retinopathy, vasculitis retinae and age-related macular degeneration, congenital glaucoma, and retinitis pigmentosa,作者: PACK 時間: 2025-3-23 01:10 作者: 苦惱 時間: 2025-3-23 02:49
Sound Currency , Full Employment,diseases in the Philippines are rare but collectively represent a significant cause of blindness. Although specialized facilities providing genetic services in the country exist, only a handful of genetic eye studies have been done in the Filipino population. Training more Filipino scientists and op作者: CAPE 時間: 2025-3-23 07:16
Medium-Term Employment Strategies,teristics, the incidence of hereditary eye disease is higher in Ningxia Region. From 2010 to 2017, our research team collected 230 pedigrees and 268 sporadic patients with monogenic hereditary eye disease, including 210 pedigrees and 250 sporadic patients with hereditary retinal diseases. Among thes作者: Urea508 時間: 2025-3-23 11:43
,The Norman Conquest, 1066–1100, consanguineous, large sibship families was exploited with overwhelming results particularly using homozygosity mapping methodology. The project came to standstill due to limited funding and complicated logistics to work in field in India. Even though the struggle started with multiple barriers and 作者: Intractable 時間: 2025-3-23 14:07
https://doi.org/10.1007/978-1-349-23648-0 cone-rod dystrophy, Stargardt disease, etc. Establishing a molecular diagnosis in IRD is important for proper diagnosis, genetic counseling, predicting prognosis, and clinical trials of retinal gene therapies. In this chapter, recent studies using gene panel-based next-generation sequencing in Kore作者: 瘙癢 時間: 2025-3-23 20:28 作者: defendant 時間: 2025-3-23 22:10 作者: 淘氣 時間: 2025-3-24 02:41
,Conrad Ferdinand Meyers religi?se Welt,share of the adult eye diseases component that particularly affects the neurovascular retina. More than 100 genes are known to cause Mendelian types of retinal degenerations including syndromic and non-syndromic RP, and it is presumed that this constitutes only 60% of all the genes known so far, and作者: 依法逮捕 時間: 2025-3-24 10:35 作者: 積極詞匯 時間: 2025-3-24 10:55 作者: 一個攪動不安 時間: 2025-3-24 15:38
https://doi.org/10.1007/978-3-476-04082-4onses and an extinguished electroretinogram (ERG). LCA accounts for 5% of inherited retinal degenerative disorders worldwide. To date at least 30 genes are known to either cause or be associated with this condition. The genes perform a structural or functional role in the visual pathway. Mutations i作者: notification 時間: 2025-3-24 22:31 作者: 編輯才信任 時間: 2025-3-25 01:44 作者: 殺子女者 時間: 2025-3-25 06:25
Essentials in Ophthalmologyhttp://image.papertrans.cn/a/image/150100.jpg作者: 攀登 時間: 2025-3-25 07:54
A Bibliometric Analysis of AEGC Scientific Outreach,logy of ophthalmic diseases and work toward clinical care and treatment. Bibliometric analysis of ophthalmic genetic publications in Asian countries provides a tool to better understand research strengths and challenges.作者: 手榴彈 時間: 2025-3-25 11:38
Advances in Vision Research, Volume II978-981-13-0884-0Series ISSN 1612-3212 Series E-ISSN 2196-890X 作者: deceive 時間: 2025-3-25 18:08 作者: monogamy 時間: 2025-3-25 22:41
https://doi.org/10.1007/978-981-13-0884-0Genetic eye research; Asian population; Genome-wide association analysis; Asian Eye Genetic Consortium; 作者: CBC471 時間: 2025-3-26 02:08 作者: 刺穿 時間: 2025-3-26 04:18 作者: 思考才皺眉 時間: 2025-3-26 12:28 作者: 注意力集中 時間: 2025-3-26 14:47 作者: infatuation 時間: 2025-3-26 19:40
Opportunity for Population-Based Eye Research in Asia and the Middle East: An NGO Perspective,pulations, the NGO sector can be an ally in building the capacity for research among service providers. This chapter frames this opportunity and offers recommendations to genetics researchers who seek to broaden their array of research options.作者: 令人苦惱 時間: 2025-3-26 22:39
,Ophthalmic Genetics in India: From Tentative Beginnings in the 1980’s to Major Achievements in the challenges, it was one of the most successful stories that a team of ophthalmologists and vision scientists in India and New Zealand enjoyed. These sincere efforts have led today towards promising gene therapy. This is a narrative story of those yesteryears.作者: 壓迫 時間: 2025-3-27 02:22 作者: MEN 時間: 2025-3-27 06:26 作者: enfeeble 時間: 2025-3-27 10:39
Matthias M?lleney,Sunnie Groeneveld improved our understanding of inherited eye disease, and validated new molecular diagnostic technology. eyeGENE. can serve as a model for creating a research resource to advance the study of rare, inherited diseases.作者: ACTIN 時間: 2025-3-27 16:27 作者: 遵循的規(guī)范 時間: 2025-3-27 18:08
https://doi.org/10.1007/978-3-319-57324-3 novel gene mutations is a challenge to our consortium to identify all disease-causing mutations within the time frame of research funding. JEGC is also responsible to identify molecular mechanism of disease onset for each mutation and apply these seed information for therapeutic development.作者: 犬儒主義者 時間: 2025-3-28 00:32
Emerging Market Companies as Globalizers,ovel variants in many genes. Understanding the population-specific genetic disease spectrum and clinical phenotypes, as well as a knowledge of regional ancestry and iwi (tribe), aids in simplifying the diagnostic process.作者: 魔鬼在游行 時間: 2025-3-28 04:22
https://doi.org/10.1007/978-3-319-57324-3ay reveal the consanguineous marriage history and will help diagnosing genetic eye diseases. Thus proper utilization of health system will not only ensure eye care of patients but also to create opportunities of research with data generation providing magnitude of eye disease with a focus to genetic eye disorder in this large population.作者: 陰郁 時間: 2025-3-28 07:37
Die Conrad Ferdinand Meyer-Forschung,tant for better diagnosis and management of eye diseases. Each population is accompanied by a unique patient data set and needs elaborate and well divided study. Area wise description of patient population in Asia for genetic eye research has been provided in the following chapter.作者: Creditee 時間: 2025-3-28 12:39
https://doi.org/10.1007/978-3-476-04082-4pulations. We have investigated ., ., ., ., ., ., ., ., and other genes in Chinese patients with retinal diseases including age-related macular degeneration, polypoidal choroidal vasculopathy diabetic retinopathy, retinitis pigmentosa, Best vitelliform macular dystrophy, and Stargardt disease.作者: 不滿分子 時間: 2025-3-28 17:27
,Inherited Ocular Disease in the New Zealand Māori: Novel Genetic Mechanisms and Founder Effects,ovel variants in many genes. Understanding the population-specific genetic disease spectrum and clinical phenotypes, as well as a knowledge of regional ancestry and iwi (tribe), aids in simplifying the diagnostic process.作者: 琺瑯 時間: 2025-3-28 21:32 作者: TOXIC 時間: 2025-3-29 00:45
Unique Patient Populations in Asia for Genetic Eye Research,tant for better diagnosis and management of eye diseases. Each population is accompanied by a unique patient data set and needs elaborate and well divided study. Area wise description of patient population in Asia for genetic eye research has been provided in the following chapter.作者: nonchalance 時間: 2025-3-29 05:38
Retina Genes in Chinese,pulations. We have investigated ., ., ., ., ., ., ., ., and other genes in Chinese patients with retinal diseases including age-related macular degeneration, polypoidal choroidal vasculopathy diabetic retinopathy, retinitis pigmentosa, Best vitelliform macular dystrophy, and Stargardt disease.作者: 懶惰人民 時間: 2025-3-29 08:23 作者: 鎮(zhèn)壓 時間: 2025-3-29 12:14
,eyeGENE?: A Model for Advancing Research of Rare, Inherited Eye Conditions Through Biobanking and D improved our understanding of inherited eye disease, and validated new molecular diagnostic technology. eyeGENE. can serve as a model for creating a research resource to advance the study of rare, inherited diseases.作者: 虛假 時間: 2025-3-29 17:07 作者: 食品室 時間: 2025-3-29 20:11 作者: 挫敗 時間: 2025-3-30 02:23
Book 2019n of information on genetic eye research in western countries, more than sixty percent of the human genes involved in eye diseases in the Asian and Pacific population remain unknown. However, new efforts and a new awareness have sparked important discussions on the subject, and new plans are being i作者: 脫離 時間: 2025-3-30 05:31
Richard Savage,Michael Stauntonpulations, the NGO sector can be an ally in building the capacity for research among service providers. This chapter frames this opportunity and offers recommendations to genetics researchers who seek to broaden their array of research options.作者: 捏造 時間: 2025-3-30 08:39 作者: Bone-Scan 時間: 2025-3-30 13:45 作者: Obliterate 時間: 2025-3-30 17:46 作者: 某人 時間: 2025-3-30 23:39 作者: overbearing 時間: 2025-3-31 01:47
Lloyd Motz,Jefferson Hane Weaverocus of genetic epidemiological studies for more than two decades, and a well-documented extended pedigree has been developed for the group making it extremely powerful and informative for genetic studies. All 1292 study participants discussed in the work presented here belong to this single extende作者: Demulcent 時間: 2025-3-31 08:43 作者: Neuropeptides 時間: 2025-3-31 09:22
https://doi.org/10.1007/978-3-476-04082-4advent of next-generation, whole genome and exome sequencing in addition to gene chip technology have revolutionised genetic and molecular diagnosis. Phenotype-genotype correlation of this disorder in some instances has made the choice of laboratory diagnosis rapid and easier. An accurate genetic di作者: craven 時間: 2025-3-31 15:03 作者: dura-mater 時間: 2025-3-31 19:45
Book 2019ved in many eye diseases. All chapters were written by leading researchers working on Asianeye genetics from the fields of Human Genetics, Ophthalmology, Molecular Biology, Biochemistry, Sensory Sciences, and Clinical Research. .Advances in Vision Research, Volume II. will prove to be a major resour
